To raise enough money for Layla Rose to purchase a Nanobubbles machine from the USA to help her manage her rare skin condition.
Nelson / Tasman
This is a speech Layla wrote to compete in an inter school speech competition in Golden Bay.
My name is Layla and I am Year 4 at Motupipi School.
Icthyosis.
Do you know what this word means? It is a really rare skin condition and you say it like this Ick - thee - o - sis. Sometimes it's a really hard word to say. It is so rare I have never met another person with the same skin as me.
Do you know how I got this skin? Well, I was born with it. 4-5 times a day I have to put cream on, even at school, to keep my skin soft and bendy and to stop it cracking. The worst part is that in winter at school, I have to have the cream put on by really cold hands.
The skin on my feet is really slippery and when I jump on my trampoline, sometimes I slip and slide all over the place.
Some people stare at me and some ask me if I'm sunburnt in the middle of winter!!
When I fall over I have super powers, because my skin grows back faster than anybody else's skin. I have super skin which grows about 6 times faster than anyone else's. Because of my super skin, I shed more skin and larger pieces. Everybody's skin grows every day and everybody sheds skin all through the day and night. Actually, most dust is tiny bits of skin.
My skin condition doesn't stop me doing ANYTHING!! I go rollerblading. I can swim and dive, ride a scooter and bike. I can run really fast and this year in the Motupipi school triathlon, I got second and won the silver medal. This year I played miniball, soccer and hockey in the school team. I act in the drama club and love to sing.
Wow! I have such a busy life. I am literally jumping out of my skin!
I work with Layla's Mum Anneliese. Anneliese is an amazing young mother who has been managing Layla's rare skin condition for the past 8 years by herself. I have got to know Layla over the past few years and she has shown me how to be the best you can be no matter what. She is an inspiration to us all.
To purchase a machine from the USA called the 'Nanobubbles'.
Any extra money raised will go towards sending Layla and her Mum Anneliese to visit other children with skin conditions like her.
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