Ryan Fischer's Blog – February 2016 Archive (2)
ACTION ALERT: Urge Lawmakers to Keep Driving Progress in the Fight to End Duchenne
Urge your Lawmakers to Sign the FY 17 Duchenne Appropriations Letter!
Today and tomorrow, scores of PPMD advocates will be on Capitol Hill to urge their Senators and Members of Congress to continue supporting vital efforts that will move us closer to ending…
ContinueAdded by Ryan Fischer on February 22, 2016 at 1:43pm — No Comments
Congress Calls on FDA to Increase Efforts to Treat Duchenne
Thanks to this incredible community urging lawmakers, well over 100 Members of Congress signed and submitted a letter …
Added by Ryan Fischer on February 18, 2016 at 2:40pm — 1 Comment
Latest Blog Posts
- 70 Members of Congress Send Letter of Strong Support for Duchenne Priorities for Next Year’s Budget
- End Duchenne Tour Recap: Grand Rapids, MI
- ADD YOUR VOICE: Participate in PPMD’s Gene Therapy Survey
- End Duchenne Tour Recap: Morristown, NJ
- PPMD's 2018 Advocacy Conference | Schedule of Events
- VIDEO: Fundamentals of Access to Duchenne Therapies
- PPMD’s #EverySingleOne Tour: Boston, MA
Most Popular Blog Posts
- ACTION ALERT: Urge Lawmakers to Keep Driving Progress in the Fight to End Duchenne
- One week away from World Duchenne Awareness Day!
- Important Updates on the Duchenne Policy Forum
- ACTION ALERT: Urge House Member - Apply FDASIA Tools to Duchenne
- CALLING ALL CALIFORNIA RESIDENTS!
- ACTION ALERT: Please urge Your Senators to Sign Letter to FDA – Applying FDASIA Tools to Duchenne
- Help Protect Federal Spending on Rare Diseases like Duchenne
© 2020 Created by PPMD.
Powered by
Badges | Report an Issue | Privacy Policy | Terms of Service
