Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) 

Giving up the “combat“ is the first step. Take Part in social life is the second step. Don't isolate.

Treat it as an auto immune illness. Make sure as a bear minimum you take as many natural anti inflammatories as you can . Don't ever be fooled into taking steroids. They will embed and make the condition worse. There are loads upon loads of natural minerals and phyto chemicals to combat the effects and the most important to kill off the virus is a mix of naturals that enhance the bodies production of natural interferons able to knock the causation out. As with cancers. They have to be taken accompanied by alcohol. So that they can working the brain by crossing the brain barrier. And taking with them the necessary interferons. In the same way as gin n tonic were developed to protect and kill of malaria.......alcohol to transit the brain barrier......and quinine ( tonic ). Hence the creation of gin and tonic as a drink . Made popular in India.

M.E is not a mystery . The mystery come with the medical ignorance and baffoons that continually talk dross.

It's fibro. Phosphate retention. Read Dr st amands book 📖 😀

I feel like it’s one of the worst illnesses you can have.

Funny how our bodies ache, we fall asleep at our desks....yet....whatever this is is in our heads! But our heads aren't hurting!!!

Carnivore will help

@@angelagrant2943 Yes it does as does BodyBio's Phosphatidylcholine

AIP diet with Benfotiamine, B-complex, D-Ribose, Acetyl-L-Carnitine (all proved efficient with ME and fibromyalgia), and herbs like lemon balm, passion flower, valeriane to sleep like a baby

OMG!!! I CANT BELIEVE YOUVE BEEN SICK FOR 41 LONG YEARS!! IM GOING ON 19 YEARS IN JANUARY 2024. I KEEP TRYING TO STAY POSITIVE FOR CURE BUT THERE IS NO GUARANTEE OF A CURE. SENDING LOVE AND HUGS!! From New York, USA

42 now and age is not helping, lol If I could give any advice to other sufferers it would be definitely keep to whatever your envelope of strength is and take LOTS of Melatonin I have for many many years and I believe it has helped in a thousand ways.@@pattycolon5655

Hanging on! The truth is coming! Dark to light!

ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-R01PRRF3774.html

Did you try carnivore?

@@godloves9163 yes. I'm currently BBEB

ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-R01PRRF3774.html

It’s practically the same but is a bit worse. Mega doses of thiamine Tetrahydrofurfuryl Disulfide have massively improved my life. ru-vid.com/video/%D0%B2%D0%B8%D0%B4%D0%B5%D0%BE-R01PRRF3774.html

I believe at some point chronic Fatigue syndrome was changed in name only to fibromyalgia. Just a hunch.

@@nathandavis5730 Interesting! Thiamine deficiency is very possible. Thank you for sharing info and video. Any specific supplement recommendation that you personally like and take? Amazon maybe....

@@marioa9350 Thiamax is a good brand. I’d highly recommend you get Elliot Overton’s booklet on how to do the entire treatment so you ease into it rather than hitting hard straight out the gate

They are sister diseases and 50% of CFS patients also have fibromayalgia.

olive leaf extract might help with the flare ups and berberine(?)

@@bobbytill Thank you Bobby for replying! ☺

How are you now? I am currently learning about ATP through Dr Huberman & Attia ... I have seen evidence of Lysine being effective. Does Dr Myhill speak about Anti Virals?

@@Stak1776 Sorry, I don't remember specifically, but she does often say as most do that a viral infection is the usual main cause of MECFS. In the past, I was misdiagnosed with Meniere's disease. I did start taking L -Lysine which does help with brain clarity. I continue to take it....seems like I get less "brain fog." Hope this helps. If I were you, I would say, just buy Dr. Myhill's book. It's a tremendous reference. Miss Monique 🙂🙏💗

I’m not so sure CFS is in itself a virus, but instead it’s HOW a virus can affect the nervous system resulting in CFS. My bet is the virus you had is long gone. You may even have immunity to it now. What it left behind is the damages and inflammation that our bodies can’t fight off on it’s own. Many, many people with CFS didn’t come down with a virus first. I didn’t. For me it was chemical toxicity from chemotherapy that was preceded by emotional traumas throughout my life. I’m simply pointing this out to you to give you a different perspective of this condition and perhaps a new way to think about how to combat it. I doubt you are currently combating the original virus. People do recover and none of them recovered by depending solely on conventional medicine practitioners. I think many if not most recovered without the help of any type of medical practitioners. There are people to be found on RU-vid (search chronic fatigue RECOVERY) that are offering solutions - often it’s those who have recovered from CFS. What works for some doesn’t work for others. Some ppl need a combination of therapies. We just have to keep trying until we find what works. Healing is going to take time. There’s no magic pill. Here’s some suggestions to get you started: On RU-vid >Irene Lyons - she uses Somatic Experiencing Therapy. SET was developed by Dr Peter Levine who first used it to help veteran’s with PTSD. But don’t think it’s only for those who have been traumatized. This therapy focuses on healing the nervous system and our systems are greatly damaged. >Crappy Childhood Fairy >Raelan Agle What has helped me the most is reducing/eliminating stressors and pacing my use of energy. Other things that have contributed: Curcumin supplements (powerful anti_inflamatory, I had to experiment with doses. I take 800 mg 2x/day) eating more red meat (animal fat is good fat) high dose vitamin C, colostrum powder from Sovereign Labs, eliminating aspartame - which has been renamed, so look that up (it’s in milk but not required to be on the ingredients label) I’m working on eliminating sugar as much as possible, with the exception of quality honey and real maple syrup. I hope you’ll find this helpful.