Sent out a genetic test this morning to screen for the most common prolactinoma-associated hereditary mutations. Most interested to see if she’s negative for MEN1 (Multiple Endocrine Neoplasia type 1)

Urgent ask: Does anyone know a neuroscience clinician in New Hampshire willing to help treat an infant with a rare, devastating genetic brain disorder using an experimental antisense oligonucleotide (ASO) therapy under NH’s new Right to Try law (effective Jan 1, 2026)? The

Thank you to everyone that replied and DM'd about this! The family has leads on clinicians that can help :)