Synapticure exists to close the unmet gaps in traditional care settings for individuals and families living with neurodegenerative conditions. Through a virtual care model, Synapticure is committed to expanding access to expert-led care, cutting-edge treatments and clinical trials, and wraparound support in all 50 states–supported by a network of in-person and local partners and a deep commitment to reach rural and underserved communities.
Our founders, Brian and Sandra, started Synapticure after Brian was diagnosed with ALS. They faced the same challenges many families do—and decided to do something about it. With backgrounds in healthcare and policy, they built a company focused on making care better, faster, and easier for people living with neurodegenerative diseases.
Too many people with neurodegenerative diseases are left behind by traditional care. Long waits. Long drives. No clear answers. Synapticure was created to change that. We bring expert care to you, no matter where you live, through virtual visits and local support. Our team works in all 50 states and focuses on helping people who often don’t get the care they need.
Our name comes from synapse, the part of the brain where communication happens, and cure, because we believe in a better future. Everything we do is designed to bring patients closer to life-changing treatments and new hope.
Our Leadership Team
Our leadership team brings deep experience in medicine, policy, technology, and advocacy. Many have personal ties to neurodegenerative disease—and all are united by a shared goal: to transform how care is delivered.
Our Care Team
Synapticure’s clinical team is composed of subspecialty neurologists, geriatricians, genetic counselors, psychiatrists, psychologists, speech language pathologists, and nurse practitioners who work together to support every patient and family.
Our physicians can see new patients in less than two weeks with comprehensive care coordination support available 24/7. We’re here for you 24/7, with a care team that can answer questions, help with medications, and guide you through clinical trials and new treatments.
Whether you have a question in the middle of the night, need help finding a new treatment, or just want someone who understands, we’re here. You don’t have to face this alone. We are here for you wherever you are, whenever you need us.
Our co-founders, Brian Wallach and Sandra Abrevaya have been living with ALS for more than 6 years. Discover the journey of 'No Ordinary Campaign' and how I AM ALS and Synapticure are revolutionizing care for patients and caregivers.
