Eyeballing that amount
Saturday January 09th 2021, 9:08 pm
Filed under: Crohn's flare,Lupus

Today’s new vocabulary word: episcleritis.

Yesterday morning I thought I’d scratched my eyeball somehow in the night as I repeatedly put eyedrops in and kept trying to find where that exceptionally long sharp eyelash could be. Maybe I’d scratched the cornea again. All day long I could not make it better but I hoped a good night’s sleep would.

Eye pain kicked me out of bed early today.

My exam was my husband taking pictures and my doctor asking me over the phone if it hurts when I touch my eyeball?

I looked at the handset funny a moment. “I dunno, I don’t usually go around touching my eyeball.”

She laughed, I closed my eye and gently tried it and went oooh yes definitely.

Any discharge?

No.

She saw one of the pictures.

Yup, pretty clearly episcleritis. Start the drops and if it doesn’t get better get right back to me.

Who knew, having had lupus diagnosed half my life ago, that there could be a new complication I’d never heard of?

When I told her NSAIDs make me deaf, she considered a moment, decided some tiny amount could get in the bloodstream, and prescribed steroid drops instead.

Which flashed me back to the staggering 200 mg/day dose via IV twelve years ago that took 25% of the bone mass in my hips (I was in a study at UCSF at the time) but did absolutely nothing to fight back my soaring autoimmunity–and my GI doctor later telling me, But: just because steroids don’t work in one part of the body doesn’t mean they won’t later work in a different part for completely different reasons.

I bet Dr. R doesn’t remember telling me that but I do and it was something I was going to need to hear and today was the day. I had to try.

Forty-five minutes after that first single drop I said to Richard, It was *painful* before. Now it’s, eh. Irritated, but, eh.

Four hours later my eye told me my dose was wearing off. And then it again thanked me for that drop, even if it took me five tries that time to land one in. I am not yet good at this.

I hope there are enough doses in that little bottle for all the times I’ll miss but I’m really grateful to have it. And that it works! Yay modern medicine!


4 Comments so far
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Don’t be shy. Ask Richard to be the drop man.

Comment by Barbara 01.09.21 @ 9:24 pm

I’ll second getting Richard to put the drops in for you. When you’re not used to them (and even when you are), they can be very awkward. I’m glad they’re helping you!

Comment by ccr in MA 01.10.21 @ 8:54 am

Second that motion!

Comment by Jayleen Hatmaker 01.10.21 @ 8:57 am

I just got steroid ear drops for the itching psoriasis down in my ears, at $30 a whack and I can’t put them in.

Comment by Sharon Stanger 01.10.21 @ 12:42 pm



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