Patient Resources & Sickle Cell Support Groups | LYFGENIA™ (lovotibeglogene autotemcel)

LYFGENIA Consideration Brochure icon

Check out our Consideration Brochure

This brochure can be a great resource for learning about LYFGENIAT. Make sure to have it available and ready when talking to your doctor.

Download the Brochure

Have your questions ready when you need them

Keeping these questions handy while talking to your doctor or your QTC team can help you make informed decisions.

Download questions for your doctor & QTC team

Connect with the sickle cell disease community

Whether you’re living with sickle cell disease or a caregiver, it’s important to remember—you’re not alone, and there may be others who have a similar story. Sickle cell disease support groups or organizations are good places to meet others like yourself, get educated, and find assistance when you need it.

Explore national sickle cell
disease organizations

Are you an organization that would like to learn more about gene therapy and LYFGENIA?

Are you an organization that would like to learn more about gene therapy and LYFGENIA?

Connect with the bluebird Patient and Community Education Liaison (bPACE) team. The bPACE team provides patient education on gene therapy and LYFGENIA for local community-based organizations, support groups, and events.

It’s important to remember to always talk to your doctor for medical advice. If you are looking for individual support outside of a community-based organization or support group, my bluebird support also has additional resources to help.