Please Help Layla Rose's Rare Skin Condition.

$10,275 of $8,000 goal
Given by 168 generous donors in around 8 months

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!

Rebecca Olney's involvement (page creator)

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.

Use of funds

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.

Other page links

Read more

Latest update

Update image

Photos  27 March 2019

Photos

Share this update

Read 5 more updates

Read more

Latest donations

Takaka Infusion
Takaka Infusion on 30 Jan 2019
We wish you all the best Layla!
$60
Guest Donor
Guest Donor on 16 Jan 2019
$5
Brenda Dundass
Brenda Dundass on 13 Jan 2019
$50
Lesley and Ellie
Lesley and Ellie on 04 Jan 2019
Arohanui
$10
Miem Wapstra
Miem Wapstra on 27 Dec 2018
If we win the lotto, your the first one to benefit Layla
Private

Who's involved?

Rebecca Olney's avatar
Created by Rebecca Olney
Anneliese R Van Lier's avatar
Paying to a verified bank account of Anneliese R Van Lier on behalf of Layla Rose Roberts
Page Moderated
The page has been checked by our team to make sure it complies with our terms and conditions.

Any concerns?

Report this page
This campaign started on 14 Dec 2018 and ended on 5 Aug 2019.