Medicine · 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!
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Position in the Medicine chart (US), last 90 days.
Where Bendy Bodies with Dr. Linda Bluestein ranks today in each Apple Podcasts chart (US, Sep 18, 2026).
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!
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
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.
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.
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