If we’re ever going to gain traction as Cure Warriors, we’ve got to speak out to the various individual and organizational leaders in the spinal cord injury community. Thanks to the persistent efforts of Dennis Tesolat (also known as Mr. “Stem Cells & Atom Bombs”), there is a respectful yet pointed appeal to the Rick Hansen Foundation (RHF) that as of today boasts over 700 signatures from around the world.
The Foundation has long proclaimed its vision to be “a world without paralysis after spinal cord injury”. That’s our goal, too, so several months ago Dennis and a few of his friends sent RHF’s CEO a simple request:
- “Please outline your spending on translational research for central nervous system regeneration, i.e. a cure for spinal cord injury.”
The response failed to outline any specifics other than what’s available in their annual report, i.e. – “81% goes to charitable programs.” Dennis wasn’t satisfied, so he decided to get organized and continue to ask questions. He asked for more details on RHF’s spending, and for Rick to publicly answer the questions at next week’s Interdependence Conference of SCI leaders.
I imagine most of my readers have already signed the appeal, but if not, there is still time if you do it today. It’s an easy, one-click process from the Stem Cells & Atom Bombs website. Follow this link.
The Rick Hansen Foundation earns annual revenues in excess of $20 million, 71% of which comes from Canadian national and provincial government funds. This is an extraordinary amount of money, and with these types of resources the Foundation should respond to the wishes of the SCI community.
We respect the work that RHF has done to improve accessibility and quality of life for people living with SCI. At this point in time, however, with so much promising regenerative research on the cusp of translation, it’s time for the Foundation to turn its attention and its resources to the achievement of a cure. As survivors of spinal cord injury and family members, we have the right, and even moreso the responsibility, to speak up to those in power at the Rick Hansen Foundation.
Tags: cure, patient advocacy, regenerative medicine, Rick Hansen, SCI, stem cell research
June 7, 2012 at 11:30 am |
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May 8, 2012 at 8:23 am |
Dennis has given the spinal cord community a voice. Thank you Dennis for your perseverance in trying to break down the barriers of unheard spinal cord community.
Aggie Mom 2007 from Texas
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May 8, 2012 at 5:19 am |
imagine a “world without paralysis after spinal cord injury”…i imagine it is possible.
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