The National MPS Society exists to cure, support and advocate for MPS and ML. Since 1974, the Society has advanced its mission by funding promising research projects, student fellowships, and clinical trials at a number of prestigious university centers throughout the world. Such projects have led to critical breakthroughs in finding treatments for these diseases. The Society collaborates with other LSD patient support groups and family research foundations in funding research and supports periodic technical conferences, allowing researchers to collaborate and discuss their findings, which benefits the larger rare disease community. Although great strides have been made in research, sponsors are urgently needed to accelerate the encouraging research that is bringing therapies - and ultimately the cures - to children and adults with MPS and ML.

The National MPS Society is taking advantage of this exciting opportunity to DOUBLE the amount of funds we raise to invest in MPS and ML research. Please join us in this important endeavor by donating towards this event using the Donate Now! Button above and, if possible, by joining in the ride at the event in Philadelphia.

For more information about our mission please visit www.mpssociety.org.