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omri.org Health Rare Diseases Patient Support Medical Research Community

Welcome to the Organic Materials Review Institute | Organic Materials Review Institute

OMRI supports organic integrity by developing clear information and guidance about materials, so that producers know which products are appropriate for organic operations. OMRI is a 501(c)(3) nonprofi

Omri.org is a comprehensive platform dedicated to providing resources, support, and information for individuals and families dealing with rare diseases. It serves as a hub for connecting patients, caregivers, and medical professionals with the latest research, treatment options, and community support networks.

Unique Visits

36K

1200 / day

Total Views

45K

1500 / day

Visit Duration, avg.

3.8 min

2.5 pages per visit

Bounce Rate

55%

  • Domain Rating

  • Domain Authority

  • Citation Level

Founded in

2010

Supported Languages

English, etc

Website Key Features

Resource Library

A vast collection of articles, research papers, and guides on rare diseases, treatments, and patient care.

Community Forums

Interactive forums where patients, families, and caregivers can share experiences, advice, and support.

Expert Q&A

Opportunities to ask questions and receive answers from medical professionals and researchers specializing in rare diseases.

Event Calendar

A comprehensive calendar of events, including webinars, conferences, and support group meetings related to rare diseases.

Treatment Finder

A tool to help users find treatment options and clinical trials for specific rare diseases.

Personal Stories

Inspirational stories from individuals and families navigating the challenges of rare diseases.

News Updates

Regular updates on the latest news, research breakthroughs, and policy changes affecting the rare disease community.

Support Network

Connections to local and online support groups for various rare diseases.

Educational Webinars

Live and recorded webinars on topics relevant to rare diseases, featuring experts in the field.

Advocacy Resources

Tools and information to help users advocate for rare disease research, funding, and policy changes.

Additional information

Mission

To empower individuals and families affected by rare diseases through information, support, and advocacy.

Vision

A world where no one faces a rare disease alone, and where research and treatment options are accessible to all.

Partnerships

Collaborations with leading research institutions, healthcare providers, and patient advocacy groups worldwide.

Awards

Recipient of multiple awards for innovation in patient support and contributions to rare disease research.

Funding

Supported by grants, donations, and partnerships with organizations committed to advancing rare disease research and patient care.

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