The National MPS Society has received a generous matching gift opportunity to support the 2023 MPS Maritime Gala in Tiburon, CA on May 13! In celebration of MPS Awareness Day, this event will help us raise funds for research and family support programs for those with MPS or ML. Give today for your donation to be MATCHED DOLLAR-FOR-DOLLAR up to $5,000 total! Help us harbor hope!

Carter McGraw was born with MPS I, Hurlers Syndrome. Currently there is no cure, just tests and prayers with a lot of hope. With hope that we can raise awareness and funds to find a cure. While only on this side of the rainbow on a short time, he left a lasting impression on many.

This page has been created to honor the lives and love left by Dorian and Wynn Johnson. Born with ML2, Dori and Wynnie surpassed multitudes of challenges and expectations and left a legacy of love and courage for all that knew them.

This page is in memory of our twins Dorian and Wynn Johnson-- amazing sons, playful brothers, and loyal friends to all.

Fletcher is a handsome redheaded little boy that is a joy to be around. He is always in a good mood and up for an adventure.

CJ aid an inspiration to me every single day♥️

I’m dedicating this fundraiser to a friend I met on Instagram. He inspires me more than he knows ♥️

Colin is a sweet, fun, and loveable little three year old boy who was diagnosed with Morquio Syndrome when he was 18 months old.

I’ve met a wonderful dad and son though Instagram who have inspired me immensely with their courage & strength. I’m dedicating my page to them & all those fighting mps1.

Gage is 14 years old and has Sanfilippo type A