9K? are u kidding me??
gc-maf is for cancer patients man
gc-maf is for cancer patients man
There are at least 20 patients on this forum taking GcMAF for ME/CFS (not all of them have added their names to the spread sheet). I am one of them. I pay 35 eu per weekly dose. I am hopeful! KDM has approx. 180 ME/CFS patients on it.
Sushi
My insurance limited the hourly payments to just one hour of Dr. Cheney's time. I had to absorb the rest. Many of the initial tests were paid for. But that was over ten years ago and things have changed in the insurance industry.
Needless to say after seeing him for a few years, I was not cured. Not Dr. Cheney's fault. He is on the cutting edge of treatments. They just have not found the "it" that will cure us yet.
Lynn
Im all for Dr's making a living doing what they supposedly love, hey it's america. we all should be lucky enough to make a good living working.
But i do however have a problem with Dr's who become filthy rich from very sick patients, who feel they have no option but to scrape up the $$$ for a little pinch of hope to have a fairly normal life!!!
it's not just cheney, he's just one thats in the spotlight, several years ago there was a dr in the next town over from me who supposedly was treating cfids. you bet i went to see him, and all i saw was a quack who was testing for allergies, and giving iv albumin( spelling) and charging 1500.00 A POP FOR THE INFUSION! Ins wouldnt pay, and My ins wouldnt even pay him for the allergy testing because i was informed there was a lawsuit between him and the Ins.
i didnt do the iv's( couldnt afford it)but i saw tons of people hooked up to poles and afterwards become severly Ill from the so called treatment. when i told my Now dr about this she was stunned, said that iv albumin had been shown to not work at all, and how was those people affording that!
and like i told her, when your this sick you will do anything to be better, even go in debt and loose your home or whatever else you have.
Not trying to badmouth anybodys Dr. but Im sick and tired of all of this!!! wheres the compassion really, and he knows what it feels like to be deathly ill..... Just sayin.
Kat
whos KDM ? ?
Dr. Kenny De Meirleir in Brussels. His clinic is Himmunitas. He is both a researcher and an MD specializing in ME/CFS for over a decade. Lots of Board certified specialties and publications.
I traveled from the US to see him. He charges 70 eu for the first visit and 50 for subsequent ones. He is also in collaboration with Cheney and the other big name ME/CFS docs.
Sushi
There is nothing you cherish that this illness cannot take way. nothing
Damn, sorry to hear that. There is nothing you cherish that this illness cannot take way. nothing
you got that right! although i have a pretty decent dr now, there was a time i just knew i was going to die on a ER floor.now i cant work at a prefession i went to school and paid good money for, i have to watch as we slowly go in debt, because of me, husband probably wont ever be able to retire, i coudnt even pay for my daughters college. as much as i love working outside, i cant even plant a flower right now.
trying to look at the glass as half full all the time is hard, sorry guys. it's just one of those days;/
if you dont mind me asking do you share the symptoms I have (#17 comment)?
I have only had this for a little over 1 and 1/2 years.