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List of ME CFS Recovery and Improvement Stories - Phoenix Rising ME CFS . . . The Phoenix Rising CCI forum is here • ME CFS patient (jeff_w) was cured of his severe ME CFS by surgery to fix his craniocervical instability ( 3-level gain ) • ME CFS patient (JenB) was cured of her ME CFS by surgery to fix craniocervical instability, atlantoaxial instability and tethered cord
PolyBio - Long COVID low-dose rapamycin clinical trial | Phoenix Rising . . . Phoenix Rising (slight improvement in exercise intolerance, slight worsening of short term memory, 2 weeks) Phoenix Rising; Phoenix Rising; Phoenix Rising; Phoenix Rising; Temporary improvement r covidlonghaulers (Update: r Rapamycin) r cfs; r cfs; Phoenix Rising; Improvement (though some are only a few weeks after starting, so might have
Phoenix Rising ME CFS Forums 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
Is this an adrenal problem? | Phoenix Rising ME CFS Forums With low dhea and cortisol it's not usually an adrenal issues but a hypothalamus hpa signalling issue Signals from the brain to the adrenals are low for some reason but common in cfs
B-12 - The Hidden Story | Phoenix Rising ME CFS Forums I moved Freddd's spectacular post on B-12 from the story section to here in order to focus on it more fully Many, many people try B12 for ME CFS but few are cured Freddd was actually cured when he stumbled upon the right type of B12 for him This sparked an extensive examination of why one
List of ME CFS Recovery and Improvement Stories | Page 14 | Phoenix . . . The Phoenix Rising thread offers a rich tapestry of ME CFS recovery and improvement stories, showcasing both hope and complexity Treatments range from pharmaceuticals (Mestinon, antivirals, LDN) to supplements (NAG, thiamine, C60), dietary changes (trigger avoidance, autoimmune protocols), and alternative therapies (oxygen, cavitation surgery)
Tips for University College Students | Phoenix Rising ME CFS Forums I’m new to PR and was trying to think of some way I could immediately contribute to the community Since I’ve spent most of my adult life in academia (almost all with ME CF) I thought I’d write some tips for students These are all based on my own experience as a student, graduate student
Copper, Thiamine, Memory Loss, Adrenal Issues | Phoenix Rising ME CFS . . . Hi Everyone, I've been reading this forum off and on for years There are so many knowledgable and helpful people here My introduction post was just approved (from May), but I have other issues, and am hoping someone can help me with them, or point me in the right direction A couple months