You may find out that your child has a health condition or impairment at a scan during your pregnancy, or at the birth itself. Alternatively you may notice something in your child’s behaviour early on. Here is what you can expect to happen if your child has a disability.
If the sonographer (the professional doing the scan) finds anything unusual, they should refer you to a doctor within 24 hours and - if it is necessary - to a specialist within 72 hours. These doctors will be able to tell you more about the condition and possible treatments.
The paediatrician (the doctor specialising in care for children) at the hospital will be able to tell you about your child’s condition and possible treatment. If it’s a rare condition the paediatrician may refer you to a specialist. The paediatrician will be able to answer most of your questions. They will then write a report and send it to your family doctor (GP).
You should be given contact details of someone who can answer any questions that you have after your first discussion with the paediatrician. This could be a meeting with another doctor or specialist at the hospital, your family doctor or a health visitor. A follow-up meeting should also be arranged.
You should always be given:
You can also ask for a second opinion if you wish.
When your child’s condition is diagnosed you will be offered a social services assessment, which could lead to extra support at home, financial assistance and more.
There are a variety of benefits available to you when you become a parent, and more so if your child is disabled. Follow the links below to find out what you are entitled to.
For help and advice, parents of disabled children can call the Contact a Family helpline on 0808 808 3555 (Mon-Fri 10.00 am to 4.00 pm, and Mon 5.30 pm to 7.30 pm), or visit their website.