Enquire rolls out the red carpet

At our annual conference earlier this month we showed a new film about getting ready to leave school.  Pupils from Woodlands School in Edinburgh worked with Enquire and Media Education to make a film of their views about getting ready to leave school, post school options and learning programme made by Playback ICE called Moving on: Transition in Action.

For the official launch of the film and as a thank you to the pupils involved we held a special screening for the stars of the show.  The young people reported that taking part in the film made them feel ‘happy’, ‘proud’, a ‘bit nervous’ and ‘involved’.  They also said it felt good to talk over their feelings about leaving school. If you watch the film you’ll see how well everyone did – we think they were all amazing!

Click below to watch the film.

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Remember, if you’re worried about leaving school and want some help with this – tell someone!  You can talk to a teacher, your family, friends, social worker or anyone else you know who can help.  You can also look at Enquire’s guide called Getting ready to leave school for help and advice.

Posted in changing or leaving school, film, my life, my say, young people's views, your future | Leave a comment

Your views are important to us!

Maybe you’ve already seen our guides such as ‘Getting ready to leave school’ and ‘Going to a new school’? We are writing two new guides just now. They will be called ‘Extra help at school when you are looked after’ and ‘What happens when you can’t go to school?’

We always like to ask young people what they think when we are developing new guides. Your views are important to us as you know what works best for you.

 

 

Jeni from Enquire met with some young people from the Edinburgh Young Carers’ Project and the Maben Residential Unit to ask what they thought of the new guides.

They looked at the words, the colours, the cartoon characters and the design of the guides and came up with lots of great ideas.

Jeni says: “The young people I spoke to had lots of fantastic ideas about how we could make the guides better. I’m very grateful that I had the chance to listen to them and hear their views. They thought of things we hadn’t, like how important it is to get enough sleep and how this can make learning difficult. They thought the guides should be bright and cheerful with lots of images of young people they can relate to. I hope the guides will be more useful now. They belong to young people!”

Thanks a lot to all the young people who gave us their ideas!

We will let you know when the new guides are ready. In the meantime if you would like to look at our other guides for young people click here.

 

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Ellie’s blue ribbons

Ellie with the First Minister

Ellie is 12 years old and lives in Edinburgh.  Like many of you, she has dyslexia. She also has two sisters with dyslexia and one with dyspraxia.  You maybe feel a bit like Ellie who says “I am fed up of having to explain what dyslexia is to everyone I meet!” Ellie decided to do something about it!

She thought it would be a good idea to have blue ribbons that lots of people would wear, a bit like wearing a poppy for Remembrance Day.  She hoped this would help everyone be more aware of dyslexia and how it affects the lives of many young people.

Ellie needed to get some money to buy the ribbons and hand them out.  She heard about ‘Disney Friends For Change Grants’. Young people from all over the country can apply for money if they have an idea that shows they are trying to work to help others.  In her application Ellie said “I want people to know how difficult life can be for those with dyslexia and that people with dyslexia are not stupid.”

Ellie was given £750 to help with her plan that as many people as possible would wear a ribbon. She put the ribbons in libraries where anyone could pick one up for free. Lots of schools took them to hand out to their pupils. Ellie hopes the ribbon will soon be known as the DAW ribbon because she timed all this to happen during Dyslexia Awareness Week in November 2012.

Ellie knew it would be good if she could get some important people to wear a ribbon. She was able to go to the Scottish Parliament and give one to the First Minister and one to the Minister responsible for Learning, Science and Scotland’s languages. He was very impressed with what Ellie had done and said he would wear his ribbon with pride.

Ellie knew Sir Jackie Stewart had dyslexia so she wrote to him too. He wrote back to say he was happy to wear the ribbon so other people with learning difficulties might get the respect they deserve.

Ellie hopes to keep working on her project so that by the next Dyslexia Awareness Week in October 2013, even more people will be wearing the ribbons. We wish Ellie lots of luck for this- very well done, what a great idea! We will all be keeping an eye open for blue ribbons and will now be able to tell people what they represent.

Watch this video where Ellie explains how she came up with her idea and what she hopes her work will lead to.

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If you have dyslexia you will know what Ellie is talking about. You might find some of your schoolwork difficult.  It is important that you remember there are people who can help. These Enquire guides might help you too:

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“I’m proud of my disability”

Enquire recently chatted with Samantha, who became a wheelchair-user two years ago following an accident. She told us about the physical challenges she faced, what it was like going back to school and how she dealt with the reactions she received. Samantha’s story is an inspiring one.

Having overcome initial difficulties and adjusted to her disability, Samantha has discovered a talent for wheelchair-racing and inspirational speaking. Her ambitions include becoming an athlete, going to university and raising awareness about disability.

“Don’t ever give up on your dreams. Just because you’re disabled doesn’t mean you can’t do it ‘cos you can, you really can. You can do greater things than able-bodied people sometimes.”

You can listen to the podcast with Samantha here or you can read the transcript of what was said here:

Linda: I’m in the Scottish Borders today talking to a young person who’s just gone into her 6th year at school. She is also a wheelchair-user.  Sam, you’ve not always been a wheelchair-user.

Samantha: No

Linda: Tell me a bit about that.

Samantha: An accident occurred 2 years ago, which has left me paralysed from the waist down.

Linda: Were you in hospital for a long time?

Samantha: I was in hospital for exactly 6 months.

Linda: 6 months. That’s a long time. At what point during that 6 months did you find out you weren’t going to walk again.

Samantha: I found out that night of my accident on 2nd December.

Linda: So almost instantly.

Samantha: Yup.

Linda: So how did you deal with that in the midst of all this?

Samantha: I kind of dealt with it different to a lot of people. I never cried about my accident. I just kept saying, ‘It’s fine. It’s fine. It’s fine’ covering it with my smile which I find easier to do than letting it all out. I find it easier just to hide it, which I know isn’t the best thing to do but I find it easier.

Linda: What kind of support did you get when you were in hospital and recovery?

Samantha: Well I was in physio from 9 o’clock in the morning till 4 o’clock. Constant physio. My Physio was really, really good with me. She took me to a lot of sport and things, to loads of different things, to broaden my thing about disability. And she told me about writing a book and writing about how you feel which has helped a lot. I have a book at home that I write in whenever I feel a little bit down, whenever I feel I’m not quite happy. I just write and that helps me.

Linda: Excellent. What would you say was the most important thing to you during that period of time?

Samantha: Everyone else in the hospital because they’re all in the same boat and there’s even people..and they’re across the bed from you..and they’re a lot worse off than you. And that makes me feel so thankful that you can move your hands at least and you can move your neck. Some people can’t even talk which makes you feel very thankful.

Linda: What would you say was the most difficult or challenging part of that time?

Samantha: The physio was quite hard. I was told at the start, ‘The physio’s going to be really hard’ but I don’t think I could understand how hard it was going to be. It’s like standing every day and I had to do callipers, which is like you sweat as soon as you stand up. It’s really sore on your hands. Learning to push a wheelchair. It looks really simple to some people but it’s actually quite hard when you first get into it. I bumped into a lot of doors and stuff!

Linda: So building up a lot of strength.

Samantha: Yeah, I did a lot of gym work in the mornings. Just to be able to lift myself. I wanted to be independent so I had to do a lot of work to be able to transfer in the cars and things like that.

Linda: You must have missed quite a bit of school during that time so how did you manage to keep up?

Samantha: I missed a lot of work. In the hospital they sent me a tutor but because I was in rehabilitation all day and you’ve got people screaming all night you don’t get a lot of sleep so it was hard to keep with that. There was a man in the hospital at the same time as me and he was a PE teacher so he taught me my PE Standard Grade. I managed to sit 3 of my exams- PE, Maths and Drama and I got two 2s and a 3. When I came back to school I got tutors and I just took a lot of work home to fill in because I was going to miss a lot still with going to hospital to get check-ups.

Linda: There must have been changes that had to be made in school. Were there changes or did you find coming back to school was a fairly easy transition for you?

Samantha: I was lucky because we’d just moved into a new school so the lifts and everything were all there. It was really good. I had to go on a course for the e-vac chair, which is a chair that takes you downstairs if there’s a fire alarm.

Linda: So no real changes in the classrooms.

Samantha: Just tables as well because some are narrower so you can’t fit right in. Or they’re too high so you have windy-down chairs.

Linda: So all these things were put in place for you. Would you say it was easy or hard to fit back into school? Even thinking about friendships.

Samantha: It was hard on that kind of thing because I was scared to come back ‘cos I’d kind of got it into my head that people wouldn’t want to be the same around me. When I did come back at first everyone stared a bit, even though they all knew what had happened to me. They still stared. They were a bit cautious about speaking to me.

Linda: So do you think that was hesitation on their part because they were unsure?

Samantha: Yeah. I think they were unsure how I was coping with it. My close friends they were fine ‘cos they came up to visit me in hospital but other people weren’t sure how I was taking to it. They were just a wee bit hesitant towards me but after a few weeks they were completely fine.

Linda: What would you say were the main issues that face a young person who is a wheelchair user in a school?

Samantha: Obviously the fear of coming back and seeing people who haven’t seen you or seeing people you knew might take the mick out of people. You know they might be talking about you. I had it once. Someone said something about me and everyone ganged up on him and everyone was like, ‘That was horrible’. Nobody stuck by him and said,’Haha, that’s fuuny’. Everyone was, ‘That’s disgusting’. I was really lucky. My whole school is completely behind me. But I can understand how hard it is. When I first broke my back, I was like, ‘I don’t want to go back to school’. I didn’t want people to see me like this. I didn’t think people would accept me. I wanted to go to a school that had everyone in wheelchairs so I was the same as everyone else but my friends just said to me, ‘No, you’re coming back!’ I got no choice!

Linda: You’ve always, I’ve heard, been interested in sport. Maybe that’s changed so what kind of sport did you used to do?

Samantha: Gymnastics, ballet, hockey. I ran a lot. I really enjoyed sport. In the hospital, I didn’t really know what I was going to do. I didn’t know if there was any sport. I never watched the Paralympics. There is no-one in my school that’s disabled so I didn’t know of anyone who’d done disability sport but my Physio took me to a club in Glasgow- Red Star- that does wheelchair racing. I remember watching and I was,’ That’s amazing! I want to do that! I want to do that!’ So after I got out of hospital I went up to visit them again. I tried to get into the team.

Linda: So you had a trial?

Samantha: I said to the coach, who’s now my coach that I’d like to get into wheelchair racing. I really want to do something and I knew that sport made me smile before my accident and I knew it would make me really happy. So he got me into a racing wheelchair. This is my second time and my first with a proper coach and he just said to me, ‘ You’re in. You’re in the squad’. He just said I had a natural ability for it. I believe now I was born to do my wheelchair racing.

Linda: Ok, you’ve told us about your ambitions in your sport. What are your plans and hopes for the future?

Samantha: I hope to obviously compete. I want to be an athlete full-time but I’d like to also do…I enjoy the counselling side…Psychology. Hopefully, I’ll get to go to university and do Psychology and go into counselling. Possibly if I’m able to do my racing constantly I’d like to do inspirational talking. I go round schools the now..primary schools..and I talk to the kids and things. I’m a believer that kids should be taught about disability younger because kids are gonna stare but they’re staring because they don’t understand that we’re just the same. All they see is they’re different and they don’t like that because they’ve not been taught that they’re just the same, It’s just their legs don’t work which makes them no different. Nothing wrong with their brains. Their legs, their arms, maybe their whole body doesn’t work. It doesn’t make them any different. So I’ve been going around schools just teaching them about my sport. They really like seeing my chair. I call my racing chair Molly ‘cos I speak to it at the start of races and I say ‘C’mon Molly!’ I like naming her. And they really enjoy seeing it and they get really interested and they ask lots of questions. They love learning about disability. They just love it.

Linda: So you’re breaking down barriers.

Samantha: I’d love to go round primary schools and do that.

Linda: Do you see any barriers to achieving all these goals that you have?

Samantha: Emm…not really. My dad’s always told me that if ever I want to do anything then I can do it. Don’t let anyone tell you that you can’t. I don’t think there’s anything…nothing.. that able bodied people do that I can’t do. I maybe just do it differently.

Linda: Do you think the experiences of the last couple of years have changed you as a person in any way?

Samantha: Yeah, I think they’ve made me stronger. I don’t think I’d be the person today if it wasn’t because of my disability. I’m very proud of my disability. I’m very privileged that I’ve had the chance to be disabled and get a chance to go to the Paralympics. I don’t think I would ever have got a chance to go to the Olympics. Yeah, I’m proud of my disability.

Linda: So, final question. If you were to give any advice to another young person who maybe found themselves in similar circumstances to you, what would the advice be?

Samantha: Don’t ever give up on your dreams. Just because you’re disabled doesn’t mean you can’t do it ‘cos you can, you really can. You can do greater things than able-bodied people sometimes.

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New podcast about the Inclusion Unit in Fife

Enquire met a group of young people who go to the Inclusion Unit at Dunfermline High in Fife.

The unit is for pupils who have been excluded from school or who are at risk of exclusion. The unit helps and supports them to either go back to school or stay at school.

The pupils talked about why they were excluded, the kinds of work and activities they do in the unit, and the support they get from the staff there.

They also talk about how attending the unit has changed them for the better, and give some good advice to other young people.

Their advice includes:

“Think about what you do before you do it.”

“I used to be a proper eejit. Now I’ve grown up a bit. Now I would talk to teachers more.”

“The only one that can help you is yourself.”

You can listen to the full interview here.

If you’d rather read what was said during the interview rather than listen to it, here is the transcript. Continue reading

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We are all different colours but together we can make a rainbow

Last year 88 young people from all over Europe, including Scotland (from the RNIB youth group Haggeye and the Scottish Youth Parliament), met in Brussels. They visited the European Parliament to talk about inclusive education. Some young people had additional support needs and some had disabilities. Some young people had additional support needs and disabilities. All were being taught in mainstream schools.

The European Agency for Development in Special Needs Education arranged the event and have now produced a report – Young Views on Inclusive Education. Here are some things that the young people said:

 

Inclusive education should be about breaking down barriers.

It is learning to live together and respecting everybody with and without disabilities.

Inclusive education is good for friendships.

Inclusive education is an investment, we must invest in people; people are our only resource.

It is important to receive support without needing to fight for it.

We are all different colours but together we can make a rainbow.

The young people also made posters about inclusion. The Scottish entry was blank; the delegates said:

The poster is deliberately blank. We wish to show that for many children and young people living with sight loss, posters and other learning materials are not accessible. For many of us, the printed word cannot be recognised and visual displays, like this, appear completely clear. This, it can be argued, is in itself not inclusive. We believe this is the strongest message we can give.

Have a look at the other posters here.

You can get a copy of the report from Children in Scotland.

 

 

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New film about domestic abuse by young people

Voice Against Violence (VAV) have made a brilliant new film to tackle domestic abuse called One Voice at a Time – Tackling domestic abuse through the voice of the young.

In the film they talk about how domestic abuse affected them. They tell education and other professionals how important it is to understand what helps. They also explain why they ‘went to the top’ to make changes that will improve things for others.

VAV is a group of eight young people who have experienced domestic abuse. They worked for over two years to encourage the Scottish Government and the Convention of Scottish Local Authorities to stop domestic abuse from happening in Scotland.

VAV members want to make sure that if you are experiencing domestic abuse you get the help you need. They say:

‘Don’t believe people don’t care and don’t give up hope – there’s so much good support out there’

Have a look at the film and all the great advice and information on the VAV website.

 

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We all struggle with some things!

Enquire recently met Chantelle, a young Gypsy Traveller who has been working with Article 12’s Gypsy Traveller Lives Project, and Jill Keegan from Article 12 who is the Participation Officer.

Going to school isn’t always easy for Gypsy Traveller children – especially going to secondary school. Chantelle told Enquire about her time at school and what she thinks would make school better for Gypsy Traveller children. She also explained how working with the Young Gypsy Traveller Lives project helped her…..and how she is using her experience to help others to think about what it’s like to be a young Gypsy Traveller.

We asked Chantelle about issues young Gypsy Travellers face at school.

“People say things like ‘oh, the Gypsies are coming to school – make sure you’ve got your school bag with you because they steal.’ People hear things like that on TV and in the newspapers but if they spoke to us they’d realise that we’re not like that.

Now that I’m older, I think the settled community and Gypsy Travellers need to come together and try to break boundaries. If settled people got to know Travelling people – and the other way too – they’d realise we are not bad, not like the people you read about in the papers and on the TV. It’s like getting settled people, parents and teachers all together and saying ‘We are all the same, we all struggle with some things.’

Bullying and discrimination are big issues. For instance, the way that Traveller girls dress is really different from settled communities. The abuse the girls get just for wearing short skirts or low tops, just because they wear different clothes. It’s like tarring us all with one brush.”

We asked what would help young Gypsy Travellers in school:

  • More awareness raising and training in schools, trying to challenge the way young people think
  • Training for teachers
  • More flexibility in how education is provided. Teachers could come out to the sites so that young people feel safe within their own community
  • More Gypsy Travellers teaching
  • More support to ask for help!

Chantelle’s school came up with the idea of Gypsy Traveller School in the local community centre; a teacher from the high school came and taught her and some of her family.

And finally, some advice from Chantelle:

“Go to high school, stick it out, get all the grades you can. Get the education you can get and do the best you can!”

Read the full interview below.

Enquire: Hi Jill. Could you tell us a little bit about the Young Gypsy Traveller Lives Project?

Article 12 has been funded for the next four years to work with young Gypsy Travellers, giving them skills to help them be part of decision-making at local and national level.

We do lots of different work. We work with Gypsy Traveller communities, building contacts and getting young Gypsy Travellers involved with the project. We have a core group of young Gypsy Travellers who have been trained as peer educators to deliver awareness raising workshops to schools, local authorities and other groups. At the heart of all our work is making sure Gypsy Travellers know their rights so we can help them have a say about things that matter to them. In doing this, young Gypsy Travellers will be able to get involved and hopefully inform Government policy and legislation that affect them and their community.

Enquire: Hi Chantelle. Thanks for coming to talk to us. Could you tell me a little bit about yourself and how you got involved with Article 12?

My name is Chantelle and I’m 25. I’m involved with Article 12 as a sessional worker.

When I was 15, I was a young person volunteer with Save the Children until I was about 17 or 18. Then I became a worker and worked on a lot of projects on a Gypsy Traveller site at Larkhall. I worked on different projects like Healthy Eating and Diet Projects because a lot of people didn’t know much about that sort of thing. We had healthy eating days, trying to get younger kids to eat apples instead of crisps.  We took them swimming and to the gym and gave them information about healthy eating and exercise.

After that project finished we felt that, as young Gypsy Travellers, we wanted to go further. We got involved with Article 12. We felt we basically wanted people to know that not all Gypsy Travellers are bad, that we do still need help with the issues we’ve got, like discrimination and things like that.

Enquire: What have you got out of working with Article 12?

It’s been brilliant working with them. I’ve learned more working with Save the Children and Article 12 than I feel that I did in primary school. I’ve got a lot of confidence, to stand up for myself as a Gypsy Traveller and not hide who I am. Just basically knowing my rights and learning about things like planning permission and things like that. I didn’t know any things like that before.

Enquire: Could you tell us what it’s like being a Gypsy Traveller and going to school?

I went to primary school until P7 but I only did a couple of months of high school and then my school came up with the idea of Gypsy Traveller School which was in the local community centre.

So it was me and my brother and my cousins who all went and a teacher from the high school came and taught us. You were only meant to be there until you were 16 but I was there till I was 17.  I used to pop in and help as well, as my wee brother and my cousins were there as well.

Enquire: What issues do you feel young Gypsy Travellers face at school?

We face barriers like when people say things like ‘oh, the Gypsies are coming to school – make sure you’ve got your school bag with you because they steal.’ People hear things like that on TV and in the newspapers but if they spoke to us they’d realise that we’re not like that.

Now that I’m older I think the settled community and Gypsy Travellers need to come together and try to break boundaries. If settled people got to know Travelling people – and the other way too – they’d realise we are not bad, not like the people you read about in the papers and on the TV.  It’s like getting settled people, parents and teachers all together and saying ‘We are all the same, we all struggle with some things.’

The bullying and discrimination are big issues. For instance, the way that Traveller girls dress is really different from settled communities. The abuse the girls get just for wearing short skirts or low tops, just because they wear different clothes. It’s like tarring us all with one brush.

Enquire: What sort of things would help young Gypsy Travellers in school?

Suggestions for making things better?  More awareness raising. Not so much in primary schools but in high schools. In primary schools, children don’t really know but in high school they are seeing the news and reading the papers and start thinking that Gypsy Travellers are these bad people. If Gypsy Travellers were going into schools and saying this is who we are, we can’t change it. Yes, fair enough we have different lifestyles but at the end of the day we still need our education too.

I’ve been involved in training up north in Aberdeen. I’ve being going into one of the high schools and giving pupils information about being a Gypsy Traveller, trying to challenge the way they think about us. We did some work using before and after cards.  Before we started the session we ask them to fill in the cards with 3 things they think about Gypsy Travellers and then once we are finished the session we ask them to do the same. What a big difference between them!

We also did things like give them lots of statements about Gypsy Travellers like ‘They don’t want an education’ or ‘They don’t pay tax’ and asked them whether they agreed or disagreed and then talked about it. We asked them to imagine a Gypsy Traveller community moving into an area beside a settled community and got them to think about what their fears would be, both as a Gypsy Traveller and somebody from a settled community. The answers were quite similar – things like fears for the safety of the children and things like that.

Another thing that would help is training for teachers. Teachers also only hear the bad stuff. We need young Gypsy Travellers teaching teachers about our lives, what they are like, what we deal with.

Also, more flexibility in how education is provided to Gypsy Travellers. Like teachers could come out to the sites so that young people feel safe within their own community, that they won’t be made of a fool of because they can’t read and write.

In my area there is something called Universal Connections, which is open on a Wednesday and Thursday and you can drop in for anything to do with your education. They do loads – Maths, English, Art and Geography. More of that sort of thing would be great.

Also if there were more Gypsy Traveller people teaching, maybe like me teaching the younger Gypsy Traveller children. We’re a community, like a family, so I might be teaching cousins or nephews or nieces but that might help. The barriers wouldn’t exist and they might be able to say they were struggling if it was somebody they felt comfortable with. Maybe even if it was like a wee unit in school, then they would have to go to school five days a week but be taught by people they were comfortable with, instead of not going or only going a couple of days.

Also, more support to ask for help. We are not good at asking for help as we feel like we’ll be made a fool of.

Enquire: What advice would you give to other Gypsy Traveller children about school and getting support in school?

Coming from me? Go to high school, stick it out, get all the grades you can. Get the education you can get and do the best you can.

Enquire: Thanks very much, Chantelle, and Jill, for coming to speak to us today and sharing your experiences.

 


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Haggeye is 5!!!

Haggeye – the forum for blind and partially sighted people in Scotland – wants you to come to their 5th birthday party.

It is in Glasgow on Saturday 15th September from 1pm – 4pm. Call Caitlin on 0131 652 3154 or Mo on 0131 652 3146 for more info or email haggeye@rnib.org.uk

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Three young people talk openly about how being homeless affected their education

Lots of young people have to try to keep going to school even when they don’t have a settled home. This can be a tough time for them and they’ll maybe even have to move away from their friends and go to a different school. Shelter Scotland say there are thousands of children in Scotland who are homeless.

Shelter Scotland and Children in Scotland have written a report called ‘Homeless Not Hopeless’. This is to help adults working with homeless young people to understand how they feel and what would help make it easier for them in school. Sometimes even just a wee change can help lots.

You might be in this situation or one of your friends might need help. Maybe you are worried about going to a new school and having to make new friends. Maybe you think you would be bullied because you don’t have a proper home just now. There’s a good website with a video of three young people talking about what they found hard and what helped them to feel better about school.  Have a look at it!

It’s not the children’s fault they are homeless. I hope all the adults read the report so they can find out how the children feel and what will help make it easier for them to keep going with their education.

Have a look at Enquire’s guide for more info about people who can help you in and out of school.

Posted in changing or leaving school, friends, my say, Uncategorized, young people's views | Leave a comment