There are many ways to support and connect with people with SCD and their families.
Scroll down to browse by type of activity that inspires you.
Get involved in our programs that educate, inspire, and mobilize individuals to create change.
By joining our programs, you can help raise awareness and share your experiences and expertise.
Join people with SCD and their families in person and online,
or lend a hand as a volunteer at our Sick Cells-hosted events.
April 20 - 21, 2021
All Day
Sickle Cell Disease Association of America, Inc. (SCDAA) 2021 Annual Advocacy Day event is an opportunity for patients and caregivers affected by sickle cell disease to learn how to advocate for issues that are important to them. Participants will learn about the key legislative issues that are important to individuals living with SCD and their families, including promoting stable funding for research, better healthcare access, and increased education and awareness for the sickle cell community throughout the country.
Learn More: HERE
Register for Day 1: HERE
Register for Day 2: HERE
April 21, 2021
2:00 pm - 3:00 pm
Brought to you by National Organization for Rare Disorders (NORD), this webinar looks to explain the process of transitioning from pediatric to adult care for people with rare diseases.
This webinar is intended for patients, caregivers, medical professionals, students and the general public.
Register: HERE
Donate today to help us continue this powerful work and make a difference for people with SCD.
For mail donations, please make all checks payable to:
Sick Cells
1042 Maple Avenue Ste 103
Lisle, IL 60532
Please consider a gift today by donating online at the link below:
