A Pocket Guide to Rare Disease Advocacy
Tony Castaldo
President & CEO, US Hereditary Angioedema Association
“HMCW has helped us design and successfully implement a comprehensive public policy advocacy program for over a decade. The leadership and staff know how things work in Washington DC, and get things done.”
Janet L. Hiesthetter
Executive Director, Dystonia Medical Research Foundation
We have benefitted from the brilliant guidance and expertise of the HMC team for over 20 years. They have helped us in numerous ways to develop significant relationships with Congress and navigate federal agencies to help serve our patient community. We are very fortunate to partner with them in the service of those affected by dystonia.
Julie Flygare
Founder, Project Sleep
Working with HMC was the game-changer for our advocacy efforts. This relationship elevated our advocacy program to the next level and led to tangible results that we could report back to our community to show that their efforts are truly making a difference in advancing our cause.
We’d be lost without the expert guidance of HMC team. They have guided us with incredible poise, professionalism and patience.
The HMCW team brings the most sophisticated real-time knowledge of what is happening on Capitol Hill today, along with decades of experience and connections.
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