As a rare disease patient, you are rare by definition. Rare disease patients do not have the numbers to spur the extensive clinical trials of more common diseases. We recognize how you must manually manage endless medical data from different doctors, keep track of test results, and push for diagnostic testing. You must advocate for yourself in ways patients of more researched diseases often don't have to. The course of action for your recovery or treatment is typically undefined or even unknown to you doctor which forces you to have to search for doctors that are familiar with your disease.

Honeycomb Health will empower patients suffering from rare diseases by providing the ability to securely store, access, and share your health information all in one place. You will be able to share your data with health care providers, loved ones, and future generations. By owning your data and uniting with other patients, you will have a better chance at pushing for- and participating in- clinical trials.

Honeycomb Health will be the hub where large groups of patients afflicted from the same disease can connect with the organizations with the means to help them. Let's end the isolation and wait-time so many rare disease patients face daily.