So here we are, at the end of April again. For one month, autism gets attention with all the flyers and reels on social media. In April, everybody suddenly remembers autistic people exist. But when April finishes, autistic people and their families still have to face the daily challenges of life in T&T, and like always, many simply do their best to manage with whatever support they can find.
I do not want to spend this week repeating that awareness is not enough. I said that already, and it is true. What I want to ask now is something more important: what are we actually prepared to do for autistic people after April? Not in theory or in speeches, but in real ways.
A few years ago, whenever parents and caregivers expressed disappointment on social media that not enough was being done for autistic people, the response was along the lines of, “allyuh make child and expect the government to mind dem.”
Parents and caregivers were made to feel like they were demanding too much rather than asking for access to basic rights for their children. Some people were quick to say that we have “many” policies in place, but I say again, policies that are not implemented are just a waste of time.
One of the typical answers to any demand for improvements and access to opportunities has been that the country has no money.
I understand that the economic situation is not very good right now, but I am not buying the “we have no money” excuse anymore. You know why? Because we find money to wine and jam while a child does not even have a school to attend. We place priority on everything else but our autistic children. So no, the issue is not money.
The issue is wrong priorities. It is very easy to say that we are a developing country, or a lesser developed country, and use that as an excuse for not having proper structures in place. But our development status cannot continue to be the excuse. Being a developing country does not mean we must have nothing. It means we have to use our resources better and put them where they can actually change lives.
And let us be honest, there are countries with fewer resources than T&T that are still trying to put practical systems in place. For example, Rwanda’s Special Needs and Inclusive Education Policy includes improving access to schooling, strengthening support services, and building the capacity of teachers and specialised personnel for learners with disabilities.
Even Bangladesh, with far fewer resources than T&T, has developed a National Strategic Plan for Autism and Neurodevelopmental Disorders and taken part in regional efforts to strengthen health, education and social care support, showing that the issue is not only money but whether a country chooses to plan seriously for autistic people.
One of the first places where T&T can do better is in schools. We do not have to wait on some perfect system to begin making changes. If teaching posts become vacant, then the Ministry of Education should start using some of those opportunities strategically so that, over time, every school has at least one teacher trained in special needs education. That alone would make a major difference.
Teacher training is also an area that can be done at little or no cost, given that the Student Support Services is supposed to have qualified personnel who can facilitate training. Partnerships with professionals and NGOs can help too.
We also need to make public spaces easier for autistic people to use. Sometimes it is simple things that matter most: clearer signs, quieter waiting areas and staff who know how to speak calmly and respectfully.
A mall, a clinic, a government office or even a public event can feel overwhelming for an autistic person. We have to start thinking about how people actually experience these spaces and how we can update and upgrade our spaces. UNICEF’s guidance on disability-inclusive spaces makes the same point: access is not only about ramps and buildings, but about practical design and usability for children with disabilities and their families.
Healthcare is another area that needs serious attention. Families should not have to wait long and be stressed every time they carry a child for an appointment. The system needs more flexibility and better communication. Staff should be trained to recognise sensory distress, and that should include auxiliary staff and security guards too. Basic dignity should not depend on whether a family happens to meet one kind person on a good day.
And we really need to stop talking about autism as though it is only about children. Autistic children grow up to become teenagers and adults.
We can create access to employment; the OJT system is already in existence and we can expand it to include persons with disabilities. There are specific career paths for which autistic adults can be trained, including data entry, graphic arts and other jobs that may suit people who prefer calmer or more structured work settings. We can also offer employers incentives to hire persons with disabilities.
Let us remember that autism does not disappear when April ends, and neither do the challenges. Our commitment cannot disappear either.
Autistic people do not need one month of attention. They need a country prepared to include them every day.
