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699 total results
Comments (657)
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
I understand how scary it is to get those results. I’ve had ANA+1:320 speckled patterns for...
https://connect.mayoclinic.org/comment/1445835/
But I also have ME/CFS (Chronic Fatigue
@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
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
@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
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).
@bbj2009 There is an article on Phoenix Rising called, "The reason why antivirals like Valtrex and...
https://connect.mayoclinic.org/comment/1472051/
Valcyte take such a long time to work in ME ... /CFS (or don't work at all), according
@law59 these symptoms are just so bizarre. My cardiologists gave me new diagnosis of inappropriate sinus...
https://connect.mayoclinic.org/comment/1427722/
My cardiologists gave me new diagnosis ... Next step is getting the ME/CFS and ... Showering has been challenging for me
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.
There is no test for M.E./ Cfs. They say it is diagnosed by exclusion. If your...
https://connect.mayoclinic.org/comment/1164136/
./ Cfs. ... things they understand they call it me ... /cfs. ... To me it says they don’t know what is ... Like ME/CSF, EBV also is a mystery
Helo! I'm new in this online gathering and I have questions about Xanax. I am 74...
https://connect.mayoclinic.org/comment/1154332/
I developed ME/CSF in 2022 and the struggle ... they took my history and recognized ME ... /CFS. ... ME/CFS is almost unknown in this country
Gjul16 I’m sorry I’m really foggy as I’m crashing tonight. I don’t understand your post. Hope...
https://connect.mayoclinic.org/comment/135184/
Most of the causes of ME/CFS are from
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