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I'm glad your docs are working on it and it's not a stroke Momma. Have you had any med changes lately? Are you sleeping okay? Do you feel different? Did you just start slurring? I don't know where I'm going with all the questions . I hope someone has an answer for you.

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I wonder where I can research problems with speech. It's not as easy as it would seem. I was taking 30 to 40 mgs. of Oxycontin 3 times a day for good coverage of my pain. Also Xanax - which was changed to Ativan - and 21 mgs of mirtazipine. The doc seemed to think it was the pain meds and wanted to put me on a Fentanyl patch for even better pain coverage....but somehow I was afraid of that. Pain specialist put on MS Contin 30 mg and hydromorphone 4 mg for breakthrough pain and she is VERY strict. This really does not begin to cover my back and knee pain but I refuse to take more because I am just afraid of the effect it could have on me. Has anyone heard of long term pain meds causing problems with speech??? Momma

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In answer to Confused questions.....I have developed some sleep problems........I do feel different......the slurring and trouble pronouncing certain words began suddenly, I think, about a year ago. I had severe pain problems, but the thing that was driving me f------ crazy was a type of Akathesia. Have Restless Leg Syndrome and it seemed to effect my whole body....24/7.....the only relief I seemed to get was when I was sleeping. Xanax used to relieve it but that stopped being effective soon. I am presently taking a new drug meant for RLS....Horizant 600 mg time release once a day. (Gabapentin plus another drug) It has made it clear that the Akathesia was definitely connected to the RLS but it comes with it's own set of problems. I have a few good days, then a few bad with nausea, fatigue, and shakiness. But it is worth ANYTHING not to have the Akathesia. My life is so diminished by all of these problems. I cannot take proper care of my house and garden or have much social life at all. I constantly worry about bad things happening. Thank you so much for anyone bothering to read this drivel and to Confused especially for trying to help me.

Momma

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Confused says: I think your questions might get lost down here.......do you think I ought to be posting somewhere else instead of side effects? I can try that.....

I was just thinking you could start a new thread in this forum. Maybe it's a stupid idea. people may have already read Cuttle's post and not scroll down.

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  • 1 month later...

When I was slurring words in the beginning of everything when diagnosing the MI, it was becaused the pdocs had me dosed up on too much of everything. Things got better and I was more alert on lower doses. Currently I am on some different meds than before, but now i tend to stutter/stammer words a lot.

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