Peripheral Neuropathy vs Nephropathy
Has anybody heard of having nephropathy before diagnosis of diabetes? Where can I find documentation of this? Thank you
Interested in more discussions like this? Go to the Neuropathy Support Group.
Has anybody heard of having nephropathy before diagnosis of diabetes? Where can I find documentation of this? Thank you
Interested in more discussions like this? Go to the Neuropathy Support Group.
@tigreyes2004
I don't remember what every med I tried, but Lyrica is one that had dramatic side effects. I was incoherent, had some stroke symptoms, tachycardia, memory loss - enough to alarm the ER doctor so they admitted me. The last med I tried was desipramine, and I had to urinate up to 24 times a day - not an acceptable side effect. I started taking imipramine last Sunday, and so far no bad side effects, and it seems to be working on my foot pain. Cross my fingers.
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1 ReactionKeep me posted on how you do on that imipramine please. I notice since I'm on the Cymbalta that I urinate like your doing. I wonder if that is a side effect. My kidney dr. told me I had to have my electrolytes checked being on this med. I hope that pill works for you.
I have Stage 3 Kidney disease and shattered my ankle in 2011. I was told a few years ago that I have Peripheral Nephropathy, so cannot take anything for pain but Tramadol, doesn't help the pain much, and wondered what else there is. I heard from my Kidney Doctor that Medical Marajuana is ok because it is natural, but have not tried that yet. Also have Diabetes now.
I was just in the Henry Ford Hospital with pneumonia and someone sent a neurologist to see me. I was diagnosed in October 2015 with guillian barre. He said something to me that stuck in my head. It was something to the effect of I will most likely get polyneuropthy since I had guillian barre. Can anyone give me more info to help me understand??? My local Doctors just really do not have a clue.
Hi @sandyhill, Welcome to Connect. I found some information that may provide some help in understanding the condition.
University of Chicago - Guillain-Barré Syndrome / Acute Inflammatory Demyelinating Polyneuropathy (AIDP)
-- http://peripheralneuropathycenter.uchicago.edu/learnaboutpn/typesofpn/inflammatory/guillainbarre.shtml
There is another discussion that you may want to read through and post any questions you might have:
> Groups > Neuropathy > Anyone been diagnosed with CIDP? It's very rare
-- https://connect.mayoclinic.org/discussion/has-anyone-on-this-feed-been-diagnosed-with-cidp-its-very-rare/
Are you able to share a little more about your symptoms? I'm sure other members with similar symptoms may be able to share what helps them.
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