Our beautiful daughter, Liwsi, from a small village called Cefneithin in Llanelli, was born on 31st October 2023. She spent her first days in the NICU needing respiratory and feeding support. A routine chest X-ray revealed that she had only 11 sets of ribs instead of the usual 12. Doctors reassured us this wouldn’t affect her, but they suggested running genetic tests just to be safe.

Three weeks later, we received the devastating news that would change our lives forever. Liwsi was diagnosed with not just one, but two rare genetic conditions. With little information available, our world turned upside down. We left the hospital feeling completely lost and alone.

Since then, our journey has been full of hospital stays, countless appointments, and the children’s ward becoming like a second home. The nurses now know Liwsi’s details without even asking. At just 21 months old, she has faced more than most of us will in a lifetime.

Liwsi lives with global developmental delay, milestone regression, learning difficulties, low muscle tone, and respiratory challenges—to name just a few. Yet despite everything, she continues to light up every room she enters. She tackles life with determination, a joyful spirit, and the most radiant smile.

Unfortunately, while the NHS provides wonderful medical care, many of the things Liwsi needs to have the best chance at independence and quality of life—such as specialist equipment, therapies, and accessibility support—come at an overwhelming cost. These are essential to help her reach her potential and live as fully as possible.

We are reaching out for support to help fund the vital therapies, accessibility equipment, and intensive therapies that will make a real difference to Liwsi’s future. Every single donation, no matter the size, brings us one step closer to giving her the opportunities she deserves.

From the bottom of our hearts, thank you for helping us give Liwsi the best chance at independence, happiness, and a brighter tomorrow.

Follow Liwsi on Instagram

Info for donors