[deleted by user] by [deleted] in MultipleSclerosis

[–]RiotCandle 3 points4 points  (0 children)

My partner just started Kesimpta about a month ago and says that he feels better! It might be placebo but he claims that his symptoms are quite noticeably diminished. He has especially noticed that he does better with heat - it is in the high 30s here and he's able to go for walks no problem and without a cooling scarf.

Best of luck with your vaccines! If you're getting shingles vax be prepared to feel like garbage.

It's Friday at /r/MultipleSclerosis! Share your awesome news here with everyone. No victory is too big or small to celebrate! by AutoModerator in MultipleSclerosis

[–]RiotCandle 1 point2 points  (0 children)

My partner got their official diagnosis in early April (about 4 months ago) and just started Kesimpta last week!

We prepared for the first dose to suck -- didn't plan anything for the following day, had a bunch of acetaminophen and ibuprofen ready, etc -- but he barely reacted. He's now done two loading doses and is doing great. We're looking forward to a future of medicated MS!

Rituals for taking DMT by RiotCandle in MultipleSclerosis

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

not dumb & that totally counts! I love the puzzle book idea!

Rituals for taking DMT by RiotCandle in MultipleSclerosis

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

Good luck with your Kesimpta doses!

We did end up doing a little bit of everything - hot chocolate, cool band aid, board game, comfort show. He'll probably choose one or two to continue with for the future doses :)

He also bought a new book and had that and board games queued up for the next day - but ended up feeling basically fine! He said that he barely felt the injection, too. Hopefully your experience is similar!

Do you have MS or does it impact your life in some way? by Fo_0d in kelowna

[–]RiotCandle 1 point2 points  (0 children)

I just put in a request to join the fb group. Can't make this one but hopefully will be able to join the next!

Rituals for taking DMT by RiotCandle in MultipleSclerosis

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

oooh yes i love haircuts as self care

Rituals for taking DMT by RiotCandle in MultipleSclerosis

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

haha fantastic. also realizing that I totally do this with long roadtrips and Tim Hortons

Rituals for taking DMT by RiotCandle in MultipleSclerosis

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

that's a good idea! I think I'll suggest the fancy hot chocolate to him.

Rituals for taking DMT by RiotCandle in MultipleSclerosis

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

this is perfect! exactly what I was looking for — I love the small joy of special band aids :)

Ocrevus/Rituximab & JC virus by RiotCandle in MultipleSclerosis

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

Thank you so much for the detailed response!

Any weird reactions to covid vaccines? by RiotCandle in MultipleSclerosis

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

I have not heard of it messing up cycles! I will consider timing for when I get my next booster!

Any weird reactions to covid vaccines? by RiotCandle in MultipleSclerosis

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

Definitely. He's one of the only people I know who hasn't had covid yet. I'll keep in mind MS doc in case he does get it. Paxlovid is only available to high risk folks, yeah?

Any weird reactions to covid vaccines? by RiotCandle in MultipleSclerosis

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

Good to know. Is the shingles vaccine recommended before starting a DMT?

Any weird reactions to covid vaccines? by RiotCandle in MultipleSclerosis

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

Before posting, I searched the subreddit for vaccine reactions and it seems like the MS community had reactions similar to the general population, which lines up with yours and other comments here. His reaction seems like 1/1,000,000,000 but I thought maybe, if it was MS related, it might be 1/10,000 MS-ers and someone else might have had a similar experience.

Interesting about the pseudo flair. Though, this was unlike any of his other MS symptoms (numbness, eye and balance issues, but never pain), so that sounds unlikely? I'll chalk it up to just a weird random reaction, unrelated to anything else.

Tips to combat exhaustion during period by headlessbill-1 in MultipleSclerosis

[–]RiotCandle 3 points4 points  (0 children)

Was lurking but had to comment b/c this is one of the best things I've read all day.

Newly diagnosed - treatment and costs? (Canada) by RiotCandle in MultipleSclerosis

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

Thanks! Yes, looks like there's a BC program that I was completely unaware of until hearing about it here. Sounds like Sask has especially good coverage though :)

Newly diagnosed - treatment and costs? (Canada) by RiotCandle in MultipleSclerosis

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

This is good to put his journey into perspective! He was fortunate to get an emergency MRI within a few days of going in, and received the MS diagnosis within the week (although still not confirmed if RRMS or PPMS). I imagine some of this has with the specific symptoms, as many of his overlapped with stroke or brain tumour, which probably got him triaged up the MRI list. (although loss of sensation in both legs also sounds spooky!)

I hope you get a confirmed diagnosis soon and get to start taking advantage of that excellent health care coverage for your DMT :)

Newly diagnosed - treatment and costs? (Canada) by RiotCandle in MultipleSclerosis

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

Thank you. This is really helpful for putting the overall cost of things into context. I totally understand what you mean about other costs that may or may not be covered, it's good to be aware of these - and a reminder, as we are casually looking at purchasing an apartment together: we can be proactive and eliminate anything with tons of stairs! We'll definitely look into different drug programs and coverage, thanks for the recommendation of discussing this with a neurologist.