About National MPS Society
National MPS Society is a Healthcare company based in Durham (United States) founded in 1975. Non-profit organization aiding families with MPS and ML through research and support programs. It operates on a Non-profit Fundraising model in Healthcare and Government & Social Sector sectors. National MPS Society offers products and services including Family Support Programs, Research Grants, Educational Resources, and Advocacy Events. Its focus areas include Rare Diseases, Genetic Disorders, MPS and ML and Non-profit.
Company details
The National MPS Society is a non-profit dedicated to curing, supporting, and advocating for individuals with mucopolysaccharidosis (MPS) and mucolipidosis (ML). Based in Durham, North Carolina, it provides educational resources, family support programs, research funding, and events to connect affected families and raise awareness. The organization collaborates on clinical studies and advocacy to advance treatments and improve lives of those impacted by these rare genetic disorders.
Products & Services of National MPS Society
National MPS Society offers a comprehensive portfolio of products and services, including Family Support Programs, Research Grants, Educational Resources, and Advocacy Events.
Programs providing aid and resources for families affected by MPS and ML
Funds projects and studies aimed at developing treatments for rare diseases
Offers booklets, fact sheets, and podcasts on MPS and ML conditions
Organizes races and conferences to promote awareness and fundraising
Apps and channels of National MPS Society
its YouTube channel National MPS Society has 305 subscribers and 30 videos.
Videos from National MPS Society
The most watched videos on National MPS Society's YouTube channel, National MPS Society (305 subscribers). Click a video to play it here.
More on National MPS Society.
People of National MPS Society
2 people are tracked at National MPS Society (2 in leadership).
| Name | Role | Group |
|---|---|---|
Terri L. Klein | President and CEO | Leadership |
Sharon King | Chief Operating Officer | Leadership |
Complete people profiles for National MPS Society
Full employee and board profiles, team structure, tenure and professional contact details require an active premium plan.
- Full employee list
- Team structure
- Board tenure
- Professional contacts
Verified entity values are shown only after access is granted.
Top companies in Rare Diseases
3 companies that operate in the same segment as National MPS Society (Rare Diseases) in United States, ranked by their profile score on The Company Check.
| Company | Description | Founded | Location | Total funding | Revenue | Employees |
|---|---|---|---|---|---|---|
mRNA-based therapeutics for diseases including cancer and infections are developed. | 2010 | Cambridge, Massachusetts, United States | USD 2.78 B | USD 1.94 B | 5,800 | |
Gene therapies for rare diseases including retinal dystrophies are developed. | 2013 | Philadelphia, Pennsylvania, United States | USD 82.8 M | USD 64.73 M | 822 | |
Therapeutics for genetic diseases are developed through targeted interventions. | 2015 | Palo Alto, California, United States | USD 434.2 M | USD 502.08 M | 730 |
Unlock complete access to The Company Check
Get unrestricted viewing across everything we track — from companies and brands to investors, funding rounds, acquisitions, financials, and more.
- Unlimited viewing on all profiles Companies, investors, financials, funding, acquisitions & directors
- Full access to every database India & global coverage, advanced filters and rich profile details
- Always-on access from your team account Single premium plan for everything you see on the portal
Frequently Asked Questions about National MPS Society
National MPS Society was founded in 1975.
National MPS Society is headquartered in Durham, United States. It is registered at Durham, North Carolina, United States.
The National MPS Society is a non-profit dedicated to curing, supporting, and advocating for individuals with mucopolysaccharidosis (MPS) and mucolipidosis (ML). Based in Durham, North Carolina, it provides educational resources, family support programs, research funding, and events to connect affected families and raise awareness. The organization collaborates on clinical studies and advocacy to advance treatments and improve lives of those impacted by these rare genetic disorders.
National MPS Society offers Family Support Programs, Research Grants, Educational Resources, and Advocacy Events.