We are thrilled to invite you to join us in celebrating a momentous milestone – the 70th birthdays of two INCREDIBLE women who have made an indelible mark in the realm of medicine, patient advocacy, and our #PHamily. Dr. Katy Phelan, PhD, FACMG, one of the first publishers about a simple deletion on the long arm of Chromosome 22, and Sue Lomas, one of the visionary founders of the Phelan-McDermid Syndrome Foundation (PMSF) and Sammy’s mom, are turning 70!
To honor their exceptional contributions and dedication to the Phelan-McDermid Syndrome Foundation community, we are hosting “Katy & Sue’s 70th” Birthday Fundraiser. This event is not only a celebration of their significant birthdays but also an opportunity to support ongoing efforts to improve the lives of individuals and families affected by Phelan-McDermid syndrome.
The journey began when Dr. Katy Phelan, then Director of Cytogenetics at Greenwood Genetic Center, identified and characterized 22q13 deletion, a rare genetic disorder that affects neurological development. Her pioneering work led to the first family gathering and has paved the way for crucial research and enhanced understanding of this condition, offering hope and support to countless families around the world.
Sue Lomas, driven by her passion and determination to make a difference, founded the Phelan-McDermid Syndrome Foundation along with a few other parents. Through her tireless efforts, PMSF has become a beacon of support, education, and advocacy, providing vital resources and creating a sense of community for families across the globe who are facing the challenges of Phelan-McDermid syndrome.
We invite you to participate in “Katy & Sue’s 70th” Birthday Fundraiser to help us honor their impact and continue the vital work in the field of Phelan-McDermid syndrome. Your support will contribute to research initiatives, family support programs, and educational campaigns aimed at raising awareness about this syndrome and empowering affected individuals and their families.
…And a very happy belated 70th birthday to Dr. Curtis Rogers, another pioneer in the world of Phelan-McDermid Syndrome Foundation. He and Dr. Katy were co-authors on their first (and several later) publications characterizing deletion 22q13 and Phelan-McDermid syndrome. Dr. Rogers has been an active participant in the initial 22q13 Family Support Group Meetings and in the subsequent PMSF International Family Conferences and zumba classes.”
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