Having your child diagnosed with dyslexia isn’t the end of that journey, and none of the problems will just disappear after an assessment. Rather, getting the diagnosis is only the first step. Here is a list of ten things that you need to know about your journey after your child has been diagnosed with dyslexia.
10 things that happen after your child is diagnosed with dyslexia
The next steps in your journey include getting hit with a wall of emotions first and then doing research online to understand the jargon in the diagnosis. You may join groups on social media, and you will become your child’s fiercest advocate and make sure they get the schooling and help they need even if the school doesn’t make it easy. Finally, you will have lots of fun with your child and appreciate your child for the unique and wonderful person they are.
Key takeaways
- There are 10 things that you need to know when your child is diagnosed with dyslexia including the range of emotions that you will go through.
- You need to know that you will not understand much of the report and you will spend most of your time researching dyslexia or joining Facebook groups.
- You may start to focus on the negative aspects of your child or that the school will provide lots of 1 on 1 extra help.
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Your school district must evaluate your child free of charge if you ask in writing, whatever your income and whatever the outcome (US, 34 CFR 300.111 and 300.301(b)). That route takes time and answers a different question than you do. This one starts today, from what you already know.
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A screener is a starting point, not a diagnosis. If your child might need formal accommodations (an IEP or 504 plan), or you suspect a vision, hearing or medical cause, pursue a professional evaluation too. That is the only route to those supports.
