"Ignite an Era of Renewed Awareness to
Sickle Cell Disease"
Advocacy and empowerment
This program is supported via a grant from Global Blood Therapeutics, Inc.
* If you miss this meeting date, you still can be an advocate. Join our Training Sessions.*
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.
Broaden public awareness about sickle cell disease
Advocate for patients and families for access to quality compassionate healthcare
Educate to empower
Establish a comprehensive Sickle Cell Disease Care & Resource center in San Francisco for people living with sickle cell disease to improve care and relations.
Their pain is real.
Let them know you care.
All Proceeds Go Towards The Sickle Cell Care & Resource Center