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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
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
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
Cort Johnson, the Founder of Phoenix Rising, Returns to Lead the Forum! Phoenix Rising is beginning a new chapter as Cort returns as administrator and owner of PR, with immediately effect! Cort, a person with ME CFS FM, founded the Phoenix Rising website in 2004, and the Forums in 2009
About Phoenix Rising | Phoenix Rising ME CFS Forums Phoenix Rising maintains the largest ME CFS online community forum on the web, with a huge database of articles and forum posts about ME CFS On our forum, members will discuss the latest scientific research on ME CFS, help answer the questions of newly-diagnosed ME CFS patients, and the forum provides a source community support and chat for
Anxiety - Well yes! | Phoenix Rising ME CFS Forums So, I have had CFS symptoms since age 7, diagnosed at 24 and am currently 39 I work part time with half a day in the office, the rest WFH The half a day messes with my CFS and causes anxiety As anyone who paces knows, you’re constantly weighing the odds of your energy levels On a good day