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The Willow FoundationWho They Are Anna was a community nurse based Anna found that when she had something to look forward to, her pain was reduced, her spirits lifted and she'd feel better. Treats, days out, concerts, shopping trips and just being with friends, simple distractions from her illness, gave Anna the adrenalin, strength and determination to keep fighting. She wanted quality of life, quality of time and most importantly, when she became ill, she wanted to be treated as 'normal'. The Willow Foundation's aim is to replicate the positive impact that Special Days had on both Anna and her family during her treatment, by providing the same opportunities for other seriously ill young adults throughout the UK. In 2003 the Wilsons stepped back from the day-to-day running of the charity, however Bob Wilson remains a trustee and Megs Wilson is Founder President. They're both still heavily involved in fundraising activities and are kept informed of every Special Day organised. What They Do Every Special Day is chosen by the recipient and tailor made to their specific needs. The Willow Foundation endeavours to fulfil each request, however imaginative, and whenever possible to exceed expectations. To date, the charity has organised and funded Special Days for young adults living with a wide range of serious conditions including: cancer, motor neurone disease, cystic fibrosis, Huntingdon's, organ failure and later stages of multiple sclerosis. Their long term aim is to be able to offer a Special Day to every seriously ill young adult in the UK. |
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From Med to Sled © Suzanne Meiklejohn.
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