National MPS Society
National MPS Society is a national nonprofit for people and families affected by MPS and ML diseases. It gives information, family support, grants, scholarships, medical travel help, advocacy, events, and research funding.
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This provides information, support groups, materials and workshops to individuals and their families affected by an MPS or ML disease, promoting public and professional awareness, and significantly increasing participation by regions.
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What they offer 11
- Not yet verified
Workshops/Symposiums * Health IssuesService
- Recently verified· Jul 1
Extraordinary ExperiencesGrant
Gives grants up to $1,000 for life-enriching experiences.
- Recently verified· Jul 1
Bereavement Expense ProgramGrant
Provides financial help to families who have lost a loved one with MPS or ML.
- Recently verified· Jul 1
Pathways ProgramProgram
Helps newly diagnosed people and families get information and support for MPS or ML.
- Recently verified· Jul 1
Continuing Education Scholarship ProgramGrant
Provides post-secondary education scholarships for people with MPS or ML and certain family members.
- Recently verified· Jul 1
Family Assistance ProgramGrant
Offers grants up to $3,000 for specialized equipment or medical aids not covered by insurance.
- Recently verified· Jul 1
Medical Travel Assistance ProgramGrant
Reimburses some travel costs for out-of-town, non-recurring medical appointments more than 125 miles from home.
- Recently verified· Jul 1
Journey Assistance ProgramGrant
Provides grants up to $500 for items that make daily life easier.
- Recently verified· Jul 1
Research GrantsGrant
Funds MPS and ML research through several grant levels, including fellow-initiated research.
- Recently verified· Jul 1
Family and Scientific ConferenceEvent
Annual conference for families, researchers, and the MPS community to connect and learn.
- Recently verified· Jul 1
Regional Social Events GrantsGrant
Provides grants up to $750 per year to support regional family social events.
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