"In 2018, our family welcomed our youngest daughter, Raelin, into the world. From the moment she was born,...
The Wain family’s journey with MPS began in 1987 when their firstborn, Matthew, was diagnosed with MPS I....
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"MPS II, also known as Hunter Syndrome, has been a part of my life for as long as I can remember. I grew...
DURHAM, N.C. (February 5, 2025) – The National MPS Society is pleased to announce the appointment of Dr....
For most of his 10 years, Jacob has been a puzzle. Born prematurely, he faced challenges from the start....
Angels Among Us: Remembering Our Loved Ones Each year, we remember individuals with MPS or...
Autumn M. was diagnosed with Mucopolysaccharidosis VI (MPS VI) at just 18 months old, at a time when no...
