Jolandie

+27 83 264 0439

Robin

+27 83 414 1191

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jolandie@fancsa.org.za

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Community Story

June 8, 2026

Robin Lewis

I am a firm believer that the body tends to follow the mind and always try to find the silver lining in every dark situation. To me, there’s always a reason for things happening the way they do, even my FA diagnosis (believe it or not).

Read now

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Community Story

June 8, 2026

Robin Lewis

I am a firm believer that the body tends to follow the mind and always try to find the silver lining in every dark situation. To me, there’s always a reason for things happening the way they do, even my FA diagnosis (believe it or not).

Read now

Blog Image

Community Story

June 8, 2026

Robin Lewis

I am a firm believer that the body tends to follow the mind and always try to find the silver lining in every dark situation. To me, there’s always a reason for things happening the way they do, even my FA diagnosis (believe it or not).

Read now

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March 11, 2025

Marlene Stals

Fast forward to 12 hours later, the same little girl lying hooked up to machines, blood and platelet transfusions and a bone marrow biopsy booked for first thing Saturday morning. This is our story in Hayleigh’s journey with Fanconi Anaemia.

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March 11, 2025

Marlene Stals

Fast forward to 12 hours later, the same little girl lying hooked up to machines, blood and platelet transfusions and a bone marrow biopsy booked for first thing Saturday morning. This is our story in Hayleigh’s journey with Fanconi Anaemia.

Read now

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Reece Smit

I was diagnosed with Fanconi Anaemia (FA) when I was five years old and received a bone marrow transplant at age ten. I got graft-versus-host-disease (GVHD) the same week of my transplant and it was a tough three years of recovery.

Read now

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Reece Smit

I was diagnosed with Fanconi Anaemia (FA) when I was five years old and received a bone marrow transplant at age ten. I got graft-versus-host-disease (GVHD) the same week of my transplant and it was a tough three years of recovery.

Read now

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Supporting patients and families affected by Fanconi Anaemia in Southern Africa.

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  • +27 83 264 0439

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  • 083 264 0439

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FANCSA Logo

Supporting patients and families affected by Fanconi Anaemia in Southern Africa.

Link

  • Home

  • About

  • Support

  • Resources

  • Donate

  • Contact

Info

  • +27 83 264 0439

  • +27 83 414 1191

  • jolandie@fancsa.org.za

  • support@fancsa.org.za

  • robin@fancsa.org.za

  • 083 264 0439

    WhatsApp us

Newsletter

Sign up to get updates & news.

© 2026 FANCSA. All rights reserved.

Privacy Policy

FANCSA Logo

Supporting patients and families affected by Fanconi Anaemia in Southern Africa.

Link

  • Home

  • About

  • Support

  • Resources

  • Donate

  • Contact

Info

  • +27 83 264 0439

  • +27 83 414 1191

  • jolandie@fancsa.org.za

  • support@fancsa.org.za

  • robin@fancsa.org.za

  • 083 264 0439

    WhatsApp us

Newsletter

Sign up to get updates & news.

© 2026 FANCSA. All rights reserved.

Privacy Policy