Hypermobility and Me: My Story

WE'RE BACK — with guests!🤩

And for this very special first episode, the tables have turned… and I’m the one being interviewed😅

Joining me is my dear friend Hannah (who shares her own experiences online living with hEDS, POTS, and a histamine condition). Today, she’s asking me about:

• my personal journey to getting an hEDS diagnosis (finally!) last summer
• what "the dark days" in my early 20s were like when I had no idea how to manage my symptoms and no support
• why I’ve been quiet on social media this past year
• and my upcoming book, Help! I’m Hypermobile: Your How-To Guide for hEDS, HSD, and Life in a Hypermobile Body (coming April 2026!🎉)

It’s been a lot lately to be entirely honest, but the podcast has a special place in my heart and I'm so happy to be back on here with all of you. I hope you enjoy the expert guest interviews and patient stories this season as much as I do!

Thank you for being here🙏

And remember: incurable does not mean untreatable!❣️

📚 Join the waitlist for pre-order information for the April 2026 release of Help! I'm Hypermobile (and get your free PDF companion guide in the meantime): hypermobilityhq.com/book
📸 Follow us @hypermobilityhq and subscribe on Instagram, Tiktok, and Youtube
🎙️ Learn more about the podcast: hypermobilityhq.com/podcast

💌 For guest info, media, or resources visit my blog at hypermobilityhq.com/blog/