by donatesctpn | Sep 1, 2025 | Advocacy & Education, Community Support, Health Education
Sickle cell disease isn’t just African—it’s a HUMAN condition. Sickle cell disease does not know borders, race, or ethnicity—it touches people from the Mediterranean, Middle East, India, Asia, Latin America, and across North America. Yet, too often, it is...
by sctpn-new | May 23, 2022 | Advocacy & Education, Community Support, Leadership
A new executive team officially began its role on October 4, 2021. The Sickle Cell Thalassemia Patient’s Network (SCTPN) welcomes Teresa Ginger Davis, President; Richelet “Rich” Jean, Vice President; and Tashiika McClain, Treasurer. Jocelle Marius is the Assistant...
by sctpn-new | Jan 6, 2021 | Advocacy & Education, Community Support
2020 was a challenging year indeed; one where stumbling blocks were turned into stepping stones. One where our true character was brought to the fore, and our tenacity was put to the test. We have lost many family and friends, much pain was experienced, and hope...
