09/04/2025
August was strange.
I got diagnosed with lupus/UCTD in July, and started on medications for it. Suddenly I’ve gone from not even liking to take ibuprofen to taking six pills every morning. But, you know what, if it actually gets me my life back, I’m all for it.
I’m always really impressed by people who can live blog their diagnoses. I’m still trying to figure out how much I’m comfortable sharing. I feel like this whole year has been a parade of doctor’s appointments and feeling like I’m constantly falling down a bottomless hole. I’m still trying to find my way out.
I’m grateful for having a good doctor, who listens. I’m grateful for clients and work and my partner, who rocks, and my weird dog and the stray spooky cat who may or may not agree to being adopted by us.
Chronic illness sucks but I’m nothing if not obstinate. So, I keep working on the plan. Keep looking for things I can do anyway. Because I want to keep doing things, even if looks different than the things I did before.
If you’re here, thanks for being here. I’m really glad you’re here.