20/08/2026
This Is Why We Must Keep Campaigning for Government Intervention
For a long time, I used to think Nigeria was the only place where parents of children with special needs were left to carry an almost impossible burden alone. But the more stories I hear from parents around the world, the more I realize that this is not just a Nigerian problem. It is a global crisis that demands a global conversation and collective action.
I came across a post from a mother whose child has cerebral palsy. She shared that she was asked to pay ₦100,000 every week for therapy sessions. Her question was simple but heartbreaking:
“Where am I supposed to get that kind of money from?”
Eventually, she said she had no option but to hold on to her faith and pray that she would not die before her daughter.
Read that again.
A mother is not asking for luxury. She is asking for her child to have access to therapy.
How did we get to a point where receiving basic rehabilitation and developmental support has become a financial burden that can push a family into hopelessness?
The healthcare sector has suffered years of neglect, and children with disabilities are among those who pay the highest price for it. Physiotherapy, occupational therapy, speech and language therapy, behavioural intervention, assistive devices, medications, special education and other forms of rehabilitation can be expensive, yet many of these interventions are not optional for children who need them to develop, communicate, move, learn and participate in society.
And we must think beyond today.
What happens to these children when their parents can no longer afford therapy?
What happens when a family has to choose between feeding the household and paying for rehabilitation?
What happens when a parent dies or becomes physically and financially exhausted from carrying the responsibility alone?
Some children may eventually be abandoned. Some may be hidden away. Some may end up on the streets. Others may grow up without ever receiving the intervention that could have significantly improved their quality of life.
This is not where we should be.
Governments must recognize disability and rehabilitation as a serious public health and social responsibility.
We need policies that provide substantial government-funded support for children with disabilities and their families. We need hospitals and rehabilitation centres that are properly equipped and accessible. We need trained professionals, affordable or subsidized therapy, early intervention programmes, assistive devices, inclusive education and stronger social protection for families.
And this should not be limited to Nigeria.
If parents in different parts of the world are facing the same struggle, then our advocacy must become bigger than borders.
We must continue to speak.
We must continue to tell these stories.
We must continue to demand that policymakers listen.
Because parents should not have to choose between feeding their children and helping them walk, communicate, learn or become independent.
A child's disability should never become a sentence to a life without opportunity simply because their parents cannot afford the cost of therapy.
Children with disabilities deserve access to care. Parents deserve support. Families deserve dignity. And governments have a responsibility to act.
This is why we cannot stop campaigning.
This is why we must keep speaking.
This is why the advocacy must continue , locally, nationally and globally.