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Comments (667)
Thanks for your kind reply. I see a naturopath and you are right that regular doctors...
https://connect.mayoclinic.org/comment/1307542/
regular doctors know nothing about ME ... /CFS or Long Covid. ... My former doctor, a specialists in ME ... /CFS (who unfortunately passed away) ... treated ME/CFS with something called
@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
Hi sueleerock, "Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a serious, long-term illness that affects many body...
https://connect.mayoclinic.org/comment/183180/
/CFS) is a serious, long-term illness ... People with ME/CFS are often not able ... At times, ME/CFS may confine them to ... People with ME/CFS have severe fatigue ... ME/CFS may get worse after people with
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
PS typo- it's ME/CFS. Myalgic Encephomylitis/ Chronic Fatigue Syndrome.
https://connect.mayoclinic.org/comment/1151552/
PS typo- it's ME/CFS.
Hi @haarvee and @covidstinks2023 , I’ve had ME/CFS for 40 years and developed severe axonal Polyneuropathy...
https://connect.mayoclinic.org/comment/1460368/
and @covidstinks2023 ,
I’ve had ME ... /CFS for 40 years and developed severe ... other stuff. )
When I first got ME ... /CFS following an Epstein Barr virus ... The neuropathy and ME/CFS are both definitely
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
@fse1973ap People taking 25-50 mg of naltrexone are taking it for addiction usually. LDN is taken...
https://connect.mayoclinic.org/comment/1467171/
LDN is taken for long COVID, me/cfs
@jeindc Hello JE, Thank you for sharing all this and I’m so sorry you have developed...
https://connect.mayoclinic.org/comment/1469257/
I’m 74 and have had ME/CFS for 40 years ... You probably know that ME/CFS and LC ... When I got sick with ME/CFS I tested ... /CFS. ... Why some people would get ME/CFS or
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
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.
@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
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?
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
Hello Spenjen, you are describing several symptoms—such as oxidative stress—that are commonly seen in people diagnosed...
https://connect.mayoclinic.org/comment/1493281/
commonly seen in people diagnosed with ME ... /CFS and Long COVID, often linked to
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.)
@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?
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
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
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