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702 total results
Comments (660)
Most helpful in the understanding of why more help/answers are NOT forthcoming from the Medical Profession...
https://connect.mayoclinic.org/comment/96452/
viewing of "UNREST" a documentary about ME ... /CFS on INDEPENDENT LENS---Ch. 9.
@dlydailyhope thanks for the input. I have large fiber Idiopathic Axonal sensors-motor Polyneuropathy. Neurologist said it’s...
https://connect.mayoclinic.org/comment/1416282/
I’ve had ME/CFS for 40 years that was
Hi. I am sorry you are going thru all of this. Have you had an endoscopy...
https://connect.mayoclinic.org/comment/751494/
I have ME/CFS which is a post viral ... might want to check out Long Covid or ME ... times but therapy and my faith bring me
I'm so sorry - I live in south Jersey, and my PCP is in north Jersey...
https://connect.mayoclinic.org/comment/1039465/
willing to join an appointment with me ... She focuses on LC and ME/CFS.
I think you nailed it. Any person, website, institution or organization that promises a cure is...
https://connect.mayoclinic.org/comment/1235115/
causes the symptoms of Long Covid or ME ... /CFS or Long Lyme or any of the post-infectious
My new neurologist just prescribed Gabapentin but I refused to take it. I’ve been on Low...
https://connect.mayoclinic.org/comment/1348112/
LDN has worked well for me with all ... I also have severe ME/CFS and fibromyalgia ... Gabapention would be a disaster for me ... It took me 2 years to wean off Xanax
@daisy17 Re the price. I just read an article about Tonmya vs cyclobenzaprine (Flexeril), written by...
https://connect.mayoclinic.org/comment/1426174/
article by Health Rising blog (re ME ... /CFS & Fibro), says Dr Clauw, Director
CFS/ME center at Stanford University. Long waiting list there and you have to meet the criteria...
https://connect.mayoclinic.org/comment/837569/
CFS/ME center at Stanford University ... How did they diagnose you for ME/CFS
Gratefully, I am not incontinent. I often have to wait a bit and focus to urinate....
https://connect.mayoclinic.org/comment/1402967/
Also, 30 years of ME/CFS.
Yes. I have these. As far as I can tell these are caused my microclots that...
https://connect.mayoclinic.org/comment/794744/
Long-COVID parallels and seems identical to ME ... /CFS. ... Teitelbaum had recovered around 3,000 ME ... and get folks out of Long-COVID and ME ... /CFS.
@lauracbaker Your suggestion is not offensive at all! I am a person diagnosed with me/cfs, fibromyalgia,...
https://connect.mayoclinic.org/comment/1433768/
I am a person diagnosed with me/cfs, ... There are MANY reasons for me to increase ... trigger a flare up that will land me
Gosh, I sure hope you do. Good to hear that other symptomes hve gone. There is...
https://connect.mayoclinic.org/comment/801450/
been used in many diseases, including ME ... /CFS155, and has also shown promise ... shown to reduce autoantibodies in ME ... /CFS161. ... /CFS literature
-Prófa
A small
Hello after an illness (upper respiratory) I developed an autoimmune disease for which I am seronegative....
https://connect.mayoclinic.org/comment/727801/
Mayo was a very important visit for me ... finally found out what was wrong with me ... ME/CFS, sleep apnea, autoimmune diseases
@palepa, fatigue and breathlessness are debilitating and real. They are also symptoms of a wide-range of...
https://connect.mayoclinic.org/comment/1198097/
encephalomyelitis/chronic fatigue syndrome (ME ... /CFS).
@ arcuri24 I have been on low dose naltrexone (3mg) for 10 years. It does wonders...
https://connect.mayoclinic.org/comment/1361630/
pain but the pain associated with ME ... /CFS and fibromyalgia. ... have any pain, but that the LDN keeps me
Dr Susan Levine Infectious Disease doctor in NY. She takes insurance (she’s nutty but I’ve been...
https://connect.mayoclinic.org/comment/1231260/
And she is a ME/CFS and Long Covid specialist
ME and CFS are considered by some scientists to be autoimmune conditions triggered by a viral...
https://connect.mayoclinic.org/comment/706598/
ME and CFS are considered by some scientists ... Autoimmune wellness Stories of Recovery ME ... CFS (or spell out those conditions.
Hello @chistiania, There are some discussions that you might find helpful learning more about the risks...
https://connect.mayoclinic.org/comment/774808/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments:
https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
I am now on sirolimus, generic for Rapamycin, which is used off-label for ME/CFS, but is...
https://connect.mayoclinic.org/comment/948274/
Rapamycin, which is used off-label for ME ... /CFS, but is actually a drug for anti-rejection ... Health Rising blog about a dr with ME ... /CFS who was sick with it for 10 years
There are many ways to mitigate the suffering we are experiencing however, to my knowledge, there...
https://connect.mayoclinic.org/comment/183100/
your condition, knowledgable about ME ... /CFS? ... that not one of them was able to give me ... each of them what best worked for me ... /CFS.
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