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45 Years On: Are Children with Disabilities Still Fighting for Education?

 

In 1980, my daughter Kaye was born and diagnosed with Moate Downs Syndrome. That same year, the 1980 Education Act was passed, promising equal opportunities for all children. Yet, despite this legislation, I faced an uphill battle to secure Kayes right to an education that met her needs. I fought tirelessly through endless meetings, appeals, and moments of frustration just to ensure she had access to the support she deserved.

Now, 45 years later, I am saddened to hear from parents who are still experiencing the same struggles. Parents tell me how exhausting it is to fight for adequate educational provision, how difficult it is to navigate the system, and how frustrating it is to see their childrens potential being overlooked. Why, after so many years of progress in disability rights, are these battles still ongoing?

Education should not be a privilege that only a few manage to fight for it is a right for every child. We need real, meaningful change. Schools must be truly inclusive, funding for support services must be accessible, and parents should not have to become full-time advocates just to secure basic rights for their children.

I would love to hear from other parents, carers, and educators. How has your experience been in securing the right education for your child? What challenges have you faced, and what changes would you like to see? Lets keep this conversation going because every child deserves to thrive.