
If you sense there is something not quite right with your child, or there is something about your child or their development you are generally right.
Trust your gut instinct.
You know your child better than anyone else.
However, there is a big difference between having an inkling that there may be something not quite right and taking the steps to checking.
It is understandable the hesitation and fear.
Having a concern that was a potential delay or disability confirmed with a diagnosis can be very confronting, daunting and overwhelming all at once.
It can also be confusing to know where to start and what to do.
It can seem complex so we suggest the first place to access help in a diagnosis is your Doctor.
The process of identifying a child’s disability or delay can vary a lot depending on the individual child, their age, the developmental delay or disability and the process of diagnosis.
Diagnosis can happen at any age, however, it is proven that the earlier it is diagnosed the better the outcome for the child as intervention can occur.
Allow yourself the time to take it all in.
You are entitled to feel many emotions at this time, including disbelief and grief.
While it may be daunting to get a diagnosis from a qualified professional we recommend seeking help sooner rather than later.
Not only can you start to heal and accept the new reality, but sometimes the process you need to go through to find out whether your child has a delay or disability may take some time until completion and a diagnosis is provided.
There are many support agencies that offer free support to families and they take into account the whole family and the individual needs of the child with special needs.
Generally a case worker/family support worker/etc will be assigned which means that they will be able to provide the support, information and assistance to you.