<p><span style="font-family: Times New Roman; font-size: small;"> </span><span style="font-family: Calibri;"><span style="font-size: small;">As most of you know the MPS Society is personally close to me as my daughter has MPS type 1.<br /> <br />The MPS Society has been fundamental in shaping the research and treatment in to this disease and continues to do the same today.<span style="mso-spacerun: yes;"> </span></span></span><span style="font-family: Calibri;"><span style="font-size: small;">They provide Advocacy Support for families that is fundamental along with providing fun weekends for children effected by these diseases and their siblings.</span></span></p> <p><span style="font-family: Times New Roman; font-size: small;"> </span><span style="font-family: Calibri;"><span style="font-size: small;">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.<span style="mso-spacerun: yes;"> </span>Please dig deep and give what you can. </span></span></p> <p><span style="font-family: Times New Roman; font-size: small;"> </span><span style="font-family: Calibri;"><span style="font-size: small;">If you would like further information about the MPS Society then please visit </span><a href="http://mpssociety.co.uk"><span style="font-size: small;">http://mpssociety.co.uk</span></a><br /><br /><span style="font-family: Times New Roman; font-size: small;"> </span></span></p> <p><span style="font-size: small;"><span style="font-family: Calibri;">Thank you for your support</span></span></p> <p><span style="font-family: Times New Roman; font-size: small;"> </span><span style="font-size: small;"><span style="font-family: Calibri;">Dan Taylor</span></span></p> <p><span style="font-family: Times New Roman; font-size: small;"> </span></p>