Since 2016, our team has worked to provide bespoke solutions to industry stakeholders. From advisory board planning and hosting to cultivating meaningful and actionable data from qualitative patient data, the Dash Connect team is committed to amplifying the patient voice with an array of impactful services and tools.
Connect with us to learn how we can help support your efforts and help achieve your goals.
We know the key to sourcing solutions in the rare disease community is collaboration. Rare72 is a virtual hackathon-style model designed to tackled to unite the international rare disease community while addressing common challenges in rare disease.
Learn more at Rare72.
Launched in 2018, The Rare Fair was the first-ever virtual event for the global rare disease community. In 2020, we welcomed over 1,600 registrants to the event, representing over 95 disease groups.
In 2021, we hosted the first annual 24 Hours of Rare, a global celebration of the rare disease community highlighting developments across the world.
Coming in January 2022, we'll launch an expanded Rare Fair agenda, with two days of educational content on January 12-13, and Rare72, a hackathon-style event on January 14th.
On January 15th, we'll launch the first-ever virtual event for kids and parents, "The Rare Fair: Junior Edition".
In celebration of world rare disease day on February 28th, we'll be travesing the globe time zone by time zone to celebrate patients, advocates, and changemakers in a 24 hour marathon event.
Register now at www.therarefair.com
We know how important it is to keep patient and research communities connected. That's why we work with non-profit organizations and industry stakeholders globally to host affordable ground, virtual, and hybrid events.
From research meetings to product launches, we leverage our expertise to help host impactful virtual events.
Learn more about what we do here.
Interested in hosting a virtual event for your community? Contact us at firstname.lastname@example.org.
Designed to bring the latest news and developments in the Rare Disease community to its global stakeholders, "The Striped Spot" features insights from leaders across the spectrum.
From everyday stories about patients and families to advocates leading the charge for inclusion and scientists making cutting-edge discoveries, this is the "spot" for all things rare in five minutes or less.
A medical diagnosis can be overwhelming for both kids and their parents. MediPals is a platform designed to help families navigate the intricacies of a diagnosis by providing education and support to chronically ill kids via a crew of helpful forest friends.
Details coming soon!