03/27/2026
Sharing magnificent news from a very special family that is dear to our hearts. 💙
Back in 2018, we met Kalel a young super hero indeed, affected by MPS (Mucopolysaccharidoses). and his incredible family. From the moment we learned about Kalel’s journey, we knew we had to be part of something bigger. Without hesitation, we joined their cause, not only to help Kalel fight and live, but to help bring hope to so many other children facing similar battles.
Throughout the years, our Giving Gators team has done everything we could to support The MPS Superhero Foundation in reaching their mission. And today, we are overjoyed to share that we received truly amazing news! ✨
While we celebrate this milestone, we know there is still important work ahead. We remain committed to this journey and will continue to stand with the MPS SuperHero Foundation every step of the way. 💜
We ask our community to keep supporting, keep believing, and keep spreading hope. Together, we are making a difference, one child, one family, one miracle at a time. ❤️💜
From: Monica Anaya (Kalel’s Mom)
MPS Superhero Foundation.💜
Hi Day, I wanted to personally thank you for your support of our foundation and family in the past years. Because of people like you, we just experienced a HUGE milestone this week. Kalel’s treatment was officially approved this week.
This moment is bigger than us, it’s hope for so many families. Your support helped us get here, and we are forever grateful. There’s still work ahead, but today we’re celebrating this HUGE WIN!
I would love to get the crew together to celebrate. You guys were a huge part of this and what kept our faith and hope strong and it would mean a lot to be able to celebrate with you all.💜