2 months ago
Travel Trade Crusade
An additional donation for this very worthy cause. Toot Toot.
2 months ago
An additional donation for this very worthy cause. Toot Toot.
3 months ago
+ £5.00 Gift Aid
This is a brilliant thing to do and such a worthy charity. Well done Rachel!
3 months ago
+ £5.00 Gift Aid
Well done ladies
3 months ago
+ £9.50 Gift Aid
A very worthy cause…congratulations to you all.
3 months ago
+ £5.00 Gift Aid
Well done! x
3 months ago
+ £5.00 Gift Aid
Well done 👏
3 months ago
+ £5.00 Gift Aid
Well done 😊
3 months ago
+ £5.00 Gift Aid
Well done!! x
3 months ago
+ £5.00 Gift Aid
Good luck Rachel and Janet you crazy ladies.
3 months ago
+ £2.50 Gift Aid
Bravo, well done!
Event dates: 4th July 2024 – 8th July 2024
The Butterfly Babes are raising money for DEBRA
We are embarking on a really fun car rally across Europe in order to raise money for Debra. We will be driving through 6 countries in 3 days and taking part in challenges and treasure hunts. Rachel Tredwell, a travel consultant, is mother to Simon who was born with Epidermylosis Bullosa, Janet is a fellow travel consultant who was a former paediatric dietician and worked with children with EB and Carla is a very close friend to the Tredwell clan.
In 2003, Rachel's world turned upside down with the arrival of a 3rd son, Simon. It had been a straight-forward home birth and all appeared normal. Sadly, 3 days later, Simon started breaking out in blisters all over his tiny body. After 3 days in hospital and none of the medical team being able to diagnose the problem, Great Ormond St were called in. They came down to Surrey and performed a biopsy. 3 weeks later, the Tredwell family were given the awful news that Simon had Epidermylosis Bullosa (EB for short). It is an incredibly rare condition that very few people have heard of. His care used to take 4 hours a day to burst his blisters. He suffered a great deal of pain, but was incredibly lucky to have one of the less serious types of EB. There are 3 main types - the first type is usually fatal within the first year of life, the second type gives a vastly reduced life-span and Simon's type has a normal life-span. All are very painful.
Debra is the charity that helps to look after the families and children living with EB. They do a wonderful job of fundraising to carry out research and offer much needed support and specialist services to these families. Please give generously.
Thank you for checking out our page. Making a donation is fast, easy and secure thanks to Give as you Live Donate. They'll take your donation and pass it onto DEBRA.
Your donations will help the great work DEBRA do.
Donate now