I just have to chime in here, too. I agree with the sentiments posted here. I am still in undiagnosed limbo. I recall all too well the PANIC I felt when my neuro suggested it could be the onset of
MND.
For along time, I just lingered and read, until I felt it was safe to share my journey. I've made some friends along the way and gained a greater appreciation of humankind to know that there are REAL people suffering and still willing to lend an ear or a cyber shoulder- and many laughs. It's NICE to know we are not alone with neuromuscular issues and that the PALS/CALS dont kick us off their site. I think it boils down to RESPECT and ADMIRATION for bravery and courage shown by PALS/CALS and their willingness to share their input.
I have learned to use the search feature and also to look at the DATES on when a thread was started.
I think what MUST BE LEARNED ON HERE and maybe posted up somewhere in BOLD along with the SHOCKER POP-UP is that you are NOT going to get a diagnosis of ANYTHING on this forum. It is a communication portal and NOT a SUBSTITUTE for a Dr. visit or a neuro visit-
With love and admiration-
Cindy