Caregivers Wear Plaid: Together in the Storm: A Caregiver’s and Thrivers' Guide to Living with Lupus

$34.95
by Sean Lowther

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Caregivers Wear Plaid is 264 pages, 33 chapters, of in-depth life experiences of Patty Dunn living with Lupus and her first love, Sean Lowther, her caregiver/advocate. Patty served as Board Chair and then CEO/President of the Lupus Foundation of America's North Carolina Chapter from 2003 to 2008. I came onto the board in 2010 and served as Chairman of the Board from 2015 to 2016. Patty was diagnosed with Lupus when she was 26 years old. Looking back, we both realized she had lupus when we were dating in high school. On June 20, 2025, Patty passed at the age of 82. She made a significant difference in many people's lives over the years by helping them understand and improve their quality of life with lupus. Caregivers Wear Plaid is one way we keep the mission moving forward by reaching out to those in need and understanding. Dr. Neal Taub, Board-Certified in Pain Management, says, “Caregivers Wear Plaid is a terrific book not only for caregivers but for their loved ones, and I dare say medical professionals, too. For caregivers, this book is the best I have seen for those caring for someone living with Lupus or other unimaginable diseases. Caregivers Wear Plaid is enlightening and brings common-sense awareness to the everyday needs, management, and understanding for the caregiver and their loved one to live a better quality of life together.” Dr. Robert Bowen II, MD, Primary Care, says, “An effective caregiver is an essential member of the healthcare team. In his book Caregivers Wear Plaid, Sean Lowther encourages and fosters successful caregivers as he shares his insights gained through his vast personal experience.” Patty and I recommend that you and your loved one read each chapter together, discuss what you have read, and share your thoughts with one another. This process will help you better understand lupus, the circumstances you are facing, and enhance communication between you and your doctors. There is nothing more important than a knowledgeable Lupus Thriver and their caregiver/advocate for the quality of care.

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