Thank you so much for this podcast. I learned so much more about hypermobility and all the aspects. My daughter soon will be 36 and we are just now being diagnosed.

…that I find super applicable and helpful. Love that it specifically covers the entire spectrum. Host and speakers are very high quality.

As someone who is in the process of being diagnosed with hEDS (confirmed HSD and many other things) the amount of information online is overwhelming to say the least. This podcast as a whole has been incredibly helpful-I actually come from the Bendy Bodies podcast which also has some great episodes. Episode 22 has been my favorite so far, I absolutely loved hearing from Mellisa. She is so positive but realistic and hearing her story and all she’s accomplished was incredibly empowering to me. Thank you.

Despite living right outside NYC, it’s still hard to find providers who know how to actually care for hEDS and don’t leave their patients feeling mentally worse. This podcast has helped me beyond words and has helped me stand up and be an advocate for myself. I love the interviews, hosts, I have learned so much and I look forward to each episode. This podcast is one of my favorites and I recommend it to friends, coworkers and even my doctors! Thank you for all that you are doing! 🖤

Kerry’s podcasts have empowered us to engage in vitally important conversations about hEDS and it’s comorbid manifestations (MCAS and POTS). Each of her episodes has reinvigorated our search and determination to find the answers to our most difficult challenges of living with an invisible chronic illness. Unlike other available resources, her podcast focuses on the most positive ways to live a life fully despite challenges. Each episode is truly uplifting and encouraging. Most importantly, she has helped us feel heard, validated, and has given us hope, reminding us that we are not alone!! Thank You for this vital resource! You are truly doing sacred work!

Life changing information! So glad I found this podcast and very grateful for Dr. Chopra’s knowledge and sharing of his findings and what has worked with his patients. Makes it seem possible to find solutions to many of the issues we experience. Thank you both!!

I was first diagnosed with hEDS in 2018 after a long journey seeing many providers. Being an RN and having done years of my own research, I thought I knew pretty much all there is to know about hypermobility. That said, I have learned so much from this show! They do a great job going over basics in a way that is easy to understand, but what I have really loved are all the interviews and deeper dives into HSDs.

Great guests and topics. I have learned so much about how my differently-built hEDS body works and how to take care of it.

If one is new to chronic pain, hypermobility, and EDS, this podcast might be helpful. I was disappointed by the levels of overgeneralization and the way mental health was dismissed. I also find that the host doesn’t add a lot or push interviewees to elaborate when they have not answered the question. I really wanted to like this podcast because I think it’s so important, but it did not meet my expectations.

I have hEDS and I’m still learning how to live a stable life. This podcast has helped me so much already and I haven’t even listened to all the episodes. Thank you!