An unexpected kneecap dislocation revives concerns about bleeding

Originally published on Hemophilia News Today by BioNews, Inc.

Managing bleeding disorders and Ehlers-Danlos syndrome can be challenging

I’d enjoyed several months without any bleeding problems until I experienced an unexpected ankle bleed last week. The elevator at my condo was out of service, so I had to climb four flights of stairs multiple times a day, which put additional strain on my joints. Just when I thought things couldn’t get any worse, I started having issues with my knee.

I was diagnosed with Ehlers-Danlos syndrome (EDS) as a teenager. My hematologist, who’d previously diagnosed me with von Willebrand disease (VWD) and hemophilia B, explained EDS as a connective tissue disorder that made my joints hypermobile.

While hypermobility may offer unique advantages for gymnasts and ballet dancers, EDS presents many challenges, including frequent joint dislocations.

During my teenage years, my kneecap often dislocated. I underwent two surgeries, and eventually, it stopped popping out of place. I’ve learned to navigate life with EDS and bleeding disorders by avoiding activities like tennis that could strain my joints.

As an adult, I’ve experienced little trouble with EDS other than hernias and an odd finger dislocation while making a bed. I’ve learned to protect my joints and adapt my lifestyle accordingly.

A familiar sensation

On Sunday, all of that changed. While sitting sideways on my recliner, my kneecap suddenly slid out of its track as I moved my leg. Although familiar, the feeling caught me off guard. Then, just as swiftly, it popped back into place. I hadn’t felt this sensation in over 30 years, yet I knew exactly what was happening.

To say I freaked out is an understatement. The mere thought of reliving that unsettling dislocation without warning fills me with dread. I don’t want the bleeding problems that come along with joint dislocations. Looking back, I recall the distressing times when my knee needed draining because of bleeding and swelling.

I’m not the only person who’s been diagnosed with VWD and EDS. Research has even established a connection between EDS and bleeding problems. My diagnoses are a trifecta of bleeding disorders. As a hematologist once told me, I’m lucky I don’t have more problems.

I’m trying to adopt a positive attitude. Treatment has come a long way since my teenage years, and I feel like I can address bleeding issues should they arise. I’m good at the RICE method, which stands for rest, ice, compression, and elevation. I have medications on hand to infuse into a vein if needed. To help put my mind at ease, I’ll talk with an orthopedic surgeon next week about how to protect my knee and prevent another dislocation.

©Jennifer Lynne, 2024, All rights reserved

Jennifer Lynne

Jennifer is an entrepreneur specializing in digital marketing, a self-professed computer nerd, and a nationally competitive Scrabble player. Jennifer has strong ties to the bleeding disorder community; she was diagnosed in 1975 with hemophilia B and Von Willebrand’s disease at age 10.

She is a graduate of the University of Wisconsin, Madison with a BA in marketing and journalism, and MIT’s Birthing of Giants Fellowship Program. A native of Brookfield, Wisconsin, she now resides in sunny Punta Gorda, Florida. Jennifer hopes that her column will raise awareness for hemophilia and other bleeding disorders, especially among women.

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