Help Lexi Fight a Rare and Aggressive Cancer

Hi everyone, Louise here please take a moment to read our story.

This is one of the hardest things we’ve ever had to write, and to be honest, we’re still trying to process it all ourselves. Our closest family and friends have been an incredible support through the last few weeks and we hope you’ll understand why we’ve kept things private until now—it’s been overwhelming, emotional, and so very hard.

Our beautiful, strong, and brave youngest daughter, Lexi Collins, just 13 years old, was diagnosed at the end of June 2025 with a rare Cancer, Angio sarcoma.

Before her diagnosis, Lexi underwent an open-heart procedure where doctors performed a debulking biopsy and fitted her with a permanent pacemaker. Since then, she has completed her first cycle of chemotherapy, with many more treatments, tests, and scans ahead.

Her medical team has been absolutely amazing, and they’re even consulting with specialist doctors in the USA who have experience treating this rare cancer. There may be options for treatment abroad that could give Lexi the best possible chance and we will seek and exhausted every option, as a parent that’s our main priority-but these treatments can come at a huge cost.

That’s why I have created this GoFundMe. We’re asking for your help to raise funds to cover potential treatment overseas, travel, and the enormous expenses that come with this fight. Every single donation, no matter the amount, and every share of this page makes a difference.

Please help us give Lexi the best shot at beating this awful disease. From the bottom of our hearts, thank you for your kindness, love, and support, Louise and Stuart Collins

Let’s fight this together—for Lexi.