Guest guest Posted February 6, 2004 Report Share Posted February 6, 2004 ----- Original Message ----- From: DOLFAMILY@... Antonucci@... Cc: tmbayuk@... ; bridgfl@... ; dominicpb@... ; RCrognale@... ; chrdana7@... ; Joefialli@... ; gfinestone@... ; Angelspjk@... ; AL1212@... ; bob.mazz@... ; Iwavva@... ; NASTYJC64@... ; reidkmr@... ; jokerswild0041@... ; Shaebevan@... ; vze2n8tr@... ; DCatbird37@... Sent: Thursday, February 05, 2004 6:14 PM Subject: If the facts are true, troubling for MS Dear friend,As a follow up to email earlier with the link to the Myelin Repair Foundation,the following points they presented as facts:Historically, the focus of government and non-profit organizations are looking for the "cure"They do not have a mechanism to allow or even encourage collaborationThey prefer to fund incremental "sure thing" experiments not innovative, higher risk, breakthrough oriented researchFor FY 2001, the NMSS spent 19% of their $156Million budget on researchThe NMSS spent less than 0.5% of their budget on research related to any type of CNS repairNIH allocated less than 0.3% of their budget on research with any relation to MSIn terms of research funding, MS ranks 48th on NIH's priority list of diseases. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2004 Report Share Posted February 6, 2004 At least there is some quite recent good news regarding the NMSS and funding for research into CNS repair. (Since I'm not on all these lists, I apologize if this has already been discussed on some of them.) Go to http://www.nationalmssociety.org/Research-2004Jan30.asp to read this news story. Galoux Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.