I’m so fucking angry. For the first time since diagnosis I have new lesions. Nearly eight years with nothing new on my #MRI and suddenly multiple new lesions. I’ve had a day to sit with it so I no longer feel like I’ve been punched in the gut. But even still. I’m so disappointed. I’d almost tricked myself into believing it was going away. Fuck you, MS. #fums #rrms #ms #multiplesclerosis #pwms #chronicillness #brainlesions

#MSAwareness: Many like me with #MS have invisible symptoms.

We may not use wheelchairs or canes, so it’s not obV… but we’re still facing life-altering dysfunction nonetheless.

2mil ppl in the US have MS.

Still no cure; researchers can’t even agree on root cause.

We MSers still must live with it, and that includes dealing with pain, fatigue, and bodies and brains that don’t work the way they’re supposed to.

Or sometimes we succumb (my goddaughter lost to MS last week at age 36).

#FUMS

All the warm white lights are up and on, but I have no energy to put the ornaments (cat toys) on the pre-lit tree that’s been up for two weeks. #MultipleSclerosis #FUMS

I am so frustrated by the tingly and numbness that I’ve had recently. Shooting down my arms to my fingertips. It was getting better and then I got #covid and it’s now much worse. Anyone else with #multiplesclerosis deal with this and find something that makes it go away? Usually I just wait it out. #fums #PwMS #numbness #chronicillness

#TaskForce #DFB #FUMS #Satire
https://www.facebook.com/fums.magazin/photos/a.353065868183797/2335080293315668/

ISO other folks with #multiplesclerosis to follow and engage with. Figure a random toot is worth a shot. #fums #mssucks #ms #neuroscience

Zuerst auf Mastodon! Nicht das jemand behauptet ich würde alles immer gleich posten.

#FumsDieShow kommt am 17. November in die Centralstation! Es wird viel Liebe geben, Geschenke und vor allem: Die #Lilien Timeline kommt zusammen!

Kommt alle 🥰⚜️💙
#sv98 #fums #fragfug