BWS Awareness Day

Even though Beckwith-Wiedemann Syndrome (BWS) is rare—
affecting about 1 in 10,000 births worldwide—

that still means thousands of families across the globe 🌍

And with IVF, the likelihood is higher.

Rare doesn’t mean small.
It means often unseen.

Let’s change that 💚💛

Did you know?

Children with Beckwith-Wiedemann Syndrome (BWS) often need
regular tumor screening in early childhood.

This may include:
• Ultrasounds
• Blood tests

Early monitoring can detect risks sooner—
and save lives 💚💛

Awareness makes this possible.

BWS Awareness Day is moving across the world 🌍💚💛

Join in—where are you from? 👇

Share. Wear green & yellow.
Spread awareness online + in your community.

✨ Awareness moves across the world—because of you.

BWS Awareness Day is moving across the world 🌍💚💛

Starting in Samoa, and flowing through:
New Zealand 🇳🇿 Australia 🇦🇺 Asia 🌏
The Middle East & Africa 🌍
Europe 🇪🇺 UK & Ireland 🇬🇧
South America 🌎
Eastern & Central North America 🇺🇸
and ending on the Pacific Coast 🌅

A wave of awareness is building—one voice at a time.

No matter where you are, you can be part of it.

Simple ways to participate:
💚 Share this post or create your own
💛 Wear green & yellow
💚 Start a conversation
💛 Support a family or organization
💚 Spread awareness online and in your local community

Drop where you’re joining from 👇
Let’s fill this space with voices from around the world 🌍

Together, we make Beckwith-Wiedemann Syndrome visible 💚💛