The Cystic Fibrosis Foundation is powered by the work of dedicated volunteers. Through their fundraising, CF patients are enjoying longer, healthier lives. But some CF patients are still dying before their time. This video, produced and directed by Dan Sonnett of the Sonnett Media Group, is a call to CF volunteers to strengthen their commitment to fight CF.
The Cystic Fibrosis Foundation video podcasts present the stories of CF patients, families and volunteers. The Cassalina family shares their experience of losing their daughter, Jena, to CF and encourage others to help find a cure for CF patients like their son Eric.
The Cystic Fibrosis Foundation video podcasts present the stories of CF patients, families and volunteers. Frank Deford, sports commenter, noted author of "Alex: The Life of a Child" and CFF Chairman Emeritus, recalls how he came to realize his daughter Alex, who died of CF at age 8, was a true hero.
Former NFL player Boomer Esiason talks about the importance of participating in clinical trials to advance the search for a cure and control of cystic fibrosis.
The Cystic Fibrosis Foundation strives to advance the search for a cure for CF by funding promising scientific research at medical centers and biotech companies nationwide. Frank Deford narrates this look at the Cystic Fibrosis Foundation's innovative approach to moving new treatments for CF into a pipeline that promises a better quality of life for all CF patients.
Congressman Cliff Stearns (R-FL), co-chair of the Congressional Cystic Fibrosis Caucus, speaks as the US House of Representatives supports cystic fibrosis awareness.
The Cystic Fibrosis Foundation depends on the efforts of dedicated volunteers to help raise funds for the search for a cure for CF. Since the first GREAT STRIDES walk in 1989, more than $180 million has been raised to support the vital research and care programs of the Cystic Fibrosis Foundation. To find out how you can participate, visit http://www.cff.org/g reat_strides.
Congressman Ed Markey (D-MA), co-chair of the Congressional Cystic Fibrosis Caucus, speaks as the US House of Representatives supports cystic fibrosis awareness.
The Cystic Fibrosis Foundation video podcasts present the stories of CF patients, families and volunteers. CF patient Caryn Silliman talks about the challenges of managing her illness as an adult and her plans for the future.
The Cystic Fibrosis Foundation is dedicated to helping the 30,000 people living in the United States with cystic fibrosis. Find out how you can help by visiting http://www.cff.org or by calling 1-800-FIGHT-CF.
New Experience Retirement Website - PR.com Montpelier, VT, September 07, 2008 --( PR.com )-- National Life Group recently launched its new consumer retirement resource website, www.ExperienceRetirement.com. This interactive and easy-to-use site is focused on the retirement planning needs for ...
FCMB pumps N300m into Legacy Pension Managers for 25% equity - Businessday ... I n a move to further enhance the level of service delivery to customers of Legacy Pension Managers Limited, First City Monument Bank plc (FCMB) has announced the acquisition of 25 percent equity stake in one of the leading Pension Funds ...
What's a peripatetic worker to do at the end of the walk? - International H... Europeans who spend their careers in more than one country may wonder if the treaties safeguarding the free movement of people and money have an asterisk in the fine print about pensions. With the regulations of retirement systems, and especially the ...
Saving for retirement is for women, too - Kansas City Star More women than men outlive their savings, partly because they tend to live longer. But women’s work histories also set the stage for financially pinched retirement years. As a group, U.S. women work fewer years than men, and they’re more likely ...