Disability Roadmap CIC

Disability Roadmap CIC Positive advice and support to look at life with long term illness or disability

Disability Roadmap CIC

Community Interest Company 14027143

Unpaid Volunteer Director
Alison S enabled by Ehlers Danlos Syndrome and Aspergers Syndrome (powered wheelchair user). www.disabilityroadmap.co.uk - positive advice and support to look at life with long term illness or disability. Bookable services available by email: business_manager@disabilityroadmap.co.uk

x Bespoke disability user feedback and testing - for web developers
x Online advice and signposting to enhance your quality of life
x Public education speaker - lived experience of disability
x Online small business promotion

13/01/2026
09/10/2025

Our very own Alison K Schofield is donating her time into creating some gorgeous personalised diamond art pictures for our cashforkids fundraising! All she needs is a good digital photo and she can get cracking, however because these pieces take a lot of materials, time and energy, Alison is charging £18 pounds per picture with the hope that you’ll add more money on top, which will be the money that gets directly donated to the Cashforkids fund!! So say you decided to pay £30, £12 pounds would go to the cashforkids campaign!!

🏀

05/10/2025
15/09/2025
📚 Snuggle up with "The Little Lost Robin" – now with an extra 10% off! Use code CUSTOMERTHANKU before 27 Aug 2025. Perfe...
13/09/2025

📚 Snuggle up with "The Little Lost Robin" – now with an extra 10% off! Use code CUSTOMERTHANKU before 27 Aug 2025. Perfect for storytime and learning! 🌟🐦

https://ebay.us/m/69gqCS

Address

Halifax
HX1

Opening Hours

Monday 11:30am - 4:45pm
Tuesday 11:30am - 4:45pm
Wednesday 11:30am - 4:45pm
Thursday 11:30am - 4:45pm
Friday 11:30am - 4:45pm
Saturday 11:30am - 4:45pm
Sunday 11:30am - 4:45pm

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Why Disability Roadmap matters...

Hi my name is Alison S I set up Disability Roadmap to help all of us to have a better quality of life.

As an individual from Halifax, West Yorkshire, UK who became disabled in 2012, after suffering with a rare genetic syndrome since birth and undiagnosed high functioning autism. I found that society places many barriers and obstacles to accessing life and public services that everyone else takes for granted. After 11 years of feeling lost with increasing pain and fatigue – an unknown rare syndrome Ehlers-Danlos was taking over my life with very little NHS treatment or support available.

Finding out how to access advice, funding and support is complicated and wasted many hours of my time and added to my anger and frustrations of becoming newly disabled.