"Ignite an Era of Renewed Awareness to
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.
Advocacy and empowerment
Self Advocacy is the ability to speak one's needs and make informed decisions about the support necessary to meet those needs.
This program is supported via a grant from Global Blood Therapeutics, Inc.
Educate Yourself, Be An Advocate
Next Meeting: May 2, 2020
Dr. Robert W. Hagar, MD of UCSF BENIOFF-OAKLAND
Topic: PRIMARY ADULT CARE
** If you miss this meeting date above, you still can be an advocate. Go to our sign up page.**
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.
Shop Amazon with SCAA
When You Shop, Amazon Gives!!
AmazonSmile is the same Amazon. Same products, same prices, same service. Amazon will donate 0.5% of the price of your eligible AmazonSmile purchases to Sickle Cell Anemia Awareness whenever you shop on AmazonSmile.
Help Us establish a Sickle Cell Care & Resource Center By Donating Now!