Crippling Electrical Burning and Twitching

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I've had a burning tongue since mid October. It comes and goes, just get more sleep and watch your diet. I think it is caused by malnutrition. It always tends to go away for a while right after I eat.
 
It sounds like parasthesia. Have you checked your vitamin b12 levels? Maybe, because you can't absorb nutrients well through your digestive tract, you may ask your doctor about vitamin b12 injections if indeed you are deficient.
 
i was, i was fine as never in the last years. had almost no twitching anymore - until x-mas time, since then i face symptoms and frequency i never had in my three years since onset.
 
I know you may most likely not believe it, but I am sure that these things are not the sign of anything sinister, neither ALS, MS, polyneuropathy, cancer or whatever, your anxiety is miles high and your body is stressed and somatisation can do all that to you, it can even cause much worse symptons actually
 
However I would not overcall anxiety, I agree that this does not sound like anything sinister (polyneuropathy is not sinister from that point of view) but due to acute worsening it might be worth to get it checked in order to treat it in this stage.
 
it is NOT anxiety. as i wrote before, i was calm and good and relaxed like never when this new stuff began. definitely not linked with anxiety.
 
No, I am just as relaxed as I could be , actually I think I am one of the most relaxed "newbies" here but I am a bag full of symptoms. Anxiety is not the answer. Somatisation is not anxiety disorder
 
what then? i am really tired of this crap. just held a plate between the index finger and the thumb and got this burning nerve sensation on that point where the plate meets the skin. I am fed up with this, with my vitiligo, my rheuma, my possible thyroid problems, my beard hairloss. life is not what it was years ago, is not a pleasure anymore.
 
now i have chronic crampy pulsating pain in my left foot and in the right tibius anterior near the shine. the one began last night, the other one this night. permanent now:-(((
 
You need to find a really person to talk too like a very good psychologist like I have who will help you calm your body internally. Your symptoms are real but most likely somitization. You say you have been relaxed before but the smple fact that you still think you might have Al's and the fact that you know somany little things about it like a certain cramp could be a symptom means you are looking at too many websites and are panicking. You need to calm your internal body. Go get a great massage, do some yoga, focus on a project. Do anything to take your mind off things. We are all in your shoes.
 
this *beep* burning needle sensation mainly in feet and hands continue. what is this crap? i refuse to visit a doctor as those butchers don't have a clue at all about anything.
 
They know what they learn in school or bythemself , I wouldn't be so irritated with doctors I wanna believe that they want to help just not always know why... If You thing that tibetan dc knows more? Go for it! I don't know that... Get help whenever you like it. Wish you will get better soon :)
 
Hey LaurentHow disabling diseases can be, they dont have to control your mind like they do to you right now. I once read an ALS-patient who stated something like: "Even though i live with ALS i try to make it a part of my life. Not my whole life."Wise words from a very ill person. The doctors who look at you say its a benign condition. Its annoying, it hurts etc. but try to make it a PART of your life. Not the whole life. Even dying persons can find joy in life. Play a game, go to the movies, visit friends. Do the things normal people do and you will see that your life will improve. You have to get out of this mess you are in. You are not deadly ill. But if you where, it would be plain stupid not to live life to the fulliest. BFS is now a part of your life...Regards
 
Hey LaurentHow disabling diseases can be, they dont have to control your mind like they do to you right now. I once read an ALS-patient who stated something like: "Even though i live with ALS i try to make it a part of my life. Not my whole life."Wise words from a very ill person. The doctors who look at you say its a benign condition. Its annoying, it hurts etc. but try to make it a PART of your life. Not the whole life. Even dying persons can find joy in life. Play a game, go to the movies, visit friends. Do the things normal people do and you will see that your life will improve. You have to get out of this mess you are in. You are not deadly ill. But if you where, it would be plain stupid not to live life to the fulliest. BFS is now a part of your life...Regards[/quotethis is a great response foxrun, well said ?
 
you are right. however even if i don't die from it instantly i don't find anything benign in having as, bfs or whatever it is, vitiligo, alozea, morbus biemer and hashimoto all together.
 
my sudden electrical needle pains get worse and worse. first they were in the feet and hands but now they appear everywhere. cannot sleep a night through anymore and loose my motivation to struggle this new stuff what i think is a neuropathy of unknown origin.:(((
 

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