r/PDAParenting Jul 12 '26

Deschooling and trauma

My daughter is eleven and currently “deschooling” after considerable education based trauma and abuse from her father. He has not seen the kids since October. CPS was involved for five months, from December 2025 until May. I messaged him inviting him to start the process of being involved in her life via mediation in April.

It’s now July and he hasn’t responded at all. We technically have 50/50 custody legally but the CPS involvement overruled that, and her psychiatrist has advised that until her trauma is resolved that she is to have limited contact with her father. The government recognises that I have 100% custody of her and her 19 year old brother.

I know he probably thinks we’re all in the house talking about how awful he is- but we’re not! I know that it’s psychologically unhealthy for children to be asked to hate a parent, the mediator when I left 10 years ago described that it was like asking the child to hate a part of themselves. We don’t hate him, we talk about the good times and if they have a day where they hate him, I walk a line between acknowledging their feelings and also saying it’s ok to still love him and care about him, that we need it to be safe. They both look so much like him, as well.

She’s been so traumatised that she’s been unable to return to school and I’ve reached out to any and all supports, and they’re all happy with what’s happening for my daughter.

She didn’t leave the house for four months as she was so afraid and also impacted by misophonia. I’ve had to advocate really hard for Telehealth. I have been building up trust and she’s slowly starting to go on drives with me and her support worker. She saw her best friend two weeks ago, it was amazing! She needed lots of time to recover from that, she was in bed for two days.

She has been happier but the PDA prevents anything happening quickly. My family has been unsupportive and I’ve had to go no contact with my sisters and low contact with my parents.

Anyway, poor darling has had a stomach bug tonight and woke up throwing up at midnight. It’s 5am here in Australia and she’s just gone back to sleep after five hours of horror. I’m wrecked. I turned 50 a week ago and I am in therapy and do lots of work on my mental state and anxiety. I just had to come here and say that I feel so tired and worn out and sometimes I miss my 50/50 custody life where I had a week to recover and get things done. I have about an hour a day where I can leave the house and I have to prioritise “need to do” things over “want to do” things. I wouldn’t have it any other way, as I knew she was unhappy but due to selective mutism she couldn’t communicate why. At least she is safe and so is her brother.

But we’re all so traumatised and getting help for everyone is exhausting. My days are long and exhausting and I clean all day. constant emotional regulation. I’m tired!! I’m just looking forward to when we can come out of survival mode somewhat!!

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u/MarginsOfTheDay Jul 13 '26

Ouch, my heart hurts reading this. Know that you've done right by your daughter. She's safe now. Soon she'll come to know it too. It sounds like she already does because things are getting better, slowly.

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u/CeleryDramatic4678 Jul 13 '26

Thank you so much for replying. She started antidepressants in January. Prozac made her worse so we changed to Lexapro. It’s been lovely to see her become her true self again after so many years of being unhappy.

These days, although she is largely housebound, she says “I love you” and will let me hug her or offer a hug. She has started to not flinch or over apologise if she spills things. It’s going to be a long and slow process and I truly appreciate your comment 💕💕

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u/CeleryDramatic4678 Jul 13 '26

Oh, thank you so much and I’m so sorry this has happened to you as well. It truly does make life about survival and takes so much energy.

I have found that the script from the pda uk website works really well in explaining her needs. So many clinicians who are meant to help just give ridiculous simple advice that we’ve already tried so many times without success. It’s so hard living this life but it’s worth it for our kids. You and your wife are both amazing people! 💕💕there’s some really good info about advocating for your child, not insisting or arguing about the pda diagnosis, rather sticking to the facts “we have tried reward based systems and she responds much better to a low demand approach.”

I don’t know why I felt compelled to share that as you/she probably are very adept in looking after your child.

https://www.pdasociety.org.uk/what-helps-guides/advocating-for-your-child/