The Emily-Ann Foundation

12/10/2026

💙 GIVING HOPE JUST GOT EASIER! 💙

We at The Emily-Ann Foundation are excited to introduce a new, convenient way for you to support our mission through our partnership with SnapScan! 📲💙

You can now simply scan our QR code and make a quick, easy donation to support one of our projects and help us continue making a difference in the lives of children and families living with rare autoimmune diseases, complex health conditions, autism and ADHD.

Every contribution, no matter the size, helps us move one step closer to creating awareness, providing support, and bringing hope to families who need it most. 🫶🏼

To our incredible donors and everyone who has participated in our projects so far — THANK YOU! 🥹💙

We see you. We appreciate you. And we are grateful that you choose to stand with us and be part of this journey.

Together, we can make a difference, one act of kindness at a time. 💙

📲 Scan. Donate. Make a Difference.

Want to support a specific project or partner with us?
Get in touch!

Empowering families. Raising awareness. Supporting healing.

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12/10/2026

Just a little over a year ago today!♥️

We are honored to be a guest feature on Jiksel Radio Station with Lynn K 🎙️.
During the segment, we’ll be sharing more about the Emily-Ann Foundation, what it’s like to raise a child living with a rare disease, and why community awareness and support are so important. 💙

We’ll also be talking about our upcoming projects and how together, we can make a lasting impact for children and families who need it most.

Tune in and join the conversation — let’s spread awareness, hope, and love across our communities!

12/10/2026

Almost a year ago today!♥️⚓️
For every rare warrior. For every hopeful heart.

CHOC and the Emily-Ann Foundation are rewriting what education looks like for children whose classrooms are hospital beds

05/10/2026

Lets celebrate warriors.💙🥹💖

"Behind every adult with a childhood-onset rheumatic disease is a brave child who learned to live, grow, and never give up. Because rheumatic diseases may begin in childhood, but their story unfolds throughout a lifetime, with the combined efforts of patients, families, and healthcare professionals." Dr Jordi Anton

As we approach WORD Day 2026, let’s remember every child and young person with a rheumatic disease, and every adult with a childhood-onset rheumatic disease who is living with their condition day in, day out and never giving up. You inspire us every day.

When times are difficult, you show your strength. When times are good, you demonstrate hope. No matter how difficult things are, remember that you are not alone - there are other people out there with the same condition, and patient organisations who can provide support and information.

Researchers and clinicians are working together with patients and families to better understand rheumatic conditions, and to develop treatments and services throughout the whole life-course - making sure they reflect the different stages of your life as you grow up and the different needs of children, young people and adults.

05/10/2026

💙

As you know, this year’s WORD Day campaign has been sponsored by PReS - the Paediatric Rheumatology Europe Society. We are grateful for all their support.

PReS are collaborating globally to change the future for children and young people with rheumatic diseases.

As part of the campaign, we’re spotlighting PReSTaR an international network supported by PReS, which is working to advance collaborative, patient-centred research in paediatric rheumatic diseases.

By connecting clinicians, researchers, and families across the world, PReSTaR and PRES are strengthening partnerships, sharing knowledge, and driving research that aims to improve outcomes and long-term futures for children and young people living with these rare and complex conditions.

Because when we work together globally, collaboratively, and inclusively we can create lasting change for young people with paediatric rheumatic diseases.
Learn more at www.pres-tar.org

05/10/2026

Let Celebrate October Month💙 and spread awareness.
Two kids within the Foundation have two different types of Arthritis: JIA & JDM .
For ever rare warrior. For every hopeful heart. 💙

05/10/2026

Navigating a complex medical diagnosis or neurodivergence can feel overwhelming—but you don't have to do it alone. 💙

The Emily-Ann Foundation, we are bridging the gap within the healthcare community for families, parents, and children facing chronic illnesses, rare autoimmune diseases, and Autism/ADHD.

We know how stressful it can be to fight for answers, face potential misdiagnoses, and search for the right tools. That is why we are proud to offer our Virtual Family Consultations & 30-Minute Coaching Sessions.

What our virtual sessions provide:

💙Dedicated 1-on-1 Parent Coaching: Live guidance tailored to understanding your child's diagnosis and daily challenges.

💙 Healthcare Navigation Support: Helping you bridge the gaps, reduce misdiagnoses, and find accurate answers.

💙 Resource Center Connection: Direct access to expert guidance, specialized toolkits, workshops, and support groups.

Let's empower your family’s health and well-being together.

Book your virtual session today🫶🏻🇿🇦

02/10/2026

Bridging the Gap, One Partnership at a Time 💙

We believe that making a difference should be as seamless as possible. That is why we are thrilled to announce that supporting our mission just got even easier with SnapScan.
Simplifying giving so we can focus entirely on what matters most: the COMMUNITY.

As we head into the final stretch of the year, we still have a few vital projects left to close out strong:

💙Our Clinic Drive: Bringing vital awareness, education, and resources directly to local clinics.
💙School Hope Bag Initiative: Equipping children with the basic stationery & socks they need to stay in school and thrive.
💙Rock Your Socks for Hope: Continuing our tireless advocacy for children facing rare diseases.

Are you ready to make an impact with us?

We are actively looking for passionate partners and collaborators to join our fight against misdiagnoses in children with rare diseases, and to support our upcoming workshops for parents and children in need.

Whether you want to sponsor a school bag, collaborate on a workshop, or contribute via our new SnapScan portal, every bit of support helps us close the gap.

Let’s connect!
Drop a comment below, send a DM, or reach out to explore how we can collaborate before the year wraps up.

30/09/2026

We seeking volunteers for the month of October to join us on our clinic drives. If you are interested please let me know.
Virtual Training will be given .
Dates for October Clinic drive will be posted.
We have over 90 clinics in Western Cape, in the Northern Suburbs there are about 20iesh.
October Month we will be at Brighton Clinic 💙

Dont forget to join our Whatsapp Community.

‎Open this link to join my WhatsApp Community:

01/09/2026

Our rare warriors are always cool!

Its YOU that must be cool with them!

Drop a word of encouragement for their hearts and support in the comment section.🌸