sensory symptoms

  1. L

    Unresolved symptoms

    Hello all! I've been a silent reader of this forum for months and appreciate the quality of discussion and people who dedicate their time to helping and consoling others. In my case, I've reached a point where I feel I need more than just being a passive observer, so please pardon me if my...
  2. M

    hello

    Dear All Hello , I have been suffering from a progressive neurological illness for the past 14 months . started with tingling/pins and needls in my little finger July 2010 which progressed up my arm and then a buzzing in my rt foot, I have had every blood test you coud list low B12 ( now i...
  3. notme

    So, you think you might have ALS?

    Welcome New Person, You're here for one of several reasons. You're scared because some symptoms you've had popped up as ALS on Dr. G o 0 g 1 e. Or, perhaps you've already seen a doctor and that doctor has suspicions that have sent you looking for answers. The Sticky Posts have great...
  4. A

    Bummer...

    I am in the process of being diagnosed with a genetic variant of MND, and it seems to have brought about a myriad of co-infections, (i.e unusual sensory symptoms, floaters rash) which were initially thought to be indicative of dermatomyositis, and upon treatment temporarily ceased. My atrophy is...
  5. T

    mmn without conduction block

    new emg today. The most awful thing is wondering what the outcome will be. Pretty much the same results as last time. Neuropathy without Conduction block. Probable MMN or at least auto-immune neuropathy, positive antibodies responding to IVIG. Obviously glad it is treatable. Frustrating that...
  6. A

    Signs appear consistent with juvenile ALS, but very strange sensory symptoms as well?

    Hello, I'm Alastor, 18 and new here. :) I think I should just let you guys know beforehand: I am not the average Google monkey who is a hypochondriac and is also terrified of various occult illnesses due to nonspecific symptoms(i.e, fascics all over body, no weakness, twitching), although I do...
  7. C

    Could this be ALS?

    Hi everyone, I'm new to this forum and would like to post a list of symptoms that I've experienced recently. Thanks to anyone in advance who could help shed some light on this :) Okay, in the last 3 months I've had a wide range of sensory and seemingly neurological symptoms. This list is...
  8. M

    Progression of symptoms with no diagnosis. Sound familiar

    In July 2009, I posted the following: "I have been reading this forum for about two months now and am so impressed by the support and information provided by the members. I am hoping to learn more and share my own experiences now as a member. I aoplogize in advance of for the long post but it...
  9. S

    Desperate

    An update. This is going to be long. Please*bear with me. And thank you for reading in advance. (to prevent confusion, if you want, you can view my previous thread 'What is a clean EMG in layman's term'. for my complete history. Thanks) So after my abnormal first EMG last May 6 (no offense...
  10. A

    early onset symptoms?

    Hi Everyone. This is my first post, but I've been "lurking" for a while now. I want to start with saying that i am in awe of the positive and informative responses. I would also like to say that I respect what people living with ALS and their caregivers and loved ones go through daily. I...
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