@ashhleyanne: When ms symptoms are endless it’s hard to differentiate #multiplesclerosis #mswarrior #multiplesclerosisawareness #msfighter

666 :

Do u get confusion / brain fog?

Debra Jo Dunbar :

My new one is hip flexor cramp/spasm

ケイト :

Anyone else wake up with a numb leg and arm this morning. Or just me?? 😭😂

Literally a Brine Shrimp :

Safest bet is just to go with it being MS

Debbie 1982 :

i have MS and FND but also IBS , every day is fun 😳

🫧MimikMew :

How often is the progression looked at?

bogos binted :

playing this before i was diagnosed and still playing it after

Tessa 🌼 :

I’m to the point of wondering if my symptoms are MS or something new bc they’re wild man! Like very bizarre. I guess we’ll never know

Shalane :

Every day 😫 your make up looks great by the way!

chronicallyillgirlypsa :

Ugh I unfortunately had this thought with my psoriatic arthritis and turned out I had MS too! I’m glad I listed to my body!

𝓑𝓪𝔂𝓫𝓲𝓮 :

I’ve had so many different symptoms for almost 10 years that didn’t make sense. I’ve gotten tested for a number of different causes over that time and finally had an mri done in January and found out there’s lesions on my brain and spine that point to MS according to an ER Dr but haven’t been able to get into neurology just yet. I’m terrified of the outcome but I just want answers. Sending prayers girl!

harley :

I have ms also can't eat gluten if lactose

🧡Kristin & 🐕‍🦺Dax the Dood :

Every day.

BuddyRise :

Such a fun game 😂 get it

Graceinprogress :

This is the post of the year!!! I ask myself this everyday 🧡

Evie 🔅🦋🌼 :

This!!! 😫

RamblingRanchWife :

everyday. every single day.

🖤🌹Sweet T🌹🖤 :

dude its exhausting 😴

Freshly Milled | Lauren :

It’s a daily struggle ❤️

marubo88 :

💚TESSA💚 :

I have MS too!

Kayani :

😳