I have interviews from family members, of those who lost their - TopicsExpress

I have interviews from family members, of those who lost their battle to MND & research on Motor Neurone Disease, accumulated during university. I need one last thing: An interview with someone willing to talk to me about living with MND. I could NOT believe this insidious & cruel disease was near the bottom for grants & donations. This is due to cost/benefit analysis. Simply put NOT ENOUGH PEOPLE DIE FROM MND to warrant government funding. So good one you Mr. Daniher & Sharnie for speaking out & giving MND a Voice. Public donation is incredibly important. It is strange that the positivity of these people, the unwillingness to cave in to MND/ALS, has inspired people to support the fundraising for MND research. So make bets with friends, grab a few bags of ice and have an ICE BREAKER FUNDRAISER. Just like Kermit.

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