Most Americans are not aware that a child is born every 30 minute with a lysosomal storage disease. MPS (mucopolysaccharidosis) is one of these rare diseases. Children are diagnosed each day and suffer physical pain before they lose their battle.

The National MPS Society has been working for 36 years to support these children and their families from coast to coast. We provide hope and support for affected individuals and their families through research, advocacy and awareness of these devastating diseases.

On October 3, 2010, come walk and run in Knott's Berry Farm Park and Walk for A Cure for MPS and related diseases. Every single dollar raised is directed to research. Help us in the fight against rare diseases. Come make a difference, because children have a right to life.

NOTE: You can now have your own LA Run fundraising page here on active!

Step: 1. Click on "Become a Fundraiser" on this page (below the logo).

2. Pick a page name and password (IE "Team Tami")

3. Follow the active step up.

It is easy and only takes a few minutes to make a difference in a child's life! Have a great time and thank you for support our children!