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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.
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A vast collection of articles, research papers, and guides on rare diseases, treatments, and patient care.
Interactive forums where patients, families, and caregivers can share experiences, advice, and support.
Opportunities to ask questions and receive answers from medical professionals and researchers specializing in rare diseases.
A comprehensive calendar of events, including webinars, conferences, and support group meetings related to rare diseases.
A tool to help users find treatment options and clinical trials for specific rare diseases.
Inspirational stories from individuals and families navigating the challenges of rare diseases.
Regular updates on the latest news, research breakthroughs, and policy changes affecting the rare disease community.
Connections to local and online support groups for various rare diseases.
Live and recorded webinars on topics relevant to rare diseases, featuring experts in the field.
Tools and information to help users advocate for rare disease research, funding, and policy changes.
To empower individuals and families affected by rare diseases through information, support, and advocacy.
A world where no one faces a rare disease alone, and where research and treatment options are accessible to all.
Collaborations with leading research institutions, healthcare providers, and patient advocacy groups worldwide.
Recipient of multiple awards for innovation in patient support and contributions to rare disease research.
Supported by grants, donations, and partnerships with organizations committed to advancing rare disease research and patient care.
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