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666 total results
Comments (626)
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.
@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
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
@vostie Its always good to hear LDN success stories. I’ve been on it for 10 years...
https://connect.mayoclinic.org/comment/1384983/
I’ve been on it for 10 years for ME/ ... CFS, arthritis, fibromyalgia, and severe
@jubilee That’s great to hear you’re doing better! Neuroplasticity is important in every disorder/disease. It gave...
https://connect.mayoclinic.org/comment/248336/
It gave me hope I could improve, but ... unfortunately for me until they find ... I wish there were in person ME/CFS groups
My son is seeing significant improvement from IVIG infusions. He has had 3 infusions so far...
https://connect.mayoclinic.org/comment/1154231/
has had 3 infusions so far and his ME-CFS
This is so interesting. The med that really helps me is a 200 mg. tablet of...
https://connect.mayoclinic.org/comment/1373403/
The med that really helps me is a 200 ... nothing and low dose aspirin makes me ... But, I had ME/CFS for many years before
@erickthompson I think my burning sensation comes from "focusing" / trying to understand what I read...
https://connect.mayoclinic.org/comment/1456311/
New paper: The top treatments for ME ... /CFS and Long-COVID
https://youtu.be ... Patient-reported treatment outcomes in ME ... /CFS and long COVID
https://pubmed.ncbi.nlm.nih.gov
@amber3212 I will attach a link for great articles on new research on CFS. There is...
https://connect.mayoclinic.org/comment/238507/
great articles on new research on CFS ... new-harvard-chronic-fatigue-syndrome-me-cfs-research-center-fulfills-crucial-need
As soon as I was diagnosed with stage three CKD, my rheumatologist sent me to a...
https://connect.mayoclinic.org/comment/707992/
three CKD, my rheumatologist sent me ... also have labile
blood pressure, ME ... /CFS, and Graves disease.
Hi. Yes you can take the two together. My Stanford LC/ME/CFS clinic started me on LDN...
https://connect.mayoclinic.org/comment/1244823/
My Stanford LC/ME/CFS clinic started ... me on LDN and after a number of months ... They then started me on Abilify - again ... very low does (0.1mg/day) and had me
I am so sorry to read about all you have gone through. I was first diagnosed...
https://connect.mayoclinic.org/comment/1305520/
I was first diagnosed with ME/CFS by ... I still have ME/CFS and LC, but after
Hi @webdog, thanks for starting this discussion on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). I'd like to...
https://connect.mayoclinic.org/comment/200368/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS).
I saw your post and I can relate to everything you’re going through post covid. For...
https://connect.mayoclinic.org/comment/1443602/
For me, I was healthy and fit before ... Your symptoms also seem to mirror ME ... /CFS.
Hello @jacii, welcome to Mayo Clinic Connect. I noticed you also created another new discussion in...
https://connect.mayoclinic.org/comment/239836/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments
— https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
I became disabled with ME/CFS (Chronic Fatigue Syndrome) following an acute Epstein Barr Virus infection almost...
https://connect.mayoclinic.org/comment/1356077/
I became disabled with ME/CFS (Chronic ... Still have ME/CFS.
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