MS awareness Archives - Tripping On Air

Tag: MS awareness

Mobility Aids 101: How To Cope, What To Get

Welcome to March, Trippers. It’s MS Awareness Month (at least in the US, so basically, everywhere), and I have mixed feelings. I’m all for advocacy,

March 9, 2023 • 13 Comments

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Trippers of Toronto! Let’s hang out October 5th

Trippers of Toronto! Let’s hang out October 5th 😍

Presented by EMD Serono, #SoThisIsMS is going to be an awesome day full of connections for ppl with MS.

Register at the link in bio and I hope to see you there! 😘

TFW all you wanna do is cry and eat chocolate and

TFW all you wanna do is cry and eat chocolate and then you realize you're about to get your period and you're like, oh thank god, that explains it 😮‍💨

well, PMS and OCG (the Ocrevus Crap Gap) must have gone to the same school of fuckery bc that's what it's like when symptoms are flaring and you suddenly remember you're due for your infusion 🤦‍♀️

Time to close the crap 💉

#ocrevus #crapGap #thisIsMS

These legs are mostly decorative. #legs #weDoWha

These legs are mostly decorative.

#legs #weDoWhatWeWant 🤷‍♀️

ID: ardra is seated on a Rollator in a photo that was not taken today because today she is still wearing the shirt she slept in #thisIsMS

When the accessible bathroom is fancy, you take a

When the accessible bathroom is fancy, you take a selfie 📱

#thisIsMS #accessibleInThe6ix #toronto #disabilityStyle #disabilityVisibility

September is for pumpkin spice and getting my shit

September is for pumpkin spice and getting my shit together, which means skipping the pumpkin spice and finding my way back to physio.

From MIA to TMI: I’m back spilling tea and everything else for that matter. Link in bio.

trippingonair.com

#newPost #thisIsMS

Spent the day with the man behind the voice, Alex

Spent the day with the man behind the voice, Alex Hajjar 🎙️

We have big plans for Season 2 of Tripping On Air podcast. Coming soon!

If you’re new to the pod, I recommend checking out episodes like “the worst symptom of MS” or “the top 10 myths about MS”

Is there a topic you wanna dig into? Leave a comment! We wanna hear from you.

You can find episodes at the link in bio and thanks to everyone who subscribes! Your support means a lot. 😘

#thisIsMS

Finally made it to the spa after sitting on a gift

Finally made it to the spa after sitting on a gift card for months bc when you have MS, even a day of pampering can be exhausting.

Getting dressed/undressed/dressed again is a slog & I try to limit the number of times p/day I have to put my legs through leg-holes. 😮‍💨 #legday

Climbing onto the high massage table makes for an awkward scene but turning myself over on that narrow slab while someone half my size holds up a sheet is like an extreme trust-fall exercise 🤞

Sometimes we have to rally even to get some r&r. Spent the day with my bestie and the effort was totally worth it. 🖤

#thisIsMS

#MS #spaDay #SPMS #namaSlay #chronicIllness #FMS

Kale doesn’t cure MS but can a burger? 🤔 Let’s find out.

Every year @awcanada raises an F-tonne of money with their Burgers to Beat MS campaign 🙌

$2 from every Teen Burger sold tomorrow goes to supporting Canadians with MS 🙏

Round up your bill, donate your change and help make a difference.

Thanks A&W for your ongoing support of Canadians with #MS and for the awareness this campaign always brings. 🍔 🧡

#burgersToBeatMS