My Nonprofit Reviews

I found out I am a carrier in 2008 after having a post mortem testing of my mothers brain tissue. I was in a yearly research testing program with a local university for about 9 years. I was told I could not participate anymore since my contact person was not available on their time. So I heard about VCP org. and started following. I have learned more from them than I did in my research years. No results were given from my years of testing. No information was shared with my PCP or specialist. I now have info cards that I share with my doctors , thanks to Cure VCP.org.
Please support this much needed patient care organization.