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Rare Disease Week
BTG at Rare Disease Week in Washington D.C., learning and sharing about a rare disease that is dear to us, Sickle Cell Disease. We also learned that there are over 10,000 Rare Diseases in the world. In the picture is Cherryl Cannady, our Project Manager, along with Pam White, CEO and Founder of BTG and other amazing Sickle Cell Disease Advocates.
BTG Christmas Event 2022
We had an amazing time at our 2022 "Connecting For Change" Christmas event! Check out more pictures from the event on our "Events" page. Hope to see you there next year!
About Us
Our Mission
To Enrich and improve the quality of life of individuals with Sickle Cell Disease, Thalassemia, and related blood disorders.
Our Vision
To aspire to a Sickle Cell Disease Community where medical, educational, and social resources are readily available; to help Sickle Cell
Disease families live a limitless and less challenging life; and see beyond the pain, dream pass the disease, and move forward in spite of.
Our Goals
- To provide services, programs, and opportunities that will improve the lives of Sickle Cell Warriors
- Enhance quality of life through access to quality health care, patient-oriented services
- Increase participation in the community with partner organizations
- Inspire Sickle Cell Warriors to acquire skills necessary to create their desired life
We Are A Member Of SCDAA
Partner with us!
Your contributions will help us to carry out our mission and our vision!
