Events
MPS Members find events are invaluable for connecting with the MPS community, sharing insights and experiences and knowing they are not alone in their journey.
Upcoming Events
We Care October
An evening of candid conversation and camaraderie facilitated by the wonderful Angie Lombardo, an MPS I parent herself…
Past Events
Recordings, presentations and photos from our past events can be found here. Select any of the event postings to access them.
MPS Cup Anniversary Celebration
We want to extend our deepest gratitude to everyone who attended, volunteered and donated to the MPS Cup event supporting those affected by MPS. Your participation made our event a huge success. If...
We Care – June
Join us at We Care – a Gathering for Parents and Caregivers. – A NEW DAYTIME SLOT. 10-11:30 AM PST. (1-1:30 PM EST)
May is the month for MPS awareness!
Every year May 15 is observed internationally, to raise awareness against mucopolysaccharidoses (MPS). MPS are rare genetic disorders in children and adults caused by the absence of a specific...
We Care – April
Join us at We Care - a Gathering for Parents and Caregivers. Following great feedback from the last We Care - a Gathering for Parents and Caregivers, online session for our members: the Canadian MPS...
You’re Invited to “WE CARE”
Join us on Wednesday, 25 January, 2023. A Gathering for MPS Parents and Caregivers
November Fireside Chat
The Canadian MPS Society will be hosting a series of online “Fireside Chats”, providing an opportunity for our members to connect with each other in an informal confidential space to share personal...
Canadian MPS Society AGM
The 2022 Canadian MPS Society Annual General Meeting will be held on: Monday 26 September 2022
Canadian MPS Society National Family Conference
This popular event takes place every 2 years. This year's is scheduled for July 21 - 23, 2023 in Calgary Alberta. See our National Conference page for more details!
2021 National Family Conference and Gala
Our bi-annual conferences give families affected by MPS & related diseases an opportunity to learn about new research, treatment and care, and to share information and experiences with other...
Resilience in Rare Diagnosis
As part of the Virtual Education and Connection Series, listen to our very special speakers talk about their unique and resilient stories regarding a rare disease diagnosis....