Raremark Foundation

09/06/2026

At Raremark Foundation, we define a hero by the service they give and the hope they inspire.

Whether in the community, the hospital, or supporting from the sidelines, if your actions move us closer to a future where no Warrior walks in pain and every child has the chance to be born free from Sickle Cell Disease, you are a hero.

03/06/2026

Today, we look back at the history of
the Martyrs and remember that
sacrifice shapes the future.

We see that same unyielding spirit of sacrifice
reflected in the daily lives of our SCD
community, in caregivers who stay at
bedsides past exhaustion, nurses who
run on hours of little rest, and
advocates who continue to ensure
that awareness around never
goes silent.

Your sacrifices are building systems
that endure.

01/06/2026

We’re stepping into one of our most biggest months yet.

From surgical camps to global awareness days, we are showing the world what happens when we work together.

The mission is in motion, and it only grows stronger with every hand that joins in.

So we ask, what role will you play this month?
🤝 Partner with us.
💸 Fund programs.
📣 Share our story with your world.

27/05/2026

27/05/2026

☪️Eid Al Adha Mubarak

May the sacrifices you make for this community be met with peace, purpose, and lasting impact.

21/05/2026

Not every day does the Sickle Cell community witness a moment like this.

The launch of Uganda’s first Hydroxyurea manufacturing plant yesterday at Quality Chemicals Limited by the Ministry of Health- Uganda is a major milestone in improving access to treatment for Sickle Cell Warriors. For many, treatment has been financially overwhelming and difficult to access, local production now brings hope for affordability and availability.

Diana, a Warrior, shared her lived experience during the event:
“Living with SCD has never been easy. There were days filled with pain and endless hospital visits. I’m grateful to be a part of the Warriors’ community at Raremark Foundation that has empowered me to use my story to educate others.”

Her story deeply moved the audience and earned a standing ovation, highlighting that behind every policy discussion are real people and real journeys.

She also shared the impact of awareness campaigns:
“I’ve seen remarkable results through campaigns like Raremark’s many of my family didn’t know their genotypes until I started to speak up.”

“With the right support, it’s possible to live a full life. I stand as a 26-year-old woman with a job, living independently, and still choosing to dream beyond my condition.”

A powerful reminder that progress is possible when advocacy, awareness, and policy come together.

20/05/2026

To us, every program, conversation, and partnership is designed to leave a lasting footprint in Sickle Cell Disease awareness and support.

From workplaces to schools and communities, we believe in sustainable change through combined efforts.

We are actively collaborating with organizations, institutions, and individuals committed to measurable, long‑term impact.

Let’s expand reach, strengthen awareness, and improve outcomes together.
📩 [email protected]
🌐 https://raremarkfoundation.org/

14/05/2026

For a Warrior living with pain, timely access to medication can mean the difference between enduring another painful day and finding relief to simply get through it.

Micro-giving may seem small, but it makes a real difference.

With just UGX 5,000, you can help ease a Warrior’s pain. Every contribution, no matter the size, is a reminder that no Warrior walks this journey alone.

Make a difference today.

12/05/2026

The greatest inheritance you can give your children is good health.

Knowing your genotype means protecting your child’s tomorrow before it begins.
And, we are here to help you ensure their future is a healthy one:

📞 +256 791 246663
📩 [email protected]

Book your free screening today, gift your children a healthy lifetime.