485. Gut wrenching.

I have low self esteem. I often see the very very worst in myself. I didn’t know that as part of my discharge/care plan that OH had agreed that I would have no unsupervised contact with little man.

OH didn’t actually tell me, but I’ve had several follow up calls from various professionals who kindly dropped this little bombshell on me. I don’t think OH was ever going to tell me.

When you feel like the crappest mum in the entire world, and then you’re told; ‘we don’t want you to be alone with your son” , it’s quite frankly devastating, heartbreaking and a real kick in the gut.

I would never ever ever put my little man in harms way. I’ll jump through whatever hoops I need to, to get my life back on track, but sorry social services, this is just cruel!!

Where was all this “help’ and ‘support’ this past 12 months when I’ve been literally crying out for it?

Loopy x

458. When family come to visit.

My family came to visit us today. Mum, Dad, my sister and her 3 children. It was nice seeing them but………

Here’s an insight into why I’m ^damaged^

I bring out shortbread to go with their cups off tea. Mum looks at the packet, turns to me and says; “aw, sure they’re not Scottish*. 1st disapproval off the day.

Later the kiddos had lunch and chocolate cake. The floor a mess, I take out our broom. Mum takes it, sweeps one stroke; “you think you’d buy a decent brush’ 2nd disapproval of the day.

A little while later I give my sister the grand tour. As she’s coming down the stairs she remarks “oh I love your Garland. Mum quickly pipes up; ^sure there’s not even any lights on it!”

There we have it folks, the trifecta. I could go on with the negative gripes that spewed today, but I can’t be arsed. Sometimes I’m accused of black and white thinking, but honestly folks if she had muttered even just the slightest off positive remarks, I’d shout it from the friggin tree tops! Not my Mum, not now, not ever.

It was still nice seeing them all though. I can manage a day, just about

Loopy x

450. Neglect

I’m an awful, awful AWFUL parent. I’m not sleeping, I’m tired and I’m short tempered. Today has been hell! It started with pure child neglect on my part. Little man was coughing so couldn’t go to preschool.

He got up at his usual 7am. OH was working, and I was in bed. Little man took himself downstairs. I could hear him, as all the doors were open, but I could not muster any energy to join him. I’m not sleeping. I’ve been zopiclone free now for almost two weeks. we briefly tried temazepam, but then we switched to prazosin. It’s prescribed off label for PTSD type presentations, to supposedly aid with sleep. It does fuck all.

Anyway about half 8 I dragged myself downstairs and little man, who is only 3 (nearly 4) had made his own breakfast, poured a bowel of cornflakes, added some milk, and successfully chopped up strawberries and blueberries with a sharp knife from our kitchen drawer. To be fair the mess was minimal, the chopped up fruit were fine, and there were no severed fingers or anything.

I felt sad though, worthless, unprotective, uncaring, and neglectful. My 3 year old is more capable and self sufficient than me at the moment. He deserves better. He needs someone other than me in his life. I’m going to damage him. I’ve already damaged him.

You’d think that such a stark realisation this morning, would spur me on to do better, for the rest off the day. You’d think I’d play with him, give him love and care, but no. Today I couldn’t stand to be around him. Today every laugh, or shout or cry for attention grated on me terribly. Today I fobbed him off with good old parent iPad.

I just want him to go to bed now. I want him to shut up. I want the noise to stop!!!

I can’t face another day tomorrow.

Loopy x

445. Mortality

I’m going to die young.

Regular self burning , will one day give me skin cancer. The repeated damage and neglectful care, don’t help. With skin cancer though, I guess you have a fighting chance.

Then there’s my drug use, prescribed (although I’m forgetful with it) and the non prescribed. Taking higher doses of zopiclone nightly and now using my built up stash of Valium to manage stress {work mostly] and sometimes to help stay calm with little man

The problem with all these drugs, is they are processed by our livers and our kidneys. The liver may at least fight back a little being our only organ that can regenerate itself. Let’s face it though I’m on a path to cirrhosis and renal failure. The other problem with all these meds, is their longer term effects on the nervous system. Gradual decline in nerve function, memory loss and neurodegeneratiin await.

Did I mention the Orlistat? (now that’s my pancreas gone}, and the purging. It’s sooo harsh on my guts, my oesophagus and throat. Oesophageal and colon damage, and disordered eating won’t help my nutrition state. I just crave carbs!!

To sum up, I’m always tired and am full off aches and pains, and the colour off my pee is concerning. I’m muddling along with all those things but they will kill me……..

I’m comfortable with dying young. That’s the saddest thing off all.

Loopy x

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444. Should I cry, or ….

laugh hysterically.? I’m lost for words.

Today I had a follow up call with the lovely lady from social services. She informed me that my CMHT are planning to discharge me from their care. It’s frigging laughable. I’m not much further on, they’ve done nothing to help me and now I’m just being dumped!! The CMHT haven’t told me this yet, but I guess it’s coming.

This little nugget of information was concerning enough to the lady from SS, that she is recommending a transfer to SS care. She is recommending that we have more input and family support. I guess she fears for little man. I do too.

As for the CMHT, fine, absolutely fine, FUCK OFF!!! I’m done with you anyway!!

Loopy x.

442. A lot to take in.

I’m almost too tired to blog. Today has been a rollercoaster.

Little man started preschool, we had a meeting with our health visitor and then to top it off we had a social services assessment with my new care co-ordinatior from the CMHT team in tow. Oh yes another new fecking care co-ordinator! I’d only met my latest one for the first time yesterday to then be immediately told, ‘oh you’ll have someone different from tomorrow.’ I nearly walked out the door right then..

I’ll never have them back, and I need to let them go, but oh my god, I miss L and C. The ladies who co-ordinated my care before we moved home to fix our lives. FFS Loopy, move on, it’s been more than a year!!

The lady from SS was lovely to be fair but jeepers it was quite in depth. She arrived and 3.30 and wasn’t gone til near 6.

Now we have the age old question to think about, by Monday. ‘What would help you?’

I’m exhausted, physically and emotionally.

Loopy x