Taylor MacLean inspiring video Cystic Fibrosis

[TheDucky89]

Great work Team MacLean! I see you guys at the walk every year!!

Breathe Easy!!

love,

Bush's Team Breathe

[TatianaSword]

1#Cystic Fibrosis

[mackenma10]

the full name of pep is physiotherapy

[anestheticroses]

does she have boneitis?

[biggbuddz]

i am a cf patient i am 19 i 2 agree not enough people know about it taylor is lookin gud and all i can say is keep up he good work as i do i am. at the mo am in aussie n my hols it isnt easy but u have 2 keep goin stay well and look after urself keep goin strog

[oddsnenz]

I too have a 13 year old daughter who has Cystic Fibrosis. Her name is Taylor also. I think this video is WONDERFUL. You keep up the fight Taylor. My daughter and I will pray offten for you.

[ROBBO1978OVBLYTH]

There should be more public awerness about CF

[Wbita]

Joel, Taylor (and the other 2!) are beautiful. I have not heard from you for a long time, but judging from this, and with supportive, involved parents like you, she is doing amazing. She looks active, and healthy, Perfect! I wish you much success on Great Strides. People should do this for the good of themselves to support, and for others who need their support to help fund treatments, and find a cure! Congrats on your dedication!