Doctors,
I aplogize greatly for the twitching question, but I need to hear it from a qualified person. I have posted questions here before regarding my ALS
fearsFears and phobias. I am now past the one year mark with my twitching. I twitch EVERYWHERE. Feet, calves,
handsHand or foot spasms
Hand tremor, TOUNGE (most distressing), arms....you name it. My feet and calves are 24/7. Being that I am only 33 years old, coupled together with me twitching for a year w/o any clinical
weaknessWeakness, do you think i can put this ALS
fearFears and phobias behind me? I know doctors can never answer a medical question with 100% certainty because there are exceptions to every rule, but could you be 99.9% certain?
LivingAdvanced care directives in constant
fearFears and phobias for over a year is the pits. I have seen Psychologists, Psychiatrists, MD's....all about this twitching stuff. No matter what I do.....it still hangs around like one of those unwanted guests at a party. I appreciate any input/reassurance you might be able to send my way. Thank you so much for you and your collegues services....they are invaluable.
Best regards,
B-Man
***@****
My fasciculations are a little heightened (maybe 20-40 /hour and I have a little twinge on my tongue for the first time that I'm attributing to my visit to the doctor today-because they (fascics) will flare up for a day or so after a treatment on the warts). But, Like many of you I've worried about ALS MS etc. but for now I'll try this route as it is working pretty well and I'm hoping that I'm at the end of this thing (head to toe eradication) within a month or so.... I'm not a doctor but maybe someone is in the same boat as me and if this helps one person improve their situation i'll be grateful for what I've learned.
Take Care... I'll update this in a couple of months as you have to go back for treatments every couple of weeks to make sure what they treated is gone...Hopefully this is the end of this.... God Bless.....
You could be exactly describing my symptoms. from top to bottom i have exactly the same problem...twitching buring tingling.I have been living with the twtiches for over 5 years (the buring and tingling followed 2 years later) (Lucky me). They come and go. Have you seen a neurologist yet?? You should have them test your B-12. I went through a battery of tests and the only thing they found ws a major b-12 problem. Seems my body can not matabalize this vitamin at all - and b-12 is responsible for development and health of the nervous system. I have been getting b-12 shots monthly for a few years now and the twitching has abated a bit. It comes and goes but I can go a month or two with little to no twitches. If I'm stressed it can come back alittle bit.Also - make sure your sleeping. If you're not sleeping at least 7 hours a night (cuz I know those darn twitches can freak you out enough that you can't sleep) -go to the doctor and get something to help. I am on trazadone to help me sleep. It's a mild antidepressant that is used to help people sleep - it doesn't really work as an anti-depressant - they seem to only give it out for sleep.
I'm still on the hunt for answers - because I will have flare ups of the burning and tingling and ocassionaly the twitches. I am just hoping to find a diagnosis - as living with a mystery illness is no fun - which I am sure you know.
No, I`m not B-12 deficient. They checked my blood and it all came back normal. They did a brain MRI - Normal, strength test - Normal, nerve conduction test - nerves conducted slightly slow, but basically normal. They recently did a neck MRI, but I haven`t gotten the results yet, I hope it`s normal too. All of this started after the birth of my daughter. I think it`s mainly from the stress that the pregnancy put on my body. My twitching seems to be improving. I`m hoping it`s just benign. Thanks for your comment, and good luck!