Stories of adults with PIDs

Here we share the experiences of adults who live with primary immunodeficiency.

Rebecca’s story of living with Panhypogammaglobulinaemia

Hamish’s story: My CVID diagnosis

Graeme’s journey with CVID

Leah’s experience with APDS 2

Emma’s story of her CVID diagnosis

Jamie’s story about having APDS

Mitch’s CVID story

Paul’s hypogammaglobulinemia diagnosis

Danny’s story of living with CVID

Jenna’s experience of complement C7 deficiency

Hannah’s diagnosis of primary immune dysregulation disorder

Danielle’s journey with hypogammaglobulinemia

Simon’s experience of living with XLA

Claire’s CVID story

Jodi and Jessi’s story of living with CVID and bronchietasis

Ellie’s experience of MBL deficiency

Alison’s experience of IgA deficiency and DiGeorge syndrome

Elisabeth’s MBL deficiency diagnosis

Jen’s journey with hypogammaglobulinemia

Dani’s experience living with CVID

Richard’s CVID diagnosis experience

Kirsty’s CVID diagnosis journey

Charlotte’s story of living with MBL deficiency

Jenny’s CVID story

Hannah’s hypogammaglobulinaemia diagnosis

Kirsty’s story of living with a PID

Alison’s experience with immune dysregulation

Tommy’s story of living with hypogammaglobulinemia

John’s XLA diagnosis

Michael’s experience with Wiskott–Aldrich syndrome

Diane’s journey with CVID

Rachel’s experience with CVID

Fiona’s story of living with IgG2 subclass deficiency

Peta’s journey with CVID

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