News
Enjoy CSC’s Summer 2018 Newsletter!
Posted on August 21, 2018
In this edition of the CSC newsletter, read about the Martin family’s inspiring journey with Kleefstra Syndrome. Also in this issue is the story of Margaretha whom the Clinic […]
Amish Nemaline Myopathy Natural History Study Finds Promise for Gene Therapy Treatment
Posted on August 13, 2018
STRASBURG, PA- A new comprehensive natural history study about Amish nemaline myopathy (ANM) in the Old Order Amish population focuses on the promise of gene therapy for this lethal disorder. […]
‘Clinic Seeks Solutions for Rare Gene Disorder’ by Lancaster Farming
Posted on June 7, 2018
Eugene and Jeanette Horning sat down with Lancaster Farming news to talk about their unique journey raising a special child living with a random gene deletion, only found in 15 […]
Thank you to Dr. Katie B. Williams for her service to CSC
Posted on June 5, 2018
Dr. Katie Williams spent her last day at CSC on June 1st, traveling this week to continue her pediatric practice in her home state of Wisconsin. We would like to express […]
Register here for our FIRST annual Clinic for Special Children 5K Run/Walk/Jog – September 22
Posted on May 10, 2018
Please join us for our FIRST 5K Run/Jog/Walk to benefit Clinic for Special Children! Enjoy a 5K, free refreshments, a silent auction, and crafts for kids among the many family-friendly […]
CSC featured in Boston Globe Media’s STAT for role in helping to create pathways for access to specialized care
Posted on May 8, 2018
Published by STAT of Boston Globe Media on May 8, 2018, CSC and Dr. Kevin A. Strauss were featured in a national article highlighting financial barriers the Plain community faces […]
A New Service Available: SMA Carrier Testing
Posted on April 30, 2018
After months of development, the CSC laboratory is proud to announce two new tests for spinal muscular atrophy (SMA), tests that have significant implications for the services and care we […]
Please enjoy CSC’s spring 2018 newsletter!
Posted on April 18, 2018
In our spring 2018 newsletter, read the intimate story of Ken and Joanna Weaver’s journey with rare genetic disease, raising four boys with spinal muscular atrophy (SMA) in a vision […]
Dr. Strauss special feature published by Lancaster Newspaper and LancasterOnline
Posted on April 11, 2018
Published this weekend by Lancaster Newspaper and LancasterOnline, read Dr. Kevin Strauss’s special feature written about CSC’s practical application of genomic medicine to develop innovative therapies for children living with […]
CSC’s 2017 Annual Report – Your Impact
Posted on March 16, 2018
Each year, CSC releases an annual report, expressing gratitude to all of our supporters and relaying the impacts of their generosity through stories. Today we are releasing our 2017 report. In […]