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Alchoholic neuropathy

I am a 38 year old woman who has been experiencing the "symptoms" of peripheral neuropathy ( Tingling, numbness in hands and feet, odd parathesias, etc) for almost a year. I have been thoroughly tested for MS,PN and ALS( brain and cervical MRI's, evoked potentilas, EMG, nerve conduction, etc) plus blood work - lupus, Sjorgrens, arthritis, etc. All were normal. It recently occurred to me that  I have slipped into a pattern over the past few years of having 2 1/2 to 3 glasses of wine every evening while preparing dinner . Since I have never considered myself having a drinking problem, it never occurred to me that this amount of drinking could be having a toxic effect on my nerves. ( I am 5' 3" tall and weigh 112 lb.). Do you have any information on how much drinking could casue PN?I am cutting way down, but if my problems are due to alcohol, is the damage permanent? Also, my b-12 was on the very low normal side.
Any info would be greatly appreciated.
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Avatar universal
i have pereiphal neuropathy due to diabetes and now it feels likr someone poured gas on me and lit it.  is there anything that will give releif.  i was told to use a capsacin creme and that only made it worse
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Avatar universal
If you want to find people who's fasciculations preceded diagnosis with ALS, just check the archives of Discuss ALS - Doug's forum.  Unfortunately, all people with fasics do not have the benign variety.  If you do, you are one of the lucky ones.
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Avatar universal
I am curious and it occurred to me to ask....of all the twitchers that have posted to this forum over time, or read it to find out info about fasiculations, etc... I KNOW you are out there and read any thing about ALS and twitching that you can...... has ANYONE been subsequently diagnosed with ALS? I am referring to the folks that have had either months or even years of just fasiculations and maybe some parathesias -  no real weaknees or other symptoms normal neuro exams normal EMGs - essentially those of us told we most likely have Begign Fasic....


thanks
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Avatar universal
Thank you for your kind and caring posts. I will follwo up . Gee, what a releif if this is actually what it is. Thank you again.
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Avatar universal
Hi Anonymous,

Go to the Mass General Neurology Web forums. Look on the General Neurology or Peripheral Neuropathy forums for posts from Rose.
There are specific tests that should be run when the B12 is low normal to determine if there is B12 deficiency due to absorption problems or utilization. Depending on the reason, the treatment is slightly different. She posts references to reliable sources of information.

Start taking b12 today even while you wait to see the Dr. If you also take folic acid and are over 50 take 100Mcg B12 which is about 50 times the RDA. From this month's readers digest.

Best of luck.

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Avatar universal
Dear Anonymous:

Sorry to hear about your parasthesias.  Whether alcohol could cause your symptoms is yes.  However, it might be due to a side effect of alcohol, that of reduced nutrition as seen in a low vitamin B12 level.  I would bet, that this more than the alcohol is the reason for your parasthesias (only a guess).  Usually we see alcohol induced parasthsesias in chronic alcohol abuse, which really doesn't sound like you.  The parasthesias can be as you describe but also burning in nature.  Even with a low normal we see vitamin B12 problems of neuropathy.  I would talk to your neurologist about vitamin B12 shots/therapy and see if the symptoms do not resolve over time.

Sincerely,

CCF Neuro MD
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