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~
Passing on Sickle Cell to your Children
Passing on Sickle Cell to your Children Warrior parents, can you relate to feeling like this? How do you cope? What helps you get through these feelings about passing on sickle cell? Jourdan Dunn feels as if she passed sickle cell disease on to her son, Riley Dunn. The model-turned-actress recently told The Sunday Times magazine about…
Make Happiness a Habit – 5 Ways to help
Happiness isn’t always easy to catch and hold onto. Yes, some relationships can provide deep joy, and material possessions might offer a short-lived thrill, but these sources of happiness are somewhat out of your control. To nurture and sustain feelings of happiness, develop routines you can rely on no matter what else is going on in…
Emergency Care not Ideal for SC Patients
New survey finds that treatment in the emergency room for patients with sickle cell disease is not ideal. This is a longstanding issue, but warriors now demand justice. It will be addressed by #BlackHealthMatters initiative
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
English
Afrikaans
Albanian
Amharic
Arabic
Armenian
Azerbaijani
Basque
Belarusian
Bengali
Bosnian
Bulgarian
Catalan
Cebuano
Chichewa
Chinese (Simplified)
Chinese (Traditional)
Corsican
Croatian
Czech
Danish
Dutch
Esperanto
Estonian
Filipino
Finnish
French
Frisian
Galician
Georgian
German
Greek
Gujarati
Haitian Creole
Hausa
Hawaiian
Hebrew
Hindi
Hmong
Hungarian
Icelandic
Igbo
Indonesian
Irish
Italian
Japanese
Javanese
Kannada
Kazakh
Khmer
Korean
Kurdish (Kurmanji)
Kyrgyz
Lao
Latin
Latvian
Lithuanian
Luxembourgish
Macedonian
Malagasy
Malay
Malayalam
Maltese
Maori
Marathi
Mongolian
Myanmar (Burmese)
Nepali
Norwegian
Pashto
Persian
Polish
Portuguese
Punjabi
Romanian
Russian
Samoan
Scottish Gaelic
Serbian
Sesotho
Shona
Sindhi
Sinhala
Slovak
Slovenian
Somali
Spanish
Sudanese
Swahili
Swedish
Tajik
Tamil
Telugu
Thai
Turkish
Ukrainian
Urdu
Uzbek
Vietnamese
Welsh
Xhosa
Yiddish
Yoruba
Zulu