A PANS/PANDAS diagnosis can leave families with more questions than answers. Whether you’re trying to understand a diagnosis, find care, afford treatment, or connect with someone who understands, we’re here to help you find your next step.

Symptoms, diagnosis, testing, treatments, and research.

Financial assistance for eligible PANS/PANDAS treatment and travel.

Connect with clinicians familiar with PANS/PANDAS and neuroimmune disorders.

Join free virtual conversations with families who understand.
When insurance denies physician-prescribed treatment, Be The Hope Foundation helps eligible families access the care their children need.
Grants may help cover IVIG, Rituximab, TPE (plasmapheresis), and qualifying treatment-related travel.
Want to help another family access treatment? Support Our Grant Program
Join other parents navigating PANS/PANDAS for free virtual IVIG Coffee Talks. Share experiences, ask questions, and connect with people who understand what treatment can really look like.
First + third Friday of every month via Zoom
Button: Join an IVIG Coffee Talk →
Finding a provider familiar with PANS/PANDAS can be one of the hardest parts of navigating a diagnosis.
Explore the Mind Global Council directory to connect with clinicians and specialists experienced in PANS/PANDAS and related neuroimmune conditions.
Explore research, diagnostic guidance, treatment information, and educational resources to help you better understand PANS/PANDAS and prepare for conversations with your child’s care team.

A step-by-step guide to PANS/PANDAS diagnosis and treatment based on symptom severity.

Clinical guidance developed by a multidisciplinary team of medical experts for evaluating children with suspected PANS.

Research examining treatment outcomes among 55 children with severe PANS/PANDAS following IVIG treatment.
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