As a rare disease advocate for over a decade, I’ve attended some of the nation’s best rare disease conferences and summits. These events have always left me inspired, recharged, and ready to take action. The only downside? The number of missed connections.
It can be a challenge to travel with a rare disease diagnosis. From traveling with medical equipment and supplies to covering the high cost of flights and hotels, physical conferences can make it virtually impossible for patients and caregivers to connect with the resources they need.
Enter The Rare Fair, a first-of-its-kind virtual health fair designed specifically for rare disease patients and caregivers. We specifically designed our fair to mimic a traditional physical conference, but in a virtual space. From keynote speakers and exhibitor booths to breakout sessions and attendee swag, we’re covering all of our bases to give attendees a truly one-of-a-kind experience.
We hope you’ll join us as we take this important step towards building a bigger network for all rare disease patients, caregivers, and stakeholders.
To your health,
Founder & CEO, My City Med