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Fashion & Tea at Tiny Boutique to Benefit the CF Foundation

Ashley Sullivan

Tiny is a charming boutique located in the heart of Charlotte offering a unique collection of clothing, accessories, and toys for children of all ages!

On Wednesday, July 17th, from 6-8PM they’re hosting a fashion show to benefit the Cystic Fibrosis Foundation, and Sel de Vie is honored to be a featured designer in the show!

Some of our current Juniors pieces will be on display, as well as some brand new custom designs created especially for the little models in the show!

This is an open event and we’d love to see you there! Please RSVP at the number listed on the invitation below if you're able to attend.

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Jewelry Designer, Mallery Horton | Sel de Vie Jewelry 

Guest Speakers:
Nicole Sconce
JanEllen Brown
Pam Stowe

Please tell your friends!
Donations are GREATLY appreciated!

Life With CF: Palmer's Fight for a Better Future

Ashley Sullivan

Palmer’s story was recently featured as a part of Levine Children Hospital’s new marketing campaign (see the video in the previous post)! This week they highlighted her on their website. Check out her story below!

“Palmer Horton isn’t in kindergarten yet, but you don’t need to simplify things for her. She’s 5-going-on-11 and knows so much medical jargon, she keeps even her doctors on their toes.

Unfortunately, just as Palmer challenges her care team with her spunky attitude, she has a rare, lifelong lung condition that presents challenges of its own. She was born with cystic fibrosis, which causes her body to produce a thick mucus that can clog her lungs, making it difficult to breathe…”


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Levine Children's Hospital

Ashley Sullivan

Kids don’t want to be sick. Kids just want to be kids!

Levine Children’s Hospital continually works to find new ways to provide the best care and always treat kids like kids. For the 12th year in a row, they’ve been named a Best Children’s Hospital by U.S. News & World Report. They’re the only children’s hospital in Charlotte to be recognized, and this year, they ranked in more pediatric specialties than ever!

Palmer was so lucky to be born in such a wonderful hospital and has received top-notch care at Levine during her many stays over the years. We’re proud that she was featured in their video below, celebrating their designation as one of the best! Way to go, Levine!

CF Foundation Video: Palmer's Story

Ashley Sullivan

Grab some tissues! Earlier this year the CF Foundation produced a video sharing Palmer’s story, and it’s officially live! Palmer is the inspiration behind Sel de Vie, and if you didn’t already know why, we’re sure you will understand after watching this video. We love you, Palmer!

Palmer's Live Auction Art

Ashley Sullivan

The CFF-Charlotte Master Chefs fundraising event was last weekend, and one of the live auction items was created by our very own SDV inspiration, 5-year-old Palmer! The painting Palmer created sold for $36,000 at live auction! Check out the news story about the event (and see the painting!) below!


Myers Park Life Magazine

Ashley Sullivan

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Our Co-Founder Mallery and her family were so happy to be asked by Myers Park Life Magazine to share their story + everything they are doing to find a cure for Cystic Fibrosis! Thank you, MPL Magazine, for bringing more awareness to the cause so near and dear to our hearts. To read the article, click here!

CF Portrayed on Hulu's Show "Zac & Mia"

Ashley Sullivan

Who’s heard of the show “Zac & Mia”, now in its second season on Hulu?!

"Zac and Mia" (based on the novel with the same name by A.J. Betts) is about two teens battling cancer in the same hospital. In the real world, Zac and Mia would have pretty much nothing in common, but in the hospital, where they're the only two teens on the ward, they develop an unbreakable bond. If cancer is the variable that changed everything, the only constant is their ever-deepening need for one another…

Also included on the show is a character named Ashley, who lives with Cystic Fibrosis. Here’s the crazy part…

Ashley is played by SDV co-owner, Mallery’s, childhood best friend, Kelsey Formost! What are the chances?!

We’re so proud of Kelsey and grateful that her role gives everyone living with CF a chance to see someone who understands their day-to-day reality portrayed on screen! If you have Hulu, the show is worth your while!