NASHVILLE, Tenn. (WTVF) — Cystic Fybrosis is scary.
About 30,000 people are currently suffering from the rare genetic disease that impacts the lungs and digestive system. And, it can require a lot. Lots of pills per day. Often times a machine that helps shake the mucus in the lungs so those who suffer can breathe better.
In short, it costs a lot for care and there's no federal funding.
So, in comes my new friend Vera Smith. Vera is the President of "Cure for Our Friends," an organization assisting in providing assistance to families who need help affording all that's required to care for loved ones suffering from CF.
She's putting on what is now the 10th annual "Cure for Our Friends Golf Outing" where 100 percent of the money raised goes right back to families in need.
"lt's an all day event we have a 7:30 tee off and a 1 o'clock tee off. We have catered lunch in between that," said Smith. "Whataburger is bringing breakfast out for the AM tee off after the golf rounds. Then we have live entertainment and a big after party to celebrate our CF families."
You can still register, by the way! The tournament is this Saturday.
It's $600 to enter as a team, or $150 per player. In addition to what Vera mentioned, there's snacks and beverages on the course, along with a Big Machine Vodka Bloody Mary bar!
You can also become a sponsor if you're not able to play.
Our viewers are the best! When Hannah McDonald highlighted the plight of Serenity Sumler, so many of you immediately stepped up. Serenity stopped to help a driver after spotting a wreck and was hit by another car, resulting in terrible injuries. Without the funds to pay for physical therapy, she was at a loss. Because of the kindness of others - she now can rehab and get back to school. Best of luck to her as she trains to become a chef!
- Carrie Sharp
