Since 2004, we’ve never stopped thinking of new ways to expand our lineup of custom silicone wristbands. Today, we are giving a shoutout to a couple specialty wristbands that have actually been around for awhile, and have been super popular in our long history of making awesome wristbands!
Lots of motocross and biking groups order custom tire bands annually. On the other hand, the golf bands are a great way to memorialize someone or to do a fundraiser or charity event. One thing is for sure–no other wristbands look quite like these!
For more ideas on how to customize your next masterpiece and to share your message with the world, head over to Reminderband today and see just how creative you can get!
Alexis Teixeira was diagnosed with Lupus at age 14 and has fought for many years through testing and treatments to get proper help. When she was eventually married, she was currently receiving exams but developed preeclampsia after becoming pregnant with their daughter Gianna. Lupus played a part in her high-risk pregnancy and Gianna was born prematurely.
Thankfully, Gianna is doing quite well and is almost four-years-old. Alexis’ husband Luis saw the need for a great deal of awareness that Lupus just wasn’t getting; so he took matters into his own hands. Since his epiphany, Luis has used his rally driving career as a way to promote better awareness for Lupus. His race team Wicked Nasty Motorsports took to representing Lupus awareness (purple) in their team colors. This has allowed the whole family to share the message of awareness and the struggles of Lupus with many, many others.
“So often we overlook the loved ones of those suffering from Lupus who are living through the difficult experiences with them.”
Alexis says her husband’s efforts to raise awareness is a good example for the community, and that everyone can help.
Part of their campaign to raise awareness includes handing out Reminderband wristbands at the racing events, which have been designed with the Wicked Nasty Motorsports logo along with “Lupus Awareness”.
If you would like to learn more about Lupus, head over to lupus.org.
We wish Alexis and her family all the best and we thank them for sharing their story with us!