About the trust
The
Trust wishes to help to relieve the needs of
children & young with Cystic Fibrosis their
families and carers by:-
-
Providing information and support.
-
Providing grants and days out, holidays and other recreational activities
-
Funding of equipment which will improve quality of life whilst in hospital care.
In 2007 Michelle and Jeremy Cotton founded the
Chloe Cotton Trust Fund in memory of their
daughter Chloe, who lost her brave battle to
Cystic Fibrosis aged 12.
Having lived with Cystic fibrosis ourselves we
are fully aware of the impact it has on every
day life and the whole family. We want children
and families to have some of their most
memorable moments and quality times together.
In our experience when children with CF have a
distraction from the daily regime of medication
and physiotherapy, it seems to lift their
spirits and determination. It is these
experiences that the trust aims to replicate
through the provision of special days and
holidays for children with Cystic Fibrosis
living throughout the UK.
Trustees
-
Michelle Cotton (chair)
-
Jeremy Cotton (secretary)
-
William Randall
-
Barbara Ansell
-
Jenny Flint