Understanding how we deliver support to our community through a structured approach.
Top of the mountain in Jasper, Canada – before the MND really had it’s teeth into my mobility.
Discover our commitment to advocating for not only research into Motor Neuron Disease, but we would prefer our role to be more hands-on relating to the dissemination of information to people and their families affected by MND, particularly as regards early planning and preparation if such a catastrophic event ever affects you or your family in the future.
Our Services
About Us
Founded by Andrew Marcovich and (Delaray) Paul Havemann, Andrew has firsthand experience living with Motor Neuron Disease since birth, although only formally diagnosed in 2003, his form of MND is genetic. Our mission is to assist patients and their families better prepare, far in advance where possible, to face the ever increasing difficulties which present themselves as the disease progresses.
