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How I followed my dreams and started my own business

Image of Jack, a young man holding an award. There are two other photos of Jack's metal art - a bird feeder made with an exhaust pipe, and a house number '5' inside a horse shoe.

I’m Jack, I’m 28 from Clydebank. I work as a metal artist/sculptor who creates art from car parts, horseshoes and mild steel and I’m the business owner of Salvaged Metal Art.

When I was about eight years old I helped my uncle weld hinges onto an old gate post. Not thinking this would make an impact on my future I just concentrated working on and learning about cars for the next number of years, as this is what I wanted to do as a career. My experience at both primary and secondary school was not a positive experience as I was bullied throughout my time there due to my cerebral palsy. My cerebral palsy affects me on a daily basis as it restricts me on some things I would like to do by myself. I often suffer sore backs and stiffness due to my cerebral palsy.

My experience at college wasn’t positive either as I was bullied in college as well when I got into the mechanics course. During the year long course I was bullied on a daily basis. A month or so before the course was due to end two of the lecturers spoke to me to tell me that I couldn’t get onto the next level of the mechanics course. This is when I told them I could try welding. They told me this would be too hard for me as well, but they didn’t know that my uncle who has been a welder for 40+ years was willing to take his time to teach me no matter how long it would take.

That year my mum and dad bought me a small mig welder to learn with and this is where I started to get a passion for welding. My first welding project was a  welding cart which I still have to this day, after a number of times practicing my welding I said to my uncle “how about combining car parts and welding to create unique pieces of art” and this is where my Prince’s Trust journey began.

In 2017 I read about a group called Street League who help people find jobs, so I joined and this is how I contacted the Prince’s Trust with my idea about setting up my business. I was given support and met new people which gave my confidence a massive boost which encouraged me to start my own business.

Jigs for making horseshoe candleholders
Jigs for making horseshoe candleholders

I continued with the Prince’s Trust which led me to me becoming a young ambassador in 2018 – that was the same year that I got involved with Improving Lives. When I attended the improving lives open day in 2018 I met the Clydesider. I have done a few pieces for their magazine in the past three years and this has also helped me with my confidence.

In 2019 I was awarded the Prince’s Trust Scotland’s Young Achiever of the Year for the work and progress that I had made. This was the highlight of my year as I got to meet my inspiration artist/blacksmith Kev Paxton who informed me that I had won the award.

A vice clamp and jig that Jack made to help him with a number of things.
A vice clamp and jig that Jack made to help him with a number of things.

During lockdown I continued to grow my business by gaining local customers and selling garden pieces such as firepits. I also got involved with Epilepsy Scotland, donating pieces for their online Christmas craft fair. Since then I’ve continued to support them by doing a sponsored 60k walk, over six weeks and a 5k during Christmas. I’ve done this since 2020 and it’s made me feel a lot better both physically and mentally.

Fast forward to 2022, I won the Prince’s Trust Young Achiever of the Year award at the Pride of Scotland Awards held in Edinburgh. I also done two collaborations with Kev Paxton, who continues to mentor me to this day. Both collaborations got auctioned off for the Prince’s Trust at their biggest fundraising event called ‘Lunch with an Old Bag’.

Two adaptations made by Jack for creating his work, called 'third hands'
Two adaptations made by Jack for creating his work, called ‘third hands’

In 2023 I expanded my range of pieces which led to me supplying a company in South Queensferry called Craigies Farm Shop and Deli my horseshoe candleholders for their gift shop. I continue to supply these and they have now extended their range of my pieces.

This year I’m aiming to grow my business even more by getting my work into Arnold Clark dealerships (who are one of my suppliers). I also want to continue with my charity work and continue to break down barriers by creating new pieces of art to show people that cerebral palsy isn’t a disability, it’s just a different ability.

I am still involved with the Prince’s Trust and would not be in the position that I am in if I hadn’t got involved with them.

My personal reason for supporting Cerebral Palsy Awareness Month is to make people aware that just because you have cerebral palsy this should not stand in your way of following your dreams and to never give up through tough times. I feel more needs to be done to tackle the bullying that people suffer on a daily basis for having a disability, it affects all aspects of your life.

I feel more needs to be taught about disabilities and more disabled role models should be speaking out.

This is what has led me to want to be a motivational speaker to encourage people to follow their dreams and knock down the barriers that I have faced.

You can follow Jack on Facebook via Salvaged Metal Art and through his motivational speaker page where he shares lots of content regarding cerebral palsy, epilepsy, motivational quotes and work/life balance.

My views on disabled access – Faith Wright

As part of Cerebral Palsy Awareness Month, we have teamed up with Euan’s Guide to ask our content creators their views on disabled access. 

Euan’s Guide is the disabled access review website where disabled people, their families, friends and carers can find and share the accessibility of venues around the UK and beyond. The website shares thousands of experiences and is the go-to tool for many disabled people. Euan’s Guide believe in making the world more accessible one review at a time. Thousands of people use Euan’s Guide every month to find and share disabled access information. Euan’s Guide recently published their Disabled Access Review where 6,000 people gave their views on disabled access. The review found that 91% of disabled people try to find disabled access information before visiting a new place.

My views on disabled access – Faith Wright. 

What do you do beforehand to prepare for an accessible day out with your friends and family?

We try to do as much research about the venue or place as we can beforehand. Usually look for information on the websites etc if there is any sometimes we have to phone or email. Then determine if my manual or electric chair is best. Make sure I have straws!!

What information do you look for from a venue before visiting?

If they have wheelchair access or if there is stairs etc so I know if I can get in and if so which chair is most suitable. What the accessible toilets are like.

How do you feel if you know that someone with similar access requirements has visited the venue before?

Definitely puts me at ease a little and means I’m more comfortable/likely to go if I know what to expect or if I’ve heard positive feedback

How does this help you to feel more confident or prepared to go out with your friends and family?

Because I then know what to expect and have a better understanding of what obstacles I might face and how to avoid or prepare for them.

What is the most important piece of information for you when you visit a venue for the first time with your friends or family? The most important thing is if the venue actually accessible to me.

What do you think venues could do to improve your experience as someone with Cerebral Palsy? Educate themselves on what accessibly actually means and how everyone may need something different. If a problem is reported with the accessibility then they should take the time to learn, research and do better!

What is the number one thing that you would like people and venues to be aware of about cerebral palsy to help them improve their disabled access and disability awareness? We want to be treated like everyone else we are just customers like everyone else. Having access issues can really make us feel like we don’t matter and are invisible and that really affects us when we are trying to have a nice day. So please try to be patient and kind and accommodating where possible.

You can find out more about Euan’s Guide, read some access reviews or even write your own review on their website here – Euan’s Guide – Disabled Access Reviews (euansguide.com)

Read more results of the Euan’s Guide Access Survey –https://www.euansguide.com/get-involved/access-survey/

Tags: Advice Information and Support, Cerebral Palsy, Disabled People

My views on disabled access – Christina MacLean

As part of Cerebral Palsy Awareness Month, we have teamed up with Euan’s Guide to ask our content creators their views on disabled access. 

Euan’s Guide is the disabled access review website where disabled people, their families, friends and carers can find and share the accessibility of venues around the UK and beyond. The website shares thousands of experiences and is the go-to tool for many disabled people. Euan’s Guide believe in making the world more accessible one review at a time. Thousands of people use Euan’s Guide every month to find and share disabled access information. Euan’s Guide recently published their Disabled Access Review where 6,000 people gave their views on disabled access. The review found that 91% of disabled people try to find disabled access information before visiting a new place.

My views on disabled access – Christina MacLean. 

What do you do beforehand to prepare for an accessible day out with your friends and family?

Travelling can be quite overwhelming and I tend to stress myself out as I struggle with the hustle and bustle. When I moved for college and university, my mum and sister would do a “test journey” with me. This would include them travelling from my flat to university for example so I could get used to the route. This made it a little easier when I had to travel on my own.

What information do you look for from a venue before visiting?

I am a young woman with mixed cerebral palsy and talipes (club foot). I also suffer from chronic migraines and trigeminal neuralgia. I do not require any walking aids but can sometimes be clumsy especially when I am tired. When going to a concert or theatre for example, I will check the layout of the venue online before booking tickets. I can sometimes find stairs difficult especially if they are steep as they may be a tripping hazard. I sometimes also check where the toilets are. I struggled at university when I did not get shown around as I did not know where the toilets were.

How do you feel if you know that someone with similar access requirements has visited the venue before?

Unfortunately, I have not been to a venue that I’ve known another person with cerebral palsy has been to. However, this would make me feel comfortable if I did.

How does this help you to feel more confident or prepared to go out with your friends and family?

I would say I am always apprehensive when going to a venue. It all depends how I feel on the day, what time I have to be there and if I need to travel. My family and friends are patient and understand that I might be feeling stressed. When I am with my friends we may get an uber together to make travelling less of a worry. My family and friends sometimes discuss a plan of what we need to do on the day, for example, get the bus, grab a coffee, go around the shops, have lunch and go to the venue. I find a routine to be extremely helpful and if it is planned out in advance I find going to a venue a bit easier.

What is the most important piece of information for you when you visit a venue for the first time with your friends or family?

I know this sounds a bit silly – but if the floor is level. Some flooring I find difficult to walk on. How steep the stairs are and where the toilets are.

What do you think venues could do to improve your experience as someone with Cerebral Palsy?

When I was at university it would have been helpful to receive a tour of the buildings I needed to attend. This would make me feel comfortable and less worried when starting.

What is the number one thing that you would like people and venues to be aware of about cerebral palsy to help them improve their disabled access and disability awareness?

That not all disabilities are visible and that we may all require different accessibility.

You can find out more about Euan’s Guide, read some access reviews or even write your own review on their website here – Euan’s Guide – Disabled Access Reviews (euansguide.com)

Read more results of the Euan’s Guide Access Survey –https://www.euansguide.com/get-involved/access-survey/

Barry’s holiday to Sandpipers Southport

As part of Cerebral Palsy Awareness Month, Barry shares his experience on a recent respite holiday to Sandpipers in Southport. Barry is currently writing his own e-book that will be published online to raise money for Cerebral Palsy Scotland.  

Who I am.

My name is Barry Smith, and I am 45 years old, with Cerebral Palsy which is a physical disability, down to me suffering from I am in a Power wheelchair, and I use an SL50 Lightwriter. I live by myself, but I get support for the things I couldn’t do for myself.

Going on a respite holiday

On the 12th of February of this year, I got a cab to Irvine railway where I booked the ramps to let me get on to the Glasgow Train by myself, I had my bag on the back of my wheelchair with everything I needed for the week in it. When I was doing this I remember I felt so happy. As soon I got off the train in Glasgow, I went for the London train before I did this I asked if could I go to first class because the staff on the train came round to ask do you want food and drink, When the person came to ask would I like anything I typed on my lighterwriter by using my big toe, this is because I hurt my fingernail one day before this and has a bandage over it, down to me doing this it is hard to type on my communication aide what I want to say to them.

When the train man came I asked if could I have a coffee and can he could put my straw into it for me. When I was on the train for about two hours, my stop was Wigan North Western then I had a sort five five-minute walk over to Avanti West to get my last train on to Southport, by this point I was feeling so happy. As soon as I got over to the next train I was told by the train man the train wasn’t on to Southport because of this we were going to put a bus service on to Southport. About an hour later, I got to Southport. As soon as I got off the bus in Southport, I made my way to Sandpipers by walking because I had been in Southport for four years, I noticed some of the shops and the pubs have closed down.

Picking the right room is a big part of having a great holiday. Here is a guide to the rooms at Sandpipers, including their many features and facilities, to help you make the ideal choice. Revitalise Sandpipers offers full board accommodation on the shores of Southport Marine Lake. Take in lovely water views, go for a dip in the hydrotherapy pool or simply enjoy the newly refurbished R Club Lounge and restaurant.

At the end of the day, retreat to your fully accessible room. All en-suites have wheel-in showers and there are also two separate bathrooms for assisted bathing with hoists and bariatric equipment, and Arjo baths.

Amenities and Accommodation

  • Heated indoor hydrotherapy pool
  • Licensed bar and entertainment area
  • Hair and therapy salon*
  • Internet access and WiFi
  • Sun terrace with balcony overlooking the Marine Lake
  • Gardens
  • Souvenir shop
  • Full board only
  • 30 single rooms
  • 4 twin rooms
  • All rooms at ground level
  • En suite accessible shower room
  • Call system
  • Television
  • Pressure relief mattresses
  • Airflow mattresses
  • Profiling beds
  • Overhead and manual hoists

You can find more information on respite holidays at Sandpipers here – Sandpipers | Revitalise

Tags: Accessible Holidays, Advice Information and Support, Cerebral Palsy, Disabled People, Physical Disabilities, Sport and Leisure, Support for Adults, Wellbeing Services

Christina’s academic journey as a person with Mixed Cerebral Palsy

As part of Cerebral Palsy Awareness Month, Christina shares her experience of education as a person with mixed cerebral palsy. 

As part of Cerebral Palsy Awareness month, I would like to share my experiences of education and the challenges I have had to face. I was diagnosed with Mixed Cerebral Palsy when I was 2, now 26. Throughout nursery and primary school, I received educational support to help with subjects like maths and English. However, this stopped before I got into high school.

Transitioning from primary into high school is difficult for both neurotypical and neurodiverse students – new friends, teachers and subjects can be overwhelming for us all but for me it felt like a nightmare. I found it difficult going between classes, corridors full of students pushing and shoving to get to class on time. I do not use any walking aids, I am VERY clumsy on my feet which means I am prone to falls. Amongst all of that, I struggled with the change of teachers due to the various teaching styles. I had maths teachers who would get frustrated and angry if I did not understand an equation and would sometimes shout. This always made me feel uncomfortable and embarrassed as some students thought I was “DUMB” and my teachers thought I did not study. I had to constantly explain “I have Cerebral Palsy” and “please be patient with me”.

This was sometimes ignored. One teacher told me… “I would never make it in life”. Most days I would go home in tears… school became such a negative place. Those comments have always stuck with me and made me doubt myself. I became extremely anxious about going to school which ended up effecting my mental and physical health. This had an effect on my exam results to which I failed most of my exams.

However, not all teachers were bad in fourth year, I had an amazing English teacher who would always make sure I understood my work and took time to go over anything if I needed it. He made the time to listen to what I had to say and was very patient – I will be forever grateful for his support. The music department was the place I felt most comfortable and where I would spend most lunchtimes. I was a member of the school choir, took part in various competitions and always enjoyed singing for our local community.

Once I finished school I went to college and then university to study music. I have a BA(Hons) in Popular Music and will hopefully receive my dissertation marks for an MScR in Music. I am looking at PhD applications and hoping to apply soon! Though education continues to be a challenge, I would like educators to receive training about the different types of Cerebral Palsy and how it may affect individuals learning abilities.

If you are a parent or carer supporting a child in education, there’s is a range of organisations you can go to for support and advice.

  • Contact in Scotland – Talking About Tomorrow: Contact in Scotland 
  • Enquire – The Scottish advice service for additional support for learning

If you are thinking about raising awareness of cerebral palsy in your school, we have a short powerpoint presentation aimed at primary school children explaining cerebral palsy and how it affects each person differently, you can find this here.

Tags: Advice Information and Support, Disabled People, Education, Physical Disabilities, Support for Adults, Support for Young Adults, Wellbeing Services

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