This is my first time having the flu diagnosed with MS. The funny thing about it (well,not really) I’ve been in a flare and while I was going to steroid infusions I started to feel like maybe I was catching a cold or that it could be sinuses.
Then out of nowhere like a Mac truck it hit me so hard and I was having issues walking, breathing and extremely fatigued. I was delirious and barely holding on.
I can’t speak for everyone’s MS but I know for me, fatigue is something I battle with almost daily. I also get frustrated and sick of things happening to me that lately I’ve been wanting a timeline for every crazy thing that happens to me.
I found some helpful tips to help count down the days of the flu on the CBHA website and I figured I would share them here.
Even though it’s not a fix all hopefully it can be some sort of guide to hope of feeling better.
I hope whoever reads this feels better soon, drink lots of fluids, try to eat and hang in there, we got this!! Even when we feel like we don’t. Keep fighting and don’t give up.
Happily Ever Amber 