For 100 years, we have been addressing the critical and complex public health issues of populations through innovative science, education, and leadership - locally & globally.
They are not looking in the right areas of the body. ME/CFS/FMS/POTS = Adrenal gland illness. It's our adrenal glands that aren't able to work right because of a physiological stress. Not emotional. It's our blood sugar imbalance that is kicking the crap out of our adrenal glands. High carbs, not enough protein, skipping meals, and more are like a karate kick to your adrenal glands. Balance your blood sugar 24/7. Omit blatant sugar, add healthy protein and fat with eat meal. No caffeine, nothing but water to drink. Those are the basics. Do that for a week, see how much more better you feel. For those with Leaky Gut, bc LG is usually present with adrenal gland iisues, chopping raw garlic and putting in food will do wonders for your micro biome. Probiotics are a waste of money. I did this for 4 months and felt the best I've felt since I was a kid. Then I had a dessert then the next night another until I couldn't balance my blood sugar anymore. Immediately, my insomnia returned then all of my symptoms returned. Take my word for it, I was diagnosed with cfs in 1987 and fms in 1994. The adrenal glands are taxed and stressed. Fix your diet, balance blood sugar and see a huge improvement. To me its like diabetes of the Adrenal Gland. I have to eat as if I am diabetic. Your cfs/me/fms/pots can be reversed.
This woman keeps mentioning a blood test, but doesn't actually reveal what that test is. Is she merely hinting that there is a blood test in progress? This video was made 9 years ago, so there has to be a test at this point. Does anybody actually know?
Omg I just burst out in tears bc this is so me! I struggle with back pain from schuermanns disease and mild chronic scoliosis but I've got my back pain back to a manageable level but my stomach and internally I'm shaking, jittery, and feel like I want to puke every single day! I have the muscle pain and tenderness and I feel like I'm plugged into an electrically outlet bc my mind is always racing and I have a millions things I want to do but I don't feel like doing them. I never want to go out around people bc I always feel so bad so I have no friends and I'm basically home all the time. I try to work as much as possible but it's so hard to hold anything bc I'm waking up throwing up some night's and just break out in sweats after I throw up. It's miserable bc I have acid reflux on top of it and widespread pain which I think is a bad form of arthritis bc my grandma had it as well and died from bone cancer. My pepaw died at 52 from liver cancer, uncle died at 52, and my dad died at 58 with throat cancer which Dr thought was from acid reflux and Zantac but he was dead bf we could do anything and the Dr retired and we didn't see the Email in time so both our records were destroyed!
Italian here: during COVID i got a bad Epstein Barr infection, i was laying on my bed for 9 months. ALL i was able to eat were literally homemade (by me) low/zero carbs and high fats protein based (whey - casein - whole milk) based shakes/ puddings / smoothies /creams / etc with high quality fats and essential vitamins, omega 3, etc for a daily total of more than 5k calories. Results? Laying in bed for MONTHS and eating 5k calories and i lost 18kgs (39Lbs). ALL the governments /angencies recomendations are literally LIES lol. I mantained low carb diet and i never gained back a single pound btw
I take 30mg. of Adderall XR daily and still have no energy. If I quadruple my medication, I have enough energy. The problem with that is I'm only prescribed 30 pills for 30 days.
I'm so sick of Doctors telling me I need anti-depression medication,,,,, B-12, D-3 Exersice more Etc..Etc . Etc Anyone on here know of a place to go for Help???
My wife's CFS symptoms began in 1993 at age 48 (31 years ago). She was a patient of Dr. Cheney and another top clinician in those early years. She began using a wheelchair in 1994 and has been totally housebound since 2005. We do the best we can but, at age 79, she now is totally incapacitated. A severe life sentence for both of us.
Video sucked. Multiple times she mentioned that there is evidence and a blood test, but no indication of what that evidence is or what the blood test would be. Absolutely useless for anybody who thinks they might be in this category or might know someone in this category. Thanks for nothing asshat
She doesn't even say what the blood test is! My doctor thinks fibromyalgia and chronic fatigue are the same thing. I have never heard of a blood test for chronic fatigue and this video is 9 years old.
So 9 years later, what has your "Robust Evidence" done now? Still do not know what this "blood test" is and my doctor says there is no test. So again I get no help!
Just name the blood tests and the distinct stages by which one could come to next outcome, making these ridiculous statements are of no use, I scrolled through comments sections to find the names of blood tests, etc and all I could find is morning of folks including me.
After the way the govt gaslighted us about getting the clot shot for covid which is just another virus similar to the flu, I no longer believe BIG MEDICINE i.e. the medical establishment. I've known one person in my life who claimed to have CFS and she was addicted to opiates at the time. Of course she couldn't do anything (work, play, live) because she was so drug-addicted she was barely functioning. I thought at the time her problem was completely psychological. I still don't understand why NOTHING seems to work with people who claim to have ME/CFS. I saw another vid here at yt where a physician was claiming it's a sort of brain inflammation yet they can't find any inflammation with multiple types of testing. I just don't understand the "disease" at all. What is society and the world supposed to do with people who can't work and can't sleep and are in so much pain? Do all these patients go on full disability from a young age and then never work again? How is this managed? Still unsure why exercise, fresh air and sunshine is strictly poo-poo'd as a possible treatment for the symptoms of ME/CFS. It's probably better than a lifetime of opioids like Fentanyl.
Love how nobody wants to talk about how the medical industry has been gaslighting millions of people with the same old crap for decades, you're not working hard enough to manage your symptoms, your diet, your lifestyle, it's in your head blah blah blah. It's so vile and disgusting. This needs to stop. Millions of people are not lying about their symptoms for fun. What a shame of a world we live in right now.
My beautiful wife suffered with fibromyalgia and chronic fatigue for years. It took it's toll until she could no longer keep up. She overdosed*sed on her prescription pills last October.
Ive had it since 1989 and an expert used to gove me 3 monthly vitamin B6 injections. He said "one day off 2 days on" Was helpful. Never push it too far. It has affected my muscles giving pins and needles in arms legs and feet. Tiredness dp bad i just zonk out for day. My immune system is compromised.
Much love and strength to you. I'd like to give you this quote by Anthony William: "CFS-or whichever name for it speaks to you-is neurological fatigue from an ongoing and chronic Stage Four Epstein-Barr virus (EBV) infection. Any of the over 60 varieties of Epstein-Barr virus, accompanied by toxic heavy metals such as mercury and aluminum, create viral neurotoxins that inflame and drain the central nervous system, creating an exhaustion that’s far more pronounced and limiting than simply being tired. In its more aggressive forms, the neurotoxins cause a mild encephalitis (which is undetectable by MRI or CT scan), which creates even heavier fatigue. This neurotoxin inflammation of the central nervous system can eventually weaken the adrenals, liver, and digestive system, and create the feeling that you have a low battery."- I reccomend his book "brain saver
@mandil.7255 thank you so much you have gone to a lot of trouble with this reply. Yes you are right it seems to originate in the glandular fever viral infection although i also had ROSS RIVER FEVER long ago. It stuffs the nervous system and retards the immune one. I was in a CFS ME SOCIETY for years and shared info. I read all i can on this but am resigned to, at an older age now, living with the rotten thing. Again thankyou. Appreciate your caring attitude. God bless.
Meanwhile, I'm coming here from a video five days old about how a girl died with ME after being told it was all in her head by NHS "doctors". And she's just one example of what people are facing presently. The medical profession really is a sham more often than not. These idiots with degrees should be much more rigorously tested for competence and knowledge. I've been to so many GPs who seem to have a lesser functional knowledge of the human body than I do with training as a remedial massage therapist. I've had to educate specialists on procedures that were as novel as five or ten years old because these professionals couldn't be arsed to stay informed in their own lucrative field. Just keep bangin' out the patients using that same old procedure that rakes in the bucks even when there's far better options with fewer adverse effects available. It's disgusting. These people have a license to print money and so often they're inept and ignorant.
A diagnosis is futile because under the NHS Nice guidelines England theres zero treatments. This is a Fact. i was watching the news on tv in England uk tonight and a father was on because his 27 year old daughter recently died from M.E and the hospital stated there is no palitive care in any hospital within the UK for any person dying from M.E doctor stated more needs to be done for M.E but it must come from the highest level meaning government. UK government has denied it exsists and wont look into it. Unless the government change the NHS Nice guidelines then the NHS can offer no treatment that means millions of people who suffer from M.E are being denied hospital treatment and care. Its a scandal.. The health care minister Savid had his own family member with M.E and ge promised money and research into it, but hes no longer the health minister now. They promised people with long covid which is similar to M.E new research etc but thats now been scrapped For 30 plus years this disease has been ignored denied covered up by British government and the NHS Its criminal. I have a family member with it. Its heartbreaking 💔 and shocking 2024.....i write this in 2024..
Much love and strength to you. I'd like to give you this quote by Anthony William: "CFS-or whichever name for it speaks to you-is neurological fatigue from an ongoing and chronic Stage Four Epstein-Barr virus (EBV) infection. Any of the over 60 varieties of Epstein-Barr virus, accompanied by toxic heavy metals such as mercury and aluminum, create viral neurotoxins that inflame and drain the central nervous system, creating an exhaustion that’s far more pronounced and limiting than simply being tired. In its more aggressive forms, the neurotoxins cause a mild encephalitis (which is undetectable by MRI or CT scan), which creates even heavier fatigue. This neurotoxin inflammation of the central nervous system can eventually weaken the adrenals, liver, and digestive system, and create the feeling that you have a low battery."- I reccomend his book "brain saver
@mandil.7255 a new recent study by uk researchers into long covid has said..when a person gets an infection the body changes something within the Iron levels and red blood cells that provide oxygen and energy to a person but it gets stuck in the wrong place meaning red blood cells keep dying leading to anemia but the person doesnt have anemia but the iron in our body's gets shifted in the wrong gear leading to long covid or long term disease the red blood cells also help white blood cells people with long covid describe symptoms similar to M.E Chronic fatigue such as utter exhaustion muscle pain migranes etc etc..if this study and research is true..its lack of oxygen within cells that cause the sufferer to have zero energy supplies..a German Dr also said the same thing..Germany offer a medical treatment for this called cleaning the blood google it..its expensive and can't be done anywhere in the uk
I take both these supplements and at first there was a subtle difference, but now I don't notice anything. By the way, it's not "caused" by the lack of any supplement - there's an organic cause. Just because it hasn't yet been discovered doesn't make it non-existent.
Much love and strength to you, hope you get beeter. I'd like to give you this quote by Anthony William: "CFS-or whichever name for it speaks to you-is neurological fatigue from an ongoing and chronic Stage Four Epstein-Barr virus (EBV) infection. Any of the over 60 varieties of Epstein-Barr virus, accompanied by toxic heavy metals such as mercury and aluminum, create viral neurotoxins that inflame and drain the central nervous system, creating an exhaustion that’s far more pronounced and limiting than simply being tired. In its more aggressive forms, the neurotoxins cause a mild encephalitis (which is undetectable by MRI or CT scan), which creates even heavier fatigue. This neurotoxin inflammation of the central nervous system can eventually weaken the adrenals, liver, and digestive system, and create the feeling that you have a low battery."- I reccomend his book "brain saver
