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ADVOCACY & EMPOWERMENT SESSIONS ARE BACK!

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February Blood Drive

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"Ignite an Era of Renewed Awareness to 

Sickle Cell Disease"

Advocacy & empowerment
sessions

February 8, 2025

11am - 1 pm

Art Grant

Retired Attorney

TBD

Next Meeting:

Time

Presenter

Affiliation

Topic

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Our Mission

Learn more About Sickle Cell

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.

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. 

Partnership/ Sponsor

To bring change, we need your help.

Join us in making the everlasting impact.

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Donate now

news

SCD patients remain VOC-free for at least 1 year after Casgevy

June 2024

The beauty and pain of growing older with sickle cell disease

June 2024

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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Lyfgenia Treatment: Gene Therapy

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Contact Us

Email: crisis@scaasf.org

Phone: (925) 494-1274‬

Please send us an email if you find any inconsistencies in our website. We deeply value your opinion.

Sickle Cell Anemia Awareness of San Francisco (SCAASF)

A registered 501(c)3 non-profit organization.

EIN: 47-1268974

Hours, Closures, About Us

This website is dedicated to my son, Kareem Marcellas Jones

© Copyright 2014-2024 By Sickle Cell Anemia Awareness of San Francisco SCAASF. All Rights Reserved. (Please view in Desktop Mode if on mobile device)

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