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Lugnutz

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Posts posted by Lugnutz

  1. On 1/8/2017 at 2:20 PM, ChrisR said:

    And we in America have all learned that "Foster's" is how Australians say "Beer"!

    (Though in fact it sounded a lot more like "Beeyah" at the Woolloomoolloo Bar)

    According to a few Aussies I met, Fosters is garbage.

  2. An update for you from where I'm at currently.

    My landlords are God-like and can do no wrong according to me. I got a care package from them today and the whole family was here to celebrate. I'm leaving everything wrapped until Christmas because it would be a crime to open them sooner. I'm very patient and can wait.

    And I'm going nowhere and am here for life. This is the most secure I've been in a long time. It feels good. I'm rooted and comfortable.  Help is only a phone call away.

    Finances are tight but things work out. I get limited help which I'm eternally grateful for. I won't turn down help be it finances or something else.

  3. What to mention this time? It always comes down to money or the lack of same.

     

    The state decided to cut it's funding to help me. This means that I'll have zero income as of January 2017 even if I got only $200.00 per month before, it helped cover bills. This came to be because I am no longer with MRS (Michigan Rehabilitation Services) and they decided to stop my help there. This is what happens when you're honest. I got it to see if there was anything I could do reliably and ended up failing miserably in the end. I checked out several driving jobs this side of the state but never got past that point. I just didn't want it biting me in the backside if I did fib and messed it up. I'm still getting food help so my complaint isn't with that. It was the limited help I was getting from the state financial wise.

     

    I had zero use for Facebook two years ago before I was diagnosed but I can't live without it now. I originally got it as a sales tool for my Gofundme but sidelined that almost from the go for the MS information out there. A lot of good MS information is given and received and more importantly, friends that you can talk with that share this decease. Some of them are local. When I was finally diagnosed with MS (Multiple Sclerosis) in January 2015 I finally knew what the problem was and how unique it was to each person. I was getting worse and looked very bad. Not any longer. I figured this was my new start so go about it positively and not seeing the dark side as it was for several years before this.

     

    In the end, it comes down to funding and what little I've got.

    I know that it's not great for everyone out there. Can you help if you can?

    tongue.jpg

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