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First steps to understanding your child’s vision impairment

Finding out that your child has vision impairment can feel overwhelming. These steps can help you to understand your child's vision, find the right support and feel more confident about what to do next.

A child bouncing on a trampoline while holding a bunch of balloons.

Children and young people with vision impairment have different needs and may face unique challenges compared to their fully sighted peers. Understanding your child's vision and needs is an important step to ensuring they're supported, in helping them develop and take part in the things they enjoy.

A new diagnosis can bring lots of information, appointments and meetings. Take your time and give yourself space to process everything. It's normal for it to take up to a year before things feel more settled, and you don't have to understand everything straight away.

Helpful resources at the point of diagnosis

We've brought together some first steps resources to help you get started after your child's first specialist eye health appointment. They'll help you build your understanding and find out what support is available.

Bookmark this page so you can come back to it as you need. You might want to focus on one step at a time, before moving onto the next. You may need to occasionally return to a step if something changes.

After you've completed the steps below, you can use them alongside our wider 'Information for Parents' and 'Sensory Play' guides. These guides explain how the eye works, detail medical conditions that cause common types of vision impairment, and give more in-depth advice about helping your child to grow and develop.

Information for children, young people and families.

Your first steps

These seven steps will help you understand your child's vision impairment and find the support that's right for your family.

If you need help at any point, get in touch with the RNIB Helpline.

1. Find out about your child's vision

It can take time for you and your child to understand your child's vision impairment. Your child's vision may change as they grow, and they may also become better able to describe what they can see.

With help from specialist professionals, you'll learn to understand your child's vision and decide what, if any, adjustments need to be made.

It can sometimes be difficult to find out the cause of a vision impairment, but it's important to know as much as you can about your child's eye health and associated medical conditions: Find out about your child's vision impairment.

2. Attend a Parent Pathways course

Meeting a small group of parents and carers who are at a similar stage of their journey can help you feel less alone and give you the opportunity to share your experiences in a safe, supportive space.

RNIB's online Parent Pathways course helps you build your understanding of how to support a child with vision impairment. The course includes two 90-minute sessions with a week between each session to give you time to reflect and consider what you've learned.

You'll also receive a free course booklet with information and resources to support your learning. After the course, you'll have the opportunity to ask questions in a follow-up call.

Find out more and sign up to Parent Pathways.

3. Find out about health, social and education support

Learn more about the different services that can support you and your child. These include:

  • health services, such as opticians, GPs and hospitals
  • social care services, including your local Sensory Service and wider social services
  • education services, such as a nursery, school, college or university, as well as the Sensory Service.

The Sensory Service can provide support across both social care and education. Your health services may refer you to the Sensory Service for additional support.

All three services should work together to support your family. You and your child should be able to contact them regularly to ask questions, discuss the support being offered and decide what's right for you.

Emotional wellbeing resources are also available at any point from each of these services and other organisations.

In hospital, you may meet different eye care professionals, particularly during the time when your child's eye condition is being diagnosed. Our “Who does what in eye care? A guide for parents” explains the different professionals you may meet and how they can support you and your child.

We also have an Eye Clinic Appointment Guide for Parents to help you prepare for appointments.

If you have any specific questions or want to know more about eye conditions, certification and registration, or looking after your child's eye health, you can find more information in our Eye Health section.

4. Look after your emotional wellbeing

Make sure you’re looking after yourself and your family’s emotional needs.

A diagnosis of vision impairment can bring up lots of different emotions for your child and your family.

Our Tough Talks resource can help you talk with your child and others about your child's vision impairment. You can also listen to our Emotional Wellbeing podcasts, which cover topics that parents of children with vision impairment frequently ask about.

Visit our emotional support resources.

We’ve also got a specific page for young people and their feelings about vision impairment.

Your child's hospital or education setting may have an emotional support or counselling service that can work with your family.

RNIB’s Sight Loss Counselling Service is available to children with vision impairment aged 11 and over and their families. You can refer yourself to the service.

Find out more about RNIB's Sight Loss Counselling.

5. Connect with other families

Parents and carers tell us that one of the best things they've done is meet other families in similar situations.

RNIB's Parents and Carers Facebook group is a great place for parents and carers to ask for advice and guidance, share stories and learn about other organisations and communities.

RNIB Parents and Carers of VI Children Facebook group.

If you're aged 18 or over, you can join one of our regional Facebook groups to connect with other people in your area.

Find out more about RNIB's social networks.

6. Find out about education support

All children and young people with vision impairment aged 0 to 25 should receive specialist support from a Qualified Teacher of children and young people with Vision Impairment (QTVI).

QTVIs work for the local authority or education authority's Sensory Service. They have a mandatory qualification in teaching learners with vision impairment and can work with your child, their teachers and other education staff to make sure that their education is accessible.

Find out more about getting the right support in education.

When you’re done here, you might want to look at our other education resources, including RNIB Bookshare and the Curriculum Framework for children and young people with Vision Impairment.

Education and learning tools for children with vision impairment.

7. Get sensory support from Social Services

Your local authority or education authority will assess the support your child needs at home after their diagnosis.

This service can support your your family with child development, learning new skills and accessing wider social care services.

This may include:

  • play, learning and developing life skills
  • moving around your home and local area
  • specialist equipment and adaptions at home
  • accessing benefits, concessions and grants.

This support may be provided by a Habilitation Specialist (RQHS) if your child is aged 0-17, or a Rehabilitation Specialist if your child is aged 18 or over. A specialist social worker or other social care professional may also be involved, if needed.

More resources

You can find some more detailed information in our children, young people and family resources.

More resources

You can find some more detailed information in our children, young people and family resources.

Further support

RNIB provides free, specialist advice and support for children and young people with vision impairment – from birth to age 25 – and their families.

If you can’t find what you’re looking for, or you’d like more information about anything mentioned on this page, we can help.

We offer:

  • family, early years and transitions support
  • support for education professionals
  • advice about accessible books, toys and learning materials
  • opportunities to meet and talk with other families.

Please contact our Helpline on 0303 123 9999.