Loopy
I was a first-grade teacher and was diagnosed in 2015. I had all these aches, feeling tired all the time, and I was forgetting everything. I would come home, take a shower, go to bed. That was my life. Luckily I was diagnosed early on. Things got better when I became a school librarian, but the stress and long days still affected me. When I could, I retired. Feeling much better and can nap or be “loopy” (brain fog) with a supportive family.
This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Lupus.net team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.
Join the conversation