Hypermobility MD
Expert diagnosis & treatment Ehlers-Danlos Syndromes. Bendy Bodies podcast host. 🚫 medical advice. and others at increased risk of hypermobility disorders.
Dr. Linda Bluestein has been practicing medicine for over 20 years and has helped countless people restore function and improve their quality of life. As a former ballet dancer and instructor, she has a special interest in treating flexibility athletes (dancers, gymnasts, acrobatic artists, etc.) As an integrative medicine physician with certification in Performing Arts Medicine, Dr. Bluestein tak
"What's the best exercise for someone with Ehlers-Danlos Syndromes?"
Morgan Groover's answer might not be what you expect.
"What do you like to do? What do you want to be doing?"
On the latest episode of Bendy Bodies, Morgan, joined by cohost Dr. Dacre Knight of UVA Health, explains that rehabilitation isn't about finding the "perfect" exercise.
It's about finding a goal that's meaningful to you.
For many people living with Ehlers-Danlos Syndromes (EDS), Hypermobility Spectrum Disorder (HSD), and chronic illness, that's easier said than done. Pain and limitations can make it hard to imagine what's possible.
But if your movement plan isn't connected to something you care about, consistency becomes much harder.
And consistency is what creates change.
If your symptoms improved tomorrow, what's one thing you'd love to get back to doing?
📌 This content is for educational purposes only and is not medical advice. It does not establish a physician-patient relationship. Please consult your own healthcare professional for personalized medical care.
ID: Video clip from the Bendy Bodies podcast featuring Morgan Groover discussing exercise for people with Ehlers-Danlos Syndromes. Joined by cohost Dr. Dacre Knight, she explains that the best movement plan is one that aligns with a patient's personal goals and supports long-term consistency.
Episode 200 feels especially meaningful because it brings us full circle.
For this milestone episode of Bendy Bodies, I’m joined by the same two people who launched Episode 1: Jennifer Milner Bodies In:Motion and Dr. Moira McCormack.
Moira brings an extraordinary perspective as both a former professional dancer with The Royal Ballet and the company’s former Lead Physiotherapist.
Together, we talk about a lesson that applies far beyond dance:
Being flexible can look like a gift.
Until you realize how much work it takes to sustain it.
Many hypermobile people are praised for what their bodies can do, whether in dance, sports, music, circus, athletics, or everyday life. But what others don’t always see is the strength training, recovery, pacing, body awareness, and decision-making required to keep going without breaking down.
Success often comes down to learning how to work with your body, not against it.
That means respecting fatigue.
Building stability.
Prioritizing recovery.
Listening earlier.
And understanding that more isn’t always better.
The people who last aren’t necessarily the ones who push the hardest.
They’re often the ones who learn how to balance performance with preservation.
💬 What’s one thing you’ve learned about working with your body instead of against it?
📌 This content is for educational purposes only and is not medical advice. It does not establish a physician-patient relationship. Please consult your own healthcare professional for personalized medical care.
VD: Dr. Linda Bluestein, Jennifer Milner and Moira McCormack discuss how hypermobile dancers have to work harder and rest more to be successful.
Thank you Cynthia Thurlow for having me on your excellent podcast, Everyday Wellness to speak about EDS, HSD, MCAS, POTS and so much more ! Link to episode in comments. 🎧🧬❤️🩹
06/16/2026
Happy Pride Month. 🌈
Everyone deserves to feel safe, respected, and heard when seeking healthcare.
Yet research shows that many LGBTQIA+ individuals experience delays in diagnosis, dismissal of symptoms, or avoid medical care altogether because of prior negative experiences.
For people living with Ehlers-Danlos Syndromes, hypermobility, or chronic pain, those barriers can make an already difficult journey even harder.
As clinicians, we have an opportunity to listen without assumptions, create affirming spaces, and recognize that every patient's experience is shaped by more than a diagnosis alone.
If you're part of the LGBTQIA+ community and searching for answers, you deserve care that sees the whole person, not just the symptoms.
What does affirming healthcare look like to you? I'd love to hear your perspective.
📌 This content is for educational purposes only and is not medical advice. It does not establish a physician-patient relationship. Please consult your own healthcare professional for personalized medical care.
ID: Rainbow-themed Pride Month graphic discussing inclusive healthcare for LGBTQIA+ individuals living with Ehlers-Danlos Syndromes, hypermobility, and chronic pain. The post emphasizes respectful, affirming care and the importance of listening to the whole patient.
06/15/2026
What if your migraines, GI symptoms, dizziness, flushing, and reactions weren't separate problems at all?
That possibility is one reason I was honored to contribute to a newly published review on mast cell activation syndrome (MCAS), a condition that remains widely misunderstood and, in many cases, underrecognized.
For many patients, the journey looks familiar. They see multiple specialists, receive multiple diagnoses, and are told that their testing is "normal," yet no one explanation seems to connect the dots.
MCAS is not simply an allergy disorder. Mast cells interact with the immune system, nervous system, blood vessels, connective tissue, and gastrointestinal tract, which means symptoms can affect multiple organ systems.
This is particularly important for those with Ehlers-Danlos Syndromes, where MCAS, dysautonomia, and gastrointestinal dysfunction frequently overlap.
Recognition matters because the right diagnosis can change the conversation and, for many patients, the treatment plan.
I've shared a deeper analysis, along with downloadable graphics and resources, in this week's newsletter. The link is in my bio.
Have you ever had multiple seemingly unrelated symptoms that were eventually connected by a single diagnosis? I'd love to hear your experience.
📌 This content is for educational purposes only and is not medical advice. It does not establish a physician-patient relationship. Please consult your own healthcare professional for personalized medical care.
ID: Educational graphic discussing mast cell activation syndrome (MCAS) and why it is often missed. The post explains that MCAS can affect multiple body systems, frequently overlaps with Ehlers-Danlos Syndromes and dysautonomia, and highlights the importance of recognizing patterns that may connect seemingly unrelated symptoms.
200 episodes.
I’m honestly overwhelmed by these messages.
When I started Bendy Bodies in 2020, I never could have imagined where this journey would lead.
What began as a passion project to help educate and empower people living with hypermobility, Ehlers-Danlos Syndromes, POTS, MCAS, and related conditions has grown into a community that has touched lives around the world.
To celebrate this milestone, I was deeply honored to receive these incredibly kind messages from some truly extraordinary people who have generously shared their expertise, wisdom, and stories on the podcast over the years.
My heartfelt thanks to Lara Bloom, Dr. Dacre Knight, Dr. Ina Stephens, Jill Miller, Kate Colbert, and Katie and Andrew Dettelbach for taking the time to record these thoughtful messages. Your words mean more than I can adequately express.
Each of you has played a meaningful role in helping Bendy Bodies become what it is today. More importantly, you have helped educate, support, and inspire countless individuals navigating complex medical conditions, often during some of the most challenging periods of their lives.
I am profoundly grateful not only for your friendship and support, but also for your willingness to share your knowledge, experience, advocacy, and heart with this community.
And to every guest, listener, viewer, subscriber, patient, client, colleague, family member, and friend who has been part of this journey: thank you.
Bendy Bodies has never been about me.
It has always been about bringing together brilliant minds, lived experiences, and meaningful conversations that help people feel seen, heard, understood, and empowered.
Two hundred episodes later, that mission feels more important than ever.
If Bendy Bodies has helped you feel less alone, understand your body better, or find language for your experience, I would be so grateful if you shared what the podcast has meant to you in the comments.
Here’s to the next chapter. 💙
06/10/2026
She was told it was anxiety.
Depression.
Maybe she just needed stronger pain medication.
But that was not the whole story.
On last week’s episode of Bendy Bodies, I spoke with Dr. Gregory Plotnikoff, joined by cohost Dr. Dacre Knight of UVA Health about why we have to look deeper when symptoms do not make sense.
Dr. Plotnikoff shared the unforgettable story of a 35-year-old mother of two whose pain and weakness kept getting worse.
For years, she searched for answers.
Her symptoms progressed to the point where she could barely stand at the kitchen counter.
And still, the explanation she kept receiving was that this was anxiety, depression, or a pain medication problem.
When Dr. Plotnikoff met her, he recognized something others had missed:
Severe vitamin D deficiency.
With appropriate treatment, her health dramatically improved.
Of course, most cases of vitamin D deficiency are not this dramatic.
And weakness should never be assumed to be “just” vitamin D deficiency. Progressive weakness deserves a careful medical evaluation, including neurologic assessment when appropriate, to look for other possible causes.
But this story is still a powerful reminder:
Symptoms deserve thoughtful evaluation.
Especially when someone has been dismissed.
Especially when the story does not add up.
Especially when the answer may be hiding in something as “basic” as a nutrient deficiency.
Have you ever had a diagnosis, deficiency, or medical explanation discovered only after years of being dismissed?
📌 Medical information shared for educational purposes only. This post is not medical advice. New, worsening, or progressive weakness should be evaluated by a qualified healthcare professional.
ID: Screenshots from the Bendy Bodies podcast featuring Dr. Gregory Plotnikoff speaking into a microphone with a headset while discussing medical dismissal, progressive weakness, vitamin D deficiency, and the importance of looking deeper for underlying causes.
06/09/2026
Migraine is not "just a headache."
It is a complex neurological condition that affects more than 1 billion people worldwide, making it one of the most common and disabling health conditions on the planet.
Yet many people living with migraine still hear things like:
"Have you tried drinking more water?"
"Maybe you're just stressed."
"It can't be that bad."
Migraines can affect work, relationships, sleep, concentration, physical activity, and overall quality of life. And because they are invisible, many people suffer without others understanding what they're experiencing.
The good news? Understanding your unique patterns can make a meaningful difference.
Tracking symptoms, identifying triggers, prioritizing sleep, managing stress, staying hydrated, and working with a knowledgeable healthcare professional can all be important parts of a comprehensive migraine management plan.
This Migraine & Headache Awareness Month, let's help increase understanding, reduce stigma, and support those living with migraine and other headache disorders.
💬 If you experience migraines or chronic headaches, what is one thing you wish more people understood about them?
Save this post for future reference and share it to help spread awareness.
📌 Medical information provided for educational purposes only and is not intended as medical advice. Please consult your healthcare professional regarding your individual situation.
06/08/2026
Don’t miss this exciting new MCAS peer-reviewed journal article led by the incredible Dr Lawrence Afrin. I’m honored to be a coauthor! 🌟🌟🌟🌟🌟
Have you read "Progress in mast cell activation syndrome: the global consensus-2 diagnostic criteria at six years?"
Grateful for the continued MCAS research, patient care, and advocacy of Dr. Afrin, Dr. Blitshteyn, Dr. Bluestein, Dr. Dempsey, Dr. Maxwell, Dr. Miller, Dr. Nagy , Dr. Nugent, Dr. Schofield, Dr. Weinstock, Dr. Xi and Dr. Molderings.
https://www.degruyterbrill.com/document/doi/10.1515/dx-2026-0016/html
06/04/2026
“The lower the vitamin D, the higher the risk of injury and the slower the recovery.”
On today’s episode of Bendy Bodies I spoke with Dr. Gregory Plotnikoff alongside Dr. Dacre Knight of UVA Health about the critical role vitamin D plays in muscle function, bone health, tendon health, recovery, and overall performance.
Dr. Plotnikoff explains why vitamin D deficiency is often overlooked, especially in artists, athletes, performers, and highly active people who may be dealing with recurrent injuries, fatigue, pain, or prolonged recovery without realizing a deficiency could be contributing.
He also shares why vitamin D is one of the simplest things to evaluate proactively.
As Dr. Plotnikoff explains, no one wants to miss performances, training, competitions, or months of practice because of a preventable deficiency-related issue.
Vitamin D is not a cure-all, but it can be an important piece of the puzzle for some patients.
Have you had your vitamin D level checked? Did it seem to unexpectedly impact your symptoms, recovery, or overall health?
📌 Medical information shared for educational purposes only. Always consult your healthcare provider for personalized care.
VD: Podcast reel featuring Dr. Gregory Plotnikoff speaking into a microphone with a headset while discussing vitamin D deficiency, injury risk, recovery, muscle function, and why vitamin D testing may be important for athletes, performers, and active individuals.
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