Research fund for LDN & MS
Posted: Wed Aug 31, 2005 9:30 am
Hi everybody, you’ve all heard from me as I’ve have been recovering from secondary prog. MS for 1.5 years on low dose naltrexone. I attended the 1st annual LDN conference in NYC, and spoke on the LDN advocates panel. In addition to the exciting news that international researchers are going to start trials for MS, I met Art Mellor of Accelerated Cure Project, and he agreed to help organize a fund raising effort for trials in the US. Please see the details at http://www.ldninfo.org/research_funding.htm and contribute if you can. The organizing group started this off with $200 dollars each. Dr Bihari & Dr Gluck have given us their endorsement. Tell everyone you know about this!
To get major research going, all we need is a $20,000 seed fund to get a major academic institution to do some preliminary research, then take that to NIH to trigger a major study. Dr Agrawal, who wrote the first hypothesis on how LDN may affect MS, is also involved as an organizer, so we have some excellent guidance.
SammyJo
My story is at http://LDNers.org
To get major research going, all we need is a $20,000 seed fund to get a major academic institution to do some preliminary research, then take that to NIH to trigger a major study. Dr Agrawal, who wrote the first hypothesis on how LDN may affect MS, is also involved as an organizer, so we have some excellent guidance.
SammyJo
My story is at http://LDNers.org