“How I Got My Home Funding”
Orlagh Woods- CVID my story …. “How I Got My Home Funding” I’m now almost 22 and I’m still figuring things out as I go, especially when it comes to…
News
World Primary Immunodeficiency Week – Newsletter
IPIA WPIW Celebration – Family/Conference Meeting April 21st Dublin, Saturday 21st April, 2018 – The Irish Primary Immunodeficiency Association (IPIA) joined the efforts of organizations across the globe to promote awareness of primary immunodeficiency diseases…
Oliver and Luke’s journey through their Bone Marrow Transplants at NewCastle-UK
Oliver and Luke’s journey through their Bone Marrow Transplants at NewCastle-UK Final Diagnose : Zinc Transporter Cell Defect My name is Colin and I’m here to share our family’s story…
Primary Immunodeficiency in Ireland Equal Access to Home Therapy & Lifesaving Treatment – IPIA – Conference Meeting 2018
IPIA’s Press Relase Primary Immunodeficiency in Ireland Equal Access to Home Therapy & Lifesaving Treatment – IPIA – Conference Meeting 2018 – Dublin, Saturday 21st April 2018 – Today the Irish…
IPIA Season Greeting 2017
Happy Holidays
NEWBORN SCREENING
SCID Newborn Screening SCID Newborn Screening Severe Combined Immunodeficiency (SCID) is the most severe form of PID and a paediatric emergency. Patient organisations around the world and IPOPI strive to ensure that…
IPIA Legal Status
IPIA Legal Status IPIA is now a registered company: “Irish Primary Immunodeficiency Association Company Limited By Guarantee” Directors: Martha Gouldsbury and Jim Colan Chairman: Rosa Aguiar Catraio Committee: Martha Gouldsbury,…
Women’s Mini Marathon – 5th June, 2017
COME AND RUN WITH US GET SPONSORS OR SPONSOR OUR RUNNERS Register here Women’s Mini Marathon – 5th June, 2017 Please sponsor our runners All the money collected will be…
Orlagh Woods- CVID my story
Orlagh Woods- CVID my story I wouldn’t say my diagnoses of CVIID was a ‘normal’ diagnoses. I wasn’t constantly sick when I was young, or on antibiotics every other week.…
