Do you notice constipation as a side effect of Parkinson's meds?

Posted by classylady71 @classylady71, Sep 12 8:20pm

This is my question: Is there any evidence linking clinical trial drugs with cancer? I did not have constipation or rectal bleeding until I was started on the Rytary. In fact, it was the opposite. I had fecal incontinence at times but there was no bleeding spotted ever.

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Thank you for asking I don’t feel quite as alone. About 2 yrs ago I began falling regularly so I went into my primary care doctor and he said it was Parkinson’s referred me to Neurologist he did some in office tests and sent me for an MRI that confirmed it. This is all unknown to me. He prescribed Amantadine. My biggest concern is my balance I was an avid walker and hiker for decades I don’t have the strength in my legs to go very far. I do balance exercises and ride a stationary bike most everyday. It feels like the disease is progressing slowly but steadily even though the exercises help. This here is a godsend being able to get information from others in the same boat.

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Profile picture for diparvij2359 @diparvij2359

My Gastroenterologist suggested using Myralax daily it really helps and now I’m basically regular

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Hello @diparvij2359, and welcome to the Parkinson's support group on Mayo Connect. Many with PD do have problems with constipation.

How long ago were you diagnosed with Parkinson's? Are your symptoms well-controlled now?

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Prune juice works along with the Mediterranean Diet, be careful of too much sodium found in most foods Read labels, especially with processed foods, including red meat, Return to basic foods.

Research this: Keep total salt to 1500-2000 mg daily. If possible, exercise a hour per day. Stretch. Stay off the couch and TV where most programing and news centers on "people hurting people". Instead as you read or just doing t he dishes, listen to soft piano music found on YouTube.

here is no perfect answers, for sure.

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Profile picture for diparvij2359 @diparvij2359

My Gastroenterologist suggested using Myralax daily it really helps and now I’m basically regular

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So did my husband’s hematologist and it has really helped him. They also have the little travel packets when are very helpful.

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prune juice and dried prunes...use only as needed. Experiment.

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My Gastroenterologist suggested using Myralax daily it really helps and now I’m basically regular

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Actually, constipation is one of the symptoms that is ongoing. Of course, medication can add to it. I have a Yeti filled with water wherever he goes. At home, I will put out 4 oz. of water in a small cup as he has a hard time remembering how much he has drunk. I just started this a couple of weeks ago. He is drinking more and he is having less constipation. He does not even realize that he is drinking more. He was showing me his abdomen and saying" Look I have a softer stomach". Of course, I smiled.😊

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I think that's pretty much a given. Try asking that on "myparkinsonsteam" where it's a constant complaint from new members. I distinctly remember seeing a GI doctor in the 2000's, was treated unsucessfully for many years (30 or so years), and not diagnosed as a Parkinson's sufferer until 2021. The MPT, as members call it, offer their own personal constipation treatments, obviously having found none suggested by the medical profession.
Right now I'm in limbo, trying to fix a mess-up caused by a hospital stay.

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