The All Party Parliamentary Group for Muscular Dystrophy (APPG for MD) is conducting a six-month inquiry into  the need for and access to psychological support for people affected by muscle-wasting conditions - this includes SMA. We want to make sure your views are heard.
 
We will collate all the replies we receive and will not use any of your personal identifying information in the summary unless you have given us permission to do so. We will share the results with Muscular Dystrophy UK who will collate all the replies they receive and report to the APPG for MD. We will also publish the results on our website
 
You can say as much or as little as you like. We expect the survey to take about 10 - 30 minutes to complete. 

If you have more than one child with SMA, please complete a separate survey for each child.
 
Closing date for replies is Friday 27th April 2018
 
Thank you.

* 1. Who is completing this survey? (please tick as many as apply / that you wish to tell us)

* 2. How old is your child / young person with SMA?  Please tick one

* 3. What type of SMA affects your child / young person with SMA?

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