Guest guest Posted May 3, 2010 Report Share Posted May 3, 2010 It would be great if those of us diagnosed with M.S. could all flood this site with a statement about how LDN helps and that the Foundation site http://erasems.org/contact/ should check into funding this low cost drug that works for a large number of people and is affordable. Thank you Larry for the info. Shana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2010 Report Share Posted May 3, 2010 I've done that, although I'm in England and have no idea about that programme, but commenting anyway! Good luck. > > It would be great if those of us diagnosed with M.S. could all flood this > site with a statement about how LDN helps and that the > Foundation site <http://erasems.org/contact/> http://erasems.org/contact/ > should check into funding this low cost drug that works for a large number > of people and is affordable. Thank you Larry for the info. Shana > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2010 Report Share Posted May 3, 2010 I just added my husband`s story to the comment page. It`ll be very interesting to see if anyone contacts any of us regarding all this. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 4, 2010 Report Share Posted May 4, 2010 I left some comments regarding LDN & MS at the Foundation's site: http://erasems.org/contact/ Let's keep the ball rolling and get the LDN word out some more. A lot of folks out there could benefit.On May 3, 2010, at 11:37 AM, shana spooner wrote:It would be great if those of us diagnosed with M.S. could all flood this site with a statement about how LDN helps and that the Foundation site http://erasems.org/contact/ should check into funding this low cost drug that works for a large number of people and is affordable. Thank you Larry for the info. Shana Quote Link to comment Share on other sites More sharing options...
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