Michelle's fundraiser for Action For Pulmonary Fibrosis
Michelle Scarsbrook is raising money for Action For Pulmonary Fibrosis
In memory of Emma Walker
Story
Emma was a lovely, kind, thoughtful friend. Her light shone brightly. We are taking on the Yorkshire 3 Peaks on 2nd August 2025
Siân, Emma's daughter, story
After my mum (Emma Walker) passed away, Colin and I decided to take on The Three Peak Challenge, a goal we discussed with her when she was with us. Since we shared our plans, many have generously offered to participate in raising both funds and awareness for Action for Pulmonary Fibrosis.
Emma was diagnosed with Pulmonary Fibrosis in 2022, and by July of that year, she was placed on the double lung transplant list at Papworth Hospital in Cambridge.
She required 24/7 oxygen support through various methods. Due to the breathlessness this caused, she found it impossible to go anywhere without her wheelchair. Over the next few months, with no progress toward a lung transplant, her body needed increasingly more oxygen to survive. She fought valiantly during her battle with this illness, never losing her sense of humour, love for others, and appreciation for life. Unfortunately, she wasn't strong enough to continue and passed away in the hospital on March 21st.
Those fortunate enough to know Mum recognise that she was truly the most special lady in the world; words can hardly convey the profound impact she had on so many of us.
This charity holds immense significance for us, and we wish to express our gratitude for the support we received throughout Mum's journey.
Also, as a side note, I would like to plead with you to take the time to talk to your family and loved ones about organ donation.
Here's a little more information on the charity:
Action for Pulmonary Fibrosis (APF) is a growing community of patients, families, researchers, and healthcare professionals striving to find a cure for pulmonary Action for Pulmonary fibrosis so that everyone affected by the disease has a better future. We provide personalised support to patients and families and raise awareness of pulmonary fibrosis through campaigning, fundraising, and education. We are also committed to funding research to improve the quality of life for people living with pulmonary fibrosis today and tomorrow.
APF is a national UK charity. We bring people together to drive change so more people affected by pulmonary fibrosis (or lung scarring) can live well for longer. People living with lung scarring, their loved ones and the professionals caring for them are at the heart of everything we do.
They provide expert support, information, education, help a growing network of support groups and raise awareness of pulmonary fibrosis. We collaborate to drive change that improves health and care and we provide vital resources to researchers, bringing hope for new and future treatments for this devastating disease.
Around 15,000 and 20,000 people a year are diagnosed with lung scarring. Despite pulmonary fibrosis being as deadly as some cancers, it takes too long for people to get diagnosed, treated and supported. This shortens and devastates lives and leaves people feeling alone, confused and frightened.
Together, we will stop lives being lost to pulmonary fibrosis.