Federal Updates:
HELP Copays Act: While S. 1375 was tabled during the May Senate Health Education Labor and Pensions Committee markup on PBM’s, the bill is up to eight cosponsors. NHF continues to solicit…
The Tennessee Hemophilia & Bleeding Disorders Foundation (THBDF) is a 501(c) 3 non-profit organization that was formed in 1970 by patients, parents and health care professionals to provide support, advocacy, and education to families affected by…
The MASAC Recommendations Regarding Physical Therapy Management for the Care of Persons with Congenital Bleeding Disorders provides comprehensive information to assist Physical Therapists at all levels in caring for persons with bleeding disorders (…
For the past four years, Marble Slab Creamery locations in the metro Charlotte region have partnered with NBDF to fundraise for inheritable blood disorders. Every summer, locations rally around Marble Slab Creamery franchisee, Ryan Griffith, his son…
The family of George King reflect on their longtime involvement with the foundation, and how their personal connection to the blood/bleeding disorders community has inspired their work.
Kelly Wornall, Granddaughter of George King…
A review published in the Journal of Thrombosis and Haemostasis (JTH) suggests gene therapy as a potential novel approach to achieving immune tolerance induction (ITI) in patients with hemophilia A and an inhibitor to factor VIII (FVIII). The…
Corporate Giving 101Speaker: Teecee HutchersonNHF's Wednesday Webinars are a free education series open to providers and community members. Register to attend and learn about the latest in research, breakthrough developments,…
Gene EditingSpeaker: Julian GilmoreNHF's Wednesday Webinars are a free education series open to providers and community members. Register to attend and learn about the latest in research, breakthrough developments, and more.…