Sickle Cell Warrior Death Inquest Reveals Gross Negligence in Hospital This makes me so mad. Rest Pain-free Mr. Evan Smith, Your death will not be in vain, you will save many warriors, I promise. Shame on you North Middlesex Hospital. All their excuses don’t matter. This young man lost his life due to poor medical
SC Warrior Death due to Hospital Negligence Read More »
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!
Pre-Registration for LiveStream Read More »
Register here for the new Mental Health Initiative, a free benefit provided by the Sickle Cell Warriors, Inc., community. The program details are below. This program is for warriors, by warriors, to warriors and funded with donations from the SCW community.
Mental Health Initiative for Sickle Cell Warriors, Inc. Read More »
Learn more about the sickle cell scholarship sickle cell disease. This education scholarship is for sickle cell warriors scholarship whoo are pursuing higher education. Will help with tuition for school.
Tuition Scholarship: First Annual Read More »
Preregister for the Sickle Cell Disease Therapeutics Conference right here. Watch the livestream here on the Sickle Cell Warriors website.
GBT Livestream Registration Read More »
To best serve you during this trying year, Sickle Cell Warriors, Inc. has developed a short study. Data received will be used to guide program development and education. This falls under our mission objectives of Research, Advocacy & Education.
COVID Sickle Cell Warriors Impact Study Read More »
Connect with over 25,000 patients and we are still growing! Sickle Cell Warriors is the largest patient-run global advocacy organization for sickle cell disease. Connect with us today!
Connect with SCW today Read More »
Knowledge and Confidence to Tackle SCD Sickle Cell Disease is well known for the pain that it causes. What isn’t widely researched is the emotional stress that families go through due to the unpredictable episodes of pain, hospitalizations, risk of death, and more. Treatment options are few, and curative therapies like bone marrow transplants and
SC Handbook for Parents and Caregivers Read More »
Sickle Cell Data Collection Program “Unite Sickle Cell: Collaboration and Community in Sickle Cell” Wednesday, September 18, 2019 1:30 – 3:00 PM PDT Register now: https://attendee.gotowebinar.com/register/2843093377260613389  Presented by Dr. Nik Rashid and Ms. Linetta Barnes from Nevada and Ms. Mary Brown and Ms. Jennifer Fields from the Sickle Cell Disease Foundation of California. Tracking California’s
SCDC Webinar: Unite Sickle Cell Read More »
