An Open Letter to Dads Living With Hemophilia and Raising Daughters
Dear Hemophilia Dad, I am writing to you today to protect the health of your beloved daughter. Trust me, I…
Jennifer Lynne is an entrepreneur specializing in digital marketing, a self-professed computer nerd, and a nationally competitive Scrabble player. She has deep roots in the bleeding disorder community, having been diagnosed with hemophilia B and Von Willebrand’s disease in 1975 at the age of 10. A proud graduate of the University of Wisconsin–Madison with a BA in marketing and journalism, Jennifer also completed MIT’s prestigious Birthing of Giants Fellowship Program. Originally from Brookfield, Wisconsin, she now lives in sunny Punta Gorda, Florida. Jennifer is the founder of GirlsBleedToo.com, a platform dedicated to raising awareness about bleeding disorders in women and girls. Through her writing, she hopes to educate, advocate, and amplify the voices of those—especially women—living with these often-overlooked conditions.
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Dear Hemophilia Dad, I am writing to you today to protect the health of your beloved daughter. Trust me, I…
Kendall Fitzpatrick and I have much in common. Like me, she has hemophilia B and von Willebrand disease.
I recently watched the eight-episode Canadian drama miniseries “Unspeakable,” which was inspired by real events and first televised a…
I have von Willebrand disease (VWD) and hemophilia B, a less common form of hemophilia that arises when a…
Hurricane Ian, which battered the southeastern United States and the Caribbean in late September and early October, nearly destroyed…
Greetings! I’m writing from Orlando, Florida, my temporary oasis from the wrath of Hurricane Ian. Last week, my mom and…
Well, hello, Ian. Please go away. As I write this, the track of Hurricane Ian has shifted south from Tampa,…
The end of 2022 is rapidly approaching, and I’ve made nary a dent in my fitness and diet goals…
“It’s my party, and I’ll cry if I want to, cry if I want to, cry if I…
Shared decision-making in healthcare was a topic at the National Hemophilia Foundation’s Bleeding Disorders Conference I attended virtually last week.
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