Hi, I'm Bev. In 2014, I was diagnosed with Lipedema, a genetic disease I'd never heard about before. This is my journey as I manage and live with a health condition that not only affects your body, but your psyche as well. The purpose of this blog is to help others learn about Lipedema. In addition, I hope to offer support and encouragement to other women who are suffering from this rare, incurable disease.
Tuesday, June 27, 2017
The (lipedema) woes of summer
I'm not a fan of summer. I don't care for hotter weather in the first place, but my lipedema appears to get worse during the summer months. :(
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