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Advice for new PEGers.

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    Advice for new PEGers.

    If like me you have well meaning carers who syringe copious amounts of air along with your meds help is at hand. Get an empty syringe, I use a 60mil, take the plunger out and screw onto end piece. Lie as flat as you can and raise the syringe straight up. Release clamp. Tense stomach. Hear a satisfying blop in the syringe. Repeat as required. Get someone to help if any of this is beyond your capabilities. We are locked in not out. Stay Strong. πŸ‘πŸŽ—οΈπŸ™πŸ€—xx
    Bulbar started Jan 2020. Mute and 100% tube fed but mobile and undefeated. Stay Strong πŸ€—πŸ˜˜πŸ€—πŸ˜xx

    #2
    this is just a new way of farting. admit it

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      #3
      Or tell your carers *not* to pump you full of air in the first place, it's uncomfortable and shouldn't happen... It's easy to expel air from a syringe beforehand!

      πŸ€—πŸ˜˜
      ​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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        #4
        I have told till I'm blue in the face. You can lead a horse to water......... 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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          #5
          Sometimes I've noticed some bubbles coming through. Stephen loves the idea of extra wind. He has no shame.

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