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#1 | ||
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Junior Member
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Hi everyone:
This is a bit of a sensitive topic so hope it's ok to discuss here. My H has PPMS and is in a wc most of the day. So far he can still stand laittle, but can't walk. Can transfer, toilet himself. He doesn't have constipation or loose bowels so that's not a problem. In other words he's not incontinent. I know bowel issues can come as ms progresses. Does anyone here have problems in this area and does a bowel program and taking certain meds really help? I just want to understand and be prepared. thanks! |
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#2 | |||
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Senior Member
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I sit a lot but not in a wheelchair. I just use Miralax as needed.
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#3 | |||
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In Remembrance
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Sometimes the meds he takes may cause diahrea/constipation. I eat Activia/yogurt every other day and it seems to keep me regular.
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ Last edited by SallyC; 07-27-2011 at 01:02 PM. |
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"Thanks for this!" says: | dmplaura (07-27-2011) |
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#4 | |||
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Wise Elder
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I started eating yogurt daily. I had to play around with brands until I found the one that worked best for me. Additionally, when I get "backed up" eating canned pears has been the best for me. I swear by them and I know others on here have mentioned having success with the canned pears. Plus, it's "natural" and has vitamins and nutrients we need anyhow. I also found that the canned pears worked the fastest, faster than any of the stool softeners I have used and prunes or prune juice.
This is an issue for many of us MSers and I know others will be along with suggestions and things that have worked for them. |
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"Thanks for this!" says: | dmplaura (07-27-2011) |
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#5 | |||
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Senior Member
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i eat yogurt too! Had not heard about canned pears, thanks. TK.
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"Thanks for this!" says: | dmplaura (07-27-2011) |
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#6 | ||
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Junior Member
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Thanks for the tips! I hadn't heard about the canned pears. H takes Accuflora and eats yoghurt. So far so good.
Appreciate any more info anyone has. ![]() |
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#7 | |||
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Elder
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I have occasional urge incontinence from both ends...comes on suddenly. I am RRMS though, and was dxd with IBS years ago, which is bothersome.
It is one of the more aggravating symptoms, since it makes me hibernate in the house, afraid I'll have an accident while I'm out.. ![]()
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Instant Karma's gonna get you-gonna knock you right in the head...John Lennon |
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"Thanks for this!" says: | dmplaura (07-27-2011) |
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#8 | ||
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Junior Member
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I eat Yoplait Plus yogurt almost everyday. So it doesn't get so boring, I sometimes add some granola or fresh fruit. I eat prunes every now and then...keep them in the fridg. It also helps to keep hydrated.
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#9 | |||
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Grand Magnate
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Dried Apricots are a nice change once in awhile
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Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
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#10 | |||
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Magnate
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Yogurt, Fiber One bars daily. Drink a LOT of water (as much as possible). Metamucil "Simply Clear" for more fiber in the diet.
I eat a lot of vegetables too - as much as I can get. I eat 1 apple daily. With my yogurt (daily too), I combine raisins and other dried fruits - sometimes prunes and dried apricots, plus a few pineapple tidbits. Magnesium supplements. I drink at least 2 liters of water daily, and at least 30g daily of fiber in the diet. I take stool softener when it gets to the point that I've literally gone days without movement. I have difficulty having a regular BM, period. I don't know what to do myself at this point. I've followed all the suggested methods! I believe mine may be more related to my medication, versus the MS.
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2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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"Thanks for this!" says: | SallyC (07-27-2011) |
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