Cumulus

At Cumulus, we are working to unite the global rare disease community and all stakeholders through the creation of a virtual hospital that seeks to provide education and access to faster, more accurate diagnoses and precision treatments.

Cumulus is a virtual medical campus designed to expedite the diagnosis and treatment of rare diseases through collaborative centers designed to meet the specific needs of different stakeholder groups.

Cumulus Campus Overview

Rare disease patients are an underserved population as a whole. From access to knowledgeable doctors and disease education to diagnostic testing and treatments, rare patients struggle to create care plans. 

Cumulus seeks to remedy these issues by providing all stakeholders access to our virtual community and the many tools offered on our campus. 

We are rare disease parents and caregivers since 1993. We understand the burden a rare disease diagnosis can place on a family and the agony of living without a diagnosis. 

We seek to help other families avoid the situation we have lived through.

We hope to expand our footprint in the market and signpost to existing best practices and resources.

We are a global platform. We welcome and have participants from several countries other than the USA. We have hosted and presented to a highly diverse group in the rare disease space.

Our business model will be a subscription based service that will allow patients, doctors, researchers, and industry professionals a secure and private platform to interact, share information, follow resources, learn in a global environment, and find solutions on a global scale.

We are subscription based service.

Promotional presentations to key stakeholders in the chronically ill and rare disease community.