International network. Founded 1999. Provides support and education for families of children with Morquio Type A. Helps educate health care professionals about this lysosomal storage disease. Funds research. Maintains database of families. Referrals to physicians and medical information, pen pals, phone support, conferences and newsletter, online guestbook and helpful links. Write: Morquio Support Group PO Box 64184 Tucson, AZ 85728-4184 Voice: 520-744-2531 Fax: 520-744-2535 Website: http://www.morquio.com E-mail: mbs85705@yahoo.com Verified: 10/9/2008
National. Founded 1974. Provides support and hope for individuals with mucopolysaccharidoses or mucolipidoses (and their families) through research, advocacy, public education and parent referral service for support networking. Write: National MPS Society 4220 NC Highway 55, Suite 140 Durham, NC 27713 Voice: 919-806-0101 Website: http://www.mpssociety.org E-mail: info@mpssociety.org Verified: 10/8/2008
This information does not replace the advice of a doctor. Healthwise disclaims any warranty or liability for your use of this information. Your use of this information means that you agree to the Terms of Use. How this information was developed to help you make better health decisions.