top of page

Upcoming event!

Educate Yourself

Treatments

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

best_crop_4a2f0d30eb4f922efddd_mini_magi

To bring change, we need your help.

Join us in making the everlasting impact.

image5.png

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.

ucsflogo.jpg

Resources from the
National Institute of Health

Subscribe to Our Newsletter

Thanks for submitting!

  • YouTube
  • TikTok
  • White Instagram Icon
  • White Facebook Icon

Contact Us

​

Email: crisis@scaasf.org

Phone: (408) 372-7694

​

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)

bottom of page