From: Hugh Watkins on
have just seen a UK ITV documentary about this

"My child can't stop eating." tells the shocking stories of three
youngsters who suffer from Prader Willi Syndrome (PWS). Only 2000
people in the UK suffer from this rare condition which is caused by
damage to a chromosome

http://www.itv.com/page.asp?partid=3023



http://www.nlm.nih.gov/medlineplus/praderwillisyndrome.html

http://www.med.umich.edu/1libr/yourchild/praders.htm
caused by a disorder of chromosome 15. and affects one in every
12,000-15,000 people of both sexes and all races and ethnic groups.

http://www.pwsausa.org/syndrome/Genetics_of_PWS.htm
defined in 1956
not usually an inherited condition; it just happens

Although every case of Prader-Willi syndrome is due to the baby failing
to receive active genes from a specific section of the father's
chromosome 15, there are three different ways that this can happen
http://www.geneclinics.org/profiles/pws/

When hyperphagia begins or weight centiles are increasing (often age
two to four years), a program of a well-balanced, low-calorie diet,
regular exercise, and close supervision to minimize food stealing
should be instituted to prevent obesity and its consequences. The same
program is appropriate if obesity is present at any time. Consultation
with a dietician and close follow-up are usually necessary, and locking
the kitchen, refrigerator, and/or cupboards is often needed. The energy
requirement of people with PWS, which rarely exceeds 1000 to 1200
Kcal/day, should be considered in planning daily food intake.

<<<< food pyramid

http://www.pwsausa.org/syndrome/foodpyramid.htm

this is very much the food triangle I know from Denmark and use myself

http://www.pwsausa.org/images/Image15.gif

my weigh in day is going to be thursdays for the next few months

Hugh W