Rosemary Richings is a writer, author, and advocate who was diagnosed in the mid-90s, when she was 4 years old. Her writing and advocacy work helps dyspraxics and other disabled people feel more represented, loved, and supported in our society. Rosemary is a co-founder of Dyspraxic Alliance and is on the board of trustees of Dyspraxic Me, a charity that provides a supportive peer group for dyspraxics ages 16-25.

1. Dyspraxia in childhood
2. Adolescence and dyspraxia
3. Secondary school and preparing for university
4. 1st and 2nd Year university challenges
5. The effect of stigma on self-esteem and body image
6. Coping and persevering
7. Aging out of my dad's health insurance (and the school system)
8. How having a disability motivated my decision to pursue self-employment
9. Developing healthy relationships with others
10. Why do people rarely know what dyspraxia is?
11. The mental health impact of having no support
12. When do people need to know about your dyspraxia?
13. Why do some dyspraxics avoid driving a car?
14. Travelling abroad with dyspraxia: can it be done?
15. Creating your own dyspraxia community: pros and cons