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446 total results
Comments (422)
Thank you everyone for your posts. I really appreciate feedback because I don’t feel like I...
https://connect.mayoclinic.org/comment/716188/
It seems to be similar to ME/CFS. ... My symptoms seem to fit more with ME ... /CFS partly because I don’t have the ... I have read a lot about ME/CFS and watched ... in my head, I’m like no that’s not me
Had similar experiences with exercise. Most rheumatologists seem to prescribe this. They also seem to forget...
https://connect.mayoclinic.org/comment/731793/
malaise is a typical symptom of the ME ... /CFS. ... If my body tells me to stop, I stop. ... If you truly have ME/CFS, you won'
I so far haven't had COVID, I have a billion other health problems but not that....
https://connect.mayoclinic.org/comment/1079199/
pains were just like fibromyalgia, me ... /CFS, thyroid issues, chronic inflammation
Unfortunately fascinating story. My symptoms are not as bad. However, every so often another develops. Because...
https://connect.mayoclinic.org/comment/677955/
However, I suspect those of us with ME ... /CFS have felt like pests for years.
Just wanted to shout out to both you (sueleerock) and seekay. I do follow these threads,...
https://connect.mayoclinic.org/comment/183182/
post is interesting as stating that ME ... /CFS may get worse with people trying
Systemic exertion intolerance disease is the new name for ME/CFS (myalgic encephalomyelitis/chronic fatigue syndrome). It is...
https://connect.mayoclinic.org/comment/135066/
intolerance disease is the new name for ME ... /CFS (myalgic encephalomyelitis/chronic
My son has had LC ME/ CFS symptoms since summer of 2022. We have tried several...
https://connect.mayoclinic.org/comment/966146/
My son has had LC ME/ CFS symptoms
Hello @christine32, Welcome to Connect. I know it must be difficult trying to find clothing that...
https://connect.mayoclinic.org/comment/977963/
Distinct Type of Pain in Fibromyalgia and ME ... /CFS: https://www.verywellhealth.com
@pluckyn welcome to the group!! Mals... well it is a significant surgery and one that is...
https://connect.mayoclinic.org/comment/131197/
controlled after the surgery, for me ... contributes to a lot of symptoms but so does ME ... /CFS.
You are absolutely not crazy, I hear it as well. It’s usually when I am transitioning...
https://connect.mayoclinic.org/comment/1038045/
started with a lot of confusion and ME ... /CFS, also highly anxious, depressed
Also have extremely high Epstein Barr titer. Have had it for 30 years. After all sorts...
https://connect.mayoclinic.org/comment/716868/
diagnosis is Chronic Fatigue Syndrome or ME ... /CFS as it's now known.
I am now 71 years old and still no diagnosis. (My symptoms seem to line up...
https://connect.mayoclinic.org/comment/207076/
(My symptoms seem to line up with ME-CFS ... doctors and my increasing age makes me ... The doctors I have seen want to push me ... Thank you for allowing me to vent.
Very important study, and yet small N, no control group, and expectancy effect may be at...
https://connect.mayoclinic.org/comment/745136/
let us know and if any other tx for ME ... /CFS and POTS please keep us posted.
My heart goes out to you. I know what it feels like to have illness that...
https://connect.mayoclinic.org/comment/1039662/
inflammatory condition), CRPS and, perhaps ME ... There is also an online publication on ME ... /CFS that may guide you, too.
To me, the hardest part of LC is the lack of recognition from doctors that it...
https://connect.mayoclinic.org/comment/1029939/
To me, the hardest part of LC is the ... It really throws me that now, 4 years ... POTS, orthostatic intolerance, PEM, ME ... /CFS, cognitive impairment as well as
I have vibrations now since shots as well, (along w so many long covid me/cfs symptoms)...
https://connect.mayoclinic.org/comment/896127/
well, (along w so many long covid me ... /cfs symptoms) they fade in to the background
@karina77 , Hi Karina, I'm afraid I can't answer your questions about IV therapy having never...
https://connect.mayoclinic.org/comment/255456/
that I've read new information on ME ... /CFS that I would like to discuss at
Hi, I'm in the same position. I'm worried at the idea of 10yrs on Tamoxifen. I've...
https://connect.mayoclinic.org/comment/1070034/
I've had Fibro ,CFS & and migraines ... hear from others with Fibromyalgia, Me ... & CFS to see how they are on Tamoxifen
Hi Barbara, To my knowledge, Post Interferon Syndrome (PIS) has only been recently been acknowledged by...
https://connect.mayoclinic.org/comment/183086/
have better luck finding help with a ME ... /CFS specialist as the PIS is a subset ... of ME/CFS. ... /CFS. ... Each of these doctors have helped me
John, Thank you for reaching out. Actually, I have been to many doctors and have very...
https://connect.mayoclinic.org/comment/750710/
In 2011, a rheumatologist diagnosed me ... accepted that diagnosis and treated me ... The new diagnosis became ME/CFS, which
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