Mya’s return to the USA to fight MS

We are returning to the States in a couple of months to get further help, testing and treatment for Mya.

Mya was diagnosed 4years ago with pediatric onset Multiple Sclerosis. Being very rare and minimal options here, we found a medical team in Arizona. We traveled there 3 years ago and stayed for 6weeks. It was phenomenal to say the least, we were and still are grateful for that opportunity. It was planned for us to go back in the same year but Covid happened.

We have continued the same medical treatment plan from our American team for the last 3 years. Mya has MRIs every 3 months, every thing has been going great except the last 6 months with new lesions appearing. From the outside Mya is thriving and taking life on in full force, but the silent battle inside is starting to build. Anything can change at anytime. We have been doing some maths and trying to put together a plan to help Mya not just for now but for her future.

I hate doing this and putting it out there but we only want the best for our girl, to have a long, happy, healthy life. But we need and would love some help. We are working as hard as we can to come up with the funds but there is a short fall.

We are so grateful for our little village of people around us that are always there and make things a little bit easier!

Love you all x

Kurt, Lauren and Mya