Redefining Sickle Cell Patient Education

Welcome to the
Sickleverse

The digital universe for sickle cell education, community and support.
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MEET THE FOUNDER
Dr Lewis Thomas smiling outdoors, founder of Sickleverse and sickle cell educator
MEET THE FOUNDER

Dr Lewis Thomas

Medical Doctor & Sickle Cell Patient

Why I created the Sickleverse?


"Whether you’re living with sickle cell or caring for someone who is, you deserve clear, trustworthy information so you can understand the condition and advocate confidently for your care."

Learn More About the Mission

Explore the Sickleverse

One Community, mutliple access points
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Join Sickleverse Live Masterclasses

Join live teaching sessions and ask questions.

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Watch on YouTube

Search educational videos on sickle cell topics.

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Read the Blog

Short weekly articles explaining key topics.

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Join the WhatsApp Community

Connect with others living with sickle cell.

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Free Resources

Download practical guides and tools.

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Sickle Cell Pedia

Need an answer right now? Ask Sickle Cell Pedia.

Sickleverse Live Masterclasses

Upcoming Live Masterclasses
May 26, 2026

Stroke Risk in Sickle Cell: Awareness & Prevention

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Watch Past Replays

March 25, 2026

Understanding Prescribed Sickle Cell Medications and Therapies

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March 18, 2026

See It Early, Save Your Sight A Practical Guide to Sickle Cell Retinopathy

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Latest Insights

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You're not alone in this

Sickleverse gives you support in two ways.
Talk to people who understand what you're going through or get instant answers when you need them most.
Connect with others

Join a moderated WhatsApp community where you can ask questions, share experiences, and learn from others living with sickle cell. Dr Lewis is there too to guide conversations and offer trusted input when it’s needed.

Join the WhatsApp community
Ask a question now

Get clear, reliable answers to your sickle cell questions in seconds. Sickle Cell Pedia is built from trusted medical knowledge, so you can get guidance anytime you need it, even when a specialist isn’t available.

Ask Sickle Cell Pedia

Stay Connected with the Sickleverse

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