Become an Ambassador
You'll learn how to advocate for the sickle cell community on a new level.
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Sick Cells is dedicated to developing programs that educate, inspire and mobilize
individuals to create community and policy-level change.
All advocates need timely and accurate information, to feel empowered to make a difference. Take a look at how we’ve activate the community to take on important challenges within policy and legislation.
We help sickle cell advocates prepare to attend Medicaid DURB and P&T meetings to provide public comments and improve access to treatments.
We partner with organizations to conduct research and surveys that help drive our advocacy work.
You'll learn how to advocate for the sickle cell community on a new level.
We're looking for leaders that can provide recommendations and advice to our staff.
Throughout the year we take on new interns who gain valuable experience.
We're love to hear from members of the sickle cell community - people living with SCD, their family members, caregivers and friends. Share your story to help us show just how diverse this powerful community is.
Every donation helps us better serve the community.
We love to share what we've learned. Let us know how we can partner with you at your events.
We do our best to round up the latest in treatment and policy news and spotlight SCD warriors in our monthly newsletters. Read through our latest newsletters.
This month, Sick Cells highlights why raising funds = raising awareness as we kick off our Summer Bash Fundraisers for Sickle Cell.
This month in our Minute with Marqus we reflect on a message from Marqus on what it means to be a sickle cell warrior. This month we also share our latest reports, an upcoming Summer Bash campaign and highlight the Mastering Advocacy Through Personal Branding and Earned Media Strategies discussed at our PTMs.
This month, we discuss DURB and P&T meeting updates including an upcoming Town Hall, provide some News You Can Use, and hear from Francesca Valentine in our Minute with Marqus.
Elevating the voices of the sickle cell community. #sickcells #facesofscd #scdsurvey
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