wdc

Our Co-Founder Jewel Darbone Interviews On WDC Radio Show About Living with Sickle Cell Disease

How would life be if we could prevent another child from being born with the Sickle Cell Disease or

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BLFSC5news

September is Sickle Cell Awareness Month

A friend on Instagram tagged numerous women including myself to participate in #BoldLipsForSickleCell photo challenge as a way to help raise awareness of the disease and

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BLFSC5news

Pucker Up and Take the Challenge for SCD Awareness!

Have you heard about the ALS “Ice Bucket” Challenge? I’m pretty sure you have. After all, everyone from Cookie Monster and Bill Gates to Rihanna and Derek Jeter have

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sickle-cell

This Is Why We’re Rocking #BoldLipsForSickleCell: A Quick Guide To Sickle Cell Disease

If you’re a fan of ours on Facebook you should know by now that September is Sickle Cell Awareness Month, and while we’re

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reauth

SCDAA Launches White House Petition for support of Reauthorization of Treatment Act

The White House Petition to bring national attention to the Sickle Cell Treatment Act – H.R. Bill 5124 is up

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