My very personal thoughts...

Please help me understand….

Please help me understand what all the FDA and Canadian health CCSVI angioplasty fuss is all about?

So the FDA won’t even acknowledge the procedures existence and the Canadian health system won’t do it as part of their MS treatment as to not offend or affect the interests of BIG pharma…what else is new? Everybody who suffers from this terrible disease knows this right? 

There are thousands of people who suffer from MS that have travelled as far away as Poland, India and Italy and as close as the U.S. and Mexico to seek the proven CCSVI angioplasty procedure who are now enjoying a much better quality of life, of this I am absolutely certain as I have witnessed this with my own eyes…My name is Andrés Brakke and no, I am not a doctor…I am the coordinator at Dr. Rafael Moguel’s Clinics of the Heart in Mexico and I have seen just over 600 people mostly from Canada experience almost immediate and mesurable improvements , many of their most nagging symptoms disappear or drastically improve, again, I have witnessed this in amazement  with my own eyes… but hey, don’t believe me…there are hundreds of testimonials on youtube and websites including ours…Would it be better if you could receive this proven treatment as part of your health care system in your own country? No question, but at this time, that’s not the case and if BIG pharma  and the neurology industry have their way it will probably never will be possible…so please help me understand…what in the world are you waiting for? Will a few thousand dollars stand in your way of enjoying a better quality of life?  It breaks my heart to read all the sad stories on Facebook and on dedicated blogs and portals like the CCSVI Locator but I fail to understand how someone would opt to wait for change in government to happen or harder yet,  for the neurology industry and BIG pharma to accept the proven CCSVI angioplasty treatment. This is not a sales pitch, I don’t care where you get treated…but GET TREATED YOU MUST! Life is short enough, so little time, so much to do…travel to where you wish to travel, go to the clinic of your choice…talk to people who have had the proven CCSVI angioplasty procedure and take that “leap of faith” that thousands of people with MS have taken before you…don’t let a few dollars stand between you and a better quality of life!

The proven CCSVI angioplasty is a simple and safe procedure and it is worth every penny I promise you that…

So, in conclusion…can anyone out there explain to me why more people with multiple sclerosis are not seeking treatment abroad? Why are they not fundraising in order to get this proven treatment? The time and energy spent  fighting this losing battle vs. BIG pharma and the neurology industry would be better spent talking to folks who have