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SCDF Staff
Sep 103 min read
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...
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SCDF Staff
Jun 173 min read
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.
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SCDF Staff
Jun 173 min read
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
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SCDF Staff
May 161 min read
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
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SCDF Staff
Feb 213 min read
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...
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