Bendy Bodies with Dr. Linda Bluestein artwork

Medicine · Dr. Linda Bluestein

Bendy Bodies with Dr. Linda Bluestein

by Dr. Linda Bluestein

Whether you’re bendy with all the benefits or hurting in all the wrong places, you’ve come to the right place for all things hypermobility. Connective tissue disorders like Ehlers-Danlos Syndromes (EDS) are often dismissed or overlooked by healthcare providers as a cause of chronic pain. But if you or someone you care about struggles with the life-altering symptoms of hypermobility, you should know YOU ARE NOT ALONE! At the Bendy Bodies Podcast, we understand. Each week, join Dr. Linda Bluestein (The Hypermobility MD) as she pulls back the curtain on how to prevent injury and unnecessary suffering in “double-jointed” individuals seeking a more comfortable life in their unique, complex “bendy bodies.” When you tune in, you’re engaging in more than a podcast. Both on-air and online, you’re joining a supportive community where patients, caregivers, and healthcare professionals trade insights, life hacks, and inspiring stories to embrace our Bendy Bodies journey together!

Latest episodes

Showing 20 · updated from the feed

Hand Pain, Numbness & Weakness in EDS: Missed Nerve Problems with Dr. William Ericson | Ep 214

#9 trending · Medicine

What if your hand pain, numbness, weakness, or grip problems aren’t actually coming from your hand or wrist? Orthopedic hand surgeon William Ericson, MD, joins Dr. Linda

Sep 17
1 h 04 min

What AI Gets Wrong About Your Health with Michael Turken, MD (Ep 213.5)

Patients are already asking AI the questions they cannot always ask their doctors. That creates enormous opportunity, but also real risk. AI can help people organize com

Sep 15
1 h 06 min

EDS Medical Gaslighting, MCAS & Migraine with Dr. Ina Stephens | Ep 213

What happens when doctors misunderstand Ehlers-Danlos syndromes (EDS) and hypermobility spectrum disorders (HSD)? Sometimes the consequences go far beyond frustration or

Sep 10
1 h 18 min

Unpredictability in EDS: Flares, Shame & What Actually Helps | Office Hours

Why can you feel almost functional one day and completely wrecked the next with hypermobile EDS, HSD, POTS, or MCAS? And how do you know whether you need more treatment,

Sep 3
58 min

Is Brain Inflammation the Missing Link? Brain Inflammation Collaborative & Dr. Ina Stephens | Ep 211

What if some of the most disabling symptoms in EDS, HSD, POTS, MCAS, ME/CFS, and long COVID are being driven by something we still struggle to see on standard testing? I

Aug 27
1 h 02 min

Flexibility as a Liability: What Circus Teaches Us about Hypermobility w/ Dr. Emily Scherb (Ep 210)

What if being “naturally flexible” is actually the thing putting you at risk for injury? Dr. Linda Bluestein welcomes back Dr. Emily Scherb, known as The Circus Doc, for

Aug 20
1 h 16 min

Tongue Tie, Trauma, Menopause & More: Your EDS Questions Answered with Dr. Dacre Knight (Ep 209)

Tongue tie and POTS? EDS without obvious hypermobility? Perimenopause making symptoms worse? And tongue numbness after a nerve block? In this listener Q&A, Dr. Linda Blue

Aug 13
1 h 02 min

Is the Ehlers-Danlos Umbrella Helping... or Hurting? with Abbey Phillipson (Ep 208)

Could lumping every type of Ehlers-Danlos syndrome under one umbrella actually be doing more harm than good? In this thought-provoking episode, host Dr. Linda Bluestein,

Aug 6
1 h 25 min

Are EDS Treatments Moving Faster Than the Evidence? with Dr. Dacre Knight (Ep 207)

Are surgical risks in EDS exaggerated, underestimated, or simply misunderstood? And how can patients tell the difference between a promising treatment and an expensive pr

Jul 30
34 min

Medical Cannabis, hEDS, and the Sensitized Nervous System with Professor Dave Nutt & Lucy Stafford (Ep 206)

Why do some people with hEDS or HSD report meaningful relief with medical cannabis, while others feel worse, notice no benefit, or experience side effects? And what might

Jul 23
1 h 11 min

The Hidden Link Between Long COVID, Lyme Disease & Hypermobility with Dr. Ina Stephens (Ep 205)

Can a single infection permanently change your health, or does it simply reveal something that was already there? In this episode, host Dr. Linda Bluestein, the Hypermob

Jul 16
1 h 27 min

What Most Doctors Never Explain About EDS | Office Hours (Ep 204)

If you could listen to just one conversation about Ehlers-Danlos syndromes (EDS), hypermobility spectrum disorders (HSD), postural orthostatic tachycardia syndrome (POTS)

Jul 9
1 h 06 min

Why Small Wins Matter More Than Miracle Cures in EDS and HSD: The MENS-PMMS Method™ with Dr. Dacre Knight (Ep 203)

What does it really take to build an effective treatment plan for a condition that touches every system in the body, when there is no single magic pill? In this episode,

Jul 2
1 h 10 min

EDS Information Overload: How to Know What to Trust | Ep. 202

Too many diagnoses. Too many opinions. Too many tabs open. Not enough clarity. If you've ever felt overwhelmed trying to navigate Ehlers-Danlos syndromes (EDS), Hypermob

Jun 25
1 h 04 min

Physical Therapy for EDS: Why It Fails and How to Make It Work | Ep. 201

"Exercise is good for EDS." So why do so many hypermobile people get worse when they try it? In this episode of Bendy Bodies with the Hypermobility MD, Dr. Linda Blueste

Jun 18
1 h 09 min

Hypermobility Then and Now | Episode 200

What happens when the original voices behind Bendy Bodies come back together 200 episodes later? In this special milestone episode, Dr. Linda Bluestein reunites with her

Jun 11
1 h 28 min

Fatigue, Pain, Poor Sleep? It Could Be Vitamin D. | Dr. Gregory Plotnikoff & Dr. Dacre Knight (Ep. 199)

Could one of the most overlooked drivers of chronic pain, fatigue, poor sleep, and slow recovery be hiding in plain sight? In this episode, Dr. Linda Bluestein and co-ho

Jun 4
1 h 10 min

Why Lipedema Resists Diet and Exercise with the Lipedema Foundation (Ep 198)

You have been told it is just weight. Just diet. Just effort. For millions of women with lipedema, that is not just wrong. It is decades of unnecessary suffering. In th

May 28
1 h 13 min

Why Everything You've Been Told About EDS Lifestyle Is Wrong with Dr. Dacre Knight (Ep 197)

Most people with EDS or HSD have been told to "exercise more," "eat better," and "sleep on a schedule," usually by someone who has never tried to do any of those things i

May 21
1 h 09 min

Too Flexible to Fix? Orthopedic Surgery and Hypermobility with Dr. Jocelyn Wittstein (Ep 196)

What if being too flexible is exactly what makes surgery fail? And what if your doctor thinks your shoulder is fine because you can lift your arm to 90 degrees, not reali

May 14
1 h 10 min

Chart trend

Position in the Medicine chart (US), last 90 days.

#13
all-time peak
498
days in the top 50 since Nov 2024

Chart positions

Where Bendy Bodies with Dr. Linda Bluestein ranks today in each Apple Podcasts chart (US, Sep 18, 2026).

#34 ▼ 1 Medicine US

What listeners say

A curated, balanced selection of Apple Podcasts reviews.

Always a great listen. So informative and it helped/helps me continue to learn more about my condition. Appreciated hearing Dr. Knight and Dr. Stephens recently as one of the new patients at the UVA center!

Knatash · Feb 2026

I’ve felt like a medical mystery for decades as I’ve had test after test and seen specialist after specialist. Then I was diagnosed with CRPS in 2017 and most doctors I see blame CRPS for anything they can’t explain. My GP has always had my back, and we’ve gone through it all together. Then recently she told me she’d been listening to this podcast, Bendy Bodies, and that I was the first person she thought of. She thinks I have EDS, MCAS, & POTS. Listening to your podcasts and your guests (like Dr. Chopra), it’s like I am finally seen. I can’t thank you enough for your excellent work in sharing your valuable knowledge about EDS & more. Excellent podcast

24lernin71 · Jul 2025

I have felt very alone on my health journey, as I live in an area where no one really even wants to recognize hEDS, POTS, MALS or MCAST ( I also have FMD) I have nearly lost my life twice to ruptured aneurysm, spontaneous subdural Bleed and now living with pretty sure MCAST of which I feel so pushed aside because none of my Drs want to even recognize it is a thing. ….. Thank you so so so so much for all of your information. It is encouraging to know someone hears me, and so many like me.

gardengirl100 · Jul 2025

Thank you Dr Bluestein for sharing your wealth of knowledge. After my hEDS diagnosis I found few resources or people talking about what can be done. Hearing you and your guests have made me feel less alone and help me navigate what is going on with my body.

Kate-Dee · Jun 2025

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