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583 total results
Discussions (35)
Mayo Clinic Rochester: Shuttle services between buildings
Just wondering if anyone can tell me ... how far it is to the FM/CFS building
Support Group: Visiting Mayo Clinic
Last active: Jun 23, 2020
Have Had Mono-Like/CFS Symptoms for 15 Months: Need Help
Have Had Mono-Like/CFS Symptoms for ... m looking for a specialist to help me ... limit this dosage and wanted to put me ... (The CFS clinic did confirm the active ... effects of herpes viruses and told me
Support Group: Infectious Diseases
Last active: Aug 2, 2023
Desperate for answers
desperate to find out what is wrong with me ... I was diagnosed with CFS but I feel ... more symptoms than what a person with CFS ... has.The last thing my primary care told me ... to do was find a support group for CFS
Support Group: Autoimmune Diseases
Last active: Feb 23, 2019
Falling Asleep While Eating Lunch!
Daytime sleepiness for me, is becoming ... Anyone else with fibromyalgia, or CFS
Support Group: Autoimmune Diseases
Last active: Jun 26 6:18pm
When your doctor stops prescribing prednisone
later now these doctors don't want me ... I have debilitating cfs spasms, pain ... other things, This medicine works for me
Last active: Apr 29, 2022
Hi and thank you for all you do for us. Regarding a post from July2011
: "Why doesnt anyone write me ... 24, 2011 why doesnt anyone write me ... not surrender to this…..someone give me ... any feedback tht might help me…….. ... that I don't have tons of (I have CFS
Support Group: Just Want to Talk
Last active: Dec 30, 2022
message from my dr about my long term covid so sad now
insurance would cover it. he gave me ... it upsets me so much that i live with ... throat hurts and my chest hurts and my CFS
Last active: Jan 11, 2023
Autoimmune? Post-COVID?
My neurologist told me he had no clue ... ve been in a clinical trial, seen a CFS ... wasn’t sure what was going on with me ... - but I didn’t meet criteria for CFS
Support Group: Brain & Nervous System
Last active: May 17, 2023
Are the symptoms in my head? Polycythemia Vera + Mastocytosis (age-23)
Bladder with Urinary Retention - ME ... /CFS - Allergies, asthma, eczema - ... Hematologist tentatively diagnosed me ... and make me itchier, so the air or ... eating, which is VERY abnormal for me
Last active: Dec 27, 2024
EBV Labs. Am I contagious, are results serious or am I crazy?
NP tested me for EBV and ran labs through ... Yesterday she diagnosed me as having ... CFS and suggested Remeron for depression ... She had just diagnosed me with CFS a ... since she sent me to ID.
Support Group: Infectious Diseases
Last active: Nov 28, 2024
PATCH TESTING! NEGATIVE REACTION!
Series, the first round was put on me ... from the partical that was given me ... The allergist tells me that she needed ... nauseated terrible, around I have CFS ... not been the same, physically since, CFS
Support Group: Just Want to Talk
Last active: Oct 28, 2021
Has anyone else had their chronic pain disappear while on Paxlovid?
Like, CFS, right hip avascular necrosis ... That, doesn't happen for me, with ... colds, do we tested me (at home) for ... few days ago, and that sure gives me
Support Group: Chronic Pain
Last active: Jan 19 10:08pm
Feeling down but hopeful
viral infections. 2018- A tick in me ... Antibiotics always make me feel ‘normal ... CFS or ME Or who knows.
Support Group: Autoimmune Diseases
Last active: Apr 23, 2023
Need to find out what's wrong with me
Need to find out what's wrong with me ... I've also had IBS and CFS thrown into ... few years ago, sever ones that put me ... ml a day, mostly at night to help me ... only eat oatmeal, even that gives me
Support Group: Autoimmune Diseases
Last active: Oct 16, 2022