Real People. 
Real Experiences.

Hear about the LYFGENIA treatment journey from people who have experienced it firsthand.

Real People.
Real Experiences.

Hear about the LYFGENIA treatment journey from people who have experienced it firsthand.

Through Their Eyes: Caden and Francita’s LYFGENIA Journey

Explore LYFGENIA stories

Choose a video below to begin watching.

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Through Their Eyes: Caden and Francita’s LYFGENIA Journey

Hear the personal story of Caden, 19, and his mother Francita—from navigating the challenges of sickle cell disease as a family to choosing gene therapy with LYFGENIA for him. And see what Caden’s life is like now, beyond VOEs.*

SCD Voices

SCD Voices: A Conversation About Gene Therapy With Francita and Elle Cole

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Francita, the mother and caregiver of a LYFGENIA recipient, joins Elle Cole, an SCD advocacy leader, to share her family’s gene therapy journey. Hear how they made the decision to move forward with LYFGENIA, what the treatment process was really like, and the difference it has made in her son’s life.

*VOEs=vaso-occlusive events, also known as sickle cell crises.

Ready to take the next step with LYFGENIA? Ready to take
the next step
with LYFGENIA?
Connect With a Patient Navigator
From the moment you decide to explore gene therapy with LYFGENIA, a dedicated Patient Navigator is here to answer your questions and support discussions with your doctor.
Find a Qualified Treatment Center
LYFGENIA is provided at carefully selected Qualified Treatment Centers (QTCs) to ensure you get the care you deserve. See if there’s a QTC near you.
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