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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.

Annie Pienaar

PiNSA is on the IPOPI Board!

Congratulations to Annie Pienaar, Chair of PiNSA for having been elected onto the IPOPI Board. It is great have representation again at international level and we are sure she will make a great contribution to IPOPI Well done Annie!

mariana-annie-and-joy

PiNSA has a new Chair!

The PiNSA Committee is happy to announce that Annie Pienaar, a long serving committee member and a stalwart of the association, has accepted the office of Chairman of PiNSA. Joy Rosario has stood down and is now Vice-Chair and Chantelle Richards continue as Treasurer. Mariana Du Toit also continues as…

rarex-james-martine-annie-and-monika

The Rare Diseases Conference | 19 – 22 October | Cape Town

  The Rare Diseases Conference | 19 – 22 October | Cape Town, South Africa. The first Rare Diseases Conference to be held on the African continent; RareX 2016 was held in Cape Town, South Africa at the Spier Conference Centre from 19 to 22 October and was proudly hosted by Rare Diseases…

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