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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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Hi Lou,
I think I have some questions left to answer. I will ASAP. Right now I am feeling awful. i think GcMAF is kicking in, and I am suffering from die-off, IRIS, or whatever it is...
Best,
Sergio
can we get a list of who is now on GcMAF? and when they started. if you send me the names, i'll keep adding them to this list. or you can cut and paste the list and add it yrself to yr own post.
== Past ==
Joey (no response, but it was only a limited trial of a pre-curser of GcMAF)
== Now ==
Canasado, source unknown, Fall 2010
Overstressed: Oct 2010??
CindyWilliams: Dr. Sharp, Nov 2010??
Nabo: Dec 2010
Lou: direct fr BGLI, Jan 2010
Ronan: KDM, Dec 2010
Garcia: KMD, Jan 2011
Froufox: KDM, Jan 2011
== soon ==
Sergio: KDM, Jan 2011
Sushi: KDM, Jan 2011
Vli: KDM, Jan 2011
Just spent hours reading entire tread.
1. Why no one is testing vitamin D3?
GcMaf has side effects, if you don't have any sucks to be you - you are using fake version and wasting money.
I don't have any updates on my situation because i just took my first shot and other than a lot of heavy side effects i can't report on anything but will let you know the progress once i have blood work and see numbers, i just hope i will turn out as good as friend of mine! so i keep my fingers and toes crossed
Here is the link to Joey's spreadsheet again if you guys want to update it:
https://spreadsheets0.google.com/ccc...CIH8jqcC#gid=0
Froufox and Garcia,
Since you are both in England, I was wondering if you could tell me whether your GP let you do the vit D testing through the NHS, at all. Or are you both paying for it?