
Karina Sturm
Writer and Journalist at Freelance
Freelance #journalist and #chronicillness advocate living with #EhlersDanlosSyndrome besides others. She/her. Profile Pic: @ohrenflimmern
Articles
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Aug 14, 2024 |
chronicpainpartners.com | Karina Sturm
Over the last year, the Ehlers-Danlos Syndromes have been increasingly present in media. Several films have depicted different aspects of the lived experience of families with Ehlers-Danlos Syndromes and comorbid conditions around the globe. The following is a dynamic list of documentary films on EDS and its comorbid conditions based on the release date.
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Jun 11, 2024 |
chronicpainpartners.com | Karina Sturm
Norris Lab Finds HEDS Gene: Kallikrein Chronic Pain Partners is excited to share a significant breakthrough from the Norris Lab regarding hypermobile Ehlers-Danlos Syndrome (hEDS). After a long wait, the research, spearheaded by Dr. Cortney Gensemer, identifying a genetic variant associated with hEDS has been published, pinpointing mutations in the Kallikrein gene family.
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Jun 2, 2024 |
chronicpainpartners.com | Karina Sturm
Podcasts on Ehlers-Danlos Syndrome With growing awareness about the Ehlers-Danlos syndromes, varying resources in different types of media developed over the last years. Our Chronic Pain Partners’ Team is collecting their favorite books, podcasts and films on EDS and its comorbid condition in a series of listicles you will find on our website over the next months.
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May 4, 2024 |
mtdialog.de | Karina Sturm
Ein Bereich, der verstärkt in den Fokus der Forschung gerückt ist, betrifft die Auswirkungen von COVID-19 auf das zentrale Nervensystem und die folgende mögliche Assoziation mit neurodegenerativen Erkrankungen wie M. Alzheimer. ZusammenfassungInmitten der anhaltenden COVID-19-Pandemie haben Mediziner als auch die Betroffenen nicht nur mit den akuten Auswirkungen des Virus zu kämpfen, sondern auch mit den Langzeitfolgen.
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Apr 22, 2024 |
chronicpainpartners.com | Karina Sturm
A Mother’s Day Shout Out from An EDS Mom and The Producer of Complicated As a parent, it is hard to witness your child suffering with symptoms and physical pain. As mothers, we are often looked to, to make everything better, right? When my kids started having medical issues, I quickly learned that there was no parenting book to teach how to comfort and support your child when an entire institution designed to help and care for them fails.
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Wir lesen in Cuxhaven aus unserem Buch “Stoppt #Ableismus” vor! https://t.co/NuOnb6CiDs

RT @EDSawareness1: We're happy to see @karinasturm 's short #EDS film Much More Than That get picked up by the “International Black & Diver…

🗓 6. März 2025, 20:00 Uhr – Sonderveranstaltung der Kollagen-VI-Community der DGM! Ich spreche über die Überlappung zwischen Kollagen-VI-Muskeldystrophien und #EhlersDanlosSyndromen. Meldet euch per PN oder Mail, wenn ihr teilnehmen wollt. #KollagenVI #SelteneErkrankungen https://t.co/f3YmuvIztC