Care Beyond Limits- Microcephaly Africa Foundation

27/07/2026

The signs to watch for. SAVE THIS POST.
At birth & early life:
📏 Head smaller than expected
🧠 Delayed sitting, walking, talking
👁️ Feeding, vision or hearing difficulties
⚡ Seizures or uncontrolled movements
💪 Muscle stiffness or weakness
🗣️ Speech & communication delays

These signs don't always mean Microcephaly - but they always deserve professional attention.
Don't wait and see. Act now.
Friday: what to do if you notice the signs. Follow so you don't miss it.

21/07/2026

This week we are sharing three posts that could change a child's life.

Episode 01: What is Microcephaly?
In plain language - a condition where a baby is born with a smaller-than-expected head because the brain hasn't fully developed.
Cause: infections during pregnancy, genetics, malnutrition, or unknown.
Common? Approximately 1 in 800 births globally. Higher in Africa.
Cure? No. But with early support - children with Microcephaly grow, learn, and thrive.
Save this. Share this. Come back Wednesday for the signs to watch for.
Africa

17/07/2026

15/07/2026

We refuse to stay silent. 🔴

We refuse to let stigma win.

We refuse to accept "there's nothing you can do."

We refuse to watch governments do nothing.

We refuse to leave caregivers alone.

We refuse to stop.

Not today. Not ever. Not on our watch.

What do YOU refuse to accept? 👇

06/07/2026

They showed up before it was easy. They stayed when it got hard. They gave everything; time, heart, and hustle to a vision they believed in before the world did.
To our incredible volunteer queens at Care Beyond Limits, today is YOURS. 👑
We see you. We celebrate you. We are nothing without you. 🌍🙌🏾
Tag a woman who gives her all to something bigger than herself 👇
WomenWhoLead AfricanWomen SheShowed Up ThankYou 💛

02/07/2026

When I think of Africa's children, I feel...
Finish this sentence in the comments 👇 We want to hear from YOU.
No wrong answers. Just honest ones. Let's go.

30/06/2026

Meet our lovely ladies from the care beyond limits microcephaly Africa team.Raising awareness is one of the key things we love doing especially to our children in the society.Microcephaly is a rare disease that most of the times people forget that such people exist and need our help so we really appreciate parents,schools,churches and other institutions that allow us to educate the children on microcephaly and how it comes about,how they can help or even go about related situations😊

25/06/2026

Yesterday we were invited to a neighbourhood school sports day in Nairobi and we turned it into a community awareness moment. 💛
Parents, teachers, and children learned about Microcephaly. Questions were asked. Conversations were had. Stigma was challenged.
This is our work. Not just in boardrooms and policy papers, but on dusty fields, in communities, face to face.
Every conversation is one step closer.
🔗 Link in bio to learn more or support our work.
NairobiKe BreakTheStigma

23/06/2026

A picture of pure hope.

​Last week, we checked in on beautiful Gianna and her mom. Thanks to consistent therapy, Gianna is hitting incredible milestones; her spine is getting stronger, and soon she’ll be sitting up on her own! Seeing her happy and thriving is everything.
​Even better? Her mom is doing well mentally, and her small business is keeping them afloat. When we support the mother, the child thrives. We are so incredibly proud to witness this journey.

​ SupportMoms

19/06/2026

MYTH: "Microcephaly only affects the child."
Not even close, sis.
It ripples through the whole family:
The caregiver- carrying everything, often alone
The whole family- emotionally, financially, socially
The community- where stigma and isolation do real damage
That's why CBL supports everyone. Not just the child.
Join us → Link in bio.