Angie Rowe, Interim Executive Director, Global Genes
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Connecting Rare Disease Patients
Angie Rowe, Interim Executive Director, Global Genes, talks about the 10th anniversary of the rare disease organization and its vision for the future.
PV: Over the past 10 years, what impact has Global Genes had on the rare disease community?
Rowe: When Nicole Boice started the organization, her goal was to connect people. She had a good friend whose son’s rare disease went undiagnosed for many years and Nicole saw the isolation of this experience. Nicole watched the very long journey to diagnosis and was bothered by the fact that her friend had no way to connect with other parents going through a similar journey.
The goal of Global Genes was, and still is, to connect people to one another so they would not feel so isolated. Well, fast-forward 10 years and those connections and the engagement and inspiration that Global Genes provides to patients and caregivers has taken off tremendously. We’ve been a catalyst for patients and families to find the power to shape their own future.
We have connected more than 6 million patients and advocates in more than 100 countries. We’ve educated 75,000 advocates, connected 15,000 rare disease stakeholders, and we have now more than 500 nonprofit partners that we work with through our Foundation Alliance Program.
We’re empowering patients to take control of their rare disease journey moving forward. No matter where they are in their journey, Global Genes wants to be their partner in helping them to get the tools and the resources they need to be an advocate or accelerate therapies or start a nonprofit.
PV: What are the goals of the organization for the next 10 years?
Rowe: The role we play is providing connections, so we aim to continue helping patient communities find one another or be found by researchers or medical specialists or companies that may be working in their disease areas. We want to continue to connect and educate these communities on how to become a player in the process.
The role of patient advocates is vastly expanding; they have more responsibilities and opportunities when it comes to serving their communities. Global Genes will continue to help advocates move forward and to teach them how to leverage data to drive innovation and gain access to therapies.
Some of the groups we work with might only have a few patients, so their voice can be small, but Global Genes aggregates all those voices, and educates all those voices on how to mobilize and be activists allowing for a whole movement to happen. An organization that represents all 7,000 rare diseases has a lot bigger voice and a lot more impact because of the sheer number of people we represent.
PV: What is the Patient Impact Grant Program?
Rowe: Now in its fourth year, the Patient Impact Grant Program is a funding program exclusively for our Foundation Alliance membership organizations. Member nonprofits have an opportunity to receive a grant to fund their support or innovation projects. Since its inception, we have provided over half a million dollars in funding. Foundation and support groups can join the Foundation at no cost. Our next grant cycle opens in May 2019.
PV: How does Global Genes partner with industry?
Rowe: We have a corporate alliance that is membership-based. Our corporate alliance and other industry partners provide the support for our major educational initiatives where we bring patients together, such as our annual Patient Advocacy Summit, our Drug Development Symposium that we do in partnership with the University of Pennsylvania, and our RARE on the Road tours that work in partnership with EveryLife Foundation, to name a few. In addition, we work with industry to create opportunities to connect, engage, and build capacity of rare disease patient communities.
PV: Tell us about Global Genes’ new hub.
Rowe: We have a new online portal that launched in February. Our new hub is a way to connect even more patients and patient communities. People on the hub can identify themselves as a caregiver, a patient, an advocate, and/or a supporter, and they can connect to resources, clinical trials, and other information about different rare diseases and support groups. Patients can also share resources and information about events. The platform allows people around the world to connect, share, and find rare disease information 24 hours a day.(PV)