pseudobulbar

  1. A

    Feeling of crying

    Hello I am worried as I have been twitching body-wide for 3 years, but now recently, I don't know if its is a placebo but I am conscious about my emotions and lately iv'e been having a sense of crying but have not actually cried. Could this be an early indicator of the pseudo-bulblar affect...
  2. E

    My Mom's Diagnosis- Sporadic Bulbar Onset ALS

    It was sometime last spring when my Mom's voice started sounding hoarse. She discounted it as being sick since she typically loses her voice once a year for a couple weeks when she gets a cold. In June, my best friend got married and she couldn't stop crying. She said she was just tired ,but...
  3. W

    This is for anyone who is currently scared out of their shorts

    I'd like to preface this by saying I am a self-proclaimed lurker on this site who also just endured what to me, in my limited little world, would consider to be the worst three weeks of my life. Out of respect for those who have a confirmed dx of this terrible disease, I never did dare to start...
  4. Duker52

    Nuedexta for non-pseudobulbar affect

    Is anyone taking Nuedexta for slurred speech, swallowing, or excess saliva problems? I'm interested to hear your experience and whether or not it is relieving any of these problems. My neurologist prescribed it at my suggestion and I took my first dose yesterday. I'm just wondering if I can...
  5. A

    Confusing EMG appt

    Hi, Last I wrote my husband had an appointment with his new neurologist where he had diagnosed him him with bulbar palsy (per report we received) and was questioning bulbar onset ALS. This past week he went and had an EMG. We are so confused now because at the end she said she was thinking...
  6. M

    Rapid progression of friend

    I don't know all your abbreviations as I am new to this forum. And if I break any "rules" it is certainly not on purpose. I am a psychiatric RN and have become very close to another RN on my unit and her wife. In the course of 1 year, her wife has lost the ability to speak and swallow. She got a...
  7. S

    ALS Progressive Bulbar Palsy/Primary Lateral Sclerosis/Progressive Pseudobulbar Palsy

    My husband has been going to the neurologist for now almost a year, taking all kinds of tests and he believes it could be ALS. We have now gone to UofMI and hopefully they will find out what is happening. He thinks after the first visit it may be Progressive Bulbar Palsy or Primary Lateral...
  8. azwxman

    My Intro

    Hi all, Mark here. Diagnosed on June 2, and got a second opinion from a neuromuscular specialist at University Medical Center (U of A) on the 10th. I'm 58 today, retired Air Force after 20 years of service and lucky me, spent nearly a year in Saudi Arabia during the first Gulf War (and have...
  9. 1

    So many questions!

    My husband was diagnosed with primary progressive aphasia on 6/28 after I began noticing first a change in the tone of his voice and the slurred speech and it seemed difficulty finding the words. We saw a local neurologist and received this diagnosis then to UPMC Pittsburgh where he was...
  10. M

    Newly diagnosed and I have a few questions

    I am 41 years old, married male with two young boys ages 3 and 7. I've always been a very physically active person in perfect health. Other than the Bird Flu and and an appendectomy in 2010 I've been in perfect health my whole life. I ran cross country and track all through high school and...
Back
Top