I'm so sorry to have to tell everyone this. Molly sadly passed away suddenly on Sunday July 24th. Just to let everyone know we will be using all of her fix me fund donations to give her the best goodbye she deserves. I hope this is OK with everyone xxx
We are raising £5000 to purchase an adrenal pump which will give life sustaining medication. Like diabetics need insulin Molly needs hydrocortisone to stay alive. The adrenal pump is not available on the NHS
Hi im Rachel Mollys mum,
Molly has been a poorly girl all of her life. Undiagnosed with a life threatening illness for 14 years Molly was poorly every 3 to 4 weeks throughout her childhood, not having the hormones to repair herself from simple colds Molly would just get worse & end up with pneumonia. Molly is 23 now and getting no better. She now takes all replacement hormones she needs but because she has been so poorly so many times her body is shattered. She also has ME so this combination means she sleeps for most of the day and can only walk a short distance before becoming exhausted. She is now showing allergic reactions to her life sustaining medication. At the Moment Molly takes 4 tablets a day to stay alive. She is showing reactions to these. We are raising money to send her to London to get an adrenal pump fitted. This means the medication will go straight in to her blood stream and should give her a better quality of life. The adrenal pump is not on the NHS and including all private care this would be around £5000. We have successfully raised funds before through my artwork and the tree of hope children's charity. Unfortunately the charity can only help those up to the age of 21. Please visit www.mollysmiracle.co.uk for more information about Molly & her condition. Please follow our Facebook page Mollys miracle adrenal insufficiency awareness.
I have also released a series of Children's books with all proceeds going to this fund.
Many thanks for your donation