Author Archive

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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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Use caution when selecting a Website Design and Developer Services.    5 points to consider.

Posted on February 10, 2022

Many Non-profit and for-profit organizations are considering creating or updating their website.  We receive many promotions each day.  As with all businesses there are good, OK and bad companies promoting their services. This article is intended to give you some general guidelines for selecting and managing a reliable Website Service Provider.   Finding a reputable […]

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February Ehlers-Danlos News & Updates

Posted on January 28, 2022

        The Funny Bone News   Because with EDS, every bone is a funny bone.    Hi everyone!    I hope your new year started well!  We skipped the January newsletter, because like almost every year, I was sick in bed over the holidays, and John & I have been working on some […]

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