As most of you know the MPS Society is personally close to me as my daughter has MPS type 1.
The MPS Society has been fundamental in shaping the research and treatment in to this disease and continues to do the same today. They provide Advocacy Support for families that is fundamental along with providing fun weekends for children effected by these diseases and their siblings.
During these difficult financial times we all face it is obviously more difficult for charitable organisations due to government cuts and individuals feeling the pinch. Please dig deep and give what you can.
If you would like further information about the MPS Society then please visit http://mpssociety.co.uk
Thank you for your support
Dan Taylor
