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568 total results
Comments (533)
Yes, meds take longer to help. I am so glad to hear you also take cymbalta!...
https://connect.mayoclinic.org/comment/169903/
With CFS you get a lot of joint pain ... second, but the fatigue is what keep me ... may not be able to eat a lot, but to me ... Let me know if you try the diet, I would
@kariulrich thanks for getting back to me. I take Cymbalta. I was given that years ago...
https://connect.mayoclinic.org/comment/169902/
kariulrich thanks for getting back to me ... I was given that years ago for the CFS ... Well stay positive and keep me posted
I, too, am getting fed up at present with the Constant pain which comes from no-where...
https://connect.mayoclinic.org/comment/89663/
.........such is the Fibromyalgia, ME ... and CFS... ... is destroying our lives, please let me
I was diagnosed with CFS in 1980 having several cramps a day in legs, feet and...
https://connect.mayoclinic.org/comment/1190091/
I was diagnosed with CFS in 1980 having ... An interesting point, CFS is not supposed ... Subsequently, my neurologist is enlisted me
Hi Jeffmarc, Thanks for your thoughts and reply. Do a little reading on TESTOSTERONE to see...
https://connect.mayoclinic.org/comment/1188824/
and brain surgery which did assist me ... Although TRT isn’t prescribed for CFS ... without utilizing TRT already places me ... I’ve made have worked out well for me ... time and thoughts you’ve shared with me
Thank you for your reply on my condition. I understand what you are talking about pushing...
https://connect.mayoclinic.org/comment/1144118/
But she does believe I have CFS/ME. ... yesterday Mayo Rochester got a hold of me ... Cardiologist and they agreed to refer me
I do not know if FM/CFS or Osteoarthritis react differently for different people. Climate change does...
https://connect.mayoclinic.org/comment/1140556/
I do not know if FM/CFS or Osteoarthritis ... As for me, if the Barometric Pressure ... and humidity does not seem to affect me ... For me, mid August our summers ever ... cold of winter months really affect me
Back in 2016, I had a whole bunch of those, all up and down my spine...
https://connect.mayoclinic.org/comment/1132241/
She explained quite a bit to me, when ... They shifted me to chiropractic, only ... room, and had me pull down my pants ... They laid me out, and lifted me up carefully ... with CFS, but I had to go off the herbal
I use St John's Wort which is classified as an MAOI. That's the oldest form of...
https://connect.mayoclinic.org/comment/1127806/
because I have a new diagnosis of CFS ... John's worked very well on me and ... if the Cymbalta gives me troubles, ... it and have the doctors treat the CFS ... records, they had so little respect for me
I’m coming to you as someone who has both PMR and Fibro for 15 years! That...
https://connect.mayoclinic.org/comment/1122408/
For me, pain is where my body touches ... My dr got me on Kevzara injections recently ... messed up my immune system and started me ... I also have CFS chronic fatigue syndrome
Hello to all of my fellow men dealing with Prostate Cancer. I was diagnosed at age...
https://connect.mayoclinic.org/comment/1078739/
also been severely debilitated from CFS ... effectively and measurably address CFS ... Also of great importance to me was to
Correction to my post I meant to say RE activation not deactivation. But I think you...
https://connect.mayoclinic.org/comment/1072239/
My doc is trying to get me on Valacyclovir ... forerunner for treatment protocol for CFS
I found this article fascinating and self-descriptive - I had CFS (diagnosed by Mayo) in the...
https://connect.mayoclinic.org/comment/1068376/
fascinating and self-descriptive - I had CFS ... has obviously stopped working for me
Please do check out the post-viral-infection syndrome website at www.solvecfs.org This is the US nexus for...
https://connect.mayoclinic.org/comment/1033017/
research into infections like long-COVID; CFS ... Syndrome, and you'll also see ME
I was in my best shape and best life before getting Covid Dec 2020. Never had...
https://connect.mayoclinic.org/comment/1032755/
Gods funny humor showed me to be careful ... It took me 3 months to “feel normal ... the neurologist said he can’t help me ... original rheumatologist diagnosed me ... exertional malaise) that is associated with CFS
Hi- I know this is an older post, but thought I’d try reaching out. I was...
https://connect.mayoclinic.org/comment/1021762/
I don’t have CFS, but I have fatigue ... Initially, all my specialists told me ... original neurologist who diagnosed me
I have, thank you so much for your time and help. I am just really frustrated,...
https://connect.mayoclinic.org/comment/1016286/
find more specific answers about the CFS ... Rochester clinic because they have a CFS ... The Rochester clinic did accept me as ... had something beneficial to offer me ... tele-medicine appointment with the CFS
Myalgic encephalomylitis>( medical name for CFS). I hate the name CFS. It is not a good...
https://connect.mayoclinic.org/comment/960692/
encephalomylitis>( medical name for CFS ... I hate the name CFS. ... ppl has been caused by the use of CFS ... I have used the nam,e of ME for yrs.
ALL providers SHOULD be more covid literate but sadly they are not. With a few exceptions...
https://connect.mayoclinic.org/comment/958993/
Have gone thru this BEFORE as a CFS/ ... ME survivor of over 46 yrs.
HI, I traveled to a specialist in Boston for SFN and he started me on LDN....
https://connect.mayoclinic.org/comment/943229/
specialist in Boston for SFN and he started me ... in, but had a dramatic effect on mt CFS ... I have a lot of pain, so for me, using
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