Louise, Claire, Laura and I are aiming to walk over 1.2Million steps in May to raise awareness of Pulmonary Vasculitis.

As many of you know, our Mum has pulmonary vasculitis and life has changed drastically in the past 15 months.

Mum now needs to use oxygen 24 hours a day and can struggle with day to day tasks. However, Mum’s determined not to let this interfere with living life to the fullest and we couldn’t be prouder of how well Mum and Dad are dealing with their new normal.

Vasculitis is a rare disease, and pulmonary vasculitis even more so, at around 20-100 per million. The following link gives you a brief overview of vasculitis: https://www.vasculitis.org.uk/wp-content/uploads/2019/07/understanding-vasculitis-factsheet-june-2014.pdf

Any donation is welcome to try and support The Lauren Currie Twilight Foundation which serves alongside Vasculitis Scotland.

May is Vasculitis awareness month so please give what you can, share this page when you can & ask us anything. We are still learning and trying to understand pulmonary vasculitis, and we hope to pass our understanding on to as many people as possible

Thank you so much!

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