TYMES TIDINGS 2014 NOW AVAILABLE! READ ALL THE LATEST...
CAMPAIGN TO DISTRIBUTE NEW 'FALSE ALLEGATIONS OF CHILD ABUSE' BOOKLET
ME - The Truth about Exercise and Therapy by Jane Colby FRSA, Guardian Letters
Follow our Executive Director Jane Colby on Twitter @JaneCColby
|NO, YOU DON'T KNOW BEST||/ DON'T MAKE ME FAIL AT SCHOOL|
|PLEASE DON'T WAKE ME UP||/ ME IS JUST FATIGUE, RIGHT? WRONG|
|STOP DAMAGING EXERCISE TREATMENT FOR CHILDREN WITH ME|
|Recognition of our work and messages of support for the children.||
A webinar by Jane Colby
The Young ME Sufferers Trust
Poster available from Tymes Trust
|Supporting the cause.|
|Includes a full list of the charity's services.|
|Information booklets and magazines.|
|Reports, guides and other information about ME.|
|Get full access to our services.|
|By credit card, debit card or Paypal.|
|Jane Colby's new book. Free pages & Stripeysocks blog.|
Young Hearts is a collection of inspirational poetry by over 40 children and young people with ME aged 7 to 26. Foreword by Terry Waite CBE. All profits will be used for the Trust's services. This book was originally the dream of Tymes member Jade Louise Scarrott who was so tragically taken from us in a road accident at the age of 14. She wanted to raise awareness and understanding of ME in children. A review was recently published by Special Children magazine.
To commemorate Jade Louise Scarrott we present the ITV Central News feature on childhood ME (broadband version - 11.4MB) (dialup version - 1.05MB) which was prompted by the publication of Young Hearts. Includes interviews with Jade's mother Karen and Jane Colby. If you have problems viewing Windows Media files, download this version - 2.75MB.
Having recently attended the 2014 Pride of Essex Awards Ceremony, at which Jane Colby received an award, I am delighted to have the opportunity to offer to all the supporters of the Tymes Trust my best wishes and warmest Christmas greetings.
I have long been an admirer of the Trustís work and Janeís award is a well-deserved tribute to all that it does to support young ME sufferers. I hope that you will all continue to support the cause and do what you can to spread the word further.
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