Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
LIVING with Sickle Cell RVA is a fully functional 501 (c) 3 non-profit organization located in Richmond, Virginia. The organization was founded in 2015 by a mother of five who has two children LIVING with the disease.
The organization’s mission is to help kids and families affected by Sickle Cell Disease to LIVE through Education, Advocacy & Empowerment.
Education about Sickle Cell Disease as well as Sickle Cell Trait is provided to patients, their families, caregivers, educators, and anyone else that would like to learn more.
+myBinderRelated Content
-
Dominique FriendDominique Friend is a 43 year old living...
-
Rare Disease Week on Capitol HillNow in its 12th year, Rare Disease Week ...
-
Malik was Cured From Sickle Cell Disease (Teaser)https://www.youtube.com/watch?v=RddQ_qvh...
-
How can Implementation Science Frameworks Help Implement new Born ScreeningHow can Implementation science framework...
-
Joining hands: SCDAA and Emmaus medical partner to fight sickle cell diseaseIn observance of World Sickle Ce...
-
COVID-19 Resources for Non-Profit Leaders and the Community | National Organization for Rare DisordersThe health and safety of those with rare...
-
@SCDadvocateLakiea Bailey, Ph.D Sickle cell disease...
