Help researchers learn more about caring for a loved one with methylmalonic acidemia (MMA)

If you care for a child or adult diagnosed with MMA, you may be eligible to participate in research interviews and receive compensation for your time.

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Connect with researchers

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After my son’s diagnosis, I had so many questions and didn’t know where to turn for answers. Know Rare provided incredible support... Can’t thank them enough for giving us hope for the future!


Fran, Mom of Diego
Diagnosed with Acidemia

Meet our team

We’re on a mission to help people with rare disease feel empowered

Our team of dedicated nurses are here to guide families to vital studies, offering solace and support. Know Rare's global impact is a testament to its team who have been impacted by rare disease and are focused on turning their pain into purpose, touching countless lives with empathy and determination.

Get in touch now to help advance research in MMA

Andreya Fletcher, Nursing Assistant

Recently I had the privilege to be a clinical research assistant where I helped with various aspects of clinical trials such as collecting data, recruitment and specimen processing.  I’m also personally connected to rare disease as my mom is diagnosed with Glanzmann Thrombasthenia which is a rare blood clotting disorder. Through learning from my mother’s experiences and supporting her in her journey, I understand how scary it can be to live with a rare disease. My personal experience combined with my professional experience in clinical research has given me the skills and insight needed to help people affected by rare disease.

Get in touch now

If you are interested in learning more about participating in research interviews, we encourage you to contact us by filling out this brief form: