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570 total results
Comments (535)
Does anyone know if the Phoenix Mayo now treats those with ME/CFS & fibro? I read...
https://connect.mayoclinic.org/comment/948271/
Phoenix Mayo now treats those with ME ... /CFS & fibro?
Hi @lukek and welcome to Mayo Clinic Connect. My suggestion would be to visit your local...
https://connect.mayoclinic.org/comment/720322/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments: https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
I have very debilitating ME/CFS and would love definitive answers to help me. I started with...
https://connect.mayoclinic.org/comment/632780/
I have very debilitating ME/CFS and ... would love definitive answers to help me ... I started with CFS 50 yrs ago.
Yes, your dr is correct. 4.5 mg is the normal dose. I have been on it...
https://connect.mayoclinic.org/comment/948251/
have an NP who only treats those with ME ... /CFS, Fibro, POTS, Long Covid (so fatigue ... So I read the research she gave me & ... formost researchers in the US for ME ... /CFS, etc.
It seems a mystery to me why ME/CFS remains a mystery to doctors. The research being...
https://connect.mayoclinic.org/comment/692631/
It seems a mystery to me why ME/CFS ... /CFS people. ... ME/CFS seems to have a mystery origin ... clue how to heal autoimmune," ME ... /CFS sufferers ARE THE CLUES.
Hello @rarelybees2889, Have you seen the following discussion? You might want to post any questions you...
https://connect.mayoclinic.org/comment/289136/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments
-- https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
Hi @brynna20, I would like to add my welcome to Connect along with @ethanmcconkey. There is...
https://connect.mayoclinic.org/comment/270456/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments
-- https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
Welcome @eabbott, I'm sorry to hear that the muscle twitches have been getting worse. I do...
https://connect.mayoclinic.org/comment/733638/
you have Chronic Fatigue Syndrome (CFS ... Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments:
https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
According to the English, ME/CFS is the same thing. The ME means the brain lining is...
https://connect.mayoclinic.org/comment/677383/
According to the English, ME/CFS is ... The ME means the brain lining is inflamed ... re sick, you may feel like you have CFS ... since not much has been learned about ME ... /CFS is 40 years or so, we're sort
@tamiwright, I thought you might find the following video helpful. What happens when you have a...
https://connect.mayoclinic.org/comment/225254/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments
— https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
No they cannot infect people. It just means they never recovered from covid. Those with LH...
https://connect.mayoclinic.org/comment/727982/
symptoms similar to other illnesses like ME ... /CFS, POTS, MCAS.
Yes. Probably those told they have me/Cfs should ask to be tested. At least knowing its...
https://connect.mayoclinic.org/comment/1164109/
Probably those told they have me/Cfs ... be, if doctors label a patient with ME ... /CFS or similar maladies they stop
Hi, @sundance6 Haven’t heard from you in a while! I thought that maybe you were doing...
https://connect.mayoclinic.org/comment/1092856/
information from Mayo Clinic about ME ... /CFS. ... state has a program or clinic for ME ... /CFS. ... hope your doctor can do for you and CFS
@colleenyoung An antiviral (Valtrex) and low dose Naltrexone have been helpful in reducing symptoms. I'm very...
https://connect.mayoclinic.org/comment/200393/
by doctors who did not understand ME ... /CFS. ... I went from mild/moderate ME/CFS to ... moderate/severe ME/CFS. ... /CFS.
You need a specialist with Two fellowships: Infectious disease Immunology. At Stanford in California you need...
https://connect.mayoclinic.org/comment/1033526/
It is called PACs and me/cfs center
Post Exertional Malaise - this is the term I first read about on a different thread...
https://connect.mayoclinic.org/comment/899509/
you going -
https://www.cdc.gov/me-cfs ... treating-most-disruptive-symptoms.html
https://www.cdc.gov/me-cfs ... Managing-PEM_508.pdf
https://www.cdc.gov/me-cfs
Hello @wandahondaconda -- Welcome to Connect. I'm glad you found us. Connect is a safe place...
https://connect.mayoclinic.org/comment/207077/
Encephalomyelitis/Chronic Fatigue Syndrome (ME-CFS ... Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments
-- https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
I'm not sure that there is a specialist type of doctor that treats ME/CFS if that...
https://connect.mayoclinic.org/comment/867587/
specialist type of doctor that treats ME ... /CFS if that is what you have based ... encephalomyelitis/chronic fatigue syndrome (ME ... /CFS): https://www.mayoclinic.org/diseases-conditions
Hello @herder42, I would like to add my welcome to Connect along with @covidstinks2023 and others....
https://connect.mayoclinic.org/comment/1345678/
quite a few other discussions on the ME ... /CFS condition if it sounds similar ... search=ME/CFS.
I’ve been on 3 mg LDN for 10 years. It’s the only pain med I need...
https://connect.mayoclinic.org/comment/1348123/
sensory motor axonal Polyneuropathy, ME ... /CFS, and fibromyalgia.
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