Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Sickle Cell Thalassemia Patients Network
1139 St. John’s PlaceBrooklyn, New York, United States
Email Phone Web
Since April of 1992, the Sickle Cell Thalassemia Patients Network (SCTPN) has been providing education, advocacy, referral services, and support for individuals and families living with sickle cell disease, thalassemia (Cooley’s Anemia), and other inherited blood disorders. SCTPN, is a 501 (c)(3) tax-exempt organization, which provides education, advocacy, referral services, and support for individuals and families living with sickle cell disease (SCD), thalassemia (Cooley’s Anemia), and other inherited blood disorders.
Public education programs and webinars are provided to help increase awareness of hemoglobin disorders. These programs also provide non-medical information that empowers individuals to take control of their health and thus enjoy a better quality of life. Advocacy is provided for families as they migrate the sometimes complicated healthcare system. Referrals for related services are also provided.
+myBinderRelated Content
-
Tandua Washington, MDDr. Tandua Washington has been a practic...
-
Sickle Strong InitiativeThe Sickle Strong Initiative is an organ...
-
Effort set to help sickle cell patients manage medsVanderbilt University Medical Center is ...
-
Shalonda WarrenShalonda is Chief Executive Officer at S...
-
Webinar Series: Sickle Cell Science: Path to Progress – Bone Marrow Transplants, Other Therapies, and Sickle C...To commemorate Sickle Cell Awareness Mon...
-
SCD Clinical Trials Network Workshop – New York, NYJoin us for an afternoon of fun acti...
-
Halloween Health & Safety TipsHalloween is a time for spooky thrills a...
