02/28/2025
Today, on Rare Disease Day, we stand together in solidarity with families around the world affected by rare conditions. At the MFDM Foundation, we are dedicated to raising awareness for Mandibulofacial Dysostosis with Microcephaly (MFDM), a rare genetic disorder that affects fewer than 200 individuals worldwide.
Through our efforts, we strive to provide support, community, and resources to those impacted by MFDM. From our private family support groups to our conferences, we create a space for families to connect and share their experiences. Together, we are stronger.
On this Rare Disease Day, we honor the strength of our MFDM families and all rare disease warriors. Join us in spreading awareness and advocating for rare disease research. Together, we can make a difference.
To learn more about MFDM, visit [MFDMfoundation.org](https://www.mfdmfoundation.org)
The MFDM Foundation serves families that are affected by Mandibulofacial dysostosis with Microcephaly.
