Help Kacper from Durham

Kacper from Durham dreams of running, playing and enjoying life just like other children his age. Sadly, progressive foot deformities caused by spina bifida make everyday life much more difficult. This is his story.

A Difficult Start in Life

Kacper was born with spina bifida (myelomeningocele). Shortly after birth, he was admitted to intensive care and later transferred to Great Ormond Street Hospital, where he underwent a major operation to close the spinal defect.

Since birth, he has also faced neurogenic bladder and bowel problems. Because he has limited control over these functions, he still relies on nappies or pads. Recently, he started intermittent catheterisation four times a day and takes daily medication to support bladder function.

His childhood has been filled with hospital appointments, medical tests, rehabilitation and ongoing treatment.

Growing Problems with Walking

When Kacper was around five years old, he began tripping more often. His family searched for answers and requested further investigations, including hip assessments and an MRI scan of his spine. Despite numerous appointments and rehabilitation attempts, they struggled to get clear answers.

During this time, Kacper's feet became increasingly deformed. The family waited almost a year for an orthopaedic appointment in the UK. Later treatment with casts caused painful wounds and skin problems. More consultations, casts and orthotics also failed to bring the improvement they had hoped for.

Finally, a Diagnosis and a Treatment Plan

It was only during a consultation in Vienna that the family finally received an explanation. Doctors confirmed that Kacper has complex neurogenic foot deformities related to spina bifida and requires specialist treatment.

Kacper has already undergone surgery on his right foot. He now needs an operation on his severely deformed left foot, as well as further correction of his right foot.

A Long Road Ahead

The surgeries are only part of the journey. Kacper will also need:

• casting and regular cast changes,
• specialist orthotic devices,
• intensive rehabilitation,
• ongoing medical reviews and follow-up care.

Because of the nature of his condition, the deformities may return over time, meaning he will require specialist support for many years. The goal is to improve the position of his feet, his walking ability and his overall quality of life, giving him the best possible chance of an active and independent future.

Simply Kacper

Behind this story is a cheerful, brave and determined young boy.

Kacper loves football, supports FC Barcelona, enjoys playing Minecraft and likes swimming. He wants to have fun, stay active and explore the world just like any other child. Despite the challenges he faces, he never gives up and continues to approach life with curiosity and courage.

How You Can Help

Kacper faces more surgery, rehabilitation and a long period of treatment. Every donation, share and kind word brings him closer to a more active and independent life.

You can help by:

• making a donation to support his treatment,
• sharing Kacper's story with family and friends,
• helping spread the word to people who may wish to support him.

❤️ Support Kacper through GoFundMe.
❤️ Support Kacper through SiePomaga.

Thank You

Every contribution, no matter how small, makes a real difference. Thank you for supporting Kacper and helping him take the next steps towards a brighter future. ❤️