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563 total results
Discussions (34)
ME/CFS and loss appetite
ME/CFS and loss appetite ... and the thought of eating also makes me ... incredible support from those closest to me
New diagnostic test for ME/CFS
New diagnostic test for ME/CFS ... to share with those who suffer with ME ... /CFS (or Fibromyalgia as these two disorders
LDN dosing for fibromyalgia and ME/CFS
LDN dosing for fibromyalgia and ME/CFS ... Naltroxone (LDN) for Fibromyalgia and ME ... /CFS. ... My local doctor wants me to just take
Yale Paper: Long COVID/ME/CFS
Yale Paper: Long COVID/ME/CFS ... article posted, some 'grab' me
Online Conference on ME/CFS and LC in May
Online Conference on ME/CFS and LC in
Wheelchair for axonal polyneuropathy & ME/CFS: So freeing
/CFS: So freeing ... I’ve been disabled with ME/CFS (Chronic ... /CFS and pain associated with that, ... /CFS or PN. ... My ME/CFS still greatly limits my activity
Multiple Myeloma: Could fatigue and breathlessness be ME/CFS?
Could fatigue and breathlessness be ME ... /CFS? ... fatigue and breathlessness is caused by ME ... /CFS?
Possible medical markers for ME/CFS, Long Covid
Possible medical markers for ME/CFS, ... As a long time ME/CFS patient of Dr.
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) treatments
/CFS) treatments ... found any treatments that help with ME ... /CFS. ... So I guess that would be moderate ME ... /CFS.
Idiopathic Polyneuropathy: Do you have fatigue?
https://connect.mayoclinic.org/discussion/idiopathic-polyneuropathy-do-you-have-fatigue-with-your-s/
But, I also have ME/CFS (which I’ve ... my fatigue is due to neuropathy or ME ... /CFS.
Myalgic Encephalomyelitis and Chronic Fatigue Syndrome Support
Why isn’t there a support group for ME ... /CFS?
Managing Post-Exertional Malaise (PEM): What can help?
common with Long Covid same as with ME ... /CFS?
TurnTo app is a great resource
out to be an invaluable resource for me ... towards people with Long Covid and ME ... /CFS and provides user-generated information ... personal experience with Long Covid and ME ... /CFS.
How to talk to my doctor & share research/knowledge I have found?
Two years ago I was diagnosed with ME ... /CFS.
Recover Covid Initiative Study - Discussion via Zoom
Understanding metformin use and Long COVID and ME ... /CFS following COVID-19 infection: Insights
Can I expect coordinated care from Post COVID Rehabilitation Program?
Took me 6 months to confines my Doctors ... , sleep apnea and narcolepsy, have me ... shared that That I think, I my have Me ... /CFS with Fibromyalgia and they basically
Massive Retrocerebellar Arachnoid Cyst
#39;s I was finally diagnosed with ME ... /CFS, dysautonomia, and small fiber ... debilitating or particularly concerning to me
Short Term Disability: What info or medical records helps approval?
few weeks ago at Mayo that I have ME ... /CFS and fibromyalgia with the long ... company that manages our STD is scaring me ... records, which she wants to discuss with me
Possible Autoimmune…undiagnosed
him I didn’t want meds prescribed to me ... ; was told “no specialist will see me ... I’ve even looked into ME/CFS & asked
Mayo Clinic Rochester: Shuttle services between buildings
Just wondering if anyone can tell me ... how far it is to the FM/CFS building
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