Funding Research to Treat MSIn MS circles all over the Internet, I've noticed many positive themes regarding hope for a cure through research. Thankfully, huge strides have been made into understanding the disease process and effectively treating various multiple sclerosis symptoms. When I was diagnosed in the early 90's, my treatment options were very limited, and were not particularly effective. Within the past few years, people with MS have been able to avail themselves of a variety of new medications to manage their symptoms-or better yet-to possibly thwart the progression of the disease. These rays of hope are due in large part to the exciting research undertaken by the scientific community. What I wanted to know, however, is precisely how research funding decisions are made. Specifically:
FUNDING SOURCES Non-Profit Funding
The NMSS spends more money on MS research than any national voluntary health agency in the world. This year, for example, the Society will invest $25 million to support the more than 300 MS researchers working in the U.S. and abroad. Since 1946, the NMSS has invested over $284 million in MS research.1 Although the NMSS is a primary funding source, other governments, foundations, non-profit organizations, and agencies contribute to the overall funding pie as well. Public Funding
The copyright of the article Funding Research to Treat MS in Multiple Sclerosis/MS is owned by Pamela Martin. Permission to republish Funding Research to Treat MS in print or online must be granted by the author in writing.
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