In this blog Kate speaks about life growing up with PWS and what her life is like now. This blog has been reproduced here with permission from Kate and Aruma where the blog was first posted.

It was hard work for my parents when I was young. Having a child with special needs was a bit daunting at times, and it was an emotional strain for them to try and fit me into a “normal life” in “normal society”.

I was basically a loner at school, I kept to myself. At lunch instead of being outside with the other kids, I would go to the library and read a book.

I loved learning and I loved school, but I hated the kids there. I had one friend right through primary school who would always stick up for me. She would say to the others, “Kate’s just like us, treat her with respect. Why don’t you just get to know the person on the inside?” We’re still friends to this day!

In primary school, I began to put on weight and the names I was called I don’t want to repeat. I coped with the bullying through food, comfort food, meaning not so good food. Chocolate bars, doughnuts, and all that kind of thing.

A lot of teenagers these days commit suicide because of bullying. I have tried that. When it got very difficult I thought, can I do this? Can I end it? I was in grade 5. Year 5 and 6 was when the bullying got bad, I was preadolescent and my weight had become more noticeable.

Growing up there weren’t many treatment options, so I just had to try really hard not to eat, and to exercise as much as I could.

Food is always hard for me. People with Prader-Willi syndrome have an unsatisfied hunger meaning they always feel hungry. They don’t have the signal that comes from the brain, the lightbulb going on saying, hey you’re full!

It’s also much harder for people with Prader-Willi syndrome to lose weight as we have low muscle tone, so it’s difficult to move around and get our muscles to work.

Growing up, my brother and sister had to be ok living in a house where there were no chocolate bars, biscuits, or sweets because I couldn’t have them, or have them around me.

At times people with Prader-Willi syndrome can even become desperate for food.

I have eaten out of bins before. And being around food in shopping centres is very hard. I have to admit, I have stolen food from shops when I didn’t have any money, but thankfully people have been understanding at those times.

Before I moved into my current home, I lived alone which meant I had a lot of time, time to go to the neighbours to get extra food, or down to the shops. It was at this stage in my life that my weight increased, and my health started to suffer. I then decided I had to do something or otherwise I would end up being 6 feet under.

This is when I decided to move to a group home run by Aruma to give me more support. Since moving in two years ago, I have lost 45kgs. Each day I do cycling in the morning, cycling in the afternoon, as well as walking throughout the day.

I now have carers that manage my meals for me. If the temptation is taken away, it’s much easier. I don’t go into the kitchen, it’s a no go zone. I need this structure around food, to live in an environment where there is no temptation.

It is a lot harder to live with Prader-Willi syndrome than people realise. The food and weight is hard, but it’s also hard to make friends, and to keep friends.

I hope one day to be able to go to schools and share my experiences with the students to raise awareness of Prader-Willi syndrome and the damage that bullying can cause.

A lot of people who have Prader-Willi syndrome do not feel comfortable talking about it, but I want to share my experiences so people can understand. People should never judge a book by its cover, but instead get to know the person on the inside.

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