Sickle Cell & Thalassemia Society
About Us
A community-driven organization working for awareness, early diagnosis, counseling, dignity, & better healthcare access for families affected by Sickle Cell Disease & Thalassemia.
Our Story
Built with a vision to serve families & communities.
We work closely with communities, healthcare professionals, educational institutions, & government agencies to promote prevention, early detection, & better quality of life. Through awareness drives, screening camps, counseling, health talks, & patient support, we aim to create a healthier & more informed society.
Awareness
Screening
Family Support
Advocacy
Our Purpose
Awareness. Care. Hope.
Late Padmashri Sampat Ramteke Sir
Late Padmashri Sampat Ramteke Sir was a visionary social reformer & tireless advocate for individuals affected by Sickle Cell Disease & Thalassemia. His lifelong dedication transformed countless lives by bringing awareness, dignity, & hope to patients & their families.
Through his relentless efforts, advocacy, & commitment to social justice, Sickle Cell patients gained recognition & important protections under the Rights of Persons with Disabilities Act, along with several other rights & welfare measures that improved their quality of life.
His mission was not merely to fight a disease, but to restore hope, dignity, & equal opportunities for every life affected by Sickle Cell Disease & Thalassemia.
Our Vision
A society where every individual has access to awareness, screening, treatment support, & a life free from discrimination due to genetic blood disorders.
Our Mission
- Create awareness about Sickle Cell Disease & Thalassemia.
- Promote screening & early diagnosis.
- Provide counseling & support to affected families.
- Organize health camps & educational programs.
- Advocate for better healthcare access.