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Mickaela Sickle CELL Foundation

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Mickaela Sickle CELL Foundation

MSCF is a nonprofit creating awareness about SCD and supporting children and families affected by it.

04/02/2024

It is raining a lot lately. Please check on your friends who are warriors. Reached out to them, it means a lot to them.

23/01/2024

Do you know your sickle cell status? If you don't, please go to the nearest hospital and have a test done.

15/01/2024

Here a few things one can do for a sickle cell patient:

05/09/2023

In Sickle Cell Awareness month, Mikaela Sickle Cell Foundation is collaborating with Bugembe Health IV to raise more awareness about Sickle Cells and reach out to more patients.

18/07/2023

Our Programs Coordinator Ms. Immaculate Kamakune met with Religious leaders of Jinja Diocese. MSCF is collaborating with the church to raise more awareness about sickle cell disease and how best to help sickle cell warriors.

19/06/2023

🌟 Celebrating Sickle Cell Warriors! 🎗️

June 19th is World Sickle Cell Day, honoring the strength of those battling Sickle Cell Disease (SCD). 💪

💙 Let's raise awareness, support research, and show love to all SCD warriors. You inspire us with your resilience! 🙌

17/06/2023

🔬 Sickle Cell Disease: What You Need to Know! 🔍

💔 Sickle Cell Disease (SCD) is an inherited blood disorder affecting red blood cells. Here are the key facts:

1️⃣ What is SCD? It causes red blood cells to become hard and sickle-shaped, leading to poor oxygen supply and circulation.

2️⃣ Common symptoms: Episodes of extreme pain, fatigue, anemia, infections, delayed growth, and organ damage.

3️⃣ Management: SCD has no cure, but early diagnosis and management can improve quality of life. Treatment includes medication, blood transfusions, and lifestyle modifications.

4️⃣ Complications: SCD can lead to strokes, organ damage, vision problems, and other serious complications. Regular check-ups and preventive measures are essential.

5️⃣ Genetic counseling: If you have a family history of SCD, consider genetic counseling before planning a pregnancy to understand the risks.

6️⃣ Education & support: Stay informed about SCD, connect with patient communities, and seek professional help for emotional and mental well-being.

❤️ Share this post to spread awareness about Sickle Cell Disease and support those living with this condition! Let's make a difference together!

(Note: This post is for educational purposes only and should not substitute medical advice. Consult a healthcare professional for personalized information.)

17/05/2023

🌟 Introducing the Mickaela Sickle Cell Foundation 🌟

We are thrilled to launch the Mickaela Sickle Cell Foundation, a platform dedicated to spreading awareness and support for individuals affected by Sickle Cell Disease. Our mission is to empower, educate, and uplift those living with this condition while fostering a community of understanding and compassion. Together, we can make a difference! 💪
🎗️ Join us in raising awareness about Sickle Cell Disease! 🎗️

Address

Box, 1887 Jinja
Jinja
0256

Telephone

+256775979640

Website

facebook.com

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