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Subcommittee on Neurological Disease committee They just celebrated their first year here in Canada. As far as what they are doing, I couldn't answer that. The contact I have with them is more with Team Fox, and that's on the organization and planning of golf tournaments and getting supplies from them. I talked to them to see
November 16th, 2010Committee meeting
Greg McGinnis
Subcommittee on Neurological Disease committee What's missing or needed? I think I would go back to this drug plan. I look at the cost of some of the medications; thankfully I have my own coverage, but I do know people who don't have coverage. They're not getting the medications and they're living a very hard life. I think
November 16th, 2010Committee meeting
Greg McGinnis
Subcommittee on Neurological Disease committee I don't know if it would be common with other Parkinson's patients. I guess each company benefit program is different. I was lucky with mine. I have an unlimited amount of drug coverage, but my wife, on her plan, only has $3,000. To get the Botox formula this time around would
November 16th, 2010Committee meeting
Greg McGinnis
November 16th, 2010Committee meeting
Greg McGinnis
Subcommittee on Neurological Disease committee From my end of it, to have something like that covered would be phenomenal. Right now my drugs are covered through my benefit package, but to have something like that covered would be phenomenal.
November 16th, 2010Committee meeting
Greg McGinnis
Subcommittee on Neurological Disease committee He's pretty awesome.
November 16th, 2010Committee meeting
Greg McGinnis
Subcommittee on Neurological Disease committee As far as support goes, I've had somebody come to my house to teach me about, to help me with, the swallowing issues I have. In terms of accessing support, within our communities it's pretty good, really. We can get in contact with the proper channels. They'll come out and assess
November 16th, 2010Committee meeting
Greg McGinnis
Subcommittee on Neurological Disease committee Good morning. Thank you for allowing me to be here. Fifteen years ago, I would never have dreamt of sitting here to talk to you about Parkinson's. I was diagnosed six years ago, and they told me I have had it 10 years plus, so that puts me back in my 20s. When diagnosed, I wasn
November 16th, 2010Committee meeting
Greg McGinnis