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Welcome to Phoenix Rising!
Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.
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Blog list
In this blog, I'm going to try to document all scientific sources of information about the Davis Nanoelectronic Assay used to Diagnose ME/CFS. By...
Living with ME/CFS since the age of 16 1/2 months (1974), but diagnosed at age 17 years (1990). Was persistent enough to get three Associates...
Personal lists of symptoms, doctor's visits, progress with meds and so on.
ME since 1993. Level 3
You can find my sometimes serious/sometimes funny blog about living this life,( in which you can also check out my...
Thoughts from a lover of island life. seeking peace and solitude to live out the later years of my life where I truly want to be. With no fears...
Health copyeditor and writing tutor living with ME and Raynaud's disease. Author of Lightening the Shadow: Diagnosing and Living with an Invisible...
I am a 29 year old mother of two beautiful girls. I have had ME/CFS for 8 years. Before I got sick, I was an archaeologist for the Forest Service...
Dainty became ill as a teenager and spent 7 years mostly bedridden from ME/CFS, life-threatening MCS reactions, extreme food...
Thinking amalgams have caused my M.E due to the fact I have MTHFR, in the process of saving for specialised treatment!
Former Healthcare worker, cared for patients of all ages and their families. ME has now prevented me from doing this work. What it can't take away...
Unless completely eviscerated by fatigue I need to create. Used to make art, hands permitting, now pour my art into writing.