Zimbabwe Haemophilia Association

18/04/2026

The Zimbabwe HaemophiliaAssociation(ZHA) joined the global community to mark World Haemophilia Day 2026 yesterday 17th of April. the theme, "Diagnosis: The First Step to Care." The event brought together clinicians, policymakers, partners, and patients to strengthen haemophilia care across Zimbabwe.
They is need of intentional and systematic diagnosis, supported by a robust health system. We need more patients to be diagnosed so they can access treatment and care. Zimbabwe Haemophilia Association we are here to serve and make life better for patients living with haemophilia and other bleeding disorders

08/04/2026

🌏 ? 459,606 people worldwide have been identified with a bleeding disorder.

But WFH estimates that over 75% of people with haemophilia worldwide are undiagnosed – with that percentage even higher for other bleeding disorders.

This means hundreds of thousands of people are living without a diagnosis – missing out on basic care, treatment and support.

💜🩷🧡💛 This year, World Haemophilia Day is an opportunity for us to shine a light on the many people with bleeding disorders – including women and girls – who are still undiagnosed.

07/04/2026

Did you know? Over 75% of people living with haemophilia worldwide are undiagnosed!

The World Federation of Hemophilia (WFH) estimates that over 75% of expected people living with hemophilia worldwide have not yet been identified and diagnosed. Identification and diagnosis rates are even lower for women with bleeding disorders and for those with von Willebrand disease (VWD) and other rare bleeding disorders.

It's 10 days until World Haemophilia Day! Recognised each year on 17 April, World Haemophilia Day is an opportunity to raise awareness for all bleeding disorders – haemophilia, VWD, and other bleeding disorders. 💜🩷🧡💛

28/02/2026

Not all battles are seen.
Not all pain is understood.

Behind every rare disease is a child who wants to play.
A mother who prays silently at night.
A family holding on to hope… every single day.

Their strength is quiet.
Their courage is constant.
Their story is More Than You Can Imagine.

This Rare Disease Day 2026,
let’s choose empathy over ignorance,
equity over inequality,
and action over silence.

Because rare is not invisible.
Rare is resilient.
Rare is powerful. 💜

28 February 2026

28/02/2026

Today, Haemophilia Advocates- Zimbabwe Haemophilia Association joins the global community in celebrating World Rare Disease Day.

Behind every rare diagnosis is a real person, a real family, and a real fight for access, dignity, and care.

No one should be left behind. Not in treatment. Not in policy. Not in hope.

Together, we continue to raise our voices until every person with a rare disease is seen, supported, and served.

20/02/2026

Are you a woman or girl with a thinking about a future pregnancy?

Join the WFH webinar on March 6 to learn why preparation before, during, and after pregnancy matters. Hear from healthcare professionals and women from our community as they discuss postpartum hemorrhage, risk factors, and how to advocate for the care you deserve.

📅March 6 | 8:00 a.m. to 9:30 a.m. EST
Learn more and register now: https://bit.ly/4ape3tt

05/02/2026

Hemophilia doesn’t always show visible bleeding.
Repeated internal joint bleeds can silently damage knees, elbows, and ankles — leading to lifelong disability.

Timely testing and proper treatment can protect mobility and give children a healthy, active future.

Don’t ignore the signs.
Awareness today can prevent disability tomorrow.

02/02/2026

thank you Mr Thomas Gowa the World Federation of Hemophilia regional manager for visiting Zimbabwe 🇿🇼

11/01/2026

I have a dream, and it will come to pass 1 day of having an HTC in Zimbabwe to improve the lives and care for people living with Hemophilia.....

01/01/2026

Happy 2026 From The Zimbabwe Haemophilia Association......

09/12/2025