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Alcohol Neuropathy???

Neuropathy | Last Active: Jun 8 1:52pm | Replies (31)

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@seanywonton

Hi Amanda,

I don't really want my post to be moved to the alcoholic neuropathy section. I feel that while that is part of my question, it also seems that you are making a judgement of why I have neuropathy and jumping to the conclusion that it's from alcohol. And that's not what I'm saying. I'm saying it could only be from alcohol if I am like, 2-3 times more easily damaged by alcohol than other people are.

If people could get neuropathy that easily from alcohol use, 50% of college graduates would also have neuropathy.

I'm going to keep looking for an answer that isn't alcohol. It doesn't make sense to me...I know full-on alcoholics that aren't suffering what I'm suffering.

I'm happy for people that quit drinking, if that's what they need to do. Creating beer is my creative passion and my livelihood. I like to drink beer. I'm not cutting one more source of pleasure out of my life without good reason. This disease has already stolen far too much from me.

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Replies to "Hi Amanda, I don't really want my post to be moved to the alcoholic neuropathy section...."

@seanywonton, I share your frustration on not having an absolute diagnosis on what’s caused my PN. When I get any new theories or suggestions, I still run them by my doctors in hopes we can prove or disprove, and at this stage (6 yrs) I’ve about learned they’re running out of things to test that could add any certainty . What I have learned from them and even more from the folks on here with links to articles and research & tons of personal experience, are what things we can do to help make the most of our quality of life having been dealt the hands we have, regardless of how we got here. Many sections in this group talk about vitamins to take/avoid, exercises/physical therapies/therapeutic devices, lotions & ointments, socks & shoes, and diet.
It didn’t take long for me to learn that alcohol added no cure or help to PN, and added nothing but dangerous risk of worsening it, so I chose to drop my social drinking without doing a scientific experiment on myself to see his long it might take to prove or disprove. PN is so different every day, it would be hard to find cause or effect reliably without a very long term study. I enjoyed wine, but have no issue not drinking and being around others. We still host & attend parties and happy hours, I’ll pour and mix drinks. I find I seem to be the designated driver often and seem to be more popular because if it. I’m glad I’m keeping my PN feet able to do that! Anyway, you don’t have to give up everything you like because you no longer drink. It’s a choice as you say. You may never get “proof “ it helps you or hurts you, just like not all smokers get lung cancer, you just have to decide the best for you. If you're looking for any doctor to tell you that they see no harm in drinking beer, I think it would be like telling a smoker to keep smoking. So while I realize you’re wanting them to find something definitive and keep looking so it might discount alcohol theories, you have a good chance of being like most of us here who don’t know our causes after exhaustive testing, so we shift to finding what helps get the best quality of life for both short and long term.

I had asked my pain specialist if drinking alcohol could have been the beginning of the neuropathy (I never had more than 3 small glasses, usually 1) he (along with other physicians) have told me that you would have to be drinking a huge amount for that to be the issue.
Have you all seen anything absolutely positive about the Loma Linda treatment? So far, I have done low light lazer and acupuncture-still have it!! Does anyone else have a problem taking the meds during the day? I hardly know what my name is if I take them and definitely get nauseated
from them. Still considering Spinal Cord Stimulation - would love to hear from everyone that has had the procedure done and what their opinion is and if it was successful.