"Ignite an Era of Renewed Awareness to
Sickle Cell Disease"
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 San Francisco for people living with sickle cell disease to improve care and relations.
Plan Well Course
Meetings:
Time:
Presenter:
April 24
11am - 1pm
Leticia Vaca
MSW, LCSW (Urban Health Group LLC)
Advocacy and empowerment
Next Meeting:
Time:
Presenter:
Affiliation:
Topic:
May 8, 2021
11am - 2 pm
Vic Reynolds
Performance Entrepreneur Coach
Self Identity
This program is supported via a grant from Global Blood Therapeutics, Inc.
Intake and Assessment Program
CLICK HERE to schedule an Intake Assessment Session with one of our Community Health Workers or SCAA Support Staff
Donate now
Sickle Cell Disease Informational Needs Survey
Fill in this survey to help us find out more about gaps in information for those living with sickle cell disease.