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One year after the launch of Lightening the Shadow, my book for people with chronic illnesses and their healthcare providers, I see hope. I see hope in the form of readers who have opened up to me about their own experiences, of a tiny increase in federal research funding for ME/CFS, and of my continued ability to write and copyedit. If you haven't left a review of the book on Amazon or Barnes & Noble, write one today! Reviews are how writers reach more readers, and there are many more readers out there who need this book. If you haven't read the book, it's never too late to read it! You can get a free sample on Amazon or get a free expanded sample by emailing me. We have the most hope in ending the silent suffering of ME, fibromyalgia, and all other invisible disabling illnesses if we work together in making our experiences known.  Source: Kinden Kuo, Flickr Creative Commons Darla Nagel is a biomedical copy editor who has an invisible chronic illness. She wants to educate healthcare professionals and encourage patients. If you want to receive quarterly updates from her, email darla.nagel{a}gmail.com.
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“If plan A doesn’t work, the alphabet has 25 more letters – 204 if you’re in Japan.” —Claire Cook Darla Nagel is a biomedical copy editor who has an invisible chronic illness. She wants to educate health care professionals and encourage patients. If you want to receive quarterly updates from her, email darla.nagel{a}gmail.com.
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