This is SO relatable gene.com/stories/life-p…

I miss the days when a cold was just a cold - adding it on top of MS has it feeling more like a freight train 😱🚂🚋🚋🚋🚋

Jokes on me...when it feels worse than a cold it MIGHT just be because it’s actually the flu 🤦🏻‍♀️ Step up your game, flu shot - what good are you?! 😷 🤒 🤧

Seems like an appropriate time to bring this article from MultipleSclerosis.net back amidst all the #COVIDcraziness - in case anyone is having difficulty articulating how this all really IS different for those of us with compromised immune systems... multiplesclerosis.net/living-with-ms…

If there was ever a time to get back in the writing game, it's while having to stay homeWoman shrugging Here's some of thoughts on how lessons learned from COVID can help beyond its resolution. (And some happy news stories if you need a pick-me-up!) misstomrstoms.com/2020/04/covid-…

Don’t care where you stand politically, this thread and analogy are on point. Watching people on social media living their life like everything is fine and dandy is driving me CRAZY

Anyone have any tips and tricks that provide any relief for the lovely nerve-burning sensation? The bottom of my foot/toes feel like I stepped on a stove top 😫 (Thanks a lot, Midwest heat/humidity 🤦🏽‍♀️)

When people ruin YOUR plans because they can’t be bothered to follow the simple COVID safety guidelines 🙃 #MaskOn #SelfIsolating #SocialDistancing

So mind blown that people still think masks “don’t work” or “aren’t even necessary” amidst this still very real pandemic...is it really that hard to believe doctors and infectious disease specialists know what they’re talking about?! 🤦🏻‍♀️ #immunecompromisedlife

This shouldn’t be funny, and yet all the people still refusing to believe health experts really fuel the hilarity here 🤦🏻‍♀️😷

Wish this round-up of millennial-focused articles was something I’d found back when I was diagnosed - a great resource if you or someone you know is in need! multiplesclerosis.net/living-millenn…

One of those posts so true it hurts 😂🤦🏻‍♀️

Life with MS Cog Fog: A Summary.

...was just told visiting people/a city where no one wears masks/distances right before visiting me (high risk) is “no different than you going to a restaurant”...in our county with a mask mandate...where all staff wears masks and other patrons are distanced... *sigh*

Nothing makes my scrambled MS brain sadder than seeing Erin Condren Design no longer offers the option to customize the soft bound planner I’ve lived by all year 😭 Guess the hunt for a new favorite for 2021 starts now...

With my neurologist’s approval...THIS GIRL got round 1 of her COVID vaccine today! Gives me a little bit of relief when it comes to immunity anxiety and a whole lot of hope 💉💪🏼🦠

"The science has shown us that the COVID-19 vaccines are safe and effective. Like other medical decisions, the decision to get a vaccine is best made in partnership with your healthcare provider." #MS #COVID_19 via National MS Society nationalmssociety.org/coronavirus-co…

Back with another rec for something that’s improved my life with MS - if you have issues with temperature regulation, I’ve found the Soma Cool Nights collection is truly a game changer and I can finally comfortably sleep🙌🏼 soma.com/store/category…

Saw an upcoming app recommended that is based all around topical recommendations - turns out there’s already an MS-focused spot to share resources related to MS! phaver.com/community/2da4…

Two days into using the Embr Labs #Wave2 and I’m already obsessed - cannot recommend enough for all of us temperature-challenged MS-ers 🙌🏼 Looking forward to putting the cooling feature to work during a workout 👟👟