Our focus is patients and their caregivers

Mayra, a Bardet-Biedl syndrome caregiver, at Rhythm

Rhythm is deeply committed not only to developing medicines for rare neuroendocrine diseases, but also to helping patients with these diseases receive the education, awareness, and access they need.

Robert and Gabe, brothers living with Bardet-Biedl syndrome
A patient and caregiver meeting at Rhythm

Rhythm InTune: resources for patients and caregivers

Rhythm InTune is a support program for caregivers and people living with rare MC4R pathway diseases. The program provides resources, education, and information to fit the unique needs of individuals living with rare MC4R pathway diseases, including Bardet‑Biedl syndrome.

Our robust and active clinical trial program is constantly evaluating new treatment options for people with rare diseases that cause hyperphagia and severe obesity. 

Genetic testing may help uncover primary causes of rare genetic diseases and help inform diagnoses. Our Uncovering Rare Obesity® program is a no-charge genetic testing program that helps identify rare MC4R pathway diseases. Participants are responsible for any doctor visit, sample collection, or other costs.