My page: http://www.bmycharity.com/janelewendon
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Raised so far
Gift Aid1
| Total Raised online: | £856.00 |
| Total Raised offline: | £305.00 |
| Name | Amount | Gift Aid |
| Catherine O'Lea... | £10.00 | £2.50 |
| Anonymous | £10.00 | £2.50 |
| Michael Cadier | £50.00 | £12.50 |
| stephen robinso... | £25.00 | £6.25 |
| Simon Bourne | £26.00 | £6.50 |
| Lynda Applebee | £30.00 | £7.50 |
| Kate le Marecha... | £5.00 | £1.25 |
| rosalyn gunston... | £10.00 | £2.50 |
| Ann Stephens | £10.00 | £2.50 |
| Tim Goodacre | £30.00 | £7.50 |
CLAPA
Hello and Welcome from Jane Lewendon - London Marathon Challenge!
Thank you to everyone who sponsored me and helped fund important projects for CLAPA . If you haven't already, there is still time to donate...
Many thanks!
Why CLAPA?
Cleft lip and palate is the most common congenital condition affecting 1 in 700 babies in the UK every year. Babies born with an opening in their top lip and/or roof of their mouth will need corrective surgery in their first year and may require additional surgery as they grow. As well as visual difference, being born with a cleft can affect early feeding, speech, hearing and facial growth. I have chosen to run for the Cleft Lip and Palate Association (CLAPA) because I've seen and heard first hand from families in our area how much of a lifeline support from CLAPA can be, for parents, children and adults.
If you are a UK taxpayer and give Gift Aid consent the charity will receive an extra 28% at no cost to you.
Thank you for your support.
About CLAPA
CLAPAis the only national charity in the UK dedicated to supporting all those affected by cleft lip and/or cleft palate. We are well-established, and have been providing dedicated services since 1979. We are the voice of both the patient/parent and those involved with their care. All our stakeholders are involved in the running of the charity; people born with a cleft lip or cleft palate; parents of children born with a cleft; health professionals involved in the treatment of cleft lip and palate.
Our aim is the continual improvement in the quality of life for all those born with clefts and their families, by providing the most appropriate and to make ourselves accessible to all sectors of the community. We do this by providing:children’s support: confidence-building camps, drama workshops, young people’s magazine, internet forum site;parent support: trained CLAPA parent contacts UK-wide, extensive range of literature on all aspects of the condition, telephone advice, internet forum site; throughfeeding support: unique specialist bottle and teat distribution to families and hospitals;improving care: safeguarding best practice and lobbying for best standards in UK and Europe;raising awareness of cleft lip and palate amongst the public;grant-giving: to further cleft care in the UK and beyond; small research projects: causes and treatment; overseas cleft treatment projects.
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