Taylor MacLean inspiring video Cystic Fibrosis
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Uploaded by MrMoe07748 on Mar 20, 2007
Please go to Taylor's Great Strides page. Great Strides walk May 20th, 2007. 11:00 AM Pt Pleasant NJ http://www.cff.org/Great_Strides/JoelMaclean
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Great work Team MacLean! I see you guys at the walk every year!!
Breathe Easy!!
love,
Bush's Team Breathe
TheDucky89 5 months ago
1#Cystic Fibrosis
TatianaSword 1 year ago
the full name of pep is physiotherapy
mackenma10 2 years ago
does she have boneitis?
anestheticroses 2 years ago
does anyone here have to do pep? (around 13 year olds?)
exbhox 4 years ago
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
biggbuddz 4 years ago
Ive sent something. I hope we can finally cure this. Very best wishes to Taylor and hope she keeps well.
Stephen Maclean.
coopermania 4 years ago
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.
oddsnenz 4 years ago
There should be more public awerness about CF
ROBBO1978OVBLYTH 5 years ago
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!
Wbita 5 years ago