Muskaan Care Trust NZ

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ensuring


Our Core VALUES, MAORI TIKANAGA,
3Ps PROTECTION, PARTNERSHIP, PARTICIPATION

12/06/2026

Muskaan CareTrust at the African Health Expo

Honouring World Sickle Cell Anemia Day 2026 JOIN us for Blood donation on 20th June at NZ blood Service Manukau center h...
11/06/2026

Honouring World Sickle Cell Anemia Day
2026 JOIN us for Blood donation on 20th June at NZ blood Service Manukau center https://www.facebook.com/share/1EbxVWBPns/ Book your time for swift and blessed experience

New WHO guidance brings renewed attention to the urgent needs of   and   with   (SCD).The World Health Organization (WHO...
06/06/2026

New WHO guidance brings renewed attention to the urgent needs of and with (SCD).
The World Health Organization (WHO) has published its new consolidated for the management of common childhood illness: management of sickle cell disease in children and adolescents, an important publication that provides global, evidence-based guidance for improving SCD care.
This is the first WHO normative guideline dedicated to the diagnosis, prevention and clinical management of SCD in children and adolescents aged 0–19 years. Its publication is a particularly significant development for countries and health systems seeking to strengthen paediatric and adolescent SCD care, especially in settings where specialised services remain limited.
SCD is a lifelong inherited and one of the most pressing global health challenges affecting children in many parts of the world.
The guideline includes 15 across seven priority areas of care: early diagnosis, infection prevention, hydroxyurea, pain management, acute chest syndrome, stroke prevention and management, and screening for complications such as cardiopulmonary disease.
strongly encourages healthcare professionals, national health authorities, patient organisations and the wider haemoglobinopathy community to access, share and use this important WHO resource.
🔗 Read the WHO guideline in the comments section.
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New WHO guidance brings renewed attention to the urgent needs of and with (SCD).

The World Health Organization (WHO) has published its new consolidated for the management of common childhood illness: management of sickle cell disease in children and adolescents, an important publication that provides global, evidence-based guidance for improving SCD care.

This is the first WHO normative guideline dedicated to the diagnosis, prevention and clinical management of SCD in children and adolescents aged 0–19 years. Its publication is a particularly significant development for countries and health systems seeking to strengthen paediatric and adolescent SCD care, especially in settings where specialised services remain limited.

SCD is a lifelong inherited and one of the most pressing global health challenges affecting children in many parts of the world.

The guideline includes 15 across seven priority areas of care: early diagnosis, infection prevention, hydroxyurea, pain management, acute chest syndrome, stroke prevention and management, and screening for complications such as cardiopulmonary disease.

strongly encourages healthcare professionals, national health authorities, patient organisations and the wider haemoglobinopathy community to access, share and use this important WHO resource.

🔗 Read the WHO guideline in the comments section.

Aplastic Crisis: A Silent Emergency in Sickle Cell DiseaseWhen Parvovirus B19 hits, the bone marrow stops making red blo...
06/06/2026

Aplastic Crisis: A Silent Emergency in Sickle Cell Disease

When Parvovirus B19 hits, the bone marrow stops making red blood cells, causing hemoglobin to drop dangerously fast. Unlike a pain crisis, this is about oxygen loss. Sudden extreme fatigue, pallor, rapid heartbeat, or shortness of breath means go to the ED immediately.
Information Courtesy - Thank you

❤️ **Only 15 days left until World Sickle Cell Day — 19 June**As we count down to World Sickle Cell Day, let’s take a mo...
03/06/2026

❤️ **Only 15 days left until World Sickle Cell Day — 19 June**

As we count down to World Sickle Cell Day, let’s take a moment to learn, share, and raise awareness for individuals and families affected by sickle cell disease.

Awareness creates understanding.
Understanding creates support.
Support creates change.

Join us in spreading hope this World Sickle Cell Day.

This week is World Haemochromatosis Week - a time when patient organisations around the world unite to raise awareness o...
03/06/2026

This week is World Haemochromatosis Week - a time when patient organisations around the world unite to raise awareness of this common yet frequently under-recognised iron overload condition.

In New Zealand, 1 in 200 people have haemochromatosis, and many don't know it. Early detection makes all the difference — learn more at https://www.bloodcancer.org.nz/blood-cancer-information/haemochromatosis

Haemochromatosis International

Learn about haemochromatosis, how it affects the body, symptoms, diagnosis, treatment options and ongoing management support in New Zealand.

This World Sickle Cell Day, we come together to raise awareness, support families, and stand with every warrior living w...
03/06/2026

This World Sickle Cell Day, we come together to raise awareness, support families, and stand with every warrior living with sickle cell disease. ❤️
Blood donation can make a life-changing difference for people affected by blood disorders, including sickle cell disease. Your donation could be the reason someone gets another chance, another smile, another tomorrow.
🩸 Blood Donation Drive
📅 20th of June
⏰ 9 AM onwards
📍 116 Cavendish Drive, Manukau
📞 Call to Register: 0212318485
Be the reason for someone’s smile. Donate blood. Save lives.

📣Proud to share that a scientific article authored by Thalassaemia International Federation - TIF the  has been ranked a...
26/05/2026

📣Proud to share that a scientific article authored by Thalassaemia International Federation - TIF the has been ranked among the Top 10 most viewed papers published by the European Journal of Haematology in 2024.

The article, “Assessing Disability in Thalassaemia: A Position Statement by the Thalassaemia International Federation,” addresses an important and often under-recognised aspect of : the wider impact of the disease, its , and its lifelong on a person’s daily life, functioning, social participation, independence, and overall wellbeing.

This recognition is a meaningful acknowledgement of the global relevance of this topic and of the growing need to view thalassaemia not only through a medical lens, but also as a with social, psychological, practical, and human dimensions.

Warmly thank the , TIF authors, experts, collaborators, and the global thalassaemia community for their continued engagement and support.

Ngaa mihi
Muskaan Care Trust NZ
Thalassaemia and Sickle Cell Aotearoa NZ (TASCA NZ)
Quote Team RED - Muskaan Care at any NZ Blood Donation Center DONATE BLOOD SAVE 3 LIVES

Read the full article in the comments: 👇

India in New Zealand (High Commission of India, Wellington) Ministry for Ethnic Communities

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