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All I can say is I had an horrendous time recently with constipation I was in tears β¦. My hubby said our marriage went up another levelββββββ
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I have trouble getting carers to wash let alone touch my private parts, which can be smellier than my pits. π©β οΈπ·πxxLeave a comment:
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Ellie thank you for your insight, I guess experimentation is the way to go. Starting this evening π₯΄Leave a comment:
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Rosemary6NT It can take a few days to get into a rhythm with any laxatives, which combination, which dose, when to take them etc - but persevere and it'll pay off.
My bowels used to rule the running order of my day (and night) and, for months, was the worst feature of having ALS for me. I knew my bathroom intimately - I knew how many tiles were on every surface π I was spending way too much time on the loo, getting stressed and even tearful...
It took about 2 weeks before I landed on a 'productive' regimen of a softener (my magic pink Docusate) and a pusher (Senna). My core is weak, making it difficult for me to push, hence the combination, and I don't go every day but 3-4x per week. Any little thing can throw me off, so I take a precautionary Movicol if needed.
Could the carers tie a scarf around your middle when you're on show? It must be harder to go in a commode pan but, I wonder... did you ever put hot water in the pan to try and relax things?? Obvs not touching you bottom!
All the best for getting a routine my lovely and you're certainly not alone π€π€π€πLeave a comment:
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Deb thanks. I have just put in an order for a variety of products! The worst thing is hanging in the toileting sling with your nether regions exposed to all the world. π³π±Leave a comment:
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Oh goodness.. this struck a chord Rosemary6NT . I find the indignity of having to be helped to the loo , albeit by my hubby, really hard.
I can't use toilets when out so it stops us having long trips. I used to take imodeum to stop me going and I still do when we fly but its really not a good idea as it makes you really constipated. It just stops the worry if you have an unavoidable appointment or occasion.
My MND nurse says it is trial and error with laxatives and hopefully you should find a routine that works for you. Im not quite there yet !!
Love Debbie xLeave a comment:
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Betty May thank you. Thereβs no such thing as too much information on here, all gratefully received xLeave a comment:
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Is that code for sodium picosulphate? ππOriginally posted by matthew55 View PostLeave a comment:
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It was something that always bothered my husband. Morphine sulphate and immobility led to constipation and he had to get an enema, thereafter he would have one laxido a day and that seemed to be OK for a while. Made sure he was drinking regularly. Then the diarrhoea started, apparently for no reason that we could ever work out. Every week or ten days he would have what we would refer to as a 'clear-out' day but the rest of the time it would be normal bowel movements.
It was tricky but because I was with him nearly all of the time he could get to the loo when he needed. Once or twice I had to abandon shopping, rush home, help him to the loo and then go back shopping again! There is no way that he could have managed his toilet needs on another person's schedule as it was so irregular.
My husband's core muscles became weak quite soon after diagnosis so our nurse advised us that the softer the stools the easier it would be to pass them so we tried to keep that in mind with his diet and drinking.
It was quite common too for him to feel as though he needed to go, but when it came to it he either couldn't or didn't really need to.
Hope the above not too much info
Hope you ladies get a solution soon that works for you xx
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