Contact Kleine Levin Syndrome - a parent's guide.

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We have set up a contact form which we would appreciate if if you could fill it out. We would like to be able to let you know of any updates we add to the web site, hear about your KLS stories, share any links to relevant articles you may have and perhaps put families in touch with one another - with your permission of course.

If you would like to contact us please fill in the form below - we would really appreciate it.

Name:

KLS Patients Name:

KLS Patients Date Of Birth:

Where for you live: (county, state, country)

If you are diagnosed and have a Consultant / Hospital - please tell as as it may help others.

Email Address for us to contact you on and to subscribe you to future updates.

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Can we share your name and email address with other interested parties - please tick the relevant boxes

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Families (other KLS families in your area)

When you press the submit buttton - an email message will be created - please send the email onto us so we can add you to our mail list, many thanks.

For any more information please contact Support@KleineLevinSyndrome.co.uk

All information on this site is © Kleine Levin Syndrome.co.uk 2018 - The information included on these pages is intended to be useful to families, friends and interested parties and talks about KLS (Kleine Levin Syndrome) from a parents perspective. We acknowledge that everyone's experience will be different, and we would like you to respect that we are not a professional body offering support, none of this information is presented by a medical professional - our backgound is parenting, childcare, disabled holidays and graphic design. Our aim for the site is to share our story, get the best help and support we can for our son, raise awareness, share the resources and stories we discover on our journey, and to hopefully along the way offer information to other families. We recommend you consult your specialist for the best advice for you and your family.

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Kleine Levin Syndrome - A parent's guide to KLS - Sleeping Beauty Syndrome - KLS KLS Support Groups include KLS Foundation (US) & KLS Support UK where you can find more information...