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I live in Cardiff, South Wales with my husband and three children. In 2015, our daughter Victoria was diagnosed with Hyper IgE and the road to diagnosis was a very long and stressful one, as is the case for lots of people with PIDs. PID UK provided us with invaluable information and support when we all felt very vulnerable. I honestly cannot thank them enough. When it felt like no one else was taking us seriously they were there. The web site was a great place for Victoria to see how other people like her were managing to lead "normal" lives and there was lots of information for us as parents.