10-10-2014 09:41 PM
10-10-2014 09:41 PM
10-10-2014 10:58 PM
10-10-2014 10:58 PM
Hi Tatsinda,
Welcome to the forums, I usually hang out on the LE one but occassionally "pop over" here too as I am also a carer.
Your question is a very good one. I struggle with this myself, both personally and with my former partner who lives with us. Minimising the impact of my MI on my children is something that has always concerned me deeply.
I have been living with episodic acute depression for 35 years. I have a 17yo, a 13yo and a 6yo.
One of the things I have learned to do when I myself am very unwell and struggling with irritability, etc is tell the kids. I say to them (wording is age dependent here) "mummy's really upset/stressed out at the moment and I need lots of quiet time/time out", and this one's really important "I love you, this is not your fault and I don't want to get cross or yell at you, can you please help by giving me some space?"
With my former partner he is rarely able to do this himself, so I tell them. I think another important word is "sorry", because inevitably we will get it wrong sometimes - and being specific about why, eg "I shouldn't have yelled at you when you spilled that milk I see it was an accident".
Even my 6yo can get this, and she also has some of her own issues as a result of early childhood trauma. My older two are ok with this. They are both very well, are quite emotionally resilient and have weathered some very difficult times themselves through school, etc. They both have some knowledge about MI which I start sharing a bit of general info about in the first year of high school, depending on them and what I think they can handle.
They don't know exactly why I suffer from MI, because I don't want to traumatise them. I have told them I will answer any questions when they are older (>15), at this point my eldest doesn't want to know and that's ok.
This approach seems to have worked for us, at least with my older two. It's too early to be sure with my yougest - although recently she came and asked me if she could play a game on a DVD which she knows I often find irritating because of the noise. She offered to turn the sound way down. I gave her a hug and told her she was wonderfully thoughful and considerate - she seemed very pleased with herself.
I try to encourage my kids to see differences in people of all kinds (including with MI) as worth embracing and celebrating for the good in them whilst trying to understand those things we are less comfortable with.
I hope this is of some help.
Kind regards,
Kristin
07-11-2014 11:10 AM
07-11-2014 11:10 AM
Hi @Tatsinda
Really good question. @Melstar71 sounds like she's in a similar situation. In her post here she's looking for childrens books that cover the topic of parents with mental illness.
@Melstar71 , can you relate to Tatsinda's post?
@kristin - great insight, as usual 🙂 Always so appreciative of your generosity in sharing your experiences
Does anyone else have tips?
08-11-2014 08:10 AM - edited 08-11-2014 08:12 AM
08-11-2014 08:10 AM - edited 08-11-2014 08:12 AM
Hi @Tatsinda , @Melstar71 & @Uggbootdiva
Amazing timing of your question @NikNik - a piece of pure serendipity! You see I was given some short booklets by my Anglicare family support worker on this topic nearly 3 years ago when I was terrified I might end up in psych ward for the first time (& thankfully didn't!).
They have stayed (lost) in a cupboard since then. Just last Thursday another friend with MI came over to help me tackle some of the mess that clutters my house and head. Guess what I found? (And if you'd asked me this question before Thursday you would have drawn a blank - because I had forgotten all about them!)
So here they are - from Children of Parents with a Mental Illness (COPMI)
http://www.copmi.net.au/order-online the Family Talk & Piecing the Puzzle Together are the two which I have hard-copies of & seem most pertinent, but they have a lot of online stuff as well so I'd encourage you to check that out too.
I hope this helps!
Kind regards,
Kristin
08-11-2014 07:32 PM
08-11-2014 07:32 PM
08-11-2014 07:43 PM
08-11-2014 07:43 PM
08-11-2014 09:17 PM
08-11-2014 09:17 PM
Yes I can. Sometimes I feel like a single mum. He has an anxiety of crowds and our local area so it comes down to me to take the kids out etc. Sometimes I am just exhausted and would love "me" time once in a while. When he is in his "moods" he dosn't take much interest in his kids. He has just started seeing a social worker who I hope will put in place the right support for him to work through his fears / anxieties so he will be able to do activities with his kids in the local community and take some of the pressure off me. Our kids don't understand why daddy dosn't come out sometimes. He dosn't work, he is on the disability support pension. He see's his regular Drs as well.
Mel
08-11-2014 09:19 PM
08-11-2014 09:19 PM
Thank you so much! You guys are awesome!
Mel
08-11-2014 10:32 PM
08-11-2014 10:32 PM
08-11-2014 11:58 PM
08-11-2014 11:58 PM
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