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Welcome to Halie Chandler's Page

Halie Chandler

Halie Chandler

This year has been one of growth and change for my family and our business in many ways. Daniels + Chandler has had the opportunity to support community members to create a "better Nashville" through architecture and design and my husband and I are adding one new person to Nashville's population. I couldn't have imagined how I would be impacted by the Cystic Fibrosis Foundation this time last year, but it has been significant in many ways. While expecting our first child, my husband and I learned that I am a carrier of the recessive gene for Cystic Fibrosis. While we waited to confirm that Ben was not a carrier, I did a deep dive into the effects this could have had for our future child and the weight of this disease was immense. 

Through 30 under 30, I have had the opportunity to meet members of the CF community who are active, resilient, and inspirational. They are living with a disease that requires incredible amounts of time and money including multiple hour long treatments per day and thousands of dollars towards medications monthly. With each interaction I've had with these champions, I've left the conversation thinking "there's got to be more that we can do".

That's where you can help!

I will soon be honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding young professionals in my community. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of controlling and curing cystic fibrosis (CF).

Please help me meet my fundraising goal by making a donation. Your generous gift will be used efficiently and effectively to help support vital CF research, medical and education programs.

Making a donation is easy and secure! Just click the Donate button on this page to make a donation that will be credited to my fundraising efforts. Any amount you can donate will be greatly appreciated!

Cystic fibrosis is a devastating genetic disease that affects the lungs and digestive system. More than ten million Americans are symptomless carriers of the defective CF gene. Advances continue to be made in finding a cure, but your help is needed now -- more than ever -- to help keep up the momentum of this life-saving research. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is about 40. This is remarkable progress, but not good enough. We continue to lose precious lives to CF every day. To learn more about CF and the CF Foundation, visit www.cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!


raised of $5,000 goal

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