My Mum the Shearer

It seems that I’ve inherited my mother’s ability to find, be found by and adopt any lost sheep. In some cases, her ability is literal. We adopted a large, lost sheep. We were in Central Australia, the year I turned 9. We’d been travelling for 6 months around the country and now had taken up residence in a single carriage of a converted silver bullet train (something like this). My bed was over the hot water service in the ‘laundry’; Mum and Dad had a fold out bed in the lounge room so my brother and sister could share the double bed in the single bedroom that there was.

When cattle or sheep were rounded up, little ones would often be brought into the community, almost like a toy, and, as toys often are, they’d be discarded and forgotten. This had happened to Sheepy. He had been around the place for a while. He was no longer little and cute, but full grown, fat and fluffy. Well, he would have been had his overgrown wool not resembled a large and fibrous tumbleweed, complete with spinifex grass and felted matting. Sheepy had wandered into our yard one day and, as I mentioned, Mum is genetically predisposed to be unable to resist something or someone in need of assistance. Sheepy became her personal project. She blunted the few pairs of scissors we had, regardless of their original purpose, trying to create a coiff from a conglomerate. The community thought it was hilarious, but I could understand her concerns. Desert days are not cool and Sheepy was lumbered with inches of filthy thermal insulation. Each day, scissors of various sizes and Mum waged war against Sheepy’s many extra layers.

With time and perseverance, Mum won the war against the wool. Sheepy bore his new, attacked by vicious lawn mower, wool cut with lightness and freedom, if not pride. His accepting personality was overcome, layer by layer, with the more realistic taciturn nature of a scruffy, hot male specimen. So Sheepy left his temporary home and ran off to rejoin the community at large. And, not long after, and not shared with the shorter siblings, Sheepy made a guest appearance at a local barbecue. Such is life, I suppose.

Awkward Eating

I’m currently at the other end of the state to where I usually am, visiting my sister and newest niece.


My own children would have liked to come with me, especially the youngest. He adores babies; we (he) often stop prams simply by standing in front of them to talk to ANYBODY’S baby. So to have one of our own is a big deal…and she’s gorgeous!

Tuesday morning on the way to school and daycare, I reminded him that I was going on the plane that evening.

“Can I come, please?”

“Not this time, I’m sorry. It’s pretty expensive to go on the plane and we don’t have that much money. Everyone would have liked to come.”

🤔 “Do you have money for YOU to go on the plane?”

“Well, my ticket has been paid and so jowett I have no money. Luckily though, when I get there, Grandma and Aunty will feed me.”

🤔🤔😕 “Do you mean like Aunty feeds the baby?”

😲😲😂😂

“No. Maybe a sandwich.”

“I didn’t think it was right but I had to see if it was like that.”

Kids!

🖒🐛

Anxiety and depression – My son’s story

Some of you know and have supported Logan and I recently so I’m sharing this with you in the hopes that someone else will be helped.

Depression doesn’t always make sense and many people don’t understand it. I’m sharing because of that too. Thank you for your support whether you’ve understood or not. I’m happy to chat anytime.

Please share with anyone you think will benefit from knowing.

I’ve copied and pasted an email I wrote to some people who knew more of this earlier, in the middle of 2014, so it may not all be relevant to you, but the info and sentiments are.

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Because we’ve spoken about this before and you are aware of what’s been happening for Logan, I want to keep you updated on Logan’s situation. I’d appreciate it if you could continue to keep your eye on him, like you’ve already been doing, and let us know if you see any changes.

I took Logan to a psychiatrist on Wednesday and she agreed with my ‘mum diagnosis’ of chemical depression within 10 minutes of us all talking. After a thorough discussion, she’s prescribed him a 12 month course of daily Zoloft, which she will monitor closely with us. She believes that we will see, and Logan will experience, positive change within 3 weeks. All going as expected, he should be functioning normally within three months and in six be back to where he ‘should’ be. This is wonderful, prayed for news, which is exactly the outcome I had hoped for from yesterday’s appointment. Thank you for praying with me.

As with any medication, there MAY be some side effects and although these are mostly minor, we want to be onto them. Especially these next two to three weeks, Logan might be more tired (not sure that’s possible); have slight headaches; have more ‘body irritability’ like jumpy legs, unable to sit still and tightness or clenching of jaw or grinding teeth. None of these presents a problem, it’s just a settling in period. As I said, she’ll be monitoring him every few weeks in person to make sure that’s all. After the initial few weeks, most people have only positive change and because we often don’t see small changes from so close, you may see these more than Logan does at first. I’ll be noticing every tiny thing, I’m sure, which will be a nice change to noticing the decline, but I’d love your feedback too. Logan knows that you are aware of the continuing story and is, even now, willing to talk to you about it all. He has briefly mentioned his anxiety to his friends, but has trouble knowing what to say. As you can understand, some people have negative perceptions in relation to psych-anything, so he’s nervous about judgmental reactions.

This next is probably the most important part of my explanation today and what I hope will help others. It’s only due to my first hand knowledge of chemical depression that I’ve seen beyond what often presents as grumpy, ’emo’ teenager,Neanderthal behaviour and really known he wasn’t ok. It took a close friend’s amazing transformation recently from severe, self harming depression to normal, functional, and finally happy person, for me to seek a psychiatric referral. The psychiatrist had worked with my friend’s medication over months to achieve this and it’s been a miracle. It’s the best discovery I’ve made. I’ve been diagnosed, and improperly treated for, various types of depression for the past twenty years. I’ve been to multiple GPs and referred to counsellors and psychologists and have attended each session feeling like a fraud and a ‘mental case.’ I rarely had anything to discuss and my catch cry has been, “There’s nothing wrong with me; why is there so much wrong with me?” Why did I still feel so hopeless, helpless and lacking in any energy or motivation?

I have tried a number of anti-depressants with varying degrees of un-success, prescribed by GPs who have tried. When one suggested post natal depression when Toby was 4 years old, I wondered if I really was in the ‘too hard’ basket. My latest GP, just prior to finding out about Theo, was the first and only person to use the words, ‘chemical depression’ and she told me it wasn’t psychological, but my body’s inability to manufacture Seratonin, among other things. She said I’d likely have to be on anti-depressant medication for life and likened it to some diabetics having to inject insulin. I felt such relief at that, finally having an answer that wasn’t a mental issue. She’s been amazing, guiding and supporting me through what’s been a rough few years with pregnancy hormones and true postnatal symptoms. I’ve taken my medication as prescribed and have been ok; but only ok. Theo’s nearly two and I’m still only ok. I am so used to being flat that I’ve only really recently realise that I’m probably operating at 75% of what’s normal for me. My head’s above water, but it’s easy to go under. With the change I saw in my friend, I’ve self-referred to this same psychiatrist Logan saw. I’ll see her next week but through the tiny bit of my information I gave her today as background for Logan, she’s already determined my medication is wrong for what I have and that I have been improperly diagnosed and treated for 20 years. She has said that most people can be treated for chemical depression like this in a relatively short, finite period, easily with the right prescription; which is a psychiatrist’s specialist area. I’ve never felt such relief and frustration and anger at the same time!

Although I knew psychiatrists could prescribe medication, I had the mistaken, but disturbingly common, view that psychiatrists were the top of the mental health hierarchy: the more crazy you were, the further up you went. The thing that’s perpetuated this myth and given me what I feel are wasted decades is that no one, not GPs, counsellors or psychologist – NO ONE has ever suggested I seek a psychiatrist’s help – and they SHOULD HAVE. If they had, I’d have done so. If they’d suggested amputation, I would have gone there too in an attempt to feel ‘normal.’ I tell you this because I know I’m not the only one in my situation and although I’m finally going to get this all sorted starting next week, I’m angry at such wasted decades. The only thing I can see that makes it ok is that God has a plan for this knowledge and experience. Because of it, I’ve been able to get help for Logan early and not shrugged it off as grumpy teen. Because of this, I may (and hope to) direct others to seek the right help. And you’re some of the first I’ve told. Maybe you can pass this on to help someone else.

I so appreciate that I’ve been able to honestly share this and my experiences with you all individually over the past few years. It seems trite, but isn’t, to say thank you so much for your support and observation and care of both me and Logan. It was so good to know others saw what I did in him and cared enough to tell me. Thank you for continuing to pray for us. Please ask about and share my journey with anyone who needs it and WATCH THIS SPACE! for new and improved Ross’. Bit scary, hey?

Veritas, Eski

Sensory Overload

I am utterly blessed. In the midst of an overload of senses; no, through them; God has blessed me.

I have a hot little hand on my face as I try to read. It pokes me and twitches at the entrance to my nostril, making breathing odd. If I turn over, I’ll have, instead, little untrimmed toenails in one of two choice spots: kidneys or buttocks.

A short reach away, I hear the thunderous roll of snoring. I prod and suggest turning over and for a moment, the storm abates. But only for a moment. Without any lightning to warn of its advance, the long drawn in breath offers new meteorological mysteries.

Further distant still, the irritating whine of machinery. It’s monotony is broken only by the insidious, regular alarm throughout the night.

Dogs, ours, bark at intruding nothings. Loudly.

If I leave this horizontal plane and venture out, I will likely find lines of light break through the darkness. Here and there, I will hear more cacophony to interrupt my rest. From one doorway, little light accompanies the pings and whirs of levels unlocked by a well known Italian plumber in overalls. From another, brighter light pops out, as unyielding as the so called notes screamed by a boy-man wearing more eyeliner than I ever have as he bemoans his newly single state.

Should I turn and retreat, my hapless tarsal structure is likely to be assaulted by weaponry at floor level. Possibly this time, I will encounter the string of a cheap bamboo bow. As I lightly sidestep the threatened trip, my other foot may find the arrow; or Danish building materials with spiked edges; or an assortment of miniature bovines cavorting without care near an enclosure of even smaller dinosaurs; or a shadowy feline hoping for food.

But despite this risk; this riot; this rude interruption of horizontal calm that I say I’d prefer; I am utterly blessed.

Little fingers and toes are not a blessing all who wish it share.
Snoring means he’s here with me.
The whir of machinery speaks of luxury others do not have.
Lights and music mean my children are home safe. They can be and do just as they wish without fear of persecution, despite my musical preferences.
Even the scattered hazards of a family hall shout freedom, safety and luxury.

I am utterly blessed.

Veritas, Eski

While the cat’s away…

With two of the big kids away and Mr 17 giving a very creditable performance of a cave dwelling hermit, Theo and I have spent lots of one on one time these holidays. We’ve made much use of our Thermomix , which is a reasonably new acquisition for us. Apart from numerous jams, sauces and yummy meals, we’ve found a smooth and long lasting playdough. You can see the recipe HERE with thanks to “The Organised Housewife.”

Our pink and blue playdough, now a delightful mauve, has been stored in the ever helpful snap lock bags and has lasted about a week now. Theo has made snakes as he’s rolled out the dough and created numerous iterations of his farm yard. The unfortunate residence of which have been struck by the lightning fist of the toddler only moments after enjoying their first meals.

[Click this link for more about FINE MOTOR SKILLS development]

We’ve also started “Theo’s Wall” this week. A large, bare wall in our lounge room is slowly transforming. Yesterday’s addition is a weekly calendar. Theo knows the names of the days and this will help him learn the order as well as some tenses; today is, yesterday was etc. I’m all about building children’s ownership and responsibility, so this should help. Future inclusions to the wall will be alphabet friezes; a “Getting Ready” checklist and a chalk or whiteboard.

So, with another week left of holidays left for me and two for the kids, what other adventures will we have? What adventures are you having? Let me know in a comment below.

Veritas, Eski!