An op ed piece in Friday's Washington Post helped make up my mind re former congressman Trent Franks (R-Ariz.). The op ed author described a classic case of male privilege in action. The writer Melissa Richmond* is currently vice president of Running Start, an organization that encourages women to run for political office. Richmond wrote that she thought she'd lost out on a career in politics after an encounter with Rep. Franks eight years ago. In her own words: I’ve always been proud … [Read more...]
How to be a CLEFT HEART book booster and reap rewards.
Thought some of you Cleft Heart book fans might get a kick out of seeing a photo (top right of the collage below) of politicians Pelosi and Schumer under an umbrella in D.C, back in the day. Actually, it's my sister Barbara and me in front of the U.S. Capitol after my dad mustered out of the military as a journalist in Washington, D.C. for the Navy's All Hands magazine. My loving sis wrote last year about growing up with a brother with clefts here and here. She wanted to add to the book I'd … [Read more...]
My brother’s clefts: When birth defects aren’t defects-Compete & Cooperate
A Disability, or Not? By Barbara Schonborn I didn’t think my brother Karl had birth defects. Nor did I think his cleft lip and cleft palate were disabilities. When we were children, Karl was just my competitor or my buddy. Brother with no birth defects completes the family. Steven, my second brother, was born when our family lived next door to our grandparents Schonborn in a rural neighborhood of Puyallup, Washington. Steven had no birth defects. His nose and mouth were normal, and he … [Read more...]
My brother’s clefts: When birth defects aren’t defects – Infancy to surgery.
I didn’t think of my brother Karl’s cleft lip and cleft palate as birth defects or disabilities. These birth defects a disability, or not? Guest blog by Barbara Schonborn** Part One: From Infancy to early surgeries. A Princess Usurped. Until I was almost two years old, my life was idyllic. My mother read to me often—I sitting in her lap, a book in mine. She sewed clothes for me, cooked for my father and me, and took me to the Sunday nursery at our church in Boise, Idaho. I knew how … [Read more...]
July is National Cleft & Craniofacial Awareness month: Two special blogs coming soon.
In honor of National Cleft & Craniofacial Disorders Month, I'm planning two special posts in the upcoming weeks from a guest blogger. Stay tuned and be ready to be surprised and informed. Cleft and Craniofacial Disorders Month. Go here for information about the meaning of this July's commemoration and for info about the many organizations supporting it. Also, consider donating a copy of Cleft Heart: Chasing Normal to one of these organizations . . . or to your dentist or … [Read more...]
Cleft lip dad adopts cleft lip baby.
This cleft lip news out of Atlanta made my Father's Day last Sunday. The day had been marred by the death of my best friend's wife the day before. However, I then noticed this news about cute-as-a-boot Hattie Pierce, pictured below. Like myself and so many others, Hattie was born with a cleft lip and palate, . Hattie Pierce w cleft lip and palate. Cleft lip dad & daughter duo get surgery at same hospital. She was adopted by Brian Pierce who'd had his lip surgically restored long … [Read more...]
Thanks to fans of my book and blogs re cleft lip and palate.
I appreciate all of you who’ve followed my cleft lip and palate blogs over recent years. I'll continue to post info relevant to this most common of birth defects.I'm also grateful to those of you who've bought Cleft Heart: Chasing Normal about my experiences with my clefts regarding bullying, facial asymmetry, speech difficulties, etc.Since no good intentions or deeds ever go unpunished, I’m hoping you blog and book fans will consider giving copies of Cleft Heart to your doctor and dentist. Or … [Read more...]