| Cystic Fibrosis - Speech - 444 sec
12 year old with Cystic Fibrosis gives keynote speech at Cystic Fibrosis Fundraiser. Video quality isn't great, but I hope you agree the message is.
Auteur : jmattsrt8
Tags:Cystic Fibrosis Speech Charity
 |
| Cystic Fibrosis - 256 sec
A tribute to the people in this world with Cystic Fibrosis or know someone who has or had cystic fibrosis.
Auteur : rugby85
Tags:CF Cystic Fibrosis Tribute lung transplant
|
| Cystic Fibrosis - 593 sec
10 minute documentary final project about a day in the life of a ten year old girl with Cystic Fibrosis
Auteur : JLHarvey85
Tags:CF Cystic Fibrosis documentary soccer feeding tube
|
| Cystic Fibrosis Foundation: Sweat Test - 225 sec
The Cystic Fibrosis Foundation created this informational video about the sweat test to inform parents about the procedure.
Auteur : CysticFibrosisUSA
Tags: Cystic Fibrosis CF Foundation medicine United States help patients parents sweat test
|
| What is Cystic Fibrosis? - 91 sec
A short film on the what cystic fibrosis does to the body.
Auteur : stoelby
Tags: CF cystic fibrosis lungs pancreas feeding tube nebulizer enzymes
|
| Cystic Fibrosis - 112 sec
this is a nice little video that a friend put together as a personal project because his daughter has CF.
Auteur : rajjas
Tags:cystic fibrosis children help lungs breath
|
| Cystic Fibrosis Foundation GREAT STRIDES - 268 sec
Find out why YOU should be a part of the Cystic Fibrosis Foundation's GREAT STRIDES walk.
Auteur : hsmithco
Tags:cystic fibrosis foundation great strides walk
|
| Cystic Fibrosis on YouTube - 248 sec
Thank all of you who have shared videos on YouTube that help us all understand what life is like living with Cystic Fibrosis! Stay inspired and stay strong.
CF patient Alice Martineau's song "If I Fall" is featured in this video, in memory of the life she led fighting Cystic Fibrosis. She died in 2003 at the age of 31.
You can see all the videos featured in here on the Cystic Fibrosis Foundation's YouTube channel: www.youtube.com/CysticFibrosisUSA.
Auteur : CysticFibrosisUSA
Tags: Cystic Fibrosis Foundation CF nonprofit YouTube video videoblog patients stories
|
| A Child with Cystic Fibrosis - 146 sec
A local couple's son is diagnosed with cystic fibrosis. How early screening is helping them and their child overcome the disease.
Auteur : wdsutv
Tags: WDSU New orleans cystic fibrosis
|
| CF-Cystic Fibrosis-Awareness:Every Breath Counts - 298 sec
I know there are many other info vidz on Cystic fibrosis but i thought it was about time 4 a updated vid.This is an information video to bring cystic fibrosis:a genetically inherited & life-threatening condition, into the spotlight.CF is a common condition which need the help and support of everyone to fight against CF. At this moment in time,there is no cure for cystic fibrosis but we hope 2 find it one day with your help.Plz pass this video on to everyone you know;the more ppl that are aware of CF,the quicker we can get to finding that cure,plz help us see off CF.thank you.
[sufferer of CF]
Auteur : mizzck
Tags:CF Cystic fibrosis awareness gene theraphy lungs breath inherited help donate sponser mizzck common
|
| Cystic Fibrosis - 482 sec
Learn more about the #1 genetic killer of children and young adults in the United States, Cystic Fibrosis, and what you can do to help!
Auteur : Philanthropy1
Tags: Cystic Fibrosis Foundation Health Education
|
| Fight Cystic Fibrosis! - 186 sec
Cystic Fibrosis sucks. Kids find it tough to breathe and their lungs break down over time. There's no federal funding and no cure. Join the fight against CF and contribute to research to find a cure for this horrible disease.
Auteur : mattygee
Tags:Cystic Fibrosis CF sick ill illness cough charity disease fundraising medicine doctor transplant mucous lungs Jake team
|
| Cystic Fibrosis Video by Eva Markvoort (65redroses) Part 2 - 514 sec
Part 2 of a short film I put together this afternoon for Ms. Hall's biology 11 class. To give a little peak into the life of a double-lung transplant reciepient/ cystic fibrosis patient.
Auteur : evadien
Tags: 65redroses Cystic Fibrosis lung transplantation double transplant biology 11 Eva Markvoort Fiona Hall
|
| No Answers, No Cure: Cystic Fibrosis - 590 sec
"This is Stephen... Stephen has Cystic Fibrosis..."
The first of a series of short documentaries whose purpose is to raise awarness and activism for the cure of genetic disease.
GET INVOLVED!!! JOIN THE FIGHT!!!
Now more then ever, little people have the tools and the power to initiate GREAT SOCIAL CHANGE!!!
I receive many letters everyday from regular people just like you asking me what it is they can do to help The Fight.
If you want to help, it takes nothing more than five minutes of your time.
Simply copy/paste the following into the message box in the share video screen:
An amazing documentary that really needs your help... Please Rate, Comment, Favorite and Forward!
If you can send that message with the video attached to as many people as possible, even if it is only your friends list, you would be helping every man, woman and child who has to suffer with genetic disease tremendously.
I am but one person and due to YouTube communication restrictions - I can only do so much.
WE need YOUR help!!!
Perhaps together we can accomplish more than just having a video posted on the front page...
God Bless
Auteur : NoAnswersNoCure
Tags: CF Cystic Fibrosis Stem Cell Research Genetic Disease Nonprofit documentary grassroots outreach help please
|
| Lilly Year One Lillydrive.com Fight Cystic Fibrosis CF - 1260 sec
video created by vintage storybooks
www.vintagestorybooks.com
Year one has come and gone. This video starts the day of Lilly's birth and takes you through her first year of life right up the day of her f1rst birthday.
Please donate and get involved to help find BREAKTHROUGH treatments and cures. Nearly $.90 of every dollar donated goes directly into needed research and programs. We thank God for our challenges and try hard to look to Him in Good AND Bad times. Love wins.
www.lillydrive.com
Auteur : lillylars
Tags:Lilly lane fight Cystic fibrosis CFfun times lillydrive year one
|
| Boomer Esiason Foundation for Cystic Fibrosis in Second Life - 271 sec
The Boomer Esiason Foundation for people who have Cystic Fibrosis is now in the world of Second Life. So those with CF can now interact with each other and outsiders with out having to wear mask or worry about getting sick. Goto Esiason.com for more information and updates, also how you can get involved
Auteur : BebopVox
Tags:Boomer Esiason Bangles Second Life Cystic Fibrosis CFU BEF NSS NaturalSelectionStudios SL
|
| Cystic Fibrosis - My Story - 397 sec
My name is Katy and I am 23 years old. I just wanted to spread awareness about CF. Many people have heard of the disease but don't know exactly what it is about. Hoping that more awareness will lead to increased research and hopefully a cure in the near future!!
Auteur : lilkate424
Tags: Cystic Fibrosis
|
| A Happy Cystic Fibrosis Story! - 277 sec
My CF Story
Auteur : bennyshob
Tags:cystic fibrosis cf gemma jones
|
| Cystic fibrosis - real story - 267 sec
Cystic fibrosis is the commonest inherited disorder in the UK. One in every 2,500 babies is born with cystic fibrosis. One in twenty-five people carry the defective recessive gene. It affects more than 7,500 babies, children and young adults in the UK. 14 year old Lauren Hutchins talks about living with the disorder.
Auteur : NHSChoices
Tags:cystic fibrosis health "nhs choices"
|
| Living with Cystic Fibrosis - 256 sec
Support The Cystic Fibrosis Foundation and Help Find A Cure
Auteur : taylorscorner100
Tags: CF Cystic Fibrosis Foundation Child Cure Donation Give Charity Cause Breathe Illness Disease
|
