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446 total results
Comments (422)
Hi Annie, EBV is another of these viruses which can have long term consequences. Covid has...
https://connect.mayoclinic.org/comment/810010/
I’m sorry you’re having CFS and fibromyalgia ... articles with scientists trying to link CFS ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
Hello @gohan, Welcome to Connect. Sorry you have been battling this condition for 15 years. I'm...
https://connect.mayoclinic.org/comment/867491/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) which has symptoms that include
@curiousr regarding long haulers, it is my opinion that they are nothing new. I am basically...
https://connect.mayoclinic.org/comment/184102/
from a bad case of mono that led to ME ... /CFS. ... professional nursing journals about ME ... /CFS. ... of the mysterious illnesses such as CFS
So glad to hear from someone who feels the same way. We have to put our...
https://connect.mayoclinic.org/comment/689980/
The ME/CFS PR is terrible.
@hw43 Hi! Reading your message is like reading my own story. They diagnosed me with MS...
https://connect.mayoclinic.org/comment/793011/
They diagnosed me with MS ++ different ... the same as those associated with ME ... /CFS.
My 17 year old son is the same. We found a functional medicine doctor who ran...
https://connect.mayoclinic.org/comment/968607/
with chronic illness, long covid, ME ... /CFS have used nicotine patches with
@gsgambhir, a healthy dose of skepticism is warranted when evaluating Dr. Patterson's offerings. Do you due...
https://connect.mayoclinic.org/comment/983963/
Later: Bruce Patterson, Long COVID, ME ... /CFS/FM and the Poll (2023) https://
Hi, I apologise if this isn't the right place for a new post, I was diagnosed...
https://connect.mayoclinic.org/comment/870773/
I also have ME/CFS so my energy is very
I had similar results from an EB panel. I had mono a little over a year...
https://connect.mayoclinic.org/comment/718394/
drip and fatigue and was suspecting ME ... /CFS. ... Does this signify CFS? ... Can CFS be mild?
I can relate to what you are going through. I am almost exactly 8 weeks out...
https://connect.mayoclinic.org/comment/1027904/
the free app Visible: Long Covid and ME ... /CFS.
BINGO! Everything you said here resonates with me! I had mono 44 years ago. I absolutely...
https://connect.mayoclinic.org/comment/838103/
Everything you said here resonates with me ... I am waiting for my NP to get me in ... infectious disease doc to prescribe me ... She won't give me anything...feels ... /CFS and chronic EBV diagnoses.
I have had high EBV titer since being diagnosed with ME/CFS over 30 years ago. I...
https://connect.mayoclinic.org/comment/739683/
EBV titer since being diagnosed with ME ... /CFS over 30 years ago. ... All this is puzzling to me particularly
Thank you for this post and I am new to this blog. I guess I have...
https://connect.mayoclinic.org/comment/791884/
symptoms are the same as described for ME ... /CFS. ... My husband works and supports me and
There is nothing to take for Benzo WD. You could take something for the tight muscles...
https://connect.mayoclinic.org/comment/120844/
necessay such as those for people with ME ... CFS).
I was referred to rheumatologist immediately. He was a smart and conscientious. He, along with my...
https://connect.mayoclinic.org/comment/718429/
He, along with
my CFS doctor who happened ... At that time they didn't give me ... ME/CFS at the current moment doesn'
Yes! 1, 2, and 3 are all correct. A lot of long covid symptoms have to...
https://connect.mayoclinic.org/comment/925910/
community is learning a lot from the ME ... /CFS community - some of the symptoms
Good to hear your story Christiana. My feelings exactly. While I have followed the research on...
https://connect.mayoclinic.org/comment/793108/
While I have followed the research on ME ... /CFS, I recognize that there is no test ... my body, brain and intuition tells me
Yes, but it’s not constant. I also get large, painful knots in my calves. My shoulders...
https://connect.mayoclinic.org/comment/868250/
I’ve been diagnosed with ME/CFS because ... The ME is ‘Myalgic Encephalomyelitis
Hello all! I have Severe CAEBV. I've been steadily worsening probably since about 2014. Recently, all...
https://connect.mayoclinic.org/comment/689212/
a specialist here in CA who treats ME ... /CFS, but nothing we have done has helped ... already taken everything else from me
Hi Kari and Group, I just joined this discussion group, and have had 4 CTA scans...
https://connect.mayoclinic.org/comment/131191/
I was diagnosed with ME/CFS and am now ... symptoms that are debilitating for me
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