Hi Bestfriendstilltheend,
Thanks for the response. I suspect many of us posting here are like me in that we don't necessarily feel it's *likely* we have ALS; we're concerned it's *possible*. A worried mind imagines the worst.
Secondly, I wouldn't be wasting everyone's time with this thread if...
Hello all, and a sincere thank you for being here and sharing your thoughts--
I am curious to hear about your experience with paresthesias (burning pain, tingling, or numbness) in ALS/MND. Have any of you had paresthesias as the first symptom of ALS or other MND? How would you describe them...