National MPS Society

The National MPS Society exists to find cures for MPS (Mucopolysaccharidoses) and ML (Mucolipidosis). We provide hope and support for affected individuals and their families through research, advocacy and awareness of these devastating diseases. Since 1974 the Society has supported individuals and families affected with MPS and related diseases. MPS and related diseases are genetic lysosomal storage diseases caused by the body's inability to produce specific enzymes. While the symptoms of MPS and ML may vary from one syndrome to another, there are many similarities. Affected individuals often have mental retardation, cloudy corneas, short stature, stiff joints, incontinence, speech and hearing impairment, chronic runny nose, hernia, heart disease, hyperactivity, depression, pain and a dramatically shortened life span.


Charity Navigator Ratings

Overall Rating

(4/4)|90.29 Score

Financial

(4/4)|91.79 Score

Accountability & Transparency

(3/4)|89 Score

EIN

11-2734849


Headquarter Address

1007 Slater Rd.
Suite 220
Durham, NC 27703