Congratulations on a fantastic website. Well done to everyone involved. I'm sure that Brooke's army of support will grow by the day. Good Luck with your campaign and to gorgeous little Brooke and family.
What a beautiful website! And informative too. Lovely pics of Brooke. Such a brave little girl. xoxoxo
hi all brookes nan here shes still a constant surprize to us yesterday she had her throat dilated as her surcoffas close under for nearly 2 hours very sick when she returned from theatre but only after 1 hour shes up running around and eating
The very very best of luck. I live in Watford and my niece who is 13 has the same condition. She had a bone marrow transplant at St Mary's 5 years ago. She is now a different child - full of beans and doing so well at school. My dad (her grandad) was her main carer in the room at the hospital as Saskia's mum was breast feeding Imogen. You can get through this x
thank you do you live in watford
brooke is now 7 still transfuseing every 3 weeks has her pump attached every day but never complains , off to see one direction on friday sooooo excited , she gets to see harry in the flesh her favorite. but she never fails to surprize us with her resilance shes an insperation to all who know her l
hey Brokke I make you lots of kisses and I wish you all the happiness in the world;::: love ya!
Hi my son has this condition he is 26 this year so there is life with this condition x hope all goes well for you x
Hi Brooke, my sister had a similar condition and fought really hard to get over it so you can definitely do it too! The very best of luck from everyone in our house! (Great website guys!)
You are an amazing brave little girl and I can see that you are very much loved by everyone who meets you. I hope it won't be too long until you go home. I'll be praying for you. X
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