Raremark Foundation

Raremark Foundation A safe space platform creating awareness, educating, and breaking boundaries for and their loved ones.

Some of our programs include S for Sickle cell, an awareness branch of our foundation.

06/05/2026

Wilma shares a powerful reminder that speaking up about can save lives, break long-held stigma, and help enable earlier diagnosis.

Her story reflects what so many Warriors experience in silence, and what becomes possible when that silence is broken.

From caregivers to Warriors, there’s space for everyone in this community, and it becomes easier when we show up for each other.
So, join the conversation, join the community, and be part of the change.

Today, we recognize everyone who's daily labour helps build systems towards creating a future free from Sickle Cell Dise...
01/05/2026

Today, we recognize everyone who's daily labour helps build systems towards creating a future free from Sickle Cell Disease.

29/04/2026

At our recent Warriors meetup, we asked Warriors to share some of the wildest myths they’ve heard about living with Sickle Cell Disease.

A lot was said, from being called lazy, to people thinking they can’t have children, or won’t live long.

The facts? We’ll let you watch and hear them for yourself. But one thing is clear; it’s time to move past these myths.

As you watch this, is there any other myth you’ve heard about living with SCD⁉

28/04/2026

The JosephineEsisa Madewo Shining Star Gala is a night where all our communities come together to honor a legacy, celebrate progress, and witness the impact Raremark Foundation is driving with the support of every partner.

It’s a night where your contribution becomes a story unfolding right before your eyes.

And this year, we’re unveiling the 4th edition, bigger and more impactful.
📅September awaits, are you ready⁉️

23/04/2026

Hope lives in the smallest acts of kindness.

What you give today can be the relief for someone fighting silently.
Your support can ease the burden and change a life today.

Together, we can be the reason a Warrior feels lighter today.
Support at: +256 791 246 663 - RAREMARK FOUNDATION

22/04/2026

Collaboration and partnerships are like a puzzle🧩
Every piece is just important.

Each contribution, voice, and effort comes together to create real impact in:
✔️Closing gaps in awareness
✔️Expanding access to screening
✔️Helping more Warriorrs receive life-changing surgeries

This is how intention becomes reality, all we need is YOU.

Support and Partner at:
📩 [email protected]
📞 +256 791 246 663

Monday magic in six sticky notes.
20/04/2026

Monday magic in six sticky notes.

Caregivers, ever feel like your to-do list never ends and there’s barely time for you?‎‎Here’s your reminder:‎💙 Breaks a...
15/04/2026

Caregivers, ever feel like your to-do list never ends and there’s barely time for you?
‎
‎Here’s your reminder:
‎💙 Breaks are not a weakness
‎💙 Self-care is not optional
‎💙 Rest is part of showing up stronger
‎
‎It’s okay to pause and reset too
‎
‎💬 How do you recharge when you feel overwhelmed?

14/04/2026

Genotype knowledge gives you the power to make informed choices, protect your future, and safeguard the next generation.

The best part?
✔ Free screening
✔ Results in 15 minutes
✔ On-site education and counselling

So why wait?
Book a session for your school, church, or workplace now👇
📞 +256 791 246663

09/04/2026

Every moment shared here reflects what you have made possible.

From community screenings that spark awareness, to life-changing surgeries, to the continued care Warriors receive, ensuring support doesn’t end when the cameras go off.

Each day, the mission grows, and so does the need for:
👉 Greater awareness
👉 Stronger support
👉 More lives reached

So we ask you — will you be part of what comes next?
If yes, connect with us:
🌐 https://raremarkfoundation.org/support
📩 [email protected]
📞 +256 791 246663

Every contribution helps create another reason to smile.

Address

Ntinda Complex, Ntinda
Kampala
00000

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