That being said I think the right attitude to take is to say that I’m Living with ALS, not dying from it. So from here on out I’m going to do what I’ve always done. Live life to the fullest! There are so many emotions that I go through when I think about this. I go from angry to sad, to pissed off to afraid, to totally numb, and then I have those emotions all over again. For the past month, I thought the doctors were going to tell me that I had ALS, so getting the news today wasn’t a total shocker, but it does still mess with you. I’m trying to stay as positive as I can but if you call me on the phone or see me out and I seem a little off you’ll know why.

I’ve started building this website so I won’t have to have the same conversation over and over as it gets tiring talking about this. I feel that being able to share what’s going on in my life whether that be good or bad will still be informative for everyone out there that is affected by ALS directly and indirectly.

That being said I’m going to need help…



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