Welcome to Allison's Hope, a non profit charity fighting to improve the lives of families and children affected by Cystic Fibrosis

Tho it may be hard to think about, don't turn away from these children they need you

Hello everyone...i designed this web page  to tell you about my little girl Ally and the non profit organization Allison's Hope. Ally is a typical 4 year old little girl. All of her life she has stayed sick in and out of the hospital..after 4 years Ally was diagnosed with a disease called Cystic Fibrosis also known as CF. CF is a disease that attacks the lungs,digestive system and other organs...some kids have stomach problems,liver problems and of course lungs problems. My daughter suffers more with the lungs. The survival rate for this disease is some kids don't make it past elementary school..I've come in contact with a few parents whose child didn't..and that's not something i wanna face...if more parents would get up and work at helping to raise money so better research could be done then we might could change that survival...I 'm a parent who's trying to make a difference that's why i started Allison's Hope...losing my baby at a young age is something i never wanna face...i want to make a difference in my child's life along with the other children suffering from this disease everyday....living with CF isn't a great lifestyle to have...Ally has to take 9 different kinds of meds a day...a breathing treatment..and 3 different kinds of inhalers on a regular basis....she cant really live a normal lifestyle of a 4 year old..my little girl is so spunky and by looking at her you would never be able to tell there's anything wrong with unless she's not feeling well...although it's hard for her to keep up with her brother and other kids she tries really hard...that's just the little fighter she is...through all the test and all the blood work..through a shake vest...breathing test..she's a fighter..still smiling that beautiful little smile and letting those bright baby blue eyes sparkle....So please if you would like to help make a difference in a child's life please contact me...Ally also has a caring bridge page...WWW.caringbridge.com/allisonabbott...thank you for all you do and for being a partner in helping these children live out their hopes and dreams...please keep in contact with us...and watch for updates of upcoming fundraisers that will be held.

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 Most kids suffering with CF call  their disease 65 roses...it came from a little boy named Robert who over heard his mom on the phone talking about Cystic Fibrosis and he told his mommy i know what you're working for..and she said what honey...he said you are working for 65 roses....so that's where the name came from...it's much easier for the little kids to say.....