The Impact of Dysarthria | Niemann-Pick UK | Rare Disease Day 2023

In the following video, originally shared as part of our celebrations for Rare Disease Day 2023, National Niemann-Pick Disease Foundation (NNPDF) Board Member Cara Gilmore provides insight into her journey with Niemann-Pick disease type C and the impact of Dysarthria on her day to day life.

The video also features Dr. Robin Lachmann (UCL) who gives expert insight into how Dysarthria can be one of the ways in which Niemann-Pick disease type C can be diagnosed.

This video was made possible with kind support from Azafaros, to learn more about their company please visit: https://www.azafaros.com

At NPUK we are a charitable organisation dedicated to making a positive difference to the lives of those affected by Niemann-Pick diseases. Our central goals are to raise much needed awareness, provide practical and emotional support, advise and information and facilitate research into potential therapies for NPD.

To learn more about Niemann-Pick UK (NPUK) and Niemann-Pick disease, please visit us at our site: http//www.npuk.org

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