The research is looking into ways to enhance people’s rehabilitation journey post brain injury. This will extend our current understanding to beyond the individual with the injury. It is widely accepted that psychosocial wellbeing and rehabilitation outcomes are influenced by how the patient is able to adjust to life with a brain injury, yet the significance of the family context within which the patient is living has not been adequately addressed.
Images supplied by the contributing charity and used with permission. They may not be reused without consent.
Images supplied by the contributing charity and used with permission. They may not be reused without consent.
Images supplied by the contributing charity and used with permission. They may not be reused without consent.
The Pixel Fund is generously donating towards our Northern Hub project. The Northern Hub is a response to the continued increase in demand for YoungMinds services nationwide. Although our remit is UK-wide, our head office is based in London. Due to travel times and costs, we have limited delivery outside London and theSouth East, with work we have delivered usually being on an ad-hoc basis through temporary contracts. Pixel are helping us reach communities in need in the North of England.
Images supplied by the contributing charity and used with permission. They may not be reused without consent.
Images supplied by the contributing charity and used with permission. They may not be reused without consent.
Meningitis is a devastating disease – one in ten people who contract bacterial meningitis will die and many more are left with life changing after effects. The Pixel Fund has supported a ground breaking research project to investigate why some people are more susceptible than others to meningitis by comparing the genetic blueprint of patients with meningococcal disease alongside the genetic blueprint of the particular bacterium that cause their illness.
Images supplied by the contributing charity and used with permission. They may not be reused without consent.
PSPA is the only UK charity dedicated to supporting people living with Progressive Supranuclear Palsy. PSP is a degenerative disease of the brain and nervous system which leaves people unable to move, speak or swallow unaided. Most people with PSP will die within about seven years. There is currently no cure or any effective treatment.
Images supplied by the contributing charity and used with permission. They may not be reused without consent.
