I hope you all found this lesson helpful. For more information on Chronic Fatigue Syndrome, please check out my lesson on it. ruclips.net/video/FwiaoKrdzx4/видео.html
Here's an idea. How about you discuss damaged mitochondria and how we do not have a function e- chain and thus don't produce enough ATP, to live? Please, discuss this issue which lies at the basis of fibromyalgia and its fatigue, nay exhaustion.
dont forget syphilis, the usual cause. corresponding with penicillins invention and wide use along with vaccines everyone thought the vaccines were working while the penicillin was actually CURING. vaccines masked the symptoms but syphilis causes tuberculosis, poliomyelitis, hepatitis, macrothrombocytopenia/leukemia. we've been pathogen primed, usually shows up when your immune system is weak, when older. congenital defects meant to shorten our lifespans. less SS. Syphilis causes almost every disease and defect. that's why they used to test for it before marriage. now they make money off of them.
after I was treated with penicillin my depression anxiety muscle joint pain hair loss thyroid hormone issues, back foot pain, utis, chronic upper respiratory infections, infertility miraculously disappeared. then I got curious. the problem: cheap unreliable testing methods if docs deny false positives and negatives while testing, we were all screwed. use PCR. Err on the side of syphilis. a little penicillin never hurt. ok it did but worth it. but doctors don't cure the "manage" symptoms.
"you will not surely die, but you will suffer " the devil said to Eve the symbiotic pathogen, "snake" trickster imitator God was trying to warn us about. spirochetes. the key. represented as apples/sores in Eden. they have the ability to clone our DNA using the Y chromosome. using us to grow clone hybrids. grown, not born of God. it presents as sacral dimple, an umbilical directly to nervous system, brain. we see it now it 1 in 50 children.
Life with fibromyalgia is an agonizing slowly painful dead sentence. I have had every symptom, every pain and sometimes I'm just tired mentally that I wish I could go to sleep forever.
Check out Dr. Eric Berg on RUclips. He has helped alot of people. Don't give up. You are not alone. It's an epidemic. The food they push on us is poison.
Please take turmeric tablets. I started taking them 6 years ago and l am now 80% better. Turmeric changed my life, before that l had such severe symptoms that l wanted to die.
@@despinacharalambous1728 thank you, will try. I use acupuncture, works but expensive. I have few flare ups, maybe once a yr. I have S.A.D., summer affect.
@@robinryan3408 start taking turmeric it would change your life don't waste time. You will notice improvement immediately but with time as it builds up in your system you will feel better and better. Turmeric is inexpensive you can find it at the pharmacy store and here in Australia you can even purchase turmeric tablets or capsules at the supermarket.
I have had fibromyalgia for 30yrs. Now I had fibro B4 I had any stress or Axiety! And anyone with this exteam pain & Fatigue is bound to become a bit depressed. None of us who suffer with this real physical illness are just depressed....we have a real illness that becomes overactive to pain and hypersensitivity to how our Brain processes pain dont give up they are on the verge of a real explanation of this disease...
Also genetic…once I learned I had fibromyalgia, during menopause…I looked back at the symptoms and realized a lot of the problems I had had most of my life. I major wreak, in hard and spine, major abscess in strep throat along with tonsilitis. Dr. Passed off as flu. Very stressful life pastor’s wife. And much more has got me to the limit. My marriage is very toxic, but really have no way out. Hurt by lots of people….
So very sorry melody Hang on to the Lord the fibro feels as if caught the flu and never got rid of it ...God knows and those who dont understand try to escape toxic people and relationships it can make it worse it's not the cause but surely doesn't help may God help you 🙏💙
Did you try celery juice in the morning dont eat an hour before or after consuming it even ancient Hebrew texts consumed celery if any problem with the body or bones as celery itself is naturally formed in the shape of a bone! Take it for a week as I did and I began feeling more energetic and clarity of mind mildly euphoric also as it was absorbing into my cells. Read psalm 91 it helps me a lot in times of torment or watch a great 'Tom Loud'(channel of the same name) short video on youtube called 'psalming'(just type 'psalming' next to his name) which in simple terms will change your life for the better Amen🔥👑🕊
I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia, he has the permanent cure for all types of disease and viruses....
I think something is wrong with our nerves and fibromyalgia is a blanket diagnosis. My symptoms started after 2 car accidents. I then gradually got si joint dysfunction, sciatica, peripheral neuropathy, pseudo tumor, and then fibromyalgia. I had a 35%ejection fraction they still can't figure out why. They don't know. Every thing is a guessing game and a cope out. We need real answers
Very interesting, informative presentation. The well laid out diagrams are helpful in achieving a better understanding of the biological processes, much appreciated for work well done. Makes more sense to me now of how rheumy made the Dx. On the other hand, my immunologist scoffed at the mention of me having fibromyalgia, he doesn't believe fibro exists, but nor does he believe that lupus or other autoimmune disorders are associated with primary immunodeficiency/cvid..
i hate fibromyalgia. i have things structurally wrong with my neck and back, so the pain just from walking can trigger a flare up. But i still try. Menopause has been a blessing. im on so much medication and take so many supplements. but i keep trying.
My mom have osteoporosis reumotoid arthritis combined with fibromyalgia 😞😪for 21 years she’s always in a lot of pain nothing help’s her anymore.she suffers from depression due to her pain.thank you for the information I appreciated
No, SNRIs have NEVER helped me. At all. Like nothing. Except I get worse headaches on them, from them. Most of what doctors push are band-aids. There is something wrong at the subcellular level. Helloooo....the mitochondria. I don't have any energy. Limited amount of ATP. Like a zombie. This needs to be treated otherwise all of this stuff that is given to us won't help. It's b.s.. I am a biochemist here and I have studied pharmacology in grad school. Serotonin is not the only reason we are fatigued. We literally do not produce ATP and NADH in our cells!!! Our mitochondria is compromised.
SNRI was one of the worst experiences of my life. It worsened everything particularly depth of depression. Cessation was a literal nightmare. I believe you’re right about mitochondrial dysfunction
Read "The Mood Cure" book, take the questionnaire, fibromyalgia would fall under Chapter 3 due to a tryptophan>serotonin>melatonin deficiency. Life changer
I was diagnosed in 2002, after three years of investigations by various doctors and being told it's in my head MANY times. from a persona intimate experience avenue, this is something people who do not have it simply cannot understand, they hear pain and have differing understandings and imaginations of what that means in regards to their own experiences of pain, but it's nothing like they imagine. I'm at a point now I simply cannot remember what it was like before it started, so even I can't really explain it now as I no longer have a reference to example from. but, at the lowest level I sit at is akin to the aches you have when you have "the flu" or a bad cold, and then, given different things, be it seasonal changes, stress event, doing too much (which varies constantly and inconsistently) and sometimes, for no reason I can ascertain, it can change a little or a LOT, the high levels are.. intense, it feels as if my bones ache, you have sore spots and areas that move, morph, phase, something like a cross between a plasma ball and a wax lamp, sometimes it's so much that it just becomes a thick fog of pain, everywhere. then there is brain fog. it's like being stoned without the fun parts combines with being drunk, you get stupid, it's like trying to think through syrup, but it also HURTS to think, you brain loses the ability to connect words and even concepts at times. then throw in skin and light sensitivity the very air touching your skin HURTS, it burns, and even an electric sensation, all combined and phasing into and through each other. there's weakness, pulling muscles for no darn reason and more, one forgets some of it until you're in the thick of it. it is a hellish existence. not all fibro sufferers get the same symptoms, a lot have other conditions that make it messy to know which is which symptom. so it's hard to compare to each other and to understand each others experiences of the syndrome.
@@edensmith206 in my 20 years of going through this, I've tried all sorts of treatments and drugs, and the only thing that has any constant effect, is hot showers. it calms the whole mess down for a while, as with everything else fibro, to different levels. but generally it's a decent improvement. for a while. pain killers mostly do little, and those that do much tend to make you tired or high (which I simply do not enjoy at all) so I take low doses. at most 30mg codene x 2 tablets. no more and that I won't take more than two days running. it's too easy to build up tolerance otherwise, and too risky to form an addiction. so it's hot showers and some anti inflammatory like voltaren (also max 2). and learn the arts of distraction when at home. be it games on pc/console or something you can get into deeply so that you don't notice you're suffering, until you can't ignore it, then hot shower again. heated pools also great, with light resistance exercise while soaking I tried low dose naltrexone, it worked well for about six months and then slowly got less and less effective till I gave up. the thing to remember no two people with fibro symptoms have the same symptoms nor react the same to treatments. so keep your mind open and try them all. but, before tying any, be sure to read up on as much info as you can for each drug, especially for side effects so you can go into trying with eyes open and knowing there may be bad experiences. some I have been unwilling to try because the potential side effects are terrifying. be aware and be careful.
Approved Drugs People with fibromyalgia are typically treated with pain medicines, antidepressants, muscle relaxants, and sleep medicines. In June 2007, Lyrica (pregabalin) became the first FDA-approved drug for specifically treating fibromyalgia; a year later, in June 2008, Cymbalta (duloxetine hydrochloride) became the second; and in January 2009, Savella (milnacipran HCI) became the third. Lyrica, Cymbalta and Savella reduce pain and improve function in some people with fibromyalgia. While those with fibromyalgia have been shown to experience pain differently from other people, the mechanism by which these drugs produce their effects is unknown. There is data suggesting that these drugs affect the release of neurotransmitters in the brain. Neurotransmitters are chemicals that transmit signals from one neuron to another. Treatment with Lyrica, Cymbalta, and Savella may reduce the level of pain experienced by some people with fibromyalgia. Lyrica, marketed by Pfizer Inc., was previously approved to treat seizures, as well as pain from damaged nerves that can happen in people with diabetes (diabetic peripheral neuropathy) and in those who develop pain following the rash of shingles. Side effects of Lyrica including sleepiness, dizziness, blurry vision, weight gain, trouble concentrating, swelling of the hands and feet, and dry mouth. Allergic reactions, although rare, can occur. Cymbalta, marketed by Eli Lilly and Co., was previously approved to treat depression, anxiety, and diabetic peripheral neuropathy. Cymbalta's side effects include nausea, dry mouth, sleepiness, constipation, decreased appetite, and increased sweating. Like some other antidepressants, Cymbalta may increase the risk of suicidal thinking and behavior in people who take the drug for depression. Some people with fibromyalgia also experience depression. Savella, marketed by Forest Pharmaceuticals, Inc., is the first drug introduced primarily for treating fibromyalgia. Savella is not used to treat depression in the United States, but acts like medicines that are used to treat depression (antidepressants) and other mental disorders. Antidepressants may increase suicidal thoughts or actions in some people. Side effects include nausea, constipation, dizziness, insomnia, excessive sweating, vomiting, palpitations or increased heart rate, dry mouth and high blood pressure. Studies of both drugs showed that a substantial number of people with fibromyalgia received good pain relief, but there were others who didn't benefit. Lyrica and Cymbalta are approved for use in adults 18 years and older. The drug manufacturers have agreed to study their drugs in children with fibromyalgia and in breastfeeding women. read up on side effects before deciding.
I bend down to your feet for such a beautiful explanation how serotonin,cortisol, all immuno, endocrine mechanism affected in this case. Where i have faced.. 90 % doctors whom i came across had no idea about this disease. The symptoms endlesz. The pains itself..so many types.. .only the kind of pains i suffered i can write 2 pages. Thanks to you for such an excellent teaching. Please educate the world..about this disease, these patients are given antidepresants bcs of serotonin defficiency, patients show symptoms like depression. And naturall, with this invisible disease and endlesz pains and symptoms, with no doctors understands, as label them as psyche..also family doesnt believe. Even i suffered too much chemical sensitivity too , couldnt tolerate any allopathy medicines.. Fibromyalgia..leave the patients in a very miserable state
For all suffering from fibromyalgia should screen for celiac disease. Or should take gluten challenge test and again screen for celiac disease. I have been cured from this disease.
JJ Med, very informative video. You delivered intense breakdown of this "disease". I suffer from Spinal /Facet Joint Arthritis, throughout my spine , sites of Stenosis, SI Joint Inflammation, arthritis in my hips, worse in my knees and into my hands as well. Due to all my chronic pain and chronic anxiety (They go Hand in Hand), he diagnosed me with FM. I just started to take 5 HTP (after doing much research), at night. I'm being cautious because for many years I've made myself a Guinea Pig with a cabinet Full of Supplements : Proelytic Enzymes, Mushroom extracts, Grapefruit seed extracts, Turmeric, Ginger, Cinnaman, Alpha Lipoic Acid, Various Amino Acids, Probiotis and Prebiotics, and more. I'm 70 yo. I fractured my right femur in 1966 playing HS football. That fracture resulted in a 1" shorter right leg which was left Unaddressed for many years. Boy, was that a Mistake. That Leg Length Discrepancy has Wreaked Havoc with my Spine, and hence my Well Being. My first Cervical MRI in 2012, showed that I had a More Narrow Than Normal Spinal Canal. I am convinced that the narrow spinal canal, mixed with the degenerative disc disease (DDD), and sites of Stenosis and the Dextroscoliosis (25 Degrees), which has greatly impacted my Central Nervous and Peripheral Nervous Systems has produced the FM. I am currently weaning off Gabapentin , weaned off Prozac months ago, and I am willing to Try Anything to get out from the Hell Hole of Fibromyalgia / Anxiety / Chronic Pain.
If you truly want a better life with less pain and no poison being put into your body, go with psychedelics. Psilocybin mushrooms, DMT, LSD, mescaline they all have benefits. Find yourself a shaman or someone with lots of experience within the field. Don’t do it alone. I guarantee you will awake from your first journey a new person. It’s not about eliminating the pain it’s about accepting it for what it is. The medicine helps but you need to believe and do the work.
🙏🏻♥️ Magnesium malate + EPA-GLA is also a great way to get better from Fibromyalgia. But most of all, stay avoid stress and negative energy - find people and thing's that make your happy. ♥️ Love from Denmark
I’ve tried a couple medications to increase my serotonin and I always have an allergic reaction. It’s like my body can’t process the excess. I have Fibromyalgia and Depression so it’s very hard to find something that works.
How can i PLEASE get this excellent video in spanish? I've suffered this illness for almost 30 years and need to show my wife and family what's really happening to me. It would help a lot because they really don't understand .. i've had post traumatic stress síndrome for 40 years.
Can you use a second phone to record the audio and then have ChatGPT translate it for you into Spanish? It will be a written transcript not audio when it’s done of course.
Fantastic video!! I have fibromyalgia, melatonin before bed is a game changer in regards to sleep and increase in REM sleep. There seems to not be much research on fibromyalgia, I would love to see more. Also I wonder about a histamine response related to fibromyalgia as well as the irritation level due to overstimulation of all my senses. Doctors wanting to start testing for Functional neurological order, it seems like they are guessing these days.
Save your time. I've been sick with FM for almost 40 years. All I do is search for help but the truth is everyone will tell you their version of what they think it is bit no one can tell you how yo get better. I can tell you that all the studies and world experts I have dealt with were all wrong about their conclusion. FM has been around for hundreds of years and today April 3rd, 2021 there has been no treatment, no cure and no actually scientific fact of anything . Sorry I couldn't offer you promising news.
@@youknowcrimedontpay9257 100's of years? Where did you get a that since MF mimics so many disorders? I particularly think the problem is with all the chemicals and pesticides and who n
@@elementalsfourheaven3401 I read your comments and I don't disagree nor agree and not because you are wrong or right. ME has more of a sleep disorder association with the lack of Slow Wave Delta Sleep due to Alpha Wave Intrusion. Some studies have shown that in FM patient there is a connection to human growth hormone from the hypothalamus which is a small region of the brain. It's located at the base of the brain, near the pituitary gland. While it's very small, the hypothalamus plays a crucial role in many important functions, including: releasing hormones. These hormones play a crucial role in the body recharging its self during deep REM sleep which patients with FM do not acheive. Without Restorative sleep we are exhausted and not just tired like working too long or staying up to late. Our bodies cannot recover energy which is what we need to feel refreshed and ready to go when we wake up. No matter how much sleep we get we cannot achieve the energy we need to operate as normal. We try to explain this to friends and family but they just think oh that person needs a vacation or needs to get to bed earlier. Now not everyone with ME has any muscular wide spread pain or depression or other symptoms that they can account for. That being said, in my situation I have all symptoms of FM and ME which I personally believe are the same as each other because the initial causation is a sleep problem that has a nurological associaton. Many of us with ME / FM and or just symptoms of ME without pain try to pin point how, what, when triggered our mysterious illness. Some of us received a vaccination, some had early childhood trauma, some had physical injuries such as automobile accidents, and other potential life altering issues that could have what I think set off our illnesses. I do not believe we just got sick I believe we were born with our illness and something triggered our sickness. If you have never had a sleep study polysomography you should have your physician send you for one. Restorative Sleep is so necessary and plays a hugh role in everything we do to surrive. The lack of restorative sleep beings on pain and with a vicious cycle of nonrestorative sleep 24/7 the body is in pain and eventually the body comes to realize it will never escape this life sentence and it becomes depressed. Some doctor's believe FM / ME is FIRST a depression related issue thus depression causing the pain and then the insomnia however I think they have it backwards. Its the story of what came first the chicken or the egg. How can there be chickens without a chicken laying an egg? The term Chronic Fatigue Syndrome has been used to describe people who feel tired but ME Myalgic Encephalomyelitis is also at times believed to be the same thing. Eventually the name Fibromyalgia will be changed to Central Sensitization. FM is the Greek name for Fiberous tissue / Malgia is the Greek name for pain. When I said 100's of years we know that FM can be dated back to at least 1820 and because medical records were not so well kept further back then that I would suggest it goes back as far as humans have been alive. Fibromyalgia tender points were discovered in the early 1820s. The condition was initially called fibrositis because many doctors believed pain was caused by inflammation at the sites of pain. It wasn't until 1976 that the condition was renamed fibromyalgia. Unfortunately there is no inflammation with FM from what science thought. My theory is that ME and FM are one of the same conditions but not everyone has all the exact symptoms as each other. I hope my comments have helped even one person better understand our most mysterious illness and I certainly hope that sooner than later we all wake up one day a see that science has made the most precious miraculous medical breakthrough ever. God Speed to all my fellow people who so greatly suffer.
@@youknowcrimedontpay9257 thank you for sharing your research. Sleep is the one thing i have been complaining about for 20 years. at first they just dismissed me, probably because i was young, they said it was my "sleep hygiene" Recently, i had to have a horrible flareup that made my get so mad at my doctor that i refused to see him any longer and scheduled myself for a sleep study. As a a woman I feel that we are made to think that we are supposed to deal with chronic pain or certain issues and we.. well, at least me, start to believe it as well and push through everything... until well we can't
Keep shoulders raised and close to neck, do not wear bras. Always sleeping on the back and immobilizing the arms with pillows under the shoulders eliminates the traction of the suprascapular nerve. Limiting external shoulder rotations and arm movement can be a way of diagnosis if pain / fatigue subsides and helps relieve symptoms. The entrapment of the suprascapular nerve in the scapula produces traction on the brachial plexus. As a defense, muscle contracture is caused in the back, neck and jaw to avoid root traction. As a result of this, myofascial pain as well neuropathic pain of the brachial plexus and trigeminal appears. Fibromyalgia occurs when the local muscle contracture is not sufficient to prevent damage to the tracted / affected nerves and the body attempts to adopt a fetal position to protect the upper trunk. Movement against the fetal position of the body causes pain. Trigger points are the counted muscles, used to adopt the fetal position, and when forcing them, they produce micro-tears of fibers, triggering generalized pain. Thumbs up if it worked for you. Unverified, non-medical.
Unfortunately, some of us can't go outside without a bra as we have large breast. Otherwise thank you for your comment, I can't sleep on my back or stomach this last year and a half. Looking onto these neck pillows I keep seeing advertised to see if that can help.
Living with this fybromyalgia is like living with a death sentence. It’s notknown what actually causes it apart from trauma or major infection. I am so tired that I wish I could sleep at night which is virtually Impossible. So many illnesses are blamed for fybromyalgia. The only things it’s not blamed for is arthritis and cancer
ever tried kratom? i would highly reccomend, only for people who actually need it, it is a mildly addictive opiate but is nowhere near the strength of other types of opiates. it is a type of leaf with a long history of use in asia. it worked so well for me, normally i lay in bed all day. on kratom i could leave my house since the pain was gone. and it doesn't even get you high (although if you stop taking it, taper. it will suck if you dont)
I understand you dear,I'll advice you recommended Dr Obinyan on RUclips,he cured my wife from fibromylgia, after taking herbal supplement we got from him,my wife is totally cured from fibromylagia,my wife can now sleep peaceful with no more pains...
I’ve heard the same thing, regarding a carnivore diet, I don’t think I could do it. I’m already restricted with celiac disease. I find sugar kicks the pain in worse. I do think diet plays apart in Fibromyalgia pain, and if you have injuries the pain seems to hit those areas harder.
Fibro patients tend to have issues with Copper, either deficiency or a high NCC ratio where they have a higher percentage of free unbound copper to ceruloplasmin.
I've been in a flare for 7 months and DOESN'T want to end! I've decided I need to get back to working out before I lock up totally and become bed ridden!
I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia with his herbal supplement, he has the permanent cure for all types of disease and viruses...
@@mlou7432 no those types of meds always come at a price. Psychedelics have almost zero consequences. The bonus is that you usually only need one dose up to twice a week for extremely severe cases.
Didnt do anything for me 🤕 but ive been fighting this crap since 2016 and its so bad i have to taka opoids just so i can sleep because im in to much pain to sleep without.
The pain and fatigue...we as fibro sufferers experience is what causes the depression and anxiety over it cause it hurts more than our bodies or minds can endure!!!! Please dont blame the condition on depression or axiety!!!! Its the illness first then comes the secondary part of this horrible horrible illness 😢
That simply isn’t true. Those conditions usually contribute to the illness. Besides depression and anxiety are that of a weak mind finding an excuse to feel that way. Psychology plays a huge part in pain perception.
@@Mfield111 have you studied neuroscience and psychology? Anxiety and depression are merely that of a weak mind. The biggest thing that helped me was mindset first, then psychedelics DMT and Mushrooms in particular have a massive effect on these illnesses. Another thing that contributes to fibromyalgia high oestrogen and low testosterone. TRT helps a lot. Vitamin infusions again help a lot. What I can’t stand is when people make excuses. Oh the pain is too much no it isn’t the pain can always be overcome it’s your mind that is weak.
@@Dionysus_Athena you have the right to your own opinion! But, that is just what it is yours, not fact! God's mercy on your way the only way! And God help all those who truly suffer with all illness and diseases that cause them real pain and suffering! And only God knows what you claim to. Case over!!!
@@Mfield111 it’s not an opinion it’s a fact backed by science, medicine and spirituality. I’m guessing you’re a Christian which is why you find it so hard to believe and accept that there is more than what your book says. Acceptance is something everyone struggles with more so for Christians. Even harder for them is accepting that there is more than one god out there. Have a good day friend one day I hope your ego dies and you are reborn with true love and acceptance of all.
I am so grateful to Dr uzoya on RUclips who cured me from fibromyalgia with his effective herbal products. I will spread your good news here in the United States.
I think the Fibro... cause low level of serotonin, because Fibro... cause stress which will reduce serotonin. Increase serotonin not reduce pain , just reduce the sense of pain. The sense of pain is important of the human body operating. In this way the human system will try to cure the pain. so low serotonin is the result not the cause.
Low level of serotonin ,dopamine and nore epinephrine is caused by stress and depression actually your brain shrink if you are depress and stress so no amount of vit.intake or mineral intake will reduced these symptoms of fibromyalgia. You need to treat the root caused and it's very easy to treat it if you know the pathophysiology of how fibromyalgia and CFS/me work
Hello doll💞 Thank you for your channel 🙌. I’m a 58 year old female medical student and Degenerative Brain disease specialist, so I should know this, I have gotten rid of 9 autoimmune diseases, but Hashimoto’s is still a problem. I had continued traumatic brain injury during a physically abusive marriage and lost “ processing speed”, but the rest of the test stayed above average. I take 200 mg of tyrosine for new tropic benefit, but I wondered if you could suggest anything that works with the brain for the ability to process faster. Thank you so much for your help I pray you are blessed as much as you bless us🙏
High level of stress during a 17 years abusive mariage completely messed up my hole health. Suffering hell from severe fibromyalgia. Had a stroke five years ago. And severe endometriosis, had to take off uterus and others around. Please, excuse my bad English, French is my first language. So much toxicity and several forms of violence harmed me so much. Feeling like my life is over since many years. Only surviving for my two wonderful boys. Take care Everybody.
I’d recommend prevagen. Especially since you are an older woman. It works really well. You could also try lion’s mane mushroom but I still think prevagen would work best for you. Also remember not to take the tyrosine with food, as the nootropic properties are most powerful on an empty stomach.
Hi Jami how old were you when u enrolled into med school?and how do you like it. I’m 42 and considering career change and going to med school, Any suggestions?
Psilocybin hands down the best and most beneficial for what you are after. It not only repairs the brain at a faster rate than anything ever seen, it also creates and improves new neuropathic pathways.
I am a sufferer of fibromyalgia long time of 25 yrs. Flare up since last years. Csnnt explain the type of symptoms endles. Your vedio is very informative. I am sensitive to all medicines, chemical sensitivity is very high. Please do more vedios with diet etc which naturally can increase serotonin levels ? Or any ayurvedic treatment etc
I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia with his herbal supplement, he has the permanent cure for all types of disease and viruses..
All thanks to Dr Obinyan on RUclips,he has restored happiness to my aunt life,my aunt recommended treatment from him,to her greatest surprised,it work perfectly 💯💯🌿💚💚...
I’ve had Fibro since age 3-4, soon after my estranged father (rotting dead now) met me and tried to strangle me to death for yelling at him to quit beating the living snot out of my mother and sister. Soon after I was on the floor BEGGING mom to *cut my legs off*. I was misdiagnosed in 1985 (age 6) with Muscular Dystrophy- a DEATH SENTENCE. I was given 400, then 800mg ibuprofen for *years* while strapped in a wheelchair and “poster-boy” for a disease I NEVER HAD. At 18 I had access to the Internet (1997), found I met no MD symptoms. Square One. Went to EVERY specialist 3 times, did 3 killer 20+ session each rounds of physical therapy. I doubt this video mentions that according to everyone (professionals) PT and light exercise helps only 15% of patients. I’m 43 and due to my doctors’ giving up and/or retiring, in the worst pain ever. I want Heaven. Tried every drug in this video. Methadone helped most with a 4x/day Vicodin (then Norco), with open permission to “double up on the Vicodin if it’s bad.” My newest pain doctor picked up writing my methadone though cut Norco (this “opioid epidemic” is bull. Pure bull. If JUNKIES WANT TO DIE LET THEM. Narcan can reverse an OD in seconds. I NEVER abused my medicine. Methadone and Norco fill-in pain receptors in those WITH chronic pain. It is ONLY those without or a low level pain that ever get “high”. Let them die, because the paranoia surrounding what WORKS has scared 90% of doctors from prescribing ANY. That means zero relief. Zero. I’ve been on methadone over 20 years safely to help. Norco was cut 5-6 years ago 100%. My pain doctor (specialist) overheard me ask a nurse if other doctors were available to see at their practice and assured me they had others. Upon hearing this, my doctor FIRED ME. A VERY SCARY MAN with multiple complaints about his attitude, dehumanizing, degrading, insulting treatment of his patients. Dr. Willard of Michigan Pain Consultants. He cut me off completely. Today is my last dose of the half-strength 2 week refill he called in. He had planned to try me on morphine. I asked 3 times “if this goes bad, will you put me back on the methadone as I’ve been?” He said “Yes” all 3 times. 10 minutes later, after overhearing me ask about a doctor transfer within Michigan Pain Consultants, he said in no kind fashion “NOW YOU NEED TO FIND A NEW DOCTOR!” He *cancelled* my RX’s for morphine or anything else. He knew my history. He took an OATH AND SQUELCHED ON IT ENTIRELY. I have NOBODY. Except the street that wants sex and cash. What???? The pharmacist I asked about this was disgusted!!! Very concerned! I have a separate (?) heart condition and a month of tests ahead as my arteries are spasming (equal to a blockage, but 3-8 minutes per episode, up to 17 a night. I now have Nitroglycerin that stops them in under 10 seconds, but many tests to come). What am I supposed to do???? He LIED! His pride was more important than MY LIFE OR HIS OATH. What do I do? I don’t want to die! I’m terrified! Terrified! And I NEVER admit when I’m SCARED, but I AM SCARED! What do I do now?
I've had fibro since 2009. After many years of being on different kinds of pills & walking around like a zombie, I found that copious amounts of CBD and plain ol weed helps TREMENDOUSLY. Yes, I'm usually stoned every day, but I'd rather be illegally alive (weed) than legally dead ( pills).
@@chifreak6 God bless you kind soul!!! You’ve made me cry- but as you know, feeling *anything* emotionally is far better than the NOTHING you feel when the “professionals” are ruling your life like they are gods. They’re not gods. Their is One God, and I serve him. I also love weed. But to “pros” here they still just consider that (me) to be a junkie. Unless I take *their* junk. I live in Michigan, and pot’s both medically and recreationally legal. Except certain towns and cities like mine found a way to block its sale. It’s safer than a low-dose aspirin for Pete’s sake! I have to travel a couple hours to find it, from a Michigan based company called LUME. They are 100% legit, high tech labs, professional labs that grow organically hydroponically and their stores aren’t your old-style head shop full of hippies- they are highly (extremely) knowledgeable and have several strains and hybrids and the purest, best tested pot you ask for. Each strain is labeled with the THC content beyond decimal points in accuracy (my last, now gone, has “19.07%” printed on the bottle. They have every range of potency from 6-7%-25%, and ask what type of condition you may have or what your goal is for medicine or fun or both. I can’t wait to go back for more, and prices are actually extremely reasonable: less than 90’s college brown brick schwag for pure quality). You give me hope. Your reply means more than a text could ever mean. Thank you. God bless you, and I’m here for you anytime. Thank you, thank you, thank you! -Bryan
@@sideswipe1261 Wow. I'm sorry I made you cry...not my intention. It's ok not to be ok! Finally had to be honest with myself & realize it's ok to have days where the pain is so overbearing & relentless that you literally wonder what heaven is really like...as long as you can snap yourself back to reality and at least try to occupy your mind with more positive thinking...ha. It ain't easy. This has been my daily ritual and I mean that literally...my story is lengthy and actually thought about writing a book. In the hopes of possibly helping someone else. The big pharma peeps almost did me in. As well as many 'specialist'...and several practioners. I trust not many & am VERY selective as to who Iam able to choose for my medical care. Long story short, cbd & weed is what helped me get off ALL benzos & anti depressants. Iam blessed & very grateful that I always can get it too. I'm happy I could help you Bryan!! I wish you luck on your journey! Stay safe out there! Be blessed 🤞🙏✊✊ - Elaine
@@chifreak6 crying felt *good* after years of being a Zoloft-Zombie! I meant to thank you 🙏🏼 because after years of feeling *nothing*, finally off the Zoloft I am becoming MYSELF again! You helped me do that! I’ll always stick around if you want to chat!
I've had it since 2000. Ironically I had been on a higher dose of Prozac for a couple of years before. I have ocd and they started me on lithium than zoloft to Prozac. I felt so flatlined in emotions that I quit taking it faster than I was supposed to. It was probably only months later I started having symptoms. I'd never heard of FM. It started with burning hips and legs arms that felt like they were made of lead. It was exhausting. My husband had put me thru some things. But I also had 3 kids, lived and worked on a farm, and just thought I'd overdid it. I've been I. Many meds but the one that probably helps more is tramadol. It was somehow different. I've had a lot strong without much relief. Magnesium malate helps a lot! You'll notice more when you run out of it. My anxiety levels get bad. I stopped going places unless I had to. Brain fog isn't fun, as well as fatigue. But it's 2 am and I'm awake but tired. I'll be up by 6 I'm sure. I recently have been having trouble with my eyes. It can come and go during the day. I just happen to read on a pamphlet in my Dr's office that that's a symptom. If you sit too long you turn to stone, but don't overdo it either. Try for the sweet spot. I used to describe to people that I turn to stone and feel like a big bruise. If a child taps my legs or my pup jumps up on me it's like they pushed on a deep bruise. Another thing. When I went on an estrogen patch a few years ago I told my gyn that I swore it made my fm symptoms extremely worse.
I have been diagnosed with muscular dystrophy and kyphosis but what you have written here that's me please help some one.. can it effect your potassium levels also? x
@@R3Quency I personally have not had blood test that showed low or high potassium levels. I have in the last year been taking a potassium supplement a couple days a week. Mainly when I feel dehydrated a bit. The blood tests that showed anything were ones that showed inflammation and I also have a rheumatoid factor that's on the bubble they said. They said that means I hurt. But it doesn't indicate RA.
@@micci7795 I was unwell with tb and lost all my weight from 10 stone to 5 stone they treated it with chemotherapy , them I thought the pain was recovery from all the muscular wastage but I received a call for my doctors saying I need to go in urgent it turned out I had severe anemia, my back was really hurting I walk well strut my mum says like my dad , I used to see and osteopath who said there was something wrong with my spine.. after i was in so much pain I called my doctor about my back and they did xrays said it was kyphosis then in November I fell amd broke my hip well obliterated it. I had surgery and then I caught sepsis, it was said I may not walk again I could hear the doctors saying I dad muscular dystrophy , brittle bones and kyphosis I was saying NO its kyphosis! I was never actually told when they found I had these other issues but all are o my discharge note. After 2 months I got out of hospital with district nurses and home help and care package as I was getting more an more depressed in hospital, I was catheterisation for 8 weeks sometimes so stiff I can not get up for the toilet in time I am 45 not 95.. the pain is unbearable also whilst in hospital I got pressure sore ungradedable they are to the bone and I jeep have to have antibiotics to treat the infection in the bone but all my symptoms as like you.. please some one any one gibe me some hope or it this is life to just tell me so I ca just do things try to live not exists.. thanks for taking tour time to read this. kindest regards Carol x now I am always being tested for infections and last new symptom was my potassium levels o could not beath my chest heart I was more stiff than normally amd the list went on. sorry for tyops my motoring skills are going xx
@@R3Quency I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia with his herbal supplement,he has the permanent cure for all types of disease and viruses...
GABA helps too, especially if your norepinephrine is high and you are having a flare. Much like bipolar and diabetes, you get to regulate your own levels. Lol. Yay. Go me….If it’s pain from a depressive spell, the 5thp is invaluable, but cessation helps with that 60 day plateau. I take Kanna and Motherwort and Skullcap, but be careful with Skullcap, it actually can give serotonin disregulation.I don’t know why, but I think it had to do with cessation of several other stimulants around the same time like caffeine and add medications. I wonder if all of us really studied the half life of the substances we take, we’d fare better. It’s rather complicated isn’t it?
Having the MTHFR gene mutation must surely play into fibromyalgia and CF. Taking methylated B vitamins with 5HTP has helped. Would love a video about that connection if any.
I am taking vitamin D, managed to raise it from 50 to 77, but l take very high dose. Also taking b12, q10 300mg, probiotic, zink, selen, magnesium, Olive leaf extract. Started also recently with low dose of bento thiamine, will increase by time. I feel much better then before taking these supplements. I have found that all mentioned above could help, esp. Q10, higher dosage. I think we have some chemical inbalanse in our bodies. Also, my problems started when l had problems with gallbladder which is now even removed. But seems that metabolism of fat is not working properly. All is connected l.
For all suffering from fibromyalgia should screen for celiac disease. Or should take gluten challenge test and again screen for celiac disease. I have been cured from this disease.
I have been taking turmeric for something else. It has NOT helped with FM. What dose are you all talking about? I have been taking 500 mgs alternating days. Helps with my bad hip.
You might like to read THE INVISIBLE RAINBOW, ABOUT WHAT ELECTRICITY DOSE TO THE HUMAN BODY. It’s by ARTHUR FIRSTBURG. A HISTORY OF ELECTRICITY AND LIFE. All ATHESE SYMPTOMS ARE IN THAT BOOK!
Nope understanding human Conciousness is the answer you can help yourself Infact nothing can help like self help Sufferer for 20 yrs Believe me Iam proof 💜
I am so grateful to Dr uzoya on RUclips who cured me from fibromyalgia with his effective herbal products. I will spread your good news here in the United States.
@@Србомбоница86 I once saw a Neurologist as I've got CFS/ME/MCS & just said that it was depression......................! The actual appointment was for an under active bladder though, but as I said that had got CFS/ME/MCS he automatically dismissed it as depression.................................
Hello sir, Does thyroid medication cause low serotonin, even after taking thyroid meds there is body cramp and sleep issues and fatigue. Does this pathway get afftected with thryoid issues
My opinion is safe and affective. I have a very close friend he likes to do one heavy dose trip (shrooms) every other month. And sometimes molly, And in between he only take 5htp to level his serotonin.
I think most psychedelics psylocibin, mescaline, LSD, DMT are serotoninegic in nature so I would leave a gap of at least a few days of 5 HTP use before and after psychedelic use
Very interesrinf, I found this video because I just bought a supplement that has 5htp+magnesium and b6 and I was looking for info about 5htp, I have fibro, I been taking the supplement for a feew days and wow its awesome, I dont expect to feel this awesome for a long time but I enjoy any time it last hahaha, I have found that also helps to take creatine and aminos, helps reduce fatigue and pain I just started excercising (Just 40min per day,) again and the recovery its so much faster
Hi iv just resently detoxed off heroin and metherdone after 33 years on it i am disabeld du to a stroke i sufferd in my erly 30s i suffer from nuropaphick nerve pain down my left side i get a lot of electric shocks down my leg and arm on my left side iv got cronick fateege sindrome and i suffer with depreshon do you think i have fibromyalger ?
That's great you must not have a real bad case of it so that's nice God bless U...CFS is more than fatigue so you must have mild fibro or something else
@@Truerealism747 oh🤔💙 I've had it since 1993!!! It has gotten worse in my 60`s but Fatigue and pain the most prevalent symptoms so it's been diagnosed as ME/CFS and fibro a part of this! Sorry you have suffered it! I know ME/CFS for sure has degrees of the illness...I'm not the worse case scenario but by far not the least it is horrible God bless you
@@Mfield111 are you hypermobile? My father had CFS now ok years ago I e had it since 1997. Though now I no why diagnosed Asperger's add had I had SPD as a child.then had a accident then wind up began have your symptoms changed over the decades I've always had fatigue from birth due to being in spectrum I've found out and hypomobility
It's the nervous system is broken hardest thing to fix.. I do have connections going back to vac ines.. Was studying this, even before Co vide ones.. I think we being deliberately poisoned..
I’ve had fibromyalgia for 14 years now and I wouldn’t wish this reality on anyone. I don’t let it stop me because.. well I can’t. I work full time, I’m a single mom and I have too much depending on me. However, it’s excruciating to walk through life as a normal person when on the inside it feels like my body is attacking itself and no one but me can see/feel it. Shitty part is, I also have bi-polar disorder so I cannot take SSRIs or SNRIs. Although prior to my diagnosis, they did have me on them and a plethora of other prescriptions. Really none of them were impactful. Hot baths, reducing stress and meditation have been the only relief I’ve gotten over the years.
I'll advice you recommended Dr Obinyan on RUclips,he cured my wife from fibromyalgia with his herbal supplements, he has the permanent cure for all types of disease and viruses....
All thanks to Dr Obinyan on RUclips,he has restored happiness to my aunt life,my aunt recommended treatment from him,to her greatest surprised,it work perfectly 💯💯🌿💚💚...
I had fibromyalgia,I got diagnosed 2years ago,until I came across,Dr Obinyan on RUclips,I recommended treatment from him,to my greatest surprise it worked perfectly 💯🥰🥰
I may have fibromyalgia. I don't know for sure, but I will be scheduling an appointment with a rheumatologist soon. My symptoms come in episodes. All i can tell you when I have an episode I am in pain all over my body. My bones and joints hurt so bad. It is like I have a severe case of the flu. I am miserable when I have an episode. Yau'll I just hurt all over. It is not in my mind. I have been on Cymbalta for years and a mood stabilizer, Lamictal. I also take Trazadone to sleep and I take Synthryoid for Hypothyroidism. My grandmother has rheumatoid arthritis as well as my identical twin sister. Does anybody else experience these type of pain all over your body especially in your joints? There is sometimes that I hurt so bad I want to cry. Any suggestions would be greatly appreciated.
Was diagnosed 2009 with Fibro. Since then I have been on numerous medications. Currently on Cymbalta and Lyrica. I dont feel any better pain wise but it does help the depression caused by the pain. My best go to medication is good ol weed. Combined with copious amounts of CBD. Yea Im frequently stoned...but its way better than all of big pharmas pills. Id rather be illegally alive than legally dead ( btw its legal here now for recreational use thank God ). Someday i hope to be off of all pills but for now this is how it is.
@@chifreak6, Thank you for responding. I appreciate your suggestions. I can't smoke weed, because it gives me horrible migraine headaches. My next door neighbor smokes weed alot and when I smell it a migrane starts up and I can barely function, but i have nothing against people who do as I have friends that smoke weed occasionally.
@@prometheuspredator7971 well that's unfortunate. Im learning weed isn't for everyone. Have you looked into CBD?? I hope you can find what works best for you. Sending positive vibes 💚🤞✌
Why are you making so many videos about Fibromyalgia? Is this a medical area you are interested in? I have the disease and I am very curious. I am exploring some newer treatments in for it. If you wan to know what my docs are doing, I can let you know.
I would really like to know what license you have in medicine. There are laws about posting these things in the States when they haven't been actually proven.
You are flirting with a dangerous notion of information suppression which will lead to a dark age, just like 1000 years ago, with your non thinking and blind trust for the select few able to kiss enough butt to interpret Devine truths. Nothing is absolutely ever proven. In fact, not even laws of physics. Just certain things fit better and make better predictions, until some BETTER IDEA COMES ALONG! Everything, everything in medicine is merely theories. What passes for proof in chemistry and medicine, is idiotic to most mathematicians and people familiar with other proofs in physics....
There is WAYYYY more out there that you should worry about. This is educational and not treating the rest us as idiots like we are in the middle ages. The way that doctors practice medicine here is all controlled by pharma. Even the way professors teach. There is something very wrong when ONE doctor in a third world country can diagnose you while you need 10 here jumping from specialist to specialist meanwhile something as simple as vitamin deficiencies aren't even checked. Actually doctors don't even know much about nutrition. Its actually pathetic. So maybe you should learn from this and become a better doctor if you are really one. Also this just tells me how incompetent is my doctor.. when he hasn't paid attention in years to my chronic insomnia or acting quickly in preventing ANYTHING until some of the bloodwork comes out very bad .. there is no preventative medicine in this way of medicine. So having an adrenal crisis is find because they are all worried about having to see x amount of patients a day and have dont want to or can't put the effort in educating themselves further.
I hope you all found this lesson helpful. For more information on Chronic Fatigue Syndrome, please check out my lesson on it. ruclips.net/video/FwiaoKrdzx4/видео.html
It was very informative thank you x
Here's an idea. How about you discuss damaged mitochondria and how we do not have a function e- chain and thus don't produce enough ATP, to live? Please, discuss this issue which lies at the basis of fibromyalgia and its fatigue, nay exhaustion.
dont forget syphilis, the usual cause.
corresponding with penicillins invention and wide use along with vaccines everyone thought the vaccines were working while the penicillin was actually CURING.
vaccines masked the symptoms but syphilis causes tuberculosis, poliomyelitis, hepatitis, macrothrombocytopenia/leukemia.
we've been pathogen primed, usually shows up when your immune system is weak, when older.
congenital defects meant to shorten our lifespans.
less SS.
Syphilis causes almost every disease and defect.
that's why they used to test for it before marriage.
now they make money off of them.
after I was treated with penicillin
my depression anxiety muscle joint pain hair loss thyroid hormone issues, back foot pain, utis, chronic upper respiratory infections, infertility
miraculously disappeared.
then I got curious.
the problem: cheap unreliable testing methods
if docs deny false positives and negatives while testing, we were all screwed.
use PCR.
Err on the side of syphilis.
a little penicillin never hurt.
ok it did but worth it.
but doctors don't cure
the "manage" symptoms.
"you will not surely die, but you will suffer " the devil said to Eve
the symbiotic pathogen, "snake" trickster imitator God was trying to warn us about.
spirochetes.
the key.
represented as apples/sores in Eden.
they have the ability to clone our DNA using the Y chromosome.
using us to grow clone hybrids.
grown, not born of God.
it presents as sacral dimple, an umbilical directly to nervous system, brain.
we see it now it 1 in 50 children.
Life with fibromyalgia is an agonizing slowly painful dead sentence. I have had every symptom, every pain and sometimes I'm just tired mentally that I wish I could go to sleep forever.
Check out Dr. Eric Berg on RUclips. He has helped alot of people. Don't give up. You are not alone. It's an epidemic. The food they push on us is poison.
Look up Dr St Amand's protocol. Life saving. The root cause Is at the kidney. He saved my life ❤
Please take turmeric tablets. I started taking them 6 years ago and l am now 80% better. Turmeric changed my life, before that l had such severe symptoms that l wanted to die.
@@despinacharalambous1728 thank you, will try. I use acupuncture, works but expensive. I have few flare ups, maybe once a yr. I have S.A.D., summer affect.
@@robinryan3408 start taking turmeric it would change your life don't waste time. You will notice improvement immediately but with time as it builds up in your system you will feel better and better. Turmeric is inexpensive you can find it at the pharmacy store and here in Australia you can even purchase turmeric tablets or capsules at the supermarket.
I have had fibromyalgia for 30yrs. Now I had fibro B4 I had any stress or Axiety! And anyone with this exteam pain & Fatigue is bound to become a bit depressed. None of us who suffer with this real physical illness are just depressed....we have a real illness that becomes overactive to pain and hypersensitivity to how our Brain processes pain dont give up they are on the verge of a real explanation of this disease...
Dr schubiner.says it tms
@@Truerealism747 I was diagnosed at the very beginning with TMJS...after my accident..
Also genetic…once I learned I had fibromyalgia, during menopause…I looked back at the symptoms and realized a lot of the problems I had had most of my life. I major wreak, in hard and spine, major abscess in strep throat along with tonsilitis. Dr. Passed off as flu. Very stressful life pastor’s wife. And much more has got me to the limit. My marriage is very toxic, but really have no way out. Hurt by lots of people….
So very sorry melody Hang on to the Lord the fibro feels as if caught the flu and never got rid of it ...God knows and those who dont understand try to escape toxic people and relationships it can make it worse it's not the cause but surely doesn't help may God help you 🙏💙
Did you try celery juice in the morning dont eat an hour before or after consuming it even ancient Hebrew texts consumed celery if any problem with the body or bones as celery itself is naturally formed in the shape of a bone! Take it for a week as I did and I began feeling more energetic and clarity of mind mildly euphoric also as it was absorbing into my cells. Read psalm 91 it helps me a lot in times of torment or watch a great 'Tom Loud'(channel of the same name) short video on youtube called 'psalming'(just type 'psalming' next to his name) which in simple terms will change your life for the better Amen🔥👑🕊
Fibro is literally like a torture chamber...Everyday
I feel like a prisoner to these symptoms and the chronic pain in my body😭😭😭
So do I. It’s a hard journey, but we have to forge ahead.
@James Sophie lmao sorry scammer- I have a solid connection
I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia, he has the permanent cure for all types of disease and viruses....
I think something is wrong with our nerves and fibromyalgia is a blanket diagnosis. My symptoms started after 2 car accidents. I then gradually got si joint dysfunction, sciatica, peripheral neuropathy, pseudo tumor, and then fibromyalgia. I had a 35%ejection fraction they still can't figure out why. They don't know. Every thing is a guessing game and a cope out. We need real answers
Very interesting, informative presentation. The well laid out diagrams are helpful in achieving a better understanding of the biological processes, much appreciated for work well done.
Makes more sense to me now of how rheumy made the Dx.
On the other hand, my immunologist scoffed at the mention of me having fibromyalgia, he doesn't believe fibro exists, but nor does he believe that lupus or other autoimmune disorders are associated with primary immunodeficiency/cvid..
i hate fibromyalgia. i have things structurally wrong with my neck and back, so the pain just from walking can trigger a flare up. But i still try. Menopause has been a blessing. im on so much medication and take so many supplements. but i keep trying.
Are you hypermobile eds?
My mom have osteoporosis reumotoid arthritis combined with fibromyalgia 😞😪for 21 years she’s always in a lot of pain nothing help’s her anymore.she suffers from depression due to her pain.thank you for the information I appreciated
Your poor Mum, I understand, chronic pain can do your head in.
No, SNRIs have NEVER helped me. At all. Like nothing. Except I get worse headaches on them, from them. Most of what doctors push are band-aids. There is something wrong at the subcellular level. Helloooo....the mitochondria. I don't have any energy. Limited amount of ATP. Like a zombie. This needs to be treated otherwise all of this stuff that is given to us won't help. It's b.s.. I am a biochemist here and I have studied pharmacology in grad school. Serotonin is not the only reason we are fatigued. We literally do not produce ATP and NADH in our cells!!! Our mitochondria is compromised.
SNRI was one of the worst experiences of my life. It worsened everything particularly depth of depression. Cessation was a literal nightmare.
I believe you’re right about mitochondrial dysfunction
Read "The Mood Cure" book, take the questionnaire, fibromyalgia would fall under Chapter 3 due to a tryptophan>serotonin>melatonin deficiency. Life changer
Does this medication help ypu
I was diagnosed in 2002, after three years of investigations by various doctors and being told it's in my head MANY times.
from a persona intimate experience avenue, this is something people who do not have it simply cannot understand, they hear pain and have differing understandings and imaginations of what that means in regards to their own experiences of pain, but it's nothing like they imagine.
I'm at a point now I simply cannot remember what it was like before it started, so even I can't really explain it now as I no longer have a reference to example from.
but, at the lowest level I sit at is akin to the aches you have when you have "the flu" or a bad cold, and then, given different things, be it seasonal changes, stress event, doing too much (which varies constantly and inconsistently) and sometimes, for no reason I can ascertain, it can change a little or a LOT, the high levels are.. intense, it feels as if my bones ache, you have sore spots and areas that move, morph, phase, something like a cross between a plasma ball and a wax lamp, sometimes it's so much that it just becomes a thick fog of pain, everywhere.
then there is brain fog. it's like being stoned without the fun parts combines with being drunk, you get stupid, it's like trying to think through syrup, but it also HURTS to think, you brain loses the ability to connect words and even concepts at times.
then throw in skin and light sensitivity the very air touching your skin HURTS, it burns, and even an electric sensation, all combined and phasing into and through each other.
there's weakness, pulling muscles for no darn reason and more, one forgets some of it until you're in the thick of it.
it is a hellish existence. not all fibro sufferers get the same symptoms, a lot have other conditions that make it messy to know which is which symptom.
so it's hard to compare to each other and to understand each others experiences of the syndrome.
Man oh man this sounds horrible, I think I'm having the start of fibro and I'm so scared I can barely function 😞 I hope you've found things that help
@@edensmith206 in my 20 years of going through this, I've tried all sorts of treatments and drugs, and the only thing that has any constant effect, is hot showers.
it calms the whole mess down for a while, as with everything else fibro, to different levels.
but generally it's a decent improvement.
for a while.
pain killers mostly do little, and those that do much tend to make you tired or high (which I simply do not enjoy at all)
so I take low doses.
at most 30mg codene x 2 tablets.
no more and that I won't take more than two days running.
it's too easy to build up tolerance otherwise, and too risky to form an addiction.
so it's hot showers and some anti inflammatory like voltaren (also max 2).
and learn the arts of distraction when at home. be it games on pc/console or something you can get into deeply so that you don't notice you're suffering, until you can't ignore it, then hot shower again.
heated pools also great, with light resistance exercise while soaking
I tried low dose naltrexone, it worked well for about six months and then slowly got less and less effective till I gave up.
the thing to remember no two people with fibro symptoms have the same symptoms nor react the same to treatments.
so keep your mind open and try them all.
but, before tying any, be sure to read up on as much info as you can for each drug, especially for side effects so you can go into trying with eyes open and knowing there may be bad experiences.
some I have been unwilling to try because the potential side effects are terrifying.
be aware and be careful.
Approved Drugs
People with fibromyalgia are typically treated with pain medicines, antidepressants, muscle relaxants, and sleep medicines. In June 2007, Lyrica (pregabalin) became the first FDA-approved drug for specifically treating fibromyalgia; a year later, in June 2008, Cymbalta (duloxetine hydrochloride) became the second; and in January 2009, Savella (milnacipran HCI) became the third.
Lyrica, Cymbalta and Savella reduce pain and improve function in some people with fibromyalgia. While those with fibromyalgia have been shown to experience pain differently from other people, the mechanism by which these drugs produce their effects is unknown. There is data suggesting that these drugs affect the release of neurotransmitters in the brain. Neurotransmitters are chemicals that transmit signals from one neuron to another. Treatment with Lyrica, Cymbalta, and Savella may reduce the level of pain experienced by some people with fibromyalgia.
Lyrica, marketed by Pfizer Inc., was previously approved to treat seizures, as well as pain from damaged nerves that can happen in people with diabetes (diabetic peripheral neuropathy) and in those who develop pain following the rash of shingles. Side effects of Lyrica including sleepiness, dizziness, blurry vision, weight gain, trouble concentrating, swelling of the hands and feet, and dry mouth. Allergic reactions, although rare, can occur.
Cymbalta, marketed by Eli Lilly and Co., was previously approved to treat depression, anxiety, and diabetic peripheral neuropathy. Cymbalta's side effects include nausea, dry mouth, sleepiness, constipation, decreased appetite, and increased sweating. Like some other antidepressants, Cymbalta may increase the risk of suicidal thinking and behavior in people who take the drug for depression. Some people with fibromyalgia also experience depression.
Savella, marketed by Forest Pharmaceuticals, Inc., is the first drug introduced primarily for treating fibromyalgia. Savella is not used to treat depression in the United States, but acts like medicines that are used to treat depression (antidepressants) and other mental disorders. Antidepressants may increase suicidal thoughts or actions in some people. Side effects include nausea, constipation, dizziness, insomnia, excessive sweating, vomiting, palpitations or increased heart rate, dry mouth and high blood pressure.
Studies of both drugs showed that a substantial number of people with fibromyalgia received good pain relief, but there were others who didn't benefit.
Lyrica and Cymbalta are approved for use in adults 18 years and older. The drug manufacturers have agreed to study their drugs in children with fibromyalgia and in breastfeeding women.
read up on side effects before deciding.
Try Keto. It helped me. Dr. Eric Berg channel is the best.
@@jadedoptimist6364 too bloody expensive in Australia ha.
the price of meat has doubled in the last 2 months.
I bend down to your feet for such a beautiful explanation how serotonin,cortisol, all immuno, endocrine mechanism affected in this case. Where i have faced.. 90 % doctors whom i came across had no idea about this disease. The symptoms endlesz. The pains itself..so many types.. .only the kind of pains i suffered i can write 2 pages.
Thanks to you for such an excellent teaching. Please educate the world..about this disease, these patients are given antidepresants bcs of serotonin defficiency, patients show symptoms like depression.
And naturall, with this invisible disease and endlesz pains and symptoms, with no doctors understands, as label them as psyche..also family doesnt believe.
Even i suffered too much chemical sensitivity too , couldnt tolerate any allopathy medicines..
Fibromyalgia..leave the patients in a very miserable state
For all suffering from fibromyalgia should screen for celiac disease. Or should take gluten challenge test and again screen for celiac disease. I have been cured from this disease.
@@jalsapillodu9972there is NO CURE for fibromyalgia or celiac disease. And both are autoimmune and caused by mcas.
@@jalsapillodu9972 did you have it all over
@@jalsapillodu9972 what's gluten challenge test
JJ Med, very informative video. You delivered intense breakdown of this "disease". I suffer from Spinal /Facet Joint Arthritis, throughout my spine , sites of Stenosis, SI Joint Inflammation, arthritis in my hips, worse in my knees and into my hands as well. Due to all my chronic pain and chronic anxiety (They go Hand in Hand), he diagnosed me with FM. I just started to take 5 HTP (after doing much research), at night. I'm being cautious because for many years I've made myself a Guinea Pig with a cabinet Full of Supplements : Proelytic Enzymes, Mushroom extracts, Grapefruit seed extracts, Turmeric, Ginger, Cinnaman, Alpha Lipoic Acid, Various Amino Acids, Probiotis and Prebiotics, and more. I'm 70 yo. I fractured my right femur in 1966 playing HS football. That fracture resulted in a 1" shorter right leg which was left Unaddressed for many years. Boy, was that a Mistake. That Leg Length Discrepancy has Wreaked Havoc with my Spine, and hence my Well Being. My first Cervical MRI in 2012, showed that I had a More Narrow Than Normal Spinal Canal. I am convinced that the narrow spinal canal, mixed with the degenerative disc disease (DDD), and sites of Stenosis and the Dextroscoliosis (25 Degrees), which has greatly impacted my Central Nervous and Peripheral Nervous Systems has produced the FM. I am currently weaning off Gabapentin , weaned off Prozac months ago, and I am willing to Try Anything to get out from the Hell Hole of Fibromyalgia / Anxiety / Chronic Pain.
I'd love to know, has the 5HTP helped you?
How are you doing?
If you truly want a better life with less pain and no poison being put into your body, go with psychedelics. Psilocybin mushrooms, DMT, LSD, mescaline they all have benefits. Find yourself a shaman or someone with lots of experience within the field. Don’t do it alone.
I guarantee you will awake from your first journey a new person. It’s not about eliminating the pain it’s about accepting it for what it is. The medicine helps but you need to believe and do the work.
🙏🏻♥️ Magnesium malate + EPA-GLA is also a great way to get better from Fibromyalgia.
But most of all, stay avoid stress and negative energy - find people and thing's that make your happy.
♥️ Love from Denmark
Sure...avoid stress... yeah. How does that lead to ATP and NaDH synthesis? Molecules that give us energy? To live?
Sad for me because my stress is my partner at work 😭
@@wizqtyt1476 Get another job ❤️😘
@@minutsi I can't I'm an ofw
@@minutsi overseas worker
So many questions were answered in this lesson. Thank you so much. 💓
I’ve tried a couple medications to increase my serotonin and I always have an allergic reaction. It’s like my body can’t process the excess. I have Fibromyalgia and Depression so it’s very hard to find something that works.
Food
Me too!
Same 😪
@@elementalsfourheaven3401 which food 🙏 I know turkey, cheese, eggs
How can i PLEASE get this excellent video in spanish? I've suffered this illness for almost 30 years and need to show my wife and family what's really happening to me. It would help a lot because they really don't understand .. i've had post traumatic stress síndrome for 40 years.
Can you use a second phone to record the audio and then have ChatGPT translate it for you into Spanish? It will be a written transcript not audio when it’s done of course.
Fantastic video!! I have fibromyalgia, melatonin before bed is a game changer in regards to sleep and increase in REM sleep. There seems to not be much research on fibromyalgia, I would love to see more. Also I wonder about a histamine response related to fibromyalgia as well as the irritation level due to overstimulation of all my senses. Doctors wanting to start testing for Functional neurological order, it seems like they are guessing these days.
Save your time. I've been sick with FM for almost 40 years. All I do is search for help but the truth is everyone will tell you their version of what they think it is bit no one can tell you how yo get better. I can tell you that all the studies and world experts I have dealt with were all wrong about their conclusion. FM has been around for hundreds of years and today April 3rd, 2021 there has been no treatment, no cure and no actually scientific fact of anything . Sorry I couldn't offer you promising news.
@@youknowcrimedontpay9257 100's of years? Where did you get a that since MF mimics so many disorders? I particularly think the problem is with all the chemicals and pesticides and who n
@@elementalsfourheaven3401 I read your comments and I don't disagree nor agree and not because you are wrong or right. ME has more of a sleep disorder association with the lack of Slow Wave Delta Sleep due to Alpha Wave Intrusion. Some studies have shown that in FM patient there is a connection to human growth hormone from the hypothalamus which is a small region of the brain. It's located at the base of the brain, near the pituitary gland. While it's very small, the hypothalamus plays a crucial role in many important functions, including: releasing hormones. These hormones play a crucial role in the body recharging its self during deep REM sleep which patients with FM do not acheive. Without Restorative sleep we are exhausted and not just tired like working too long or staying up to late. Our bodies cannot recover energy which is what we need to feel refreshed and ready to go when we wake up. No matter how much sleep we get we cannot achieve the energy we need to operate as normal. We try to explain this to friends and family but they just think oh that person needs a vacation or needs to get to bed earlier. Now not everyone with ME has any muscular wide spread pain or depression or other symptoms that they can account for. That being said, in my situation I have all symptoms of FM and ME which I personally believe are the same as each other because the initial causation is a sleep problem that has a nurological associaton. Many of us with ME / FM and or just symptoms of ME without pain try to pin point how, what, when triggered our mysterious illness. Some of us received a vaccination, some had early childhood trauma, some had physical injuries such as automobile accidents, and other potential life altering issues that could have what I think set off our illnesses. I do not believe we just got sick I believe we were born with our illness and something triggered our sickness. If you have never had a sleep study polysomography you should have your physician send you for one. Restorative Sleep is so necessary and plays a hugh role in everything we do to surrive. The lack of restorative sleep beings on pain and with a vicious cycle of nonrestorative sleep 24/7 the body is in pain and eventually the body comes to realize it will never escape this life sentence and it becomes depressed. Some doctor's believe FM / ME is FIRST a depression related issue thus depression causing the pain and then the insomnia however I think they have it backwards. Its the story of what came first the chicken or the egg. How can there be chickens without a chicken laying an egg? The term Chronic Fatigue Syndrome has been used to describe people who feel tired but ME Myalgic Encephalomyelitis is also at times believed to be the same thing. Eventually the name Fibromyalgia will be changed to Central Sensitization. FM is the Greek name for Fiberous tissue / Malgia is the Greek name for pain.
When I said 100's of years we know that FM can be dated back to at least 1820 and because medical records were not so well kept further back then that I would suggest it goes back as far as humans have been alive.
Fibromyalgia tender points were discovered in the early 1820s. The condition was initially called fibrositis because many doctors believed pain was caused by inflammation at the sites of pain. It wasn't until 1976 that the condition was renamed fibromyalgia. Unfortunately there is no inflammation with FM from what science thought. My theory is that ME and FM are one of the same conditions but not everyone has all the exact symptoms as each other.
I hope my comments have helped even one person better understand our most mysterious illness and I certainly hope that sooner than later we all wake up one day a see that science has made the most precious miraculous medical breakthrough ever. God Speed to all my fellow people who so greatly suffer.
They are guessing i have been there 🙄
@@youknowcrimedontpay9257 thank you for sharing your research. Sleep is the one thing i have been complaining about for 20 years. at first they just dismissed me, probably because i was young, they said it was my "sleep hygiene"
Recently, i had to have a horrible flareup that made my get so mad at my doctor that i refused to see him any longer and scheduled myself for a sleep study.
As a a woman I feel that we are made to think that we are supposed to deal with chronic pain or certain issues and we.. well, at least me, start to believe it as well and push through everything... until well we can't
Keep shoulders raised and close to neck, do not wear bras. Always sleeping on the back and immobilizing the arms with pillows under the shoulders eliminates the traction of the suprascapular nerve. Limiting external shoulder rotations and arm movement can be a way of diagnosis if pain / fatigue subsides and helps relieve symptoms. The entrapment of the suprascapular nerve in the scapula produces traction on the brachial plexus. As a defense, muscle contracture is caused in the back, neck and jaw to avoid root traction. As a result of this, myofascial pain as well neuropathic pain of the brachial plexus and trigeminal appears. Fibromyalgia occurs when the local muscle contracture is not sufficient to prevent damage to the tracted / affected nerves and the body attempts to adopt a fetal position to protect the upper trunk. Movement against the fetal position of the body causes pain. Trigger points are the counted muscles, used to adopt the fetal position, and when forcing them, they produce micro-tears of fibers, triggering generalized pain. Thumbs up if it worked for you. Unverified, non-medical.
100
Unfortunately, some of us can't go outside without a bra as we have large breast. Otherwise thank you for your comment, I can't sleep on my back or stomach this last year and a half. Looking onto these neck pillows I keep seeing advertised to see if that can help.
nice joke🤦♂
Doesn’t work for everyone. Especially if the fibromyalgia came after body dysfunction.
Living with this fybromyalgia is like living with a death sentence. It’s notknown what actually causes it apart from trauma or major infection. I am so tired that I wish I could sleep at night which is virtually Impossible. So many illnesses are blamed for fybromyalgia. The only things it’s not blamed for is arthritis and cancer
ever tried kratom? i would highly reccomend, only for people who actually need it, it is a mildly addictive opiate but is nowhere near the strength of other types of opiates. it is a type of leaf with a long history of use in asia. it worked so well for me, normally i lay in bed all day. on kratom i could leave my house since the pain was gone. and it doesn't even get you high (although if you stop taking it, taper. it will suck if you dont)
@James Sophie Not at all I do not object
@James Sophie where is he or she based at?
@James Sophie Any idea of a price for these please
I understand you dear,I'll advice you recommended Dr Obinyan on RUclips,he cured my wife from fibromylgia, after taking herbal supplement we got from him,my wife is totally cured from fibromylagia,my wife can now sleep peaceful with no more pains...
I have a couple of friends who have greatly reduced the pain of fibro and migraine by moving to a carnivore diet. God bless ❤️🙏❤️
I’ve heard the same thing, regarding a carnivore diet, I don’t think I could do it. I’m already restricted with celiac disease. I find sugar kicks the pain in worse. I do think diet plays apart in Fibromyalgia pain, and if you have injuries the pain seems to hit those areas harder.
Research carnivore. Many testimonies of individuals having celiac improve the gut issue and alleviating FM. Check out Dr. Ken Berry channel.
Fibro patients tend to have issues with Copper, either deficiency or a high NCC ratio where they have a higher percentage of free unbound copper to ceruloplasmin.
I've been in a flare for 7 months and DOESN'T want to end! I've decided I need to get back to working out before I lock up totally and become bed ridden!
I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia with his herbal supplement, he has the permanent cure for all types of disease and viruses...
5 THP has changed my life. The pain has decreased substantially and I can sleep again.
No doubt my problem was the Serotonin
Can we take 5-htp indefinitely?
Yes that's true. My docter gave me serotonin medication against fibromyalgia symtoms. And it really helps. So happy
@@mlou7432 no those types of meds always come at a price. Psychedelics have almost zero consequences. The bonus is that you usually only need one dose up to twice a week for extremely severe cases.
@@michellehabets4568 did you have pain all over or in certain areas
Didnt do anything for me 🤕 but ive been fighting this crap since 2016 and its so bad i have to taka opoids just so i can sleep because im in to much pain to sleep without.
The pain and fatigue...we as fibro sufferers experience is what causes the depression and anxiety over it cause it hurts more than our bodies or minds can endure!!!! Please dont blame the condition on depression or axiety!!!! Its the illness first then comes the secondary part of this horrible horrible illness 😢
That simply isn’t true. Those conditions usually contribute to the illness. Besides depression and anxiety are that of a weak mind finding an excuse to feel that way.
Psychology plays a huge part in pain perception.
@@Dionysus_Athena I'm glad you have first hand data on this illness I'm sorry you suffer from it!!!!
@@Mfield111 have you studied neuroscience and psychology? Anxiety and depression are merely that of a weak mind.
The biggest thing that helped me was mindset first, then psychedelics DMT and Mushrooms in particular have a massive effect on these illnesses.
Another thing that contributes to fibromyalgia high oestrogen and low testosterone. TRT helps a lot.
Vitamin infusions again help a lot.
What I can’t stand is when people make excuses. Oh the pain is too much no it isn’t the pain can always be overcome it’s your mind that is weak.
@@Dionysus_Athena you have the right to your own opinion! But, that is just what it is yours, not fact! God's mercy on your way the only way! And God help all those who truly suffer with all illness and diseases that cause them real pain and suffering! And only God knows what you claim to. Case over!!!
@@Mfield111 it’s not an opinion it’s a fact backed by science, medicine and spirituality. I’m guessing you’re a Christian which is why you find it so hard to believe and accept that there is more than what your book says.
Acceptance is something everyone struggles with more so for Christians. Even harder for them is accepting that there is more than one god out there.
Have a good day friend one day I hope your ego dies and you are reborn with true love and acceptance of all.
I just bought 5 HPT remembering it helped me years ago w/ depression and fatigue
Do you still take it?
Very interesting to know about this topic. 👍 Thanks for sharing!
Vaginismus, knee pain, thankful for meds, prayer, this sight ❤
What you talked about at 6:34 Does that mean we are always sympathizing because of the disease? Because I think I am and it stresses me more.
I have fibromyalgia so this helps
I am so grateful to Dr uzoya on RUclips who cured me from fibromyalgia with his effective herbal products. I will spread your good news here in the United States.
I think the Fibro... cause low level of serotonin, because Fibro... cause stress which will reduce serotonin. Increase serotonin not reduce pain , just reduce the sense of pain. The sense of pain is important of the human body operating. In this way the human system will try to cure the pain. so low serotonin is the result not the cause.
Low level of serotonin ,dopamine and nore epinephrine is caused by stress and depression actually your brain shrink if you are depress and stress so no amount of vit.intake or mineral intake will reduced these symptoms of fibromyalgia. You need to treat the root caused and it's very easy to treat it if you know the pathophysiology of how fibromyalgia and CFS/me work
Hello doll💞 Thank you for your channel 🙌. I’m a 58 year old female medical student and Degenerative Brain disease specialist, so I should know this, I have gotten rid of 9 autoimmune diseases, but Hashimoto’s is still a problem. I had continued traumatic brain injury during a physically abusive marriage and lost “ processing speed”, but the rest of the test stayed above average. I take 200 mg of tyrosine for new tropic benefit, but I wondered if you could suggest anything that works with the brain for the ability to process faster. Thank you so much for your help I pray you are blessed as much as you bless us🙏
Protandim Nrf2 and Axio
High level of stress during a 17 years abusive mariage completely messed up my hole health. Suffering hell from severe fibromyalgia. Had a stroke five years ago. And severe endometriosis, had to take off uterus and others around. Please, excuse my bad English, French is my first language. So much toxicity and several forms of violence harmed me so much. Feeling like my life is over since many years. Only surviving for my two wonderful boys. Take care Everybody.
I’d recommend prevagen. Especially since you are an older woman. It works really well.
You could also try lion’s mane mushroom but I still think prevagen would work best for you.
Also remember not to take the tyrosine with food, as the nootropic properties are most powerful on an empty stomach.
Hi Jami how old were you when u enrolled into med school?and how do you like it. I’m 42 and considering career change and going to med school, Any suggestions?
Psilocybin hands down the best and most beneficial for what you are after. It not only repairs the brain at a faster rate than anything ever seen, it also creates and improves new neuropathic pathways.
How about the muscle spasms, that stay that way so you can't walk or lift things or open jars??
Very good information, in every way it was really well presented. One of the best lectures on this sunject. Thank you.
I am a sufferer of fibromyalgia long time of 25 yrs. Flare up since last years. Csnnt explain the type of symptoms endles. Your vedio is very informative. I am sensitive to all medicines, chemical sensitivity is very high. Please do more vedios with diet etc which naturally can increase serotonin levels ? Or any ayurvedic treatment etc
All your symptoms will be treated with one word "OXYGEN" BECAUSE WHAT YOU HAVE IS LOW LEVEL OXYGEN IN THE CELL OF ALL YOUR BODY.
I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia with his herbal supplement, he has the permanent cure for all types of disease and viruses..
All thanks to Dr Obinyan on RUclips,he has restored happiness to my aunt life,my aunt recommended treatment from him,to her greatest surprised,it work perfectly 💯💯🌿💚💚...
Thank you, finally a clear and in-depth explanation. When is the best time to take 5-HTP? Some say at meals, others away from these...
i have these but the worst one is deminsihing memory, so worried about it !!
Great lesson! Thank you.
I’ve had Fibro since age 3-4, soon after my estranged father (rotting dead now) met me and tried to strangle me to death for yelling at him to quit beating the living snot out of my mother and sister. Soon after I was on the floor BEGGING mom to *cut my legs off*. I was misdiagnosed in 1985 (age 6) with Muscular Dystrophy- a DEATH SENTENCE. I was given 400, then 800mg ibuprofen for *years* while strapped in a wheelchair and “poster-boy” for a disease I NEVER HAD.
At 18 I had access to the Internet (1997), found I met no MD symptoms. Square One. Went to EVERY specialist 3 times, did 3 killer 20+ session each rounds of physical therapy. I doubt this video mentions that according to everyone (professionals) PT and light exercise helps only 15% of patients. I’m 43 and due to my doctors’ giving up and/or retiring, in the worst pain ever. I want Heaven. Tried every drug in this video. Methadone helped most with a 4x/day Vicodin (then Norco), with open permission to “double up on the Vicodin if it’s bad.”
My newest pain doctor picked up writing my methadone though cut Norco (this “opioid epidemic” is bull. Pure bull. If JUNKIES WANT TO DIE LET THEM. Narcan can reverse an OD in seconds. I NEVER abused my medicine. Methadone and Norco fill-in pain receptors in those WITH chronic pain. It is ONLY those without or a low level pain that ever get “high”. Let them die, because the paranoia surrounding what WORKS has scared 90% of doctors from prescribing ANY. That means zero relief. Zero. I’ve been on methadone over 20 years safely to help. Norco was cut 5-6 years ago 100%. My pain doctor (specialist) overheard me ask a nurse if other doctors were available to see at their practice and assured me they had others. Upon hearing this, my doctor FIRED ME. A VERY SCARY MAN with multiple complaints about his attitude, dehumanizing, degrading, insulting treatment of his patients. Dr. Willard of Michigan Pain Consultants. He cut me off completely. Today is my last dose of the half-strength 2 week refill he called in. He had planned to try me on morphine. I asked 3 times “if this goes bad, will you put me back on the methadone as I’ve been?” He said “Yes” all 3 times. 10 minutes later, after overhearing me ask about a doctor transfer within Michigan Pain Consultants, he said in no kind fashion “NOW YOU NEED TO FIND A NEW DOCTOR!”
He *cancelled* my RX’s for morphine or anything else. He knew my history. He took an OATH AND SQUELCHED ON IT ENTIRELY. I have NOBODY. Except the street that wants sex and cash.
What???? The pharmacist I asked about this was disgusted!!! Very concerned! I have a separate (?) heart condition and a month of tests ahead as my arteries are spasming (equal to a blockage, but 3-8 minutes per episode, up to 17 a night. I now have Nitroglycerin that stops them in under 10 seconds, but many tests to come).
What am I supposed to do???? He LIED! His pride was more important than MY LIFE OR HIS OATH. What do I do? I don’t want to die! I’m terrified! Terrified! And I NEVER admit when I’m SCARED, but I AM SCARED! What do I do now?
I've had fibro since 2009. After many years of being on different kinds of pills & walking around like a zombie, I found that copious amounts of CBD and plain ol weed helps TREMENDOUSLY. Yes, I'm usually stoned every day, but I'd rather be illegally alive (weed) than legally dead ( pills).
@@chifreak6 God bless you kind soul!!! You’ve made me cry- but as you know, feeling *anything* emotionally is far better than the NOTHING you feel when the “professionals” are ruling your life like they are gods. They’re not gods. Their is One God, and I serve him.
I also love weed. But to “pros” here they still just consider that (me) to be a junkie. Unless I take *their* junk. I live in Michigan, and pot’s both medically and recreationally legal. Except certain towns and cities like mine found a way to block its sale. It’s safer than a low-dose aspirin for Pete’s sake! I have to travel a couple hours to find it, from a Michigan based company called LUME. They are 100% legit, high tech labs, professional labs that grow organically hydroponically and their stores aren’t your old-style head shop full of hippies- they are highly (extremely) knowledgeable and have several strains and hybrids and the purest, best tested pot you ask for. Each strain is labeled with the THC content beyond decimal points in accuracy (my last, now gone, has “19.07%” printed on the bottle. They have every range of potency from 6-7%-25%, and ask what type of condition you may have or what your goal is for medicine or fun or both. I can’t wait to go back for more, and prices are actually extremely reasonable: less than 90’s college brown brick schwag for pure quality).
You give me hope. Your reply means more than a text could ever mean. Thank you. God bless you, and I’m here for you anytime. Thank you, thank you, thank you!
-Bryan
@@sideswipe1261 Wow. I'm sorry I made you cry...not my intention. It's ok not to be ok! Finally had to be honest with myself & realize it's ok to have days where the pain is so overbearing & relentless that you literally wonder what heaven is really like...as long as you can snap yourself back to reality and at least try to occupy your mind with more positive thinking...ha. It ain't easy. This has been my daily ritual and I mean that literally...my story is lengthy and actually thought about writing a book. In the hopes of possibly helping someone else. The big pharma peeps almost did me in. As well as many 'specialist'...and several practioners. I trust not many & am VERY selective as to who Iam able to choose for my medical care.
Long story short, cbd & weed is what helped me get off ALL benzos & anti depressants. Iam blessed & very grateful that I always can get it too.
I'm happy I could help you Bryan!! I wish you luck on your journey! Stay safe out there! Be blessed 🤞🙏✊✊
- Elaine
@@chifreak6 crying felt *good* after years of being a Zoloft-Zombie! I meant to thank you 🙏🏼 because after years of feeling *nothing*, finally off the Zoloft I am becoming MYSELF again! You helped me do that! I’ll always stick around if you want to chat!
@@sideswipe1261 I'd love to chat also!
I've had it since 2000. Ironically I had been on a higher dose of Prozac for a couple of years before.
I have ocd and they started me on lithium than zoloft to Prozac.
I felt so flatlined in emotions that I quit taking it faster than I was supposed to.
It was probably only months later I started having symptoms.
I'd never heard of FM. It started with burning hips and legs arms that felt like they were made of lead. It was exhausting. My husband had put me thru some things. But I also had 3 kids, lived and worked on a farm, and just thought I'd overdid it.
I've been I. Many meds but the one that probably helps more is tramadol. It was somehow different. I've had a lot strong without much relief.
Magnesium malate helps a lot! You'll notice more when you run out of it.
My anxiety levels get bad. I stopped going places unless I had to. Brain fog isn't fun, as well as fatigue. But it's 2 am and I'm awake but tired. I'll be up by 6 I'm sure.
I recently have been having trouble with my eyes. It can come and go during the day. I just happen to read on a pamphlet in my Dr's office that that's a symptom.
If you sit too long you turn to stone, but don't overdo it either. Try for the sweet spot.
I used to describe to people that I turn to stone and feel like a big bruise. If a child taps my legs or my pup jumps up on me it's like they pushed on a deep bruise.
Another thing. When I went on an estrogen patch a few years ago I told my gyn that I swore it made my fm symptoms extremely worse.
100%.
I have been diagnosed with muscular dystrophy and kyphosis but what you have written here that's me please help some one.. can it effect your potassium levels also? x
@@R3Quency I personally have not had blood test that showed low or high potassium levels. I have in the last year been taking a potassium supplement a couple days a week. Mainly when I feel dehydrated a bit.
The blood tests that showed anything were ones that showed inflammation and I also have a rheumatoid factor that's on the bubble they said. They said that means I hurt. But it doesn't indicate RA.
@@micci7795 I was unwell with tb and lost all my weight from 10 stone to 5 stone they treated it with chemotherapy , them I thought the pain was recovery from all the muscular wastage but I received a call for my doctors saying I need to go in urgent it turned out I had severe anemia, my back was really hurting I walk well strut my mum says like my dad , I used to see and osteopath who said there was something wrong with my spine.. after i was in so much pain I called my doctor about my back and they did xrays said it was kyphosis then in November I fell amd broke my hip well obliterated it. I had surgery and then I caught sepsis, it was said I may not walk again I could hear the doctors saying I dad muscular dystrophy , brittle bones and kyphosis I was saying NO its kyphosis! I was never actually told when they found I had these other issues but all are o my discharge note. After 2 months I got out of hospital with district nurses and home help and care package as I was getting more an more depressed in hospital, I was catheterisation for 8 weeks sometimes so stiff I can not get up for the toilet in time I am 45 not 95.. the pain is unbearable also whilst in hospital I got pressure sore ungradedable they are to the bone and I jeep have to have antibiotics to treat the infection in the bone but all my symptoms as like you.. please some one any one gibe me some hope or it this is life to just tell me so I ca just do things try to live not exists.. thanks for taking tour time to read this. kindest regards Carol x now I am always being tested for infections and last new symptom was my potassium levels o could not beath my chest heart I was more stiff than normally amd the list went on. sorry for tyops my motoring skills are going xx
@@R3Quency I'll advice you recommended Dr Obinyan on RUclips, he cured my wife from fibromyalgia with his herbal supplement,he has the permanent cure for all types of disease and viruses...
GABA helps too, especially if your norepinephrine is high and you are having a flare. Much like bipolar and diabetes, you get to regulate your own levels. Lol. Yay. Go me….If it’s pain from a depressive spell, the 5thp is invaluable, but cessation helps with that 60 day plateau. I take Kanna and Motherwort and Skullcap, but be careful with Skullcap, it actually can give serotonin disregulation.I don’t know why, but I think it had to do with cessation of several other stimulants around the same time like caffeine and add medications. I wonder if all of us really studied the half life of the substances we take, we’d fare better. It’s rather complicated isn’t it?
how to increase GABA?
Having the MTHFR gene mutation must surely play into fibromyalgia and CF. Taking methylated B vitamins with 5HTP has helped. Would love a video about that connection if any.
Yes Asperger's hypomobility and adhd
Very interesting and informative thankyou so much.
I am taking vitamin D, managed to raise it from 50 to 77, but l take very high dose. Also taking b12, q10 300mg, probiotic, zink, selen, magnesium, Olive leaf extract. Started also recently with low dose of bento thiamine, will increase by time. I feel much better then before taking these supplements. I have found that all mentioned above could help, esp. Q10, higher dosage. I think we have some chemical inbalanse in our bodies. Also, my problems started when l had problems with gallbladder which is now even removed. But seems that metabolism of fat is not working properly. All is connected l.
I was taking vitamin D my reading was 123 my Dr said that’s the highest reading he’s had. 🤔
Omg thank you !!!
This makes so much sense 😃
For all suffering from fibromyalgia should screen for celiac disease. Or should take gluten challenge test and again screen for celiac disease. I have been cured from this disease.
So knowing all this cure me!
I have been taking turmeric for something else. It has NOT helped with FM. What dose are you all talking about? I have been taking 500 mgs alternating days. Helps with my bad hip.
You might like to read THE INVISIBLE RAINBOW, ABOUT WHAT ELECTRICITY DOSE TO THE HUMAN BODY. It’s by ARTHUR FIRSTBURG. A HISTORY OF ELECTRICITY AND LIFE. All ATHESE SYMPTOMS ARE IN THAT BOOK!
Can we (fibromyalgia sufferers) take 5-htp indefinitely?
Black seed capsules with water and honey 🍯
Amazing Dr...
I try do my you tube video on living with fibromyiala and mental health issues having both isn't great
Thank you very much
Nope understanding human Conciousness is the answer you can help yourself
Infact nothing can help like self help
Sufferer for 20 yrs
Believe me Iam proof
💜
Yes, Consciousness, nonduality, is the way
I was watching my playlist & in the middle of this vid it disappeared :( .. & now it's back :)
I am so grateful to Dr uzoya on RUclips who cured me from fibromyalgia with his effective herbal products. I will spread your good news here in the United States.
@@reginaldneal675 pls tell me which ayurvedic medicine sir
Would a endocrinologist be the correct doctor to look at these things?
Neurologist
@@Србомбоница86 I once saw a Neurologist as I've got CFS/ME/MCS & just said that it was depression......................! The actual appointment was for an under active bladder though, but as I said that had got CFS/ME/MCS he automatically dismissed it as depression.................................
DON'T GO TO A NEUROLOGIST. THEY WILL SAY WHAT YOU DON'T WANT TO HEAR. First appt will be telling you you need an emg test
I saw an endocrinologist to begin with and they sent me to a rheumatologist for diagnosis
A rheumatologist is best! Really!
Thanks
Frustrating to still see outdated medical theories being shared.
Brilliant.
It is hard
Tried the 5HTP but it made me sick.
Hello sir,
Does thyroid medication cause low serotonin, even after taking thyroid meds there is body cramp and sleep issues and fatigue. Does this pathway get afftected with thryoid issues
Is it safe to combine Psylocibin microdosing/ trip dosing with 5htp?
I have the same question my friend
I'm thinking about alternating the two using 5-HTP on my off days
@@user-rm1lm3rt7e Me too - does anyone have information re psilocybin microdosing w. 5htp?
My opinion is safe and affective. I have a very close friend he likes to do one heavy dose trip (shrooms) every other month. And sometimes molly, And in between he only take 5htp to level his serotonin.
I think most psychedelics psylocibin, mescaline, LSD, DMT are serotoninegic in nature so I would leave a gap of at least a few days of 5 HTP use before and after psychedelic use
Very interesrinf, I found this video because I just bought a supplement that has 5htp+magnesium and b6 and I was looking for info about 5htp, I have fibro, I been taking the supplement for a feew days and wow its awesome, I dont expect to feel this awesome for a long time but I enjoy any time it last hahaha, I have found that also helps to take creatine and aminos, helps reduce fatigue and pain I just started excercising
(Just 40min per day,) again and the recovery its so much faster
Hi iv just resently detoxed off heroin and metherdone after 33 years on it i am disabeld du to a stroke i sufferd in my erly 30s i suffer from nuropaphick nerve pain down my left side i get a lot of electric shocks down my leg and arm on my left side iv got cronick fateege sindrome and i suffer with depreshon do you think i have fibromyalger ?
Thanks for the video, any thoughts on 5-HTP helping with Polymyalgia Rheumatica?
Depression and stress with alcohol. Think about it
Milnacipran/Savella has been shown to only work for only some people.
I literally don’t understand why I don’t have any fatigue from fibromyalgia but I’m not complaining hehe
That's great you must not have a real bad case of it so that's nice God bless U...CFS is more than fatigue so you must have mild fibro or something else
@@Mfield111 I've had CFS decades but not it's more fybromyalgia seams it's changed faces
@@Truerealism747 oh🤔💙 I've had it since 1993!!! It has gotten worse in my 60`s but Fatigue and pain the most prevalent symptoms so it's been diagnosed as ME/CFS and fibro a part of this! Sorry you have suffered it! I know ME/CFS for sure has degrees of the illness...I'm not the worse case scenario but by far not the least it is horrible God bless you
@@Mfield111 are you hypermobile? My father had CFS now ok years ago I e had it since 1997. Though now I no why diagnosed Asperger's add had I had SPD as a child.then had a accident then wind up began have your symptoms changed over the decades I've always had fatigue from birth due to being in spectrum I've found out and hypomobility
Well you’re lucky in that respect, the fatigue is hard to deal with, I sleep 💤poorly which doesn’t help.
Is the cause alcolism.
@@Annedowntherabbithole here well with ve had a sip it's related to Asperger's ADHD OCD hypomobility fhtmr gene u have them all
It's the nervous system is broken hardest thing to fix.. I do have connections going back to vac ines.. Was studying this, even before Co vide ones.. I think we being deliberately poisoned..
You can get it from a chemicals being released from women getting iud alot people got it
Its a big game.
Cymbalta is useless to me
I mean I'm an alcoholic and that's what the common link is. But alcoholic is accepted.
Yes alcoholism can cause fibromyalgia due to inadequate oxygen ation of the tissue all over the body
I’ve had fibromyalgia for 14 years now and I wouldn’t wish this reality on anyone.
I don’t let it stop me because.. well I can’t. I work full time, I’m a single mom and I have too much depending on me.
However, it’s excruciating to walk through life as a normal person when on the inside it feels like my body is attacking itself and no one but me can see/feel it.
Shitty part is, I also have bi-polar disorder so I cannot take SSRIs or SNRIs. Although prior to my diagnosis, they did have me on them and a plethora of other prescriptions. Really none of them were impactful.
Hot baths, reducing stress and meditation have been the only relief I’ve gotten over the years.
I'll advice you recommended Dr Obinyan on RUclips,he cured my wife from fibromyalgia with his herbal supplements, he has the permanent cure for all types of disease and viruses....
All thanks to Dr Obinyan on RUclips,he has restored happiness to my aunt life,my aunt recommended treatment from him,to her greatest surprised,it work perfectly 💯💯🌿💚💚...
I had fibromyalgia,I got diagnosed 2years ago,until I came across,Dr Obinyan on RUclips,I recommended treatment from him,to my greatest surprise it worked perfectly 💯🥰🥰
Well done Destiny, you have a lot to deal with, working with such pain I truly admire you.
Yo the one thing that goes hand in hand with depression, stress, anxiety, agoraphobia, and so on is ,Alcohol. The gate way was their from birth.
Sharing to look at in length...
Unless you are a doctor which they really need educated it is another language.
I may have fibromyalgia. I don't know for sure, but I will be scheduling an appointment with a rheumatologist soon. My symptoms come in episodes. All i can tell you when I have an episode I am in pain all over my body. My bones and joints hurt so bad. It is like I have a severe case of the flu. I am miserable when I have an episode. Yau'll I just hurt all over. It is not in my mind. I have been on Cymbalta for years and a mood stabilizer, Lamictal. I also take Trazadone to sleep and I take Synthryoid for Hypothyroidism. My grandmother has rheumatoid arthritis as well as my identical twin sister. Does anybody else experience these type of pain all over your body especially in your joints? There is sometimes that I hurt so bad I want to cry. Any suggestions would be greatly appreciated.
Was diagnosed 2009 with Fibro. Since then I have been on numerous medications. Currently on Cymbalta and Lyrica. I dont feel any better pain wise but it does help the depression caused by the pain. My best go to medication is good ol weed. Combined with copious amounts of CBD. Yea Im frequently stoned...but its way better than all of big pharmas pills. Id rather be illegally alive than legally dead ( btw its legal here now for recreational use thank God ). Someday i hope to be off of all pills but for now this is how it is.
@@chifreak6, Thank you for responding. I appreciate your suggestions. I can't smoke weed, because it gives me horrible migraine headaches. My next door neighbor smokes weed alot and when I smell it a migrane starts up and I can barely function, but i have nothing against people who do as I have friends that smoke weed occasionally.
@@prometheuspredator7971 well that's unfortunate. Im learning weed isn't for everyone. Have you looked into CBD?? I hope you can find what works best for you. Sending positive vibes 💚🤞✌
Thank you so much. Sending you positive vibes as well 💚🤞🤞🙋♀️. I will talk to my doctor about CBD and maybe he will prescribe it for me.
Cannabis gummies decrease the inflammation in my brain allowing me to process stimuli more effectively. It also treats pain and insomnia.
iodine
👏👏
The pathway implications have far more implications than just Fiber myalgia.
Too technical to be helpful!
Syphilis
Huh?
@@inspiradorupees3029 this is a side effect of syphilis. can be cured with penicillin.
did mine
Excelle nt
Vitamin D people.
Isn't everything in this lecture pure conjecture?
Why are you making so many videos about Fibromyalgia? Is this a medical area you are interested in? I have the disease and I am very curious. I am exploring some newer treatments in for it. If you wan to know what my docs are doing, I can let you know.
whats the treatment? need it
That is a lie. It's not a death sentence. It is what you believe
I would really like to know what license you have in medicine. There are laws about posting these things in the States when they haven't been actually proven.
You are flirting with a dangerous notion of information suppression which will lead to a dark age, just like 1000 years ago, with your non thinking and blind trust for the select few able to kiss enough butt to interpret Devine truths. Nothing is absolutely ever proven. In fact, not even laws of physics. Just certain things fit better and make better predictions, until some BETTER IDEA COMES ALONG! Everything, everything in medicine is merely theories. What passes for proof in chemistry and medicine, is idiotic to most mathematicians and people familiar with other proofs in physics....
This presentation is much too complicated. I seems to be a lesson for a medical class.
one jealous...
There is WAYYYY more out there that you should worry about. This is educational and not treating the rest us as idiots like we are in the middle ages. The way that doctors practice medicine here is all controlled by pharma. Even the way professors teach. There is something very wrong when ONE doctor in a third world country can diagnose you while you need 10 here jumping from specialist to specialist meanwhile something as simple as vitamin deficiencies aren't even checked. Actually doctors don't even know much about nutrition. Its actually pathetic. So maybe you should learn from this and become a better doctor if you are really one.
Also this just tells me how incompetent is my doctor.. when he hasn't paid attention in years to my chronic insomnia or acting quickly in preventing ANYTHING until some of the bloodwork comes out very bad .. there is no preventative medicine in this way of medicine. So having an adrenal crisis is find because they are all worried about having to see x amount of patients a day and have dont want to or can't put the effort in educating themselves further.
Oh and never mind how WOMEN are Sooooo dismissed by a very patriarchal society