Being an Advocate for Your Child
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When most people hear the word “advocacy,” they think of the efforts, even struggles, of individuals who take action to influence government programs and policies. Although many parents engage in this level of advocacy, organizing to pressure policymakers and officials, advocacy can also take place on a more personal level. It means making the case that something is important and needs to be done. When families advocate for their children, that’s what they’re doing—presenting information and making requests in a focused way to ensure that something important gets done.
Why Advocacy?
In a perfect world, the specialized services that your child is entitled to receive will always be available and easy to obtain. In the real world, however, the full range of necessary services may not be available unless you request them, point out their importance, and actively work to get them unless you “advocate” for them.
Some state departments of education and local school districts may not have the money and staff to do everything you want to have done for your child, disabled or not. In particular, there is a serious shortage of specially trained certified teachers of students with visual impairments. It’s estimated that at least twice as many teachers are needed to meet today’s service demand. This shortage means many communities don’t have a teacher trained to provide the special services a blind or low vision child needs. Because there are relatively few visually impaired children in the school population, your child may be the first to need special services in your school district. That situation is particularly true in rural areas.
Working to Make Things Happen
Under the Individuals with Disabilities Education Act (IDEA), the school system is required to do what it takes to provide a certified teacher of students with visual impairments to work with your child if the goals of your child’s Individual Education Program (IEP) fall under the responsibility of this professional. The same is true for providing a certified orientation and mobility specialist. The reality is that parents need to know the types of specialized services their child may need so that they know what to request. That’s the first step in advocacy, and you may find that you have to become your child’s strongest, most persistent advocate. You may also find that the role comes naturally to you.
Being an effective advocate doesn’t require specialized skills or extraordinary capabilities. The most important ingredients are:
- Understanding your child’s needs
- Knowing the law that governs your child’s access to special education services
- Listening to others and ensuring others listen to you
- Following through so that progress is made in a timely manner
Dealing with the School System
A positive relationship with key staff members of your child’s school district is helpful and important. Aim to form a solid, cooperative team with your child’s teachers, therapists, other professionals, and district staff. Active involvement in your child’s educational team can earn respect from school personnel and offer valuable information and connections. Here are ways you can demonstrate your commitment:
- Attend all Individualized Family Service Plan (IFSP) or IEP meetings. Contact the team in advance if you need to reschedule.
- Maintain consistent communication with team members between team meetings.
- Call or email team members to keep informed about your child’s educational progress and to provide information to staff.
- Find out how you can support your child’s efforts by reinforcing IFSP and IEP goals at home.
Successful Advocacy
Here are steps to help others understand your perspective and address your child’s unique needs:
- Present clear reasons for your requests
- Provide accurate, helpful information
- Acknowledge others’ viewpoints
- Apply persistent but polite pressure
This four-point strategy lays the foundation for strong advocacy for your child. Yet, discussing with other parents and advocates adds crucial support and ideas. Engaging with parents’ groups and national bodies focused on visually impaired children and adults is also a significant resource.