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Sickle Cell Disease Foundation Kicks Off Sickle Cell Disease Awareness Month with Special Events and Toolkit Release
(Ontario, CA) – The Sickle Cell Disease Foundation (SCDF) is rallying communities, health care providers, and policymakers to recognize...
SCDF Staff
Sep 10, 20243 min read
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California Needs to Keep Funding Sickle Cell Care. Will It?
Despite cutting-edge treatments, many patients—mainly Black and brown—don’t even get basic support.
SCDF Staff
Jun 17, 20243 min read
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PAINFULLY AWARE: Understanding Sickle Cell and Its Impact on The African American Community
PAINFULLY AWARE: Understanding Sickle Cell and Its Impact on The African American Community
SCDF Staff
Jun 17, 20243 min read
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After living with sickle cell disease for 39 years, I’m both excited and skeptical about the newly approved gene therapies
After living with sickle cell disease for 39 years, I’m both excited and skeptical about the newly approved gene therapies
SCDF Staff
May 16, 20241 min read
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NCSCC: Uplifting Sickle Cell Disease as a statewide priority
The Networking California for Sickle Cell Care Initiative (NCSCC) was developed through advocacy and stakeholder engagement supported by...
SCDF Staff
Feb 21, 20243 min read
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