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Comments (559)
PS typo- it's ME/CFS. Myalgic Encephomylitis/ Chronic Fatigue Syndrome.
https://connect.mayoclinic.org/comment/1151552/
PS typo- it's ME/CFS.
Does anyone here know of a Mayo doctor who can diagnose ME/CFS and/or another auto immune...
https://connect.mayoclinic.org/comment/200371/
of a Mayo doctor who can diagnose ME ... /CFS and/or another auto immune disease ... group of individuals dealing with ME ... /CFS and they keep abreast of the latest
@colleenyoung Chronic Fatigue Syndrome is quite the unfortunate name, as it implies "fatigue" is the main...
https://connect.mayoclinic.org/comment/200395/
/CFS. ... nationalacademies.org/hmd/reports/2015/me-cfs.aspx ... And that ME/CFS patients are more disabled ... Convincing doctors that ME/CFS patients ... https://www.cdc.gov/me-cfs/healthcare-providers
I do research, but have also had ME/CFS since 1984 and Long Covid since 2022. 95%...
https://connect.mayoclinic.org/comment/1338567/
I do research, but have also had ME/ ... CFS since 1984 and Long Covid since ... /CFS or Long Covid patients. ... Research on ME/CFS can be found on the ... https://hhv-6foundation.org/category/me-cfs
Same exact situation here, the ME/CFS and PEM still persists amongst other symptoms...
https://connect.mayoclinic.org/comment/1263728/
Same exact situation here, the ME/CFS
Hi @beanie300, there is another active discussion that may be helpful for you to read through...
https://connect.mayoclinic.org/comment/225215/
Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments
-- https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
@sita Thanks for the Phoenix Rising info. I am familiar with this group, as well as...
https://connect.mayoclinic.org/comment/200374/
with this group, as well as the S4ME.info ... Your primary care doctor can diagnose ME ... /CFS. ... ME/CFS is no longer a diagnosis of exclusion ... https://www.cdc.gov/me-cfs/symptoms-diagnosis
Just read an article today from the blog Health Rising, which follows ME/CFS, Fibro, POTS reaearch....
https://connect.mayoclinic.org/comment/948269/
blog Health Rising, which follows ME ... /CFS, Fibro, POTS reaearch. ... /CFS Moment Just Occurred at…The Mayo ... it is not the right treatment for ME ... /CFS.
Mayo Clinic follows CDC guidelines for diagnosis and treatment of ME/CFS. I had the opportunity to...
https://connect.mayoclinic.org/comment/613914/
guidelines for diagnosis and treatment of ME ... /CFS. ... listen to a talk by specialist in ME ... /CFS at Mayo Clinic, who reaffirmed
Thanks so much for this information. Unfortunately getting my primary or any other doctor in NM...
https://connect.mayoclinic.org/comment/200377/
for another diagnosis rather than ME ... /CFS. ... ME/CFS is a terrible and terrifying
Please check out information on ME/CFS and POTS. I have both after Covid and both my...
https://connect.mayoclinic.org/comment/978654/
Please check out information on ME/CFS ... /CFS. ... Common co-morbid dx w/ ME/CFS and often ... Tough if she also has ME/CFS as exercise ... /CFS.)
Did you know that long Covid is similar or may trigger to ME/CFS? There is a...
https://connect.mayoclinic.org/comment/687200/
Covid is similar or may trigger to ME ... /CFS?
Hello @stress, Welcome to Connect. I think you are right in that a lot of the...
https://connect.mayoclinic.org/comment/656969/
I don't have ME/CFS but do have ... that I think speaks to neuropathy and ME ... /CFS. ... Neuropathy (SFN) Fibromyalgia and ME ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
@petuniamom567 I’ve been wondering if you have found out anything about the ME/CFS site at Stanford...
https://connect.mayoclinic.org/comment/700803/
have found out anything about the ME ... /CFS site at Stanford U?
@1634517678, did you know there is an Epilepsy group on Connect here: https://connect.mayoclinic.org/group/epilepsy-2bb359/ Your participation in...
https://connect.mayoclinic.org/comment/254284/
seen the discussions on Connect about ME ... /CFS? ... Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments
I’ve actually had active full-blown mono twice. 1st time was 1990, 2nd time around 2010. In...
https://connect.mayoclinic.org/comment/184081/
He diagnosed ME/CFS and it was my understanding ... Has your doctor mentioned ME/CFS? ... the difference is between CREBV and ME ... /CFS?
@steph24 Welcome to Mayo Clinic Connect! I’m glad you joined the site! Here is Mayo Clinic’s...
https://connect.mayoclinic.org/comment/1102529/
Here is Mayo Clinic’s information on ME ... /CFS. ... Mayo also, just opened a ME/CFS clinic
This sounds like a game changer for those doctors, including Rheumatologists, who are still skeptical of...
https://connect.mayoclinic.org/comment/881856/
skeptical of the existence of Fibro/ME ... /CFS.
For many years at the recommendation of ME/CFS pioneer, Dr. Paul Cheney, I have used Nexavir...
https://connect.mayoclinic.org/comment/1324950/
many years at the recommendation of ME ... /CFS pioneer, Dr. ... Cheney, I have used Nexavir Cream for ME ... /CFS.
Don't know where else to list this. No one is paying much attention to ME/CFS. There...
https://connect.mayoclinic.org/comment/677698/
No one is paying much attention to ME ... /CFS. ... /CFS. ... /CFS people. ... Instead, those of us who have ME/CFS
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