I was diagnosed with ALS back in 2001. They thought it might be the PLS form of it and after a few years confirmed to me that it was. I would like to know what other people are like who are living with this condition called PLS form of ALS. I am now 16 years with this. I have been quadriplegic...
My specialist assures me that I have ALS but have a PLS component or something like that. I was diagnosed with ALS back in 2000, but possibly PLS because I did not exhibit any muscle fasciculations so cardinal in ALS. After 2 more years of testing with several ALS and MS specialists it was...
als
back
bipap
brain
caregivers
diagnosed
diaphragm
emg
fasciculations
love
medicine
movement
muscle
muscles
neurologist
pls
progression
stroke
testing
work
I'm quad now with ALS and bought new computer with windows 8. I use a headmouse. Can't get my clikka mouse to work on anything except the desktop app. Any suggestions?