- Joined
- Apr 2, 2024
- Messages
- 4
- Reason
- Learn about ALS
- Diagnosis
- 00/0000
- Country
- US
- State
- IL
Hello,
I have gone through and read the stickies and while most everything makes sense, theres still a few things I am confused about so i figured I would post here. 42 year old male. As a short backstory, a year ago I lost my only parent, my mom, and had caregiven for her for two years prior. Worst stress and grief of my life. Over the past year much has changed such as chronic fatigue, but one thing was that I kept getting injured doing normal weights at the gym or normal tasks (injured hand muscle opening jar, pulled rib/lat/bicep muscles doing weights) that all happened on my right side. Most of these never truly healed. On top of that, I developed joint pains in my fingers and toes all on the right side. I chalked it all up to my body going through complete exhaustion of the caregiving stress and grief. That was until 3 weeks ago
3 weeks ago I started with a twitch isolated to one muscle in my right upper arm that would last 15-20 seconds with multiple twitches. After 3 days it started affecting multiple muscle groups in my upper right arm, except they were split second twitches. 6 days in started predominantly affecting my right thigh and knees. I would say 80% of the fasciculations are in the right knee/quad, 15% in the left, and 5% randomly in both shoulders, forearms, calves, arms, etc. They feel like little worms digging into my muscles. 4 days ago I started feeling unexplained muscle soreness in my right quad which is now also in the shin.
So far I have had CBCs taken, and basic nuero tests at the chiro (push, pull, etc). I did have an EMG of my right arm in early February (well before the twitching started) for a completely different reason (numbness/pain when sleeping on right arm) that came out clean except a pinched ulnar nerve. I would have taken solace in this knowing that nerve damage would have already accumulated by then, but since the twitching and muscle soreness is mostly in my right leg, is it possible that the ALS is affecting the leg first and that the arm EMG could have been ok but still have ALS?
The fact my muscles became so injury prone on the right side over the past year and now have fasciculations and soreness happen so rapidly in the past 3 weeks leads me to believe this is essentially unilateral. Ive read stories where the fasciculations happened first before weakness, but what I cant figure out is how long or short it takes for ALS to progress if the first symptom truly is twitching, and if so, would muscle soreness come next like mine up until a sudden inability to use the muscle? Could the constant injuries to the right side over the past year been the warning for me that the muscles are deteriorating?
I have a neuro appt scheduled for april 12th. Until then I just feel in constant fear. I was starting to hope this was just BFS but now that muscle soreness has started in the right leg my panic alarm is in absolute overdrive.
Thanks for reading, im sure I will be one of thousands here who have posted something similar thats not close to what ALS looks like, but I still feel my feelings and fears are valid, at least to me.
I have gone through and read the stickies and while most everything makes sense, theres still a few things I am confused about so i figured I would post here. 42 year old male. As a short backstory, a year ago I lost my only parent, my mom, and had caregiven for her for two years prior. Worst stress and grief of my life. Over the past year much has changed such as chronic fatigue, but one thing was that I kept getting injured doing normal weights at the gym or normal tasks (injured hand muscle opening jar, pulled rib/lat/bicep muscles doing weights) that all happened on my right side. Most of these never truly healed. On top of that, I developed joint pains in my fingers and toes all on the right side. I chalked it all up to my body going through complete exhaustion of the caregiving stress and grief. That was until 3 weeks ago
3 weeks ago I started with a twitch isolated to one muscle in my right upper arm that would last 15-20 seconds with multiple twitches. After 3 days it started affecting multiple muscle groups in my upper right arm, except they were split second twitches. 6 days in started predominantly affecting my right thigh and knees. I would say 80% of the fasciculations are in the right knee/quad, 15% in the left, and 5% randomly in both shoulders, forearms, calves, arms, etc. They feel like little worms digging into my muscles. 4 days ago I started feeling unexplained muscle soreness in my right quad which is now also in the shin.
So far I have had CBCs taken, and basic nuero tests at the chiro (push, pull, etc). I did have an EMG of my right arm in early February (well before the twitching started) for a completely different reason (numbness/pain when sleeping on right arm) that came out clean except a pinched ulnar nerve. I would have taken solace in this knowing that nerve damage would have already accumulated by then, but since the twitching and muscle soreness is mostly in my right leg, is it possible that the ALS is affecting the leg first and that the arm EMG could have been ok but still have ALS?
The fact my muscles became so injury prone on the right side over the past year and now have fasciculations and soreness happen so rapidly in the past 3 weeks leads me to believe this is essentially unilateral. Ive read stories where the fasciculations happened first before weakness, but what I cant figure out is how long or short it takes for ALS to progress if the first symptom truly is twitching, and if so, would muscle soreness come next like mine up until a sudden inability to use the muscle? Could the constant injuries to the right side over the past year been the warning for me that the muscles are deteriorating?
I have a neuro appt scheduled for april 12th. Until then I just feel in constant fear. I was starting to hope this was just BFS but now that muscle soreness has started in the right leg my panic alarm is in absolute overdrive.
Thanks for reading, im sure I will be one of thousands here who have posted something similar thats not close to what ALS looks like, but I still feel my feelings and fears are valid, at least to me.