Cystic Fibrosis Emcee: VC2

[naturegirl56]

He died about a year after this, August 21, 2010. Rest in Peace CJ! :(

[LindsayMichelle87]

@fixin2fish it's called being an attention whore. people make up stories on here all the time. is it pathetic?

[samanthasuicide1]

Cystic fibrosis is absolutely no joke. A friend of mines best friend passed away from the disease and it tore her and his family apart. It's a horrible disease that needs to be cured

[myalaynaangel]

I am studying to be an RRT... I am honored to work with people like you.

[xchrisforbushx]

Oh no, this guy passed away?

[citizenjenna]

@xchrisforbushx Yes, he passed away in August.

[superj238]

My Nephew has CF.... Unfortunatly hes got three different genes of it and two of them are very rare.. Hes only 4 months old so im not sure what to expect.. Im his caregiver and its very hard to see him go through everything.. It does give me more faith and courage knowing and reading some of ur comments on this video...

[metalcranium07]

my wife has cf and it pisses us off when we go out in public people always stare at us cause she coffs alot

[brand1818]

@metalcranium07 aaw i sorry same here with my boyfriend..

[MsJennyAnthem]

@metalcranium07 Same. My boyfriend has CF and whenever he coughs people stare or ask if he has asthma, but he is a big mouth and just goes NO I JUST HAVE CF!

[metalcranium07]

my wife has cf

[aprilcs2009]

I have Cystic Fibrosis.. yeah people can laugh or talk shit.. and make fun who cares!!!!!!! There's evil everywhere!

[mbbs5000]

damn, i heard he recently passed away. that sucks, even for someone with CF he went quite soon (often people with CF can live well into their 40's). RIP

[stylezmindone]

RIP. Everybody needs to check out his music. To deal with this and still give praises to God, truly amazing.

[michaiah14]

@stylezmindone Yeaa, it is.

Personally having CF I can see where he is coming from.

I dont understand how anyone with CF could not have faith in God.

[xchrisforbushx]

@michaiah14 Hello Stylez. I'd like to talk to you and anybody who has CF about a movement that I'm starting to raise funds around the country for people suffering with CF. My 2 year old boy has it and I've started Orion's Army on facebook in hopes that we can spread awareness and gather support from people outside the cf community. If you are interested, and I hope you are, contact me asap and we'll talk. Thank you very much for your time. Jah Bless!

[LILLEWI1]

I am a upcoming rapper. i have cystic firbrosis, please help me get famous, i will put 1/2 of my earnings to a cure for CF. i want to prove everyone wrong and show them i can make it, even with CF. Ima make the cure happen... help me!!! Rate,Subscribe, Support

[LILLEWI1]

@citizenjenna Yes?

[kolorfulkitty]

I know his momm D: R.I.P.

[soundshitter]

eff you cystic fibrosis...i want my friend back...

[soundshitter]

eff you cystic fibrosis...i want my friend back...

[smittyguy710]

My sister has CF and i see her go through ALOT! its soooo sad seeing her to the point to were she cant breath. Every breath I take I think how lucky i am! I know this is one of the many challenges in many of peoples life but god just give us these challenges to make us stonger and thats what hes doing right now in my life.

[freqazoidiac]

I know a girl who eventually overcame her CF at 32 with Apple Cider vinegar, Lugol's iodine, black walnut hull, cloves, wormwood, and lot's of hard work plus ozone/hydrogen peroxide therapy. That was 6years ago and she has had a child since and has been a new person.

[TamirasEx]

@freqazoidiac REALLY? Seriously? She had an actual diagnosis of cf? What do you mean by "overcame"? I'm just curious because I've never heard of anything like that before.

[vcdiiv]

I had 3 brothers lost to CF It blows but we had some great times. I am from a family of 5. It is My Sis and Me now. Looking for a Friend to talk to.

Vin

[Kellard18]

I'm 18 and have cf...I think it's finally catching up to me...

[michaiah14]

@Kellard18 Dont ever give up.. fight it till your last breath.

[fornydagrasfairy]

my brother recently passed away of cf at the age of 24. like you, my brother was a fighter with every breath he took. he had a double lung transplant at the age of 16. you are an inspiration to many out there with the disease. i also love the fact that even though you have a lung disease you still chose music as your passion that is great! i know its a hard life man but you always have to remember to keep your head up. tomorrow is another gift, another day with the ones you love!

[Zeivv]

have same shit 20 years...

wow nice inhalation machine bro! i wish i had one like that.

[reispirit]

Nice vid. I'm 21 with CF and just today we did a walk for Great Strides. I've never met another person with CF so it's interesting to see how other people that have CF live. Keep up the good work. ^-^

[buggerjlewis]

I love that you are doing what you love despite Cystic Fibrosis slowly killing our bodies from the inside out. . I lived with CF for 28 years and had Cepacia for over 14 years. I never gave up my dreams of acting. But Cystic Fibrosis comes with an expiration date and mine came up fast. I fought for my life and fought for a center who would give me a double lung transplant. . . . .I only had months to live maybe less. . . . . Check out my video channel to learn more about my battle with CF.

[SSDavyS]

his wife said* i love him to death * i found that yet funny and awesome thing to say :) keep on doing it :D

[Veliccia]

Should watch S.I.C.K about bob flanagan

[jharbour742509]

I use to have that machine.....the air peddle control went out on me. i had to get a new portable one since i'm goin to college now.......i have my gauges at a half an inch.....that was random but just sayin lol idk if i'll go any bigger i dn't want to have to get them surgically sewn(spelll check) back up

[MrBlomzak]

Mijn kleindochter 7 jaar heeftCystic Fibrosis.Ik steun ook alle aktie's die er kunenn toe bijbrengen dat dit uit de wereld kan woereden geholpen

[ejmerenet]

Our friends have 2 boys (Levy is 3 yeuars and Finn is 1 year old). They both have CF. In Holland they test baby's for differtent diseases and they just (with the youngest) test them for more diseases. CF is one of them. So they discovered CF after the birth of Finn and then they tested Levy, and he has CF too.

Will they ever find a cure for Cystic Fibrosis? I SURE HOPE SO!

I WISH YOU STRENGTH!!!

With love, Esther van Susteren - Renet

(Echt, The Netherlands)

[thecolormaria]

wow. and to think that i was complaining about my bad day a few minutes ago...

kinda gives you perspective.

[spitlord]

We all suffer from a terminal disease; it is called death. We all pay hospital bills, but you don't see geriatrics (except Ceryl Brickowski) bitching about it. We are all dying, stop feeling sorry for the ones who go before us; they are lucky. They got a "get out of hell free" ticket.

You can obviously see that she is waiting for him to die.  This is horrible street poetry. She even takes pictures. How sad. Her husband's family won't hear from her after he is dead. I promise.

[Keithjustinburton]

Fuck you, Spitlord. This life is all we have and trying to compare his life cut short to the general population just makes you come off as yet another anonymous, ignorant internet asshole. People who die young aren't lucky to do so. There isn't a heaven or a hell waiting for them. All they had was this planet. Life on this planet still has some good in it worth experiencing for most humans, especially if you were lucky enough to have been randomly born in, or made it to, a developed country.

[arm0083]

I am intersted in how you think, I like how you worded that "all they had was this planet". May I ask your age? I would like to talk to you more about science, religion, and this disease. My daughter is 2, she has CF.

[RyRuk11]

Hey I am sorry to hear that your daughter has CF. I was just watching this video too and he definently has great motivation and faith, thats exactly what you need when your battling cystic fibrosis. If you ever have any questions, need advice or anything feel free to ask me. Im 22 years old and have CF. Good luck to you and your daughter and dont lose faith no matter what you go through!!!

[arm0083]

Keith, my comment was directed to you

[spitlord]

"I'm a trooper" = Social Security and life insurance. Fucking twat. AND she's getting laid.

[sergio311]

this si=uxxx :( thatnks currentz !

[memxox1]

my friend has Cystic Fibrosis and we are trying to find him a new liver and money but so far no good, he is a great person

[roderelo]

Haha, its good to have a life plan

[bl0000000000]

grow a dick first

[StephonWallace]

well it looks like you are comfortable with a vagina so good luck

[Bleedingbox]

p.o

[peacebone2010]

there's nothing funny about this. grow up.

[TheBkrug]

@peacebone2010

This isn't supposed to be FUNNY!! It's NOT funny. It's his LIFE. You grow up you jerk!! If only YOU knew what it was like to have Cystic Fibrosis or to be affected by it. . . . my daughter has CF and it's a lifelong struggle. Give this guy some freaking credit. He's doing the best he can and I think it's wonderful. He CAN'T grow up - unfortunately, he will, most likely die before that happens so THINK before you post LOSER!!

[peacebone2010]

@TheBkrug what the fuck are you yelling at me for?! I told that person to grow up. don't @ reply to me. fuck.

[ColossusofVita]

wow dude...