CPF Logo
 
  Coalition for Pulmonary Fibrosis
Note New Address
10866 W. Washington Blvd #343
Culver City, CA 90232
(888) 222-8541
info@coalitionforpf.org
   
Search
 
Join the Fight
 
 
contribute today
 
fundraiser
 
butterfly ball
 
announcments
 

 
Cindy Chandler turns Grief into Celebration of Husband’s Life, Raising $30,000 to Help Others Fight PF
 
 

When Cindy Chandler’s husband Greg was diagnosed with PF – a disease the two had never heard of – in January 2007, she had no idea the sudden and severe impact it would have on their lives. The couple had no way of knowing the disease was so aggressive and could progress so rapidly.

“We didn’t know the symptoms of PF, but had we known more, we may have noticed that his breathing had changed and sought medical help earlier than 2007.” Cindy said.
As can occur, within four months after his diagnosis, Greg lost his life while awaiting a life-saving lung transplant.
Devastated, Cindy decided to become a crusader, working to change the outcome for future patients by raising research funds. The fact that nothing could be done to treat the disease and prolong his life was heartbreaking,” she said. “But I might be able to prevent that heartbreak for others by taking on the cause and driving monies to those who are seeking the answers.”

In her determination to overcome her grief, Cindy very quickly became involved with an event to raise funds for the CPF put together by her colleagues at work – that was her first effort for the CPF. At the time, Cindy talked about how grateful she was to her community for rallying on behalf of her family. That support, along with the love from her extended family, helped her deal with her loss. Still grieving but wanting to stay involved, in September 2007 she and one of her teenaged sons joined the CPF in Washington for meetings with Members of Congress during National IPF Awareness Week.

Cindy says it was the brutality of the experience of PF and the terrible inevitability of her husband’s death that jarred her into action. Knowing that PF could strike her family again motivates her to keep fighting for answers.

“Everyone has the ability to pursue fundraising and awareness efforts to further the cause,” Cindy said. “The fundraising efforts we’ve held were uplifting for our family, the boys especially. They saw such love and support for our family. Although they felt Greg’s obvious absence, they also felt that they were supporting others in this effort. The idea of taking tragedy and finding something positive is helping us to continue each day.”

Wanting to direct her time and energy in the most effective way, Cindy researched the CPF’s work to learn how funds are used and what services are available for the PF community. The CPF’s broad spectrum of services and careful peer review of research grant requests convinced her that it would be the right place to invest her efforts.
In just more than a year after Greg’s death, Cindy has held three successful fundraisers along with her sons, in her home of Webster, New York. The first effort, a concert in June, 2007 sponsored by the local middle school and their band teacher, Cindy’s friend and neighbor, Tony Britt. With just two weeks of planning, the event raised $4,000 for the CPF.
The second event was a charity basketball throwing contest in January this year that was organized by a friend of the Chandler family, Andy Spadoni, as his senior project for high school. Through pledges with the boy’s basketball team, he raised over $1,000 for the CPF.

Just weeks ago, Cindy’s family and friends celebrated their love of Cindy’s husband Greg, by holding a hugely successful fundraising golf tournament. Cindy’s nephew, Matt Solimano set up the event, also as part of a senior project. They quickly realized their original goal for the event of $10,000 and exceeded it by raising more than $30,000. More than 160 golfers participated on a rainy day in June, some waiting patiently for hours to tee off. The depth of local support was obvious when people kept arriving until the dinner tent was filled to absolute capacity.

“We were blown away by the efforts of everyone involved,” she said. “This event helped to raise awareness and also to highlight the work of the CPF.” Cindy said her goal was to make it a memorable event to celebrate Greg’s life.

 

A school principal, Cindy reached out to other administrators, students and families to help raise awareness about the disease and to raise funds for desperately needed funding.
“The idea that there is a panel of experts at the CPF deciding on the research efforts makes us feel confident that our efforts will have the most impact,” she said.
Her sons, ages 13 and 17, are equally dedicated to the cause. “One of the doctors in Philadelphia challenged the boys to ‘find a cure’. This fundraising is something we can all do now to support the research,” Cindy said.

Cindy says anyone can hold a successful fundraising event for the CPF and she shares a few tips for making an event successful:

  • Share details about the CPF and Pulmonary Fibrosis to raise awareness. The facts about PF and your personal experience with the disease seem to be key motivators for people to participate.

  • Continue to connect with others in the community that have experience with PF.

  • Pay attention to detail in your planning so the event can run smoothly and be exciting for those attending.

“Everyone has the ability to pursue fundraising and awareness efforts to further the cause,” Cindy said. “The fundraising efforts we’ve held were uplifting for our family, the boys especially. They saw such love and support for our family. Although they felt Greg’s obvious absence, they also felt that they were supporting others in this effort. The idea of taking tragedy and finding something positive is helping us to continue each day.”

Cindy says she is already making plans for her fourth fundraising event in Webster. It will be another golf tournament, likely to be held in July, 2009. “We are committed to continue our efforts until we have a cure.”

 
 
 
 
 

  All registered trademarks and trademarks that appear in this Web site are the
property of their respective owners. ©2001 - 2009 Coalition for Pulmonary Fibrosis
Site Last Updated 6/16/09
floor 84 studio

This website is accredited by Health On the Net Foundation. Click to verify. We comply with the HONcode standard for trustworthy health information: verify here.