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Neuromuscular Electrcal Stimulation (NMES)

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    Neuromuscular Electrcal Stimulation (NMES)

    Does anyone have experience of a Mollii suit?
    I guess we all suffer from dysphagia to some degree. Has anyone visited Vitalstim in Staffford?

    #2
    Would get one if they worked. Is that a flying pig in one?
    Copyright Graham

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      #3
      Could you say that again in English please? πŸ€”πŸ˜‰πŸ˜„πŸ‘xx
      Bulbar started Jan 2020. Mute and 100% tube fed but mobile and undefeated. Stay Strong πŸ€—πŸ˜˜πŸ€—πŸ˜xx

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        #4
        You know what, Bob, as long as something doesn't harm you and you want to try it, go ahead.

        It is highly unlikely that NMES will make any difference to your swallow, but if you have money to burn and it would make you feel like you're at least trying something and, providing you've researched it, go ahead. It can improve function in stroke patients, but their motor neurons are not dying or dead.

        If you have very bad spasticity, apart from buying the rather expensive Mollii suit, your GP can prescribe meds which work.

        Do your research and decide how you want to spend any money you may have, not forgetting holidays etc.

        Love Ellie.
        ​Diagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
        Eye gaze user - No functional limbs - No speech - Feeding tube - Overnight NIV.

        ​

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