Thanks for taking the time to visit my JustGiving page.
My beautiful princess Lucy has Cystic Fibrosis , she is 4 years old . Lucys day starts by taking 5 tablets when she wakes up , then physio on her chest , then a nebuliser . She then has breakfast which she also need to takes more tablets with . Lucy has to take tablets with every meal and snack she has . She will then have another nebulises when she gets in from nursery , later in the evening she will have tablets, more physio and breathing exercises followed by another nebuliser before bed . my princess is a very strong brave girl who i admire so much and takes all this treatment in her stride but it is alot for anyone just to try to stay healthy . there is no cure for Cystis Fibrosis and life expectancy is 31 years old , although there are exciting developments being made in gene therapy this is costing millions of pounds and with no government funding for this i need your help so PLEASE PLEASE PLEASE consider sponsoring me to help find a cure for Cystic Fibrosis . i have did quite a few fundraising thing since i found out about Lucy having CF at 7 months old including a sky dive and a naked calender but having ALL MY HAIR shaved is one i fear the most !!! it will be taking place on top of the Transporter Bridge in Middlesbrough on Sunday 29th May . Thank you for taking time to read this and your support . X
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