Jane Frances
19 November 2019
Jane Frances
Jane Frances is a psychotherapist and was for many years Schools Specialist and Policy Advisor in Education at Changing Faces, UK. She is an expert in the psychology of visible difference.
She tells us of how findings from psychological research can help parents and teachers of children with Neurofibromatosis to better support them.
“I have worked with a lot of children with many conditions including NF, and I’ve found that the responses by other people to visible difference is pretty standard across conditions. The advice I give is based on research. ‘Common sense’, however well-intentioned, can lead to counterproductive interventions.
For example, if a child is staring at a child with a visible difference, the ‘natural’ reaction of the teacher is to say, ‘you mustn’t stare’. The result is that children learn to turn away, and the child with the difference feels even more isolated.
A better response is for the teacher to tell the staring child, ‘if you find yourself staring, smile and say ‘Hello, my name is Jane. What’s your name?’’
It is even more important that parents or the teacher coach the child who has NF to handle other children’s curiosity. The best strategy is for the child with NF to have something to say, like: ‘Don’t mind my lumps and bumps. I’ve got NF. Have you got something interesting about you?’ It is always good to round off with a question and engage – curiosity is the beginning of a relationship.
If the child is shy and nervous, the teacher might need to say, ‘Oh you’ve noticed Timothy’s unusual face. Well that’s the way Timothy’s face is, and did you know Timothy has a pet cat?’
We know from countless studies that it is harder for a child who looks unusual to make and keep friends. This is caused not by an aversion to the unusual face, but by an aversion to the stigma. The key, therefore, is to reduce or eliminate the stigma. The conversational strategies above will help. A curious stare is a door to a conversation and possible relationship.
Teachers’ expectations are also key: they need to hold in their heart really positive hopes for this child’s future. Many studies confirm the ‘Pygmalion Effect’: that lower expectations lead to lower results. Teachers aren’t doing children a favour by going easy on them. The child needs tough, high expectations.
These are just a few tips. You can get more information and resources for tackling issues of face equality and the impact of appearance at changingfaces.org.uk.”
– Jane Frances"The best strategy is for the child with NF to have something to say, like: ‘Don’t mind my lumps and bumps. I’ve got NF. Have you got something interesting about you? "
Filter News
![](https://nervetumours.org.uk/images/made/images/common/jonnyPage-Preview-800-x-500-px_800_600_s_c1.png)
Jonny’s Story
Jonny has chosen to open up and share his incredibly brave battle with Cancer over the past year, find out more here:
Read More![](https://nervetumours.org.uk/images/made/images/common/james_2__800_600_s_c1.jpg)
James on Tour
James Wiggin is taking on the Tour de France on behalf of Nerve Tumours UK – or at least a part of it.
Read MoreNerve Tumours UK Specialist Neurofibromatosis Nurses attend the National NF1 Meeting in Manchester
Have a read what was talked about at this year's National NF1 Meeting in Manchester
Read More![](https://nervetumours.org.uk/images/made/images/common/lets-go-regional-coverPage-Preview-800-x-500-px_800_600_s_c1.png)
Let’s Go Regional/ Let’s Go Outside
Read about the website that offers new exciting opportunities to help you find a fundraiser/event that is most suited to you
Read More![](https://nervetumours.org.uk/images/made/images/common/Meet-harley-Mobile-600-x-800-px_800_600_s_c1.png)
Meet Harley
Have a read about the amazing 7 year old boy with NF1 and his fundraising family
Read More![](https://nervetumours.org.uk/images/made/images/common/PerculiarArtboard-1_800_600_s_c1.png)
Funny Peculiar
Peculiar Productions has chosen to donate all their proceedings to NTUK this year! Find out more:
Read More![](https://nervetumours.org.uk/images/made/images/common/christmas-card-website-2019Page-Preview-800-x-500-px_800_600_s_c1.png)
Christmas Card Competition 2019
Check out this year's Christmas Card Competition and how to enter
Read More![](https://nervetumours.org.uk/images/made/images/common/LanyardsPage-Preview-800-x-500-px_800_600_s_c1.png)
Sunflower lanyards to support patients and visitors with hidden disabilities
Read about the new lanyards being given out at Heathrow, Sainsbury's and Gatwick to help support those with disabilities
Read More![](https://nervetumours.org.uk/images/made/images/common/Small-Charity-NTUKPage-Preview-800-x-500-px_800_600_s_c1.png)
NTUK attends Small Charity Week
Nerve Tumours UK attended Small Charity Week, find out more about the week and why we attended here:
Read More