Sarah Willow’s Wish

Sarah Willow was born with a rare brain disorder. Just4Children are raising funds to send her to a neuromotor research centre in the USA for therapy specifically designed to treat her condition.

£29284.43
Total raised
97.61%
£30,000.00
Target
Donate Fundraise

348 donations

Recent donations

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£52.00 from Peter Austin
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£51.00 from Ken and Margaret
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£50.00 from Hill Family
"Can't think of a better cause"
£23.00 from Mike G
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£20.00 from Anonymous
"Wishing you all the best"
£210.00 from Dave and Jackie
"Best wishes for the treatment."
£46.00 from Robin S
"Amazing effort Craig for your beautiful little girl. So impressed. With huge love to you all. Lucy, Nick and Theo xxx"
£110.00 from Nick and Lucy Murchie
"I hope your blisters heal fast (I'm sure you'll have some!) - Lovely to meet the family and best wishes with everything."
£34.50 from Glen Lowerson
"Best of luck"
£HIDDEN from Anonymous
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£HIDDEN from Anonymous
"Good luck and all the best"
£20.00 from Anonymous
"Good luck, Craig. I hope your fund raising makes a real difference."
£33.00 from Chris
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£21.00 from Anonymous
"Good luck on the run, Craig! All the best."
£11.00 from Will Goulden
"We Craig's have to stick together! it's a long way but i'm sure it will also be fun!"
£20.00 from Craig Hawes
"Sounds like a massive challenge. Good luck!"
£HIDDEN from Anonymous
"Good luck with your run. Wishing lots of love and support for you and your beautiful daughter x"
£22.00 from Liz Kemp
"Loads of luck Craig - you'll smash it x"
£22.00 from Hannah Eaton
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£100.00 from Anonymous
"Good luck with the run!"
£100.00 from Clare C
"Best wishes"
£22.00 from Ed L-W
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£HIDDEN from Anonymous
"Good Luck,"
£55.00 from Anonymous
"Good luck"
£22.00 from Geetesh Patel
"Good luck."
£55.00 from Jim
"Smash the race, good luck"
£17.45 from Andy J
"Good luck Craig. I think you might need it!! You couldn't have a better (and cuter) motivation than Sarah to get you around."
£11.50 from Emma Connelly
"Good luck Craig"
£100.00 from VIMAL S
"Good luck Craig. Hope you are not planning to run in toe shoes!"
£50.00 from Anonymous
"Having walked some of those hills, I think you're mad! Good luck :)"
£55.00 from Gareth Jones
"Good luck Craig! The run sounds grim but I'm sure you'll smash it."
£31.50 from Bertie Pinnock
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£33.00 from Anonymous
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£33.00 from Jordan Cassem
"Craig, good luck - sounds like a big challenge"
£52.50 from Jem Brown
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£10.00 from Ollie Chambers
"thoughts and prayers for Willow and all her supporters"
£HIDDEN from Anonymous
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£55.00 from Louisa
"As this affects the whole family we are thinking and praying for you all."
£HIDDEN from Roger & Ann
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£22.00 from Anonymous
"For the lovebirds picture. It reminds of the never ending love and dedication you show. I hope Sarah Willow's wish comes true. Love Karen x"
£40.00 from Gardner Family
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£110.00 from Julie King
"Good Luck with your run I hope you get to the USA"
£HIDDEN from Anonymous
"Best wishes in your wonderful work."
£HIDDEN from Anonymous
"Good luck both."
£34.50 from Kath
"Good luck with the run and even more so with the fund raising"
£50.00 from Phil & Shirley Beedon
"So pleased you have this opportunity to help Sarah."
£22.00 from Anonymous
"Amazing effort Craig, make sure you actually enjoy the run too!"
£HIDDEN from Matt Boyd
"Great cause!"
£22.37 from Justin couch
"Really hope that you manage to raise the money to take Sarah to the US and that she really benefits from the therapy. Sally and Bob xxx"
£34.50 from Sally Powell

Sarah Willow was born with a rare brain disorder. Just4Children are raising funds to send her to a neuromotor research centre in the USA for therapy specifically designed to treat her condition.

Sarah Willow is aged 2 from Liphook in Hants. She has a smile and laugh that is contagious. Everyone who meets her falls in love with her gentle nature. Unfortunately, the prognosis for her genetic condition (MICPCH caused by a mutation in the CASK gene) is generally poor. If there is a chance she will one day sit unaided or walk or talk then we want to give her every opportunity to reach those milestones.

The CASK gene is found in the whole body and is needed for efficient respiration and proper development of the brain. Without the gene the neurones in the brain do not fire properly and, as in Sarah’s case, often cause epilepsy. Sarah contracted epilepsy in October 2018 and it took nine months of emergency trips to hospital and physical and mental regression before we discovered she was being treated (accidently) with an unsafe dose of epilepsy medicine and, in fact, she had a rare form of epilepsy called epileptic spasms. This type of disorder needs to be treated immediately since every seizure causes brain damage which results in loss of skills.

We feel we owe it to our beautiful girl to make up to her those lost nine months of her life.

Since being properly diagnosed and being treated with the correct medicines (at the correct doses!) she has started to develop again. Whilst researching her condition we were advised to read a published scientific paper about some children with the same condition who had undergone intensive therapy in America and had learned lots of new skills. The children gained an average of two developmental years in just one month! The therapy costs $24,000. However, we believe this could be the difference between Sarah ever being able to pick up a toy or being able to communicate with us effectively. The funds we raise will hopefully pay for therapy in October 2020 and contribute to flights and a month’s accommodation.

If you would like to get to know Sarah Willow better then take a look at her Instagram page welliesandwillow.

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