Tyler and Nerhys's Early Intervention Page


This site last updated 4th October 2000.

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Tyler's school photo. July 2000.
Read Tyler's Story
Read The Diary
Updated 4 October 2000

Hi, we'd like to introduce ourselves. We are Richard and Katherine Price and this page is dedicated to our children, Tyler and Nerhys. Tyler was born on 9 January, 1996. He has a variant of Landau Kleffner Syndrome, which is a form of epilepsy that mostly affects the language centre of the brain. Nerhys was born on 24 May 2000. She has a cleft palate. This site is dedicated to our struggle to get them the help they need and the problems we have encountered along the way. We hope to be able to help other parents in similar situations and ask that if you have any information that would help us or any other parent that you let us know either by e-mail or by signing our guest book.

Those revisiting the site will notice the addition of Nerhys. We were kind of hoping for a "normal" child but instead we have a few more challenges. Nerhys, though, has a common ailment and there is a wealth of information so we do not expect a great deal of trouble getting help. Our local children's hospital has an entire unit set up for just such children.

Nerhys at 16 weeks
Read Nerhys's Story
Read The Diary
Updated 4 October 2000

Tyler's condition has all the appearance of being caused by his immunisation. Part of this site will be dedicated to increasing the awareness of immunisation dangers (we are not anti-immunisation, we just want support when things go wrong) and part will be dedicated to getting the help once a problem occurs. Initially all of the physical support mechanisms will be centred around Sydney, Australia, and all electronic services will be world wide. We hope to be able to expand these services as we get feedback from every one.


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