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SCAASF VIRTUAL BLOOD DRIVE

DONATE BLOOD IN FEBRUARY

"Ignite an Era of Renewed Awareness to 

Sickle Cell Disease"

Spotlight:

  • SICKLE CELL SURVEY FINDINGS

  • Learn More: Vaccines & Virus

Advocacy and empowerment

March 9, 2024

11am - 1:30 pm

Kim Major & Judy Cavazos

UC Benioff

Neurocognitive Health: through the lifespan & resources 

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This program is supported via a grant from Global Blood Therapeutics, Inc.

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Who Are We?

Sickle Cell Anemia Awareness of San Francisco (SCAASF) is a 501(c)3 non-profit organization that came into existence in 2014 after our founder's son Kareem M. Jones passed away in 2013 from complications with sickle cell disease. 

Our Mission

Broaden public awareness about sickle cell disease

Advocate for clients and families for access to quality compassionate healthcare

Educate to empower

Establish a comprehensive Sickle Cell Disease Care & Resource center in the Bay Area for people living with sickle cell disease to improve care and relations.

Partnership/ Sponsor

To bring change, we need your help.

Join us in making the everlasting impact.

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news

I’m learning to embrace both natural and pharmaceutical medicine

December 2023

FDA approves cure for sickle cell disease, the first treatment to use gene-editing tool CRISPR

December 2023

Clinical Trials At UCSF

The University of California San Francisco (UCSF) is running a dozen clinical trials for people with sickle cell disease.

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Their Pain is Real

LEt them know you care

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