Interview of Julie Power, founder of Vasculitis Ireland Awareness (VIA)

Rare Stories – Voices of the 1 in 17 Northern Ireland Rare Disease Partnership Introducing Julie Power, founder of Vasculitis Ireland Awareness (VIA). Julie’s story discussed symptoms, the diagnosis odyssey, and the importance of the patient’s voice, These are the stories of the Rare Disease Community who face extraordinary challenges with strength and grace every day. By lending our ears and hearts to these narratives, we can contribute to a more inclusive and supportive society for all.