Annina's Cystic Fibrosis Fund

At 3 days old Annina had her first operation to remove the mucus from her bowel caused by Cystic Fibrosis, she was in theatre for 6 hours and came out with Stomas (her bowel on the outside of her body). After the operation she was diagnosed with Cystic Fibrosis and spent over 10 weeks in Alder Hey Hospital. She then got Bronchilitus and was on oxygen for a week in isolation. 7 weeks later she had another operation to reverse the Stomas back inside her body, after 2 and a half weeks she was finally allowed home.
Annina is on 4 medications twice a day everyday and another medication called Creon before she eats anything for the rest of her life.
Annina requires intensive physiotherapy every day to remove the mucus build-up in her lungs.

I will be cutting off my hair and donating it to The Little Princess Trust to be made into a wig for children with cancer. All money donated is going to Annina's charity.
I am raising money for vital equipment needed to improve Annina's quality of life and help her breathing. We are in the process of organising a charity day where me and George will be shaving our hair, raising extra money and announcing what we have raised for both Annina and Bobbie.

This poor girl has been through so much, is still going through it and will be for the rest of her life. Any contribution small or large is a massive help to Annina & her family! Thanks everyone for your help and support xxxx