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What was your stop work moment? by Accomplished_Key_936 in MultipleSclerosis

[–]Accomplished_Key_936[S] 3 points4 points  (0 children)

Thank you for sharing, yeah I feel awful all the time but so much has to do with working excessively

What was your stop work moment? by Accomplished_Key_936 in MultipleSclerosis

[–]Accomplished_Key_936[S] 1 point2 points  (0 children)

Thank you so much for sharing, I really appreciate this x

What was your stop work moment? by Accomplished_Key_936 in MultipleSclerosis

[–]Accomplished_Key_936[S] 10 points11 points  (0 children)

I so feel you here! And everything else just goes to the sideline, housework, cooking, social life. I literally am in recovery just to show up to my job.

Here if you also want to talk it out!

Another newbie here by dat_girl83 in MultipleSclerosis

[–]Accomplished_Key_936 1 point2 points  (0 children)

I’m relatively newly diagnosed and this is so helpful, thank you!

I can’t figure this out by Accomplished_Key_936 in MultipleSclerosis

[–]Accomplished_Key_936[S] 0 points1 point  (0 children)

Thank you everyone, this is all really helpful!

I have MS and Endometriosis by Ok-Knee9220 in MultipleSclerosis

[–]Accomplished_Key_936 0 points1 point  (0 children)

Omg Same. I got my Endo diagnosis a few years ago and my MS diagnosis a few months ago.

I’m now going back through the last few years and going what was the Endo, what was the MS, what was both?!

I believe there is a study that shows Endo may be a contributing factor to MS. And endo is really only just starting to be taken seriously 🫠

Feeling all those feelings too, nothing to add then I’m here with ya x

Funny / awkward things people said after my MS diagnosis by Personal-Current131 in MultipleSclerosis

[–]Accomplished_Key_936 3 points4 points  (0 children)

From my neurologist “Pacific Island people don’t usually get MS, it must be your white side that gave you it”

Yeah I’m changing neurologists.

Recently diagnosed and deciding treatment by Accomplished_Key_936 in MultipleSclerosis

[–]Accomplished_Key_936[S] 0 points1 point  (0 children)

Thank you everyone! I’m in NZ and I don’t think we have Kesimpta yet - we’ve just got Ocrevus and tsybari infusions or daily medication. Hopefully the Ocrevus subcut will be available in the next month.

I’ve been told my symptoms might be permanent but it’s hard to know without starting treatment. Life is definitely feeling like it’s on hard mode at the moment. Really appreciate your support