Pete and Helen Carter, parents of Hollie Carter who has Niemann Pick Type C and founders of the Hope for Hollie Campaign would like to say a huge big thank you and well done to all those who have supported the Hope for Hollie campaign since 2007, helping it to raise over £100,000 for the Niemann Pick Disease Group (UK).  The campaign continues to grow in strength and has now established a strong network of supporters who work tirelessly to raise awareness of Niemann Pick Disease and funds for the Group.   The campaign looks forward to supporting the work of NPDG(UK) in the coming years.

 

Pete and Helen would like to recognise the fact that the campaign would not be where it is today without the help of the Hope for Hollie working committee who have  given up hours of their time to help organise fundraising events and help manage the campaign over the years.  A special thank you to the following past and present committee members:-

 
Diane Waller (current)
Roger Widdecombe (current)
Alison Taylor (current)
Wendy Drewett (current)
Sarah Gale (current)
Jodie O’Grady (past committee member 2009 and 2010)
Vicky and Alastair Smith (past committee members 2008)
John Moore (past committee member 2008)
Dominic Dyer (past committee member2008)

 
This year we have even managed to rope in a few new recruits to help organise Hollie’s Midsummer Night Dream Ball taking place in June 2012 –  a big welcome to Dana Smith and Connor Dyer. 


Pictured left to right above - Sarah Gale, Wendy Drewett, Jodie O’grady, Helen Carter, Alison Taylor and Diane Waller.