Tag Archives: healing

The Secret…Friday Fictioneers.

 

“I hate you!” Alice screeched at her parents. She might’ve been difficult, but she wasn’t stupid. She knew this was another attempt to force her to “self-calm”, as the therapist put it. They’d tried everything…mediation, relaxation, mindfulness, yoga. Yet, instead of bringing inner peace, they’d only fueled an endless, inner rage. She had to scream. Smash something. Carve a stream into her arm to let the tension out.

This time, they let her run.  After all, there was nothing more to say. Yet, they still clung onto a completely irrational hope, that somehow their only beloved daughter would find her way back out of the darkness and into the light.

……

My humble apologies for going over the word limit. I don’t know why Dale’s beautiful photo prompted such despair in my piece this week. However, I’ve never been good at meditation or sitting still.

This has been another contribution to Friday Fictioneers hosted by Rochelle Wishoff-Fields. PHOTO PROMPT © Dale Rogerson.

Best wishes,

Rowena

A Journey Without Steps…Friday Fictioneers.

All this motivational quackery was rubbish. My journey of a thousand miles was never going to begin with this step, and it wasn’t going to head straight up a flight of stairs either. Surely, there was a lift? Yet, I couldn’t bring myself to ask. Twenty-five years young with the rusty joints of an eighty year old, I was done explaining. I’d shut shop. It was much easier to stay home. Yet, that wasn’t a luxury I could afford. Lingering between the lines of disability and wellness, I had to work. If only I had the wings to soar….

….

For those of you who’ve known me for awhile, I live with some chronic health and disability issues. When I was 25, I was diagnosed with hydrocephalus and had brain surgery to insert a shunt. My road to recovery felt like it was straight up the side of Everest without any safety equipment or assistance whatsoever, even though I was not alone. I really had comprehensive and loving support from my family friends and particularly my OT at Mt Wilga, who really helped me get through this incredibly hellish experience. Yet, I was the only one who could walk in my shoes. I was the only one who truly knew what it was like to put one foot after the other. I still had a job when I was going through that and yet my return to work date kept getting put back and their were complications. The valve of the shunt malfunctioned and I needed further surgery, which I really didn’t expect to survive. By this stage, returning to work seemed hopeless. My relationship had all but ended and it was a bloody hard slog. Yet, through all of that I always saw myself as a career woman. Work was very important to me. I ended up getting a part-time job and then landed what seemed to be my dream job in an advertising agency but the hours were very long and it was very stressful and one night I collapsed at Central Station from sheer exhaustion. I had to slow things down. Find a new path. One that wasn’t quite so steep and allowed me to heal. This was a huge life lesson for me and I clearly remember being told that I was a “human being and not a human doing”. I have a lot of adjustment to do and that is ongoing.

I would like to take this opportunity to raise awareness of the kinds of barriers people face when it comes to returning to work or finding a job when they have a disability, health issue or are just battling with life. How can we make their path a little bit easier? How can we reduce the load? What are we doing as a community to make their battle worse? Indeed, the finger of blame falls too quickly on the survivor instead of a helping hand.

Lecture over.

This has been another contribution to Friday Fictioneers hosted by Rochelle Wishoff-Fields. PHOTO PROMPT © Jilly Funell

Best wishes,

Rowena

 

An Unpredictable End…Friday Fictioneers.

The end was unscripted. He simply sent her a text, as cold and unfeeling as a Winter wind. Yet, her grief was brutal. A stab to the heart. A kick to the guts. She could even feel his huge mechanic’s hands tighten around her throat, along with that final gasp.

Kate was not above revenge. A crime of passion. Destroying him cell by cell with her own rat cunning. She even thought of phoning Roger.

Yet, a skerrick of reason remained. That, while she couldn’t make it better, she could always make things worse.

Now, she could only face the storm, but with renewed strength, knowing it too would pass.

……

This was my second go at this week’s prompt and it stretched so far beyond the initial photo prompt that I decided to use a different image. It looks at how we respond when someone does something terrible and unforgivable to us. Do we lose ourselves and our core values in pursuit of revenge? Or, self-destruct unable to recover from the pain?

I remember a bit of a joke from my single days: “If you can’t have the one you love, love the one you’re with. If you can’t love the one you’re with, turn out the light.”

When it really boils down to it, we really have no choice but to plough onwards through the storms of life, but there are things we can possibly do to prevent the storms from building up. Moreover, we can also be better prepared, and in peak condition when they hit. That way, we’re better positioned to be a victor, than a victim and to rise from the ashes of what ever it is that hits us.

Here is the original photo prompt thanks to :

July 18 dawn-in-montreal

PHOTO PROMPT © Dale Rogerson

This was another contribution to Friday Fictioneers hosted by Rochelle Wishoff Fields

Best wishes,

Rowena

Bob’s Left Foot…Friday Fictioneers.

Bob hadn’t even thought about his foot, until it was gone. It had simply sat inside his shoe, going wherever the rest of his body was going. Not a decision-maker. More of a follower, than a leader, although his right foot always led the way.

However, it wasn’t his right foot that blew up in the landmine. It was the left.

Now, he was leaving the fallout of war behind, and was finally moving forward. It had been a long road. Yet, come October, he would be sprinting in the Invictus Games. At last, he was starting to feel like a hero.

…..

This has been another contribution to Friday Fictioneers hosted by Rochelle Wishoff-Fields. This week’s PHOTO PROMPT © J Hardy Carroll. I encourage you to have a go and come up with your own response to this week’s prompt. Every week, these prompts stretch and challenge me in ways that are often rather unexpected and are such an encouragement.

Best wishes,

Rowena

 

“Speak even if your voice is shaking”…

The terrible thing is that for every person who takes their life, there are others just hanging on to the very edge of the abyss by the skin of their fingertips. Moreover, we often don’t find out who they are until it’s too late.

On January 3, 2018 a young Australian teenager “Dolly” Everett tragically took her life in response to cyber bullying.

At the time, I was quite surprised that this young woman would be a victim of any kind of bullying, let alone something bad enough that this was her only escape. She was a very attractive young woman, who had modeled for Akubra Hats. I don’t know. I guess it just goes to show that nobody’s immune to being bullied or its consequences.

In the days before she passed, Dolly drew a young dancer with the heading: “Speak even if your voice is shaking” and these words are now being used in a media campaign to tackle cyberbullying and bullying in general.

However, Dolly’s words came back to me today in a different context. That her advice doesn’t just apply to people experiencing bullying, but about also enduring other trials and bottling their feelings up.

After all, it’s not easy to find the words to express yourself when you’re stuck in a labyrinth. It’s not easy to reach out and say you’re not okay. To go beyond that socially acceptable “fine”, when someone asks you how you are, even when you’re feeling shattered.

I try to laugh about it
Cover it all up with lies
I try and laugh about it
Hiding the tears in my eyes
Because boys don’t cry
Boys don’t cry…

The Cure

I don’t know whether we ourselves are holding it all in, or whether it’s what society expects. Turning back the clock a bit, there was that classic song by The CureBoys Don’t Cry However, while our society has encouraged men to be more emotional, I suspect it’s also pushed women to be more controlled and to adopt the stiff upper lip. What do you think? I certainly don’t want to break down and cry. No, I’ll soldier on. Keep smiling… sunny side up. I don’t know whether it’s a case of denial or acceptance, but there isn’t a manual for how to keep living year after year with a severe life-threatening medical condition either from my own point of view, or from that of my family. We just keep going, because we have to and because we want to. I don’t want to die before I’m dead!!

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Yet, through Dolly’s words, I’ve also realized that I’ve been silent. That I haven’t been speaking up, and we as a family haven’t spoken about the elephant in the room for quite awhile. After all, we’ve been living with it for 12 years now, and it’s starting to look like we’ve established some kind of mutual stand off. That it has its part of the house, while we have ours. Yet, that doesn’t mean it doesn’t exist. That it’s not here and sometimes moves so close that I can feel it’s breath against my skin. I start to scream. Feel my life slipping away. Then, somehow the storm has passed, and we’ve back to calm seas and endless blue skies.

Yet, as hard as it is to speak when your voice is shaking, it’s not always easy to write about it either. Indeed, for the past couple of nights, I’ve been typing randomly into my computer hoping to unravel the wound up spring inside. Work out what’s eating me alive, when everyone else is asleep. What’s wrong.

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Here I am at Railway Park, Byron Bay.

 

It always seems to come back to this. I live with a neuro-muscular, autoimmune disease called Dermatomyositis, which has spread to my lungs causing fibrosis. I look perfectly fine most of the time on the outside. However, if my lungs were my face, you’d barely see my eyes through the scar tissue. Yet, I breathe. I walk. Play the violin and sometimes dance. I also love and hug my husband , my children, my Mum and Dad and the puppy dogs. I have a rich and beautiful life jam packed with love. More over, I am also able to give and care for those around me. Put my arms around the broken-hearted, and shelter them from life’s storms. Try to help them feel loved. Indeed, even in the face of all my health issues, I strongly feel that my time on the planet has only just begun, and couldn’t be about to end any time soon.

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But these are the words, the feelings, the fears, I carry on my shoulders like Atlas, because I don’t want anyone else to worry. I don’t want them to be afraid. I especially don’t want my kids growing up wondering when Mummy’s going to die. It’s much better to keep those thoughts to myself, although given my frequent coughing attacks, they must also have their doubts. I’ve been stuck gasping for air too many times and desperately holding onto that Ventolin for them not to be freaking out.

Yet, how long is a piece of string? No one knows. Not even those who think they know, get it right. Dying seems to be a very complex equation. Indeed, this week we saw death’s contrariness personified in the death of Stephen Hawking at 78 years of age, when he was supposed to die in his twenties.

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So, there is no crystal ball. You can’t predict when your number’s going to come up and to me, it’s all starting to look rather random.

So, what can we do?

I guess that’s where I thoroughly believe in Carpe Diem…Seize the Day. You need to be thankful for what’s going well and you do need to find an outlet, some way you can share those challenging days and emotions and know that your concerns will be taken seriously, respected and that someone will respond in exactly the way that is right for you…be it a hug, a bunch of flowers, a card, a poem.

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Now, I’m going to turn this around and throw the challenge back to you the bystander…”Speak even when your voice is shaking”. I have also been in the situation many times where someone I’m close to is sailing way too close to the wind.When  I know life is excruciatingly painful, and they could well pull the pin. Again, there seems to be no manual for what to say in this instance either. If you’re anything like me, you can get tied up in knots trying to think of the right thing to say. What to do. “I dunno!” Surely, something is better than nothing. A stutter or an awkward stumble, is better than silence.

In Australia, we have “R U OK Day”. This is a fantastic idea because it at least provides some kind of way to start that awkward conversation.

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That said, once we’ve asked the question, we need to be able to leave room for the consequences. Make sure we have enough time to listen. Moreover,  I believe most of us should have some basic understanding of how to handle a mental health crisis. Anyone of us could be that first responder and you’re not always in a position to call 000 or 911. I have been in this situation and I must admit that I had the peace of God around me at the time, because I am not a calm person.

As a parent of teenagers, this is a huge concern. Not just for me, but all parents of teens and all who love and care for them.

This takes me back to something Dolly Everitt’s Dad said:

“Be honest with your kids. If you can’t connect with them for whatever reason that may be, find someone that can. They’ll always have a mate they’ll always have a little buddy somewhere that knows more than mum and dad.”

– Tick Everitt

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So, I apologise that my thoughts have wandered but I don’t profess to have the answers. I just have the questions. Yet, I’m thinking. I’m trying to find a better way to handle my own hard yards, and also to reach out and be there for those within my sphere. After all, I’m only human. The rest is in God’s hands.

Please leave your thoughts in the comments, but if something is troubling you, I encourage you to turn to someone where you live who can truly be there for you.

Love and best wishes,

Rowena

PS You would think that by broadcasting my thoughts on the World Wide Web that those closest to me emotionally and also in proximity would also be the wiser. That they’d read my confessional on my blog and know what’s in my heart and mind. However, there is that cyber divide and my family rarely reads my blog. Indeed, it wouldn’t surprise me if they knew a very different me, and for those of you who also blog extensively, that this is the same for you. This is important for us to keep in mind, just as it is for parents to be aware that they don’t know what they’re children are sharing online or how they’re being treated. There are two worlds.

More About the Photos

The photos which appear in this post were taken in August, 2011 in the Railway Park at Byron Bay, NSW. Byron Bay is a stunning coastal town with such amazing natural beauty, a striking lighthouse and since the 60s, it’s been a magnet for hippies and alternative lifestylers. People who are troubled, searching and potentially experiencing mental health issues go to Byron Bay to clear their head and yet their issues only follow.

We have taken our kids to the climbing tree whenever we’ve gone to Byron Bay to stay with Geoff’s sister and family. It is our home away from home. Or, at least it was when we could get away more often.

This climbing tree is rather special because it’s fallen on its side so kids can climb it easily and given the hippy vibe of the area, it’s not surprising that people tie scarves and ribbons in the tree. We’ve even found an empty milk crate suspended from a rope.

However, on two separate occasions many years apart, we met  a lady, Mama Dee who was painting the tables and chairs and decorating the tree as a tribute to local youth who had taken their lives. Indeed, her son had accidentally died in the park through an overdose of prescription drugs. She wanted to honour all these precious young people and also brighten up the park for children and make the place happy.

I hope her gift of love will also touch your hearts as it has moved mine.

 

Life Was Meant To Be Easy.

According to the “Feel Good School of Thought”, life is meant to be easy. Adversity is a transitory thing that we can simply power through, as long as we “think happy thoughts” and “stay positive”. “If it feels good, do it. If it feels bad, give up.” However, from this perspective, we might as well pull the pin when “shit happens”. There is no reason to live.

Yet, ironically humans thrive on being challenged, using our problem-solving abilities, and overcoming adversity. We’re meant to use what we’ve got, even if some of the equipment isn’t in peak form. Indeed, adapting to these challenges stimulates the mind. After all, we were never designed to be couch potatoes, or even worse, liquid mash. Rather, we were meant to grow roots and broad branches, and stand tall on the inside, no matter what our design. Just think about how often you hear heroic stories of everyday people overcoming huge setbacks and surging forward in a new direction. Indeed, their curse can even become their blessing. The Paralympians embody such triumphs.

“I think a hero is an ordinary individual who finds strength to persevere and endure in spite of overwhelming obstacles.

So many of our dreams at first seem impossible, then they seem improbable, and then, when we summon the will, they soon become inevitable.

Once you choose hope, anything’s possible.”

-Christopher Reeve.

At a more basic level, I remember my Dad encouraging to overcome fear and have a go. His big line was: “it’ll put hair on your chest”. As a little girl, I didn’t quite get what he meant and took him quite literally and I didn’t want hair on my chest. However, these days, this sort of grit has been rebadged as “resilience”. This school of thought poses that we need to experience the bumps and knocks of life to grow stronger and prepare us for the big hit. This isn’t as much fun as thinking happy thoughts and only doing what feels good, but we do emerge more rounded and as the Scouts would say: “prepared”.

While that all sounds great in theory, it’s quite a different story when you’re lying face down in the mud with no known way of getting up. At this point, it’s quite natural to feel overwhelmed by shock, disbelief, anger and self-pity. However, if you want to move beyond subsistence, you have get yourself out of the quagmire and start thinking about taking those first few critical steps, be they literal or somehow figurative.  Staying put isn’t an option.

Rowena

This isn’t theory for me, but my own, personal experience. I have walked the talk, sometimes needing assistance.

When I was 25, I was diagnosed with hydrocephalus or fluid on the brain and six months later had brain surgery to insert a VP shunt. The hydrocephalus was pretty freaky. Although it was largely dormant for the first 25 years of my life, it rapidly became symptomatic and for the six month period in between diagnosis and surgery, I lived the bizarre and traumatic life of Oliver Sacks’s: The Man Who Mistook His Wife For A Hat. I had 6 months of intensive rehabilitation, learning how to walk and had occupational therapy to manage my life again. This all culminated in moving back in with Mum and Dad and a year off work. That in itself felt terminal. After all, when you’re living the story, you don’t know how it’s going to end. I slowly got back on my feet. Returned to work. Got Married. Had two kids. Then, the thunderbolt of medical misfortune struck for a second time. The birth of my daughter, triggered so much more than maternal joy. My hands turned raw. As it progressed, I couldn’t sit on the floor and get up again, dress myself. Eventually, 18 months later, I was finally diagnosed with dermatomyositis (DM), an exceptionally rare auto-immune disease where your muscles and skin cells attack themselves. As soon as I was diagnosed, I was put in a wheelchair and spent the next week or two in that and the next couple of weeks in a walking frame. I was only 36. Treatment made a vast improvement, but I went on to develop Institial Lung Disease with fibrosis, and affiliated chest infections nearly take me out most years. The Cough has now become such a permanent fixture, that I’ve called him Fergus.

I didn’t respond well to treatment for the DM, and five years ago, I had seven treatments of chemo. My specialist also changed my meds and I’ve been in remission ever since. Not smooth sailing, but still a relief. My kids are now about to turn 14 and 12 and still have their Mum. Moreover, I’m still an active part of their lives, even if I’ve had five years off work. I am so very thankful to be here. Yet, there are still times, especially when the cough flares up, that I get fed up. After all, I’m human, not invincible.

With the New Year, I’ve been rethinking my status quo and wondering how to get back into some paid work, while coughing like a mongrel dog and feeling dreadful in so many ways, that it’s tempting to sink underneath the waves and give up.

Prior to chemo, I had been employed as the Marketing Manager for a local IT Company one to two days a week. I’d also been working towards a motivational book about turning your mountain around. I had it all planned out. What had started out with a rather feeble New Year’s resolution to vaguely improve my heath through green smoothies, evolved into a surprisingly productive year. I lost 10 kilos, took up the violin and performed at the end of year concert, started the blog and tackled all sort of challenges at an adventure camp run by Muscular Dystrophy NSW…quad bike riding, sand boarding, para-sailing. It was incredible. I’d pulled off so many things I’d never thought possible, and was almost on top of the world.

 

All of these breakthroughs and successes were definitely book worthy and I thought my story could encourage others experiencing the hard knocks of fate, to give living a go. Living with two debilitating, life-threatening medical conditions and consequent disabilities, I was proof that it was possible to carpe diem seize the day even through times of serious adversity. However, my story wasn’t going to end there. The icing on the cake, which I intended to be the finale of the book, was skiing down Perisher’s Front Valley, in effect, turning my mountain around. Yahoo!

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Skiing in Perisher. You can see my instructor, Tom, in the background…the wind beneath my wings. I went as a member of the Disabled Winter Sports’ Association.

That was the plan. However, while I triumphantly skied down Front Valley, my “victory” didn’t match my expectations. Rather than the exhilaration of triumph, I felt my gut sink with unbridled terror as I perched precariously over the edge, with a huge drop off down the slope to the village below. I felt like fleeing straight back to the safety of the “magic carpet”. However, I had my ski instructor with me and Tom went backwards down the steep start and held my hands to ease me down. By the time I finally reached the bottom after a few spills, I was more relieved than jubilant and I was just glad it was over.

However, the story doesn’t end there. Triumph soon did a terrifying back flip, and even before we left Perisher, I’d developed a nasty chest infection, which turned into life threatening pneumonia. Indeed, one night in between coughing bouts, I actually stopped breathing.

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Playing Moonlight Sonata after chemo.

At this point, I also found out that the auto-immune disease was in a serious flare and was attacking my lungs. The Institial Lung Disease had become active and I had marked fibrosis in my lungs. Moreover, the report on my lungs read like the contents of a vacuum cleaner bag…ground glass, honeycomb. I was actually surprised there wasn’t any dog hair in there. Anyway, they started me on chemo (cyclophosphamide) a week before Christmas 2012 and I’ve got to say, I didn’t expect to be alive for Christmas 2017. I am a living, breathing miracle, which has been a comprehensive and intensive team effort.

As you could imagine, pneumonia and chemo weren’t the grand finale I’d planned for the book and the book is still on hold as I wrestle with what it really means to be a survivor, grappling with my numerous battle scars and LIVE on. I don’t merely want to exist.

This isn’t something I think about all the time. However, with the new year, I’ve revisited all of this. I’m still wrestling with THE COUGH, while also trying to get back to some kind of meaningful paid work. The two of them are looking very incompatible at the moment, but surely I can find something?

Pursuing this question further requires me to accept my weaknesses, but also to acknowledge and embrace my strengths. Know that I am not a dud. Rather, I’m human. We all make mistakes and have strengths and weaknesses. Of course, that’s something I would say with conviction to anyone else, but I struggle to find that in myself.

So, I guess this takes me to George Bernard Shaw:

“Life is not meant to be easy, my child but take courage: it can be delightful.”

When you’ve experienced adversity, how have you kept your head above water? Please leave your thoughts in the comments and links through to any posts.

Best wishes,

Rowena

This post was published on Smorgasbord – Variety is the Spice of Life.

Our Son and the Rescue Pup.

This afternoon, I was tapping away on my laptop, when I glanced over and spotted a priceless moment. Our son was snuggled up on the couch with our Border Collie pup, Zac (ie Isaac Newton)  watching The Good Doctor. It’s Sunday afternoon, which quite frankly should be declared a “snooze zone” before having to return to the realities of “The Week” on Monday. Hence, I’d slept in, and was still in my PJs. That explains how I managed to capture the moment. I didn’t need to leave the house, or even my chair. My camera was sitting faithfully by my side, just waiting.

Zac is almost 4 months old, and we’ve had him since he was a little 6 week old pup, along with his sister Rosie. Rosie was meant to be a foster pup, and simply passing through. That was before she got caught in our heart strings. Zac and Rosie have also become inseperable. After all, they’re more than brother and sister. Now that the rest of their litter has dispersed, they’re “twins”.

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Rosie (left) Zac (right). Not quite identical twins.

Of course, with such young pups, you don’t know anything about their personalities, psychology or outlooks on life. You can only base your selection criterion on things like markings and which pup comes to you first. I was the one who chose Zac, because he had distinctive black and white markings, which I thought looked more like Bilbo. Our daughter chose Rosie as she has a broad, white stripe on her face, which she thought looked like Bilbo. Rosie also has black spots on her legs, which I wasn’t too sure about, but others loved. Both dogs were looking short-haired and Bilbo and every other dog I’ve ever had, has been long haired. However, I reasoned that short hair is better suited to our beach lifestyle. It was a tough choice.

Zac was instantly “my dog”, and he was also the pup most determined to turn a  recalitrant, growling Lady, into “Mum”. Rosie palled up with the rest of the family and was a little more cautious about turning to Lady for love. It soon became clear that Zac and Rosie were inseparable, and that having both dogs could be much less work than the one. They could occupy each other.

Back at the end of June before the pups came along, our beloved Border Collie Bilbo passed away. He was 11 years old and we’d had him since a pup. Back then, our son was 2 years old and our daughter was crawling. So, not only had Bilbo seen the kids go through the childhood years, he’d also been with us through each and every up and down with my severe health struggles. I don’t know whether all of that made him a sensitive soul, but he certainly was a very special dog.

And, Bilbo was also a survivor himself. Indeed, he was only a young pup when I was admitted to hospital for about eight weeks and he went from having the kids and I at home almost every day, to me being in hospital, the kids staying at my parents’ place and Geoff getting home super late from work after touring Sydney seeing the rest of us every day. On top of that, the pup also lived through the trauma. A stress beyond stress.

 

Above: RIP Bilbo.

At least, that’s how we explain Bilbo’s act of determined destruction, which could have killed the wee pup. Bilbo went exploring under the house chewing the the wifi and computer network cables. When an exhausted and irate Geoff retraced his paw prints under the house, he found that Bilbo had even started chewing on an electrical cable and must’ve received a slight zap, which made him stop.

Obviously, that wasn’t the best of times for us.

So, when Bilbo passed away, he took a lot more than memories along with him. There was also the deepest and most compassionate empathy, and an understanding of us which came with walking through the valleys and mountain tops with us and in our hearts.

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Lady.

While we have another dog, Lady, she doesn’t have that same sense of empathy or emotional depth…and isn’t quite so melancholy either. She’ll greet you with an uber-enthusiastic wag of the tail, which could almost take your leg off. She has different talents, but she also doesn’t fetch which was a rather difficult gap for us to ignore. We are a ball throwing family and that requires a dog to fetch, even if he was an annoying, obsessed maniac  more often than not.

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Zac & Rosie when they first arrived, aged 6 weeks.

Wanting to let our emotions heal before we adopted another dog, we were going to wait until next year and get another pure-bred Border Collie. However, I got word through the pet rescue group that some Border Collie x puppies were coming in. I could also see that our son could use another dog  now. At the time, this was more of a vague hunch than a neon sign.  although until Zac settled in, I had no idea that he had such a special capacity to heal. A capacity not unique to him, but not universal among dogs either. That he has a gift.

Reversing up a bit, not long after Bilbo died, I caught the flu and a nasty respiratory infection. With my underlying health issues, such infections become life threatening and I developed a powerful, incessant cough which was absolutely terrifying. After losing the dog, the kids were particularly concerned this year and didn’t have Bilbo for support.  After all, it was hard times like this, that Bilbo had always been there for every single one of us. Shaken by such fear on top of grief, our son in particular needed the love only a special dog can give.

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That’s why I was so stoked to see our son so snuggled up and entwined with the dog today. As a parent, we so often feel like we’re flying blind.Even when we know we’re doing our best, it’s all to easy to feel like we’re floundering. That despite our best efforts and utilizing every single resource we’ve got, that we’re still getting sucked into the vortex and drowning…along with our beloved child. Seeing our son so relaxed, content fused with the dog and knowing we’ve all made it through the storm, was such a relief. An answer to prayer in a way that made so much sense and yet seems hard to put into words on the weekly praise list…RESCUED DOG SAVES TRAMATISED CHILD.

And, so I’m happy.

In addition to sharing my joy, this photo marks Day 4 of the Seven Day Black Photo Challenge, which a friend roped me into on FB. The idea is that you post a B & W photo every day for seven days and you nominate someone new to take up the challenge every day. Today, I’d like to nominate Trent from Trent’s World.

Have you have a special dog or pet who has whispered magic into your life? Please share.

xx Rowena