
Expert guidance on joint hypermobility, EDS, HSD, POTS, MCAS and chronic pain from Dr. Linda Bluestein, The Hypermobility MD.
| Platform | Pricing | Freemium | Publishes | Twice weekly | |
|---|---|---|---|---|---|
| Issues | 329 | Founded | 2 years ago | Last Issue | 2 days ago |
| Active | |||||

What happens when real chronic illness meets a social media algorithm that rewards hospital photos, medical devices, and dramatic symptom posts?
In this episode of the Bendy Bodies Podcast, Dr. Linda Bluestein, is joined by Dr. Dacre Knig...
Part 2: The Hidden Biological Contributors to Widespread Pain
Welcome back to the Bendy Bulletin!
Why are so many women with hypermobile EDS, mast cell activation syndrome (MCAS), and dysautonomia told their symptoms are “just anxiety,” and how do you tell real anxiety from a body-driven feeling of dread?
In this episode of the Bendy...
Part 1: Understanding the Science Behind Widespread Pain
“My whole body hurts.”
If an infection triggered your mast cell activation syndrome (MCAS), Sjögren’s, or dysautonomia, can treating that infection reverse it?
In this episode of the Bendy Bodies Podcast, Dr. Linda Bluestein and Dr. Ina Stephens answer a listen...
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The writers behind this newsletter.
Evidence-based insights on Ehlers-Danlos syndromes, hypermobility spectrum disorders, POTS, MCAS, chronic pain, and related conditions from a physician who also lives with hypermobility.
I am a physician assistant specializing in Ehlers-Danlos syndromes, hypermobility spectrum disorders, and complex chronic illness. My work with Bendy Bodies focuses on patient education and support for people navigating these conditions.
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