Alcohol Neuropathy???
Hello All, I just found this group and I am so thankful to have found this! I am so frustrated with our medical system here is Santa Rosa, Ca. It takes months to get an appointment with anyone.... Please read my story and any feedback or information would be so helpful. So I live in Wine Country, and last year beginning in Oct. 2017, I lost four family members, my baby brother, two sister-in-laws and my best friend just in July 019. I started to drink more and more wine everyday. Sometimes up to a bottle a night. On Jan. 2, 2020 I decided to stop, cold turkey. By the fourth day, I woke up at 3:00 am with stabbing, burning pain going up and down my legs and the bottom of my feet. My calf muscles were so sore as if I had run a marathon the day before. I went in (on a Saturday to a doctor, not my primary care physician), and explained my symptoms and that I had quit drinking just recently. She gave me a referral to have a nerve conduction test and physical therapy. I had blood work done and I don't have diabetes and my Vitamin B-12 level was VERY high, I think because I had taken vitamin B-12 supplements the day before the blood test, but all in all my blood test results were all good. I can't get an appointment for the nerve test until the end of March! In the meantime, I went to my chiropractor and explained everything to him, he said all that nerve pain was from going through alcohol withdrawal. He said I should have weened myself off instead of cold turkey. So, I went home and had a glass of wine and the next day I felt better. BUT, I am so nervous that I have damaged my nerves and I can't get help for another 6-8 weeks. Has anyone experienced this? Could this nerve pain be something else?
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Best wishes! I hope you get some answers soon.
I also have idiopathic neuropathy. You referenced “newly found indicators”…
I’m curious what those are?
Thank you.
@stallen
After having normal lab panels an EMG NCS and skin biopsy with only an abnormal skin bx I requested autoantibody panel offered by Washington U in St Louis. There is a lab req online and my blood mailed there for testing. There are panels depending on type of neuropathy. Im still waiting for my results. Good luck!
The main ones I know of are the ones Washington University is testing for that @eah mentioned. Still trying to figure out how to get tested for them myself.
There's also some stuff alluded to in this webinar, that I need to follow up on. It's the Webinar from Feb 22, 2023. https://www.foundationforpn.org/past-webinars/
There's also one on that same page I haven't listened to, on genetic testing for neuropathy, October 6, 2022. It's probably worth a listen to see if there's leads there as well.
Could you post a link to how to start this lab request? I'm having trouble figuring out that part. Thank you.
I've been reading all these posts, each of us looking for a cause. Me too.
I have been tracking my symptoms. I have no pain when I awake up,just a funny sensation from the ball of my feet to my toes. Then about late afternoon I start to feel mild to moderate burning in my toes. As the day progresses the burning increases. So by late evening my feet are on fire. By the time I get into bed, the burning is excruciatingly. Now during the day I have taken my Lyrica and started using Diclofenac gel on my feet and have taken Tramadol 50 mg as ordered.
This pattern goes on almost every day. So I find myself wondering if it is a hormonal changes during my day. I don't think it is my level of activity because my routine changes every day. Are there aphysiological changes that go on in my body that go on that influences the progression of my pain pattern. There are so many chemical changes in our bodies that we are not even aware of.
I wonder if any researchers have tracked people as the pain pattern changes through the day.
Just a thought. Does anyone know if there is any research in this area?
Hello @seanywonton. I think the chronic/consistent, long-term use of alcohol is the part where it would be feasible to point to alcohol neuropathy, and likely why your neurologist suggested it.
You will notice that I have moved your post into an existing discussion on this same topic, which you can find here:
- Alcohol Neuropathy???: https://connect.mayoclinic.org/discussion/alcohol-neuropathy/
Unfortunately, as you know, quitting drinking will not reverse already damaged nerves and neuropathy symptoms. However, will benefit you by not increasing your symptoms and/or making things worse. Regardless if your neuropathy is classified as alcohol neuropathy or not, consuming alcohol going forward could contribute to additional nerve damage.
With that said, congratulations on your two breaks from drinking! I know the challenge of sobriety is day-to-day, as my spouse just celebrated his 10th year. It has required him to change many of his hobbies centered around alcohol and drinking or at least look at doing them differently. For him, it has been worth it 100% and he is the healthiest he has been since his 20s, probably largely in part because he replaced drinking with lap swimming.
Perhaps @pippy023 @texasflyboy @tomm547 and @casey1329 could join you here to share their experience with alcohol neuropathy and what they have learned and the treatment options they are using.
Would it be more freeing to think less about how this came on and more about what choices you can make going forward now that you know you have neuropathy?
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.
@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.