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waspslegends.co.uk 

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home news what is kls about us living with kls kls leaflet case histories medical q & a's promotional material fundraising links legal contact us home welcome to kls support uk we are a small charity offering help and support to those affected by kleine-levin syndrome (also known as kleine levin syndrome or 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. there is more about us and our aims here since we are a uk small charity (and concentrate on uk information) we ask that those in other countries please contact the kls foundation . contacting kls support uk it is easy to contact us by filling in the contact us form. one of us will reply as soon as possible. we are happy to speak over the phone (after email contact). we appreciate that you have been through a traumatic time and may find it therapeutic speaking to someone who has experience of kls. we are happy to put people in touch with each other if/when they are ready (by mutual consent). we try to pair those who have similar kls experiences. we help with those seeking diagnosis and those diagnosed. for kls support uk news and updates please click here and then fill in the contact form to be subscribed to our mailing list. kls leaflet the kls support uk information leaflet can be downloaded and printed to give to gp's, family and friends, the text etc. has been approved for nhs use. we are delighted to be listed in the patient.co.uk directory - where our leaflet is mentioned. this will make it more readily available to doctors and patients alike. if you would like to just view the leaflet please right click here and open in a new window or tab. if you would like a printed copy/copies please contact us and we will post some to you. please help our small charity with funds kls support uk is the only uk small charity representing families affected by kleine-levin syndrome. trustees:- adele clarke, lachlan dunbar, danielle harris, professor beverley hunt, caron krieger. © 2018 kls support uk · log in · cookies · sitemap

URL analysis for kls-support.org.uk

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patient.co.uk
static.kls-support.org.uk

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Error for "kls-support.org.uk".

the WHOIS query quota for 2600:3c03:0000:0000:f03c:91ff:feae:779d has been exceeded
and will be replenished in 103 seconds

WHOIS lookup made at 15:31:53 05-Jul-2018

--
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Copyright Nominet UK 1996 - 2018.

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  REFERRER http://www.nominet.org.uk

  REGISTRAR Nominet UK

SERVERS

  SERVER uk.whois-servers.net

  ARGS kls-support.org.uk

  PORT 43

  TYPE domain

DISCLAIMER
This WHOIS information is provided for free by Nominet UK the central registry
for .uk domain names. This information and the .uk WHOIS are:
Copyright Nominet UK 1996 - 2018.
You may not access the .uk WHOIS or use any data from it except as permitted
by the terms of use available in full at https://www.nominet.uk/whoisterms,
which includes restrictions on: (A) use of the data for advertising, or its
repackaging, recompilation, redistribution or reuse (B) obscuring, removing
or hiding any or all of this notice and (C) exceeding query rate or volume
limits. The data is provided on an 'as-is' basis and may lag behind the
register. Access may be withdrawn or restricted at any time.

  REGISTERED no

DOMAIN

  NAME kls-support.org.uk

NSERVER

  KIP.NS.CLOUDFLARE.COM 173.245.59.128

  ZARA.NS.CLOUDFLARE.COM 173.245.58.148

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