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Small Bowel Dysmotility?


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I have this also and I think the consensus among GI docs is to use the same mades for gastroparesis (erythromycin, domperidone, etc.). I've also been advised to stay on a gastroparesis diet (small, frequent meals, low fiber, low fat, etc.). Another thing that helps is to keep your colon moving properly. I use milk of magnesia regularly.

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Hi Angela,

My son consistently has this- nexium, eyrthromycin, no dairy, and a gastroparesis diet helps him. I have it intermittently, the severity waxes and wanes for me. Controlling the reflux with ranitidine and using mega doses of Miralax keeps me feeling "normal."

I have consistently been told that the symptoms are identical to gastroparesis & the treatment is the same.

Is yours acting up? Have you tried the Miralax yet?

Julie

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Truly changed my life. I take a lot- all at night and a half phenergan to deal with the tiny bit of nausea it gives me. The phenergan helps me sleep too. In the AM, I have my coffee, and feel nature's urge :rolleyes: right after. I take around 3 doses at once now. Start with whatever dose your doc recommends. It takes a few days before it starts working. When it does- it's a miracle.

If you like sweet drinks, easy to hide in juice or soda. I hate sweets, so I have it in water flavored with lemon- not bad. My nighttime toddy :P. Yum Yum.

Good luck! I have found that once you get things moving anywhere in your GI tract, the whole thing moves :unsure: Sam's club is the cheapest place to buy it. They even have their generic form called "Clearlax"- works just like the named brand.

Cheers-

Julie

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Guest tearose

Okay cardiactec, maybe more than you want to know...

I dislike using miralax all the time for concern that it doesn't allow me to control my sphincter and I have then had accidents. Horrible "blow outs" in my pants. It is NOT diarrhea, it is just not giving steady, controllable movements. I apologize if you don't want to know, it is just the way for me, so I thought you want my experience.

I use miralax, only as needed and only when I can be near a bathroom.

Instead of getting to a stuck place, I try to get little fiber doses all day in various food sources and chewable tablets.

I was in the hospital just last May with a Small bowel obstruction. The thought was it may be from scar tissue/adhesions. I have done no official follow up since then, I have just been doing all to manage on my own. I did okay for a long time with occasional flare ups and I too did the small frequent soft meals. I also massaged the lower left pelvic area that feels like it "kinks" up.

I am due for a review since I'm having more problems with pelvic/bowel pain recently. I hadn't considered the small bowel dysmotility could be the dysautonomia. I'll have to discuss all with the doctor.

My "new" GI appointment is this Monday and I'll tell you more after.

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none of my docs have made any prediction about the future of my motility... it waxes and wanes. Miralax does help too, along with avoiding large meals. Walking helps too.

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