One Goal

[beasleyallen]

For more information on cystic fibrosis, simply type in Gibson Vance promoting Cystic Fibrosis in your youtube search engine

[organdonor5]

There is a great project to increase DONOR AWARENESS that ends Septemebr 1, 2008. American Express (credit card company) will fund the project with the most votes and I would LOVE for it to be the DONOR AWARENESS project.

It was written by an 18 yr old girl that received a transplant and is living with CF cystic fibrosis.

GOOGLE IT. It is called Member Project "Second Chances" Mobile Organ Donation Awareness.

Please VOTE FOR IT, pass the word to everyone and increase DONOR AWARENESS!

[organdonor5]

When you get to the American Express Member Project home page type UZHKO0 into the search box...it will take you right to it.

Come on people, $1.5 million could be AWARDED for ORGAN DONOR AWARENESS if we can win the VOTE!

PLEASE TAKE THE TIME AND PASS THE WORD.

[001moviemaker]

Thank you cff for this video of hope and your work against cf. Greetings from Germany

[Tory584]

u no those machines my mom has one of those when i was little i would sit with her while she bounced around on that thing lol she's my hero

[CFJJJ]

I am the proud grandmother of three of the children in this video, with God, the CF Foundation and many prayers, my grandchildren are going to live, full and wonderful lives. Thank you, CFF

[thebahrijczuks]

We are lucky enough to be parents to three of the beautiful children in this video. With your help, the CF Foundation will allow all children with CF to live long and healthy lives.

[CFJJJ]

Thank you, Amy, for sending me this video, I agree with you, there will be a cure found for the beautiful B's and all other CF children, God Bless, MeMe

[burton1rocks]

what a positive video, I loved it :] having two children with CF and one that has had to go through two double-lung transplants, a CURE is imminent. Looking for the day when CF stands for Cure Found. Great Strides Walk 2008 :]

[EllaDsNana]

I am the 55 year old grandmother of Ella Deveaux, 4 years old. The CF Foundation has been instrumental in providing the assistance, education and treatments so that my granddaughter is now a bright and healthy little girl. We have a growing nationwide network of Ella's Elite teams who have participated in Great Strides fundraising every year since Ella was diagnosed. We will use this video as an important tool in our efforts to raise funds and awareness. We too will never stop working!!

[BlackestTeardrop]

Thank you for all of your hard work. This touched my heart knowing what my dear friend Alli goes through each day with having CF. I pray that a cure comes soon . . .

[kclontzbell]

Thank you for all your hard work CFF! Our son's quality of life is so great because of all you do! Thanks!

[fugitchoo]

"money buys science" Its sad that money has so much power over our life... if i didnt already have insurance when my daughter was born with CF id be bankrupt by now. thanks for all you do CF Foundation!

[GloMtzMtz]

Godspeed! Thanks CFF for all that you do! Knowledge is power.

[kikiandtarb4ever]

So sad.... My two closest cousins have CF, and they've been living very good lives- and it's all thanks to you! Thank you so much for all you have done!

[cselliott04]

Great video to help spread the word about a disease that often goes forgotten. I am the husband of a 27 year old nurse who has CF. She has accomplished so much all ready, and thanks to the CF foundation and their pipline of drugs and therapies we are adding more time each year. We must never stop pressing toward the goal of finding a cure. Support your local Great Strides!

[mjcapable]

I am a 50 year old man with CF. I lead a relatively normal life. I would not have survived this long without the research support of this marvelous foundation. I have been involved in some clinical trials with Gene Therapies at Shands Hospital in Gainesville, Florida. To those of you out there with this disease who are younger; I never thought I would live this long, or still be this active. Keep the faith! Plan for a bright future!

[michaelrayknowles]

The CFF is a Great Organization...Keep it up... M Knowles

[MissReb6102]

Well done on the video! I'm depending on the CFF to find a cure for my 1 year old son. Your research is near and dear to my heart and we appreciate the dedication the Foundation gives to those suffering from Cystic Fibrosis. THANK YOU FOR BRINGING CF AWARENESS TO THE WORLD!

[spiritwhisperer]

Wonderful video! Our grandson, who will turn 5in a few short weeks, was diagnosed with CF at the age of 3 months. Our lives were all turned upside down. We knew relatively nothing about CF at that time. Thanks to the wonderful work and support of CFF we have been, and continue to be, educated about this disease. The CF community is one filled with love and compassion, and we are blessed to be a part of it. Keep up your great work! There are thousands counting on you.

[msteyer]

EXCELLENT video! Our daughter has CF - she is almost 21 - and very healthy!!! Thank you so much CFF! Without your research, trial studies (many of which she's participate in), new medications, and support of THOUSANDS of volunteers, she would not be alive today. Thank you!!! PS - see the youtube video her brother did with her as the star - campy video of PICC lines! Search Justin Steyer

[FCSmajor]

1st comment! We count our blessings every day to have an organization like the CFF. We keep it in our prayers every day. From one family who lives with CF, Thank you. Thank you for your work and dedication. We will continue to support you in any way we can.