I'm spanish and I'm doing a work about CF. I would really like to listen at the speech but my english level is not good enough. Can anyone show me where can I find it written? That would be easier for me. Thanks :)
I'm really interested in this, my uncle has CF and I know how horrible it can be.
"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!
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.
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!
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
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.
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
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:)
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!
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)
nice one
aseohosting 4 months ago
Super CF'er Thanks- Please keep supporting CF resurch!
GetoffyourRss 1 year ago
Hi :)
I'm spanish and I'm doing a work about CF. I would really like to listen at the speech but my english level is not good enough. Can anyone show me where can I find it written? That would be easier for me. Thanks :)
I'm really interested in this, my uncle has CF and I know how horrible it can be.
Sil5iNRoses 1 year 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!
JMMPR24 2 years ago
brave boy...well done
S888999333 2 years ago
I like this boy
airsoft622 3 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
cheesecakeman31416 3 years ago 2
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.
WANTMORE2321 3 years ago
@cheesecakeman31416 god bless you and good luck brother
shia120 1 year 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. :D
vamp666babe 3 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
xximnotdeadyetxx 3 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.
surfnakd23 4 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
thatclimberguy 4 years ago
How can I help with CF?
Diane George
dianesnewlife 4 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:)
SSDavyS 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.
dogermad 4 years ago
wow nice speach , very amazing ,good job!
tenyus 4 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
mizzck 4 years ago
I have CF and I am 19 this kid did an amazing job I wish him and all of us good luck
maddhatter7891 4 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)
nikoleham 4 years ago
Nice job :)
Bigmuck1 5 years ago
Wow, he did an incredible job. My son is 3 with CF. Thank God for all those medications.
lilhyperfingers 5 years ago
this is a amazing speech!
partyanimalxx 4 years ago