We are so excited to share that NPRNA now has an official bill # after being introduced in the Senate!
This bill was assigned to a congressional committee on February 28, 2013 (Rare Disease Day!), which will consider it before possibly sending it on to the House or Senate as a whole.
FightSMA wrote in a press release:
Introducing the NPRNA on Rare Disease Day on Capitol Hill, Senators Sherrod Brown (D-OH) and Roger Wicker (R-MS) continue their leadership from the 112th Congress by once again serving as the bill’s lead sponsors. Joining them as original cosponsors will be Senators Richard Blumenthal (D-CT), Roy Blunt (R-MO), Susan Collins (R-ME), Rob Portman (R-OH) and Sheldon Whitehouse (D-RI). The NPRNA will now be referred to the Senate Health, Education, Labor and Pensions (HELP) committee, where it is expected to be considered by committee members in the coming weeks.
Now — on to the Senate and from there to desk of the President of the United States!
As this critical legislation is considered in the Senate, FightSMA needs your help. A phone call, letter or email to your senators can make all the difference.
Please help us build this critical support in the Senate by writing your Senator through their website and also phoning the Capitol Hill office. You can copy and paste the draft letter below for email or fax. We’ve also listed talking points. Here’s a link that could be helpful:http://www.senate.gov/general/contact_information/senators_cfm.cfm . When you write or call, we strongly encourage you to mention your family’s story and experience with SMA.
(Letter to be sent via Senator’s website)
Here in [STATE], I’ve had the privilege to be involved with FightSMA, a non-profit organization of families in our state and across the country working to find a treatment for spinal muscular atrophy (SMA), the leading genetic killer of children under two. Along with millions of other families living with rare pediatric diseases, I am proud to support S.424, the National Pediatric Research Network Act (NPRNA). I write you today to ask for your support in passing this critical legislation, which will lead to increased research and enhanced treatments of devastating pediatric diseases.
(Talking points for phone call)
- I am a constituent of Senator NAME
- I am phoning today to urge Senator NAME to cosponsor the National Pediatric Research Network Act of 2013 (S. 424/H.R. 225)
- This legislation will benefit SMA and other rare diseases.
- There are nearly 7,000 rare diseases affecting 25 to 30 million people most of whom are children.
- Mention your family’s story and experience with SMA.
- The Senator’s co sponsorship of NPRNA would mean the world to me and other families across STATE
- Thank you for your consideration!
Many thanks for all that you have done to make this happen.