Articles

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Cassandra Campbell on finding acceptance as a person with EDS

Posted on July 19, 2022

For our August newsletter, the Chronic Pain Partners media team interviewed a group of people to highlight the diversity of our community and emphasize the challenges that arise when a person belongs to more than one minority. In this interview, writer Beth Miller speaks with Cassandra Campbell, a coach, author and EDS advocate. Campbell shares […]

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Interview with Dr. Norris on finding the genetic cause(s) for hypermobile EDS and much more

Posted on June 25, 2022

  For Chronic Pain Partners, journalist Karina Sturm had the honor to speak with Dr. Russell “Chip” Norris from the Norris Lab at MUSC, a research laboratory dedicated to finding the genetic cause(s) for the hypermobile Ehlers-Danlos syndrome. Sturm speaks with Norris about their current research and how it will change care for people with […]

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Jack Briar Pollock on challenges of being trans with EDS

Posted on June 23, 2022

For our July newsletter, the Chronic Pain Partners media team interviewed a diverse group of people to highlight the diversity of our community and emphasize the challenges that arise when one belongs to more than one minority. In this interview, medical writer Sarah Cook, PA-C, speaks with Jack Briar Pollock, an EDS advocate and artist […]

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Jules Machias about their EDS journey and new middle-grade book “Fight + Flight”

Posted on June 23, 2022

For our July newsletter, the Chronic Pain Partner media team is excited to introduce the EDS community to the new middle-grade* fiction book “Fight + Flight,” which features a character with EDS! Journalist Karina Sturm had the pleasure to talk to author Jules Machias about their life with Ehlers-Danlos syndrome, their career as a writer, […]

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Interview with Donna Sullivan, TCAPP, about wrongful child abuse allegations and medically complex children

Posted on June 23, 2022

  For our July newsletter, journalist Karina Sturm spoke with Donna Sullivan, board member of The Coalition Against Pediatric Pain (TCAPP). Sullivan lives with EDS and has several affected children as well. In this interview, she shares with Chronic Pain Partners her decade-long experience working with families accused of child abuse due to a medically […]

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Kaleena Deshawn on challenges as a person of color with EDS, Fibromyalgia and ME/CFS

Posted on June 22, 2022

For our July newsletter, the Chronic Pain Partners media team interviewed a group of people to highlight the diversity of our community and emphasize the challenges that arise when a person belongs to more than one minority. In this interview, journalist Jackie Saa speaks with Kaleena Deshawn, a Boston-based intermedia artist, makeup enthusiast, and zebra […]

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Interview with Dr. Pradeep Chopra regarding the psychological and psychiatric aspects of the Ehlers–Danlos syndromes and hypermobility spectrum disorder

Posted on May 20, 2022

Introduction EDS expert and pain specialist Dr. Pradeep Chopra contacted Chronic Pain Partners to speak about a recently published review on the psychological and psychiatric aspects of Ehlers-Danlos syndrome. Dr. Chopra has been treating complex pain patients with a focus on people with Ehlers-Danlos syndrome for decades and is a passionate advocate for EDSers across […]

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