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Thread: Parkinsons Disease

  1. #1
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    Parkinsons Disease

    Do any of you have Parkinsons?

    I was diagnosed yesterday after 18 mths of various medical appointments.

    Much to learn now.

    I'm already involved in 2 DVA Health/Fitness programs and have to start another physiotherapy class with Gold Coast University Hospital.

    A bloke will be as fit as a mallee bull.

    Den

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    No advice for you, RB, but 'All the Best'!
    'sit bonum tempora volvunt'


  3. #3
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    NavyDiver is offline Very Very Lucky! Gold Subscriber
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    I saw and know several long term Parkinson's survivors in my prior Medical admin/management role. I am not Medical!!

    Good news was treatments are getting better rapidly! Better news was some of the LONG term I refer to was 20+ years!

    Best of luck and chin up always mate.

  4. #4
    BradC is offline Super Moderator
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    I don't but my Grandmother did. She was being treated for severe osteo arthritis and Parkinsons. Her initial Osteo medication was seriously effective against her Parkinsons. When they moved her to different meds to treat her Arthritis her Parkinsons escalated and they wouldn't give her both the old and new. That was 11 years ago, and treatments are getting better but there's still a lot they don't know. Best wishes and a crapton of profanities in the hope you don't need them.

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    Only what I've read. And that would be out of date. It's a tough break, Den. I hope you have good support.

    Make of this what you will. I only include it because since I gave up my alcohol abuse this guy has helped me turn my life around big time. Maybe he will have something of use for you. Best wishes,

    ​JayTee

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    Sorry to hear your diagnosis. My wife was diagnosed early this year and we are both making adjustments to our lives. She qualifies for some assistance from My Aged Care, but actually getting some has involved a lot of time on phone calls and chasing round many different agencies. The medication she was put on takes a while to have any effect, unfortunately, and only slows it down. We did find quite a bit of useful information from an organisation called Fight Parkinson’s (1800 644 189), which included support groups in our area. Suggest you give them a call if you haven’t already, the lady Jeannie spoke to spent nearly an hour with her and then sent an email with plenty of information. Sadly it seems there is no cure, we just have to find a way to manage it, hopefully in a way that we can still get some enjoyment from life.
    Hope you find the support and care that you will need, and that you are able to cross off a few items on your bucket list.
    Best regards,
    Woolly.

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    Thanks Wooly and to the others who replied.

    Changes to lifestyle and social platforms have to happen and some already have occurred. The community response is very good and help/support groups are offering their assistance.

    I'm only dealing with early onset which hopefully can be maintained. The medication I am taking is Kinson , 2 tabs/day increasing to 4 , hoping to avoid side effects.

    I'm still hoping to go on a world cruise this time next year and I should be good at shuffleboard.

    Den

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    Quote Originally Posted by ramblingboy42 View Post
    I'm still hoping to go on a world cruise this time next year and I should be good at shuffleboard.

    Den
    Love the sense of humour there, Den. With that attitude you'll be fine.
    ​JayTee

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  9. #9
    Roverlord off road spares is offline AT REST
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    Quote Originally Posted by ramblingboy42 View Post
    Thanks Wooly and to the others who replied.

    Changes to lifestyle and social platforms have to happen and some already have occurred. The community response is very good and help/support groups are offering their assistance.

    I'm only dealing with early onset which hopefully can be maintained. The medication I am taking is Kinson , 2 tabs/day increasing to 4 , hoping to avoid side effects.

    I'm still hoping to go on a world cruise this time next year and I should be good at shuffleboard.

    Den
    Hi Den so sorry to be reading this, I know where you are coming from, Parkinson you do have a longer life, I wish Mario had it instead of Multiple system atrophy. I know so many people that was told Parkinson and later a few years later it turn up to be MSA because of the rapped decline I know this because Mario and I are on the MSA FB, and one guy that use to go to physio where Mario did, was told Parkinson and 3 years later they changed it to MSA. MSA you have life 6-10 years with it Parkinson you can live 20+ years with it. Mario took Kinson and really in the end a lot of meds they use where for Parkinson, as they dont have any really suits MSA. Are you able to get on NDIS. You have to be under 65, you will need to get an OT and a physio that deals with neuro. Talk to your doctor about this. Heather


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