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/Inform_800_600_s_c1.png)
First Diagnosis Survey
A survey to improve NF diagnosis support by gathering feedback on early experiences and concerns from those affected.
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen_Cockburn__Charity_Director_(3)_800_600_s_c1.jpg)
Working with the hospitality industry & creating safe spaces for everyone
Read More![](https://nervetumours.org.uk/images/made/images/common/Untitled_design_-_2025-02-03T143712.302_800_600_s_c1.jpg)
Visible Differences: Changing The Narrative
Nerve Tumours UK joins multi-organisational workshop to enhance support for those with a visible difference
Read More![](https://nervetumours.org.uk/images/common/Untitled_design_-_2025-01-29T112429.522.jpg)
Repurposing anti-retroviral drugs to treat NF2 related tumours Retreat Study
Join a brand new study treating tumours in NF2 patients.
Read More![](https://nervetumours.org.uk/images/made/images/common/Untitled_design_(50)_800_600_s_c1.png)
Nerve Tumours UK joins the Neurological Alliance of Scotland
Nerve Tumours UK joins the Neurological Alliance of Scotland.
Read More![](https://nervetumours.org.uk/images/made/images/common/Untitled_design_(51)_800_600_s_c1.png)
Brain scans to give crucial insight into childhood genetic disease
New funding secured for exciting new global research initiative.
Read More![](https://nervetumours.org.uk/images/made/images/common/Road_Banner_1_800_600_s_c1.png)
Looking Back, Moving Forward: A Message from Our Charity Director
Read More![](https://nervetumours.org.uk/images/made/images/common/461673450_10169430984830371_375012236727486905_n_800_600_s_c1.jpg)
Oliver’s Blog
Oliver Bromley shares some personal experiences of visible difference, and how education and kindness can reduce stigma.
Read More![](https://nervetumours.org.uk/images/made/images/common/Ellen3_800_600_s_c1.jpg)
Ellen’s Story
Read Ellen's story, how she recovered from 'radical surgery' and why she's raising funds for NTUK.
Read More