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Current Administration Threatens Medicaid – April 2025

Since the new administration took office in January, policy changes have been moving fast. Currently, the Republican led Congress (the House) is dangling the threat of major budget cuts to social safety nets over the senior and disabled community, leaving a lot of EDSers and others quite stressed about the continuity of their health care […]

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Why Is It So Hard To Get A Genetics Appointment For My Child?

If you are a parent who is trying to get your child evaluated for Ehlers-Danlos Syndrome, you may have already discovered that it is often not a straightforward process. The Ehlers Danlos Society estimates it can take 10-12 years on average for a diagnosis. That can be a lifetime for a child. However, obtaining a […]

A woman sitting on the floor holding her legs close to her body with eyes closed.

Understanding Your Flare Fettered Friend

Has a friend recently told you: I feel a pain flare coming on, I’m in a flare, or I’m coming out of a flare? If so, what does this mean for them and what does it mean for you? Maybe you want to help but are unsure how? In this article, guest author Avi, who […]

A collage of three images of Dr. Hollick. Two where he is wearing a bright yellow shirt and trains to run the Boston Marathon and one wear he sits at his desk wearing a white coat.

The Extra Mile: Why This 79-Year-Old Pioneering Physician Is Running the Boston Marathon

Not all heroes wear capes, sometimes they wear sneakers.  At age 79, Dr. Michael Holick is preparing to run the Boston Marathon to raise awareness for a group of patients he’s long championed: those living with Ehlers-Danlos Syndrome (EDS). It will be the second time he has completed this historic and rigorous road race. Although […]

A group of people on the red carpet at SlamDance Film Festival.

The World Premiere of Complicated: The Film That Named Itself!

It took nine years to get to that Red Carpet. In late February, our documentary film, Complicated, premiered at the prestigious Slam Dance Film Festival in Los Angeles.   The film is a call to action, an expose of some of the darker challenges that young people and their families living with complex symptoms of Ehlers-Danlos […]

A child playing with colorful building blocks looking serious. The child has brown short hair and wears a blue shirt with red stripes.

Neurodivergence and Hypermobility: The Autism-EDS Connection 

Chronic Pain Partners introduced the topic of neurodivergence and Hypermobility Spectrum Disorders (HSD) and Ehlers-Danlos Syndrome (EDS) in our first newsletter this year (January 2025), but autism has been shown to co-occur with EDS for many years, with an early published case dating back as far as 1993 and another in 2011. Neurodivergence comprises a […]

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Part Two: HEDS Researchers Explain Clinician-Associated Trauma

This is the second article in our series covering psychological medical trauma. The first article provided an introduction to what concepts of psychological medical trauma exist and the newly-created concept of clinician-associated trauma. It also introduced a study regarding hEDS patients and clinician-associated trauma. This article will look deeper into the details of this study […]

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10 clever comebacks for handling offensive comments about hEDS

Living with a rare disease like hEDS (Hypermobile Ehlers-Danlos Syndrome) can lead to misunderstandings and sometimes offensive comments from people who don’t get it. However, handling these remarks with wit and wisdom can make the situation easier and lighten the load. Here are ten clever comebacks for handling offensive comments about hEDS: “You’re just lazy.” […]