Interviews and Podcasts:

EDS Awareness Podcast with Dr. Linda Bluestein

I had the honor to be interviewed by Dr. Linda Bluestein, an EDS expert for a podcast featured by EDS Awareness. In this interview, we discuss the challenges of making ’We Are Visible’, my personal goals for the next years, and the plan for future distribution of the film. 

Video Interview with Kendra Neilson Myles for EDS Wellness

Kendra Neilson Myles, the CEO of EDS Wellness and health expert, interviewed me via Skype and we spoke about the challenges of making ‘We Are Visible’, the cast, future screenings, and my plans for distribution. 

Watch the video:

We Are Visible - Q&A with Karia Sturm about Her Recently Released EDS Documentary
Watch this video on YouTube.
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Professional Reviews of ’We Are Visible’:

Oh Twist! -- EDS Advocate and Educator

Not only was the story telling masterfully handled, weaving her own diagnostic journey into those of her six international subjects, but their stories were so moving and compelling I was sunk. Bring tissues!

Read full review here: http://ohtwist.com/becoming-visible

Jeannie Di Bon -- Physical Therapist specialized in EDS care

But not one of the six participants in the film felt sorry for themselves. Remarkable strength. The film demonstrated resilience, strength and determination – qualities I believe you need to survive in the EDS world. It shouldn’t be a fight, but for many people it is. We Are Visible is going to be a valuable tool to show the world what living with an invisible illness is really like. 

Read full review here: https://jeanniedibon.com/wellness/this-film-is-going-to-close-the-gap-on-eds-education/

David-Elijah Nahmod -- Journalist and Film Critic

It’s a profoundly moving and eye-opening film that will hopefully find an audience outside of the Ehlers-Danlos community. It’s a film that calls for compassion and understanding, and explains in no uncertain terms exactly what Ehlers-Danlos can do to a person’s body.

Read the full review here: https://belocipriani.com/disability-advocates/life-with-ehlers-danlos-syndrome-chronicled-in-new-documentary/

Press Releases and Blogs:

EDS Wisconsin

The organization EDS Wisconsin released general information about my motivation to produce ’We Are Visible’ on their blog:

EDS Awareness

The organization EDS Awareness lists several screenings on their website:

Fight Like A Warrior

‘We Are Visible’ didn’t only give a voice to its contributors. It also gave me a voice. It helped me realize that there are so many people with similar experiences to mine. All of their perspectives helped me to become a better person, a better journalist, and they made me feel validated for the very first time. 

Read the full release: https://www.fightlikeawarrior.org/post/we-are-visible-a-documentary-about-living-with-an-invisible-illness

EDS Society

 Journalists and filmmaker alike talk about these people but not with them. I wanted to change this, so ’We Are Visible’ directly involved all of its contributors in order to represent this community in an accurate and truthful way

Read the full release here: https://www.ehlers-danlos.com/we-are-visible/

Do you want to find out more about ‘We Are Visible’?

Check out the official film website

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