National MPS Society, Inc.
Organization URL(s)
info@mpssociety.orgwww.mpssociety.org
Other Contact Information
P.O. Box 736
Bangor,
ME 04402-0736
207-947-1445 (Voice)
207-990-3074 (FAX)
Description
The National MPS Society exists to find cures for MPS and related diseases. We provide hope and support for affected individuals and their families through research, advocacy and awareness of these devastating diseases.
Online Resources
- Mucopolysaccharidoses (MPS) I - Hurler, Scheie, and Hurler-Scheie Syndrome
http://www.mpssociety.org/content/4021/MPS_I/ - Mucopolysaccharidoses (MPS) II - Hunter Syndrome
http://www.mpssociety.org/content/4022/MPS_II/ - Mucopolysaccharidoses (MPS) III - Sanfilippo Syndrome
http://www.mpssociety.org/content/4039/MPS_III/ - Mucopolysaccharidoses (MPS) IV - Morquio Syndrome
http://www.mpssociety.org/content/4040/MPS_IV/ - Mucopolysaccharidoses (MPS) VI - Maroteaux-Lamy Syndrome
http://www.mpssociety.org/content/4041/MPS_VI/ - The National MSP ( mucopolysaccharide ) Society Inc.
http://www.mpssociety.org/content/4002/MPS__Related_Disorders/
Print Resources
The MPS Society publishes a quarterly magazine for its members. We also offer Syndrome booklets as well a management, Education, Anesthesia and Daily Living Guide. For more information, please contact the society.