Thank you for making this video. I got a project on CF and I figured this topic would be really boring but after finishing this project with the help of this video I have a better understanding and respect for all of the people born with CF fight on guys and girls!
I'm 18 and I have cystic fibrosis. It's not an easy genetic disease to live with and it does make many aspects of day to day life challenging. But it also motivates me to try harder and work with the disease rather than against it. If I can Change the lives of others by challenging myself and living my dreams then that'll be all the motivation I need to wake up each morning and believe that I am grateful for every day!
hi ...thats really agreat words you say ....your so aptomostic ..i also have the same age of yours ..and im stydying medicine ..and i would like ..to know you better ..and chat with you about your fisease ..and i might could have chance to help you with any thing new .. 😊 hope to get replay soon .. all the best ..for you ..💖
My dad had Cystic Fibrosis and today I am doing a presentation on it so people can vote for it and make it my houses charity for the next academic year.
my cousin just recently passed away from CF. he was 30 and was constantly in the hospital. always suffering. But he always had a smile on his face and always had a great sense of humor. He was a great guy and will be missed. The whole family is glad that hes done suffering and in a better place now. RIP Jeremiah. November 30 1985- July 31 2015
oh I'm so sorry but I know how you feel my aunt passed away at 26 2 yrs ago from CF and me and my family do a special fundraiser for her she passed away when I was 8 (I am now 10)
Stampystyleboots I send big prayers to you and your family I know how it will feel to lose someone goood luck , if she were to die don't be sad or she won't come around I was in grade 2 and I'm in grade 5 now ! Best of luck
My friend passed away from CF and at the time I didn't really known what it was thanks for posting this helped me to understand what it was about. #RiP
Cute video. Some friends of mine have a child with it. They just posted a pic of their two year old in her new "shake vest" I decided it was time for me to learn more about CF, so I did a youtube search and this is the first video I watched. It was simple and clear and know I understand quite a bit more. Thanks.
i have cystic fibrosis and if you keep up on your breathers and taking your pills you get better and better. This makes us be able to do sports better and P.E. like when your running. I play softball and im the fastest runner on my team in p.e. im also the fastest runner.
You have a chance. Never EVER give up. Now CF patients have a longer life expectancy. My cousin who has CF lived up to 32 years. The oldest person living with CF is 75. You have a great chance. :)
My 14 year old son has CF, it can be a battle at times. He takes about 35 pills a day, but has vest treatments, nebulizer treatments, and when he is coughing a lot it tears at my heart. I pray they find a cure in his lifetime.
CF sucks! I have it and i'm 15. In the middle of December, 2012, I received new lungs and now I can breathe. But I still remember all months at the hospital. I still pray for all my cysters and fibros! Keep strong and never give up! Let CF stand for Cure Found!
Really sorry about what you are going through. My son, Jamie had 2 broncs last year, and one so far this year, each followed by a 2 week stay in hospital. You are both amazing for spreading awareness of this via You Tube. God has awesome plans and purposes for your lives, keep praying and healing will come. Bless you both.
Forgot to say that people voted for my presentation and that means that all the money my house in school raises in the next year will go to the CF trust. :)
this is brilliant, a very hard topic to explain and sometimes understand. This could easily be used to help young children understand CF, thank you for such a fantastic informative video!
Great video! I don't have CF, but my brother has it, my sister had it and I am a carrier of the CF gen :( Witch means that my children might get it, and thats really scary.. My brother, who is 25 years old, is doing semi-okey, but takes alot of medicin, and is in the hospital quite often. My sister on the other hand, died a little over 9 years ago, when she was only 19. I miss her everyday♥♥
I hope that the doctors can find a cure for Cystic Fibrosis. To all kid that may suffer of CF, you are a brave soul! keep on fighting and always keep the hope up! with all the tech today a cure should be around the corner, I hope for you sake that there is, so you guys can live a healthy long life. Good luck to all
Very good video, informative indeed! But, the little kid's voice made this video so depressing, I mean, sounds like children living like adults, knowing exactly how hard their lifes already are, and how harder it will become.
they forgot to mention that people with CF can usually only live up to the age 30 my little sister Stephanie rosales just passed away and she was only 17 and her lungs just couldn't handle to work anymore :(
people say that cf makes you different from others but i say that your just like everyone else so people dont worry if you think your different because from others because of cf. I mean maybe i have to do meds and many things but that dosnt matter
I have cf and it is embarrassing when I cough up mucus. And I get winded when I run long distances. I use a vest treatment 2x a day morning/night I take enzymes every time I eat.
My Little Brothers have Cf ! its really hard to deal with and they do cough alot ! My younger older brother jack is 11 and they said he could possible live up to 30 years :c same with my baby bother ! they have to go to the doctor every month for a check up !
I have CF but somehow the mucus is only in my digestive system and only a bit in my lungs so my digestive system is pretty messed up but i try to stay positive most of the time btw i am 9
Has anyone ever tried to go vegan? I know milk and dairy made me really congested, I had chronic sinusitis (so sick they thought I had cancer) and not one doctor ever told me to go vegan. I'm doing a lot better now :o) Doctors are not really trained in nutrition. It makes me sad hearing how kids can be so sick like this. Sending positive vibrations~
Maanne Arcega there is no cure and it can't be cured, it's in our genes. I have cystic fibrosis and there is medication that is unavailable for me because it is not on the pbs. It would cost me over $300000 a year. But is unpredictable and could make cf better or worse.
I think vitamin A might help with cystic fibrosis ,because it makes good mucus all around your body so bacteria can't get a foot hold in your body making you sick and it might replace the bad mucus with good mucus.
I'm with u therainbowcupcake01 i have cf too but i'm on 10 but i never got a lung transplant because i don't want to be in the hospital for the 5th time
I'm 22 I got cystic fibrosis I got do my vest jacket every day an night be honest I go see my doctor s appointment s I exercised hurts I breath I drink slot water
Thank you for making this video. I got a project on CF and I figured this topic would be really boring but after finishing this project with the help of this video I have a better understanding and respect for all of the people born with CF fight on guys and girls!
I'm 18 and I have cystic fibrosis. It's not an easy genetic disease to live with and it does make many aspects of day to day life challenging. But it also motivates me to try harder and work with the disease rather than against it. If I can Change the lives of others by challenging myself and living my dreams then that'll be all the motivation I need to wake up each morning and believe that I am grateful for every day!
hi ...thats really agreat words you say ....your so aptomostic ..i also have the same age of yours ..and im stydying medicine ..and i would like ..to know you better ..and chat with you about your fisease ..and i might could have chance to help you with any thing new ..
😊
hope to get replay soon ..
all the best ..for you ..💖
Thank you very much, I am glad to talk to you on facebook! ask anything you wish :)
+my65roses
thank you so much 💖
My dad had Cystic Fibrosis and today I am doing a presentation on it so people can vote for it and make it my houses charity for the next academic year.
how did it go?
my cousin just recently passed away from CF. he was 30 and was constantly in the hospital. always suffering. But he always had a smile on his face and always had a great sense of humor. He was a great guy and will be missed. The whole family is glad that hes done suffering and in a better place now. RIP Jeremiah. November 30 1985- July 31 2015
oh I'm so sorry but I know how you feel my aunt passed away at 26 2 yrs ago from CF and me and my family do a special fundraiser for her she passed away when I was 8 (I am now 10)
+Emily Drysdale my auntie has it and is in hospital with her cf and pewmonia and we think she could die so I understand
+Stampystyleboots pneumonia
Stampystyleboots I send big prayers to you and your family I know how it will feel to lose someone goood luck , if she were to die don't be sad or she won't come around I was in grade 2 and I'm in grade 5 now ! Best of luck
When my aunt died in grade 2
im head over heels in love with this girl with cf, I want to understand as much as i can,
axel4clover1 hi how are you?
My friend passed away from CF and at the time I didn't really known what it was thanks for posting this helped me to understand what it was about. #RiP
Thank you so much, its simple and very informational
Cute video. Some friends of mine have a child with it. They just posted a pic of their two year old in her new "shake vest" I decided it was time for me to learn more about CF, so I did a youtube search and this is the first video I watched. It was simple and clear and know I understand quite a bit more. Thanks.
i have cystic fibrosis and if you keep up on your breathers and taking your pills you get better and better. This makes us be able to do sports better and P.E. like when your running. I play softball and im the fastest runner on my team in p.e. im also the fastest runner.
Same here, great to hear! :)
You have a chance. Never EVER give up. Now CF patients have a longer life expectancy. My cousin who has CF lived up to 32 years. The oldest person living with CF is 75. You have a great chance. :)
My 14 year old son has CF, it can be a battle at times. He takes about 35 pills a day, but has vest treatments, nebulizer treatments, and when he is coughing a lot it tears at my heart. I pray they find a cure in his lifetime.
CF sucks! I have it and i'm 15. In the middle of December, 2012, I received new lungs and now I can breathe. But I still remember all months at the hospital. I still pray for all my cysters and fibros! Keep strong and never give up! Let CF stand for Cure Found!
Really sorry about what you are going through. My son, Jamie had 2 broncs last year, and one so far this year, each followed by a 2 week stay in hospital. You are both amazing for spreading awareness of this via You Tube. God has awesome plans and purposes for your lives, keep praying and healing will come. Bless you both.
Forgot to say that people voted for my presentation and that means that all the money my house in school raises in the next year will go to the CF trust. :)
I'm so sorry for your loss. My prayers go out to you and your family.
this is brilliant, a very hard topic to explain and sometimes understand. This could easily be used to help young children understand CF, thank you for such a fantastic informative video!
Great video! I don't have CF, but my brother has it, my sister had it and I am a carrier of the CF gen :( Witch means that my children might get it, and thats really scary..
My brother, who is 25 years old, is doing semi-okey, but takes alot of medicin, and is in the hospital quite often. My sister on the other hand, died a little over 9 years ago, when she was only 19. I miss her everyday♥♥
Thx for the video, hope and pray that the scientists find its cure soon..
My sympathies to you. My family has this gene lurking in our midst as well.
God Bless😇😇😇
thank you for this educational movie. makes so much sense.
I hope that the doctors can find a cure for Cystic Fibrosis. To all kid that may suffer of CF, you are a brave soul! keep on fighting and always keep the hope up! with all the tech today a cure should be around the corner, I hope for you sake that there is, so you guys can live a healthy long life. Good luck to all
Thank you for you animation. Nice and concise. Good job.
Thanx awesome video
the end made me cry!!! =(
Very good video, informative indeed! But, the little kid's voice made this video so depressing, I mean, sounds like children living like adults, knowing exactly how hard their lifes already are, and how harder it will become.
Awe! I have cystic fibrosis!
they forgot to mention that people with CF can usually only live up to the age 30
my little sister Stephanie rosales just passed away and she was only 17 and her lungs just couldn't handle to work anymore :(
this is so nice of you, i fight it well and i will continue, i love comments like this, YOU MAKE ME HAPPY
Nice cartoon.
This is a good video. It made me learn shit. Like... in my spare time...
I have CF. And sometimes I get really depressed about it, because I sometimes think that I won't even have a future.
This is a great video :D does a good job and helping others understand us with cf :D
My thoughts are "the heck? why is that dog talking?"
My son has Cystic Fibrosis - keep praying - healing will come.
people say that cf makes you different from others but i say that your just like everyone else so people dont worry if you think your different because from others because of cf. I mean maybe i have to do meds and many things but that dosnt matter
I want to know about CF.. anyone here to tell me about it..
I have cf and it is embarrassing when I cough up mucus. And I get winded when I run long distances. I use a vest treatment 2x a day morning/night I take enzymes every time I eat.
i feel sory for those who have, it must be super hard to live on pills...
+Tanya Korotiuk It's not the pills that are difficult
+TomAndJerry87 well, yea, agree, its just everything together. :(
+Pufa Channel wow, you should move to America, I myself came from Ukraine, and I know its not any richer than your country...
+Tanya Korotiuk Uh, thx
The pills are the easy part
grande mr richard
I have cf and l'm 11 years old I had cf sense I was a baby so I will live with it for the rest of my life
My Little Brothers have Cf ! its really hard to deal with and they do cough alot ! My younger older brother jack is 11 and they said he could possible live up to 30 years :c same with my baby bother ! they have to go to the doctor every month for a check up !
Love it.
I am 9 and I have cf😢
I have cf and it’s ok but it’s hard because we get very sick at first day the second day at school I’m usually sick.. like other cfers
I have CF but somehow the mucus is only in my digestive system and only a bit in my lungs so my digestive system is pretty messed up but i try to stay positive most of the time btw i am 9
Has anyone ever tried to go vegan? I know milk and dairy made me really congested, I had chronic sinusitis (so sick they thought I had cancer) and not one doctor ever told me to go vegan. I'm doing a lot better now :o) Doctors are not really trained in nutrition. It makes me sad hearing how kids can be so sick like this. Sending positive vibrations~
Nice
I like it
hope they can find the cure of CF, my little 5 y.o. cousin died of CF exaclty 21 years ago
The end of this video made me sad :( i really hope they find a cure for CF
Maanne Arcega there is no cure and it can't be cured, it's in our genes. I have cystic fibrosis and there is medication that is unavailable for me because it is not on the pbs. It would cost me over $300000 a year. But is unpredictable and could make cf better or worse.
I think vitamin A might help with cystic fibrosis ,because it makes good mucus all around your body so bacteria can't get a foot hold in your body making you sick and it might replace the bad mucus with good mucus.
Don't you think the CF team has tried that? Come on.... At least watch more videos or search more information than just relying this shitty video....
Yeah all tried mate! They push vitamin d more than a for loads of others reasons and people with cf don't commonly have vitamin a deficiency
Omg i'm so sorry for the persona who have that😢
Thanks for your support
Imagina crea y Recuerda I have it I am 14
I'm with u therainbowcupcake01 i have cf too but i'm on 10 but i never got a lung transplant because i don't want to be in the hospital for the 5th time
Just found out that my mate has CF. Its really sad.
I loved the song! where can i find the song?
I WALK TO FIND A CURE FOR CYSTIC FIBROSIS
She's 15 and she's currently in the hospital.
If you have cf you cannot go near anyone else with cf
That was cute
I have cf. delta f508
18,000 pills A YEAR ahhhh thats tough stay strong guys
The end motto has a grammatical error it should be "tomorrow's" not "tomorrows". Anyway, you have my sympathy for the affected children
I agree with what you said but did you really have to point it out?
+Abigail Rawlins ok, don't get your knickers in twist! I was merely pointing it out.
Nope. It's actually right the way it is. It's meant to be a plural, so the apostrophe would be a mistake.
THERE'S A CURE NOW!!!
omg my name is felix too!
Oh yes there is and it's called "Atox Bio", but I'm not allowed to tell you that.
Thumbs up if you watching this because you have Cystic Fibrosis. *Thumbs up*
@Madison Wade
I have cf too :(
Omg so many pills
My cousin has CF.
I feel bad for the people
h
i have cf and im 14 my sister has it to and shes 15
+Osama Adill YOU THIIIIIIRSTY GOTDAMN BOI SHE 14
Wissam Adill if your a doctor, why do you play clash of clans on your channel?
im 14 and i have plus my brother who is 20 has is too
Anybody got any solutions for the below comment?
My friend has cystic fibrosis and I'm making my little brother watch this video to understand it a little more
I have it
I'm 22 I got cystic fibrosis I got do my vest jacket every day an night be honest I go see my doctor s appointment s I exercised hurts I breath I drink slot water
WHAT THE HELL ARE THEY DOING NEXT TO EACHOTHER!?
Dats a sh*tload of pills a year!!
And here Iam smoking a cigg FFs I'm quit info
Lmao turn on captions
Ha I'm one of them
I've got it
I only looked this up cause I have it my mum ran 12 miles so yer
So great. My 6 year old has cf. Check out my page to see his treatments.
I heard people got new lungs
ღNaomiTheGamerღ not new they are used
Bruh it's 2020 and there's no cure
my sis haz this
shes 14
My vousin Keely shay has cf just go to rebma 2882's channel and it will tell you what she has to do
hello
#cf
i have cf
I have cf
Everlast. JRE
Ewww mucus.XD. M to the O to the M-O
Dr Wallach your writing a load of crap and i cant believe your a real doctor cos if you treat a cf child in this way they surely wont live long