Cystic Videos
newest 100 cystic videos / cystic widgets / media rss:

Alex Merced Contest - Members for Charity from Alex Merced on Vimeo. Alex Merced will give 10 cents for every member of the Alex Merced Community by June 30th, 2009. He will be splitting the proceeds among the Cystic Fibrosis Foundation and Ron Pauls Campaign for Liberty. http://www.alexmerced.com http://alexmercedrocks.ning.com Cast: Alex Merced

Alex Merced will give 10 cents for every member of the Alex Merced Community by June 30th, 2009. He will be splitting the proceeds among the Cystic Fibrosis Foundation and Ron Pauls Campaign for Liberty. http://www.alexmerced.com http://alexmercedrocks.ning.com

This documentary short explores the struggles of living with cystic fibrosis. Produced by and for Current TV.

MC Chris live in louisville june 3rd 2008. MC takes a second to teach us a life lesson, and to help raise money for cystic fibrosis. Author: thoraxe514 Keywords: MC Chris cystic fibrosis Added: June 3, 2008

Bioguard and Emily Shreiver, a nine year old girl with Cystic Fibrosis, are participating in the "Splash for CF" fundraiser. Emily has raised 1.2 million dollars to date.

Jenny Davison, 39 years old with cystic fibrosis (CF), happily married, the proud mother of her 10 year-old daughter Dara. Made possible by an unrestricted educational grant from Genentech to The Boomer Esiason Foundation. Distributed by Tubemogul.

HTML clipboardTitle: Cystic Fibrosis and Starting a Family Jenny Davison, 39 years old with cystic fibrosis (CF), happily married, the proud mother of her 10 year-old daughter Dara and LIVING BREATHING SUCCEEDING on a daily basisâ A little over a decade ago marriage and starting a family seemed to be an unthinkable dream for adults with CF. Through advancements in treatment of the disease and being compliant the dream became a reality for Jenny and her husband Tim. Jenny Davison grew up in Long Island and is one of 9 children. âFamily is Extremely important to meâ states Jenny.Deciding to have a family when you have CF can be risky business butâ âStarting a family while you are healthy and always being compliant is keyââIt is challenging for a woman with CF to have a child and you and your husband should know the risks but most importantly, take care of yourself firstâ states Jenny.Jenny maintained her career as a nurse for seven months of her pregnancy and believes in the importance of a strong support system.Jenny states: âAlthough I have cystic fibrosis, Tim and I never regret having a childâ Dara has added so much to our livesâ Jennyâs advice: âHaving CF does not mean you stop your life â you just keep living and have a career, think about getting married and starting a familyâ you do what everyone else does â I just have to work a little harder at it with CFââEverybody has something and cystic fibrosis is what I haveââ This âLIVING. BREATHING. SUCCEEDING.â Podcast/Vodcast series is the 3rd of 12 made possible through and unrestricted educational grant from Genentech to The Boomer Esiason Foundation.

Author: CulinaryMedia Added: Thu, 08 May 2008 00:19:32 -0800 Duration: 211ReMARKable Palate Video #40: Taste of the World Video of the Cystic Fibrosis A Taste of the World event at New York's Chelsea Market. Over 25 restaurants and 20 wine and spirits producers gathered to raise money for CF. We speak with Arlene Weston ...

ReMARKable Palate Video #40: Taste of the World Video of the Cystic Fibrosis A Taste of the World event at New York's Chelsea Market. Over 25 restaurants and 20 wine and spirits producers gathered to raise money for CF. We speak with Arlene Weston of Maroon's and "Spike" Mendelsohn of Mai House (and this season's Top Chef) ReMARKable Palate is a production of The Culinary Media Network. www.culinarymedianetwork.com

Author: myqmya Added: Tue, 22 Apr 2008 14:19:37 -0800 Duration: 110http://www.myqmya.com/acne/index.php Acne can be troublesome and depressing. Our experts have written many solutions to questions about acne treatments, acne creams and acne medicines.

http://www.myqmya.com/acne/index.php Acne can be troublesome and depressing. Our experts have written many solutions to questions about acne treatments, acne creams and acne medicines.

Title: Relationships and CF â Episode #0063 Tiffany Christensen Speaks Out! Tiffany Christensen, 34 years old with cystic fibrosis is LIVING BREATHING SUCCEEDING on a daily basisâ With the help of todayâs therapies, cystic fibrosis (CF) patients are now living longer and achieving more than ever before. Pulmonary treatments are enabling adults with CF to pursue their dreams by entering college and the career world. In this podcast, 34-year-old CF survivor Tiffany Christianson talks about the role of CF in establishing new relationships. Tiffany is the recipient of 2 double lung transplants and the author of the book Sick Girl Speaks. In this conversation with her, she dives into topics such as the importance of remaining compliant on a daily basis as well as the tricky issue of revealing your CF to your newfound friend. Whatever you do, she says, âdonât lose your identity in a relationship and ignore your CFâ. Key messages in the Podcast include: Tiffany is a relationship driven person and believes telling about your CF is good, but that âless is moreâ at the beginning of a romantic relationship. âCF adds more layers to relationships but I am worthy of it!â says Tiffany. Tiffany has learned to âstop making my disease my identityâ and to start communicating, enjoying, and having fun in a relationship â âWe are a teamââ Relationships involve a lot of work and vulnerability â make sure you do your homeworkâ âRemember, like all relationships people may not accept each other due to certain likes/dislikes and that includes CFâ states Tiffany. âDonât search for your worth in someone elseâs armsââ says Tiffany. Tiffanyâs advice: â CF should be a motivator to get in a relationship. Relationships enhance your life! I have no regrets!â www.sickgirlspeaks.com * This âLIVING. BREATHING. SUCCEEDING.â Podcast/Vodcast series is the 1st of 12 made possible through and unrestricted educational grant from Genentech to The Boomer Esiason Foundation.

Author: splitlip Added: Mon, 11 Feb 2008 09:46:19 -0800 Duration: 1076A balance between holistic and traditional western healing of my health challenges during my morning routine.

Title: Jerry Cahill â Exercising is Key to Being Compliant with CF Jerry Cahill, 51 years old with cystic fibrosis is LIVING BREATHING SUCCEEDING on a daily basisâ With the help of todayâs therapies, cystic fibrosis (CF) patients are now living longer and achieving more than ever before. Pulmonary treatments are enabling adults with CF to pursue their dreams by entering college and the career world. âJerry Cahill â Exercising is Key to Being Compliant with CF,â features Jerry Cahill, a 51-year-old man with CF. Jerry talks about exercising as a form of CF therapy, sports improving his quality of life, exercising outdoors to keep his lungs CLEAR, and the importance of compliancy on a daily basis. Jerryâs philosophy is NEVER NEVER GIVE UP!â Key messages in the Podcast include: Jerry believes exercise and sports have made a major impact on improving his health and quality of life physically and mentally. Exercise outdoors to help keep your lungs clear. âSimple exercises like walking, jogging, stretching, push-ups, quick knee drills, and lunges help move the secretions and clear out the lungsâ states Jerry Time management is key to CF and maintaining your daily therapy routine so you can continue socializing and enjoying the great opportunities and people in life. Jerry states; âDo not let CF stop youâ just get out there and live life to the fullest!â * This âLIVING. BREATHING. SUCCEEDING.â Podcast/Vodcast series is the 1st of 12 made possible through and unrestricted educational grant from Genentech to The Boomer Esiason Foundation.

Title: Jerry Cahill Exercising is Key to Being Compliant with CF.

Skit Happens: Skitty Skitty Bang Bang: In Memory Of! Ricky Briggs gives a monologue for CF (Cystic Fibrosis).

Author: l4anyrat Added: Fri, 11 Jan 2008 11:36:44 -0800 Duration: 90Skit Happens: Skitty Skitty Bang Bang: In Memory Of! Ricky Briggs gives a monologue for CF (Cystic Fibrosis).

Skit Happens: Skitty Skitty Bang Bang: In Memory Of! Ricky Briggs gives a monologue for CF (Cystic Fibrosis).

Author: l4anyrat Added: Thu, 03 Jan 2008 13:28:22 -0800 Duration: 51Stand up comedian performs his Cystic Fibrosis (CF) joke at Club 307 in downtown Lafayette, LA. Yes Ricky does have CF.

Linda Hood, Mother of Twin Boys with CF, Talks about Transitioningâ Linda Hood from Cincinnati, Ohio talks about growing up with twin boys with CF â Keith and Kyle â and transitioning to an adult CF center. Lindaâs boys were born 4 weeks early and found out they had cystic fibrosis at 6 months of age. âFinding out my twin boys had cystic fibrosis was the most devastating thing in my lifeââ states Linda Linda states; âthe doctors told a horrifying story and said my boys would not live to 18 years of ageâ Linda and her family were proactive and started fundraising for a cure. Being a caregiver is scary due to concerns/fear of germs at school. Linda discusses making the transition from pediatric to adult CF center and the resources available to adults. Linda gets her support from her husband - âMy husband is my strength and gets me through the tough timesââ âStay hopefulâ do what the doctors tell you to doâ do not take shortcuts,â states Linda. Lindaâs advice: âLet your son or daughter be boys or girls and ENJOY LIFE!â Keith and Kyle are in college today and LIVING BREATHING SUCCEEDING.

2007 Costa Rica Classic Billfish Tournament To register or for more information on the 2008 tourney go to: www.costaricaclassic.com March 28-29, 2008 Los Suenos Marina Playa Herradura, Costa Rica

Happy New Year

Laurie McDonald Podcast Title: Laurie McDonald, Social Worker at UNC Transplant Center Makes a Difference Jerry Cahill interviews Laurie McDonald, Transplant Social Worker at UNC Medical Center in Chapel Hill, North Carolina. Laurie works closely with the medical team, patient, and family to make sure everything runs smoothly with the transplant. Laurie is involved in lung, heart, liver, and kidney transplant social work. Cystic Fibrosis disease progression is the reason for over 50% of lung transplants at UNC. âFinancial issues as well as re-locating and waiting for the transplant are the biggest challenges for patient and familyâ? states Laurie UNC Transplant Center offers support groups to patients and family that is both educational and good forum for stress release. Laurie recommends setting up a âfundraising teamâ? ASAP once you are listed to help ease the financial burden of unexpected expenses. Laurieâs advice: 1. âLive everyday /minute of your life and donât count on transplant to turn your life aroundâ? 2. âPrepare Financiallyâ? 3. âExercise â the surgery and recovery will go smootherâ?