Zambia Sickle Cell Anaemia Society - ZSCAS

Zambia Sickle Cell Anaemia Society - ZSCAS To uphold the wellbeing of sickle cell patients nationwide through Research,Advocacy& Sensitization programs. AWARENESS is the key-lets spread the WORD!!!!
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ZSCAS joins the Ministry of Health and all partners in commemorating World Patient Safety Day 2026.But today, we also wa...
17/09/2026

ZSCAS joins the Ministry of Health and all partners in commemorating World Patient Safety Day 2026.

But today, we also want to remind ourselves that patient safety must be more than a theme or a day on the calendar. It must be something patients experience every day.

For those living with sickle cell disease and other chronic conditions (NCDs) safe care means being heard when we speak, believed when we report our symptoms, treated with dignity, and given timely and appropriate care.

It means healthcare systems that understand that behind every diagnosis is a person, a family and a life.

As patients, we want to be more than recipients of care. We want to be part of the conversations, decisions and solutions that shape the care we receive.

We strongly believe that our lived experiences matter, our voices too, so is
Our safety.

As ZSCAS, we continue to advocate for care where no patient’s concerns are dismissed, no voice is ignored, and no one is left behind.

Together👏🏻, for the safety of every patient

Safe care for life must include the patient’s voice.

SEPTEMBER | SICKLE CELL AWARENESS MONTHFrom Awareness to Action: It Is Time to Change the Story.Today, the Zambia Sickle...
01/09/2026

SEPTEMBER | SICKLE CELL AWARENESS MONTH

From Awareness to Action: It Is Time to Change the Story.

Today, the Zambia Sickle Cell Anemia Society (ZSCAS) joins the global sickle cell community in opening a month of awareness, advocacy, solidarity and action.

For too long, sickle cell disease has been spoken about primarily through the language of pain, crisis and survival.

We believe the story must be bigger.

Sickle cell disease is not a sentence to a life defined by suffering. People living with sickle cell deserve the opportunity to learn, work, build families, pursue their dreams and contribute meaningfully to society—with the right care, support and understanding.

Yet across Zambia and much of Africa, too many children and adults continue to face delayed diagnosis, inadequate access to comprehensive care, medicine and blood, financial barriers, stigma, misinformation and health systems that are not sufficiently equipped to meet their needs.

And this is why awareness alone is not enough.

This September, ZSCAS is calling for a deeper commitment:

Know sickle cell.
Know your status.
Challenge stigma.
Support families.
Donate blood.
Invest in care.
Listen to lived experience.
Strengthen our health systems.
And turn awareness into action.

We also call upon governments, healthcare professionals, researchers, development partners, private-sector leaders, communities and families to recognize people living with sickle cell disease not merely as beneficiaries of healthcare, but as partners in shaping the systems that serve them.

The global conversation is moving forward. WHO’s new guidance for children and adolescents with sickle cell disease reinforces the importance of evidence-based, equitable care and reminds us that effective interventions must actually reach the people who need them. (World Health Organization)

Zambia must be part of that progress.

This month, we remember every life affected by sickle cell disease.
We celebrate every warrior, caregiver, healthcare worker, researcher, advocate and ally who continues to show up.
And we renew our commitment to building a Zambia where sickle cell disease is diagnosed early, treated appropriately, understood without stigma and supported with compassion.

To every person living with sickle cell disease:

You are more than your diagnosis.
Your life has value.
Your voice matters.
Your dreams matter.
And your future matters.

To the world, ZSCAS says:

Let this not be another month of awareness that ends when September does.

Let September be the beginning of stronger systems, greater understanding, better access and measurable change.

This is our month to raise awareness.
Our responsibility to demand action.
And our opportunity to change the story.

ZSCAS - Standing with the Sickle Cell Community.
From Zambia to the world.

Let's Friday:📌📌📌Dear parents and caregivers,📌📌📌📌We know you mean well for us; but this right here is a big NOOOO! Don't ...
08/05/2026

Let's Friday:

📌📌📌Dear parents and caregivers,📌📌📌📌

We know you mean well for us; but this right here is a big NOOOO! Don't even try it, it's a biggest trigger to most uncommon complications of Sickle Cell Disease/ Anemia and the worst exposure you can ever put your child to. No matter how desperate you may feel to help your child, DO NOT try this at home or anywhere else!

Stick to the Doctor's advise, learn the management protocols and you will be good to go. Sickle cell is a manageable condition.



18/04/2026

What was that one pointer that led to your or your child's diagnosis with Sickle Cell Anemia/Disease?👇🏿👇🏿👇🏿

17/04/2026

Did you know Some practices we carry out at home in the name of finding a solution for our warriors aren't safe?

E.g. Most of the concoctions we mix at home are triggers to some painful crises!

01/04/2026

The red cell stories box awaits you.
Please share your stories, questions and concerns with us.

What's your relationship like with DOTI/ ILOBA/ CLAY?Dear SCD Warrior Community… can we pause, reflect, and unlearn this...
28/03/2026

What's your relationship like with DOTI/ ILOBA/ CLAY?

Dear SCD Warrior Community… can we pause, reflect, and unlearn this small habit before it grows into a serious health problem- eating dirt, soil or clay locally called Doti or iloba....

This message includes me too.

For those who may be wondering what this is about: many of us in the sickle cell community experience a strong urge to eat non-food substances such as soil (commonly known as doti), paper, sponge, or even mattress foam. This condition is known as Pica.

It’s important to understand that this is not simply a “bad habit” or a matter of choice. While it can be managed, in many cases it is linked to underlying medical conditions....particularly nutritional deficiencies. For individuals living with Sickle Cell Disease, pica is often associated with low iron levels or anemia, which are common due to the body’s increased demand for red blood cells.

Let’s also demystify a harmful myth:📌

Pica is not a form of demonic possession or a spiritual attack requiring deliverance. It is a medical and nutritional issue. When the body lacks essential nutrients like iron and Zinc, it can trigger unusual cravings as a signal that something is missing internally.

⚠️ Why is it a concern⁉️

Engaging in pica can lead to:
•Infections (especially from soil or contaminated substances)
•Intestinal blockages or digestive problems
•Worsening anemia
•Exposure to harmful chemicals or parasites

💡 What then can help?⁉️
•Seek medical guidance: Get your iron levels and overall blood count checked regularly.
•Follow prescribed supplements: Only take iron or other supplements if recommended by a healthcare professional I.e the daily intake of folic acid.
•Maintain a balanced diet: Include iron-rich foods like leafy greens, beans, fortified cereals, and lean proteins.
•Stay hydrated: Sometimes cravings can intensify when the body is dehydrated.
•Find safe alternatives: Chewing sugar-free gum or healthy snacks may help manage the urge.
•Talk about it: There is no shame.....sharing helps normalize the conversation and encourages support.

Let’s continue to learn, unlearn, and support one another. What feels like a “small habit” can become a trigger of other health complications if ignored - but together, we can take control of our health with the right knowledge and care.

Let's maintain our healthy lifestyle always by excluding Iloba/ Doti.

22/03/2026

From our Red Cell Stories Box:

📮Dear ZSCAS,

We have just discovered my fiancé and I are both Sickle Cell traits. We are trying to convince our families to allow us to proceed with the marriage scheduled to take place in 2 months but parents have made it clear it can't happen! My parents keep saying love is not enough compared to to the future we want to sign up for if we proceed with this marriage. We are both confused.....

Please ask your community to help us understand this predicament we are in by sharing their views and if anyone has been through this; to please share how they solved it before we conclude on what's next. My fiancé and I will follow the comments keenly....

22/03/2026

Introducing: The Red Cell Stories Box 📮

Not every story is easy to tell… but every story deserves to be heard.

We’re creating a safe space for individuals and families affected by sickle cell to share their real experiences - the pain, the strength, the questions, and the victories.

Whether you’re ready to speak openly or prefer to stay private, our Red Cell Stories box is always open for you. Your story can be shared anonymously, with care and respect via our messages feature.

By speaking up, you’re not just healing - you’re helping someone else feel seen, understood, and less alone.

📩 Send us your story.

💬 Let your voice be part of the change.

Red Cell Stories Box - "Where courage meets community."

Address

University Teaching Hospital(UTH) Clinic 4. Hermatology Unit
Lusaka
RW1X

Opening Hours

Monday 09:00 - 17:00
Tuesday 09:00 - 17:00
Wednesday 09:00 - 17:00
Thursday 09:00 - 17:00
Friday 09:00 - 17:00

Telephone

+260955281107

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