XLH UK
XLH UK exists to help those with X-linked hypophosphatemia (XLH) and their families living in the UK. We organise events and maintain a website with resources and news. We raise awareness by sharing stories of the lived experience. We also contribute to research into the multiple aspects of this rare condition, to better inform the development of new treatments and standards for best care.
Latest income
£24k
Latest spending
£15k
Registered
2021
Trustees
- Sarah Mitsonchair
- Claire Jayne Lewis
- David Mark Bryan
- Dean William Derek Fletcher
- Jennifer Joan Carrington-Elson
- Oliver Gardiner
- Sally Shaw
Income and spending
| Financial year end | Income | Spending |
|---|---|---|
| 31/01/2026 | £24k | £15k |
| 31/01/2025 | £13k | £16k |
| 31/01/2024 | £18k | £24k |
| 31/01/2023 | £23k | £28k |
Government & lottery funding
| Funder | Date | Amount | Purpose |
|---|---|---|---|
| The National Lottery Community Fund | 06/02/2025 | £5k | XLH UK Community Day 2025 |
| The National Lottery Community Fund | 16/02/2024 | £5k | XLH Family Day 2024 |