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.
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!
Learn more about our amazing scholarship recipient, her journey is definitely worth the read and she is going to do great things.
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To Enrich and improve the quality of life of individuals with Sickle Cell Disease, Thalassemia, and related blood disorders.
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.
After realizing the immense impact the pandemic has had on many, the BTG family put in place "Warriors In Prayer." W.I.P is a network of Warriors standing in the gap for those seeking prayer.
Submit your prayer request today!
Your contributions will help us to carry out our mission and our vision!
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BRIDGING THE GAP-ADULT SICKLE CELL FOUNDATION, INC IS A 501 ( C) 3 NONPROFIT REGISTERED IN THE STATE OF NEVADA. TAX IDENTIFICATION 84-4208373 PLEASE CONTACT US VIA PHONE OR EMAIL FOR MORE INFORMATION ON THE AVAILABLE ASSISTANCE WE CAN PROVIDE TO FAMILIES IMPACTED BY SICKLE CELL DISEASE PERMISSION TO USE THE BRIDGING THE GAP ( BTG)-ADULT SICKLE CELL DISEASE FOUNDATION LOGO OR FOUNDATION NAME, IN ANY VARIATION, IS SUBJECT TO THE TERMS AND CONDITIONS EXPRESSLY AGREED UPON IN WRITING WITH APPROVAL FROM THE BTG BOARD OF DIRECTORS. UNAUTHORIZED USE IS PROHIBITED
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