Hypermobility Happy Hour

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Hypermobility Happy Hour is the first podcast exclusively dedicated to discussing hypermobility conditions including hypermobile Ehlers-Danlos Syndrome. Guests on the Hypermobility Happy Hour have included world renowned physicians, patient advocates, researchers, and individuals living with hypermobility.Listen in as we examine a wide range of topics, including treatment options for hypermobility disorders and ways to improve the doctor-patient relationship. The information provided on this podcast is for educational purposes only and not for the diagnosis or treatment for any individual. Hypermobility conditions can be complex and difficult to treat and it is extremely important to work with trained medical specialists for any diagnosis or treatment.

Recent Episodes
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Recent Reviews
  • cprhoads
    Great help
    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.
  • ba11er1na
    The only hypermobility podcast show
    …that I find super applicable and helpful. Love that it specifically covers the entire spectrum. Host and speakers are very high quality.
  • Chloe Madeleine
    Newly getting diagnosed, so much helpful info- Episode 22 so inspiring
    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.
  • Manic Insanity
    Beyond helpful!
    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! 🖤
  • אבי זהבי
    Life Changing and Life Affirming
    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!
  • Lo B hEDS
    Dr Chopra MCAS and POTS
    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!!
  • altie1004
    Great Podcast for Hypermobile People
    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.
  • Annoying V
    Helpful for newbies
    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.
  • DouKrem
    A must listen for anyone on the hypermobility spectrum.
    Great guests and topics. I have learned so much about how my differently-built hEDS body works and how to take care of it.
  • RE app reviewer
    So helpful!
    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!
  • Aupair1995
    Med student, researcher, patient
    I’m a recently diagnosed hEDS med student and a former researcher. I found it so frustrating trying to find information on my disorder and now I listen to this podcast and take notes between classes. It’s truly amazing. Great work. :) the sound quality is a little rough but Im sure it’s difficult to make podcasts in the first place. as with every podcast I wish there was a transcript I could refer back to and cite accurately but I know that would take a ton of work.
  • Grace and Peace-full
    Informative podcast for those with joint hypermobility & possible associated health issues
    This podcast has been so informative & helpful for me as I wade through my many health problems and diagnoses as well as my multitude of symptoms which I haven’t ever discussed with my health provider. I’m so glad these women have put together a podcast that helps to guide me on the path to greater health! I hope it continues a long time. I have listened to all the episodes & hope they keep producing more for years to come! ** yes, the audio was QUITE difficult to listen to in the first few episodes, but it’s much better now!
  • JacNicole07
    Normal
    Can we use the term non disabled instead of normal. Please.
  • clarkbriz
    Finally
    Its refreshing to finally have a podcast EDS!!!
  • mom1018
    Thank you so much
    When I got this diagnosis (hEDS) I was scared and yet relieved. Thank you so much for this amazing and helpful podcast.
  • milocito
    i’ve been waiting for this!
    So great to hear you talk about EDS, I have hEDS!
  • Fluffster Normalpaws
    Breath of Fresh Air
    I was dx’d w/ hEDS, head to toe osteoarthritis, neuropathy, & peripheral muscle wasting- in my 40’s, after decades of being told I was a hypochondriac. Then I saw specialists for only a couple yrs. To my surprise I was still treated like a hypochondriac, due to abject ignorance in the medical establishment. So I completely gave up on docs a couple yrs ago. This podcast gives me hope that maybe someday treatments will improve for ppl like me
  • Ann555857
    Informative and interesting
    This podcast is really helpful and informative, thank you for making the podcast!!
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