Please please please help- tongue issues

miller427

New member
Joined
Jun 20, 2025
Messages
2
Reason
Learn about ALS
Diagnosis
00/0000
Country
US
State
VA
I’m a 34yo female and I am having a very very hard time. For the last 2ish months I’ve had bad twitching body wide (legs, thighs, face, neck- all over) lately, I am really worried bc I have tongue issues daily. This includes a persistent buzzing feeling and twitches that I can see at rest- they look like little pops. I also feel like I’m starting to stumble over my words which is happening more often.

I have not been able to see a neurologist yet but I was able to get an EMG (they only did it on my left arm and leg) and that was normal however they didn’t do anything on my face or tongue. I was able to get the EMG as my rheumatologist sent in a referral for one- I do have diagnosed Sjögren’s syndrome and potentially lupus however these have been stable for years and my rheumatologist doesn’t think it’s related. I have had tons and tons of blood work done as well as an mri (my rheumatologist is great but not a neuro). The mri and most blood work (vitamin deficiency etc) have been normal.

I am a mom of 2 toddlers and I am sitting panicked daily that I have ALS based on these symptoms- especially my tongue and speech lately. I can’t get in to a neurologist for months despite calling daily to see if there are openings.

I’m feeling really hopeless and discouraged today after some bad tongue twitching and weird feeling in my mouth and throat. My tongue is also very scalloped but it’s been that way for years. Any help/advice appreciated.
 
Last edited by a moderator:
Hi there-

Make sure to read this: Read Before Posting for an explanation as to why tongue twitching and weird feelings are not enough to give a doctor concern about ALS. The clean EMG (yes, just on your limbs is adequate and appropriate, read the link) and a complete lack of clinical weakness means your twitching is pointing towards something other than ALS.
 
Would one set of Limb emg be enough to rule out bulbar als? Also haven’t had an exam with a neurologist (just my rheumatologist) but things have been worse since then unfortunately
 
Back
Top