The SMA Trust

As a result of my own experiiences with this terrible childhood disease (my son Harry died aged six in 2000), I was asked to join the board of trustees of The SMA Trust to help in the funding of research programmes in the UK and the States.

If you haven’t heard of SMA there are a lot of good sources of information, links to which can all be found on The SMA Trust website – this site is just a few holding pages at present but will be updated shortly to include details of the research projects we are currently funding and proposed projects.

Leave a comment

This site uses Akismet to reduce spam. Learn how your comment data is processed.