I’m 3 1/2 years post COVID. My life, body and mind struggle everyday. I need help! We need more Drs who care, instead of saying your just stressed and have anxiety.
I hear you. I went through a ton of severe neuro symptoms for which conventional drs. didn't have any answers. I was all on my own. A chiropractor (Dr. Perry Nickelston_ and a Gastroenterologist (dr. Ross Hauser) on you tube. they steered me in the right direction. What has helped me the most is acupuncture. I'm telling you this as I wish someone had told me what to do to prevent months of suffering. Acupuncture helps with anxiety, depression, constipation and diarrhea plus pain, and other things. I can promise you'll get help. If you can find community acupuncture, it's quite a bit cheaper. It's where they treat two people in a room at once. I'm curious to see if you try this - let me know if it works. The cost for community acupuncture is $30-$50, depending on income etc.
I was extremely ill with covid and long covid for about a year. Now, my personality changed. I am more subdued. I am tired and can get exhausted having dinner with more than 2 people. Too much to deal with all at once. I get to bed by 9pm. My favorite activity is going to bed and getting a good night's sleep. I am anxious, and depressed. I feel that I slog thru life. I don't want to be engaged. I prefer to watch the clouds stream by. I am not the same person I was before covid. It sucks.
@@danr13 Similar, I am a bit more active, but still slowed down and still easily overwhelmed with too much activity that stresses me along with too much engagement with people. Grateful to be alive. Sleeping is still a nightly challenge. I lived thru it and things are just different now...
Thanks for sharing. You have described word for word my experience of long covid. I feel exactly the same; long covid has now only affected me physically and cognitively but also my personality.
@@francesnance9110 Thank you for responding! I am sorry you are going through this. I am experiencing the same thing. Wishing you all the best. I hope we will continue to get better (or start getting better...)
Me too, a little over 1 year. My doctor just suggested a psychiatrist. WTF I work, do the bare minimum of household chores (when I can manage it) sleep. That’s my life now. 😢
Thanks for sharing. I’ve been dealing with Post Covid almost 2 years. I have shortness of breath, extreme fatigue, short term memory, as well as heart palpitations. Covid has been an unbelievable journey.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
I had these plus vertigo imbalance plus mental fogging in 2018 after 9 months of constant coughing 2018!!!! In Australia No travel history In 2022, i received my first moderna jab- 5 minutes after, i felt the mental fog lifted, was energetic cleaned out two houses snd gardens Never looked back since, had 4 other moderna jabs I had covid, i suspect in 2018!!!!
@@OMG-jv6vbay be your symptoms are not from the persistent low grade viral infection, but something else???? I really swear that within 5 minutes, after the jab, i felt a gush of blood flowed into my brain, and that was when i distinctly felt a fog was lifted off my brain. I am a medical doctor, was hesitant about taking the jabs, and i was working despite the symptoms i had, The symptoms i had were bad but they did not prevent me from working part time, and going to the gym. I also recalled there were times my face would flushed like a red balloon suddenly, A registered nurse who witnessed these flushes described them as a mast cell explosion or histamine explosion. All these have never recurred now Remember all these problems happened to me in 2018, long before any covid. The coughing i had and the post coughing symptoms were so covid-like- i did not have loss of smell but i gained heaps of fat, prior to that i was really really skinny, lean, with minimal subcutaneous fat, just born like that. I have now lost all those fat from vigorous walking on a treadmill.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@marcopoblete2592 I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@marcopoblete2592 it triggers that. Went thru 3 phases wher I thought I was dying and I even prepared my finances and told close relatives goodbye. Being under constant attack from the virus and/or spike messes up your parasympathetic nervous system. It will produce continuous stress hormones, which affects the rest of the body, then disbalance, then slew of symptoms. Resilience is my biggest strenght but I broke down. I've never suffered that much in my life. That feeling of decay and losing your senses is absolutely painful and terrifying. Be there and be supportive.
I tested positive 5 times over 2.5 years with Covid. First time was most severe but no hospitilazation. I have been dealing with long covid since. The longest time between infections was about 10 months. I had just begun to feel improvement gradually over two months, from 8-10 months in my symptoms. But then was reinfected. Right now I am three months since the last infection. Strong constant fatique, brain fog, difficulty getting deep breaths, tiring very easily moving around (for example going up stairs) then gasping short of breath, strong somewhat migrating inflammation pain - all over but particularly in the lungs and neck- intense brain fog with post exertional fatigue, headache. It gets worse and better on different days without being able to ascertain why. Exertion definitely makes it worse. I am not obese and I look good to people. Thus many do not understand. All of this is invisible on quick glance. Unless people are actually with me all day and can see the impact of having a lively conversation for two hours then leaving me in bed with confused brain fog the rest of the day, feeling miserable. This is debilitating! Few people understand. I could feel this interviewing doctor's bias and lack of awareness...jumping to that standard easy and condescending conclusion when they don't know how to explain it - 'isn't it really in their head?' - trope. So irrititating and insulting. I don't waste my time with people who have that level of bias and ignorance about this. I will finally start treatment at UCLA Med Center in October where they have a clinic for long covid. I wish us all luck.
Tu for this ❤️ am vax injured 3 times. 3years in, have xact same, but no help inRi, and too sick to go Boston.. cal has more.. would like to follow-up w u on your clinic journey, healing thoughts and prayers🙏💕😺
I’ve had chronic fatigue syndrome for over 20 years. Main problem is post exertional malaise. Now long COVID patients seem to be experiencing similar symptoms
I had covid back in August of 2023. It is now March of 2024 and i cant take it anymore. Raging headache, loss of of balance, vertigo, brain fog, insane fatigue, pain in the back of my eyes, really bad light sensitivity, muscle weakness.
Thank you to the doctor! So many were exposed to Covid at work, and later when they thought they were recovered... experienced serious cognitive issues, weakness, malaise, etc.. numbness, vision problems, etc., and were terminated. Many were unjustly judged as incompetent, treated as if they had Alzheimer's...when they were perfectly healthy before exposure to Covid at work. It's cruel, and inhumane to GIVE someone an illness, humiliate and shame them on the job for it, and then terminate them. Many lost their jobs, finances, health insurance, and were abandoned with hefty medical bills, all due to coworkers giving them the illness. Employers are too quick to judge someone who may be struggling with REAL terrifying post COVID symptoms. Employers should be educated on the REALITY of COVID's cognitive and other symptoms. I also agree that those struggling with long COVID should receive significant govt assistance. Congress can cut their huge pay raises, wasteful spending and needless multi-million dollar witch hunts to do so.
Thank you for this video. Female in her 40s…no positive Covid test but suspect I was infected several times with mild symptoms. Been suffering from so many of what I’ve come to understand as possible long Covid symptoms. Recently went through thousands of dollars in multiple tests because of elevated liver enzymes. After several months went by my labs went back to normal. I was optimistic that was the end as I was feeling better, but as had happened so many times previously, after feeling mostly well for a week or two I was knocked down with fatigue among a number of other symptoms that are only manageable because I lead a simple life and have a desk job working from home. I cannot imagine how it would look if I had the demands so many others do. Just started LDN to see if that will provide any relief. But it does seem like whatever is going on with me could be autoimmune in nature. Hugs and understanding for all those out there that have had doctors shaking their heads while escorting them out the door with a stack of medical bills and no relief.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Your enzymes got back to normal by themselves? I'm going thru a phase right now which tells me my gut aint working well, among a laundry list of other symptoms. I'm losing a lot of strenght. I used to be an athletic cyclist.
@@User98681 good advice. Intermittent fasting with a strict no carb diet and some prolonged fasting. I just got out of a 5-day fast but wasnt in good shape from the start.
@@stephangauthier911 it seems that way. Inflammation is the key word to all of this, as far as I can tell. Recently put an earthing/grounding mattress cover on my bed and have been finding other ways to ground my body. Out of all of the things I’ve tried, this one stands out as being instantly helpful. Upon waking on the first morning I felt different-in a good way. Like more rested. Visible signs of poor circulation have also been improving. Haven’t been doing it very long, but it my limited experience this is one treatment that seems to work based on my personal experience. I know exactly how frustrating it can be to feel like you can’t have fun all the ways you’re used to. I hope you find some relief soon.
I wonder if I had Cov and didn't know it as I've had severe neuro symptoms including no appetite and Im already too thin. I'm 73 yo but have had excellent health until 7 mo ago. My liver enzymes went fromm 77 to now 20 (not sure how that happened) and also other markers go up like pulse, blood pressure and blood sugar even though I don't consume a speck of sugar. Elliot Overton on YT helped me eliminate most of my IBS with B1 (Benfotiamine). I've had now a horrendous problem sleeping. I told the dr. that the sleeping pills he gave me doesn't work - he just said to try it for a month even though I sleep the same with or w/o sleeping pills. I feel like a total zombee. I checked myself into the hospital because I wanted to make sure I'm ok with shaking etc. and I was told I could stay at that hospital for 2-3 days until a bed is available at a Psych ward and at a place that's 50 miles away. Even my GP said he wouldn't advise that. Going to drs has been worthlesss and I don't even think Mayo Clinic could help these symptoms. I am going to try two things: R alpha lipoic acid (the natural kind which is 40x more bioavailable) and methylene blue (start slowly on MB, doing 1 drop/day - added to an empty capsule to avoid blue on the tongue).
I’m sorry to say this and don’t wish to offend anyone. But thank god for long Covid. Those of us who had CFS, Fibromyalgia and other autoimmune diseases that were not recognised decades earlier. We were told it was all in our heads, now they realise it is a chronic disease and hopefully we can find answers and maybe a cure.
@lranieri1disagree. many of us have suffered same symptoms as myself 30 years with cfs. we were thrown under the bus and disregarded. made fun of not taken seriously mostly because we are female. We do not want anyone else to suffer this hell of a life we have and hope long covid suffers are taken seriously and work continues to try and help them so 30 years later they are not still suffering the same thing.
Yes 30 yrs later and I still suffer the same cfs symptoms as l. covid. I have done everything under sun to return to health. Have degree in Health Ed. and even have a study published in medical journal in hopes of helping find us help in 2010. But still nothing. We don't wish anyone this hell of a life and hope they just don't keep stringing these people along with no help like they did us. But after 2+ years it's looking the same. Lots of tests., lots money made at our expense and nothing yet.
I agree. As a 66 year old retired orthopaedic surgeon who has suffered ME/CFS for 11 years, following a viral upper respiratory tract infection, I have also endured the ignominy of an “unfashionable” illness. At least I can now say “I contracted long COVID before it was popular”. 🤷♂️. Unfortunately, the attitudes and beliefs of my medical colleagues are very difficult to change.
@lranieri1 - sorry - as a sufferer of an unfashionable post-viral CSF for 11 years, I beg to differ. Your reasoning suggests that everyone with “Long Covid” should shut up too and disappear into the shadows.
The irony of people who suffer wishing that suffering on others because they are mistreated. It’s literally sick thinking. It’s like saying if you were hit in a car accident other people should be too. You were treated wrongly but you are sick for wishing that pain on others.
He just described M/CFS something most neurologists mocked and ignored for decades, Why now are they recognising post viral illnesses affect a patient neurologically?
@acebacker1 what can be done to get people who suffer from this help? I've been suffering for years, yet have forced myself to continue working as a mother with kids who was abandoned by my husband. I didn't have a choice but to work. Now the kids are out of the house, and it sure would be great to finally get some rest. But it won't happen. I work and collapse into bed every day. Why is this not taken seriously? We should be candidates for disability, but it's so easy to be gaslit.
I had Covid for the first time Sept 2023. Five months later I developed an increase level of liver levels and neuropathy from head to toe.. Out of nowhere.. Had skin test and nerve test was diagnosed with Small Fiber Neuropathy.. I’m not diabetic nor do I have autoimmune disorder. Neurologist said it might be long Covid symptom, It’s crazy
My wife has the most extreme case of LC which became worse and worse after contracting Alpha, followed by three or four other variants. She has some similar symptoms to lupus. She has been diagnosed with Inappropriate Sinus Tachycardia, POTS and Pollen Food Syndrome. She has a healthy heart muscle, but frequent heart episodes. She has bouts of extreme pain in her extremities, sleep disturbance, near dangerous levels of iron, and IGE. She has 9 specialists, and no improvement. In fact it’s getting worse. The Drs can’t approve disability status for LC in Canada and she is sick in bed. Can’t make ends meet in Toronto on one income. Really just at a loss here
I’m so sorry! I was going to ask what LC meant, but I get it. Duh. My adult son has Lyme and since he had covid, he’s had a horrible migraine 24/7 and has been having seizures and neurological problems.
Ask for ivermectin. It opens the healing pathways in the body. It's why they refused to give it out. People with neurodivergence tend to have poor healing and detoxification pathways. It affects the vagus nerve as well, which is the inflammation depression system. The nervous system and immune system work together. Taking MCAS support vitamins and antihistamines also help support the over immune response.
I am having long COVID. I was initially very ill for 2 months, then I was able to get out of bed. Before COVID I worked full time, no neurologic issues. I have ankylosing spondylitis however, and was taking Consentyx when I I fell sick. I am only now able to work 1/2 day, and have to triple check my work as I feel like I did when I had a concussion and the post concussion syndrome. I went to a grocery store twice and forgot my groceries, pretty bad stuff. I'm also exhausted I have to nap every afternoon. I was vaccinated and boosted. I hope I can hang on long enough to get better. I too had crazy heart palpitations and very blurry vision.
Wow! I’m so sorry! I’m in the same boat with Lyme, and went through covid and I couldn’t find the right words for a long time. I don’t even shop anymore, but have my groceries delivered. I also have autoimmune diseases including AS. This thing is horrific!
You need to treat inflammation. I had terrible fatigue, brain fog, memory cognitive issues after covid. I'm Still recuperating. New doctor treated me with I meg solumedrol IV steroid. Within hours of treatment the pressure I felt on top of my head lifted. Several days later I could think clearer my short term memory lapses improving. My fatigue also is much better. I nap once or twice a week once a day. Not every day twice or three times. Why do doctors ignore treating brain inflammation. It is documented on MRI scans. They know it's there but don't treat it. I thank God I finally found a doctor who treated it. Look for doctors who will give corticosteroids to treat long term covid inflammation. This is what causes long covid!
I am from Puerto Rico, female 70 years. I have been diagnosed with long Covid 19 vasculitis. I have varices in both legs, and bruises or hematomas in my arms. A constant headache with lost of vision. I was treated with paxlovid during the infection, last August. After visiting a few doctors, a hematologist-oncologist gave me this diagnosis.
Male in his mid 30's perfectly healthy before covid, Got covid bad twice in one year then a third time minor. I've had major GI issues, heart arrhythmia (AFIB and Flutter, and High and low heart Rate), pulsate tinnitus, and now weakness/muscle spasms in arms and legs. I've had pretty much every test done including MRI of heart and Brain and all come back normal. So I've been a covid long hauler for 2 years now. This all happened after my second run in with covid, which I also had the vaccine. Not which which actually caused this. I've gotten better with some things but then new things show up. It's a wild and expensive ride.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
It's weird how the symptoms change over time. I'm going thru a phase right now where my GI is very much messed up and extreme weaknesses. Feels like I'll lose my ability to walk. Scary AF stuff. You're not alone in this man. Hang tight; it's gonna be a bumpy ride.
I really believe that it was the vacine that caused all this 2 days after second jab I got sick that was July 29th 2021 still have major problems it is now may 2 2023 you should all read the physer records they wanted it to remain silent for 75 years but the court demanded they release them now and they did frighting
My exact symptoms and age. Can i ask what you do for a living. Im looking for lifestyle connections. But i agree with long fast. Also, ive heard apheresis is really working. Also you should try pepcid and zyrtec 2 times a day each. It will be huge for the GI stuff and other stuff.
For those posting here about your struggles with long covid we are going to assume that you were fully vax'd and boosted, unless you indicate otherwise!
I have been dealing with this for 3 years. My first COVID infection was January 2022. I dealt with dizziness, ear ringing, tasting salt with everything I ate or drank, racing heart, profusely sweating for no reason , randomly vomiting, terrible constipation, choking and brain fog. I saw a million doctors and no one even mentioned this was possible. After months of vestibular therapy the neurologist gave me a burst and titration of prednisone starting with 60 mg for three days, 50mg for three days, etc… it worked! I was mostly symptom free except for migraines 1-3 days a week. I had COVID again two weeks ago… and I am starting all of the same symptoms again. I am at wits end- waiting to be fired for missing work (I carry our insurance) and can’t see my neurologist until January 16, 2023. I’m so done. Just over it.
Sorry you’re having a bad run with this. I had some of the issues you’re dealing with and have been on a carnivore diet for over a year and it’s the only thing that works for me. It sucks. Just want to be normal. Not advise. Just a thought. Hope you get better.
Oh my, same salty taste on my tongue ever since my second shot. I do not believe that Covid has to be contracted but just the shots can cause the same neurological symptoms and other symptoms. I too, have severe neuropathy, heart palpitations, tinnitus, dizziness, balance issues, short of breath, pain, fatigue, anxiety attacks, weak and heavy legs, headaches, digestive issues etc. my husband had severe heart attack, both of these things happened to us after the second jab, as far as we know, we didn't have Covid.
He’s forgetting, excessive sweating 24/7 most days, thoughts that are abnormal, extreme paranoia, insomnia, and major weight loss and muscle tissue. I had mild Covid, I was told. It was terrible! 25 months later with Covid twice, I’m worse than ever!
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
The neurologist just described M/CFS something most neurologists mocked and ignored for decades, Why now are they recognising post viral illnesses affect a patient neurologically?
I got Covid beginning of December 2021. It was horrible. I got the monoclonal antibody infusion. I have never recovered my senses of taste and smell since then. My spleen is enlarged and my internal organs actually hurt. I have left side facial twitching. I got Covid again in August 2022. It wiped out my memory and caused constant fatigue, severe anxiety and depression. I am convinced that my brain is damaged and I will have a shortened lifespan because of this bioweapon.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 I do not see how fasting will help repair the damage to my olfactory bulb. I am not in the best of health. Supplements scare me. I am on thyroid meds and Zoloft. No way I can do three days existing on just water. 16 months with Anosmia and no recovery. I fear this is permanent.
@@LoveMyBoys3 3 days water fasting will cause drastic weight loss which is even more dangerous when you are already experiencing symptoms. It will only add fuel to fire.
I got covid in 2020 and not hospitalized during that moment I experienced many symptoms like loss of smell and then I started to notice ringing in my ears, acid reflux and bloating, tingling in my feet, dizziness, blurry vision and eye floaters, heart palpitations and I feel exhausted and I can't do exercise because my heart rate goes very high, until now I didn't recover and just my sense of smell recovered
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
I developed anxiety and panic attacks severe panic attacks where I would get hyperventilation and fatigue after such but now I'm taking antidepressants and I'm doing great so far
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 I've noticed that too, everytime I starve myself for a day or two, I feel fantastic on the other hand eating too much makes me feel uncomfortable
Yes thanks. Some of my family members don't understand why I am not better yet, thinking am faking my symptoms. My O2 was 41 when I went to hospital I am very lucky to be alive, but I still have a bunch of symptoms and the doctor s don't know what to do with me.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@haotang2638 I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
The neurologist just described ME/CFS, something most neurologists mocked and ignored for decades, Why now are they recognising post viral illnesses affect a patient neurologically?
My two cents from my 15 month long and counting long covid nightmare: 55 year old male, main symptoms insane fatigue, brain fog, AND THEN: one year post infection(14 months post vaccination) had first episode of supratachycardia SVT that sent me to the ER and had to get cardioversion to reset my 160 bpm resting sitting heart rate. I see "tachycardia" very often when reading about long covid aka PACS Post Acute COVID-19 Syndrome.
I’ve had these symptoms for two years now after Covid (mild). Recently had a spinal tap due to optic nerve swelling and found to have very high CSF pressure and an ongoing autoimmune response . Diagnosed with IIH and papilledema.
My ex wife had the same in optic nerve swelling, constant fever for weeks, high CSF Pressure and also received the IIH Diagnosis 3 years after getting covid in late 2019. Also her left 2nd toe has been twitching constantly for 1¾ years. Non stop. Sometimes the twitch is just more powerful than others. This disease keeps on giving even after the respiratory symptoms go away.
I've had Covid twice. I got it in February of 2021, right before the vaccines. First week couldn't get out of bed, fever, chills, aches, 102 to 104 fever for 5 days. Second week, fever broke, developed a sever cough and couldn't take deep breaths. Breathing deep hurt in my chest, and that's when I looked up the breathing exercises to do to stay out of the hospital and on a ventilator. Fortunately, I stayed out of the hospital, and it seemed to break after two weeks. Second time was March of 2023. I drove to and from Las Vegas that weekend, and Monday the 13th on the drive home, I developed a very severe headache. By the time I got home I had the chills and was feeling lousy overall. My wife said to take a test, and I was positive. I took a second one to make sure the next morning, and it was positive. I didn't get a fever the second time, but I still had chills, body aches and a headache for the first week. The second week I had a sore throat and mild cough, but most of the other symptoms were almost gone. Again, after the second week, it seemed to break and I felt close to normal. Last summer, first week of July 2023, one morning I had severe enough low back pain on the right side that my wife drove me to the ER. They were thinking kidney stones and wanted to run a CT scan. I knew it wasn't kidney stones, because two days prior to this ER visit, I had just been proclaimed to be "the epitome of health" by my primary doctor after we finished my annual physical. Two days prior, I didn't have a single medical problem, all of a sudden I'm in the ER feeling like I was being stabbed in my low back. Of course the CT scan showed my kidneys, as well as all of my other organs, were normal. No sign of stones, kidneys clear. Almost (9) months in now, March 25, 2024, I have seen (12) doctors and had multiple CT scans, Ultrasounds, and MRI's of my spine (Thoracic and Lumbar), my abdomen and pelvis (inner, for organs), my right flank and abdominal muscles from my right hip to my naval, X-rays of my right hip and spine, and not a single doctor can tell me what it is. They can all tell me what it isn't. What I'm dealing with is for (9) months, I have had pain / cramping in my right flank area, all day, every day, from when I get out of bed in the morning until I go to sleep that night. On the 1 - 10 scale for rating pain levels, my normal day is a 4 to 5 all day, as long as I'm awake. When it goes to an 8 or 9, then I have to lie down on my back. It is like having a calf cramp, but in your side. There is nothing I can take for the pain, as Norco, Toradol, and a Lidocaine patch all did nothing at the ER. So, Ibuprofen and Excedrin don't have a chance. That isn't even the end of it. My right flank area (I say "Love Handle", it gets the exact location across), the entire love handle, has been numb for the (9) months this has been going on. Totally numb on the outside, pain / cramping on the inside, (9) months, every day, all day. Not a single doctor I've seen want to touch that. They move on to something else, ignoring that I just told them I've had a body part numb for (9) months. One doctor literally almost ran out of the exam room when I told him this, he was saying my specialists had it covered, and he was sure they would figure it out. I still have pages to go, but I think the medical issue is there. There is so much more, about doctors lying to you, another blowing you off for a month (ongoing, Keck doctor ghosted me), and the ones that don't believe anything is wrong.
I went to the doc which i never did. I was crying out of nowhere. I was so tired. Scared. Something was so wrong. I forgot names was scared outside. Didn t know where i was. Light and noises hurted me. I kept working till i could not. It was long covid he said. And it feels like a relieve. No excuse and feeling guilty for dismisisng dates with friends and having no strentght. Taking my rest. Sleep as long as i want. It is healing. I am broken. And it is ok. ...
I had the first virus in early 2020. I started having peripheral neuropathy in my feet then. I then got the 2 vax in Feb of 2021. Then I got Omicron in April of 2022. I received the antibody infusion at the Mayo clinic in 2022. Neuropathy is much worse, all the way up my legs. Severe fatigue, tinnitus, brain fog, and can barely walk. I am seeing specialists through the Mayo clinic. Next test will be for arterial blockage in legs on the 20th. I am sure tired of this and wish there was something that would return me to normal.
@@LisaL-yl9zm Feet and legs are worse. Still have fatigue, brain fog, stomach issues. I just had bloodwork done last week. testing now for thyroid, hashimotos, celiac, A1C, C3 and C4, B12, etc. most came back normal except for the autoimmune stuff. Thanks for asking.
Hello, I really hope you are feeling much better now. I had the viral infection one month ago. Now having burning pain in my feet that I can barely walk. Did you have the same symptom? It’s hard to fine someone understand what I am experiencing. My GP said my symptoms are very rare.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 I tried water fasting last year, but more 2,5 days, cant say it helped alot, but I feelt better for shore, during like 4-5 days after completed fasting.
And I have Hämatomsa bloodpressure,many inflammation, Dysphagie, soaring and pain like being teared apart, walk-in,bslsnsce ? I need advice!! My partner had to take me in!! Because I could not have take care !! Can not move on some days ?? It’s like if you have some kind of phases
I do not have long covid but I have some of those symptoms. My symptoms started over 2 years ago after I got two covid shots on 2/21 and 3/21. So for the past 2 years plus I have had chills and sweats every day. The past 8 months the chills are freezing so that I have to take 3 hot showers a day just to increase my core temperature. I also have extreme fatigue and brain fog. So I am going to try some of these helpful ideas with regards to the treatment of long covid. Thank you Doctors for the information. From Don...Northwestern University Class of 1971.
Don, you have post vaccination squalae, what everyone whether caught it or inje cted is calling long covid. The entire clade is man made gov’t funded wea pon ized.
I still am suffering 2.5 years later. The worst was the jab. It's worse now that it was 1 year ago. I've tried so many things like strict diet, some products like artemesia, NAC and nattokinese, exercise, fasting. The health system is useless other than sign me a leave of absence from work (I'm nearly disabled). No tests come back positive. ECG, EEG (I had so many seizures with no priors), x-rays, complete blood tests, brain MRI.
My personal struggle has my intuition telling me that the virus attacked my vagal nerve. I almost feel it. Never had the shot, just a severe infection in early 2021, hospital for 5 days. It started a few weeks after hospitalization with crushing afternoon weakness. Right away , before a tone was talking about it I kept telling my wife that I felt like there was a problem with my central nervous system. My cyclic symptoms are numerous and from what I've learned, almost universal.
These doctors have poor investigative skills. I was an Air Force officer before falling ill and have hyper documented and reviewed all of my labs, imaging, reports… I have positive NMO antibodies (AQP4), my neurotransmitters are negatively effected (particularly Dopamine), I have numerous reactivated infections, and a lot of endocrine and metabolic dysfunction. He’s also wrong about his presumptions regarding the vaccine and it’s risk/reward. Don’t let the suit/tie and white coat fool you. These are drones with no practical sense or effective discernment. Listen to the patients. Doctors often think they have a monopoly on intelligence and yet tend to have very poor investigative abilities.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
As an orthopaedic surgeon 11 years down the track with ME/CFS after a viral infection, my advice to any medical professional (in respect of any patient interaction really) is “First, shut up and listen to the patient, and don’t interrupt them until they have finished giving you their history.” What patients give you is gold, and following that, only a few more questions may be required to narrow down possible diagnoses and guide targeted investigations. Unfortunately, after exclusion of specific diseases or disease processes, doctors have patients that have brain fog, fatigue, etc which cannot be easily confirmed - apart from perhaps functional MRI etc. And then, there is no specific treatment. Confirmation of real illness can be helpful for the mental health of the affected person, as is documentation for insurance. The most important diagnostic tool is the doctor’s ear, which if connected to an open mind not crystallised by dogma, rapidly makes the diagnosis of a post viral autoimmune problem affecting the brain. Simple really, but in my personal experience, rare.
@@User98681 Thank you for the offer. I have a small feeling I may have at one point or another attempted the recommended protocol(s). I’ve tried nearly everything and have waded deeply in multi-chronic infection treatments, autoimmune treatments, mitochondrial dysfunction supplementation, etc. But I’m always welcome to new ideas…currently in a nursing facility and suffering symptoms that cross between Sjogren’s, Systemic Sclerosis, Dysautonomia, ataxia, and more.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@Sarah_S26 i wish doctors knew what is causing it. It’s unsettling feeling like your insides are vibrating. Have you tried any meds for your symptoms??
@@marielopez2947hi , gp here , this is dysautonomia , take beta blocker or corlanor . Also associate it with probiotics. What you have is a vagus nerve dysfunction.
Thanks for this❤ best questions asked that I have been seeking answers. I am grateful that so far no one took my situation not seriously, as I lost 80-90%of my life, hope more long Covid patients being treated and heal soon. Any advice on things I need to do for faster recovery? I
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
This is a silent horrible disease. I have had diagnosis of chronic fatigue syndrome 30 years with similar symptoms. It's a soul sucking life sucking disease. Leaving patients with unpredictable symptoms that are hard to manage. Causes loss of jobs and friends and sometimes family. Not to mention life choices and possible accomplishments that put hope of getting relief out of reach, causing further depression and who wouldn't be depressed with no help from anyone only disbelief. Please help these people more then you have helped us with CFS we have been forgotten thrown under the bus.
I had Covid (that I know of) 3 times and this all tracks. Mild infections (ie was never hospitalized) was in my late 30’s/early 40’s, otherwise healthy, etc… At 41 yrs old after the 2nd bout I developed a stutter. Which I’d never had before in my life & was extremely severe at first to the point I could barely speak/string 3 words together but has improved over the last couple years. There are so many other symptoms that you mentioned and I have ALL of them but I had depression & PTSD before COVID so no one is going to take me seriously. But, I’d recovered a lot re those issues through intense treatment before that & then they got 5 times as bad after. I just always figured it was the stress of the pandemic that set me back so far. I’m still dealing w this stuff!
Everybody has anxiety and depression during a time when the world was shut down, so I don’t like when they bring it up, that’s so goofy that’s a confounding variable
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Doctors, is it possible that the neurological symptoms may be a Molybdenum deficiency? As well as other vitamin depletions from where the body is experiencing an auto immune response . I consider covid a symptom . But the disease acts more parasitic in nature. Going through cycles of wellness and illness. Similar to the illness - malaria. Could it be that with infection people loose the ability to detox ? And lack the ability to also absorb necessary nutrients to improve wellness?
Only the Chinese who created this biological weapon can answer. But they themselves are now facing karma as it has boomeranged on their own population. They can't find any antidote as the research team who created the virus themselves have perished it seems.
The virus hides in the biofilms. Not regarded in allopathic medicine, but a real, actual force in trying to recover from Long Lyme, Long Civid, and others.
I'm glad you brought up the many patients who were unable to get a covid test in the early days of the pandemic. April 1, 2020, I became sick and continued to get worse. Never could geta covid lost because I didn't have a cough. I became sicker than ever have been in my 55 years. still, was told not o came to docter or hospital unless I couldn't breath. Anyway, I have been denied access to the long-covid clinics hear me even with referral from my PCP. I'm in Alameda, CA and was denied at both Stanford and Davis. The clinics all apparently have too many pa tients. They complain that their doctors and students-doctors, are unable to do the other work they need to do because of the overwhelmcy number of LC / PASC patients. So, for that, they deny anyone without a positive PCR test just to limit access and limit number of patients. Any suggestions of where to go close to me. or at least in Californian, so my insurance can pay?
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@Liam Tytgat I do not eat much seem food since the second fax has turned me off of dinners and breakfast I eat very little but you do make sense so tired of this now it's attacting my right side knee bone hurts shoulder bones hurts all on the right side even though the second jab in my left arm was painful and she went into the bone this time I yelled in pain firt jab no problem getting really tired of this crap I will try what you suggested had this Aug 2021 bone aches just started out of the blue 4 weeks ago it is now April 28th 2023
One thing glaringly left out was the role of autonomic solutions. I took 5 doses of the vaccine in order to NOT get long Covid as I have hyperadrenergic POTS from multiple surgeries to start with. You say there are no tests for long Covid but not once was neuro diagnostic testing mentioned. Depression and anxiety very definitely occur because people are marginalized, not believed and told it is all in your head. Unfortunately autonomic neurologists are few and far between and booked months out. Simple blood pressure and heart rate readings supine and standing will establish the baseline of POTS or orthostatic hypotension. Dysautonomia International has a wealth of webinars and sites related to this. And I am also a medical professional and do know whence I speak.
@@madelinesabatello1845 Dear Madeline, I took all 5 because, for me, the chances of getting Long Covid were more daunting than the disease itself. Dysautonomia drives much of the Long Covid and Long Covid on top of dysautonomia plus an immune system that is seriously disturbed was much more of a risk than Covid-19 itself. People forget that all life on this planet works on the bell curve. There are always the outliers. So it’s always individual risks versus benefits. That’s why I did it. As well as my age, 76, dysautonomia, asthma, chronic pain syndrome. Russian Roulette at its finest. The same types of things happened other all other vaccines. And you should see clinical trials. That’s why I quit as a clinical pharmacologist, Big Pharma ethics. But the divisions in the world made it into a political issue. Be well.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
This Long Covid has taken my life away from me. I have no appetite I am in bed do to fatigue and weakness just getting dressed takes all my energy . I feel faint when I go out to my pain doctors my legs feel like rubber I feel faint & scared. What do people do that have fibromyalgia also ? I can be setting up in bed & all of a sudden I get a dizzy spell out of the blue, sleeping is hard, everything is hard to do !!! & I feel like I am dying at certain points. I have a racing heart of a 136 beats per minute , that is like this when I have to go out or try & clean , so I have stopped depression is bad & so is my anxiety Thank God for my hubby who is amazing at taking care of me, I just feel bad because our lives are at a stand still….🙏 oh I hope others can relate to my situation & have some of the same symptoms…..🙏❤️✌️🌹
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Ja mijn lichaam is ook loodzwaar inderdaad rubber met lood cellen. ik was ook een sportman en gouden handen. maar lichaam ziet er niet meer uit lijk wel 90. vrezelijk. tip spike eiwit amyloidose. denk denk attr amyloidose. dat is aanmaak verkeerd gevouwde eiwit cellen. maar hoor graag van je meissie hoe het nu met je is. klagen mag van mij ik snap je hoor voel met je mee. het is allemaal zo on eerlijk wat je mee maak. veel liefde gewenst. blijf heel dicht bij je zelf jij merk en voel wat er mis is. blijft wel tegen je zelf zeggen het komt goed het komt goed. hele universum zal luisteren.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
I still have long Covid problems. I had covid leg. My legs have gradually gotten worse. I'm starting to lose circulation. I get so weak I can't go and about pass out. My feet and legs are swelling. I've got brown and blackening on my feet and lower legs from lack of oxygen. I hurt all over. I have difficulty swallowing at times. My blood pressure runs real high at times then drops to like 80-40 at other times. Severe headaches. Isdis with my right arm now. My gall bladder and appendix are both failing. Im having those issues. I have problems breathing at times. I sleep sitting up now. Abs that's just what I know about. I'm sure I have blockages and I think I may have cancer now. I'm ready to go. I'm tired of fighting
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
what about those of us who sustained a vax injury and not a covid one ? i sustained severe small fibre neuropathy straight after and have done for past 12months - is there a possibilty of healing from this ?
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 thank liam - do you feel vax injury is just the same of long covid? the symptoms do seem to be similar but then some vary greatly - small fibre neuroapthy being my issue - i do take those supps and do infared sauna - fasting has been hit and miss based on how im feeling but will try a longer fast if possible
@@monnmar1 I am not vaccinated but suffering from LC I am about 75% back to fully healed. Vaxx injury and LC are 2 totally seperate things, both have similar symptoms. Fasting is good either way, it’s best not to get any vaccines. They are in effective and highly dangerous
@@User98681 thanks...but comments about it not being the best thing to do is not helpful when going through the ramifications of it . Plenty have been fine with their dosing....I just wasn't.... I can't go back in time and chnage that....no matter how much regret it brings
My husband and I have long covid for 2 1/2 years, I have 95% of symptoms listed by CDC. ( I was in the hospital for 31 days and then transferred to an acute rehab for 60 days.) But my husband was in the hospital for three weeks, and a regular rehab for five weeks,) He has fatigue and neurological issues. He isn't the same person that he used to be. I am so tired of the doctors telling us that they don't know much about Covid because it's a new disease. I can go on RUclips and see all the studies, why can't they? I just want my life back.
My father passed away of parsonage turner syndrome last week. It took over his entire body except his right arm. This needs more research. It started 5 days after Covid booster shot.
I am injured from 18 months, from 2nd dose of pfizer. My life is ruined, i was healthy and fit. Jabs ruined too many people... And doctors won't help people like me...
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 i ve tried 3 days... In the 3 days i was better, then when i restarted to eat way worse than before...i take nac, nattokinase, magnesium, zinc, selenium, b complex, d, c, probiotics .... From months... They seems to me useless..nervous system and immune system are damaged..
10:40 …”urban legend” yes, right, …like the vaccine injury I suffer from . …Please do not use this frase. …I can tell you a thing or two about “legends” and subsequent gaslighting!
Im not taking the jab but i do feel like im experiencing symptoms of long covid (about 8 months) is the brajn fog permanent? Is this just who I am now?
A friend of mine was told he had Alzheimer's (they assumed due to his age) and his dr told him he was "terminal" and drugged him accordingly (without any tests to confirm the diagnosis) for over a year until I kept at him to switch doctors to be tested and appropriately diagnosed. Turns out he simply has brain fog as I suspected. I've known him for over 20 years and could see that he had Long Covid like me but his ADHD & OCD made it look otherwise, but other symptoms (GI and new allergies, post nasal drip, etc) made it clear it wasn't dementia. If you are MALE you will be shuffled off to a nursing home if you are older unless you self advocate since Long Covid is less common for men. This is dangerous as far as medicine goes but that's what's happening "out there" and every one of us will have to be wary & fight against the "instant 5 min diagnosis" from the too busy doctors who are more than happy to dismiss us.
those who have severe cases of pneumonia are vastly 65+ and are vulnerable to pneumonia just based on age and shown to have a longer time for immune response, thus making lung damage more serious. those with mild cases develop an immune response quicker, we have seen that antibodies produced allow entry into monocytes and macrophages where infection and replication of non infectious but foreign proteins are created and circulate the blood stream passing many major organs including the blood brain barrier, it replicates in numbers that overactivate the immune response causing healthy cells and tissues to be attacked in the clearing of viral proteins, thus causing scar tissue on many tissues/organs and death of cells which can lead to a copious amount of lingering symptoms and debilitations.
My mom had so much brain fog she couldn't do anything and So fatigue. SO WE PUT HER ON A DEMENTIA MED AND IT HAS ACTUALLY HELPED. Now she doesn't have DEMENTIA but it's actually working
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
They are vague in a sense. The better term would be non specific. Evidence shows covid hides in the body and causes systemic damage. It's hard to pinpoint what is covid and what isn't when every system in the body is being affected. But you are right, there are symptoms that are more prevalent than others.
@rbdesigner725 whatever cluster and specific symptoms you think, may be true but in reality it is even more than that. It's not just fatigue. It affects the skin, hormones, organs, nerves, stomach. Not every long hauler will present the same way. But you're right many do. Doctors should be better at piecing the puzzle together.
Notice how the guy in yellow says do you test for x,y,z and the white coat makes it seem like no because it isn’t necessary. For example, brain MRI, EEG etc..
Hello my name is Sarah.I have Long COVID and MS it is very hard but I trust in the Lord and He is with me. I am praying for all of you on here. Trust Jesus Christ today. He is coming soon for His bride. John 3:16-18 1 Corinthians 15:1-4
Last year I had covid twice, first was in march, which caused cyst to form in by eyelid, surgery was needed to remove that and that has healed fine. Second covid was in december, now after two months from covid I have tingling and numbness in my legs and arms even after sleeping or sitting, this must be long covid attacking my nerve systems, never had these kind of symptoms so often. But what you could do for healing, eating more vitamin B ?
Get this, I'm 63, I get sick usually every year, bronchitis or the flu, since covid I haven't been sick once, I've never had one shot, so the mask is still worn in public places.
My mri I says - idiopathic intracranial hypertension but it has to be from Covid. Had it about 3 years ago no jab. That’s when the pain started. Lost my smell. Was in hospital right guy after I had Covid be cause of crazy headaches. Four days in icu.
Vaccines made my adult son worse, and now he’s had Lyme and long covid for way over 3 years with severe neurological problems, seizures, severe headaches and pressure, neuropathy, and autoimmune diseases. It’s worse than I can describe. No one will give him pain relief, and he’s trying to get ketamine treatments, but he keeps getting too ill to get to the doctor. What a shame.
I have met a number of people who were diagnosed with long covid, all had been vaccinated and those with the worst symptoms had actually had covid prior to the vaccination. How many here were and still are unvaccinated but have been diagnosed with long covid?
@ its my worse feeling. I got vaxed in 2021 but i never had a reaction at all, then got coming for the second time in January 20th 2024 and thats when all my symptoms came about. I still struggle. It will be a year on the 20th of this month
Look at all the comments and reply’s. Mine are in here. I’ve had significant improvement through addressing every function impacted and reset by SARS. I describe what I’m doing and my process for dealing with all my PASC symptoms. Improving greatly by re-regulating dis-regulated, disrupted systems. A really good younger Endocrinologist who will address valid squalae symptoms. Diagnosis Code in U.S. is SQUALAE.
I think doctors should have an objective opinion about specific individuals in their healthcare. And when the bought and paid for CDC and NIH she'll for Pfizer and moderna - and maybe doctor should look at the objective data and not blindly follow the paid for establishment
Did we know at what tissue temperature did SARS COV2 better replicate? At TWiV 659 at min29 virologist Christian Drosten indicate that to replicate SARS COV2 better ,must decrease incubator temperature. Theoretically, high mucoseal temperature decrease SARS COV2 replication May be, must not decrease fever ,If are not excesive to decrease SARS COV2 replication?
I still can't smell or taste over 2.5 years of catching covid for the first time. I had a mild sickness. I have brain fog as well and push through my fatigue. I think my daughter has problems from catching covid last year. Her legs are numb and painful and she has constance dizziness. We are not jabbed.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
The interviewer here reminds me of the jerk doctors my daughter has seen who have told her her symptoms were just her having panic attacks or some other useless crap. My 27 year old daughter after having COVID had an attack where out of nowhere she had a group of strange symptoms hit her .. From the onset many more symptoms followed . Loads of tests have been done but nothing show up yet my healthy, happy working daughter became debilitated.. For months she could not work , drive or anything that she did prior to this attack that came on the tail end of having COVID.. We finally found a rheumatologist who was willing to treat her with autoimmune meds which has helped her tremendously but NOT cured her. She has been able to get back to work , a work from home job and now drives again etc… We need to go to one of these clinics..
Is long covid due to the untested vaccinations or due to the virus as most people have had both. The vax does not stop infection like it was supposed to so it is certainly not effective may not be safe either.
My life has been a nightmare since I had the jab with neurological problems developing a month after. 36 at the time, not exactly old and perfectly healthy, not a thing wrong with me at all, ever and it's completely ruined my life, I have a permanent tremor, mostly in my face and a list of other problems, unbearable tinnitus to name a couple (that's not even the half of it). I literally have the same symptoms listed off as long covid, which funnily enough, I started getting before I got covid but I had ther jab. I did get covid nearly 4 months after the jab but these problems had already started. My guess is everyone got the jab and had covid who has these problems and it's being palmed off as long covid to protect powerful peoples interests.
@djkurtstudio Totally agree with you. I was a very fit 68yr old until I had my 1st covid shot over 2 yrs ago. Lost my ability to walk a few weeks after the jab and remain with severe balance problems and a semi paralysed right leg. Never had a covid infection so far.
It's June 2024 and I still have pain in both arms. I can show exactly, the points on both arms where they injected me with the vaxx poison! It's been three years.
I wonder if people have heard of post polio fatigue that can start to happen 20-30 years after the start of the infection. Long Covid might do the same thing.
And jut so you know this condition happens with other viral infections as well it is called Chronic Fatigue Syndrom M.E. all this fancy words for nothing...
I’m 3 1/2 years post COVID. My life, body and mind struggle everyday. I need help! We need more Drs who care, instead of saying your just stressed and have anxiety.
Find my post on what this, etc, kidney failure, etc heavily censored.
I hear you. I went through a ton of severe neuro symptoms for which conventional drs. didn't have any answers. I was all on my own. A chiropractor (Dr. Perry Nickelston_ and a Gastroenterologist (dr. Ross Hauser) on you tube. they steered me in the right direction. What has helped me the most is acupuncture. I'm telling you this as I wish someone had told me what to do to prevent months of suffering. Acupuncture helps with anxiety, depression, constipation and diarrhea plus pain, and other things. I can promise you'll get help. If you can find community acupuncture, it's quite a bit cheaper. It's where they treat two people in a room at once. I'm curious to see if you try this - let me know if it works. The cost for community acupuncture is $30-$50, depending on income etc.
Yes I agree, I am an acupuncturist and I just recently started treating myself. Thank you for you kind response
@@karreenco.beautyhealthwell9806 That's cool if you can do it yourself. I consider my acupuncturist a hero!
post vaccine or post covid?
I was extremely ill with covid and long covid for about a year. Now, my personality changed. I am more subdued. I am tired and can get exhausted having dinner with more than 2 people. Too much to deal with all at once. I get to bed by 9pm. My favorite activity is going to bed and getting a good night's sleep. I am anxious, and depressed. I feel that I slog thru life. I don't want to be engaged. I prefer to watch the clouds stream by. I am not the same person I was before covid. It sucks.
how are you now?
@@danr13 Similar, I am a bit more active, but still slowed down and still easily overwhelmed with too much activity that stresses me along with too much engagement with people. Grateful to be alive. Sleeping is still a nightly challenge. I lived thru it and things are just different now...
Thanks for sharing. You have described word for word my experience of long covid. I feel exactly the same; long covid has now only affected me physically and cognitively but also my personality.
@@francesnance9110 Thank you for responding! I am sorry you are going through this. I am experiencing the same thing. Wishing you all the best. I hope we will continue to get better (or start getting better...)
Me too, a little over 1 year. My doctor just suggested a psychiatrist. WTF
I work, do the bare minimum of household chores (when I can manage it) sleep. That’s my life now. 😢
Thanks for sharing. I’ve been dealing with Post Covid almost 2 years. I have shortness of breath, extreme fatigue, short term memory, as well as heart palpitations. Covid has been an unbelievable journey.
@RR 6 are you sure
@RR 6 I'm so hot right now I want to cry. If I do something one day the next day, I'm completely exhausted. I don't know what to do.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
I had these plus vertigo imbalance plus mental fogging in 2018 after 9 months of constant coughing
2018!!!! In Australia
No travel history
In 2022, i received my first moderna jab- 5 minutes after, i felt the mental fog lifted, was energetic cleaned out two houses snd gardens
Never looked back since, had 4 other moderna jabs
I had covid, i suspect in 2018!!!!
@@OMG-jv6vbay be your symptoms are not from the persistent low grade viral infection, but something else????
I really swear that within 5 minutes, after the jab, i felt a gush of blood flowed into my brain, and that was when i distinctly felt a fog was lifted off my brain. I am a medical doctor, was hesitant about taking the jabs, and i was working despite the symptoms i had,
The symptoms i had were bad but they did not prevent me from working part time, and going to the gym. I also recalled there were times my face would flushed like a red balloon suddenly,
A registered nurse who witnessed these flushes described them as a mast cell explosion or histamine explosion.
All these have never recurred now
Remember all these problems happened to me in 2018, long before any covid.
The coughing i had and the post coughing symptoms were so covid-like- i did not have loss of smell but i gained heaps of fat, prior to that i was really really skinny, lean, with minimal subcutaneous fat, just born like that.
I have now lost all those fat from vigorous walking on a treadmill.
Horrible symptoms. I have brain zaps, anxiety and panic, intense ear pressure, off balance, ackey shakey. This is a nightmare
Look up Miguel from chronic fatigue syndrome I'm in a practice now meditation it's very helpful
my son became suicidal for not knowing the source of his pain an panic attacks!
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@marcopoblete2592 I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@marcopoblete2592 it triggers that. Went thru 3 phases wher I thought I was dying and I even prepared my finances and told close relatives goodbye. Being under constant attack from the virus and/or spike messes up your parasympathetic nervous system. It will produce continuous stress hormones, which affects the rest of the body, then disbalance, then slew of symptoms.
Resilience is my biggest strenght but I broke down. I've never suffered that much in my life. That feeling of decay and losing your senses is absolutely painful and terrifying.
Be there and be supportive.
I tested positive 5 times over 2.5 years with Covid. First time was most severe but no hospitilazation. I have been dealing with long covid since. The longest time between infections was about 10 months. I had just begun to feel improvement gradually over two months, from 8-10 months in my symptoms. But then was reinfected. Right now I am three months since the last infection. Strong constant fatique, brain fog, difficulty getting deep breaths, tiring very easily moving around (for example going up stairs) then gasping short of breath, strong somewhat migrating inflammation pain - all over but particularly in the lungs and neck- intense brain fog with post exertional fatigue, headache. It gets worse and better on different days without being able to ascertain why. Exertion definitely makes it worse. I am not obese and I look good to people. Thus many do not understand. All of this is invisible on quick glance. Unless people are actually with me all day and can see the impact of having a lively conversation for two hours then leaving me in bed with confused brain fog the rest of the day, feeling miserable. This is debilitating! Few people understand.
I could feel this interviewing doctor's bias and lack of awareness...jumping to that standard easy and condescending conclusion when they don't know how to explain it - 'isn't it really in their head?' - trope. So irrititating and insulting. I don't waste my time with people who have that level of bias and ignorance about this. I will finally start treatment at UCLA Med Center in October where they have a clinic for long covid. I wish us all luck.
Tu for this ❤️ am vax injured 3 times. 3years in, have xact same, but no help inRi, and too sick to go Boston.. cal has more.. would like to follow-up w u on your clinic journey, healing thoughts and prayers🙏💕😺
@@brendabrenner2891 exactly, well done for getting thru the algorithms.
All this fatigue, brain fog, difficulty getting deep breaths, tiring easily, inflammation pain, headache, all worsened by j_a_b.
Inflammation here
@@brendabrenner2891 see my posts👇all labs, over & over protect kidneys.
I’ve had chronic fatigue syndrome for over 20 years. Main problem is post exertional malaise. Now long COVID patients seem to be experiencing similar symptoms
I had covid back in August of 2023. It is now March of 2024 and i cant take it anymore. Raging headache, loss of of balance, vertigo, brain fog, insane fatigue, pain in the back of my eyes, really bad light sensitivity, muscle weakness.
Thank you to the doctor! So many were exposed to Covid at work, and later when they thought they were recovered... experienced serious cognitive issues, weakness, malaise, etc.. numbness, vision problems, etc., and were terminated.
Many were unjustly judged as incompetent, treated as if they had Alzheimer's...when they were perfectly healthy before exposure to Covid at work. It's cruel, and inhumane to GIVE someone an illness, humiliate and shame them on the job for it, and then terminate them. Many lost their jobs, finances, health insurance, and were abandoned with hefty medical bills, all due to coworkers giving them the illness. Employers are too quick to judge someone who may be struggling with REAL terrifying post COVID symptoms. Employers should be educated on the REALITY of COVID's cognitive and other symptoms. I also agree that those struggling with long COVID should receive significant govt assistance. Congress can cut their huge pay raises, wasteful spending and needless multi-million dollar witch hunts to do so.
you silly sausage. research vaccine damage.
Thank you for this video. Female in her 40s…no positive Covid test but suspect I was infected several times with mild symptoms. Been suffering from so many of what I’ve come to understand as possible long Covid symptoms. Recently went through thousands of dollars in multiple tests because of elevated liver enzymes. After several months went by my labs went back to normal. I was optimistic that was the end as I was feeling better, but as had happened so many times previously, after feeling mostly well for a week or two I was knocked down with fatigue among a number of other symptoms that are only manageable because I lead a simple life and have a desk job working from home. I cannot imagine how it would look if I had the demands so many others do. Just started LDN to see if that will provide any relief. But it does seem like whatever is going on with me could be autoimmune in nature. Hugs and understanding for all those out there that have had doctors shaking their heads while escorting them out the door with a stack of medical bills and no relief.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Your enzymes got back to normal by themselves? I'm going thru a phase right now which tells me my gut aint working well, among a laundry list of other symptoms. I'm losing a lot of strenght. I used to be an athletic cyclist.
@@User98681 good advice. Intermittent fasting with a strict no carb diet and some prolonged fasting. I just got out of a 5-day fast but wasnt in good shape from the start.
@@stephangauthier911 it seems that way. Inflammation is the key word to all of this, as far as I can tell. Recently put an earthing/grounding mattress cover on my bed and have been finding other ways to ground my body. Out of all of the things I’ve tried, this one stands out as being instantly helpful. Upon waking on the first morning I felt different-in a good way. Like more rested. Visible signs of poor circulation have also been improving. Haven’t been doing it very long, but it my limited experience this is one treatment that seems to work based on my personal experience.
I know exactly how frustrating it can be to feel like you can’t have fun all the ways you’re used to. I hope you find some relief soon.
I wonder if I had Cov and didn't know it as I've had severe neuro symptoms including no appetite and Im already too thin. I'm 73 yo but have had excellent health until 7 mo ago. My liver enzymes went fromm 77 to now 20 (not sure how that happened) and also other markers go up like pulse, blood pressure and blood sugar even though I don't consume a speck of sugar. Elliot Overton on YT helped me eliminate most of my IBS with B1 (Benfotiamine). I've had now a horrendous problem sleeping. I told the dr. that the sleeping pills he gave me doesn't work - he just said to try it for a month even though I sleep the same with or w/o sleeping pills. I feel like a total zombee. I checked myself into the hospital because I wanted to make sure I'm ok with shaking etc. and I was told I could stay at that hospital for 2-3 days until a bed is available at a Psych ward and at a place that's 50 miles away. Even my GP said he wouldn't advise that. Going to drs has been worthlesss and I don't even think Mayo Clinic could help these symptoms. I am going to try two things: R alpha lipoic acid (the natural kind which is 40x more bioavailable) and methylene blue (start slowly on MB, doing 1 drop/day - added to an empty capsule to avoid blue on the tongue).
I’m sorry to say this and don’t wish to offend anyone. But thank god for long Covid. Those of us who had CFS, Fibromyalgia and other autoimmune diseases that were not recognised decades earlier. We were told it was all in our heads, now they realise it is a chronic disease and hopefully we can find answers and maybe a cure.
@lranieri1disagree. many of us have suffered same symptoms as myself 30 years with cfs. we were thrown under the bus and disregarded. made fun of not taken seriously mostly because we are female. We do not want anyone else to suffer this hell of a life we have and hope long covid suffers are taken seriously and work continues to try and help them so 30 years later they are not still suffering the same thing.
Yes 30 yrs later and I still suffer the same cfs symptoms as l. covid. I have done everything under sun to return to health. Have degree in Health Ed. and even have a study published in medical journal in hopes of helping find us help in 2010. But still nothing. We don't wish anyone this hell of a life and hope they just don't keep stringing these people along with no help like they did us. But after 2+ years it's looking the same. Lots of tests., lots money made at our expense and nothing yet.
I agree. As a 66 year old retired orthopaedic surgeon who has suffered ME/CFS for 11 years, following a viral upper respiratory tract infection, I have also endured the ignominy of an “unfashionable” illness. At least I can now say “I contracted long COVID before it was popular”. 🤷♂️. Unfortunately, the attitudes and beliefs of my medical colleagues are very difficult to change.
@lranieri1 - sorry - as a sufferer of an unfashionable post-viral CSF for 11 years, I beg to differ. Your reasoning suggests that everyone with “Long Covid” should shut up too and disappear into the shadows.
The irony of people who suffer wishing that suffering on others because they are mistreated.
It’s literally sick thinking.
It’s like saying if you were hit in a car accident other people should be too.
You were treated wrongly but you are sick for wishing that pain on others.
He just described M/CFS something most neurologists mocked and ignored for decades, Why now are they recognising post viral illnesses affect a patient neurologically?
It's about effin time.
As a 66 year old orthopedic surgeon who contracted ME/CFS after a viral upper respiratory tract infection at age 54, I can only agree with you.
@acebacker1 what can be done to get people who suffer from this help? I've been suffering for years, yet have forced myself to continue working as a mother with kids who was abandoned by my husband. I didn't have a choice but to work. Now the kids are out of the house, and it sure would be great to finally get some rest. But it won't happen. I work and collapse into bed every day. Why is this not taken seriously? We should be candidates for disability, but it's so easy to be gaslit.
I had Covid for the first time Sept 2023. Five months later I developed an increase level of liver levels and neuropathy from head to toe.. Out of nowhere.. Had skin test and nerve test was diagnosed with Small Fiber Neuropathy.. I’m not diabetic nor do I have autoimmune disorder. Neurologist said it might be long Covid symptom, It’s crazy
My wife has the most extreme case of LC which became worse and worse after contracting Alpha, followed by three or four other variants. She has some similar symptoms to lupus. She has been diagnosed with Inappropriate Sinus Tachycardia, POTS and Pollen Food Syndrome. She has a healthy heart muscle, but frequent heart episodes. She has bouts of extreme pain in her extremities, sleep disturbance, near dangerous levels of iron, and IGE. She has 9 specialists, and no improvement. In fact it’s getting worse. The Drs can’t approve disability status for LC in Canada and she is sick in bed. Can’t make ends meet in Toronto on one income. Really just at a loss here
🙏🙏🙏
I’m so sorry! I was going to ask what LC meant, but I get it. Duh. My adult son has Lyme and since he had covid, he’s had a horrible migraine 24/7 and has been having seizures and neurological problems.
Ask for ivermectin. It opens the healing pathways in the body. It's why they refused to give it out. People with neurodivergence tend to have poor healing and detoxification pathways. It affects the vagus nerve as well, which is the inflammation depression system. The nervous system and immune system work together. Taking MCAS support vitamins and antihistamines also help support the over immune response.
@@SK-jq8um👍👍🎯💯🙏🇬🇾🎉😎
I am having long COVID. I was initially very ill for 2 months, then I was able to get out of bed. Before COVID I worked full time, no neurologic issues. I have ankylosing spondylitis however, and was taking Consentyx when I I fell sick. I am only now able to work 1/2 day, and have to triple check my work as I feel like I did when I had a concussion and the post concussion syndrome. I went to a grocery store twice and forgot my groceries, pretty bad stuff. I'm also exhausted I have to nap every afternoon. I was vaccinated and boosted. I hope I can hang on long enough to get better. I too had crazy heart palpitations and very blurry vision.
Wow! I’m so sorry!
I’m in the same boat with Lyme, and went through covid and I couldn’t find the right words for a long time.
I don’t even shop anymore, but have my groceries delivered. I also have autoimmune diseases including AS.
This thing is horrific!
You need to treat inflammation. I had terrible fatigue, brain fog, memory cognitive issues after covid. I'm Still recuperating. New doctor treated me with I meg solumedrol IV steroid. Within hours of treatment the pressure I felt on top of my head lifted. Several days later I could think clearer my short term memory lapses improving. My fatigue also is much better. I nap once or twice a week once a day. Not every day twice or three times. Why do doctors ignore treating brain inflammation. It is documented on MRI scans. They know it's there but don't treat it. I thank God I finally found a doctor who treated it. Look for doctors who will give corticosteroids to treat long term covid inflammation. This is what causes long covid!
I am from Puerto Rico, female 70 years. I have been diagnosed with long Covid 19 vasculitis. I have varices in both legs, and bruises or hematomas in my arms. A constant headache with lost of vision. I was treated with paxlovid during the infection, last August. After visiting a few doctors, a hematologist-oncologist gave me this diagnosis.
Male in his mid 30's perfectly healthy before covid, Got covid bad twice in one year then a third time minor. I've had major GI issues, heart arrhythmia (AFIB and Flutter, and High and low heart Rate), pulsate tinnitus, and now weakness/muscle spasms in arms and legs. I've had pretty much every test done including MRI of heart and Brain and all come back normal. So I've been a covid long hauler for 2 years now. This all happened after my second run in with covid, which I also had the vaccine. Not which which actually caused this. I've gotten better with some things but then new things show up. It's a wild and expensive ride.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Have also tinnitus, finally found cricket sound bath by audiologist on you tube that gives relief for a while.
It's weird how the symptoms change over time. I'm going thru a phase right now where my GI is very much messed up and extreme weaknesses. Feels like I'll lose my ability to walk.
Scary AF stuff.
You're not alone in this man. Hang tight; it's gonna be a bumpy ride.
I really believe that it was the vacine that caused all this 2 days after second jab I got sick that was July 29th 2021 still have major problems it is now may 2 2023 you should all read the physer records they wanted it to remain silent for 75 years but the court demanded they release them now and they did frighting
My exact symptoms and age. Can i ask what you do for a living. Im looking for lifestyle connections. But i agree with long fast. Also, ive heard apheresis is really working. Also you should try pepcid and zyrtec 2 times a day each. It will be huge for the GI stuff and other stuff.
For those posting here about your struggles with long covid we are going to assume that you were fully vax'd and boosted, unless you indicate otherwise!
bullshit heb geen vaccins lichaam vol verlammingen en kapot. 2022 shedding opgelopen.
I have been dealing with this for 3 years. My first COVID infection was January 2022. I dealt with dizziness, ear ringing, tasting salt with everything I ate or drank, racing heart, profusely sweating for no reason , randomly vomiting, terrible constipation, choking and brain fog. I saw a million doctors and no one even mentioned this was possible.
After months of vestibular therapy the neurologist gave me a burst and titration of prednisone starting with 60 mg for three days, 50mg for three days, etc… it worked! I was mostly symptom free except for migraines 1-3 days a week. I had COVID again two weeks ago… and I am starting all of the same symptoms again.
I am at wits end- waiting to be fired for missing work (I carry our insurance) and can’t see my neurologist until January 16, 2023. I’m so done. Just over it.
Sorry you’re having a bad run with this. I had some of the issues you’re dealing with and have been on a carnivore diet for over a year and it’s the only thing that works for me. It sucks. Just want to be normal. Not advise. Just a thought. Hope you get better.
Oh my, same salty taste on my tongue ever since my second shot. I do not believe that Covid has to be contracted but just the shots can cause the same neurological symptoms and other symptoms. I too, have severe neuropathy, heart palpitations, tinnitus, dizziness, balance issues, short of breath, pain, fatigue, anxiety attacks, weak and heavy legs, headaches, digestive issues etc. my husband had severe heart attack, both of these things happened to us after the second jab, as far as we know, we didn't have Covid.
He’s forgetting, excessive sweating 24/7 most days, thoughts that are abnormal, extreme paranoia, insomnia, and major weight loss and muscle tissue. I had mild Covid, I was told. It was terrible! 25 months later with Covid twice, I’m worse than ever!
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681
Fast is the best way let me know r u vaccinated or nonvax
The neurologist just described M/CFS something most neurologists mocked and ignored for decades, Why now are they recognising post viral illnesses affect a patient neurologically?
My husbands exact symptoms. I was afraid he might have prions or rapid progression of dementia.
Check into Covid psycosis
I got Covid beginning of December 2021. It was horrible. I got the monoclonal antibody infusion. I have never recovered my senses of taste and smell since then. My spleen is enlarged and my internal organs actually hurt. I have left side facial twitching. I got Covid again in August 2022. It wiped out my memory and caused constant fatigue, severe anxiety and depression. I am convinced that my brain is damaged and I will have a shortened lifespan because of this bioweapon.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 I do not see how fasting will help repair the damage to my olfactory bulb. I am not in the best of health. Supplements scare me. I am on thyroid meds and Zoloft. No way I can do three days existing on just water. 16 months with Anosmia and no recovery. I fear this is permanent.
@@LoveMyBoys3 3 days water fasting will cause drastic weight loss which is even more dangerous when you are already experiencing symptoms. It will only add fuel to fire.
Try Magnesium chloride oil
I got covid in 2020 and not hospitalized during that moment I experienced many symptoms like loss of smell and then I started to notice ringing in my ears, acid reflux and bloating, tingling in my feet, dizziness, blurry vision and eye floaters, heart palpitations and I feel exhausted and I can't do exercise because my heart rate goes very high, until now I didn't recover and just my sense of smell recovered
same symptoms as you since june of last year plus i had panic attacks and depression, this sucks only thing i dont have is the tiredness
@@mcmaviation4486 covid 19 affected me too much because i had depression and stressed before i got infected.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
I developed anxiety and panic attacks severe panic attacks where I would get hyperventilation and fatigue after such but now I'm taking antidepressants and I'm doing great so far
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Paroxitine is fantastic for stopping panic and aniety
@@brobinson8614 I’m taking escitalopram for anxiety and anxiolitic for panic attacks
pharma has everything you need to mask symptoms of illness.
@@User98681 I've noticed that too, everytime I starve myself for a day or two, I feel fantastic on the other hand eating too much makes me feel uncomfortable
Yes thanks. Some of my family members don't understand why I am not better yet, thinking am faking my symptoms. My O2 was 41 when I went to hospital I am very lucky to be alive, but I still have a bunch of symptoms and the doctor s don't know what to do with me.
Please study long covid patients who develop POTS and PEM 🙏
That is me😢
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@haotang2638 I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
The neurologist just described ME/CFS, something most neurologists mocked and ignored for decades, Why now are they recognising post viral illnesses affect a patient neurologically?
My two cents from my 15 month long and counting long covid nightmare: 55 year old male, main symptoms insane fatigue, brain fog, AND THEN: one year post infection(14 months post vaccination) had first episode of supratachycardia SVT that sent me to the ER and had to get cardioversion to reset my 160 bpm resting sitting heart rate. I see "tachycardia" very often when reading about long covid aka PACS Post Acute COVID-19 Syndrome.
I’ve had these symptoms for two years now after Covid (mild). Recently had a spinal tap due to optic nerve swelling and found to have very high CSF pressure and an ongoing autoimmune response . Diagnosed with IIH and papilledema.
My ex wife had the same in optic nerve swelling, constant fever for weeks, high CSF Pressure and also received the IIH Diagnosis 3 years after getting covid in late 2019.
Also her left 2nd toe has been twitching constantly for 1¾ years. Non stop. Sometimes the twitch is just more powerful than others. This disease keeps on giving even after the respiratory symptoms go away.
May I ask what IIH is?
You got IIH and papillaedema from covid?
@@jonathangraham6412 Yes. Neurologist said it was an autoimmune response caused from the virus.
@@Tinyteacher1111 Idiopathic Intracranial Hypertension, aka Pseudotumor cerebri...basically increased spinal fluid pressure, the symptoms mimic a brain tumor.
I've had Covid twice. I got it in February of 2021, right before the vaccines. First week couldn't get out of bed, fever, chills, aches, 102 to 104 fever for 5 days. Second week, fever broke, developed a sever cough and couldn't take deep breaths. Breathing deep hurt in my chest, and that's when I looked up the breathing exercises to do to stay out of the hospital and on a ventilator. Fortunately, I stayed out of the hospital, and it seemed to break after two weeks.
Second time was March of 2023. I drove to and from Las Vegas that weekend, and Monday the 13th on the drive home, I developed a very severe headache. By the time I got home I had the chills and was feeling lousy overall. My wife said to take a test, and I was positive. I took a second one to make sure the next morning, and it was positive. I didn't get a fever the second time, but I still had chills, body aches and a headache for the first week. The second week I had a sore throat and mild cough, but most of the other symptoms were almost gone. Again, after the second week, it seemed to break and I felt close to normal.
Last summer, first week of July 2023, one morning I had severe enough low back pain on the right side that my wife drove me to the ER. They were thinking kidney stones and wanted to run a CT scan. I knew it wasn't kidney stones, because two days prior to this ER visit, I had just been proclaimed to be "the epitome of health" by my primary doctor after we finished my annual physical. Two days prior, I didn't have a single medical problem, all of a sudden I'm in the ER feeling like I was being stabbed in my low back. Of course the CT scan showed my kidneys, as well as all of my other organs, were normal. No sign of stones, kidneys clear.
Almost (9) months in now, March 25, 2024, I have seen (12) doctors and had multiple CT scans, Ultrasounds, and MRI's of my spine (Thoracic and Lumbar), my abdomen and pelvis (inner, for organs), my right flank and abdominal muscles from my right hip to my naval, X-rays of my right hip and spine, and not a single doctor can tell me what it is. They can all tell me what it isn't.
What I'm dealing with is for (9) months, I have had pain / cramping in my right flank area, all day, every day, from when I get out of bed in the morning until I go to sleep that night. On the 1 - 10 scale for rating pain levels, my normal day is a 4 to 5 all day, as long as I'm awake. When it goes to an 8 or 9, then I have to lie down on my back. It is like having a calf cramp, but in your side. There is nothing I can take for the pain, as Norco, Toradol, and a Lidocaine patch all did nothing at the ER. So, Ibuprofen and Excedrin don't have a chance.
That isn't even the end of it. My right flank area (I say "Love Handle", it gets the exact location across), the entire love handle, has been numb for the (9) months this has been going on. Totally numb on the outside, pain / cramping on the inside, (9) months, every day, all day. Not a single doctor I've seen want to touch that. They move on to something else, ignoring that I just told them I've had a body part numb for (9) months. One doctor literally almost ran out of the exam room when I told him this, he was saying my specialists had it covered, and he was sure they would figure it out.
I still have pages to go, but I think the medical issue is there. There is so much more, about doctors lying to you, another blowing you off for a month (ongoing, Keck doctor ghosted me), and the ones that don't believe anything is wrong.
I went to the doc which i never did.
I was crying out of nowhere.
I was so tired.
Scared.
Something was so wrong.
I forgot names was scared outside. Didn t know where i was.
Light and noises hurted me.
I kept working till i could not.
It was long covid he said.
And it feels like a relieve.
No excuse and feeling guilty for dismisisng dates with friends and having no strentght.
Taking my rest.
Sleep as long as i want.
It is healing.
I am broken.
And it is ok.
...
I had the first virus in early 2020. I started having peripheral neuropathy in my feet then. I then got the 2 vax in Feb of 2021. Then I got Omicron in April of 2022. I received the antibody infusion at the Mayo clinic in 2022. Neuropathy is much worse, all the way up my legs. Severe fatigue, tinnitus, brain fog, and can barely walk. I am seeing specialists through the Mayo clinic. Next test will be for arterial blockage in legs on the 20th. I am sure tired of this and wish there was something that would return me to normal.
How r u feeling now? I'm dealing w neuropathy in my legs for 2yrs after getting covid
@@LisaL-yl9zm Feet and legs are worse. Still have fatigue, brain fog, stomach issues. I just had bloodwork done last week. testing now for thyroid, hashimotos, celiac, A1C, C3 and C4, B12, etc. most came back normal except for the autoimmune stuff. Thanks for asking.
@@chermarie332 I just got a blood test today to see if the spike protein from c-vd is still in me . Keep u posted
Hello, I really hope you are feeling much better now. I had the viral infection one month ago. Now having burning pain in my feet that I can barely walk. Did you have the same symptom? It’s hard to fine someone understand what I am experiencing. My GP said my symptoms are very rare.
@@LisaL-yl9zmHi Lisa. Did the test showed anything. What's the name of the test. Dealing with long covid since 2022. Hopefully you're doing better.
Dr's should really stop dismissing long covid symptoms!!!!!!!!!!
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 I tried water fasting last year, but more 2,5 days, cant say it helped alot, but I feelt better for shore, during like 4-5 days after completed fasting.
And I have Hämatomsa bloodpressure,many inflammation, Dysphagie, soaring and pain like being teared apart, walk-in,bslsnsce ?
I need advice!! My partner had to take me in!! Because I could not have take care !! Can not move on some days ?? It’s like if you have some kind of phases
I do not have long covid but I have some of those symptoms. My symptoms started over 2 years ago after I got two covid shots on 2/21 and 3/21.
So for the past 2 years plus I have had chills and sweats every day. The past 8 months the chills are freezing so that I have to take 3 hot showers a day just to increase my core temperature. I also have extreme fatigue and brain fog. So I am going to try some of these helpful ideas with regards to the treatment of long covid. Thank you Doctors for the information. From Don...Northwestern University Class of 1971.
Don, you have post vaccination squalae, what everyone whether caught it or inje cted is calling long covid. The entire clade is man made gov’t funded wea pon ized.
stop taking vaccines
I still am suffering 2.5 years later. The worst was the jab. It's worse now that it was 1 year ago.
I've tried so many things like strict diet, some products like artemesia, NAC and nattokinese, exercise, fasting.
The health system is useless other than sign me a leave of absence from work (I'm nearly disabled). No tests come back positive. ECG, EEG (I had so many seizures with no priors), x-rays, complete blood tests, brain MRI.
It breaks my heart, Stephen. Looking at the amount of published papers I am pretty optimistic that we'll find something pretty soon.
I'm so sorry.... my husband is in the same disabled state after his forced vax's almost 2 years ago. Nothing is helping, especially doctors.
Why don't we have long sars for other viruses from.the same family? And why the long c symptoms are so similar to the cobra venom?
My personal struggle has my intuition telling me that the virus attacked my vagal nerve. I almost feel it. Never had the shot, just a severe infection in early 2021, hospital for 5 days. It started a few weeks after hospitalization with crushing afternoon weakness. Right away , before a tone was talking about it I kept telling my wife that I felt like there was a problem with my central nervous system.
My cyclic symptoms are numerous and from what I've learned, almost universal.
These doctors have poor investigative skills. I was an Air Force officer before falling ill and have hyper documented and reviewed all of my labs, imaging, reports…
I have positive NMO antibodies (AQP4), my neurotransmitters are negatively effected (particularly Dopamine), I have numerous reactivated infections, and a lot of endocrine and metabolic dysfunction.
He’s also wrong about his presumptions regarding the vaccine and it’s risk/reward. Don’t let the suit/tie and white coat fool you. These are drones with no practical sense or effective discernment.
Listen to the patients.
Doctors often think they have a monopoly on intelligence and yet tend to have very poor investigative abilities.
🙏💖💞💞💞👍
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Im in the same boat as you my friend. It too broke my heart when he said he said to follow the CDC recommendations. They're SO corrupt.
As an orthopaedic surgeon 11 years down the track with ME/CFS after a viral infection, my advice to any medical professional (in respect of any patient interaction really) is “First, shut up and listen to the patient, and don’t interrupt them until they have finished giving you their history.” What patients give you is gold, and following that, only a few more questions may be required to narrow down possible diagnoses and guide targeted investigations.
Unfortunately, after exclusion of specific diseases or disease processes, doctors have patients that have brain fog, fatigue, etc which cannot be easily confirmed - apart from perhaps functional MRI etc. And then, there is no specific treatment. Confirmation of real illness can be helpful for the mental health of the affected person, as is documentation for insurance. The most important diagnostic tool is the doctor’s ear, which if connected to an open mind not crystallised by dogma, rapidly makes the diagnosis of a post viral autoimmune problem affecting the brain. Simple really, but in my personal experience, rare.
@@User98681 Thank you for the offer. I have a small feeling I may have at one point or another attempted the recommended protocol(s). I’ve tried nearly everything and have waded deeply in multi-chronic infection treatments, autoimmune treatments, mitochondrial dysfunction supplementation, etc.
But I’m always welcome to new ideas…currently in a nursing facility and suffering symptoms that cross between Sjogren’s, Systemic Sclerosis, Dysautonomia, ataxia, and more.
So glad I'm still in the control group.
Me too.
I agree with you that it's mainly V injury.
However, I've gotten LC after getting C anyway. :(
And there's LC sufferers from 2020, pre V.
Covid gives LC. The vaccine is pointless at this point. It was just a waste of time and resources
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Anyone have the internal vibration after covid?? I have many more symptoms but that is is by far the most overwhelming one of all
Yes, I have that. It's been 2 years. Also, have full body numbness and tingling and sometimes burning. It's been a nightmare.
@@Sarah_S26 i wish doctors knew what is causing it. It’s unsettling feeling like your insides are vibrating. Have you tried any meds for your symptoms??
@@marielopez2947hi , gp here , this is dysautonomia , take beta blocker or corlanor .
Also associate it with probiotics.
What you have is a vagus nerve dysfunction.
@@marielopez2947
Any other symptoms?
Thanks for this❤ best questions asked that I have been seeking answers. I am grateful that so far no one took my situation not seriously, as I lost 80-90%of my life, hope more long Covid patients being treated and heal soon. Any advice on things I need to do for faster recovery? I
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@Liam Tytgat I will ask doctor and see if that is paid for in canada
This is a silent horrible disease. I have had diagnosis of chronic fatigue syndrome 30 years with similar symptoms. It's a soul sucking life sucking disease. Leaving patients with unpredictable symptoms that are hard to manage. Causes loss of jobs and friends and sometimes family. Not to mention life choices and possible accomplishments that put hope of getting relief out of reach, causing further depression and who wouldn't be depressed with no help from anyone only disbelief. Please help these people more then you have helped us with CFS we have been forgotten thrown under the bus.
IT'S REAL, yes it is! I hope GP's are watching this and stop dismissing us! I am back to about 95%, but it was a very rough ride!
Thanks for sharing. I'm in the thick of it & praying for healing as well❤❤❤❤🙏💪💋👠
I have just about beat it.. but I have night time spasms in my upper body and can’t sleep. When I get sick now… it’s two weeks long not one
I had Covid (that I know of) 3 times and this all tracks. Mild infections (ie was never hospitalized) was in my late 30’s/early 40’s, otherwise healthy, etc… At 41 yrs old after the 2nd bout I developed a stutter. Which I’d never had before in my life & was extremely severe at first to the point I could barely speak/string 3 words together but has improved over the last couple years. There are so many other symptoms that you mentioned and I have ALL of them but I had depression & PTSD before COVID so no one is going to take me seriously. But, I’d recovered a lot re those issues through intense treatment before that & then they got 5 times as bad after. I just always figured it was the stress of the pandemic that set me back so far. I’m still dealing w this stuff!
Long covid treatment centers are popping up throughout (heavily jabbed-up) California, by the dozens lately.
What does that tell you, folks?
Everybody has anxiety and depression during a time when the world was shut down, so I don’t like when they bring it up, that’s so goofy that’s a confounding variable
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Doctors, is it possible that the neurological symptoms may be a Molybdenum deficiency? As well as other vitamin depletions from where the body is experiencing an auto immune response . I consider covid a symptom . But the disease acts more parasitic in nature. Going through cycles of wellness and illness. Similar to the illness - malaria. Could it be that with infection people loose the ability to detox ? And lack the ability to also absorb necessary nutrients to improve wellness?
Bingo. Then those disbalances cause systemic symptoms by themselves.
Only the Chinese who created this biological weapon can answer. But they themselves are now facing karma as it has boomeranged on their own population. They can't find any antidote as the research team who created the virus themselves have perished it seems.
The virus hides in the biofilms. Not regarded in allopathic medicine, but a real, actual force in trying to recover from Long Lyme, Long Civid, and others.
Thank you.
I'm glad you brought up the many patients who were unable to get a covid test in the early days of the pandemic. April 1, 2020, I became sick and continued to get worse. Never could geta covid lost because I didn't have a cough. I became sicker than ever have been in my 55 years. still, was told not o came to docter or hospital unless I couldn't breath.
Anyway, I have been denied access to the long-covid clinics hear me even with referral from my PCP. I'm in Alameda, CA and was denied at both Stanford and Davis. The clinics all apparently have too many pa tients. They complain that their doctors and students-doctors, are unable to do the other work they need to do because of the overwhelmcy number of LC / PASC patients. So, for that, they deny anyone without a positive PCR test just to limit access and limit number of patients.
Any suggestions of where to go close to me. or at least in Californian, so my insurance can pay?
Be canadian and pay nothing sorry there is no cure
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@Liam Tytgat I do not eat much seem food since the second fax has turned me off of dinners and breakfast I eat very little but you do make sense so tired of this now it's attacting my right side knee bone hurts shoulder bones hurts all on the right side even though the second jab in my left arm was painful and she went into the bone this time I yelled in pain firt jab no problem getting really tired of this crap I will try what you suggested had this Aug 2021 bone aches just started out of the blue 4 weeks ago it is now April 28th 2023
@ark thank you. Agree, it's insensative. But, I'd where my N95 in that type of setting.
Find my post, what this is, kidney protection needed, all labs repeatedly, for dysfunction. Heavily censored, Semper Fi
Can the doctors distinguish the difference between Havana symptoms and the neurological conditions of long covid19?
One thing glaringly left out was the role of autonomic solutions. I took 5 doses of the vaccine in order to NOT get long Covid as I have hyperadrenergic POTS from multiple surgeries to start with. You say there are no tests for long Covid but not once was neuro diagnostic testing mentioned. Depression and anxiety very definitely occur because people are marginalized, not believed and told it is all in your head. Unfortunately autonomic neurologists are few and far between and booked months out. Simple blood pressure and heart rate readings supine and standing will establish the baseline of POTS or orthostatic hypotension. Dysautonomia International has a wealth of webinars and sites related to this. And I am also a medical professional and do know whence I speak.
Mmp
Wow, you're a medical and you still took the vaccine???? I have that condition too and my cardiologist said ABSOLUTELY NO to the vaccine from day one!
@@madelinesabatello1845 Dear Madeline, I took all 5 because, for me, the chances of getting Long Covid were more daunting than the disease itself. Dysautonomia drives much of the Long Covid and Long Covid on top of dysautonomia plus an immune system that is seriously disturbed was much more of a risk than Covid-19 itself. People forget that all life on this planet works on the bell curve. There are always the outliers. So it’s always individual risks versus benefits. That’s why I did it. As well as my age, 76, dysautonomia, asthma, chronic pain syndrome. Russian Roulette at its finest. The same types of things happened other all other vaccines. And you should see clinical trials. That’s why I quit as a clinical pharmacologist, Big Pharma ethics. But the divisions in the world made it into a political issue. Be well.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
The vaccines caused POTS - diagnosed 3 weeks later with that. Then the infection itself caused Long Covid. Can't win.
Vanessa here from Germany!! Has someone to desk with symptoms like Parkinson or MS like after the COV I have postv
are there any studies supporting patients developing focal seizures post covid
I went thru at least 60 tremor and seizure-like episodes, some of them rendered me unable to move.
This Long Covid has taken my life away from me. I have no appetite I am in bed do to fatigue and weakness just getting dressed takes all my energy . I feel faint when I go out to my pain doctors my legs feel like rubber I feel faint & scared. What do people do that have fibromyalgia also ? I can be setting up in bed & all of a sudden I get a dizzy spell out of the blue, sleeping is hard, everything is hard to do !!! & I feel like I am dying at certain points. I have a racing heart of a 136 beats per minute , that is like this when I have to go out or try & clean , so I have stopped depression is bad & so is my anxiety Thank God for my hubby who is amazing at taking care of me, I just feel bad because our lives are at a stand still….🙏 oh I hope others can relate to my situation & have some of the same symptoms…..🙏❤️✌️🌹
Hello sister r u vaccinated or unvax
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
How are you right now?
Ja mijn lichaam is ook loodzwaar inderdaad rubber met lood cellen. ik was ook een sportman en gouden handen. maar lichaam ziet er niet meer uit lijk wel 90. vrezelijk. tip spike eiwit amyloidose. denk denk attr amyloidose. dat is aanmaak verkeerd gevouwde eiwit cellen. maar hoor graag van je meissie hoe het nu met je is. klagen mag van mij ik snap je hoor voel met je mee. het is allemaal zo on eerlijk wat je mee maak. veel liefde gewenst. blijf heel dicht bij je zelf jij merk en voel wat er mis is. blijft wel tegen je zelf zeggen het komt goed het komt goed. hele universum zal luisteren.
AND IT WAS SUPPOSED TO BE SAFE AND EFFECTIVE 🧐🧐🧐
I developed RA 3 months after having COVID (previously vaccinated and boostered). No one that I know of in my family has ever had a history of RA.
I understand you I got covid last decemberber and after 2 months I developed RA too I feel sad
RA is a form of auto-immunity
what is RA?
@@ex8280 Rheumatoid Arthritis - Autoimmune disease.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
I still have long Covid problems. I had covid leg. My legs have gradually gotten worse. I'm starting to lose circulation. I get so weak I can't go and about pass out. My feet and legs are swelling. I've got brown and blackening on my feet and lower legs from lack of oxygen. I hurt all over. I have difficulty swallowing at times. My blood pressure runs real high at times then drops to like 80-40 at other times. Severe headaches. Isdis with my right arm now. My gall bladder and appendix are both failing. Im having those issues. I have problems breathing at times. I sleep sitting up now. Abs that's just what I know about. I'm sure I have blockages and I think I may have cancer now. I'm ready to go. I'm tired of fighting
Thank you for this.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
what about those of us who sustained a vax injury and not a covid one ? i sustained severe small fibre neuropathy straight after and have done for past 12months - is there a possibilty of healing from this ?
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 thank liam - do you feel vax injury is just the same of long covid? the symptoms do seem to be similar but then some vary greatly - small fibre neuroapthy being my issue - i do take those supps and do infared sauna - fasting has been hit and miss based on how im feeling but will try a longer fast if possible
@@monnmar1 I am not vaccinated but suffering from LC I am about 75% back to fully healed. Vaxx injury and LC are 2 totally seperate things, both have similar symptoms. Fasting is good either way, it’s best not to get any vaccines. They are in effective and highly dangerous
@@User98681 thanks...but comments about it not being the best thing to do is not helpful when going through the ramifications of it . Plenty have been fine with their dosing....I just wasn't.... I can't go back in time and chnage that....no matter how much regret it brings
@@monnmar1 my prayers are with you Jesus loves you!
My husband and I have long covid for 2 1/2 years, I have 95% of symptoms listed by CDC. ( I was in the hospital for 31 days and then transferred to an acute rehab for 60 days.) But my husband was in the hospital for three weeks, and a regular rehab for five weeks,) He has fatigue and neurological issues. He isn't the same person that he used to be. I am so tired of the doctors telling us that they don't know much about Covid because it's a new disease. I can go on RUclips and see all the studies, why can't they? I just want my life back.
Pray to Satan.
My father passed away of parsonage turner syndrome last week. It took over his entire body except his right arm. This needs more research. It started 5 days after Covid booster shot.
How many people with long Covid have been vaccinated?
I am injured from 18 months, from 2nd dose of pfizer. My life is ruined, i was healthy and fit. Jabs ruined too many people... And doctors won't help people like me...
Doctors are killing people. They got paid for pushing vaccine. try MMS.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
@@User98681 i ve tried 3 days... In the 3 days i was better, then when i restarted to eat way worse than before...i take nac, nattokinase, magnesium, zinc, selenium, b complex, d, c, probiotics .... From months... They seems to me useless..nervous system and immune system are damaged..
10:40 …”urban legend” yes, right, …like the vaccine injury I suffer from . …Please do not use this frase. …I can tell you a thing or two about “legends” and subsequent gaslighting!
Im not taking the jab but i do feel like im experiencing symptoms of long covid (about 8 months) is the brajn fog permanent? Is this just who I am now?
A friend of mine was told he had Alzheimer's (they assumed due to his age) and his dr told him he was "terminal" and drugged him accordingly (without any tests to confirm the diagnosis) for over a year until I kept at him to switch doctors to be tested and appropriately diagnosed. Turns out he simply has brain fog as I suspected. I've known him for over 20 years and could see that he had Long Covid like me but his ADHD & OCD made it look otherwise, but other symptoms (GI and new allergies, post nasal drip, etc) made it clear it wasn't dementia. If you are MALE you will be shuffled off to a nursing home if you are older unless you self advocate since Long Covid is less common for men. This is dangerous as far as medicine goes but that's what's happening "out there" and every one of us will have to be wary & fight against the "instant 5 min diagnosis" from the too busy doctors who are more than happy to dismiss us.
those who have severe cases of pneumonia are vastly 65+ and are vulnerable to pneumonia just based on age and shown to have a longer time for immune response, thus making lung damage more serious. those with mild cases develop an immune response quicker, we have seen that antibodies produced allow entry into monocytes and macrophages where infection and replication of non infectious but foreign proteins are created and circulate the blood stream passing many major organs including the blood brain barrier, it replicates in numbers that overactivate the immune response causing healthy cells and tissues to be attacked in the clearing of viral proteins, thus causing scar tissue on many tissues/organs and death of cells which can lead to a copious amount of lingering symptoms and debilitations.
My mom had so much brain fog she couldn't do anything and So fatigue. SO WE PUT HER ON A DEMENTIA MED AND IT HAS ACTUALLY HELPED. Now she doesn't have DEMENTIA but it's actually working
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
Big question to the viewers... How many were jabbed 2x and more?
Symptoms are not vague. THey run very similarly through all the long haulers I know.
They are vague in a sense. The better term would be non specific. Evidence shows covid hides in the body and causes systemic damage. It's hard to pinpoint what is covid and what isn't when every system in the body is being affected. But you are right, there are symptoms that are more prevalent than others.
@@shaneschommer1074 It’s not hard and it is very specific. It’s a cluster of specific symptoms and damage.
@rbdesigner725 whatever cluster and specific symptoms you think, may be true but in reality it is even more than that. It's not just fatigue. It affects the skin, hormones, organs, nerves, stomach. Not every long hauler will present the same way. But you're right many do. Doctors should be better at piecing the puzzle together.
No word on treatments…? wtf? A good summary of what LC is though, but no helpful information.
Totally agree 💯 .
Notice how the guy in yellow says do you test for x,y,z and the white coat makes it seem like no because it isn’t necessary. For example, brain MRI, EEG etc..
What will treat me
Hello my name is Sarah.I have Long COVID and MS it is very hard but I trust in the Lord and He is with me. I am praying for all of you on here. Trust Jesus Christ today. He is coming soon for His bride. John 3:16-18
1 Corinthians 15:1-4
Amen! I wish my Savior would come back now! I’m tired of this LC pain and discomfort.
Last year I had covid twice, first was in march, which caused cyst to form in by eyelid, surgery was needed to remove that and that has healed fine. Second covid was in december, now after two months from covid I have tingling and numbness in my legs and arms even after sleeping or sitting, this must be long covid attacking my nerve systems, never had these kind of symptoms so often. But what you could do for healing, eating more vitamin B ?
Get this, I'm 63, I get sick usually every year, bronchitis or the flu, since covid I haven't been sick once, I've never had one shot, so the mask is still worn in public places.
I started having allergies, headaches, diahrea,vertigo,depressed
How many of them were vaccinated?
Long covid or longterm adverse resctions to covid vaccination???
I know someone who had it 3 times since 2019 & still no recovery
My mri I says - idiopathic intracranial hypertension but it has to be from Covid. Had it about 3 years ago no jab. That’s when the pain started. Lost my smell. Was in hospital right guy after I had Covid be cause of crazy headaches. Four days in icu.
Vaccines made my adult son worse, and now he’s had Lyme and long covid for way over 3 years with severe neurological problems, seizures, severe headaches and pressure, neuropathy, and autoimmune diseases. It’s worse than I can describe. No one will give him pain relief, and he’s trying to get ketamine treatments, but he keeps getting too ill to get to the doctor. What a shame.
The devil got your son.
The devil got your son.
I have met a number of people who were diagnosed with long covid, all had been vaccinated and those with the worst symptoms had actually had covid prior to the vaccination. How many here were and still are unvaccinated but have been diagnosed with long covid?
no one will answer that....i suspect 95% lol
I got long covid from vaccination…
How are you feeling? Anyway improving?
@@marielopez2947a bit better, but it didn’t go away
@ its my worse feeling. I got vaxed in 2021 but i never had a reaction at all, then got coming for the second time in January 20th 2024 and thats when all my symptoms came about. I still struggle. It will be a year on the 20th of this month
Reading some of the comments i see that depression is a common factor which could also lead to symptoms like fatigue.
This was 7 months ago, Please tell us the results of two weeks of Paxlovid🙏🏻🙏🏻👏🏼
Do the massive changes in our lives eg. Lockdown, social isolation, have any effect?
Look at all the comments and reply’s. Mine are in here.
I’ve had significant improvement through addressing every function impacted and reset by SARS. I describe what I’m doing and my process for dealing with all my PASC symptoms. Improving greatly by re-regulating dis-regulated, disrupted systems. A really good younger Endocrinologist who will address valid squalae symptoms. Diagnosis Code in U.S. is SQUALAE.
What are you doing?? Brain retrain
Did crioglobuline occur after SARS COV2 infection?
I think doctors should have an objective opinion about specific individuals in their healthcare. And when the bought and paid for CDC and NIH she'll for Pfizer and moderna - and maybe doctor should look at the objective data and not blindly follow the paid for establishment
Did we know at what tissue temperature did SARS COV2 better replicate?
At TWiV 659 at min29 virologist Christian Drosten indicate that to replicate SARS COV2 better ,must decrease incubator temperature.
Theoretically, high mucoseal temperature decrease SARS COV2 replication
May be, must not decrease fever ,If are not excesive to decrease SARS COV2 replication?
No, the vax injured are the ones who get more rejected and more stigmatised. I hope these guys are more up to date by now.
If anything the jab may be causing or exacerbating autoimmune responses. That's the jab and not just a bout of corona virus.
I still can't smell or taste over 2.5 years of catching covid for the first time. I had a mild sickness. I have brain fog as well and push through my fatigue.
I think my daughter has problems from catching covid last year. Her legs are numb and painful and she has constance dizziness. We are not jabbed.
I reccomend prolonged fasting. DYOR on the topic and make sure your in the right health to do it safely. I have seen a great improvement in my LC after a 3 day water fast paired with supplementing RESVERATROL & QUEURCITIN. This triggers autophagy and clears the blood of spike proteins!!!! I have more supplements that will help, comment back and I will tell you!
same symptoms, no taste/smell for 3 years :/
youve been quangoed
I wish my GP would watch this.
your gp is a mug like you, no worries
The interviewer here reminds me of the jerk doctors my daughter has seen who have told her her symptoms were just her having panic attacks or some other useless crap. My 27 year old daughter after having COVID had an attack where out of nowhere she had a group of strange symptoms hit her .. From the onset many more symptoms followed . Loads of tests have been done but nothing show up yet my healthy, happy working daughter became debilitated.. For months she could not work , drive or anything that she did prior to this attack that came on the tail end of having COVID.. We finally found a rheumatologist who was willing to treat her with autoimmune meds which has helped her tremendously but NOT cured her. She has been able to get back to work , a work from home job and now drives again etc… We need to go to one of these clinics..
Is long covid due to the untested vaccinations or due to the virus as most people have had both. The vax does not stop infection like it was supposed to so it is certainly not effective may not be safe either.
🤤
My life has been a nightmare since I had the jab with neurological problems developing a month after. 36 at the time, not exactly old and perfectly healthy, not a thing wrong with me at all, ever and it's completely ruined my life, I have a permanent tremor, mostly in my face and a list of other problems, unbearable tinnitus to name a couple (that's not even the half of it). I literally have the same symptoms listed off as long covid, which funnily enough, I started getting before I got covid but I had ther jab. I did get covid nearly 4 months after the jab but these problems had already started. My guess is everyone got the jab and had covid who has these problems and it's being palmed off as long covid to protect powerful peoples interests.
@djkurtstudio Totally agree with you. I was a very fit 68yr old until I had my 1st covid shot over 2 yrs ago. Lost my ability to walk a few weeks after the jab and remain with severe balance problems and a semi paralysed right leg. Never had a covid infection so far.
It's June 2024 and I still have pain in both arms. I can show exactly, the points on both arms where they injected me with the vaxx poison! It's been three years.
Try going to an holistic doctor to detox
@@antonellal7827 I did. Nothing! Cost me $60 also.
@@aarongarcia9880the devil is within you. Be grateful.
I wonder if people have heard of post polio fatigue that can start to happen 20-30 years after the start of the infection. Long Covid might do the same thing.
You sound exactly like me, and I already had POTS so I'm a mess
And jut so you know this condition happens with other viral infections as well it is called Chronic Fatigue Syndrom M.E. all this fancy words for nothing...