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Episode Spotlight

Hand touching something.
The Tesler Family
Quotes

We’ve done so many adventures over the past year and a half—small things, big things, things most people take for granted that their kids are capable of...We wanted to do it to show you what you could do.

AJ Tesler, Magnolia's Dad

Hand touching something.
The Brady Family
Quotes

As much as they have to deal with on any given day, for us to be able to give them these kinds of experiences, when there’s so much they can’t do, they get to do something that most people will never do. That’s what I’m looking for.

Sherri Brady, Lauren’s Mom

Hand touching something.
The Brady and Tesler Families
Quotes

I’ve wanted Lauren to try this for years. But in my mind, I’m thinking: ‘How would that work?’ and ‘How comfortable would I be with that?’ Seeing the baskets and the care that they [Reach for the Stars] put into this, they really make it for everyone.

Sherri Brady, Lauren’s Mom

Jenny's Recap: Spotlight

The sun was just waking up, golden light across the horizon. We had nervously and excitedly waited for hours in the darkness, being shuttled around for the right place to launch. Finally, the moment was here. We were watching both the sun and the balloons rise.

Have you ever dreamed of floating through the sky in a hot air balloon, with the world stretching out below like a living patchwork quilt? I did. And recently, that dream took flight, quite literally, thanks to a hot-air balloon ride designed with accessibility in mind. There are less than a handful of organizations with accessible hot air balloons in the country. And we were lucky enough to find an amazing organization called Reach for the Stars out of Temecula, California.

We decided it would definitely be worth flying across the country to work with this organization. It also gave us the chance to check off our personal bucket list item: having an adventure with 2 people we have known since Magnolia was diagnosed with Rett syndrome 11 years ago. Early in the morning, we met up with Sherri Brady and her daughter, Lauren. It was dark and cold, but that didn’t stop the excitement.

There we were in the middle of an open field, watching a kaleidoscope of color come to life. Two different accessible balloon baskets: one for Sherri and Lauren, adapted for a wheelchair user, and another basket adapted with a secure seat with visibility for someone with low tolerance for standing long periods—perfect for Magnolia.

As we all checked out our baskets, we realized it would be a quick start as soon as the balloons were filled. As hot air filled the balloons, excitement filled the cool air around us.

Ruby and her dad skiing
Ruby and her dad skiing
Ruby and her dad skiing
Up there, floating in a basket of dreams, I cried a little. Tears of awe and joy about another adventure with Magnolia, adapted for her so she could be included.

Jenny Tesler, Magnolia’s Mom

Finally, the takeoff. Rising in the hot air balloon felt like a magical breath of fresh air. There was no jolt or roar, just a gentle whoosh as the ground calmly slipped away. As we climbed higher, the dreamier the ride became, and we were all in awe. Grayden (Maggie’s brother) bounced around the basket looking out all sides. Magnolia sat on her perch, enjoying the amazing view of the world below and the skies above. Up there, floating in a basket of dreams, I cried a little. Tears of awe and joy about another adventure with Magnolia, adapted for her so she could be included. Everything and nothing felt out of reach.

For those with disabilities, the feeling of inclusion is profound. Because accessibility isn’t just about ramps and seats and lifts. It’s about possibility. It’s about seeing the sunrise from 2,000 feet and knowing you belong there just as much as everyone else.

If you’ve ever told yourself, “That’s not for me,” let me tell you: The sky says otherwise.

The hot air balloon wasn’t just a ride. It was a reminder that adventure should have no barriers. That everyone deserves a chance to rise. And that sometimes, the best view of the world comes from a basket in the sky.

So go ahead—dream big!

Dog Sledding with the Bitton Family

Every day, families are making

What if We Can a reality

Share your family’s adventures—from the small victories to big milestones—with the entire Rett community and showcase the things you CAN do while living with Rett syndrome, just like Nadine did.
Submit today and show other families what’s possible! Your story might be the inspiration they need to go on their own adventures.
Dog Sledding with the Bitton Family
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Ready to create your own adventures?

Embark on your own Magnolia adventures from home with an exclusive adventure sticker journal!

What’s included:

  • A series of vibrant adventure stickers
  • Journal pages with fill-in prompts where you can document your own highlights and adaptations
  • Ideas for future family adventures
Request now

The season may be over, but you can still catch up on all of Magnolia’s adventures!