The GFPD is proud to partner with The EveryLife Foundation for Rare Diseases and several other patient advocacy groups to support North Carolina HB 736, which would require the North Carolina Department of Health and Human Services (NCHHS) to implement new screening recommendations within three years of approval to the federal Recommended Uniform Screening Panel (RUSP), which will ensure that babies born in North Carolina have the same opportunity for diagnoses and treatments as babies born across state lines. The GFPD urges our community (especially our supporters in North Carolina) to click the link below to show support for HB 736.
https://everylifefoundation.org/voter-voice/?vvsrc=%2fcampaigns%2f80975%2frespond