I saw most of it earlier tonight but, it brought me to tears as my girlfriend and I talked about what I have done in front of her. Not including all the ones I had b4 my meds helped control them alot better. I used to have 1 or 2 a month if not more and everytime I had to start over trying to remember things, such as where I am, what was I doing and so on. Its very depressing when I heard that there is more of us than people w/ M.S. and they mentioned 2 others as well that are high on the list of disabilities. And they said we amount for all three Combined if not more. So why havn't they found a C.U.R.E yet? It has been know since biblical times about people w/ our problems, So wheres the help? All over seas being spent on Wars that arn't even our buisiness to have to commit to. Men and women are returning a nd having Epilepsy when they return. Whats that? Our goverment should be taking care of it's own citizens first, especially those that have
helped make our contries what they are today. Then help those other Countries in need of True Help. Epilepsy does effect every continent I know but, if we spent the money that these "Fake" Medical Equipment Operations on a Cure they would make alot of progress. 60 billion is alot of taxpayers money going into the hands of some greedy People of all walks of Life....
____________
From: bwm78640 <bruce903@hotmail.
To: epilepsy@yahoogroup
Sent: Sun, October 25, 2009 6:17:00 PM
Subject: [epilepsy] Re: CBS 60 Minutes - Sunday, October 25th, 2009
Bumped up...
If you watched it, please post some feedback.
Bruce
--- In epilepsy@yahoogroup s.com, "bwm78640" <bruce903@.. .> wrote:
>
>
> Hello everyone, I found out about something just last night that I'd
> like to bring to everyone's attention. On Sunday, October 25, 2009 the
> CBS - 60 Minutes is supposedly going to air a segment on CURE and
> epilepsy. For those of you who don't know about CURE, it is the
> nonprofit organization, Citizens United for Research in Epilepsy, and
> you can find out more about this organization through their website, at
> http://www.cureepil
>
> This will be the very first time I have ever heard of, or even seen,
> in-depth information about epilepsy being aired on nationwide
> television. Which in my opinion and how I've seen things, means that the
> Epilepsy Foundation of America did not have anything to do with this
> upcoming presentation through the media.
>
> Now since this presentation is going to be shown on the CBS show 60
> Minutes, I would like to give everyone a "heads up" on how I've seen 60
> Minutes operate. 60 Minutes is usually scheduled to come on the air on
> the hour, such as 7 PM Eastern Time / 6 PM Central Time. However, if
> there just so happens to be some kind of sports game (football, golf,
> etc.) that has been scheduled to air at any point before the 60 Minutes,
> if the sports game last longer than expected, like if a game ends up
> going into overtime, what's being aired on TV is going to be lasting
> longer than expected. For example a game was expected to end at 4 PM,
> but winds up going into overtime and ends at 4:15 PM; what will follow
> is going to be the 30 minutes CBS Evening News, followed by 30 minutes
> of local news. If something like this does happen, 60 Minutes is still
> going to show their 1 hour-long presentation, but it will be starting at
> 7:15 PM Eastern Time / 6:15 PM Central Time. So for those of you who
> would like to record that 60 Minutes show on Sunday, October 25th, you
> might want to set your recorder for an extended amount of time, say
> maybe 30 minutes or 1 hour extra, in hopes of making sure that you
> record the entire 60 Minutes show.
>
> Bruce
>
>
>
> [Non-text portions of this message have been removed]
>
[Non-text portions of this message have been removed]
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