Cell and Gene Therapy Sessions
Your questions about gene therapy and transplant — answered by people who've been there.
No pressure.
No sales pitch.
Just honest information and real community.
Are you interested in Gene Therapy or Bone Marrow Transplantation?
Considering a bone marrow transplant or gene therapy for sickle cell disease can feel overwhelming. You may have questions about the treatment process, eligibility, recovery, long-term outcomes, fertility, mental health, finances, school, work, family planning, and what life looks like after treatment.
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At Sickle Cell Prodigy, we believe that every patient deserves access to trusted information and the opportunity to learn directly from individuals who have already walked this path.​
As the first and only nonprofit organization dedicated exclusively to supporting survivors of bone marrow transplantation and gene therapy, we are building a community where patients, caregivers, and survivors can connect, learn, and support one another throughout the transformative treatment journey.
Hear from real survivors in small group setting
Connect with people who have undergone bone marrow transplant or gene therapy and are living their lives on the other side. Sessions are intentionally small so everyone gets space to ask questions and be heard — not a webinar, a conversation.
Understand your options in a judgment free space
Learn the difference between gene addition, gene editing, and allogeneic transplant — in plain language, not clinical jargon. Whether you're just beginning to explore these options or you've been researching for years, you belong in this room.
Available in your language
Sessions are offered in English, Spanish, and French to serve our global sickle cell community. Our survivor community includes people from across the US, Canada, Europe, and beyond — bringing diverse experiences of the same journey.
Get in Touch. Stay Connected.
Fill out the form below and we'll reach out with upcoming session dates that work for you.​ By joining our interest list, you'll receive updates on educational programming, survivor stories, research opportunities, and resources designed to help you make informed decisions about your healthcare journey.