There are many well-established ALS/MND organizations in the US, UK and, Canada that focus on providing support for caregivers. But none that I’ve found in Europe or other countries. I’m often by our caregiving members who live overseas how they can connect with organizations that can offer help – – virtual, in-person or self-help programs (not fundraising or disease awareness).
If you know of ALS/MND-related (or any!) international organizations, please share names and links.