..........The Bethany May Charities Fund

''Aiming to provide financial assistance to charities established for children suffering from Neuroblastoma and to promote research into its treatment & cure''
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 "Those who bring sunshine to others cannot keep it from themselves"
 James M. Barrie
  
 
On the 21st December 2006 our lives were to change forever.
At the age of just one year and five months old, Bethany May
was diagnosed with a very rare childrens cancer, called neuroblastoma, affecting only 100 children in the UK per year and usually children under the age of five. Read My Story
 
 
She is our brave little soldier, Our love, Our hope and Our inspiration every single day.
           

Our Mission:

 

To raise money to assist funding into essential new research into improved neuroblastoma treatment programmes.  Headed by Professor Pearson at the Royal Marsden Hospital, who is widely regarded as one of the leading childhood Oncologists in Neuroblastoma. Click Here to read more


The harsh reality is that Neuroblastoma is one of the most aggressive childhood cancers yet receives very little funding into Neuroblastoma treatment and new research, the funding it does receive is relied upon solely from charitable donations as no Neuroblastoma funding is offered by the government.
 
 
Latest Updates: (Click on headlines to read more)
 
 
''CSC UK launch Christmas Card Donations Scheme'' - Nov' 2008
 
 
 
 
March 2008 saw the launch of our website, its launch and our ongoing campaign is dedicated to a very special little friend, Spencer Javi Roberts who we sadly lost earlier this year, Bethany and Spencer became the very closest of friends, he is missed every single day and will always be in our hearts. Read My Tribute to a Very Special Friend
 
 
 
 

                                      WE HAVE NOW RAISED     £15,642.45

 

 

                                   Please continue to support this worthwhile cause!