ability

  1. S

    Am I overreacting?

    Hello. I want to first say thank you for any information or insight you may be able to give me. I also wanted to say that my thoughts are with you all that have been affected by this disease. I am concerned due to a few reasons. About a week ago, I noticed something was "off" with my left foot...
  2. KarenNWendyn

    Legal signature stamp

    Question for those who are losing or have lost their ability to sign their name— is there a procedure for obtaining a legal signature stamp in the US? Is this something useful and worthwhile exploring? Looks like this problem is on the horizon for me. Thanks in advance.
  3. blitzc

    Recent Diagnosis

    Hello Everyone! My name is Cathy and am new here and trying posting for only the second time. Not so certain about how the rules and regulations work and feeling a bit apprehensive. What do I say to all of you? I am 53 years old and live in Ohio with my husband. We recently became empty...
  4. BlsdMama

    Glycine receptor antibody? Swallowing fluctuations?

    Anyone else been tested or positive? Curious. I'm positive and Mayo thought certainly a more rare variant of Stiff Person. However, thus far, have not responded to meds. My MND doc at our university thinks PLS. Mayo admitted this week that maybe MND is what it is afterall. But first we try...
  5. A

    Seeking communication support for special friend

    A special friend (David) of mine and my husbands is a 17-year survivor of ALS. David currently has a Tobii Dynavox I-15 (with eye gaze interaction – AAC device) speech generating device. His AAC device is calibrated to his eyes. David was able to communicate (with his wife and family, also with...
  6. Chincoteaguer

    Using the Hoyer for the first time

    I anticipate using the Hoyer lift within the next few weeks. My wife's ability to lift herself is steadily decreasing . We still managed to get her in a standing position but she is asking that I do most of the lifting. I was not at home when the lift was delivered so I did not get the...
  7. T

    Familial ALS

    Thank you for adding me/us to the forum. In brief, here is our story: My husband lost his mother to ALS when she was 59 years old. She had one aunt, one uncle, and two first cousins who also passed from ALS. There were a couple other family members who may or may not have had early signs, but...
  8. K

    Just looking for input

    Hi, I am posting about symptoms that I have been seeing in my father over the last 2 years. He is 73. He started having trouble swallowing his food about 2 years ago. He seen several doctors, and had a scope done, and it was brushed off as aging. He was told to chew his food better, and...
  9. F

    Muscle weakness, atrophy

    Hello all, First I would like to say my heart goes out to those struggling with this horrible disease. I’m writing today to ask opinions about my Dad’s situation. I will try to be brief, but thorough. Nov. 2017 - Dad swears he remembers falling while outside, and then getting up and moving...
  10. G

    Dirty but inconclusive EMG, family history, now bulbar symptoms

    Hi, I started a discussion here last September, right after having a mildly (but widespread) dirty EMG. I'm sincerely grateful for the support and encouragement I received from the PALS and other people in this forum, they helped a lot to get me trough a very dark phase of my life. I'm checking...
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