Hi, any suggestions for dealing with trapped wind. I feel like I need to pass wind but cannot. This is a regular occurrence. I spend almost all of my day sitting ( can’t walk any longer) which I suspect is not helping. Bowel movements are not as regular as they used to be which causes some challenges. GP has prescribed Sodium picosulphate, cosmocol and micro enemas to help with number 2s. Just need to resolve the trapped wind to be able to relax.
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Originally posted by Miker View PostGP has prescribed Sodium picosulphate, cosmocol and micro enemas to help with number 2s.
I have a feeding tube so I can vent my stomach, but peppermint tea or ginger can help too, as can massage and heat. xx
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.
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Originally posted by Miker View PostHi, any suggestions for dealing with trapped wind. I feel like I need to pass wind but cannot. This is a regular occurrence. I spend almost all of my day sitting ( can’t walk any longer) which I suspect is not helping. Bowel movements are not as regular as they used to be which causes some challenges. GP has prescribed Sodium picosulphate, cosmocol and micro enemas to help with number 2s. Just need to resolve the trapped wind to be able to relax.Diagnosed 18th May 2021 with sporadic ALS. Limb onset. Terrified of not being able to breathe easily.
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Originally posted by Ellie View PostI have a feeding tube so I can vent my stomach, but peppermint tea or ginger can help too, as can massage and heat. xx
Diagnosed October 2020 - See my blog at https://www.myneurodiary.com
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Originally posted by Ellie View PostMike, I presume you don't take all of the above at the same time - abdominal pain, bloating and flatulence are common side effects with laxatives (as if we were not uncomfortable enough already 😟)
I have a feeding tube so I can vent my stomach, but peppermint tea or ginger can help too, as can massage and heat. xxDiagnosed July 2020, ALS bulbar onset. PEG and ventilator (mainly at night), and pretty poor speech, but legs still about functioning!
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Originally posted by Heather R View PostEllie by venting do you mean the air just bubbles up when you do a PEG feed?
There is a technique to it so as the stomach contents stay put and just the air is released, but basically an empty 60ml syringe, minus its plunger, is attached to the feeding tube, held up higher than the stomach, clamp is opened and the air can escape for instant relief 👍👍
If you have a PEG Nurse or maybe a Dietitian, and want to ask them to show you or tell you about venting your stomach when you have wind, fire away. xxDiagnosed 03/2007. Sporadic Definite ALS/MND Spinal (hand) Onset.
Significant bulbar impairment - No functional limbs - No speech - Feeding tube - Overnight NIV - Eye gaze user.
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