Kellys medical fund

I need help im going to need to travel to toronto multi vistes befor my lung transplant, as of now we have to leave monday may 25th 2015 , this is going to be my 2nd  time, 


Being a cystic fibrosis child is sure a challenge. Some children have it a slight worse & im one of those.. This past 2years have been a bumpy road!! Several hospital admission, thousands of tears, hearing pull threw is pretty scary. Me as a young girl. Would love to be normal but i was made this way& ill live it!!! You have to deal with the rain if you want the rainbow
As a young child i hated school, all i wanted was to be with my mom,it got to the point my mom start coming to school with me. Yes i got weird looks&comments but its what make me feel safe.
Then junior high came my mom got the surprise of her life, as she went to get out of the car & come in with me the first day i said no. So off i went, it all went great! Finished grade 7. Grade 8 came first months was great,second was went the trouble happend. I got horrible news my doctors saying it could be my last christmas with my family. Really gave me a fright. Not knowing whats going on so back in hospital again. Got better after a couple of days of treatment, got out of hospital a few days later back in i was again. It went like that for the longest time.didnt do grade 9. Went from grade 8-grade 10 Then skip forward abit in march, i ended up in the ICU (intensive care unit) on a breathing machine,not knowing what to expected. I remember to this day every moment that happendd down there... Not good ones, hearing my doctors tell my parents they diddnt know if their little girl was going to pull threw. Still gives me chills.. My parents have to be the strongest parents out there. Also my big brother also has cystic fibrosis & luckily he dont have to go threw any of this,its hard for him to watch his little sister, gasp for air,cry,be there for when im down, then that was a long admission then april2 i had to travel to Toronto sick kids hospital to be seen for a assessment about a lung transplant..spent my dads birthday in Toronto. Then stayed there for 8dayss and got better,came home and got a bit better,then it just went down hill again. Multi admissions,surgery, cystic fibrosis has no cure, but i have to say im a strong cystic fibrosis fighter!