Cystic Fibrosis – Speech

12 year old with Cystic Fibrosis gives keynote speech at Cystic Fibrosis Fundraiser. Video quality isn’t great, but I hope you agree the message is.

Cystic

This entry was posted by admin on April 25, 2010 at 3:58 pm, and is filed under Health Conditions. Follow any responses to this post through RSS 2.0.You can leave a response or trackback from your own site.

Comments (19)
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#1 written by lilhyperfingers 2 years ago

Wow, he did an incredible job. My son is 3 with CF. Thank God for all those medications.

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#2 written by Bigmuck1 2 years ago

Nice job

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#3 written by nikoleham 2 years ago

If brave, which I believe that all kids with Cf have to be brave. My son is 4 years old and has Cf. He is very smart and very very brave. (Alot braver than mom)

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#4 written by maddhatter7891 2 years ago

I have CF and I am 19 this kid did an amazing job I wish him and all of us good luck

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#5 written by partyanimalxx 2 years ago

this is a amazing speech!

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#6 written by mizzck 2 years ago

hey everyone.i have cf 2and so dus my lil sister.i have made a cf awarness vid,plz feel free 2 check it out.thnz and pass the message on.thnx,i appreciate it.

all my luv to every1,kp well and live life to the full!
xx
saira

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#7 written by tenyus 2 years ago

wow nice speach , very amazing ,good job!

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#8 written by dogermad 2 years ago

wow i have cf too it is amazing how many people went! i’am two years old than him, he did an amazing job of talking for everyone with cf.

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#9 written by dianesnewlife 2 years ago

How can I help with CF?
Diane George

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#10 written by thatclimberguy 2 years ago

That was a great speech, a friend of mine has CF. We did a walk for CF at the milwaukee county zoo last year and are doing it again this year. It was really successful

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#11 written by surfnakd23 2 years ago

At our surf school, we taught people with CF how to surf. A Foundation sponsered it. The Ocean air and water helps their lungs. We learned alot. and the little kids were awesome. their tuff as nails.

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#12 written by xximnotdeadyetxx 2 years ago

MY best friend whos 15 has been given a year to live ,,she will die then .its so horrible ..to see her in the hospital all wired up ..its so scary .shes my friend she should be out. enjoying her having fun ..but shes not ,,i love you kate i always will..xxxx

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#13 written by vamp666babe 2 years ago

I’m a CF’er and live in Australia. I will turn 21 in 2 weeks, which is pretty exciting given that when I was born my parents were told I would live till 12. I am on the waiting list for a lung transplant, and have been since December 2007 and now am on constant o2.
CF will stand for CURE FOUND very very soon, I have hope in it!
Off for another neb now.

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#14 written by cheesecakeman31416 2 years ago

i have cf and im on oxagen and need a transplant and i am bed ridden i have two years to live but im goin to keep fighting

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#15 written by airsoft622 2 years ago

I like this boy

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#16 written by WANTMORE2321 2 years ago

Hi i too have CF however i dont have that bad of a condition. i was wondering how old you are since i am 15 and the life expectancy is in the 30′s for children born recently with CF.

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#17 written by S888999333 2 years ago

brave boy…well done

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#18 written by SSDavyS 2 years ago

hi i got systic fybrosis,and if u wanna help, i know this sounds stupid but :donating money helps, also they look for healthy persons to do tests on that might help to find cure for CF, maybe sign-up for it, i got CF and i do many tests for the bettership of cf:)

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#19 written by JMMPR24 2 years ago

“My parents thinking the trombone was probably not the best instrument for someone with a terminal lung disease, may have actually been the first parents in america to actually want their child to play drums. ” bwhahaha! Now THAT was good!

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