Brave Bears Club & Co.

Brave Bears Club & Co. Brave Bears Club creates comforting, educational companions for children navigating medical experiences like EEGs.

Founded by a mom, trusted by 75+ hospitals, and built to help kids feel!

If you’ve ever sat through an EEG with your child, you know how much it matters.EEGs are an interpretive test, which mea...
04/26/2026

If you’ve ever sat through an EEG with your child, you know how much it matters.

EEGs are an interpretive test, which means what’s captured truly matters.
It shapes what doctors are able to see, understand, and act on.

The technology, the software, the quality, the attention to detail… and the way your child is supported through it. It all matters.

At the center of it all are EEG technologists.
They’re the ones making sure everything is placed just right, watching closely, helping your child feel safe, and capturing the moments that guide what comes next.

They’re the link between what your child experiences and what doctors are able to understand.

This week and always, we’re so grateful for the care you bring to our kids. 💜





04/24/2026

anyone else? xoxo almost friday we made it ✌️

Who do you walk for? 💜Bring your Brave Bear.Walk for the 1 in 26.Find your local walk and support your local epilepsy co...
04/22/2026

Who do you walk for? 💜
Bring your Brave Bear.
Walk for the 1 in 26.
Find your local walk and support your local epilepsy community.

Love love love seeing our friends showing up for their local epilepsy communities. 💜
When you’re first diagnosed, and honestly always, it can feel really hard.
Go to your local walk. Reach out. We’ll help connect you.
It’s worth it, I promise.

P.S. Grab your bear at www.bravebearsclub.com and tag us.

Sharing a little more of what this is becoming 🤍This series is exactly what we wish we had when we were first navigating...
04/15/2026

Sharing a little more of what this is becoming 🤍

This series is exactly what we wish we had when we were first navigating everything…
real talk, real experiences, and the resources that actually help.

In these videos, we’re walking through:
• why the Clinic Courage Program was built the way it was
• how collaboration across community partners and clinical teams matters
• what actually supports families beyond the moment of diagnosis

And in the slides, we’re starting to share some of the resources and organizations that have made a real impact, both for us and for so many families.

Because this was never meant to live in one place.
It’s about connection, access, and making sure families don’t feel like they have to figure this out alone.

So many of these community partners are doing incredible work, and we’re just getting started highlighting them.

Which one should we feature next? Tell us in comments!

Series name coming soon 👀✌️





04/03/2026

Introducing the first of our weekly series of advocating with Kate… in our currently unnamed series. Help us name it.

Also, thank you for all the love and support.

As mentioned, Clinic Courage Kits are available at the link in bio, and we are so grateful to the hospitals and organizations that make it possible for children to receive them at no cost.

Will this be a podcast or just a video series I film whenever I can squeeze it in between snacks, scheduled hospital visits, and the occasional unscheduled ones? Unclear.

What is clear is this community cares, shows up, and keeps asking for this… so here I am.

We’re especially grateful to the organizations and hospitals that have recommitted this week to making our small business with a big heart available to their patients at no cost. Turns out, doing things with intention, community, and a lot of lived experience still matters.

And to the people behind the scenes… the EEG techs, child life teams, and parents who keep advocating and making this happen… you are the reason this exists.

If you’ve ever shared, commented, sent a message, or just quietly supported… thank you. That’s how this keeps going. And honestly, how I justify talking to my phone like this.

Also taking all name suggestions. Current front-runners include Raising Rare, Kate Advocates, and a few others I’d love to share… but I’m apparently running for PTO president now, so trying to stay on my best behavior.

If you want to support a hospital or bring this to yours, visit www.bravebearsclub.com to start or support a program. ✌️

Lots of new faces here, so sharing this again because you all loved the pink poodle one so much 🤍This is the story behin...
03/31/2026

Lots of new faces here, so sharing this again because you all loved the pink poodle one so much 🤍

This is the story behind Brave Bears Club.
How it started, how it grew, and why it means so much to us.🫶🫶🫶

If you’re new here, we’re so glad you’re here.
And if you’ve been here from the beginning, thank you for sticking with us… even when I’m a little annoying and throw 50 shades of purple on your screen ✌️💫

Purple Day was started by Cassidy Megan in 2008, inspired by her own experience with epilepsy. Her goal was simple but ...
03/26/2026

Purple Day was started by Cassidy Megan in 2008, inspired by her own experience with epilepsy. Her goal was simple but powerful, to get people talking, break down stigma, and remind those living with seizures that they are not alone 💜

We’re so grateful to partner with and for this special day.

In honor of Purple Day, we’re gifting a special edition Waves the Brave to a beary brave kid.

Includes a limited edition Purple Day t-shirt designed for the Purple Day Expo 💜

Because every child deserves to feel prepared, supported, and just a little bit braver.

To enter:
• Follow
• Like this post
• Comment who this would be for 💜
• Tag a friend (each tag = an extra entry)
• Optional: share to your story for an extra entry

✨ Flash giveaway
Closes March 27 at 5pm EST
Winner announced March 28

Sponsored by with love & support from 💜

Get in loser, we’re wearing purple tomorrow 💜Raise your hand if you have ever been personally victimized by epilepsy 🙋‍♀...
03/25/2026

Get in loser, we’re wearing purple tomorrow 💜

Raise your hand if you have ever been personally victimized by epilepsy 🙋‍♀️

Purple Day is for everyone 💜Not because everyone has epilepsybut because everyone can show up.Epilepsy can look differen...
03/23/2026

Purple Day is for everyone 💜

Not because everyone has epilepsy
but because everyone can show up.

Epilepsy can look different for everyone.
Some moments are big.
Some are small.
Some are loud.
Some are quiet.

And every single one deserves understanding, support, and care.

On March 26, wear purple.
That’s it. That’s enough.

Tag us if you join in 💜
🧸

Address

1001 Rose Bowl Dr
Pasadena, CA
91103

Website

https://www.youtube.com/channel/UCdeKed9cfYPRWOoKWaM1Bvw

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