Intelligent, sporty and musical, nine-year-old Amelia Crane has similar dreams and ambitions as many other young girls her age.
But the youngster from Lydney has to contend with unwanted attention and finger pointing because of the way she looks.
Amelia was born with achondroplasia, or dwarfism, and suffers from the impolite attention she gets from strangers.
Her parents Adelina Donaldson and her partner Graham Crane had no knowledge anything was unusual about their baby until a planned late scan at 36 weeks.
They want to share their experiences to help highlight the issues surrounding the condition to encourage support for Jeans for Genes Day, raising money for Genetic Disorders UK on Friday.
The charity is inviting everyone to wear their jeans to work or school and make a donation to help other families in a similar situation to Adelina, Graham and Amelia.
Nine out of ten children born with dwarfism have average-size parents. It can affect anyone and Adelina's first daughter Fiona is of average height.
Mum Adelina said the public attitude to dwarfism needs rapidly turning on its head.
"I do think that people are often kinder when they see other disabilities than dwarfism," she said.
"They don't name call or point or giggle when they see someone in a wheelchair. That's probably one of the most upsetting things for Amelia."
Amelia has the classic characteristics of shortened limbs and larger head and is far smaller than her friends. She is often in pain from her legs and lower spine and her proportions can make everyday activities and personal care difficult.
Add to that her two hearing aids and slight hydrocephalus, or fluid potentially pressing on her brain, and it seems inconceivable anyone would find her condition amusing. But they seem to.
Despite all of this, Amelia is a determined youngster busily enjoying her life, school and friends.
She sings, acts, swims and works hard at school having stated her ambition to be a vet; she chose a stick insect to join the family cat and goldfish.
She loved being in Beavers where she was awarded a sleeveful of activity badges before recently moving up to Cubs.
"It wasn't always that easy achieving them all," added Adelina.
"But she did it in the end. Cubs may be even more of a challenge. She is very happy at her school where she has lots of friends and everyone loves her but she does have problems with the new younger children who start each year.
"They can stare or be hurtful. But overall school is a more positive experience than not."
At her mainstream school Amelia has a one-to-one carer. There's a provision of step stools as well as a rail in the toilets and recently a sink was installed at a height she could wash her hands.
Before that the carer had to fill a bowl of water for her and so she wasn't self-sufficient.
Adelina said: "We try not to wrap her up but get her out there. It's a question of getting the balance right.
"Her friends are great and, for example, will run a bit slower so she can join in games, but I do worry about secondary school.
"Those can be tough years and youths can be nasty. As can younger ones; on one hospital visit a younger child refused to believe she was older and called her a liar.
"She didn't know how to handle that, for example. So we're trying to build up her confidence now.
"We haven't made masses of changes at home. We've quite a number of step stools around the place, and grabbers so she can reach things she wants.
"Amelia enthusiastically bashes the light switches with sticks and sometimes I wonder, how long is that switch going to last?"
Amelia, and her family, carry cards explaining her condition that she can hand out to curious adults and children who stare at her or when she might be in a situation needing extra support.
And she is constantly learning new skills to cope as a smaller than average person.
Her dad Graham installed a bidet which she's learned to use. Fortunately he's very practical. He adapted a bicycle so that she can travel in a trailer with back support when we all go out.
She has an adapted bicycle that she rides but she couldn't keep up on a long ride with the rest fo the family.
As for the future Adelina believes academic studies will help Amelia have a fulfilling life.
"I tell her it will give her more chances in a competitive world," she said.
"And there are teachers and doctors like her. I just wish there were more positive roles for people with dwarfism in programmes and films, such as presenters or news readers."
The Restricted Growth Association is a Jeans for Genes Day 2014 grant charity.
It will receive £5,000 from funds raised on Jeans for Genes Day to fund an activity weekend for children with restricted growth and their siblings.
Sign up for a free fundraising pack at www.jeansforgenesday.org.
![Unwanted attention for Amelia Crane, 9, who is living with dwarfism and just wants a normal life in Lydney Unwanted attention for Amelia Crane, 9, who is living with dwarfism and just wants a normal life in Lydney]()