Posts tagged with: disability

Scary things that go bump in my brain

It’s a good night to talk about terrifying things, right? No. I’m not talking about creepy baby dolls or marionettes or ventriloquist’s dummies or even movies about satanic possession or... Read More

Bethy Bright and Dark 2.0

Here’s the thing about putting all your business on the Internet (as my mother calls what I do)…it means when bad things happen you feel compelled to share the news... Read More

Quick update

The Great Scott himself called me before I could call him this morning. As it turns out, my labs were completely normal. No UTI indicators at all. No indicators of... Read More

This Little Miggy is teaching me to look up

I’m not really sure what I want to write about. This is unusual for me. I usually have at least three or four posts swimming around in my brain at... Read More

When your switch won’t flip

It’s still off. My switch. It hasn’t gone back on. It’s a real conundrum. First they tell me, rest! Your body is healing, silly person, you’ve just put your body... 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 subtle art of not panicking

When I decided to go for this new approach to my treatment, I made some promises to myself. Maybe they were more like challenges that I presented to myself than... 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