Glenn’s MND Fundraiser
Donation protected
Hi my name is Ben this page has been set up to assist my cousin Glenn Cogan with his fight with MND.
This page has been set up as a result of people wanting to not only support Glenn in terms of his medical costs but also Glenn’s wish to also raise funds and awareness for MND research. As such 50% of all funds raised here will be donated to Macquarie University to assist in funding Professor Rowe’s MND treatment research. The other 50% will go towards helping Glenn’s fight including equipment, trial medications etc.
Glenn’s story:
Earlier this year Glenn was diagnosed with Motor Neuron Disease (MND). He has already lost use of his legs and only has minimal use of one hand, recently his speech has also started to decline.
Most of you that are reading this will know Glenn Cogan if you don't he is an amazing Dad to son Finn and we think a pretty good Husband to Mel. Glenn is a very well-known creative having worked in major movie production, with NBN for many years, before starting Enigma with business partner Lisa to more recently founder of Toybox Films with business partner Aaron.
MND - Motor Neuron Disease is a disease which affects the brain and messaging through the body that affects movement such as walking, swallowing, talking and breathing. There is currently no cure for MND and life expectancy from diagnosis is sadly short. In Australia every day 2 people are diagnosed with a form of MND and each day 2 people die from MND.
Please support and share where possible ❤️
Organizer
Ben Neil
Organizer
Kahibah, NSW