Patient-Focused Nonprofit Generating Awareness About Sickle Cell Disease, a genetic disorder that primarily affects BIPOC minorities
Welcome to Sickle Cell Warriors™, Inc.
We Made It!
September Is Sickle Cell Disease Awareness Month!
Our Time to Shine!
World Sickle Cell Day on June 19th
Sickle Cell Awareness Month
Don’t call me a sickler, I am a warrior!
~Get Latest News About Sickle Cell Disease Curated by Sickle Cell Warriors™ for You & Your Warrior Family~
By Brooke Pillifant |
The Sickle Cell Disease Coalition (SCDC), is developing fact sheets on sickle cell disease (SCD) therapies for the community and would appreciate your help reviewing the draft resources. As background, the SCDC formed to amplify the voice of the SCD stakeholder community to improve outcomes for individuals with SCD and Sickle Cell Warriors, Inc. is a…
We are the innovators of the term Sickle Cell Warrior© a word that has been adopted by patients all over the globe.
Our mission is to provide education, awareness, empowerment, advocacy, research access & support for those living with sickle cell disease. We do this through digital media, events, and conferences. We help to amplify the voices of patients, caregivers, and families battling this genetic rare disease.
Share Your Story
First of all, if sickle cell has touched your life in any way, you are a warrior. Are you a sickle cell warrior living life to the fullest regardless of sickle cell? Are you a mother, father, or grandparent caring for a sickle cell warrior? Are you in school, working or managing a household? Would you like the your sickle cell story featured on this website?
Written by Warriors for Warriors
SCW has the largest peer-curated online collection of articles dealing with the personal nature of sickle cell disease.
Join the movement to end Sickle Cell Disease.
Want to be featured as a Warrior in the Spotlight? Share your story here and inspire others.
We work with incredible organizations around the world.
Want to collaborate?