Living with Cystic Fibrosis

[kimberlymerrygold1]

just saying the singing is funny in that vibrations

[holly459]

aww wen she was singing de vest made her sound so funny :)

[Trumpettier17]

Cute video! Somebody is impersonating you on twitter though! :/

[sammelina12]

LOL awwwwww when she started singing!! haha <3

[yvonnespearing]

this is a awesome girl?goooooooooooooo girl.xx

[moviemakergal03]

my friend has cystic fibrosis. isn't it a funny thing that people with CF, cancer, or really any deadly disease never think about it? they are always so happy and cheerful. they live life to its fullest.

[francipc123]

1235aw112451245 4 45 5 545 45 4 5 1 21 1 2 451. 

[romallica]

If all people like her with bad genes servive we'll soon all be like that :/

[zookybeans]

Great going Chelsea. God Bless you child :-)

[zackyv08]

Heya, im a person from ireland with CF and were doing a facebook event to raise awarness of Cystic Fibrosis and also to get a Guinness World Record, if ye all could join and spread the word it would be great. just type into facebook "make cystic fibrosis aware by trying to break a world record". All support would be very greatful

[trix1498]

One of my bestfriends has this.. :/ I hope they find a cure

[MsDelicateflwr]

Take heart, CFers! God willing, I'll be 41 in a couple of weeks - was diagnosed when I was 12. Just keeping taking the meds, eat well and exercise as much as you can possibly push yourself to do so!

[rocker10050]

Keep on pushing with you people with cf be brave

[rocker10050]

I have to help those in need I feel so sad for them

[MusicDirects]

i have CF i live in the uk and im 16 years old i was diagnosed with cf when i was born there has been some hard times as all families will know but we are here for a reason and one day there will be a cure just keep taking your tablets and doing your nebs when you become a teenager it becomes alot harder to keep on track of your drugs but make a routine because if your one of the ones who is fit enough and well enough you be able to have a long and amazing life

[Drewry5]

I have a 8 year old daughter with Cf also, these kids are truly amazing. Always fighting the battle with a smile on there face. Maci is wanting to meet Taylor Swift also.:)

[emoserfier]

your cute. i hope u feel better

[Germancanadianly]

Oh yeh and your so lucky to do the vest I wish I got to do the vest

[Germancanadianly]

I feel really sorry for you !!!I have CF and I'm thirteen. NOT FOR SYMPATHY but how bad is my CF comparison because I'm not sure if I'm sicker thuan I should be. I take 36 pills daily I do three physios daily each 30 min three pulmonary tubes daily and 4 of the blue buffers and orange puffers daily. I visit my doctor every three months

[jackieinthebox1]

Thanks for sharing and educating the rest of us! Good bless beautiful girl:)

[Jessica141996]

Your a stroung HAPPY girl, I really hope treat mentis working!

[gleeisthebest1000]

Idc

[EMTgirl4ever]

you are a strong girl, keep fighting :)

[ditalydo]

MY DAUGHTER Has c/f and i have a youtube channel i happened on these videos of kids with c/f and my 9 year old that has c/f was so excited she has never known anyone else with the issue because they arent supposed to hang out but i can see from her reaction that just seeing kids on here is therapeutic for her so please subscribe to my Chanel so she can see all your precious little ones new videos and vise versa(sub, ditalydo)

[Taconut7]

I hope that your daughter will stay strong and make it through this! This disease does not define who she is! She can do everything else other kids can do! God Bless you!

[MNU1978]

This country will put its most brilliant minds to work for decades, spending trillions of dollars developing nuclear weapons that can obliterate an entire nation and new aircraft carriers every 20 years.

If our government devoted as much time and the same amount of money to finding cures for the diseases that plague our planet, the United States and all of humanity would be much better off.

God bless this sweet child!

[RennanizedRen]

Haha she sounds like she's having fun. I get bored when I'm using the vest. Once I fell asleep. Stay healthy girl!

[bjriley]

If Taylor Swift wasn't such a jerk she would reach out to this kid.

[frannyj33]

I have CF and just celebrated my 45th Birthday!!! I am happy 2 hear u get to meet Taylor swift.. Well at this posting you prob. met her already! Ur 2 cute, sound like the chipmunks singing :-) Keep on coughing that stuff out! I think that is the key to living a long life w/ this disease. I am one of the oldest pts at my clinic! Blessings 2 u & ur family.

[TatianaSword]

1#Cystic Fibrosis

[ToXSiiiK]

My uncle, Josh. Well he was my aunts boyfriend had CF. He died 10-14-10. He was 25.

[nattxo0]

my bestfriend just died of CF she was16 she was waiting for a transplant and she had caught a cold and it was too bad for her body to fight off

[WanfzMakaGraceDroo]

My older brother passed away from CF at 27 :( I was only 4 years old..

[jesssallison]

omg thats exactly like me when i was 8! actually i still sing while im doing the vest LOL

[blob1029]

aww she is so cute. i hope she gets better

[ABCsofCPT]

I really hope you make her cough the secreations out of her lungs after the vest. So many people just shake them up with the vest and then leave them in there. Makes no sense to me.

[lp4ju]

such a brave little girl....CF seems like such a terrifying illness I can't imagine having to live with it...

[TheBkrug]

So cute! She sounds like my daughter when she's on her VEST! lol. My 7 year old has CF too. Best wishes for a cure to be found soon. Glad she got to go see Taylor Swift!!

[pyrskorp]

The vest has no effect on cf mucus! long time since we in sweden stopped shaking.

[bearjean]

You are a very strong little lady.

[amp9081]

I also have only been admited 2 times in the hospital within 13 years one in last october and when i was 3 years old. so i am very lucky because most by the time there my age they are usually in the hospital at least 9 or 10 times. I have to thank my grandma because she is the one that has taken care of me for 13 years and i love her and i would hate to see her go i am also the healthiest CF kid in toledo well for all the kids that go to the hospital

[amp9081]

this is really sad but someone that i know has just been killed by this disease he died last month he was only 19. I have the disease to and it is hard to live with i sometimes dont feel right and just somtimes have know where to turn but im 13 and living through it

[wagnerholly5]

Beautiful Girl, we wish you the best. That's our CF video down there!

[Chelciebugu145]

Hi Chelsea. My Name is Chelcie, im 16 years old. I have CF also. It got really bad and i was admited to the hospital. On July 13, 2009 I had a Double Lung Transplant. Im doing great now! Your a brave girl. CF is not easy. Just keep going strong and you will continue to do great. Bless you! :)

[stingerz1]

I wish you all the best in life...i have a niece that has CF so i understand what

you have to go through ..she seems like

a very happy young lady as is Lauren my niece...God Bess You..kindest regards

[lookstolove]

You are so adorable! It's great to see that you have such a postive attitude! Keep singing and thanks for sharing this with us! :)

[LVG4GOD]

i LOVE when she sings as she shakes thats soooo funny lol it made me laugh. She seems really positive. =)

[shouldbestormplaya27]

i also have cf and i also do the vest and pulmazime. i also do the tobi and i take mt ultrase 12 with my food... i usualy take 7 to 8 pills in a meal and take them all at once lol. haha once i got dared to put the veat up to the highest level and it was not fun!!!

[cnat1117]

God bless you and may you live a long and full life. (sort of resemble "Paris" Micheal Jackson's daughter)