speech

  1. P

    Bulbar Specific Questions - Old Thread Closed

    Hello - I have posted before about symptoms (https://www.alsforums.com/forum/do-i-have-als-als/38110-follow-up-questions-old-thread-closed.html) and my experiences thus far. I am posting again because I am currently away from home and do not have access to a neuro. I was hoping to get some...
  2. D

    I'm new, this is me and my uncertainty...

    Hello, I am new to this forum, and wound up here after experiencing another symptom that I have recently had in a list of others to keep pointing me to ALS... I am currently un-diagnosed, but have started clinical testing. I'm hesitant to continue because I personally can no longer afford the...
  3. Erika

    One year ago this crazy ride began....thank you for all the information and support!

    My mom was diagnosed one year ago today. So much has happened and yet, I remember those days leading up to the day and "the" day like it was yesterday.* I had already been told it was likely ALS a week prior, but I only told my parents we were being sent to another doctor who knew more about...
  4. S

    Slurring speech or no?

    hey everyone, i have a problem with my speech that id like to ask you guys about. i felt like i was having problems speaking and i googled slurred speech and it ended up bringing me here. nobody else has noticed it and i have been asking people every day for almost two months now. my parents...
  5. E

    Is this als? Worried

    Hello everyone, 28 year old female, I started twitching all over my body when I first read als symptoms, I went to a nero and he did an emg and it was clear, after 3 months, one day I started to twitch again and that time I had no als fear, I went to ny nero again and it was clear too, 2 days...
  6. D

    possible nerve problem

    i was diagnosed in the singapore hospital possible bulbar problem but after 41/2 yrs i went for my muslces tissue biopsy tests and confirmed that it was a nerve problem at such is affecting my speech, my execessive saliva and swallowing problem his three has been a hell of problem to me sir can...
  7. H

    Seeking Guidance

    I have been seeing a top neurologist for several months. He has told me that I might have ALS, although I might also have some other MND or some form of neuropathy. I would appreciate any thoughtful reactions based on the following facts. I realize that any views expressed have limits, but at...
  8. N

    It's been 13 months...

    Hi Everyone, It's been 13 month's since my husband's diagnosis. It's been a really long time since I've posted on here. I just wanted to update everyone on how everything is going, but first I would like to THANK ALL OF YOU :) You were my support system with your encouraging words of wisdom...
  9. A

    ALS on a teenager? Surface EMG?

    AGE: 18 Sex: M Height: 5'3 Weight: 75 kg Race: Asian Duration of complaint: 2 years and 2 months since i first twitched My twitch started 2 years ago and now it's all over my body mostly on my left foot no weakness though but I can twitching. Like when I put my feet on a cross position it gets...
  10. F

    Finally asking

    Hello all, I'm finally asking I've been a long time lurker and I can't help but ask your opinion now. I've been worrying about ALS since January of 2016. I was 18 then and not I just turned 20. For almost a year and a half I was worried about atrophy between my thumb and forefinger, but I...
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