Tonya Lantis

Miles for Amelia here! I am just a spunky little girl that is working on being two years old. I have a brother named Liam, a puppy named Jeter, & my mommy and daddy whose names are Tonya and Devin. Fun facts about me are I love my ranch, I enjoy watching Cruella Deville while I do my therapies, I can really throw a ball, I throw food even further after I am done eating, I like flushing toilets, currently Nutella stuffed mini pancakes are my favorite breakfast... I could just go on and on about what I love! 

Now Amelia's mommy here, hello it's Tonya! Miss Amelia  was born in October 2020. She has been a little rockstar with everything with her condition of cystic fibrosis, & let's not forget outside of it as well, because more than anything she is still a sweet, crazy little girl. Miss Amelia has currently mastered taking her pills whole with applesauce, she loves her food (for the most part), she runs around and is very curious of her surroundings, and she likes to challenge her brother with his own basketball. Amelia currently takes her enzymes with any food containing fat or protein. She does physio therapy twice a day. She takes her vitamins with her breakfast. Amelia also sees her team at Riley every three months for check ups. We are beyond thankful for this team and they are always there with any and all questions and concerns! 

This is just a little bit about our Millie and there's many more kids and adults fighting this same fight that we are as well.  We hope you will join us in this fight against Cystic fibrosis and help us find a cure. A donation, sharing our story, or even simply taking the time to understand what this genetic disease is- will mean so much to us. 

We appreciate you taking the time to read this and we hope you and your family have a healthy, happy, and beautiful 2022!

There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?

Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.  

Please support me!

We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!