FOCUS ON PKU
LIFE WITH PKU: WORK IN PROGRESS Sharon Buckley BSc, MSc, MBPsS
In this article, Sharon shares memories of bringing up children with PKU and reflects on the difficulties and demands through the years.
Sharon is a lecturer of cognitive psychology with published research in The Journal of Brain and Cognition. She is currently conducting research in psychology and treatment adherence in PKU
Recently, I asked both Charlotte and Adam, what their childhood was like growing up with PKU. The consensus was that, having PKU as young children did not mean very much to them in terms of negative experiences; neither of them could recall feeling excluded or different to other children. I am thankful, that whilst I was frantic with the demands of managing life with PKU (creating and baking low protein substitute foods, ordering/ collecting prescriptions, scouring supermarkets, educating those involved in their care such as for parties, sleepovers, tea at a friend’s, holidays and school trips etc), all that passed them by. Thus, as a parent I
Sharon is a parent to two young adults withPhenylketonuria (PKU); her daughter Charlotte is 20 years old and remains on the diet, whilst her son Adam is 18 years old and is off diet (though he makes valiant attempts to get back on diet).
had been successful in my endeavours to reduce the impact that PKU had on their childhood and, therefore, had enabled them to lead a ‘normal’ life. In a study that examined the parental experience of caring for a young child with PKU, Carpenter et al1 identified that striving for a normal life for a child was a coping behaviour often carried out by parents of young children with PKU. Though the parents experienced immense pressure, the result of watching their child engaging in a normal life, enabled the majority of parents to be accepting of the PKU diagnosis within the lives of both themselves and their child.
Adam’s story When Adam began high school, he shied away from letting people know that he had PKU, he felt different and wanted to be able to eat the same foods as his peers. Subsequently, from around the age of 14, his phenylalanine levels were recurrently beyond the target range. This was not as a consequence of eating high protein foods, but because he would over eat chips, chocolate and crisps (foods that are allowed, but have to be restricted). As his teenage years progressed, Adam gained a substantial amount of weight, though the summer before his 16th birthday he did lose nearly three stone on Slimming World (green days). However, we had not consulted his PKU clinic before commencing the weight loss programme and when we did, the clinic considered that our approach was incorrect, for example, we should not have been giving him the calorific supplements. The clinic told Adam that as he would be going to adult clinic and compliance was an issue for him, that to aid his weight loss he could make the decision to come off the PKU diet. As yet, there is no approved prevention, or treatment intervention for overweight and obese people with PKU.2
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A month after coming completely off the PKU diet, Adam began to gain weight; he was unable to be selective amongst such a wide range of foods that he was now ‘allowed’. Less than 10 months after stopping the PKU diet, Adam had gained three stone. Within a year of being off diet, whilst on a family holiday to Spain, Adam became feared for his safety; he believed he was going to be robbed, kidnapped or blown up. His paranoia
www.NHDmag.com May 2018 - Issue 134