Find a Cure for Hunter Syndrome!

About this campaign

I am raising money for the MPS Society. The MPs Society helps families and individuals affected by MPS & MLS. Our son was diagnosed with a form of MPS; MPS II also known as Hunter Syndrome when he was only 1 1/2 years old.
I have made it my mission to spread awareness about this condition and help as many people as I possibly can by creating awareness and openly speaking about my son’s diagnosis and our life since finding out.
I started doing the 5K as a way for people to know more about Hunter Syndrome and to hopefully ask questions for themselves or maybe someone they know whom they think may be at risk or affected by this and has yet to be diagnosed.
I chose to donate to the MPS Society because they advocate for our boys, for the families that can’t afford treatment, they help us find the support that we need not just for our boys but also for us as caregivers.