Patient-Focused Nonprofit Generating Awareness About Sickle Cell Disease, a genetic disorder that primarily affects BIPOC minorities
Welcome to Sickle Cell Warriors™, Inc.
Warriors,
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~
New Blog with Great Resources
By Brooke Pillifant |
Micromattie.com is launching a blog focused on recent developments and best practices in healthcare for Sickle Cell patients. Check it out!
Register for SCDTC LiveStream
By Tosin Ola |
pre-register and watch the sickle cell disease therapeutics conference here live sickle cell disease awareness month warriors
Pre-Register for LiveStream Here
By Tosin Ola |
Click here to register and watch the sickle cell disease therapeutics conference. Watch live here on Tuesday; sickle cell disease awareness month is for warriors, it’s our time to shine!
We are the innovators of the term Sickle Cell Warrior© a word that has been adopted by patients all over the globe.
Our Mission
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?
Advice on Living with Sickle Cell
Join Live Conversation on #SickleCellDisease
Connect with Sickle Cell Warriors online via one of our social media portals
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