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 make a difference. Take a look at how we’ve activated 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 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.
The SCDC program is in jeopardy. We are asking the SCD community to mobilize and take action.
This month we hosted our Annual SCD Policy Forum with SC3, celebrate Woman’s History Month, and hear from Mariah Scott in a new blog.
This month, we recap our time at Rare Disease Week, congratulate Talana Hughes, and highlight an article by former staff member Mariah Scott.
Elevating the voices of the sickle cell community. #sickcells #facesofscd #scdsurvey
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