The Emily-Ann Foundation

The Emily-Ann Foundation Empowering kids with rare diseases & Chronic Illnesses | Rare but Real | Partner with us to make an impact

We’re so excited to share the first-ever issue of our Dear Emily Digital Magazine! 🌼Discover stories of courage, hope, a...
04/11/2025

We’re so excited to share the first-ever issue of our Dear Emily Digital Magazine! 🌼

Discover stories of courage, hope, and impact through the Emily-Ann Foundation.
Read here → https://heyzine.com/flip-book/185d39c215.html
Password: October2025

We’d love to hear your thoughts - comment, share, and tag us to spread the word! 🌈

Caleb Express Tours is on the move for our rare warriors with our limited edition branded socks.💚Need your way around th...
10/10/2025

Caleb Express Tours is on the move for our rare warriors with our limited edition branded socks.💚

Need your way around the beautiful City of Cape Town?

They’re one of the best-rated tour companies with incredible reviews and unforgettable packages! 🌿

Thank you, Caleb Express Tours, for supporting the movement of hope and awareness for our rare warriors!

💙 Celebrating Arthritis Awareness Month! 💙What an inspiring day with Family Redemption Church, where faith met hope and ...
10/10/2025

💙 Celebrating Arthritis Awareness Month! 💙

What an inspiring day with Family Redemption Church, where faith met hope and community came together in strength at Kraaifontein Old Age home.

The Emily-Ann Foundation was honored to join in — sharing love, encouragement, and special goodies to remind our warriors they’re never alone. 🌸

Our brave little fighter, Emily-Ann, showed up with her radiant smile and powerful testimony, proving that even in the face of Juvenile Dermatomyositis (JDM), courage wins every time. 💪🏽

In partnership with The Arthritis Foundation, we hosted empowering talks and workshops — from fun exercises to practical health tips on managing arthritis, nutrition, and understanding the different types of arthritis.

Have questions or need support?
We’re here for you — reach out to us anytime!

Awareness Brings Hope 💚🧠Some children wake up one day completely changed - gripped by sudden anxiety, OCD, tics, or emot...
09/10/2025

Awareness Brings Hope 💚🧠

Some children wake up one day completely changed - gripped by sudden anxiety, OCD, tics, or emotional outbursts. This isn’t bad behavior… it’s PANS or PANDAS, a serious autoimmune condition where the immune system mistakenly attacks the brain after an infection.

These are our hidden rare warriors - fighting battles no one can see. With early diagnosis, medical care, and understanding hearts, healing is possible.

Let’s spread love, not judgment. 💚
Let’s speak up for children who can’t explain what’s happening inside.

Meet Nkuli Mosethe - a young, vibrant man with a heart full of purpose! This morning, he sent us a photo rocking his lim...
06/10/2025

Meet Nkuli Mosethe - a young, vibrant man with a heart full of purpose! This morning, he sent us a photo rocking his limited edition socks to work to show his support for our rare warriors.

Nkuli believes in the power of inclusivity and continues to advocate for our little warriors with passion and pride.

Rock your socks for hope! 🌈
Have you got your pair yet?

Message us and get yours today - wear your socks with boldness for our young warriors!💛

Rock Your Socks for Hope! 🧦Our volunteers are rocking their socks for HOPE — because every step counts, and every rare w...
05/10/2025

Rock Your Socks for Hope! 🧦

Our volunteers are rocking their socks for HOPE — because every step counts, and every rare warrior matters. 💙

Introducing our limited-edition “Socks with Purpose” - created in collaboration with Sexy Socks and our dedicated manufacturing partners. Together, we’re walking for awareness, inclusion, and the rare disease community that inspires us every day.

Each pair tells a story.
Each step makes an impact.
Each sock represents a child, a family, a fighter.

Are you ready to Rock Your Socks for Hope?

Get your limited-edition pair and help us step forward in unity for all rare warriors.

This Heritage and Braai Day, we celebrate the colours of South Africa — our unity, diversity, and the spirit that brings...
24/09/2025

This Heritage and Braai Day, we celebrate the colours of South Africa — our unity, diversity, and the spirit that brings us together. Just like the many cultures and traditions that make our nation unique, there are many different rare diseases… but at the heart of it, we are all one. 💙💚🧡🤍♥️💜💛🖤🩵🩶🤎

At the Emily-Ann Foundation, we walk in purpose to support every child, every family, and every community. Because together, we can build a future of hope, dignity, and care. 🧦🔥

We have stock! Introducing the Emily-Ann Foundation x Sexy Socks — Ultimate Active Sock Made for movement, built for pur...
18/09/2025

We have stock!
Introducing the Emily-Ann Foundation x Sexy Socks — Ultimate Active Sock

Made for movement, built for purpose.
92% polyester | 8% elastane
✔️ Anti-blister
✔️ Moisture-wicking
✔️ Shape retention
✔️ Quick drying

Features you’ll love:
Long length design
Cushioned cotton-touch heel & toe
Arch support
Breathable mesh

Perfect for walking, running, padel, soccer, cycling — or any active lifestyle!

And here’s the best part:
For every pair you buy, Sexy Socks donates school socks to a child in need.

👉 Partner with us as a business or grab your pair today! Together, we step forward for every rare warrior, every hopeful heart. 💙

DID YOU KNOW???Children living with rare diseases often face not only the physical challenges of their condition but als...
05/09/2025

DID YOU KNOW???

Children living with rare diseases often face not only the physical challenges of their condition but also the emotional burden of feeling different. Many struggle with exclusion, bullying, and isolation—and in some heartbreaking cases, this leads them to feel hopeless or even suicidal.

No child should ever feel that being rare makes them less. Every child deserves to be included, celebrated, and supported. 🌈

At the Emily-Ann Foundation, we are working to build communities where kids with rare diseases are not defined by their diagnosis but embraced for their strength, courage, and uniqueness. 💙

Together, we can:

✅ Raise awareness about rare diseases.
✅ Educate schools, communities, and families about inclusion.
✅ Create safe spaces where every child feels they belong.

This weekend, while we cheer for our Bokke, let’s also cheer for our rare warriors—because their fight is every bit as powerful.

Just like the Bokke, we believe in strength, unity, and never giving up. 💚💛 This weekend, let’s rally behind our boys AN...
05/09/2025

Just like the Bokke, we believe in strength, unity, and never giving up. 💚💛 This weekend, let’s rally behind our boys AND the kids we support through the Emily-Ann Foundation.
One team. One nation. One mission. 🏉🇿🇦

Hey, We did it in 7 days! The Emily-Ann Foundation has officially reached our first 50 sock orders for our Rare Warrior ...
04/09/2025

Hey, We did it in 7 days!

The Emily-Ann Foundation has officially reached our first 50 sock orders for our Rare Warrior Socks! Every pair sold brings hope, raises awareness, and supports children living with rare diseases. 💜

A huge thank you to our amazing supporters – together, we’re keeping feet warm, spirits lifted, and futures brighter.

Let’s keep walking for hope – every step counts!

Address

Kraaifontein
Cape Town

Opening Hours

Monday 09:00 - 17:00
Tuesday 09:00 - 17:00
Wednesday 09:00 - 17:00
Thursday 09:00 - 17:00
Friday 09:00 - 17:00
Saturday 09:00 - 17:00

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