Bruton Designs

We love collaborating with other local small business friend and make their ideas come to life 😍😍 this is officially our first sign and I’m in love! This is a combination of white board, black board, and acrylic… I can’t wait to see it on her beautiful new cart!

One of my favorite things is making gifts for ppl I love! 🫶🏼 these will be on the site soon 💕

If you haven’t yet been to you should go! It’s awesome by itself, but you can also go check out our shelf 🫶🏼 #25

Trucker hats up at 🧢🧢🫶🏼 or message us to create your own 😊

NFL Kick Off Event at last week 🫶🏼🏈🍷We took door prizes, and Evan won bingo 🏆

I’m super jelly of all you folks getting to go to Zach Brian this weekend!! I realized his amazingness too late for decently priced tickets, but now he’s on repeat all the time!

Hats on hatssssss 🧢 …. Check us out at !!

Made myself a cute Masters inspired coquette shirt to match my Mother’s Day present 🫶🏼🏌🏼‍♀️🌺

Paulding Board of Realtors High Achievers Awards were last night and we got to supply a Wine and Whiskey wall auction item 🫶🏼🍺

We also added our Fat Heads to the website last night!
Get ready for your next event to cheer on your people … or embarrass them 🤣

Www.brutondesigns.com/products/fathead

Added some cutie little Easter Basket Tags to the site last night. These will need to be pick up only to ensure they make it to their homes before Easter. 🐰🐣✝️
Www.brutondesigns.com/products/easter-basket-tag

We were able to help support Lejla, my dear friend of 24 years daughter who has Champ1. She is 1 of 120 people in the world diagnosed. To see the love and support for Lejla at her school makes my heart so happy!



To donate: https://funraise.org/give/Champ1-Research-Foundation-Corporation/b724481c-caa3-4727-b738-2306a5b0e719/

CHAMP1-Short for Chromosome Alignment- Maintaining Phosphoprotein. CHAMP1 an ultra rare genetic disease discovered in 2015. It is located on chromosome 13 and is said to be crucial in cell division called mitosis. The mutation of the CHAMP1 gene is refered to as Haploinsufficiency, this means out of the 2 alleles the mutation causes a loss of function to one leaving those affected with a single functional copy. Patients with CHAMP1 have a reduction in the CHAMP1 protein below the 50% which is necessary for proper neurological Function and development.