• Navigating Disney with POTS: Magic is Possible (With a Little Planning)

    As much as Disney is about magic, it’s also about making the impossible possible—and that includes navigating the parks with a chronic illness like POTS.

    I’ve always dreamed of spending a day in the parks, just soaking in the atmosphere and enjoying the magic. But when I was first diagnosed with POTS, I wasn’t sure how that would work. Would I even be able to stand in line for rides? How would I deal with the heat and crowds? Disney isn’t known for being a “chronic illness friendly” place, right?

    Well, spoiler alert: Disney magic does exist for people like us. It just takes a little planning, some pacing, and a lot of self-compassion. Here’s how I’ve been able to enjoy Disney even with POTS—and how you can too.


    Plan Ahead

    If you’re like me and need to manage energy levels and avoid overstimulation, planning is key. Before every trip, I take time to map out which rides and attractions are must-dos, and I make sure to schedule breaks throughout the day. Here’s my usual routine:

    • Arrival Time: I try to get to the parks early when crowds are thinner and I’m still feeling fresh.
    • Rest Periods: After every 1–2 hours in the park, I find a quiet spot to sit and hydrate. Whether it’s a bench, a shaded area, or even the indoor seating of a quick-service restaurant, it’s important to rest—not just when I’m tired, but preemptively.
    • Slow Pace: Disney is exciting, but it’s not a sprint. Don’t rush, take time to soak it all in, and give yourself grace to go at a slower pace.
    • Come Prepared: Bring any medications you may need, a pulse oximeter, a cooler bag with water bottles and snacks, electrolyte packs, anything you think you may need…BRING IT!!!
    • Dress Comfortably: Wear comfortable shoes, in the summer wear light weight clothing, in the cooler months bring a light jacket/cardigan, and in the winter be prepared for it to be cold one day and hot the next!
    • Locate First Aid in Each Park: I know where they are located now, but I had to take the time to locate them on the MyDisneyExperince app, they are also listed on the paper maps, and you can ask any cast member for help finding it!

    🏰 Navigating Rides Without DAS

    Disney used to offer the Disability Access Service (DAS) to guests with conditions like POTS that made standing in long lines difficult. But as of 2024, DAS is now only offered to guests with developmental disabilities who can’t tolerate or understand long waits—so it’s no longer available for most chronic illnesses. (I have tried to get it four times)

    To help manage the parks, Disney introduced two new options: Lightning Lane Multi Pass and Lightning Lane Single Pass.

    The Multi Pass lets you book up to three attractions in advance, and once you’ve used your first one, you can keep making more reservations one at a time throughout the day. It’s great if you need flexibility and want to avoid long lines in the heat.

    The Single Pass is available for those really popular rides and can be bought individually. It’s a good option if there’s a must-do ride on your list with a long wait.

    Both of these options can help make the day easier to manage—especially if your symptoms come and go or standing for long periods is tough.

    💧 Hydration is Key

    I cannot stress this enough: water, water, and more water. Dehydration is one of the worst triggers for POTS symptoms, so staying hydrated is my number one priority at the parks. I always carry a refillable water bottle with me, and there are plenty of water refill stations around the parks.

    Don’t be shy about asking for ice water at any counter-service restaurant or quick-service stand—they’ll give it to you for free! And I always pack snacks too—anything that’ll help keep my energy levels stay steady throughout the day.

    🌞 Heat Management

    Florida heat is no joke, especially if you have POTS. For me, staying cool is crucial. I’ve learned to:

    • Wear light clothing that lets my skin breathe and helps keep me cool.
    • Use cooling towels (they work wonders) and keep a small fan in my bag for when it’s extra hot. I also have recently started carrying gel cooling patches with me!
    • Avoid the midday sun by taking breaks indoors, preferably in air-conditioned areas like the shops on Main Street or the indoor seating areas at some of the restaurants.

    🎢 Managing the Rides

    One of the hardest parts of Disney with POTS? Rides. While some roller coasters and spinning attractions might be off-limits for me due to dizziness, there are still so many that I can enjoy without issue. It’s all about knowing what works for your body. I’ve learned to:

    • Avoid intense rides that could trigger dizziness or a heart rate spike.
    • Focus on low-impact rides that are still magical, like It’s a Small World, The Haunted Mansion, and Peter Pan’s Flight.

    That said, there are still some thrill rides I can handle, especially if I take the right precautions and listen to my body.

    💖 Enjoying the Magic, No Matter What

    Even with all of the planning and self-care, there are still moments when my body doesn’t want to cooperate. But that’s okay. The magic of Disney is not just about the rides or the shows—it’s in the atmosphere, the details, the little moments. And sometimes, I find the most magic in slowing down and truly enjoying the experience in my own way.

    Whether it’s watching fireworks from a bench, meeting a character, or just being in the middle of the parks with all the music and sounds around me, there’s always a little magic waiting for me, no matter how many breaks I need to take.

    🏰 Final Thoughts

    Navigating Disney with POTS is not always easy, but it’s definitely possible. With the right planning, self-care, and some flexibility, you can still enjoy all the magic Disney has to offer. And remember: the magic isn’t just about how many rides you get on—it’s about making memories, enjoying the moments, and embracing the adventure, no matter how it looks.

    Thanks for visiting POTSofMagic—may your days be magical (and upright)! 💫

  • My Disney College Program Experience: Living the Dream (and What I Wish I Knew)

    There’s a special kind of magic that lives inside Walt Disney World—and for a while, I got to help create it.

    Growing up, Disney was more than just movies and parks—it was my happy place, my escape, and a huge part of my identity. So when I got accepted into the Disney College Program, it felt like my dream was literally coming true. I packed my bags (probably way too many ears) and headed to Florida, ready to make magic.

    ✨ My Role in the Magic

    During my time in the DCP, I worked in merchandise at Hollywood Studios on Hollywood Boulevard. Every day, I got to interact with guests from all over the world and be part of moments they’d remember forever. Whether I was giving someone a first visit button, or just giving a warm smile to a tired parent, I knew I was part of something bigger.

    Some of the most magical parts of my experience weren’t even on stage—they were the behind-the-scenes laughs, the spontaneous character sightings on breaks, and the friendships I made with other cast members.
    A few standouts:

    • One time, I got to help a little princess dressed as Belle pick out a toy as a reward for riding Slinky Dog Dash for the first time. We sat on the floor next to the plush wall and went through all the stuffed animals until she found the perfect one—a weighted Simba plush. She held my hand as I walked her to the register, and while her family was paying, I made matching “I’m Celebrating” pins for her and Simba that said, “I’m celebrating riding Slinky Dog Dash!” It was one of those moments I’ll never forget.
    • I was also part of the group of cast members who got to see Fantasmic! return before it reopened to the public after the pandemic—and I got to preview TRON before its official debut. I even had some unforgettable backstage character interactions. One day, on my way into work, Pluto grabbed my hand, spun me around, and we did a little dance before he kissed my hand and sent me on my way!
    • I made lifelong friends during my program—people I still talk to every day. Later this year, I’m even flying out for one of their weddings. I found my people during my program, and I couldn’t ask for a better group.

    🌧️ The Reality Behind the Magic

    It wasn’t always easy. I was horribly homesick the first two weeks. The hours were long, the Florida heat was brutal, and the fast pace could get overwhelming. Looking back, I now realize I was already experiencing symptoms of POTS (though I didn’t know it at the time). There were days my body just didn’t want to cooperate—but I pushed through, not knowing the bigger picture yet.

    📝 What I Learned (and Wish I Knew)

    The DCP taught me so much:

    • How to show up and give your best, even when you’re tired
    • The importance of boundaries and self-care
    • That it’s okay to say “no” when your body needs rest

    I wish I had known more about listening to my body—and had been kinder to myself during those hard shifts. If you’re planning to do the program, take care of YOU. Hydrate, rest, and ask for help when you need it. The magic will still be there.

    🏰 Where That Experience Took Me

    The DCP gave me confidence and lifelong memories, but more importantly, it helped me believe in dreams again—even the tough ones. Today, I carry that same magic as I work in the legal field and prepare for law school (with my chronic illness in tow). I may not be working at a theme park now, but that pixie dust is still part of my story.

    Thanks for visiting POTSofMagic—may your days be magical (and upright)!💫

  • Disney Dreams and POTS Realities: Welcome to My Blog

    Hello, and Welcome to My Blog!

    I’m so glad you’ve found your way here! My name is Morgan, and I’m excited to share my story with you. This blog is a blend of my love for all things Disney, my journey with POTS (Postural Orthostatic Tachycardia Syndrome), and my aspirations to one day become a lawyer, all while navigating life with my many pets and some incredible experiences along the way.

    Disney: A Lifelong Dream

    Growing up, Disney has always been more than just entertainment—it was magic in its purest form. My love for Disney started at a young age, and that passion led me to an unforgettable chapter in my life: working at Walt Disney World through their College Program. I was able to live my dream, working in the heart of the magic I’d adored for years. Disney taught me to believe in the impossible, and I carry that spirit with me every day.

    A Bumpy Road: My Spinal Fusion and Diagnosis Journey

    At age 11, I underwent a spinal fusion surgery for scoliosis, a life-changing experience that shaped who I am today. I learned a lot about resilience and strength during that time, and while it was difficult, it sparked my determination to keep pushing forward through any challenge life throws my way.

    In October 2024, after four long years of struggling with symptoms that no one could explain, I was finally diagnosed with POTS. It’s been a challenging journey, but it’s also been empowering to put a name to the condition and learn how to manage it. I’ll be sharing my experience and what I’ve learned along the way.

    My Four-Legged Friends

    Along the way, I’ve had the love and support of my pets—three cats and four dogs. They’re my daily reminder of the simple joys in life, and they bring so much comfort as I navigate the ups and downs of living with a chronic illness.

    Dreams of Law School and My Career in the Legal Field

    I’ve always had a passion for justice and helping others, which is why I’m on a journey to become a lawyer. Currently, I work in the legal field, and while it’s tough with my disability, I’m determined to keep moving forward. One day, I hope to be a lawyer who helps others navigate legal challenges, just as I’m learning to navigate my own.

    What You Can Expect

    In this space, you’ll find a mix of posts about my Disney experiences, my personal health journey, tips for others living with chronic conditions, and the path I’m walking toward law school. My hope is that my story resonates with you, that we can find magic in the tough moments, and that we can share our journeys toward overcoming challenges.

    Thank you for joining me on this adventure! I’m excited to connect with all of you. ✧༺♥༻∞