“It’s an honor to lead an organization that listens to the migraine community, supports groundbreaking research, and works every day to improve lives.”
Carrie Howell stepped into the role of CEO at the American Migraine Foundation in January, bringing more than 20 years of nonprofit leadership experience and a deep-rooted commitment to patient-centered care.
In her first few months, she has focused on listening to the migraine community, strengthening AMF’s partnerships, and shaping a bold, collaborative vision for the future. With passion, purpose and empathy at the core of her leadership, Carrie is guiding AMF into its next chapter—one grounded in connection, advocacy and impact.
“Carrie brings a people-first approach that aligns beautifully with our mission and community,” said Dr. Christine Lay, Board Chair of the American Migraine Foundation. “Her leadership is thoughtful, inclusive, and exactly what AMF needs at this exciting moment of growth.”
A Foundation in Advocacy
Carrie has spent her career leading mission-driven organizations that focus on serving vulnerable and underserved communities. Before joining AMF, she served as Executive Director at Hospitality House, Dup15q Alliance, and a therapeutic home for teen girls—bringing a strong background in both direct service and strategic leadership.
She holds a Master’s degree in Counseling from Southeastern University and is a Certified Fundraising Professional (CFRE). Carrie has also served in leadership roles on several nonprofit boards and was recognized as one of the 50 Most Influential Women in Charlotte, NC. Her contributions to the nonprofit sector earned her the prestigious Brava Award from SmartCEO.
Throughout her career, she’s been guided by a core belief: that the people most affected by a condition or challenge should be at the center of decisions that impact their lives.
“I think [my last role] really solidified my passion for medical nonprofits and being in this space where I can advocate for people who may not be able to advocate for themselves,” Carrie said.
Supporting the Migraine Community
Since stepping into her role at AMF, Carrie has spent her time listening—meeting with team members, healthcare partners, and members of the migraine community to better understand their experiences and needs.
“We want to be representative of the patient voice, and as we work on our strategic plan over the next year or two, we really want to bring patients to the table and make sure we hear what needs are not being met,” she said.
Carrie’s leadership at AMF is focused on expanding access to education, strengthening support resources, and investing in research that centers the needs of people with migraine. She is also committed to building trust through transparency and ensuring that all voices in the community are seen and heard.
A Message From Carrie
In a recent video, Carrie shared her hopes for AMF and her gratitude for the work already being done across the migraine space. She also invited the community to share what matters most to them—what kind of support, resources, or advocacy efforts would make the biggest difference in their lives.
“Please don’t hesitate to reach out. We are here for you,” she said. “I’m so excited that you’re part of the community, and I just really appreciate you letting us be part of your journey.”
We’re excited about the future of AMF under Carrie’s leadership and look forward to all the ways she’ll help grow our mission and impact.
About the American Migraine Foundation
Founded in 2010, the American Migraine Foundation is a nonprofit organization dedicated to advancing research, raising awareness, and providing free doctor-verified resources for the millions of people living with migraine and other disabling conditions that cause severe head pain. Through education, advocacy, and community support, AMF serves as a central hub of hope and empowerment for individuals navigating life with migraine.
The American Migraine Foundation is committed to supporting people living with migraine and advancing research that will one day lead to a cure. We provide education, resources, and community for the millions of people living with this disabling disease.
For more information and to get involved, visit americanmigrainefoundation.org.
