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I developed this in 2019 when I turned 16 I am a male. Happen one month after a viral illness this lasted like a year then it started to fade very slowly. Until 2022 is when I rarely had episodes however that left me with anxiety but I managed it and felt 100 better until 7 weeks ago caught covid and again feeling like in 2019 😢

Doctors have little to no clue, unfortunately.

Google image vitamin compatibility chart (it is a picture of Red Yellow and Green squares)// these combinations are for the nervous system (also mental health) B1 (Thiamine) + B5 (Pantothenic acid/avocados) // The reason there is 4 or 5 different clusters is because if you look at this chart some vitamins cancel the other ones out// B6(Pyridoxine/ causes lucid dreams), B2 (Riboflavin/ dairy products), B3 (Niacin), Zinc /// B12, B9, B5, Calcium, Magnesium/// Vitamin D + potassium ( this is a good combination after work really easy 10,000 IU vitamin D and a banana/// Vitamin E, beta carotene (carrots/synthetic vit A is toxic) , Alpha Lipoic Acid, Vitamin C// To make red blood cells you need Iron + Vitamin C and then two hours later B9 and B12// Vitamin C destroys Vitamin b12 and vitamin C makes Iron absorbable// Good luck with the leap of faith trusting this information!! More red blood cells = Faster healing

The only precident for treating latent ebb, cms, hhv6 is the work by Martin Lerner and confirmed by Kogelnik and Montoya. Valtrex + valcyte early treatment in CFS yielded most favorable outcomes.

I have long COVID and it’s been 17 months I think. I get sick every single month for 3 weeks. Bad headaches, dizzy spells upon standing, racing heart. Out of breath , coughing and runny nose constantly. I can no longer breathe out all my air. My breathing function is not functioning very well. Scars on my lungs. Do I have Pots? Great question.

Best thing I did, when I started experiencing this, is, not going to a Doctor and getting a "diagnosis". I researched how the human body works, relating to my constantly growing symptoms. I understand enough now, thanks to the various natural health doctors on RUclips, that I'm 75% improved. The brain inflammation was becoming dibilitating, before I found anything to touch it. High dose Bromelain gave me immediate relief. I didn't have to lie down ALL day anymore. High dose B1 (thiamine) and electrolytes also helped me. Now, I'm on the Carnivore way of eating, for 6 weeks, along with the aforementioned supplements and iodine. My organs are functioning again, though my energy is limited. Carnivore is handling the inflammation I had and nerve dysfunction (peripheral neuropathy) is 80% better. My brain is the final hurdle. I feel hopeful now. I think Carnivore is helping my whole body heal.

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There are a lot of PubMed articles linking long Covid with parasitic infections! Oh and don’t bother doing a stool test through your GP. They are SO flawed because they only tested for certain parasites and only do a 1 day stool test. A 3 day stool test is really what is needed for accuracy! My naturopath just ordered the GI Effects test from Genova Diagnostics at my request because I believe this could be what’s driving my long Covid for over 3 years now. I have done so much reading and research over these years trying to get to the bottom of this! My husband and I have spent close to 100 k trying to figure out what’s wrong with me! 😫😭🤬 It truly is criminal!!

You should come to NH and interview me. I’ve been suffering debilitating, systemic symptoms for over 3 years now. Tell me I haven’t wanted to end my life more than a few times… 😔😫😭🤬 I’m anxious, depressed, extremely sad, and pissed the F off for having to live with this for so long and ZERO help from “Pharmaceutical agents”…. 😒 I used to be so active and loved hiking the White Mountains of NH with my husband. I was happy, vibrant and active! Now I can barely get up a flight of stairs. The last slap in the face for me was being denied SSDI. I am 43. I got Covid 2 months after my 40th birthday, in April 2021. I guess they figure I’m too young. I had to leave my job by Dec 2021 because I couldn’t function. I waited 2 years to file for SSDI, trying all the while to get better, get healthy and go back to work! I changed my diet and lifestyle, make all my hygiene and cleaning products to cut down on the toxic load. It’s now Aug 2024 and I’m still suffering just as bad! I will now be getting an attorney to take them to court. We should not have to suffer like this, not be able to work and then be made to feel like it’s not that bad. Talk about insult to injury!!! 🤬🤬

thank god for an amazing doctor!

I feel so much for Kelcey. I am going through the same thing. Haven’t been the same since getting Covid the first time (had x3 now). Found out I have Lyme disease too, along with Hashimotos … it’s been 2ish years of hell.

F our government for doing this to people. Absolute travesty.

Gotta throw a rainbow 🌈 person in there- For the algorithm- Such a crock of shi+

We are losing muscle mass, you fooking evil tyrants.

What is she dying from?

Mes commentaires sont effacés, d'après les commentaires je trouve qu'il y a un maximum de personnes qui sont accrocs aux médicaments et la vaccination 😂😂 Prenez vous en charge sinon bigpharma se fera un plaisir de s'occuper de vous

So I found out that a lot of tachycardia events is connected to things with the gut but also connected to this dysautonomia I noticed when I'm super hungry or need to have a bowel movement my heart rate would increase slightly (which never used to happen before covid ) but if I eat late and go to bed late I'll wake up with tachycardia that kinda actually wakes me up out of my sleep and as a person who has experience anxiety at 16/17 now at 30 I've never felt my heart beat so fast during those moments and thats how i knew it was definitely not anxiety but 6 years into the pandemic and still no absolute answers.

Me too.

I think the only thing that could keep me going, is the fact that someone in the world is actually trying to find an answer or treatment for this terrible condition. I don't suffer from this, but i have chronic pain and many days i don't find my life worth living. But hearing how you handle your illness, gives me ideas to handle mine.

Interesting!

Im sorry you had an Abortion. Thats so Sad. I hope you make a full recovery. Doctorsnaee not God. Remember that.

I've had ME/CFS for 27 years, plus diabetes type 1 for 30 years now. I was 3 years when I was in a diabetic coma because the doctor said it would just be an "inflammation of the bladder". By the time I got ME/CFS, I was 6 back then, I already knew that nobody would help me, I had experienced the same even with diabetes type 1 already... After 23 years of having ME/CFS I diagnosed myself as it got worse from a new infection. This was before Covid, in 2018, that I had this infection, and I found out in 2020 that I have ME/CFS; and even with the current infection in 2018, doctors still said I would just be lying because I would be lazy. Doctors who had never seen me before! Meanwhile I have found a doctor who has diagnosed ME/CFS, but only 2 or 3 months ago this year, in 2024. This is incredible, really. And I found a therapist who knows what's ME/CFS, very exactly, I found her online at the beginning of this year during my daily research since 2020. After 27 years I have doctors who believe me and don't say I would be a liar. Incredible. The only one who never said I would be lying with being so sick is my diabetologist, I have had her since 2014, only doctor I have ever trusted until this year. I live in South Germany.

Well done. The answer to being valued, having a purpose, contentment, and joy is found only in Jesus Christ. He is our creator, Colossians 1.18. He loves us. ❤

I have had long flu for 24 years

Long Covid is reactivated EBV.

The globalistOccult is Hell-bent on Geneti-cide,& enslavement of humanity(like the days of Noah,& "man of perdition"👹 comes before Jesus' 2nd coming) We must get right(if not yet), w/Jesus Christ/Savior, He paid our sin debt❤ on the cross& arose again, so we can spend eternity in Heaven-

The jab should never have included the entire spikeprotein/ most dangerous part- look up how to detox from spike& miniclots etc. I've heard about zeolite, immunoglobulin treatment,& ivrmctn. Also a detox for metals- May you be well soon!

I’ve never seen the medical profession ignore and gaslight people that are very sick like they are now! Sick for three years now from one vaccine and NEVER caught Covid! We were lied to and therefore could not make a informed decision about the vaccine.

Long covid is a TORTURE, until i'm still suffering all these symptoms that it make me unstable and unable to do my daily task like i use to, long covid ruined my life...

I didn’t leave my apartment for two years! Saw no one! I’m retired and was terrified. I had the first two shots and no more. Never got Covid. Still not. I have PTSD now and at 73 I had a heart attack”thing” with A-Fib last month. I think it was brought on due to depression. My strength is starting to get better. 🤞

This long term trauma I lay at the feet of Donald J Trump! PERIOD…!!! He needs to be held accountable for this and all the deaths…!!! The Hague needs to put him on trial. He KNEW IT WAS BAD AND DID N O T H I N G !!

The immune system is over shooting and has problems shutting off. 3 reasons 1 you need vitamin D blood levels to be adequate (50 to 100 ng/ml) 2 Glucose metabolism (from eating carbohydrates) and high insulin is inflammatory. 3 overweight is also inflammatory. You can start by taking at least 10.000 IU of vitamin D3 daily. Eat only meat no plants, drink only water. This low carb diet will also get you in ketosis and help you lose weight especially liver fat and belly fat.

I wanna know if it’s hereditary too

I have dysautonomia since the vaccine, Covid long exists and vax long too. good luck to every body, it is an awfull desease

It has been around 31 years now since I started to have symptoms of ME/CFS when I was in my twenties. I received all sorts of discouraging and hurtful comments from many doctors. People around me, family and friends with good intentions tried to help and came up with different suggestions, they probably ended up being frustrated that I didn't make any efforts to get better. They didn't know that the illness were so complex. I really couldn't follow their advices. By the time I got diagnosed was almost 15 years later. At the time there were only a few doctors who were seeing potential patients. I had to travel far to see one and the journey itself made me felt so sick every time. The CBT helped me to manage my life from day to day. I could cope with the illness better until the menopause symptoms added to the existing conditions. I got so depressed, may be due to hormonal imbalance. I felt like giving up and almost let go of my life. From the beginning until now, I haven't had any help from any welfare. The doctor who came to review my conditions years back didn't give me an approval for any state help because he met me when I was slightly better e.g. could have showers myself, etc. It would help to have a badge for my then husband to park nearer to the buildings, when I used a wheelchair. Now I don't really have friends. My conditions automatically made me a fussy and an unreliable person to talk, meet or arrange anything with. My friends are mostly my carers whom I pay everything privately. I also just got divorced because it must be very hard after all these years for my ex-husband. Everyone who encounters this illness has each of their own stories. We have to endure but life goes on I guess. Thank you all the people in this episode for enhancing the awareness of these conditions and hope both ladies and other sufferers whether it was from the COVID or from other causes will get better. Apologise for the long message, it did take me a few rests to write:)

Shedding is a problem for me. I’m exhausted.

Guess what? Shedding is real. I’m exhausted. Doctors gaslight all of us. I’ve had tremors ever since someone used my nose spray without my permission or knowledge.

EVIL... vax 🙏🙏🙏🙏🙏🙏🙏

The nose blowing transitions, was it intentional?

Are the covod survivors with POTS all VACCINATED? THEY DONT SAY!

Is she vaccinated? They wont say......

Just for the video, TAKE OFF THE MASK!

Unvaccinated people don't get LONG COVID....

All people with Long COVID are VACCINATED.

This video was so beautifully done. God bless you for making it, and may an intervention be found soon that can help to pull those with Long Covid out of this. Research parameters should be followed in the future, not given a nod and moved offshore. Thank you so much for your work.

I got Covid in 2020 , it lasted a year & half , it was the worse period of my life

I'm dealing with ME dysautonomia x 30 years now. I am glad you have each other!!! The majority of people lose their partners and family

Using ANU figures for long Covid and the ME/CFS support organisation there are an estimated 1.5 million Australian sufferers but nobody is talking about this.

I just stumbled upon this episode and am now scrolling through channel. I am 3.5 years in. PASC (Long Covid) MECFS POTS. Hashimotos. Psoriasis. Asthma. It’s amazing these shows are out here but the gaslighting is still going on. It’s upsetting.

I sympathize with this young lady. I’m not in a wheel chair yet but have had my share of major problem since the vax in 2021. There has not been one Dr that takes me seriously so I just get sicker. All of these Drs that refuse to help people should have their licenses revoked. I realize that these Drs do not know what to do but do they not have the drive as a Dr to just take some time to do some research And at least try to help? I have been gaslighted and dismissed so many times that I don’t want to see another Dr! The medical field has failed the American people!!!!!!’n