Your friends are fundraising. Don't miss out, opt in.

Step Up For BPAN 2026!

Campaign by Action for BPAN

Join us as we climb Snowdon on the 20th of June to support BPAN research! Help raise awareness and funds for this rare condition as we conquer the mountain together. Every step brings us closer to a better future for those affected #StepUpForBPAN

Step Up For BPAN · 20 June 2026 ·

Be a fundraiser

Create your own fundraising page and help support this cause.

Start fundraising
Action for BPAN was created by two mothers who's daughters have been diagnosed with this rare Neuro-degenerative condition. As the UK's first charity for BPAN we want to fund the vital research for a cure or treatment and give a voice to this rare community of wonderful children and parents.

Story

We are proud to launch our second Step Up For BPAN fundraiser on June the 20th 2026! Born from both grief and necessity, our charity is the first of its kind in the UK, dedicated to raising vital funds for research into treatments and a cure, supporting families living with BPAN, and being a strong voice for our girls and children like them.

Beta-propeller protein-associated neurodegeneration (BPAN) is a diagnosis we have both received for our daughters, Isabella and Emily. From that initial moment of devastation, we managed to find one another and, together, discover hope in what first felt like an utterly hopeless situation.

So, what is BPAN? BPAN is a rare and devastating condition that impacts every aspect of a child’s life. Its symptoms are heart-breaking: as iron builds up in their brains, children with BPAN often lose their ability to walk, talk, and move. They endure complex, prolonged seizures, severe motor difficulties, and cognitive decline. As the condition progresses, they also develop symptoms of Alzheimer's and Parkinson’s disease... illnesses typically associated with old age.

Watching our daughters, and other children like them, face these challenges at an age when they should be playing and carefree is truly devastating. It’s a future we simply refuse to accept.

Our efforts have already helped fund the initial stages of ground breaking gene therapy research at Great Ormond Street Hospital. This pioneering work offers hope for a potential cure that could transform the lives of children like Isabella and Emily.

This is where we need your help. This climb isn’t just for Isabella and Emily, but for every person and family affected by BPAN. It’s our chance to raise the vital funds needed for research and to spread awareness of this devastating condition.

This climb symbolizes our determination to never stop fighting for our daughters, for every child with BPAN, and for every family who feels as lost and helpless as we once did.

Please step up for BPAN and climb for a cure because every step brings us closer to life-changing treatments. Whether you donate, share our story, or join us as a fundraiser on the climb, your support matters so much, every step counts.. #ActionForBPAN #StepUpForBPAN

Kelly Sayers & Nicole Harper

Co-founders of Action for BPAN & Mums of Emily and Isabella

Donation summary

Total
£7,312.37
+ £1,321.25 Gift Aid
Online
£7,312.37
Offline
£0.00
Direct
£3,019.22
Fundraisers
£4,293.15

Charities pay a small fee for our service. Learn more about fees