Chronic Fatigue Syndrome IS LONG COVID? | Dr Sarah Myhill 

Yes and how does one no what's what

@@Truerealism747 a blood titers test should be able to show exposure, either latent or acute, to viruses. If you have access to ME/CFS aware doctors, you can request that test and the results should give an idea of the overall viral load by an IGM/IGG blood serum test. (The titers blood test)

Not sure if this will help, but I was sure I had either CFS or fibromyalgia. It all started with constant cold like symptoms then progressed to more flu like symptoms. I was back and forward to the Dr's for few years. I had cameras down my throat, chest xrays, ECGs, bloods etc, but everything came back normal, Dr's said there's nothing wrong with me. But I'd begged to differ, my symptoms got worse after having my second child in 2018 and by 2019 I was bed bound most days and constantly in pain. Any way, I started looking into things as my little one had bad eczema and found not too good things about a lot of the synthetic chemicals that are in almost everything we use. I started changing up things, food/drinks, cleaning products, hygiene/beauty products etc to more natural and/or organic. But what I found was that I myself started to get better as a result of these changes. I now fully believe we should be living more on the natural side and try to eliminate as many synthetic chemicals as possible out of our lives. I really do believe these things wreak havoc in/on our body. If they don't appear naturally in nature our body isn't used to living with them. We have like little eco systems in and on our body and these chemicals tend to be disruptive to them. I know it might seem a bit too much for some, but it has cured my little ones eczema and I truly think this has saved my life. I can do normal day to day things now and have a life. I think food was the main player in my health, so it may be a good idea to look at what you eat and if possible change it to atleast 80% organic. Make sure meat and dairy is from organic grass fed animals or at the least grass fed. Cut out processed foods and try to cook from fresh. Cut out veg and seed oils, especially oils with low smoke thresholds, never cook with them. Hippocrates was right, "let food be thy medicine and thy medicine be thy food." Sorry its so long winded, just wanted to cram in so much to try and help and to be honest, I've barely scratched the surface with things here lol. Hope this helps you hun, don't give up. Peace and love

Have you had your am cortisol levels checked? When I first developed ME in 2004, due to my very low cortisol, I was given low dose hydrocortisone and agreed, much help. Now years later my levels have been normal but upon a recheck they were borderline low. You may need to see an endocrinologist for that. If low enough, a low dose would be Indicated.

@@joeynarciso94 did the help with the muscle pains

​@@129babehas your muscle pain gone

​@@joeynarciso94found out I have autism heds and sleep problems related to cortisol to CFS fybromyalgia b26 years same condition will a endo treat for this

Get checked for hypomobility rccx gene theory

yes, me too- My CfS got extreme right after I took Covid Vaccine for some reason. I had it for years from a severe car accident then whiplash event, now after covid vaccine I cannot even have energy to drive it walk to mail box. Keeps getting worse & no one to understand or help me as every time O have gone to hospital E R with extreme weakness, they just say they don’t find anything then put me in a wheel chair in waiting room for hours to have taxi take me home. Now I don’t go there because I don’t have the strength to do the taxi ride and then get home and get myself cleaned up and to bed. I can’t even have strength now to take shower with a shower stool last year and half… I don’t know what to do or where to turn for help as doctors can’t diagnose it & O am not 60 years old. There needs to be a special clinic and place for people with this condition in my view-

@@Blubirdmoon111 there is a clinic in London but it's getting in and liverpool.ive had it 27 years my father has it to reason it's git worse for you is mcas take look at this having sleep apnea test next week to

what is mono amine?