Searcher
Active member
- Joined
- Oct 17, 2008
- Messages
- 68
- Reason
- Learn about ALS
- Country
- US
- State
- MD
- City
- Gaithersburg
A little over 2 years ago, while having some speech and swallowing problems and noticing what appeared to be some subtle changes (new erosion) on tongue, I asked the speech pathologist evaluating me to take some pictures of my tongue. I also took a few. Yesterday I looked at the pics online and the prints I had made up. It is very evident that there are new wavy, hilly areas on the top, anterior portion of the tongue that were not on those pictures. This, on top of a rheumatologist this week confirming that, indeed, one side of tongue has more grooving and less tissue and is somewhat weaker on that side. And this all fits with the recent difficulty in articulation and vocal fatigue and mildly increased difficulty eating. I occasionally feel twitches in tongue.
I realize I've had some speech, swallowing and other symptoms going back maybe 27 years, and specifically speech and swallowing difficulties going back at least 20 years. However, my speech never was this bad for this long a time and while these symptoms have fluctuated or remained essentially the same over many years, my tongue is clearly having progressive atrophy. Can anyone tell me any reason to think this is not evolving into ALS? What else could it be, regardless of past symptom history? Needless to say, after so many false alarms, so many times crying wolf, it now seems that the real thing is at hand and it is surreal and existentially shattering. My best hope, I feel, is that given my unusual history, the progression will be slow (in fact I think some of the tongue atrophy was present at least 16 months ago) or that maybe it is something else which is mimicing ALS, like an unusual form of MMN.
I don't have a neuro appt. for another 4 weeks but may see if I can get a speech pathologist consult before then. Does that make sense?
What do others do to deal with the anxiety? I'm upping klonopin (more times per day) and occasionally taking a beta blocker (though not supposed to take it every day due to too low a heart rate).
Thanks for any thoughts
Searcher
I realize I've had some speech, swallowing and other symptoms going back maybe 27 years, and specifically speech and swallowing difficulties going back at least 20 years. However, my speech never was this bad for this long a time and while these symptoms have fluctuated or remained essentially the same over many years, my tongue is clearly having progressive atrophy. Can anyone tell me any reason to think this is not evolving into ALS? What else could it be, regardless of past symptom history? Needless to say, after so many false alarms, so many times crying wolf, it now seems that the real thing is at hand and it is surreal and existentially shattering. My best hope, I feel, is that given my unusual history, the progression will be slow (in fact I think some of the tongue atrophy was present at least 16 months ago) or that maybe it is something else which is mimicing ALS, like an unusual form of MMN.
I don't have a neuro appt. for another 4 weeks but may see if I can get a speech pathologist consult before then. Does that make sense?
What do others do to deal with the anxiety? I'm upping klonopin (more times per day) and occasionally taking a beta blocker (though not supposed to take it every day due to too low a heart rate).
Thanks for any thoughts
Searcher