My Sickle Cell Research Xplained Stories
Stories based on people with sickle cell disease, their experiences and advice to others on how sickle cell research has played a role in their lives.
Blogs and Podcasts on Sickle Cell Disease Research
Check out the latest blogs and podcasts for helpful topics on sickle cell disease research.
To see all of our blogs, click here. To see all of our podcasts, click here.
Blog 8 – Basics Behind Gene Therapy
Episode 2 – Progress in SCD Research and Potential New Treatments
Join Our Facebook Community
We've created a private Facebook community to discuss sickle cell disease research. Join the community to stay up to date on content added to this website about sickle cell disease research!
Meet the Experts
Meet the experts who helped create the My Sickle Cell Research Xplained content. We’ve got a pretty great panel. Check out their bios to learn more!
Amber Yates, MD*
Shirley Miller, MA*
Nirmish Shah, MD
Mary Brown*
Medicine X Story
Working as a medical doctor, I realized that far too many people may be confused about their diagnoses, their conditions, and their treatments. There can be a disconnect between the language that health care providers use, and what many individuals understand. This can make you feel anxious at what is often a very difficult time in your life.
We believe there is a better way. We believe all people, regardless of age, gender, culture or condition, should have access to medical information they can understand! Everyone should feel informed and empowered, in order to engage with their health care providers and be involved in making medical decisions.
This is why Medicine X was created.

Dr Kim Chilman-Blair
Founder, Medicine X
About My Sickle Cell Research Xplained
Dedicated Team
The Medicine X team is made up of doctors, artists, and creative writers who work together to make sure the information provided on this website is medically correct, up-to-date, and easy to understand.
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