Our Pledge:
understanding, awareness, support
Our commitment to people living with rare genetic disorders of obesity 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 rare genetic disorders of obesity, and to drive positive change with others.
Solomon. living with Bardet-Biedl syndrome, and his brothers
It took so much longer than it could have. There’s not a one-size-fits-most diagnosis.
Olivia, mother of Solomon, diagnosed with Bardet-Biedl syndrome
We are committed to improving the understanding of severe obesity that results from specific genetic disorders, 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.
Healthcare professionals can explore the science at Uncommon Obesity.
Leigha living with Alström syndrome,
Helping to open doors to diagnosis
Genetic testing may help physicians diagnose some rare genetic disorders of obesity in individuals who may suspect there could be a specific underlying genetic cause of their obesity. However, access to genetic testing can be costly and is frequently not covered by insurance.
To help expand access to testing in the United States, Rhythm launched the Uncovering Rare Obesity program. The program is for individuals who suspect there is more driving their obesity than diet and lifestyle, and includes a free* genetic test for several rare genetic disorders of obesity conducted by PreventionGenetics, an independent DNA testing laboratory. As part of the program, licensed genetic experts are available to advise both participating individuals and healthcare providers. (Participating individuals may choose up to 2 free counseling sessions–one before the test and one after to review results.)
*Covers cost of test only for eligible individuals; additional restrictions apply. Click on the links below to learn more.
Our hope is to spark great change for this community.
Jill Spencer, Director, Patient Engagement and Advocacy
Small company, BIG vision
Supported by a dedicated Patient Advocacy team, we are helping to turn big ideas into real change for people living with rare genetic disorders of obesity.
Our team focuses on making a meaningful difference for those living with these rare disorders by:
- Acting with transparency and the highest ethical responsibility
- Understanding and supporting the community
- Shaping internal business practices with a focus on the patient
- Supporting the vital work of advocacy groups, both nationally and internationally
- Helping to raise awareness of rare genetic disorders of obesity
To reach us, please contact Patientadvocacy@rhythmtx.com.
Giving back
We proudly support education, professional society and advocacy conferences, research initiatives, and awareness efforts designed to improve the lives of people impacted by rare genetic disorders of obesity.
Email our grants team to submit a grant request