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PiNSA is a non-profit association formed to support patients with PID and their families. It is made up of volunteers. It was formed in 2001 and has over 100 members.

World PI Week 2021

To all our Primary Immune Deficiency Warriors and families,As you may know World Primary Immunodeficiency Week will be celebrated from 22-29-April-2021. We are excited to share that PiNSA will be sharing in these celebrations!The theme we have chosen is “Live your life in Colour” inspired by Kyle Henderson who was…

Report any adverse reactions to IG products using this form

To all our members It is vital that you, or your treating doctor/nurse use this form to notify SAHPRA of any adverse reaction that you might have from using IG products. This information is vital for several reasons including the following: If your treating doctor recommends alternative IG products due…

PiNSA present at Allergy Carnival!

Allergy Carnival on Saturday 1 April at Red Cross Children’s Hospital in Rondebosch in Cape Town. We had an opportunity to tell people all about PiNSA, thanks to AFSA – Allergy Foundation of South Africa.

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