View the presentation by Dr Laura Madeley - Guy’s & St. Thomas’ NHS Foundation Trust
What is KLS ?
KLS is a rare disorder characterised by recurrent bouts of excessive sleep associated with reduced understanding of the world and altered behaviour. KLS usually starts in the teenage years but can occur in younger children and adults. Each episode lasts days, weeks or months during which time all normal daily activities stop. Individuals are not able to care for themselves or attend school and work. People with KLS coming out of episodes will have little or no memory of what happened during an episode. Between episodes they have normal sleep, understanding and behaviour. KLS episodes may continue for 10 years or more. KLS is sometimes referred to in the media as "Sleeping Beauty" syndrome.
Give Donation
KLS Support UK is the only UK small charity representing families affected by Kleine-Levin Syndrome. Please help our small charity with funds.
Donate NowBecome a Fundraiser
Become a Fundraiser for KLS Support UK and raise money to support medical research with the aim of finding the cause, treatment and ultimately a cure for KLS.
Fundraise NowTake part in an Event
KLS Support UK promote events that allow fundraising for this cause. Events include runs, cycling and treks. Why not get involved and help our cause.
Find EventOur Mission & Goals
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Awareness
Raise awareness of KLS in the UK amongst the medical profession and the general public.
Learn moreMedical Research
Support medical research with the aim of finding the cause, treatment and ultimately a cure for KLS.
Learn moreWork with other Groups
Co-operate with other KLS groups around the world to further these aims.
Learn moreLatest News
We are reaching out with a plea to the KLS families who attended the 2015 KLS Conference in Atlanta and those families engaged on the KLS Facebook page.
Happy Volunteers
Become a Fundraiser to this great cause. Why not take on a personal challenge, organise an event or celebrate someone special who is bravely forging through life despite coping with KLS? Thank you for supporting KLS Support UK.



