PKS UK relies on fundraising and donations in order to support and educate those who are affected by PKS. Every penny really does make a difference, so if you are thinking of raising some funds for us please get in touch. We currently have no paid staff and are run by a dedicated team of trustees who are all family members of someone with Pallister-Killian Syndrome.
PKS UK is registered with the Charity Commission. Please use form below or visit our just giving page to donate.
