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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
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
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
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
List of Reliable Prescription-Free Online Pharmacies | Phoenix Rising . . . Phoenix Rising does not endorse the information provided in this thread Some information and resources listed in this thread may provide services and products which are illegal in some countries It is the user’s sole responsibility to determine the safety, veracity, legality, and trustworthiness of sources listed in this thread
Thoughts on the Perrin Technique? - Phoenix Rising ME CFS Forums My sister is a massage therapist and has suggested that I look into ther Perrin Technique My experience with many treatments has been that some 'types' of ME CFS respond to some treatments and others to others (i e theres no uniform treatment - LDN for example messed my up for 6 months, whereas