clonus

  1. G

    Is anyone complaining of a nagging cough

    Hello, My husband was diagnosed three years ago with PLS. However, I am not so sure it has remained PLS. He has progressed a lot this passed year. He has clonus right foot, and now left also. He has babinsky in right knee and now left knee is buckeling. His right had is so week he can hardly...
  2. T

    What is going on with me?

    I have posted before, but since the beginning in march i get more and more symptoms: March: fasciculations and cramps in calves April: continuous fasciculations and cramps in calves; isulatied in arms and abdomen End of April: Clinical Exam=> Brisk reflexes, Low CMAP in NCV, high MUAP in the...
  3. M

    UMN symptoms

    Sorry for posting two questions in one day, but I hate feeling anxious. I had a question about UMN symptoms. When I went to my neuro for my latest check up, I mentioned to him that I had noticed that my right foot felt really uncoordinated. He asked what I meant and I explained to him that I...
  4. Sammantha

    So close yet so far away

    Went to my appointments.. The resident and doctor saw me. They were not concerned about my thymoma or cat scan print out, he wanted the actual CD so i have to mail it to him. He then checked my muscle strength and what not. He sat down and told me that my symptoms were atypical for...
  5. hopingforcure

    The Twitching or the Egg?

    It seem's that we spend so much of our time on this forum questioning the twitching weakness, atrophy question: It is this simple TWITCHING on it's own is meaningless....................................................... I feel like for MOST people that have a MND or something Malignant, the...
  6. sdsyd

    The saga continues!

    Hi everybody! Just wanted to update again and get any thoughts anyone has. This might be long so I apologize in advance. I dont know if updated since my spinal tap, but there were no antibodies for CIPD, so the neuros felt they werent ready to "hang their head on a diagnosis" OR begin IVIG...
  7. awieleba

    My als/ neuro appt

    Well, I will try not to make this to long but I have a bit to say and those that know me, know that I can get a little long winded..... So, Ihad my repeat emg and saw the other head nuero at als universty (whom has been in als for 30yrs). He did the emg himself and it was perfectly CLEAN...
  8. J

    New Here

    Just thought I would chime in and proclaim my presence. I started having problems with my legs 7 0r 8 years ago. I mentioned it to my Gyno and he sent me to the Rheumy who sent me to a Neuro. The first Neuro told me it was depression. :roll: I knew better. The second Neuro did the tests and...
  9. M

    New to this-diagnosed of PLS

    Hi. I have been reading these threads for about 6 mths now but haven't actually shared my story. As briefly as possible, I started noticing slurred speech during the summer of 2006, made worse by a half a glass of wine. Also, I was an avid runner and started to feel "cloddish" in my thighs while...
  10. S

    extreme clonus

    Hi everyone. I was diagnosed about a year ago- for the passed few months I have what I call extreme clonus. My legs will shake and my clonus will not stop unless I change position of my legs. Can you guys tell me about your clonus issues and what are you taking for it.I have trie clonozepan and...
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