Fighting spirit

After a full on week of discovery, some good results some not so good, this family is taking a well earned break, and a trial camping trip, in preparation for our upcoming adventure holiday. We took off to the beach for a night to chill out, & to ensure that everything "works". I'm a controll freak and I need to make sure that everything is 'just right' not easy to do when you are taking off for a month camping around Australia, but I'll do my darndest to make sure it's all great. 

So just after I'm admitting to being s controll freak I'm now going to tell you just how out of controll our lives really are. 

So Toby, Larissa & I all headed to Sydney to the Royal Institute of the Deaf & Blind Children RODBC where they put us up for the best part of a week to do some assessments on Toby, to hopefully assist him and his teachers for school next year & for setting up his eyegaze computer and for us to best help him with his hearing and communication.  Communication is a huge thing for us, given Toby is deaf and non verbal he has never really had an issue getting his needs across to us. But those that dont know him struggle to 'talk' to him and understand him and he can't just 'ask to go to the movies' or something outside of what we pre empty for him. For us this is unacceptable. We want & have always wanted him to be able to communicate as effectively & independently as possible for him & that's why he's soon to get a super computer that he can use with his eyes.  But currently he has a special book. A PODD book that uses specialized pictures to help him tell us his needs but it hasn't been working that well. 

This week we found out that although his actual vision is ok he has a Cortical Vision Imparememt. Which means that his brain struggles to understand what he is seeing and it can be hard especially in times where there is lots going on & lots of noise for him to make sense of what he is seeing therefore his current PODD book, just won't work for him, there's simply too much information on each page, makes sense, that's why after 12 months he is still struggling to use it propperly. 

Yet another "diagnosis" yet another thing our poor little man has to coap with, but for us this diagnosis although crappy, is kind of positive. It explains a lot!  It's what I knew for a while, without actually knowing what it was. I knew the book was too much & have been fighting with speech therapy for a long time over it so in a way it's nice to know I was right & now we have the proof and can focus our energies towards the right way to el Toby!   That was discovery number 1!  That was ok.  I can deal with that, something not so good, but not so bad either. 

The next discovery....... Not so good. 

While we were away Kent stayed home & was off to the Drs for an ultrasound on his hip.    He's had inconsistencies with his pain since having his hip replacement in June. He was recovering well but then started to get more intense pain, we were worried it was the return of his cancer and he went off for X-rays, ct scans and bone scans. Amazingly all came back clear for Cancer in his bones, we wre greatly released but still concerned that something was amiss as he is still requiring lots of pain relief & struggles to do most things.   

This week he went off for an ultrasound after he pushed the doctors saying it feels like a giant "corky" something has to be up!   

The results weren't great. They were horrible. Although one could say it was expected it's still Another huge blow to our little family. It showed 2 small metastatic densities mixed up in the scar tissue. The cancer is now in his skin cells. He can't have any more radiation as he's had too much for that site, & we aren't interested in chemotherapy until we get back from our trip as he wants to be as fit & healthy as possible. & chemotherapy would make him Ill & potentially even hospitalize him while we are away, it's also not guaranteed to do a lot anyway so we decided to take the risk.   A crazy risk, one should never have to decide between a family holiday & chemotherapy,  it just sux!  There is no other word for it, no more to say!   It sux! 

So after that week we have taken time out and taken to the beach one of our favorite places. Time to just be! 

Climbing those steps

A few days ago, we attended a christmas break up party for the children in our Deaf community. It was held at the local water slide, which is an interesting place to hold this kind of event, given the children can not use their hearing aids / devices in or around the water. so the deaf children, are…Deaf.  I mean ,they can not hear properly without their aids. Anyway, so we arrive at the slide, knowing full well that it was also a totally inappropriate place for my child for other reasons. He cant walk, or sit up, or hold his own body up at all so, how was he going to get to the top on the slide? last I heard there weren't many watersides with lifts to the top so that the physically disabled could have fun too.  

Despite it being inappropriate for Toby physically, it was totally appropriate for him developmentally and this created a painful issue for us.  Toby cant walk to the top, and his daddy couldn't get up those stairs either, with out much puff its hard to climb stairs. Aimee came with us but she isn't strong enough to carry him, so that left me. All good Im happy to work hard, except I also have a medical condition, a very bad back from a work injury. I struggle to lift Toby now simply into and out of his bed is hard. However I have found that if I throw him over my shoulder like a “fireman's carry” then I can lift him for longer distances, but this was going to be a challenge, there are some serious steps leading up to the waterside. But how could I not, how could I let him become left out? I have worked so very hard for Toby to be included, and he wasn't going to miss out on a simple childhood pleasure, like the water slide, he’d been on them before when he was much lighter, and we know that he just loves anything like this, anything that creates a thrill excites Toby. 

So with a big deep breath, over the shoulder he went, one step at a time, up the slide I climbed, I wouldn't let it defeat me. I new what would surely be waiting for me at the end. As I climbed the stairs I realised again that this was just one of the many sets of steps that I would have to climb for our Toby, in a world that is designed for the abled, there are no elevators to fun for the disabled. Never thought about, until Toby entered our world, never questioned the lack of facilities especially in our home area, the North West Coast of Tasmania,  we don’t even have a disabled friendly playground, there are no slides that Toby can slip down, not without breaking his mummas back. there are no seesaws, or forts that he can enjoy, there is a Liberty swing, in our local park, but it has been dumped there, no thought as to its location,  dumped off to the side, so to play on it Toby would again be segregated from his peers, yet another reminder of all the things he struggles to do. 

Back to the water slide,  so I was climbing up the stairs and all the children seemed to love that Toby was joining in, he’s a bit of a celebrity it seems, and they all were delighted to see him climbing the slide, they let him in, allowed him to jump the Que., (thankfully as he is sooooo heavy) Carefully sitting down, I lowed him to my knees, his little body so tight with excitement, he was gasping the air into his little lungs, as I pushed us to start the slide.  Out came the biggest giggles,  a laugh so infectious, it made all the physical pain of climbing those stairs worth it, it made all the  emotional pain of climbing stairs for the last 5 years, worth it. and thanks to that laugh, to his jiggling, little giggle, I know I will continue to climb those stairs for him, I will do my best to break down those barriers that prevent him from having the same fun as his friends, as why shouldn't he?

Im not sure I’ll be able to get a lift put on every water slide, Im not sure what will happen in the future, as this is most likely the last time he will get to experience a water slide, truthfully, he is too big for me to carry now, but I do, Its sad to think that this could be his last time.. but I know, 

I’ll always be doing my darndest to hear that laugh, to see that smile, to be infected with his love, over and over. He is my inspiration, now…. back up those stairs for another turn :)

Travel.

Coming up to christmas our little family prepare for a BIG holiday. In a little over 4 weeks we will be embarking on the holiday of our dreams. For a very long time Kent and I have dreamed of travelling and camping our way around our beautiful country. we dreamed of long trips, and just pulling over to camp wherever we felt we wanted or wherever looked nice. we dreamt of long walks along beaches and refreshing splashes in little picturesque water holes. Originally our dream would be to take a few months off and just wander whoever our hearts took us. As time passed this dream has been broken down and when Kent was diagnosed with cancer it was put on hold and almost forgotten about. 

But we have decided to do it. My sister who lives in Darwin is travelling to Queensland for christmas to spend it with her partners family, and we decided, on a whim, to kick up our heels and just do it, we are going to meet her and her family in Queensland for Christmas. The kids Finnish school and then we are out of here. We jump on the Spirit of Tasmania for a day sail in on the 20th december, and then, camping our way up, we have just 3 days to get to Queensland, as we have planned to spend christmas eve at the fun parks, and to camp, with my sister, christmas Day. 

Its going to be tough, we have little money and both Kent and I suffer form chronic pain, and Toby doesn't sit well for long periods in a car seat. However, we are going to give it out best shot, well stop when we need and drive when we can. Our Plan is to call into Summer Bay (Palm Beach) so the kids can see where Home and Away is cast. and go for a swim on the beautiful beach.  just some great photo opportunities and something special to do. other than that we have no plans. Just driving, Camping and Family time. and I just can not wait for this. 

Our trip will see us spending christmas in QLD with my twin sister and her beautiful family, and on boxing day, I will fly back to Tasmania with my 3 other children, bringing them back to spend time with their father, and I attending, my best friends wedding before jumping back on the plane to meet Kent and Toby at Rockhampton.  There we will spend a night with my cousin on her beautiful property, before heading on the Townsvill, travelling and camping with my sister.  before breaking apart and leaving just Kent Toby, and myself to find our way back,  Kent, Toby and I have around 3 weeks to get home, and not plans as to how we will do it.  WOW, 

I just can't wait, we are thinking that we will head back through the center to South Australia and then back along the great ocean road before boarding the Spirit of Tas to come home again.   Talk about the holiday of the life time.  I am so looking forward to early morning sun rises, splashes in the ocean, the smell of salt air, as well as the heat of the sun as it lashes the harsh terrain of outback Australia. the many animals that we will see, the many flora that we will smell. I cant wait to teach Toby and the others all the Real things in life. all the beauty that there is in our world.  I cant wait to take our time to do whatever takes our fancy that day. I cant wait to do the fun parks and to see the wonder and excitement on my children's faces, oh man, I just cant wait. I feel so very blessed to have this opportunity. To have the time to spend together as a family, to have the option to complete a long awaited dream of ours. the memories that we will make, will stay with us for a lifetime. I am so very thankful that myself and the children will remember this holiday with Kent well past the day that he is no longer with us. This is our chance to make memorise. our chance to be family our chance to explore our amazing country, 

Just cant wait!!!

About 2 weeks ago we were having a battle with Toby not wanting to wear his Cochlear Implant Processors, we thought that is was due to that fact that we have to tape them to his hear, and double sided tape to his ears. we thought it was because the tape pulled, and we were trying to think of ways to help him, but really the only way to hold them on his ears is to tape them there. But one of my special Face Book Friends (a mother of an older child with severe CP) suggested that we actually ask Toby why he didn't want to wear them. Duh!  why didn't we thing of that. 

So we pulled out his special PODD communication book, and asked him why? expecting to know the answer we were both shocked and completely heartbroken to hear him say that he didn't want to ware them because they made him different. wow, how do you handle that? 

For the first time ever Toby had expressed sadness due to his disabilities. I knew that it was coming, I knew that one day we would have to deal with it, I just wished that one day was a long way off. To hear this from Toby, brought about our sadness for him and stirred up many suppresses emotions, grief for all the things that Toby would never be able to do, for all the dream that have had to be altered or forgotten as his abilities differ so much to our dreams and hopes for our son. 

To hear that at just 5, he was starting to understand that he is different and to start to reject that was just heartbreaking. 

Immediately we knew that we were our of our depth, we sought help with a social worker with the RIDBC, (Royal, Institute of Deaf & Blind Children) in Sydney, and I have a very informative session with the psychologist. who deals with non verbal children all the time. she explained that although it was a sore spot for Toby that we  had to make him put on his cochlear implant processors just like we would make him brush his teeth, we had to make it, a NO option subject, as if we give him an option he will be loosing valuable hearing time and could develop tinnitus due to the hearing nerve trying to search for sound.  

Kent and I didn't like the idea of pushing him to do something he didn't wish to do, as Toby is such an easy going boy and doesn't normally make a fuss. We have been working so hard to give him a voice, that we didn't like that we would be taking it away form him by forcing him to wear him processors against his will.  now we have such a tough decision, 

He does not complain, he does not wish to run, to play rough & tumble with the other boys, he never gets upset over his lack of ability to do the tasks that we all take for granted,  he very rarely even gets frustrated,  so for us to ignore this reaction is a very tall task.  Although for the greater good, maybe, he just doesn't want to hear? It is interesting that, with all his differences, and all his disabilities, that he has chosen this… his hearing to be the first upsetting factor.  it is probably one of the only ones that we can actually fix for him! 

Kent and I thought that we needed more guidance regarding this, and upon discussion which his school, they too could use more guidance upon Tobys actual condition and different ways to help get the best out of him. so we have decided a visit to the RIDB centre in Sydney would be worth while. we video conference with a speech therapist from there once a week for a therapy session, but a Trip to the centre would provide a full assessment, including medical, physiotherapy, speech therapy, occupational therapy, ophthalmological assessment, and psychological assessment. it could give us a good map for the next few moths to help lay good foundations for early next year in prep and beyond. This trip is a must.   So next week we will be bound for Sydney, to help us answer some uninsured questions and to help us deal with the many hard days with Toby to come, as he learns to accept his different abilities and the many differences between himself and his class mates. heartbreaking as it is, we are thankful that we have the help of a fully prepared team, who are there just to help us as we need. despite a few teething issues, they are all there to help us on this journey. Without them we would be lost.  

Travelling,

Always been a hard thing for us to do, both Kent and I have always love to get out and about. When we first met we use to take every opportunity to  get away, a long weekend, or any weekend, we would take off, traveling around we would try and book a spa cabin so that we could stay in luxury, it was our thing, to jump into the spa together and enjoy a bottle of wine or two, Cradle Mountain, picturesque Stanley, Hobart, anywhere we felt the need, we love to go camping we can rough it with the best, however over the years we have managed to build up some pretty crush equipment and now we camp in luxury. I remember we got engaged on a trip to Wickham where we were visiting with his sisters. Ever since Toby came into our lives, our travelling has slowed down a lot, we still go camping, we still fly, but we don’t very often get the chance to take off for a weekend spa. 

Our Travel has changed,  it now comes down to matriculate organisation. we have to carry spares of just about every thing, as with with us, we have realised over the years that, what ever can go wrong will usually go wrong. Im siting her at the airport typing this, we are waiting to get on a plane to Sydney,  without Kent this time, he's not well enough to travel and asset me with Toby, so Iv taken Larissa this time, she's our pac mule. 

We have carry on bags, we have toby in his chair, we have drinks, the laptop, iPads, I phones, handbags, the list goes on, and somehow we have to carry all this, plus Toby up into the waiting plane, balance Toby precariously over my shoulder in a Fireman’s like carry, while I hand over our boarding passes.  No one help you, they wouldn't dare, for they might get sued if something goes wrong,  don’t get me wrong they do mean well but they don’t actually help, This time we are getting the lift to the top of the stairs, but I still have to carry Toby, he’s too floppy to get into the aisle chair that they airlines have. we have booked a upper torso harness this flight although I needn't bother as it wont really hold him in place,  nothing really holds him, but Ill sit him between myself and Larissa and well squash him in. Well support him up the whole 2 hour flight to Sydney, then be the last to disembark, waiting in the heat, hoping with everything that they will have his wheelchair waiting at the gate for him. hoping it hasn't been lost. 

Travel has become harder, It involves, making sure we all have enough medication, making sure we have batteries and chargers for Tobys hearing aids, he is tube fed too so that includes tubes and feeds to take to keep him nourished, this trip we are staying for a week and Toby is on a blended diet that means that we blend real food up into an oblivion and then push that through his gastrostomy, so Today we have a blender packed in out bags, just incase there isn't one at the school we are staying at. 

Toby needs his nappies and snacks and oh we must take his PODD book, his words… next trip Im guessing well be taking his Eye gaze computer too. it never ends. we could fill a trailer full if we could carry it. oh in fact we are taking a trailer on our next trip,  but its loaded full of camping gear and will be u much more enjoyable trip than this. 

Flying with a special needs child is hard,  Flying with any child is hard,  but one that cant walk, cant talk, cant sit… its so draining. but its worth it. when we get to Sydney we have lots in store for Toby, lots of assessments this trip, we are visiting the RIDBC, the Royal Institute for the Deaf and Blind Children for Toby to undertake a series of assessments, so that the school can assertion exactly where he is at with his learning, and the best ways to get the most of him. We are hoping for big things, we are hoping that the eye gaze computer that is coming will assist with this, but we are really looking for his motivators and how best to help him move forward. Im also looking forward to the heat of Sydney, most people dont like the stifling heat but love it, it makes my back feel so much better, I an move more freely and I feel so much happier.  bring on the learning and the warm weather,  stay in touch, to see how we go…..

heartbreak

About 2 weeks ago we were having a battle with Toby not wanting to wear his Cochlear Implant Processors, we thought that is was due to that fact that we have to tape them to his hear, and double sided tape to his ears. we thought it was because the tape pulled, and we were trying to think of ways to help him, but really the only way to hold them on his ears is to tape them there. But one of my special Face Book Friends (a mother of an older child with severe CP) suggested that we actually ask Toby why he didn't want to wear them. Duh!  why didn't we thing of that. 

So we pulled out his special PODD communication book, and asked him why? expecting to know the answer we were both shocked and completely heartbroken to hear him say that he didn't want to ware them because they made him different. wow, how do you handle that? 

For the first time ever Toby had expressed sadness due to his disabilities. I knew that it was coming, I knew that one day we would have to deal with it, I just wished that one day was a long way off. To hear this from Toby, brought about our sadness for him and stirred up many suppresses emotions, grief for all the things that Toby would never be able to do, for all the dream that have had to be altered or forgotten as his abilities differ so much to our dreams and hopes for our son. 

To hear that at just 5, he was starting to understand that he is different and to start to reject that was just heartbreaking. 

Immediately we knew that we were our of our depth, we sought help with a social worker with the RIDBC, (Royal, Institute of Deaf & Blind Children) in Sydney, and I have a very informative session with the psychologist. who deals with non verbal children all the time. she explained that although it was a sore spot for Toby that we  had to make him put on his cochlear implant processors just like we would make him brush his teeth, we had to make it, a NO option subject, as if we give him an option he will be loosing valuable hearing time and could develop tinnitus due to the hearing nerve trying to search for sound.  

Kent and I didn't like the idea of pushing him to do something he didn't wish to do, as Toby is such an easy going boy and doesn't normally make a fuss. We have been working so hard to give him a voice, that we didn't like that we would be taking it away form him by forcing him to wear him processors against his will.  now we have such a tough decision, 

He does not complain, he does not wish to run, to play rough & tumble with the other boys, he never gets upset over his lack of ability to do the tasks that we all take for granted,  he very rarely even gets frustrated,  so for us to ignore this reaction is a very tall task.  Although for the greater good, maybe, he just doesn't want to hear? It is interesting that, with all his differences, and all his disabilities, that he has chosen this… his hearing to be the first upsetting factor.  it is probably one of the only ones that we can actually fix for him! 

Kent and I thought that we needed more guidance regarding this, and upon discussion which his school, they too could use more guidance upon Tobys actual condition and different ways to help get the best out of him. so we have decided a visit to the RIDB centre in Sydney would be worth while. we video conference with a speech therapist from there once a week for a therapy session, but a Trip to the centre would provide a full assessment, including medical, physiotherapy, speech therapy, occupational therapy, ophthalmological assessment, and psychological assessment. it could give us a good map for the next few moths to help lay good foundations for early next year in prep and beyond. This trip is a must.   So next week we will be bound for Sydney, to help us answer some uninsured questions and to help us deal with the many hard days with Toby to come, as he learns to accept his different abilities and the many differences between himself and his class mates. heartbreaking as it is, we are thankful that we have the help of a fully prepared team, who are there just to help us as we need. despite a few teething issues, they are all there to help us on this journey. Without them we would be lost.  

exciting times

Coming up to christmas our little family prepare for a BIG holiday. In a little over 4 weeks we will be embarking on the holiday of our dreams. For a very long time Kent and I have dreamed of travelling and camping our way around our beautiful country. we dreamed of long trips, and just pulling over to camp wherever we felt we wanted or wherever looked nice. we dreamt of long walks along beaches and refreshing splashes in little picturesque water holes. Originally our dream would be to take a few months off and just wander whoever our hearts took us. As time passed this dream has been broken down and when Kent was diagnosed with cancer it was put on hold and almost forgotten about. 

But we have decided to do it. My sister who lives in Darwin is travelling to Queensland for christmas to spend it with her partners family, and we decided, on a whim, to kick up our heels and just do it, we are going to meet her and her family in Queensland for Christmas. The kids Finnish school and then we are out of here. We jump on the Spirit of Tasmania for a day sail in on the 20th december, and then, camping our way up, we have just 3 days to get to Queensland, as we have planned to spend christmas eve at the fun parks, and to camp, with my sister, christmas Day. 

Its going to be tough, we have little money and both Kent and I suffer form chronic pain, and Toby doesn't sit well for long periods in a car seat. However, we are going to give it out best shot, well stop when we need and drive when we can. Our Plan is to call into Summer Bay (Palm Beach) so the kids can see where Home and Away is cast. and go for a swim on the beautiful beach.  just some great photo opportunities and something special to do. other than that we have no plans. Just driving, Camping and Family time. and I just can not wait for this. 

Our trip will see us spending christmas in QLD with my twin sister and her beautiful family, and on boxing day, I will fly back to Tasmania with my 3 other children, bringing them back to spend time with their father, and I attending, my best friends wedding before jumping back on the plane to meet Kent and Toby at Rockhampton.  There we will spend a night with my cousin on her beautiful property, before heading on the Townsvill, travelling and camping with my sister.  before breaking apart and leaving just Kent Toby, and myself to find our way back,  Kent, Toby and I have around 3 weeks to get home, and not plans as to how we will do it.  WOW, 

I just can't wait, we are thinking that we will head back through the center to South Australia and then back along the great ocean road before boarding the Spirit of Tas to come home again.   Talk about the holiday of the life time.  I am so looking forward to early morning sun rises, splashes in the ocean, the smell of salt air, as well as the heat of the sun as it lashes the harsh terrain of outback Australia. the many animals that we will see, the many flora that we will smell. I cant wait to teach Toby and the others all the Real things in life. all the beauty that there is in our world.  I cant wait to take our time to do whatever takes our fancy that day. I cant wait to do the fun parks and to see the wonder and excitement on my children's faces, oh man, I just cant wait. I feel so very blessed to have this opportunity. To have the time to spend together as a family, to have the option to complete a long awaited dream of ours. the memories that we will make, will stay with us for a lifetime. I am so very thankful that myself and the children will remember this holiday with Kent well past the day that he is no longer with us. This is our chance to make memorise. our chance to be family our chance to explore our amazing country, 

Just cant wait!!!

So where are we now?…..

Toby has been attending Kindergarten at our local mainstream school, and he has been accepted as just another child. The school have been amazing at including him, and both his teacher and teachers aids are amazing, they work tirelessly to ensure Toby doesn't miss out on a thing. 

Toby is bound to his wheelchair. he can not sit without the special support that it provides. Toby can not stand, walk, or even talk. however he does not miss out. His cognition is amazing and he understands everything that is going on. he is like a little sponge, absorbing all the information, but he has trouble getting it out. being non verbal, he uses a special book to communicate, but that is all about to change. Thanks to a very special man we were able to purchase him an eye gaze computer. at a cost of around $20,000 it was way outside our reach, but Ian decided to help us, a organised a fundraising marathon. He ran 42km and raised all the money needed to purchase this special computer. It has now been ordered and we are anxiously awaiting its arrival.  Toby will be able to use this computer with his eyes. in the coming weeks he will learn how to use it and how to make it talk for him, as it will have special software on it that he can use for a voice. just like his special book he has now, but he will be able to use it independently, and for us that is a huge thing, all we ever wish for, for Toby is to be as independent as he can. and personally I hated his special book. Although it has given him a voice, he has always needed to rely on someone else to turn the pages.  Now   with this special computer system, for the first time, Toby will be able to communicate on his own. That is so empowering.  Amazing,  and we will be forever grateful for Ian and all of those who helped to fundraise the money. 

Those that know Toby, know that he is a cheeky boy with a wonderful sense of humour and despite all of his obstacles he has never let anything get in his way. Inside he is a typical 5 year old, he loves to play with his friends and at school, he has lots of “girlfriends”. the girls like to play dress ups with him. Toby can count, and he can spell his name. he just does things differently to the other children. His Teacher aid is great as she assists him in every way, including in play. But the children, they are amazing. Times have truly changed, Toby is a star in his class, and nobody sees his wheelchair. They talk with him though his book, and the girls love to help him thought his morning routine of unpacking his bag and putting his drink bottle away. They help him choose his name to put on the board and they share there weekend stories with him, just as they would a typical child. Toby just “fits” into his class and the school. 

He is learning how to use his powered wheelchair, he has a head switch that enables him to use it independently. He is greatly encouraged on by his little friends at school, who are all amazed by his technology, and are eager to help Toby in any way they can. 

Earlier this year our resolve was tested again, as minor back surgery went wrong for me, casting me back into the world of pain and subsequently onto workers compensation again. deemed unfit to return to work, I was lucky enough to be able to negotiate an agreement with my new employer that allowed me to have 6 months leave to hopefully sort out my back issues, so I can return to work.  

In some cruel twist of fate, It was fortunate that I have this time off work as not too long after, we discovered that Kent’s cancer had spread to his bones, he had to have a partial hip replacement as the cancer had eaten away the top of his femur, The surgeon, a friend of ours promised that he cut and scraped away as much of the cancer he could, and he must have done the job as just last week after an intensive review we got the all clear of cancer in his bones. However the cancer in his lungs, continues to grow, and he will need more chemotherapy early in the new year. 

Kent still battles with lots of pain from his surgery, scar tissue is causing him a lot of concern, but his doctors are fantastic and are on to it with providing lots of pain relive medication. Despite his pain, we continue to try to live a normal life. As normal as we can anyway, fitting in as much as we can but also allowing for rest time. Me with my crappy back, fighting depression and Kent with his crappy lungs and bung hip, & Toby in his wheelchair, we must be sight to see walking up the street, hobbling, limping, and wheeling away. but we get on with it. Thats what makes us special. despite adversity, together we make it. and our love has never waned. Together we can fight any battle. 

Oh and we are whole again, my family is complete, Larissa has come home to live and I couldn't be happier. All of my children are amazing, all of them have had to deal with so much more than most adults, and yet they still stand. Love keeps us together, Love keeps us strong. Together we are Family!

SO now you are all just about up to date. 

I have  given you the short version, 

Mental Health

Chemotherapy continued for a few months, and Kent became unwell from the treatment, initially it wasn't too bad, a few aches and pains but after a few doses he was becoming really sick, Ill never forget the day he couldn't get out of bed, in all my years of knowing him Iv never seen him so sick, it was scary, he was so weak he struggled to get to the toilet. These days were not fun but we managed through, with the help of our families, we were living with my family, up stairs in my old family home, and although we needed the help and have so much appreciation for my parents for taking us in, my nerves were fried, I struggled with every day. 

Personally I was suffering with depression well before Kent’s diagnosis, with a long standing workplace back injury I had struggled with the time I had taken off work and the different treatments for my injury, I was a mess before that horrid Christmas, in fact that christmas day was marred with my moodiness and scars that I am sure I have left on my family by my behaviour, Suffering from depression and severe anxiety, but trying to hide it as I felt ashamed, I was so ashamed already at being off work on workers compensation that I didn't want to admit to myself or to anyone else that I had depression too.  I was angry that I had a back injury I was angry that I had constant pain and I was angry that I couldn't work the career that I loved and worked so hard to get to where I was.  I was severely depressed and about to seek help but once we got Kent’s diagnosis I pushed it all behind me. I needed to help him, and he needed me. he needed me to be strong, so some how, I have no idea how, but I pulled myself together and just got on with it, I did whatever I needed to do to keep us afloat, those months went by in a blur, and so I wont go into too much detail, mainly because I cant remember most of it, I think Iv blocked it out. But once Kent’s Chemo was finished, and all treatment had been given, everything stopped & we had to just wait for a while, just wait to see what happened next.  I didn't do well with that, My world came spiralling down, I burned out. The depression came rushing back to me hitting me with full force, however this time I sought help. I remember not knowing how ask, I felt ashamed that my husband was fighting so hard to stay alive, he wanted to live so much yet every inch of my body I just wanted to throw away, I didn't want to be here, I didn't want to be living through this, how do I explain to someone who is doing everything possible to survive that I didn't want to?  So I sat down, and wrote a letter to my husband, & to my doctor, as I knew that I didn't have it in me to say the words out loud, I handed the letter to him with shaking hands, not knowing what to expect, I just felt ashamed. 

I needn't have, he held me close, he comforted me, he understood.  and together we went to the hospital. I admitted myself to a private clinic so that I could get the help I needed to keep going. For a while I had to hand over control, I had admitted defeat, I was in a bad place. 

I spent several weeks in the hospital, recovering, and learning ways to control my anxiety and my fears of the future. but I really just needed the time out, that was what my mind craved, time to just shut down and press the restart button. During this time, I pushed people away, I alienated some of my family members, and I hated myself for this, at the time I needed them the most, I pushed them away. and to this day, the damage has been done, and is seemingly irreparable. I have to live with that. and for now that is ok. 

A period of shut down time was just what I needed. I was suppose to be learning ways to control my anxiety, learning self awareness, and enduring Cognitive Based Therapy. however I don't do well with quietness, I don't do, “self awareness”, I just needed time out. 

Im not even sure I felt better when I came out,  I was semi refreshed, recharged and ready to continue fighting. but feeling better within myself? I don't think so.  That was over 12 months ago now and I still suffer with this horrible depression, every day is a battle for me, every day I get up I put on a mask, and I pretend that it is all ok. I hide my thoughts, keep them locked away during the day only for them to come flooding back with a vengeance at night, but at least I can get through the days. I still have the strength to get up each day, I just manage my way through, any way I can. whatever it takes to get though. I keep telling myself I am ok. so for now I am OK