Hi my name is Kim Fisher and our son name is Jaxon Campbell.

Little Jaxon faced challenges from the moment he was born, He had a Major Exomphalos which contained his stomach, bowel and Liver. This unfortunately led to Pulmonary Hypoplasia and Pulmonary Hypotension and like the little warrior he was, he fought with the determination and strength every single day. No matter what obstacles came he pushed through them all in the hopes of coming home with mummy, daddy and his big sister Lottie.

Unfortunately on 9th of February 2024 Jaxon gained his angel wings in the arms of his parents. Some battles are just too overwhelming for such an angel. He spent 3 months in the NICU at Kings College Hospital where they made us feel at home with him.

Spending a little over 3 months in the NICU Morning, Day, Night Early hours, we got to witness countless things many positive and some not. We would like to raise money with the soul purpose of helping to enhance the neonatal unit experience for parents and siblings.

My goal is support parents and siblings like us throughout there NICU journey. We have already successfully purchased a Kangeroo chair, Bought books for every baby and family at Christmas. Bought Easter eggs and stuffy bunnies for every baby at Easter and we want to do much much more.

Help us make Jaxon's wish to help and support all his Neonatal friends. Lets make a positive impact on this world and keep Jaxons memory eternal.

Jaxons little steps may leave a beautiful footprint on the world.