Earlier this week, Dr. Francis Collins,
director of the National Institutes of Health (NIH) fulfilled his
promise to Alzheimer’s advocates to designate $40 million from his
2013 budget for Alzheimer’s research. I was one of more than 700
advocates at the Alzheimer’s Association Advocacy Forum, where Dr.
Collins made the announcement that he was taking this unique step to
show the NIH’s commitment to finding a cure for a disease that has
baffled scientists for decades.
During his keynote address on April 23
at the forum, Dr. Collins said, “I so wish it could be more, but I
hope you hear in this kind of a commitment the way in which we at NIH
see this as an opportunity and responsibility. We also hope that
moving forward we can put medical research back on the stable track
that is needed in order to support the research and the researchers.”
The story in last week’s New York
Times and USA Today both report that an additional $5
million has been designated by the National Institute on Aging (NIA)
to provide support for innovative clinical trials.
Among the trials being supported
through these additional funds is the Dominantly Inherited
Alzheimer’s Network Trials Unit (DIAN-TU) trial at Washington
University, St. Louis. Dr. Randy Bateman is the team leader. I met
Dr. Bateman several years ago when he accompanied Missouri advocates
on our visits with our legislators at the Alzheimer’s Forum in
Washington, D.C. Hearing firsthand the possibilities of research to
find therapies or a cure for early onset Alzheimer’s is encouraging
in a way that reading about it cannot touch. Dr. Bateman is
passionate about his work, confident, and optimistic that a cure can
be found for the hereditary form of Alzheimer’s that can strike
during early adulthood.
The APOE4 trials being conducted by
Drs. Eric Reiman and Pierre Tariot at the Banner Alzheimer’s
Institute in Phoenix will be fully funded in 2013. Several other
trials are being funded to move them forward. An Allopregnaolone
Regenerative Therapeutic study at the University of Southern
California will evaluate the safety and tolerance of a natural brain
steroid to treat Alzheimer’s disease. Other studies will analyze
data collected from volunteers to identify promising therapies, test
existing drugs currently used for other conditions for effective
treatment of Alzheimer’s, and treatment based on targeting the
immune system.
In a letter I received as an
Alzheimer’s Ambassador, Alzheimer’s CEO Harry Johns said that the
fulfillment of NIH’s pledge is historic. “In addition to fueling
much needed research toward treatment, prevention, and ultimately a
cure, it shows the growing recognition that our cause is receiving at
the nation’s highest levels.” Johns praises hundreds of
Ambassadors and hundreds of thousands of advocates for making the
case in Washington, D.C., and in communities nationwide. In the
Alzheimer’s Association news release, Johns said, “These studies
are examples of the quality research in the pipeline that needs
further funding in order to prevent and effectively treat Alzheimer’s
disease by 2025 as outlined in the National Alzheimer’s Plan.”
Kudos to NIH and NIA for taking this
first step toward prioritizing research for Alzheimer’s. Now, we
need to keep pressing our legislators to take a proactive approach to
finding a cure for this disease.
Alzheimer’s is an equal opportunity
disease. It affects people without regard to race, religion,
financial status, political party, intelligence, education, or any
other classification you can think of. No human is immune to
Alzheimer’s. It could happen to you or to someone you love if it
hasn’t already.
It’s not a question of whether we can
afford the research for Alzheimer’s, the real question is—can we
afford not to fund research? Does it make sense to spend only $484
million on research that costs this country more than $140 billion
annually in Medicare and Medicaid? Alzheimer’s is the sixth leading
cause of death in the United States, yet the funding is minuscule
when compared to research spent on other diseases which received
billions annually to fund research.
Some of us have spent years advocating
for Alzheimer’s research dollars. It can be frustrating when
funding is stagnant, or worse yet, the years funding was cut. By
hanging tough, advocates have fought for treatment equity for those
living with Alzheimer’s and other dementias.
This is not the time to rest on our laurels, it is the time to step up our advocacy while the focus is on research. The ultimate goal is a world without Alzheimer’s, and it can be done.
This is not the time to rest on our laurels, it is the time to step up our advocacy while the focus is on research. The ultimate goal is a world without Alzheimer’s, and it can be done.
Copyright (c) September 2013 by L.S.
Fisher
www.earlyonset.blogspot.com
Resources:
http://www.alz.org/documents_custom/nih_grant_announcment_final.pdf
http://www.usatoday.com/story/news/nation/2013/09/18/alzheimers-disease-research-funding/2832865/
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