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711 total results
Comments (667)
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
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.
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
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.
@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).
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
@sandguy I’m sure sorry you’ve got LC now. Your story is so interesting because I knew...
https://connect.mayoclinic.org/comment/1473231/
also got the “yuppie flu” followed by CFS ... also believe LC is likely the same as ME ... /CFS.
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
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.
@ 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
All that you say is true and I've experienced it all over the years. I am...
https://connect.mayoclinic.org/comment/1398813/
patient who they'd diagnosed with ME ... /CFS (Myalgic Encephalomyilits/Chronic ... It frustrated me to hear that, thinking ... why didn't you say something to me ... My issue had also been called ME/CFS
@2011panc , @JK Volunteer Mentor, @grandmar , Thank you for your thoughts. It's difficult for me...
https://connect.mayoclinic.org/comment/254272/
It's difficult for me to talk to ... I also realize that ME/CFS is poorly
@cjd72 and @hraka13 , LDN is not an opioid- it’s actually an opioid antagonist and was...
https://connect.mayoclinic.org/comment/1436305/
kinds of pain including fibromyalgia, ME ... /CFS, osteoarthritis, and severe Polyneuropathy ... It’s been a game changer for me and
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.
I sincerely hope you did not construe my comments as negative. They are not meant to...
https://connect.mayoclinic.org/comment/610676/
(famous author) has suffered with ME ... /CFS for decades, as have many, many
Dr. Paul Cheney and his partner first identified a cluster of very sick patients (who were...
https://connect.mayoclinic.org/comment/1296500/
sick patients (who were later labeled ME ... /CFS) in their Lake Tahoe practice in ... from all over the world including me
ME/CFS would be physically and emotionally hard, navigating how much one can exert oneself and diet....
https://connect.mayoclinic.org/comment/1287775/
ME/CFS would be physically and emotionally
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