sensory symptoms

  1. J

    Acute Onset and Rapid Progression of Symptoms

    Hello, First of all, thank you for those that are diligent to post and answer questions on this forum. It appears that many are very helpful. My thoughts are with those that have been diagnosed and those still searching for answers about their conditions. Secondly, I do have a few questions...
  2. L

    Everything I thought I knew about als was wrong. Worst fears confirmed.

    I was already expecting the worst, but hearing it officially was like someone punched me in the stomach. My father in law was diagnosed with als today. All the researching and reading and desperately searching for reassurance all this time was all for nothing, as everything I'd read about or...
  3. A

    This is freaky....

    The wait is just killing me right now and I can't concentrate on anything else. I had a dirty EMG on Tuesday (forearm and triceps showed abnormalities while hand and biceps were completely normal) in my left arm. The nuero suspects that I have a pinch nerve. However, I'm also experiencing...
  4. M

    Tests and other stuff

    Hi, everyone, those of you who have read my earlier posts will be familiar with my symptoms and the testing I am undergoing to unearth the cause. As I mentioned, I am having some additional tests over the next few weeks for the possibility of MS, although the neuro noted I do not have sensory...
  5. L

    I'm afraid for someone high risk

    I'm really scared. Not for me, but for my 79 year old father-in-law, who has had problems with the same leg on and off for years. He's had both circulatory problems as well as nerve pain. 5 years ago was my last time of intense worry, when he was having pain in the leg. They never did figure...
  6. S

    Another ALS Imitator

    Just an FYI: Still trying to pinpoint what may be wrong with me (as I'm having another hard day with fascis, my head feeling like a 50 lb. bowling ball, etc. and can't seem to accept BFS as the answer) and found this on Medscape. Thought it would be of benefit to the Forum: Synopsis: "A...
  7. M

    update since Cleveland visit

    Hi, everyone. I haven't posted in quite a while, but I visit the forums often (especially when my symptoms really bother me). Here's an update ( I guess you can look at old posts for my symptom chronology and a rundown of all of the testing I've had so I won't be longer than necessary!): I...
  8. J

    Could you experienced people please answer this question

    I had a diagnosis of ALS 5 months ago. Symptoms; Fast Reflexes Fasciculations: Arms, Chest & Legs Muscle wasting and loss of some functions of Hand. Note: I think that the diagnosis was way too quick. After the diagnosis I had an EMG which showed normal nerve conduction ( except...
  9. B

    Progressive symptoms of ALS - no diagnosis

    Hello all, I'm a first time poster (27y, m) from Melbourne, Aus, and would appreciate any feedback. I am pretty sure I have ALS, but haven't been officially diagnosed yet. My symptoms started mid July, when I noticed a burning feeling in my toes. Over the next month this had spread all over...
  10. K

    Concerned about ALS (long!)

    Hi: I am a 29 year old male, non-smoker, occasional drinker. Excellent health until my symptoms flared up. Last thanksgiving, I woke up with an intense neck pain, exacerbated by moving my head. Symptoms resolved within a week. Now fast forward to mid-May. I started experiencing tingling...
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