Hey Kathryn, yes I know it's very hard, hang in there and keep up your treatments - they are working really, really hard to get to this cure. Keep smiling, you're a blessing to those around you. Thanks for the comment.
This made me really teary, i am 16 and i was diagnosed when i was 2-3 weeks old, so i woulnt no what its like to live with out it. All i can say is that is hard, and lets just hope someday someone will find a cure.
Hope this can bring you some hope; My wife was diagnosed with CF as a baby. She's into her 30's now and we have two beautiful boys who do not have CF, but do carry the gene. Keep smiling. X
Olivia was diagnosed at 5 as well. AND she's now 14 too. Active in soccer and swimming. Hope you're doing well - keep those treatments up! Thanks for the comment :)
the love of my life has C.F. it's hard to deal with but I have hope and so does. The most important thing is to believe. C.F. doesn't make the person who they are, it's just a part of life. It's worth all the procussions, and medications, and inhalations. Everything is worth it! Keep active and keep smiling. God's watching over you.
my daughter has c/f and is looking for support i am going to put more of her life on my channel and less of the rest of us plz subscribe it would mean allot to her she loves watching these other videos now that we know they are out there sub, to ditalydo
my older cuzin has cystic fibrosis and for her and u and all the others with it i hope they find a cure fast because 2 many ppl are dieing everyday from it..... :~(
im in high school english III and we have a report to do for class. i chose CF because i had read a book where one of the characters had CF. the book moved me as did this video i am happy that i chose CF as my topic so i can get more people involved with searching for a cure. i will pray for olivia and your family.
What a beautiful video. My two cousins aged 12 and 5 years have CF. I live with them and have to watch them struggle every day. I've been to hospital with them, it's so tough, but they are fighters. God bless you Olivia. xxxx
Thank you for this video. My daughter Eliza is 4 and has CF. She was diagnosed at 4 months. . . she was almost diagnosed too late. She is doing remarkably well now. We will pray for you Olivia and your family and pray for a cure! God Bless.
Thank you Joanna - They've come a long way in the CF battle and Eliza being only 4 stands a great chance to benefit from all the advances - keep praying, stay strong, and press on!
@angels4eliza There is no such thing as being diagnosed too late! Under my command your daughter is now immortal!!! God Bless you and your family! I am 13 and have Cf and I was diagnosed when I turned seven. I remember it all too. Let Eliza know she is loved by all.
I''m in College preparing to do a report on CF, and stumbled across this vid. This is very moving. Very well put together and the song is very powerful. Good luck with everything.
Beautiful video! I too wish for a cure, although no one in my family, nor me myself have the disease, I have a friend who has passed away from it and not a day goes by that I don't wish that she could have cured before it has happened. Grow up strong and big Olivia and maybe by the time you're a grown up and have children of your own you will be free of the disease.
BTW, what is the name of the song? It is beautiful and I am quite fond of it.
Well... I'm 19 and have CF... I met a person that's 88 years old and with CF... Just gotta work out, follow your treatment and you'll be ok! Actually, after a few days of treatment, I feel 40% better! Fellow CF people... Keep on fighting and remember if you put your mind into it, it's not that bad!
You're such a cutie ! You remind me of my daughter, Breanna who also has CF and is 11 years old. I am determined to do whatever I need to help find a cure for you, for my daughter and for everyone with CF, every day we're a step closer to a cure :)
GREAT video....well done..very inspirational..i am sure u have a long way to go with such great support too little grl..keep the faith....I have CF age42...
Unbelievable how wrong people can see the way God has plans for everybody..
I have CF myself.. and the fact that you can even think about being a freak for trusting God in His ways when you have such a disease.. thats even sicker!
This is gorgeous, and it was so great to see some of the CHOA staff on the video! Our son has CF and we're fighting for a cure right along with you. God bless.
Oh my goodness, your video had me nearly in tears. I am also a sufferer of Cystic Fibrosis. We do need help from the American population to find a cure for this wretched disease. One cannot achieve a large goal single handedly, it takes support and motivation. To everyone with Cystic Fibrosis, stay strong and never give up no matter what life throws at you. "It doesn't matter if the whole world is pulling you down, with Christ you have everything." -Nicholas Jonas
yay for Christianity, a frankenstein creation of numerous pagan religions that started thousands of years before christianity. It is called will power and strength of character to keep yourself going, not divine intervention. This brings me to another topic.... if your god created the heavens and the earth and shaped us in his image, why is there disease? Also, why have the type of body systems that we have. They are so complex and can go wrong in so many ways.
Couldn't a god who could create the heavens and the earth in 6 days create a far less problematic system for life? Religion has, throughout the ages, only brought about war, chaos, bigotry, and hatred.
@TomAndJerry87 That's a pretty big assumption there. Also, relevance? P.S. I'm not negative TOWARD life, I'm negative toward a collective of ignorance and intolerance that has a great deal of power in this country, as well as countless other countries.
Thank you for sharing that and for sharing it with your class. It's a small population disease and doesn't get the coverage that others do - so thanks for helping educate others. :)
I love those folks at Children's Hospital of Atlanta!! I got to meet them about 6 weeks ago ... my 3 month old has CF ... I pray for a cure every night ... and this video as hard as it made me cry, gives me hope because you have hope ... Thank you!!
When I usually watch these kind of videos I dont normally cry but I actually did in this one. The video gives a clear message to all people even young ones, and I hope they will find a cure.
My best friend has CF and I love her so much so I hope they find a cure fast enough to save you both from this horrible disease.
i cried so hard when i watched this..i am so sorry i never knew what i had untill i saw this. and i never knew how darn greatful i should be before i watched this video. i am so sorry olivia. be strong, and never give up you will make it through.
//eng.wavegenetic.ru/
superhope03 2 months ago
This has been flagged as spam show
I've seen hundreds of CF awareness videos, but this by far, is one of the best made videos I've ever seen!!
Breathe Easy, Cure Cystic Fibrosis.
TheDucky89 4 months ago
I've seen hundreds of CF awareness videos, but this by far, is one of the best made videos I've ever seen!!
Breathe Easy, Cure Cystic Fibrosis.
TheDucky89 4 months ago
I've seen hundreds of CF awareness videos, but this by far, is one of the best made videos I've ever seen!!
Breathe Easy, Cure Cystic Fibrosis.
TheDucky89 4 months ago
Hey Kathryn, yes I know it's very hard, hang in there and keep up your treatments - they are working really, really hard to get to this cure. Keep smiling, you're a blessing to those around you. Thanks for the comment.
taylorscorner100 5 months ago
This made me really teary, i am 16 and i was diagnosed when i was 2-3 weeks old, so i woulnt no what its like to live with out it. All i can say is that is hard, and lets just hope someday someone will find a cure.
Lucykathryn1994 5 months ago
Hope this can bring you some hope; My wife was diagnosed with CF as a baby. She's into her 30's now and we have two beautiful boys who do not have CF, but do carry the gene. Keep smiling. X
JonahFro 6 months ago
i have cf and im now 14 we found out when i was 5 thanks you for this it means alot :)
josephinejo1996 10 months ago
@josephinejo1996
Olivia was diagnosed at 5 as well. AND she's now 14 too. Active in soccer and swimming. Hope you're doing well - keep those treatments up! Thanks for the comment :)
taylorscorner100 10 months ago
the love of my life has C.F. it's hard to deal with but I have hope and so does. The most important thing is to believe. C.F. doesn't make the person who they are, it's just a part of life. It's worth all the procussions, and medications, and inhalations. Everything is worth it! Keep active and keep smiling. God's watching over you.
wrobinsonx19 11 months ago
I have cf and i am 12 years old i got diagnosed when i was 5 x
123NatJade 11 months ago
my daughter has c/f and is looking for support i am going to put more of her life on my channel and less of the rest of us plz subscribe it would mean allot to her she loves watching these other videos now that we know they are out there sub, to ditalydo
ditalydo 11 months ago
beautiful video.
ryanholbert 1 year ago
my older cuzin has cystic fibrosis and for her and u and all the others with it i hope they find a cure fast because 2 many ppl are dieing everyday from it..... :~(
purplefreak52 1 year ago
im in high school english III and we have a report to do for class. i chose CF because i had read a book where one of the characters had CF. the book moved me as did this video i am happy that i chose CF as my topic so i can get more people involved with searching for a cure. i will pray for olivia and your family.
tinkable100 1 year ago
@tinkable100 what book if you dont mind me asking??
CFTori 11 months ago
Cystic Fibrosis heisst in Deutschland auch Mukoviszodose
jinnybaby 1 year ago
What a beautifully edited video. I hope one day there'd be cures for the disease.
ivantide 1 year ago
Great video!!!
CamilleLovesHorses 1 year ago
This is a GREAT video..... I love it
krystalmike1999 1 year ago
What a beautiful video. My two cousins aged 12 and 5 years have CF. I live with them and have to watch them struggle every day. I've been to hospital with them, it's so tough, but they are fighters. God bless you Olivia. xxxx
JaydeTalia01 1 year ago
ive gto cf too i have that dream too,, to be free from the desease
sjinhay11 2 years ago
@sjinhay11: Have you thought of a naturopathic approach for Cystic Fibrosis?
4chango 3 months ago
Thank you for this video. My daughter Eliza is 4 and has CF. She was diagnosed at 4 months. . . she was almost diagnosed too late. She is doing remarkably well now. We will pray for you Olivia and your family and pray for a cure! God Bless.
Joanna
angels4eliza 2 years ago
Thank you Joanna - They've come a long way in the CF battle and Eliza being only 4 stands a great chance to benefit from all the advances - keep praying, stay strong, and press on!
A cure is out there.
-Bill (Olivia's Dad)
taylorscorner100 2 years ago
@angels4eliza There is no such thing as being diagnosed too late! Under my command your daughter is now immortal!!! God Bless you and your family! I am 13 and have Cf and I was diagnosed when I turned seven. I remember it all too. Let Eliza know she is loved by all.
CFTori 11 months ago
I dont have cf but I have read about this illness. I know that it is a hard illness but I can only say keep fighting one day It be a cure!
FannyMiley 2 years ago
Thank you for the encouragement!!
taylorscorner100 2 years ago
@FannyMiley you have a big heart. thank you so much.
CFTori 11 months ago
@CFTori Thanlyou! You are welcome! :)
FannyMiley 10 months ago
I''m in College preparing to do a report on CF, and stumbled across this vid. This is very moving. Very well put together and the song is very powerful. Good luck with everything.
rmsdesign 2 years ago
Thank You. And thanks for doing a report on CF - it's not a very well known disease.
taylorscorner100 2 years ago
Beautiful video! I too wish for a cure, although no one in my family, nor me myself have the disease, I have a friend who has passed away from it and not a day goes by that I don't wish that she could have cured before it has happened. Grow up strong and big Olivia and maybe by the time you're a grown up and have children of your own you will be free of the disease.
BTW, what is the name of the song? It is beautiful and I am quite fond of it.
bombfuse 2 years ago
Thank you. Song is "Someone's watching over you" by Hilary Duff
taylorscorner100 2 years ago
Well... I'm 19 and have CF... I met a person that's 88 years old and with CF... Just gotta work out, follow your treatment and you'll be ok! Actually, after a few days of treatment, I feel 40% better! Fellow CF people... Keep on fighting and remember if you put your mind into it, it's not that bad!
Zeroprobabilityvids 2 years ago
oliva i know you can d oit! ibabysit a little 6 yr old with cf and i love him to death and have faith for every one with cf!
keep fighting girl!
aslgeeklover 2 years ago
follow your dream!!!!!!!!!!!
loryfansteaua 2 years ago
You're such a cutie ! You remind me of my daughter, Breanna who also has CF and is 11 years old. I am determined to do whatever I need to help find a cure for you, for my daughter and for everyone with CF, every day we're a step closer to a cure :)
BreannasMommie 2 years ago
be strong i have CF to i am only 12 and docs. say i will only live to 16 but i will stay strong as long as you will! (:
living0with0cf 2 years ago
Don't believe them... I'm 22. I have another friend who is 29 with CF.
aslchick1 2 years ago
be strong.kiss from greece!
trelozombie 2 years ago
Dear Olivia.
I have Cystic Fibroses to
it's not easy be strong hun.
Im only 14 i have lived past what the docto's said i would pass away.
think highly of urslef (:
god bless u
cheritaylor6 2 years ago
hey does anyone know a cf clinic in lafeyette lousiana?
my papa and i have too move there too male more money cuz the meds are so exspansive:(
5ta46az3 2 years ago
i know how hard it is to have that, i have it too i hope there will be cure
4eva542 2 years ago
GREAT video....well done..very inspirational..i am sure u have a long way to go with such great support too little grl..keep the faith....I have CF age42...
S888999333 2 years ago
42 - awesome. Where do you live? Any additional tips on staying healthy?
taylorscorner100 2 years ago
for me plenty of these - I call the
6 S's - Sleep, Sun, Surf, Salt-air,Salt-tabs,Supplements.......
...and...no alcohol, no drugs, no stress,
,....and PTG.....Prayer to God for strength, support and thanks :)
S888999333 2 years ago
yay for Christianity, a frankenstein creation of numerous pagan religions that came about thousands of years before christianity. lol
direngrey4569 2 years ago
get a life direngrey4569..go away!
S888999333 2 years ago
Whatever you say man
direngrey4569 2 years ago
Unbelievable how wrong people can see the way God has plans for everybody..
I have CF myself.. and the fact that you can even think about being a freak for trusting God in His ways when you have such a disease.. thats even sicker!
Thnx for the tips S888.. ;)
martindemik 2 years ago
I'm 13 and I live right next to the beach and all the salt air is good for me and that's how I stay healthy! And of course I eat a lot haha
1moe7 2 years ago
what an awesome , well put together video -- gave me more info than a lot of other videos and was really easy to understand -- thankyou@
lovinlifekyles 2 years ago
This is gorgeous, and it was so great to see some of the CHOA staff on the video! Our son has CF and we're fighting for a cure right along with you. God bless.
marchetbutler 2 years ago
Oh my goodness, your video had me nearly in tears. I am also a sufferer of Cystic Fibrosis. We do need help from the American population to find a cure for this wretched disease. One cannot achieve a large goal single handedly, it takes support and motivation. To everyone with Cystic Fibrosis, stay strong and never give up no matter what life throws at you. "It doesn't matter if the whole world is pulling you down, with Christ you have everything." -Nicholas Jonas
uhcougar12 2 years ago
another quote:
"There's always a way to find hope."
-Nicholas Jonas
uhcougar12 2 years ago
yay for Christianity, a frankenstein creation of numerous pagan religions that started thousands of years before christianity. It is called will power and strength of character to keep yourself going, not divine intervention. This brings me to another topic.... if your god created the heavens and the earth and shaped us in his image, why is there disease? Also, why have the type of body systems that we have. They are so complex and can go wrong in so many ways.
direngrey4569 2 years ago
Couldn't a god who could create the heavens and the earth in 6 days create a far less problematic system for life? Religion has, throughout the ages, only brought about war, chaos, bigotry, and hatred.
direngrey4569 2 years ago 2
@direngrey4569 but It has also brought love, hope, peace, and friendship
TomAndJerry87 1 year ago
@TomAndJerry87 and genocide, murder, and intolerance. whether you are willing to admit it or not, the bad outweighs the good.
direngrey4569 1 year ago
@direngrey4569 why are you so negitive towords life?
TomAndJerry87 1 year ago
@TomAndJerry87 That's a pretty big assumption there. Also, relevance? P.S. I'm not negative TOWARD life, I'm negative toward a collective of ignorance and intolerance that has a great deal of power in this country, as well as countless other countries.
direngrey4569 1 year ago
I played this video for my class to show them what cf was and a few of the girls cried. Tears mean good job because people are actually getting it.
SaraWiley 2 years ago
Thank you for sharing that and for sharing it with your class. It's a small population disease and doesn't get the coverage that others do - so thanks for helping educate others. :)
taylorscorner100 2 years ago
I understand becz i have Cf also! if you ( littlegirl) are the director of this username plz connect with me! i wanna talk w/ sumone w/ cf also !
Hreedproductions 2 years ago
This has been flagged as spam show
For more information on cystic fibrosis, simply type in Gibson Vance promoting Cystic Fibrosis in your youtube search engine
beasleyallen 3 years ago
I love those folks at Children's Hospital of Atlanta!! I got to meet them about 6 weeks ago ... my 3 month old has CF ... I pray for a cure every night ... and this video as hard as it made me cry, gives me hope because you have hope ... Thank you!!
CLM21585 3 years ago
as the song say don,t give up
teiubesc36 3 years ago
When I usually watch these kind of videos I dont normally cry but I actually did in this one. The video gives a clear message to all people even young ones, and I hope they will find a cure.
My best friend has CF and I love her so much so I hope they find a cure fast enough to save you both from this horrible disease.
AlisonJeanNeil 3 years ago
This video is soo sad. I am so sorry Olivia They will find a cure for the diesese someday. Stay strong!!
sparky21737 3 years ago
My two year old son has CF...
Great work on the video, and I loved the song as well. Blessings!
lonespuce 3 years ago
i cried so hard when i watched this..i am so sorry i never knew what i had untill i saw this. and i never knew how darn greatful i should be before i watched this video. i am so sorry olivia. be strong, and never give up you will make it through.
AlexAndKatie1622 3 years ago
my friend died a few days ago from cf
she was an amazing girl and raised lots of money
her name was haley palmer
she fought hard managed 12 years before dying.
i know now that she is in heaven with her maker.
stay strong!
tayyxlorr 3 years ago 2
im sorry... :(
NiaMiaDramaQueen 3 years ago
You are wonderful. We know what cf is as well. My nephew has cf and we love him and we love you! God bless you and your family...Ian
yannybaby 3 years ago