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I was feeling triggered after reading some reports about my eldest child. I will admit, this podcast might present as an incoherent rant, but essentially, I want to communicate how much my son has been let down…and how so many families have been let down. Our system is baffling and in great need of change. How can it be justified that a child who needs such high levels of support has been denied educational, health and social interventions? How many children and families are experiencing the same issues? You need a diagnosis to be considered for specialist provision (and it might not even be adequate), but diagnosis is inaccessible to so many people. Please don’t be afraid to reach out if you are going through the same challenges. It’s emotionally draining and so exhausting. (Apparently I referred to being in 2020 when it is clearly still 2021…just. I meant that when the professional looked at me blankly when I mentioned PDA…it was 2020. Also, the EHCP assessment was applied for in 2020…so it is shocking that in that time, no real efforts have been made to adequately assess and get to know my child.)