Living With MPS2

video uploaded from my mobile phone

video uploaded from my mobile phone

This tutorial features a simple braided bun updo.

the story of how Logan was diagnosed with Hunters Syndrome

Support the National MPS Society and help find trreatment and cures for rare disorders.

You are invited to participate in the second annual "Dream for a Cure" fundraiser to benefit MPS disease research. This event will be on Saturday, ...

Surgery can't keep Zachie down!!

He's Amazing!!!!

Hoy martes 16 de noviembre es un día de gran celebración para nuestra familia y para muchos amigos que han acompañado a Kemuel durante estos cuatro...

I was interviewed on Canada AM becasue of the interest generated by the video Steve and I made. Thanks to Seamus O'Regan for his interest

VIDEO SLIDESHOW OF BOYS WITH HUNTER SYNDROME!!! LOTS OF LOVE TO ALL OF THE BOYS IN THIS VIDEO AND A SPECIAL PART OF MY HEART GOES TO PEYTON AND HI...

Hunter Syndrome, or MPS II, is a genetic disorder that leaves a person at risk for organ damage, respiratory distress and a vastly shortened lifespan.

A few photos about my son, David, now 15, and grandson, Daniel (20 months), who live with MPS 2, or Hunter Syndrome, one of the many forms of lysos...