Strongbones is a nationally registered charity celebrating 25 years of supporting children and young people who are full‑time wheelchair users and live with conditions affecting the bones and muscles including Spina Bifida, Scoliosis, Spinal Muscular Atrophy (SMA), Cerebral Palsy, and Muscular Dystrophy. Our mission is to reduce social isolation and increase independence by providing essential disability and educational equipment, fully accessible respite and residential opportunities, and practical and emotional support for families.
Why Your Support Matters
The funding landscape has become increasingly challenging. Grant rounds have reduced, competition has intensified, and fewer resources are available across the sector. As a smaller charity, these pressures have directly impacted our income for year‑end 2026. Without renewed support, our ability to deliver life‑changing equipment and services will be severely limited. Your help is crucial.
The Families We Support
Many of the families we work with are among the most vulnerable in society. Parents often provide 24‑hour complex care to their children on the palliative pathway, relying on carers allowance of just £86.45 per week while managing suction, medication, catheters, personal care and night‑time support. Rising living costs and gaps in statutory provision push families to breaking point. Strongbones exists to stand beside them — turning isolation into inclusion and giving children the chance to participate in everyday life.
Led by Lived Experience
Our charity is guided by people with lived experience of disability and caring, ensuring every grant we provide is safe, practical and genuinely transformative.
What we do
Below is an extensive list of the work Strongbones carries out, but the trustees are always open-minded to innovative projects exclusive to children under our criteria.


