Living with MMN: Hope, Treatment, and Advocacy

In this episode Jay shares a personal update on his MMN (multifocal motor neuropathy) journey — from insurance and treatment wins to a restorative solo cruise and the physical challenges that follow. He explains MMN, common tests and treatments like IVIG, and the importance of plasma donors. Jay also calls for awareness during MMN Awareness Month, encourages support for the GBS CIDP Foundation, and offers hope, faith, and advocacy for others living with rare nerve disorders.