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Old 05-05-2010, 02:02 PM
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MelodyL MelodyL is offline
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Join Date: Aug 2006
Posts: 8,292
15 yr Member
MelodyL MelodyL is offline
Wise Elder
MelodyL's Avatar
 
Join Date: Aug 2006
Posts: 8,292
15 yr Member
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Quote:
Originally Posted by kpRN View Post
Just to re-cap....I was diagnosed with mixed axonal and demyelinating peripheral polyneuropathy on my 50th birthday (although I was having symptoms as far back as 1996 or 14 years ago.) I was initially put on Neurontin 300 mg at bedtime. Around the first part of April 2010, I started to experience severe burning on the palms of my hands and in my fingers. This was unlike any burning I have ever experienced. Just air circulating would send me into a frenzy. I could not stand to touch anything or have anything touch my hands. I went to my GP because my neuro is 150 miles away. He gave me a "burst" of steroids, started me on Cymbalta 30mg to start and now 60mg, and increased the neurontin to 600 mg at bedtime. After about 7 days, the burning started to decrease and has eventually disappeared. I wonder.....was it the steroids, the Cymbalta or just the PN coming and going as it usually does?

Another weird thing, I have begun to have feelings like electrical shocks in my fingers and toes. Very painful for the few seconds that they last. I haven't figured out if anything exacerbates them, just know that it hurts like heck.

My main reason for posting is an unpleasant side effect, possibly from one of the meds. I am having terrible constipation as of the last month or so. I eat very well, I walk 3 miles at least 3-4 times/week and I am trying very hard to increase my fluids, especially water (yuk). Just wondering if anyone else has experienced this with Neurontin or Cymbalta?

I do have an appointment with a neuro at Cleveland Clinic on June 14th. He specializes in neuropathy so maybe he can shed some light on this "idiopathic" booger that is wreaking havoc on my (our) life. Will share what I find out after the appointment.

Until then......I want you all to know that this forum serves as a source of comfort to me. (not to mean that misery loves company, at all!!) I check in daily to see how everyone is getting along. Your words of encouragement and advice to each other warms my heart. I am fighting this as hard as I can and remind myself often that there is strength in numbers.
Hi.

I have friends who try Miralax and they said it works wonders.

I myself do the benefiber thing. Two teaspoons in my coffee in the morning, and two teaspoons in a glass of water in the pm. You would NEVER know you are taking this stuff. It is clear and dissolves completely. You just can't put it in any kind of soda. So I use a packet of something called True Orange which are crystals and pour two little packets in a glass of water, and BAM, you have an orange drink with no sugar, no nothing. Very refreshing. I add my benefiber to this.

I do take stool softeners sometimes, but no laxatives. I GO EVERY DAY.

so give it a try.
Melody
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"Thanks for this!" says:
DejaVu (05-29-2010), kpRN (05-06-2010)