Dear All,
maybe I am not writing in the right topic... maybe this should go in the DIHALS topic.
This is my hopeless scream on the internet, for strangers.
I should be the caregiver of my mother, but I am not...
This is the story of our family (with some off-topic, not ALS-related threads)...
age
anxiety
back
caregiver
children
cured
depression
diagnosed
diagnosis
dihals
drugs
emg
eye
familial
familial als
family
father
fatigue
fell
fingers
foot
hours
kids
life
mad
muscles
problems
speech
story
symptoms
testing
twitching
vision
weakness