WHO WE ARE

At HAS Foundation, a registered 501(c)(3) nonprofit, Our mission is to advance care for those impacted by ALS, brain trauma, and other serious neurological conditions through science, compassion, and legally grounded collaboration.

We don’t work alone—we bring together medical professionals, legal experts, researchers, and community partners to close critical gaps in care. We serve as a bridge—connecting individuals affected by neurological conditions to the people, resources, and systems that can support their healing, recovery, and long-term well-being.

Through our conferences and events, we create spaces for collaboration, raise public awareness, and highlight emerging research and care practices—ensuring these conversations translate into action.

We are committed to:

• Supporting families and caregivers by offering financial assistance program, linking them to vital community resources, and providing thoughtful, non-clinical guidance throughout the care journey.

• Promoting innovative research in neuroscience and neuroplasticity, and advocating for access to evidence-based treatments and rehabilitative approaches.

• Collaborating with healthcare professionals and institutions to strengthen ethical care coordination, facilitate informed decision-making, and foster patient-centered care.

• Ensuring unrepresented patients—those without family, legal surrogates, or advocates—receive the protection and support they need through legally compliant partnerships, including guardianship facilitation and advance directive planning.

At HAS Foundation, we don’t replace the system—we connect it. With compassion and integrity, we work to ensure no one falls through the cracks.