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  1. Bradkl
    09-04-2016 01:28 AM - permalink
    Bradkl
    So sorry if I offended you. I really did not have that intention but can see how this can be seen that way and that is my fault. I think that section of the site is indeed a difficult one for people to have to read anxieties of others that don't have the same or anything like similar problems and it is incredible that people even take time to read the posts let alone respond to stories like mine in hindsight. I really wanted to say thanks as you are so right and extremely caring to have responded and taken the effort to do so. I wish you love. Brad
  2. Scotiaspirit
    06-06-2016 10:58 AM - permalink
    Scotiaspirit
    I can relate to the F word too. Too often really. I was dx back in Nov 2015. Just this week, I can no longer reach my R-Hand to the mouth..... it happened literally overnight a few nights ago. I felt a sore numbness in my R arm the night before and my fingers got really spastic on my R hand. When I awoke the next morning, I have lost approx. 30% of the movement in my R arm, literally overnight. It is the constant change of having to mourn a loss of a movement which happens all too often now. This disease is tough on the psyche. A constant change in continuous motion. Hope you can keep your symptoms at bay for as long as possible. Scotiaspirit (Paul)

About Me

  • About faithandlove
    What's your relationship with ALS/MND?
    I have been diagnosed with ALS.
    If diagnosed, when was the diagnosis?
    06/2016
    City
    Reno
    State or Province
    NV
    Country
    US
    Biography
    Worked in court system for 35 years, married with two adult children, and four grandchildren
    Occupation
    Retired

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  • Last Activity: 06-03-2017 05:40 PM
  • Join Date: 05-22-2016

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