Alexgb81
New member
- Joined
- Feb 15, 2025
- Messages
- 1
- Reason
- Learn about ALS
- Diagnosis
- 00/0000
- Country
- UK
Hi all.
Just like everyone else here I’m worried sick and feel terribly selfish. I’m M43 usually fit and healthy.
Full disclosure, a good friend of mine died from ALS several years ago and a colleague has recently been diagnosed.
Approx 2-3 weeks ago my left hand started feeling odd; no pain or sensory loss, but clumsy (e.g. struggled to hold a knife straight at dinner) No clinical weakness or wasting noted. It seems to have progressed (certainly got no better) and become more clumsy and less coordinated but strength remains normal grossly and no wasting. I think it’s the thumb and index finger that are affected.
Right hand has also started feeling “clumsy” in the same manner (again no weakness or atrophy) and has started twitching/fasiculating of the thumb muscle.
No other symptoms noted.
I’m unsure if this could be “early” ALS or if I’m massively overthinking things, especially with history of being close to people with ALS.
The medical system where I live means I have a family doctor appointment in 2-3 weeks and am unable to see a health professional until then.
Any advice taken gratefully
Thanks.
Just like everyone else here I’m worried sick and feel terribly selfish. I’m M43 usually fit and healthy.
Full disclosure, a good friend of mine died from ALS several years ago and a colleague has recently been diagnosed.
Approx 2-3 weeks ago my left hand started feeling odd; no pain or sensory loss, but clumsy (e.g. struggled to hold a knife straight at dinner) No clinical weakness or wasting noted. It seems to have progressed (certainly got no better) and become more clumsy and less coordinated but strength remains normal grossly and no wasting. I think it’s the thumb and index finger that are affected.
Right hand has also started feeling “clumsy” in the same manner (again no weakness or atrophy) and has started twitching/fasiculating of the thumb muscle.
No other symptoms noted.
I’m unsure if this could be “early” ALS or if I’m massively overthinking things, especially with history of being close to people with ALS.
The medical system where I live means I have a family doctor appointment in 2-3 weeks and am unable to see a health professional until then.
Any advice taken gratefully
Thanks.