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568 total results
Comments (533)
@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
Discussion: Functional Neurological Disorder (FND)
Support Group: Brain & Nervous System
Posted: Feb 26, 2019
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.
Discussion: Stage 3 chronic kidney disease (CKD): What specialists do I see?
Support Group: Kidney & Bladder
Posted: May 13, 2022
@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
Discussion: Chronic Fatigue Syndrome and Temporary Paralysis?
Support Group: Just Want to Talk
Posted: Jan 4, 2019
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
Discussion: What helps longhaulers dealing with Chronic Fatigue?
Support Group: Post-COVID Recovery & COVID-19
Posted: Feb 24 5:02pm
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
Discussion: Difficult case, several diagnosis, no solution yet
Support Group: Autoimmune Diseases
Posted: Mar 9, 2019
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
Discussion: Epstein Barr Nuclear AG AB IGG result of over 600
Support Group: Infectious Diseases
Posted: Oct 28, 2024
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
Discussion: Going off of Xanax
Support Group: Depression & Anxiety
Posted: Oct 9, 2024
@prn2016 - I've had ME/CFS since 1986 and have been on LDN for 6 years. LDN...
https://connect.mayoclinic.org/comment/845798/
@prn2016 - I've had ME/CFS since ... has helped lesson the pain from FM, CFS ... back down to find the sweet spot for me
Discussion: Low dose Naltrexone for POTS helping alot
Support Group: Post-COVID Recovery & COVID-19
Posted: Apr 19, 2023