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Lydia explains what enrolling in the Genetics Project entails at the Weinberg Family CP Center.
Lydia tells her story as someone growing up with cerebral palsy and creating your own norm.
7 things I want to encourage the CP community with when it comes to advocating for inclusion and life with CP
Webinar – 10.1.20 – A discussion for caregivers, patients, and providers on how to make better-informed long term care decisions regarding neurological and orthopedic treatment of cerebral palsy.
The 74th Annual AACPDM Virtual Meeting will feature presentations and research from a number of Weinberg Family CP Center staff, affiliates, and researchers.
The WFCPC is CPRN’s first site in New York City and provides a large and diverse patient population, including children and adults, for the studies conducted by CPRN.
A cross-sectional study of adults with CP at a single institution compared the patient characteristics of patients with and without CSS.
The Movement Recovery Lab at the Weinberg Family CP Center, led by Jason Carmel, MD, PhD, has recently been awarded a grant to continue its research into a clinical trial.
As I got older, my disability started affecting me in new ways and that took a lot of getting used to. With that being said, I would like to share with you what I’ve learned up until now.
The social work team at the Weinberg Family CP Center is here for you. They share some general “tips” on coping with social distancing.