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/Siobhan_Harding-Lester_370x280_800_600_s_c1.jpg)
Meet Siobhan, our new Specialist Advisor for Northern Ireland
Meet Siobhan from Northern Ireland, our newest Specialist Advisor
Read More![](https://nervetumours.org.uk/images/made/images/common/Poppy_1_370x280_800_600_s_c1.jpg)
Poppy’s NF1 story
Poppy describes growing up with NF1 and fundraising for future research & treatment
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_4646_370x280_800_600_s_c1.jpg)
Meeting Alpha FX
NTUK Head Office visited Alpha FX to give a presentation on our work & how their support & donations help the NF Community
Read More![](https://nervetumours.org.uk/images/made/images/common/NA_logo_370x280_800_600_s_c1.jpg)
Nerve Tumours UK joins the Neurological Alliance
A coalition of over 70 organisations working together to transform quality of life for people with neurological conditions.
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_4791_370x280_800_600_s_c1.jpg)
Nerve Tumours UK Conference 2021
The first meeting since 2019 with our Specialist NF Advisors & Nurses, Head Office & Members of the Board of Trustees
Read More![](https://nervetumours.org.uk/images/made/images/common/Wing_Walk_Ailsa_photo_on_wing_waving_370x280_800_600_s_c1.jpg)
Tricia’s Wingwalk fundraiser
Tricia describes her wingwalk experience in celebration of her 75th birthday and in memory of her daughter Sarah, who had NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/834872_1052_00091_370x280_800_600_s_c1.jpg)
Stuart’s Schwannoma Story Part One
Stuart describes how certain symptoms led to a Schwannoma discovery
Read More![](https://nervetumours.org.uk/images/made/images/common/image1_370x280_800_600_s_c1.jpg)
Joy’s NF1 story
Joy describes living with NF1; her son's diagnosis and support at school; fundraising and shining a light on NF
Read More![](https://nervetumours.org.uk/images/made/images/common/1_Onno_Faber_at_a_meeting_this_summer_to_organize_his_hackathon_OF_370x280_800_600_s_c1.jpg)
A man on a mission: Onno Faber and his NF2 journey
Onno Faber - since NF2 diagnosis aged 33, Onno is a man on a mission. Article courtesy of NEO.LIFE
Read More