Caring for a child with a rare disease like MPS can feel isolating at times – but you don’t have to go it alone. We’re bringing together a compassionate group of parents and caregivers who have been there and can offer a listening ear, share advice, and uplift each other through shared experiences.
We’ll gather online for an evening of candid conversation and camaraderie facilitated by the wonderful Angie Lombardo, an MPS I parent herself. Consider this your invite to take a break, and build meaningful relationships with others walking a similar path.
Thursday, October 26, 2023
We’ll meet from 5-6:30pm PST (8-9:30pm EST) on Zoom.
This is a judgment-free zone focused on mutual understanding and support. It’s completely free for Canadian MPS Society members – Just bring your open heart.
Register now on Eventbrite to receive the session link >>