"Ignite an Era of Renewed Awareness
Sickle Cell Disease"
ADVOCACY AND EMPOWERMENT PROGRAM
Self Advocacy is the ability to articulate one's needs & make informed decisions about the support necessary to meet those needs.
In January 2020 SCAASF will launch the Advocacy and Empowerment Program (AEP) with sessions once a month at the South Beach Harbor Community room located 3 blocks from AT&T Ballpark in San Francisco.
The program is comprised of two primary activities. The first part consists of 3 intensive workshops held once a month designed to introduce clients to the purpose of the year-long program, present core educational content on SCD, and explore self-advocacy. The second part is the implementation of the educational content learned, with journaling and role playing along with discussions pertaining to their real world experiences. We are in need of 30 patients/clients.
· Refreshments will be served at all sessions
· $50 Gift Card & Health and Wellness bag at the end of the program
· Transportation Assistance available
· Contact NeDina Brocks-Capla --
(415) 720-4458 or email reference AEP.
This program was supported via a grant from Global Blood Therapeutics, Inc.,
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;
and, lastly create a SCD Care & Resource Initiative in San Francisco.
DID YOU KNOW?
When You Shop, Amazon Gives!!
AmazonSmile is the same Amazon you know. 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.
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