Andjelam
New member
- Joined
- Oct 7, 2019
- Messages
- 3
- Reason
- Learn about ALS
- Diagnosis
- 00/0000
- Country
- CA
- State
- ON
- City
- Toronto
Hey everyone! I’ve been following this forum for a while since started twitching and having weird numbness 10 months ago.
I am a 25 year old female registered nurse. I have had clean MRIs ruling out MS. I had an abnormal somatosensory evoked potential in my right tibia that my neuro did not know what to make of. I finally had an NCV and EMG last week where the neuro pointed out that my right foot Extensor Digitorum Brevis muscle is completely atrophied and produces no signal at all. I of course started to freak out but she said that if it were ALS the rest of the muscles would show dennervation on EMG. She said my NCV showed some more slowing at the knee, but the EMG was done super quickly and she seemed to think nothing of it. She is scheduling me for a follow up EMG in three months.
I am now paralyzed with anxiety because I cannot think of one thing that would cause a foot muscle to atrophy in isolation (apparently my lumbar spine is clear). I have no noticeable weakness and the atrophy has been present for at least 6 months according to photos. This muscle is an accessory muscle so it’s atrophy would not affect function.
Has anyone had a similar situation/can offer any advice on next steps? Thank you!!
I am a 25 year old female registered nurse. I have had clean MRIs ruling out MS. I had an abnormal somatosensory evoked potential in my right tibia that my neuro did not know what to make of. I finally had an NCV and EMG last week where the neuro pointed out that my right foot Extensor Digitorum Brevis muscle is completely atrophied and produces no signal at all. I of course started to freak out but she said that if it were ALS the rest of the muscles would show dennervation on EMG. She said my NCV showed some more slowing at the knee, but the EMG was done super quickly and she seemed to think nothing of it. She is scheduling me for a follow up EMG in three months.
I am now paralyzed with anxiety because I cannot think of one thing that would cause a foot muscle to atrophy in isolation (apparently my lumbar spine is clear). I have no noticeable weakness and the atrophy has been present for at least 6 months according to photos. This muscle is an accessory muscle so it’s atrophy would not affect function.
Has anyone had a similar situation/can offer any advice on next steps? Thank you!!