Sending Office: Honorable Mark Pocan
Join Reps. Gallagher, Pocan and Gutiérrez for a Briefing on the Importance of the DoD CDMRP to Find Cures for Neurofibromatosis (NF) and Beyond
Friday December 1, 2017
CVC Congressional Meeting Room South
Currently, there are no effective treatments and no cure for neurofibromatosis (NF), a genetic disorder affecting 1 in 3,000 people. Through research conducted by the NF Research Program within the CDMRP, research at the National Institutes of Health (NIH),
and other public and private research partnerships, we know we will find solutions for NF patients as well as 175 million Americans suffering from traumatic brain injury, cognitive delays, various cancers, persistent pain, nerve damage and amputations.
Please join us for a briefing in collaboration with the Littlest Tumor Foundation on the value of the CDMRP to finding treatments for NF and other deadly diseases.
- Naba Bora, PH.D., Neurofibromatosis Research Program at Department of Defense CDMRP
- Jill Morris, PH.D, Program Director, Neurogenetics at the National Institute of Neurological Disorders and Strokes (NINDS)
- Annette Bakker, PH.D., President and Chief Scientific Officer, Children’s Tumor Foundation
- Lynn Black & Gregg Erickson: NF Parent and NF Network
When: Friday December 1, 2016 at 1:00 p.m.
Where: CVC Congressional Meeting Room South
Refreshments will be served. We look forward to seeing you there.
Member of Congress
e-Dear Colleague version 2.0