Bubba23
New member
- Joined
- Jan 29, 2017
- Messages
- 1
- Reason
- Learn about ALS
- Diagnosis
- 00/0000
- Country
- US
- State
- VA
- City
- Ashburn
Appreciate all the folks who take the time to respond to scared folks who come to this forum.
I am looking for some helpful thoughts about some of my issues.
I have been twitching for about five years now. Also bad headaches. Mostly in my calves, but at times all over. Throughout this entire time I’ve been an active weight lifter. When this all started I went to a local neuro who checked me out, nothing of note on EMG or neurological exam other than brisk reflexes (all over though). The twitches seemed to come and go, definitely a positive sign.
However, around 2018 I started to experience some weakness with my left thumb. I would often get a very fine twitching/burning feeling in the FDI. This seem to progress until the summer of 2019 when I went to a hand doctor and some atrophy was noted mostly around the APB. At the end of the summer after a heavy bench day I noticed my tricep was completely numb. Got a new EMG Which indicated radiculopathy from the C6 C7. MRI agreed. I got a cervical fusion that September. Fixed the headaches but I continued to twitch. My tricep felt much better at the time, but not my thumb. Life went on. Still twitching.
Fast forward to August of this year, I started having Difficulty with a few lifts on the arm that was affected. I noticed that my triceps and biceps looked somewhat deflated. My hand also does not look any better. The FDI Looks OK, but the intrinsic muscles and ABP seem to have atrophied more. I went back for another EMG which thankfully did not show any active denervation. With all that said you might be asking why I’m posting, without active denervation I would most certainly think motor neuron disease is excluded. I did notice on the EMG report that remote radiculopathy was noted, I don’t really understand what that means. It also noted +1 poly on the PronatorTeres and a >12 duration in the tricep. The arm that feels somewhat atrophied and weak continues to be very sensitive, like an electric current continuing to run through it. Lifts have been much harder.
I guess I’m just asking, is it at all possible for radiculopathy to be confused with MND? What is the difference on EMG, and would it be obvious? Does it matter which part of a muscle the needle goes into for the NCS?
It just concerns me that I’ve atrophied a bit and experiencing these issues after my fusion, I was really hoping I’d get better and wish I could explain the continued issues. Had I not been a twitcher then I don’t think I would’ve thought much of it. The logical part of me just points that this was a lack of recovery after the ACDF or some continued nerve irritation.
Thanks for taking time.
I am looking for some helpful thoughts about some of my issues.
I have been twitching for about five years now. Also bad headaches. Mostly in my calves, but at times all over. Throughout this entire time I’ve been an active weight lifter. When this all started I went to a local neuro who checked me out, nothing of note on EMG or neurological exam other than brisk reflexes (all over though). The twitches seemed to come and go, definitely a positive sign.
However, around 2018 I started to experience some weakness with my left thumb. I would often get a very fine twitching/burning feeling in the FDI. This seem to progress until the summer of 2019 when I went to a hand doctor and some atrophy was noted mostly around the APB. At the end of the summer after a heavy bench day I noticed my tricep was completely numb. Got a new EMG Which indicated radiculopathy from the C6 C7. MRI agreed. I got a cervical fusion that September. Fixed the headaches but I continued to twitch. My tricep felt much better at the time, but not my thumb. Life went on. Still twitching.
Fast forward to August of this year, I started having Difficulty with a few lifts on the arm that was affected. I noticed that my triceps and biceps looked somewhat deflated. My hand also does not look any better. The FDI Looks OK, but the intrinsic muscles and ABP seem to have atrophied more. I went back for another EMG which thankfully did not show any active denervation. With all that said you might be asking why I’m posting, without active denervation I would most certainly think motor neuron disease is excluded. I did notice on the EMG report that remote radiculopathy was noted, I don’t really understand what that means. It also noted +1 poly on the PronatorTeres and a >12 duration in the tricep. The arm that feels somewhat atrophied and weak continues to be very sensitive, like an electric current continuing to run through it. Lifts have been much harder.
I guess I’m just asking, is it at all possible for radiculopathy to be confused with MND? What is the difference on EMG, and would it be obvious? Does it matter which part of a muscle the needle goes into for the NCS?
It just concerns me that I’ve atrophied a bit and experiencing these issues after my fusion, I was really hoping I’d get better and wish I could explain the continued issues. Had I not been a twitcher then I don’t think I would’ve thought much of it. The logical part of me just points that this was a lack of recovery after the ACDF or some continued nerve irritation.
Thanks for taking time.