Feel free to explain further!!
My entire life people have been chiding me to speak more clearly “just slow down” etc, etc. Recently got diagnosed with FND, now I’m realising it’s probably been that all along. I’ve always been really embarrassed of my voice and how difficult it is for me to speak, hopefully now that I have a diagnosis this will change.
I’ve never seen younger people using canes. That is why I use my cane with pride so that I may be the person that assures another that they have a right to stability. They have the right to the independence and support of a mobility aid. I hope that by living my life as I choose I may be able to drown out some of the rampant ableism being fired at the youth of our community.
Does anybody else with FND/coordination issues go to take a drink out of an open water bottle (one without a straw, just an opening to drink out of) then accidentally spill it all over themselves?
It never occurred to me that you could get a seat for showering. I’ve been stumbling around and sitting on the floor this entire time. Woahhhh….the wonders of modern technology.
mxmorbidmidnight reblogged
Shoutout to people with Functional Neurological Disorder
Shoutout to people with functional tics
Shoutout to people who have dystonia
Shoutout to people with Psychogenic non-epileptic seizures
Shoutout to people with paralysis and or weakness
Shoutout to people with tremors
Shoutout to people who shut down/unresponsive episodes
Shoutout to people who have walking difficulties
Shoutout to people who have numbness
Shoutout to people who have speech problems
Shoutout to people with vision problems
Shoutout to people with hearing problems
Shoutout to people with memory loss
Shoutout to everyone with FND
Was nice to see this after being diagnosed a few days ago.