Posts tagged with: working with MS

The blog post that almost wasn’t

Here’s the unfiltered truth about why writing this blog has been helpful to me. It’s not about helping others. Or even helping myself, really. It was mostly about the fact... Read More

Inspiration or desperation

I’ve had a really bad couple of days. I could feel it coming in the parts of me that hurt worse when a bad day is looming. I could see... Read More

And then she rested

I like to play a little game sometimes now that I’m in my post-Lemtrada recovery period. I call this game Recovering or Just Lazy: You Be the Judge. While I’m... Read More

The Story of Day 3

Day three is in the bag. No more gagging on handfuls of nasty-tasting pills a couple of times tomorrow. That last handful of Prednisone I took earlier this evening had... Read More

4.6 + 11 + 1 = one hot mess

I’ve never been good at math. I was a writing major in college. Even more, I was a creative writing major (with a minor in political science but who cares... Read More

Update from my bubble…Inside the mind of one house-bound MS’er

Patient, calm, Zen-Beth has left the building, folks. She’s been replaced with Can-We-Get-This-Show-On-The-Road-Beth and you know that’s not a good thing. Not a good thing at all. Let’s see…where have... Read More

The unexpected upside of Lemtrada

Before anyone gets too excited, I use that image above ironically at best. I mean, I’m not laying in bed moaning or weeping but I’m also not out skipping in... Read More

And then she slept

I’ve been meaning to update the blog with my post-Lemtrada experience sooner than this but here’s the thing: I’ve been asleep. If you’re a regular reader of this blog you... Read More

Musions on Infusions: 40% Down

I When I started this Lemtrada journey on Monday I had every intention of doing a daily blog describing the day-by-day experiences of the treatment. After my first day I... Read More

It finally happened

This whole thing was bound to catch up to me. Eventually. I knew the day would come when I’d be forced to face the fact that this disease I’m still... Read More