Announcement

Collapse
No announcement yet.

Advice for new PEGers.

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

    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
    when i can think of something profound i will update this.

    Comment


      #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.
      Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user
      .
      ​

      Comment


        #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

        Comment


          #5
          Sometimes I've noticed some bubbles coming through. Stephen loves the idea of extra wind. He has no shame.
          when i can think of something profound i will update this.

          Comment

          Working...
          X
          👍