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    Jasia

    My wife Jasia passed away on March 3rd, just before this pandemic was a reality for all of us. I was out of the country when this happened and I was unable to be at her funeral (for travel restrictions mostly). Today, five years ago we got married. It was also around that time that she got...
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    Swollen upper lip

    I can't rule it out, but it does not seem like that is the cause. Her jaw muscles are weak, so very often her mouth is open (since she is unable to close it). It might be that. I was just wondering if anyone here has had any similar experiences.
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    Swollen upper lip

    For a few days now, my wife wakes up every morning with a swollen upper lip. She has a trach for more than a year now, so there's nothing touching her lip during the night. I wonder if anyone else has a clue about this, there seem to be no other symptoms (i.e., not swelling in other places, no...
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    Behavioral changes

    My wife was diagnosed two years ago, and the progression has been quite fast. Right now she is almost completely immobile, has a PEG and a vent since a little more than a year. She used to be really smart, both in the academic and the emotional sense, had a great sense of humor, and used to be...
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    Dreams

    My wife also talked/threw punches etc. in her sleep often prior to diagnosis. She also grinded her teeth a lot. I have no idea if these things can be related, but it is interesting to see that others had the same.
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    A podcast about a PALS

    Hello, I came across this episode of a podcast that I sometimes listen to, in this episode they interview a young ALS patient: https://gimletmedia.com/episode/88-second-language/ The story starts around 16 minutes in. I would love to hear your impressions about it.
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    Vent and trach

    My wife was trach´d in April, and had the PEG since November of last year. She is now almost 24/7 on the bed. She has not lost a lot of weight recently, but has severe constipation problems.
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    Don't mean to hijack...

    I have also feel that at times I am not as afectionate as I could be to my wife. I feel that this is because, as the main caregiver there are already a lot of things that I have to do for her (including handling -for lack of better terminology- multiple body secretions), to on top of that being...
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    Losing myself

    When my wife was diagnosed, I did some research about this disease and the first thing that you learn is that "The average survival from onset to death is three to four years". Of course this does not cover the fact that if the patient is ventilated and feed thru a tube, they can live many more...
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    no words

    Sorry to hear about your wife. I don´t have a lot to contribute, but I can relate of having a (relatively) young wife affected by this disease.
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