understanding, awareness, support
Our commitment to people living with rare MC4R pathway diseases extends well beyond the development of potential medicines. We embrace a responsibility to listen to the community, to help bolster both individual and collective understanding of these diseases and help transform their lives through optimal and stigma-free care.
We are committed to improving the understanding of severe obesity that results from specific MC4R pathway diseases, and we have developed resources to help share knowledge, recognize symptoms, and aid in diagnosis.
We invite people to learn more at LEAD for Rare Obesity.
And learn more about our genetic testing program Rhythm’s Uncovering Rare Obesity.