Design a site like this with WordPress.com
Get started

Winter End Garden Tour

I have shared about myself and what my life has been like over the past few months living with CPTSD. It seems to me writing here assists me so much. Seeing my thoughts/activities/feelings in print help me see how far I have come in my life with this illness. Learning to live my life accepting how I move through each day no matter how and what is happening in my life and life around me. I am proud of myself that I keep moving forward no matter how minuscule it may be.

Lets look at what is happening in the garden. Here in the Southern Hemisphere we being our Spring Season very soon; the problem tends to be I along with many others feel the days lengthen and see the weeds growing all the new growth everywhere. I feel the urge to sow seeds. I have to hold myself back and wait wait.. which I have been doing, today I intend to plant a few in pots to germinate in side.

Lets go for a walk around my gardens in the last few days of the yearly Winter season.

I feel like I have done very little during winter, yet when I review the photos I have been doing small things. On top of this each day I walk around and pull weeds out of the paddock area.
We have had a very wet few weeks very wet. This has made it more difficult to continue to clear around the fruit trees as the ground is too wet.

The joy of my garden and the hope that I will get seeds in and growing for my own vegetables and food. Rain and colder days are on the agenda for a few more days.

The chooks ahh the chooks sadly I have three roosters, and only five girls. Rupert has been amazing with the chicks but they have all grown up now and I have to attend to reducing the number of roosters, as they will be to much and to mean for the few girls I have. Sadly only one of the female chicks have survived to now. I also lost one of my original hens one of the brown girls. Penny I am not holding out any hope that she is nesting anywhere. My neighbours have also got new hens, and both my neighbour and I have noted that a Sea Eagle has been flying around everyday. This may be part of why my hens have disappeared along with one of the rooster chicks (perhaps not so bad one less for me to attend).

I have been taking my vitamin D as down here we have such low levels of sun over this time of year it is a necessity. It also helps with mood and lessening seasonal affective disorder. (SAD)

It is great to wake up each day, to see how beautiful my garden is looking. I am so thankful to have such a great area to create my space.

I am thankful to those of you who read my posts, blessings to You all. Tazzie

All things beginning with C.

I think it is Tuesday March 17th, just checked and it is. it is 13:20 on a stunning Autumn day in the Huon Valley my home region in Tasmania. I have taken a while to get a sense of what happened recently the after affects impaired me and I felt no desire to do or be anywhere, to be with anyone, just being with my dogs, chooks and at home is the recovery and medicine I have required. It has taken time, and a lot of management strategies to not sink towards the black hole, it would have been so easy. I work constantly at not going back.

I moved on from beating myself up and began to consider what a really good person I am. Compassionate, to empathetic and kind. Would I change myself NO. No I am me, and I honestly do like me more and more. I am so very very fortunate to be able to be totally myself and still part of such an incredible community. I sigh as I write and know that I am so very very fortunate. I m safe here. What an incredible gift that is.

I look at the horse tail wispy clouds with the blue sky listening to the hum of bees, and flies, the chug of a Aquaculture vessel coming up the river and feel the sun beating on my legs as I watch cabbage moths trying to find unprotected brassicas to lay her eggs on. My dogs are chewing bones near bye. I am aware of the European wasp that has invaded Tassie. As it will seek out any meat left outside as too flies. I know that is why the blowies (blow flies) are zooming about Miss Treacle as she is eating hers. Busby’s is all gone.

A wattle bird just let out a call that is hard to describe and was answered by another. This morning I have let out the chicks and Frida Kahol too free range in the chook run with everyone else. She is an incredible Mamma, I am a bit fearful as I lost two chicks in one fowl swoop to a grey Goshawk two weeks ago. The decision was made by Frida as I had put a fence (I use it on the deck to keep the wallabies off it at night) around their chick house. I had let them out and was tending to the other hens and Roopert when I heard much distressed chirping Frida Kahol had flown the coop! The smallest of the chicks, a bantam I feel as it is a great deal tinier than the others, had managed to get through the bars but the other six chicks were not able to follow their Mamma.

I had to remove the fence and allow nature and Frida to take their chances with the remaining seven chicks. I have noticed that Henny (the darker of my two brown hens her sister is Penny) is broody and I am working hard to ensure that I do not have more chicks this season.

I have also it seems been able to keep all the poultry in the run. I do miss seeing them outside in the paddock, I do not miss the digging up of plants and seeds, and dust bathing hollows they leave in my garden and paddock where I can stumble into them unwittingly.

It is green looking over the river and at parts of my paddock grass, yet here on this side of the river we have had little rain compared to across the river. It is very surreal to be sitting here in March with almost full rain water tanks (from a couple of weeks ago) and green grass. It is normally dry and I ponder if I need to consider buying water.

Am I repeating myself. Maybe its Ok, Pretty normal for me after being triggered.

Life has not stood still even with the emotions and dealing with the aftermath of being triggered. I have shared previously that I have been waiting on being notified of when I will be having a colonoscopy, unlike the USA in Australia you do not automatically have one on turning 50. Here it is only if there is a concern. I was listed in the highest priority case due to symptoms. I had not heard anything and the timeline I should have heard had passed.
There are some things having been an RN helps with, and that is feeling able to contact the appropriate department to inquire. So last week I did phone them to discover my file was in a drawer, and who knows if I had not called when I might have heard. (off course my mind has taken me to dying with colon cancer and all that goes with it in the months I have been waiting). Knowing that Australia has one of the highest rates of colon cancer in the world does not help. Early diagnosis is the best help to survival.
I rang and was rung back the next day first thing in the morning. I am booked in soon. I have recieved all the instructions in the mail, and I feel that the actual preparation will be far worse than the procedure, having worked in colonoscopy as a casual RN I am very aware of what occurs and I am not too concerned about the procedure. My only concerns were with what to do with my dogs.

The thing that is extremely difficult for me with my CPTSD is actually telling people in the first place and then asking for someone to assist me in anyway. I find it almost impossible to ask for help.
At first I thought right I can not bare the thought of telling anyone, and I can not bare the thought of being away from my dogs. I wanted to drive myself there and back both things not supported by the hospital or I imagine my insurance. So I considered a dog friendly B and B for two nights. (My hospital wants you to be with someone overnight after the procedure, as its policy). That is not going to happen. I am not having a general anesthetic, it is a twilight one. While it is not safe enough to drive myself home, I do not need anyone with me overnight.
I did share with someone who has kindly offered to drive me and bring me home. The appointment is made and I will be away from home less than 6 hours all up (proviso that all goes well). My dogs are quite content to be at home as long as they have had a run and used their bowels. So I put logic and fugal me in charge and will be home before and after the procedure.

I am now aware of how much distress was on me with not having any acknowledgement other than the letter advising me I was highest priority a date range that had past and me taking the bull by the horns and following up.
I am so pleased I found the courage to do that. If anyone in Australia is in a similar situation contact the Endoscopy unit and ask them when your procedure will be please.

I have also been accepted for the National Disability Scheme (NDIS), and have a meeting with someone from their in the near future to see what I might need. As my mental illness/s has seen me accepted on the Disability Support Pension (DSP) it means that I can request my psychology appointments be on the NDIS, and that means my Psychologist can bulk bill me. I am not sure how she has been charging me before this, as I have paid nothing to see this wonderful woman.
The veggie garden is doing OK my tomatoes the few I have picked have been delicious, I noted this morning something has taken two green tomatoes and pecked them I am blaming the blackbirds or starlings. I have pumpkins, and a couple of zucchinis. My peppers are fruiting but will they ripen before the cold sets in? Not a cucumber or tomatillo has appeared. I have at some stage to pull up the sweet potatoes. I hold no hope for any this year. I will cut some slips for next year. I have not emptied my last pot of potatoes as they have not flowered yet.
It has been a better year this year for veggies than last year and I learn as I go. I am averaging 3 eggs a day. I will be winter glassing a lot of eggs. To provide me with eggs during the off season. I do not want to burn my girls out with keeping them laying or year. As hens only have as many eggs in their systems as they will lay over the course of their life.

I have not showered in way too long, and will be soon, I have been eating a bit better, and generally getting to bed early. Dogs are walking I am driving. Right now I am really just focusing on the things I need to do for next period of time and as too diet I have to follow instructions nearly every thing I actually eat is not on my menu for next period of time. Clear broths, clear juices, I have minimised my coffee in take already. I have noticed that the preparation fluid for the colonoscopy has aspartame in it sigh I really dislike any artificially sweeteners, but I have no choice. Thankfully I can take my medication.

While I know I am anxious about what is still to occur and the results. Just knowing the date and time it is going to happen is a relief.

blessings to You, Tazzie.


When you really go backwards.

May be triggering and language some may find offensive. Please do not share or use any of the following without consent of Echidna Home. (C)

Living with a mental illness such as Complex Post Traumatic Stress Disorder is so shit at times. I have been moseying along living life in way that has been good. I was out for a day with a friend on Saturday all day and it was really lovely we went to a town further a field. I was so exhausted afterwards. I have to say being with her is quite relaxing as their is nothing like being with someone who really understands what having a mental illness is like. We shared a lot it was really interesting, though at one point she mentioned that she often felt suicidal. This just blew me away, we talked and shared (as we both have had too many people we know and love succeed in suicide. )

Yesterday Sunday (it is a long weekend here in Tasmania). I was just at home and perhaps just switched totally off I am not sure even what I did. Yet I woke feeling good.

I needed to go and get some chook food so drove int Huonville. I did the little bit of shopping I needed too, and stopped for a bite to eat and coffee at one of my faviourite cafes. Sitting in the lane with my dogs, a small disagreement with another dog, sorted and my dogs under the table. His dog near his and all fine. Thy moved the dog and it blocked the access for the staff to bring drinks and food out. One staff member spilled coffee another almost dropped a dish, then the dog jumped up and tried to take food from a plate a staff member was bringing to another table.
These people made no effort to move the dog, they never apologised to the staff. I suggested they move the dog form between the stairs and table, they saw no problem.. I was triggered and ended up just loosing it. I could not believe anyone would put anyone else at such risk to conducting their work. I even said it was a health and saftey issue. They just laughed at me and my escalation telling me I should leave. Of course I responded and it went on..I just could not shut up and fucking was used by me numerous times it seems to go with the course. Then one of these people said in a loud voice that I had obviously missed my medication as I was crazy. Well that was just the final trigger. Mocking mental health! I just kept on at her. I was shaking and crying red in the face.

When they were leaving after a very uncomfortable silence had settled whilst some of them finished their food.

It was ugly and horrible and I feel so ashamed, I lost it completely I was so so disappointed as I have not had anything like this occur in over a year. Sigh. I know I know I have a mental illness. I get triggered and when I am triggered I say fucking a lot. Positive is I will be speaking to my psychologist later on this week.

I feel so ill and so tired from all this. I hate this illness. Not being in control and all the work and effort is so tiring so all consuming. I feel I am growing I know I am moving forward I know all this. Yet an experience like this is just frustrating and now takes so much work to not let my self loathing feelings of shame and disillusionment and all those delights that come after such an episodes.

For me where I am now right now is that I do still have insight, I still know that I am so much better than I have been. I am still moving forward. I know I am improving and this is just a small set back.

It taught me that there are some truly wonderful people out there who when someone with a mental illness is falling a part I had someone who stood bye me and cared. For this I am so very thankful.

blessings to You, Tazzie

Living with CPTSD

Wondering sometimes if sharing so much of my own life and experience with this mental illness can cause some anxiety.
I ponder often if I just kept living my life in private would I be better off.

My answer is a resounding No.

I have not posted for a while and that is partly due to life, and more to do with not being so well. As for many people the holiday period can be unsettling. Yet mine personal experience has been more about what I have been hiding from myself.
I missed the time with people I care about and love, those I have welcomed into my life not necessarily those by birth. I do not celebrate ‘Christmas” the church holiday, nor am I a big fan of the commercialised concept.

After gorging on almost 3.5kg of Toblerone (darn supermarket had the huge huge blocks so cheap)plus a whole lot of other highly processed food. Over a couple of weeks, I realised I was not well. Yes physically but also mentally.

I had been with people on boxing day (26/12/2020) and it was really lovely.
Yet I had a dark area forming in my moods. I began to sink slowly not wanting to be but not really being able to stop. Feed my face feel angry, eat more, feel upset, eat more, yet no comfort did I feel from my emotional eating.

I feel my psychologist was aware that I might have been heading for a bit of a backstep. In combination with COvid and all the lockdowns seeing an increase in mental unwellness our Federal Government increased the number of visits to a psychologist/psychiatrist/counsellor you could have to 20 a year. Prior to this it was 6 having over the past few years gone from being 12 to 6. So I am seeing my psychologist more often.

Shortly into the new year I had my first appointment. I really did not want to do a zoom, or talk to her. In the morning as the approaching time came my neck began to itch unbearably. As our meeting began, it became to so extreme I could not talk all I could do was rub my neck, jawline and cheeks. I had welts and rash from this, and it just was so intensely and utterly uncontrollable I just had to scratch. She offered to reschedule but I knew I wanted, to no needed to talk about what ever this was.

As I began to talk I just let the words come and what I discovered was I really wanted to have people over, to decorate my home for Yuletide(even though here it is summer). I wanted to celebrate the season, to share in what is in the northern hemisphere the returning of the sun and longer days. (Maybe I need to look at celebrating it in winter down here..lol ). Now we can not celebrate sitting around a fire (total fire ban) and daylight goes until nearly 10pm. But..the idea of just being a group and yes of women friends. Sitting sharing and talking about their passions. Being thankful for all we have.

As I really thought about it, the itchy remained and I was scratching and rubbing. Very aware of it, but also of the feeling or overwhelming sadness. tears rolled down my face as I began to have memories of wonderful times at my grandparents home. 40dC/104dF the combustion (wood fired stove) going cooking Christmas lunch in a tiny 2 bedroom fibro house with 9 people inside around the fan and a water filled air conditioner.
It was not just about being with my grandparents. It was something more. It was not perfect. It was simple it was hard work for my grandmother and mother.
I think it was that my Grandparents had decorated their tiny home with so much delight. There was a real feeling of wonder.
Perhaps that is just a simplistic childlike memory of a better time in my childhood. Yet it is a deep memory that has come out and changed me.

It was not instantly. I did not toss or give away the remaining highly processed food, nor get immediately back on my routine. (Yes I was totally off every aspect of my routine). Are you sick of my routine yet?

I have been kind to myself. I have not punished myself, or done the negative self talk as much as possible. I have sat with the feelings, working through them now rather than emotionally eating in an attempt to keep what ever my mind and body needed me to get out. As small and simple as this new knowledge been to me as I worked through all that was happening internally and externally, yes the hives continued for a week even with anithistamines. I now know more about what I need for myself.

Pushing myself to talk and work through the incredible discomfort of this as with so many other times on my path towards managing and maybe healing my mental illness. Is hard, intense, extraordinarily emotional and confronting at times yet worth it. For me my life now is about living my best life. MY LIFE.

What my CPTSD has taught me so far is that as a child my brain was so incredible at creating ways to keep me safe and living by just pushing all the screwed up shit that was my childhood so often deep inside me. I lived two lives the one at home an the one at school, the one where I tried to make friends, to be a friend yet even as a small child I was filled with rage and anger at what had been done and was being done to me.

Finally I am really aware that I love being alive. Even on my really bad days. I love that I am moving through so much that has happened in my lifetime, but especially in my childhood and adolescence. As hard as draining and scary sometimes letting these hidden experiences feelings and emotions out is, the understanding that each time this happens is a step forward for me to BE ME. As corny as that sounds.

So yes I will keep sharing my personal journey. My life. Its warts and all that happens. I am currently a mature aged woman who has Complex Post Traumatic Stress Disorder, who is not so afraid of the blackness as I was because I am learning that the blackness is all my trauma, all my fears, known and unknown. That part of my healing is working bloody hard to accept and let these fears,and emotions of my life experiences out. To just burp the bottle a bit at a time. Not every appointment with my psychologist is such. However for me it is the time after where I really develop understanding and can really explore what has happened in the appointment are where the biggest shifts in my life are. Where the new strength is and where my adult self is able to speak up. Say and do what I want not just need to live my life as I chose.

The other reason I keep sharing the good the bad and the unwell, is that not so many years ago the word Cancer was never said, then it was whispered about if someone had it as if it might be contagious. Well I see similarities with mental illness. As statistics say
•Mental illness is very common. One in five (20%) Australians aged 16-85 experience a mental illness in any year. The most common mental illnesses are depressive, anxiety and substance use disorder. These three types of mental illnesses often occur in combination. For example, a person with an anxiety disorder could also develop depression, or a person with depression might misuse alcohol or other drugs, in an effort to self-medicate. Of the 20% of Australians with a mental illness in any one year, 11.5% have one disorder and 8.5% have two or more disorders. Almost half (45%) Australians will experience a mental illness in their lifetime
. Australian Bureau of Statistics. (2009). National Survey of Mental Health and Wellbeing: Summary of Results, 4326.0, 2007. ABS: Canberra

By Rubina Kapil on February 6, 2019

Mental health and substance use challenges can take many forms. There’s depression, anxiety, schizophrenia, addiction and the list goes on. Some of these challenges are more visible and you might recognize them immediately. Others can be harder to see when you’re not looking for them. But, they are still there.

These statistics provide a look at how many people face a mental health or substance use challenge, whether we see it or not:

  1. In the United States, almost half of adults (46.4 percent) will experience a mental illness during their lifetime.
  2. 5 percent of adults (18 or older) experience a mental illness in any one year, equivalent to 43.8 million people.
  3. Of adults in the United States with any mental disorder in a one-year period, 14.4 percent have one disorder, 5.8 percent have two disorders and 6 percent have three or more.
  4. Half of all mental disorders begin by age 14 and three-quarters by age 24.
  5. In the United States, only 41 percent of the people who had a mental disorder in the past year received professional health care or other services.


So when you look at these figures my personal feelings are we need to be talking openly and honestly about our illnesses. This brings more understanding to others going through it, to family and friends of people who are dealing with CPTSD and PTSD. It makes the politicians more aware of the impacts on work experiences, prejudices of some employers, how difficult life really is, costs to individuals and families emotionally financially, more one on one services and packages for those of us unable to afford access to psychologists and psychiatrists. It may help to reduce suicide. Family issues. Our own issues. Employers/businesses will really understand why we might behave or respond in situations. Also Schools may begin to realise that so much of how and what they encourage as ‘normal’ is really not for everyone.



It may also help those younger folk who are not ‘fitting in’ to what society says is ‘normal life’ If I had known for me living out of town and not having heaps of social activities and lots of friends was perfectly normal and OK for me at a much younger age it may have been helpful.

blessings to You, Tazzie




Reality of Living with CPTSD Complex Post Traumatic Stress Disorder and unexpected reaction.

Having a mental illness of any kind is so frustrating and hard at times. Even when as I have been feeling really well, and yes I would still say that I am pretty well in the mental states compared to where I have been even now. Yet this does not stop being hit hard, knowing that I need to fight with every tool I have learnt and utilised in my treatment of CPTSD management too remain moving forward no matter how miniscule that move is.

I am waiting for a colonoscopy. Here in Australia you will only have you have symptoms that may be indicative of problems or potential cancer concerns in your colon. I have been listed as a priority. Which means my symptoms are concerning enough that I need to be seen within a fast time frame. I have a friend who was told needed a colonoscopy. My friend has been placed on a lower level of priority and has up to 12 months to be on the waiting list. (It may be sooner it could be longer). Depending on lists and what happens to my friend’s symptoms.

I was a Registered Nurse and no that the majority of colonoscopies are benign. Yet even with this knowledge for me with my anxiety my mind catastrophises. Of course it will be bad, I am going to die.

I mention this as the trigger for my mental health decline. I have again resorted to sitting on the lounge, and eating comfort food. I have huge insight into this as being a starting point to heading towards the darkness and am struggling but fighting it. My house is going backwards, I have been driving my car and the dogs run ahead. Instead of walking them. All my normal reactions to things I can not handle. I am trying not to think about what is ahead. So loose myself in Youtube and games. All normal for my mental health illness. All symptoms of my illness flaring up.

I look about the house, garden and routine and am very aware that I am not following my routine. Which for anyone who has not read previous posts is pretty simple. Walk my dogs everyday. Have a shower every two days. Go to bed lights out 22:30. Do one thing in the house to improve it every day. Eat healthy. Be thankful.
nothing extreme in that list. Yet for me it is as if I am attempting to climb Mt Everest every day without oxygen.
How do you explain that to anyone who does not understand? Fortunately I do not have to explain it to anyone else. I no longer have to work due to my mental illness.

Yet this morning I woke after going to bed bye 22:30 and up after a good sleep, though I am sleep well most of the time. Once the dogs rose, I went and let out the chooks.

I decided to walk the dogs. I don’t walk them miles it is just up the road and back about 1km or a bit less. We did this, and as usual I felt so much better for doing it.
My well mind says this is so easy and has such benefit for you Tazzie. Then I hear other voices of my past and have to fight them. The berating of parents and teachers the pressure when I could not do what they expected. When I am unwell it is these voices and memories I struggle with. Along with if you lost weight you would be so pretty.. and you are lazy, you never finish anything, you are a slob, you don’t care, why cant you be more like your siblings if you had been the first there would have been no other children in this family, you were a lot of trouble before you were born and still are. I become their expectations. I hated myself and never felt a part or accepted. (that is a whole other story).
Even as I type these words, I have tears for the smaller me and for Who did defend herself and was beaten viciously and punished.

When I reread these words above I realise that I am falling under the battery of abusive demeaning words that were the background of my childhood. Along with other physical abuses. I continue to work constantly daily to let go of these and know that these words no longer have power over me. So it is hard to realise for last month or two this is playing over in my head again, “see you got what you deserved..you are all these things”. So subliminally along with the fear of what if I have cancer, no one for support, I am all alone (which is not fact) but reality and logic kind of go out the window here. Fear and tapes in my head are so detrimental and the response to withdraw and comfort eat, is my treatment.

Filling in the hospital paperwork, next of Kin? I do not have any next of Kin that I want contacted. I do not want anyone to know not because I am ashamed or embarrassed just because I do not. Privacy is important to me. I have told one or two people and here that is enough. Then who is going to pick me up and be present in my home overnight post the colonoscopy? Well I was going to drive myself but know that I can not rationally. (Thankfully a friend has offered to take me and bring me home.) No one will be with overnight. As No One comes inside my home.

These are things I believe that hospitals just do not understand. So I will probably be less than truthful about filling this in if I am not allowed to leave it blank. This is part of my mental illness that is difficult for even hospital administration to understand.

Just sharing this here, writing it all down has always assisted me to really see how my illness is the cause of my reactions and responses.

I have forgiven all the people (mostly family members) for the way I was treated and abused. Not for them and they are not aware of this fact. It was only ever for me. As I hated the anger that accompanied the tears and frustration of my triggers. The triggers still happen as I have documented and no matter where I am on being able to manage my responses to them. It is only with insight that I can process accept and move forward.

So my personal treatment plant of withdrawing and comfort eating, being aware that my routine is slipping but not gone are all OK and acceptable. I have not failed I have not fallen back into the deep hole I have been climbing out of. I have loved and soothed myself in perhaps not the best way, yet every day I have had insight and awareness that it will be OK, and I will be able to get back into the garden and connect again in ways that help me as seen by writing here again. Living with a mental illness is an ongoing thing.
Like being a diabetic if I can stick with my life time treatment plan medication, routine and utilising my management tools I will be living a great life for me. I know this from when I am even better than I am right now. It is worth it and for anyone who is finding the best medication, the psychologist, what works for them as an individual to live the life you want and no one else’s. It is a lot of effort and there will be I am sorry to say periods where you are not doing as well as you have.
You will have gained insight and know that you are unwell due to your illness and triggers, through no fault of your own. You will be able to move forward and live the life you want.

I have struggled for too many years attempting to fit into family, school, work, and community. Where I am accepted as I am is my community and when I go out into it when I choose is wonderful. When I withdraw they generally understand. I have people who check in on me, and wonderful unobtrusive neighbours.

I like who I am and am very proud of who I am. I am thankful that I am doing well even when it feels like I am not. When I read back my jottings over the years I see where I have been and where I am now. I love waking up each morning and going to sleep each night. I am thankful I did not kill myself when I tried. I am thankful for all I have. I am thankful to be able to share my life with my mental illness warts and all.


blessings to You, Tazzie

Complex Post Traumatic Stress Disorder and Me.

Even when life is so positive it can be quite a challenge when you have CPTSD or PTSD to manage when some bumps appear.

The difference for me now in my management and coping with my mental illness is I can usually work out or understand why behaviours and reactions occur and aspects of my life which had seemed under control, are obviously just under the surface and are ready to jump out and catch you when you are challenged.

I have to have a colonoscopy, and my GP rated it as urgent. Of course I read up on what and why I have had this rating. I find it very very interesting, and thankful that this is happening when I am so greatly improved and healthy mentally. Also having had some huge stress taken off my shoulders financially and dealing with Australian Government bureaucracy every fortnight to now not needing to do that.
I at least understand my instinctive reaction and am not dumping heaps of shit on my shoulders.

I have been working on emotional eating, and eating healthily. Unfortunately this situation has seen me comfort eating plus plus plus. Now I say that it is plus plus plus, when in actual fact for me what I am eating now is very different to what I would have been eating earlier this year. It is no where near the volume. Yet it is so much and of course with that the shame and frustration can begin to become an issue.

I have not let that happen. I acknowledge it is happening. I allow myself to eat and do what settles me right now. The difference is I am totally aware of everything I am eating. The best part is I begin to feel ill. Something in the past that did not happen. It is an acknowledgement that somewhere in my brain a part is aware this is too much. So instead of wolfing down 1 litre/2pints, of ice cream a huge packet of chips, and bags of lollies or biscuits I might eat 475ml/1pint of ice cream, half a pack or less of chips and maybe no biscuits or lollies, or just a handful. That is progress.. but most progress is I am aware of the whys, and understand the reason.

I am so anxious and frightened of what might be, even though my rational logical self which is very present knows it may be something or it may be only hemorrhoids or nothing really. It is a positive that I have chatted to my GP about it, it is a positive that the hospital has contacted me with forms to fill in.
My anxiety rose though as I filled in the forms. Next of Kin, I do not want to list any next of kin, I have to have someone pick me up. It is only a day procedure and probably only a couple of hours. The fact I have an hours drive after is the issue. I also have begun to be concerned for my dogs. Remember there is no date yet. Yet here I am my anxiety building. Deep breath.

Today I have thought about a few ways to manage this. My dogs can be left all day on their own at home. I have had to do it before. Non of us like it but…lol
I have to find someone who can bring me home, I am happy to catch a bus up to Hobart.
Or I put the dogs in a kennel overnight where I know they will be fine. I book into a hotel or bnb for the night after. Or see how much a taxi costs to bring me home post procedure it may be not a lot more expensive.lol

I feel it may be a huge step for me requiring me to ask for help. (memories of the last time I needed someone to help with taking me to my gp appointment when I had no car and no one would could help). A stranger ended up doing it for me. I was so touched.

The other part of the paperwork is the weight issue. I am morbidly obese I have no idea how much I way. I have lost a lot of inches over the last 12 months, which is great. threes sizes in chest and one in trousers blasted tummy.. and I was feeling so good. This requirement has me back in a place where I reach for comfort eating sigh. Like my depression I do not have any desire to go back there.

The overwhelming sense of dread, of firstly telling people that I need help, and secondly knowing that people will want to know the outcome. Deep breath.

The information wanted is too much for me. As I will not be having anyone in my home overnight, and I doubt I would need it…but they ask this question.
The next of kin stuff, and the person to pick up. Perhaps I will just advise them that I do not know at this point but will have someone on the day?

There really are so many assumptions made about people and the realities of people having others about them. Family, and close friends.

The weirder thing is I would be there for someone in a heart beat if I was up to it. To do it for someone else.

I just want to drive myself up and back.

See how someone with a mental illness like CPTSD thinks and looks at things. The reality of living with this illness for me.

This is just the filling in of the paperwork..lol I feel a call to my social worker next week is the logical thing.

I am trying very hard to keep moving forward, no matter how small. It is a struggle. But I am my routine a bit loose.. and the emotional eating. But again I am aware, I know why and what and will work through it.

As bad as this sounds. I am not so fearful of the end result it is as so often the not knowing. Since I saw my GP it is a bit like until I know my life is on hold in some manner. It isn’t totally I am doing some things, and am working in a manner to get my routine back on track.

I am fortunate in so many ways, thankful for all I have about me.

blessings to You all, Tazzie

Sexual betrayal, differences in a relationship and trauma. (may be triggering)

The following post may be triggering to some. If you wish to share this or any part of the following post you must acknowledge that the writing below is the opinion and comment of Tazzie Gee at https://echidna.home.blog/ .
The following is my response to another bloggers Post. All information on Martys blog is at the end of my post.

“What incredible research and statistics. My partner and I tried to be as honest and open in all areas of our relationship. Yet I feel as being his third long term partner, and one after a relationship with a woman who treated him terribly, our honesty and respect unconditional love and not fearing how our words would be taken wrongly allowed us to have a very deep level of love.

My partner had had prostate cancer and this impacted his ability at times, he was deeply ashamed of this. Worried how I would react. We were totally open about it. things improved greatly and he shared that with me he never felt in adequate or a need to perform.

I feel so little real information is shared honestly and openly about sex. The crap that is written in magazines and on TV in movies many books. Expectations and that it will be wonderful. The shame of body image. Aging, odours, natural odours that have the pheromones being sanatised and destroyed by chemicals.

The pornogrpahy industry showing ridiculous situations fantasies, and all that goes with it. Fictional and not reality but often the only way many see the sexual act displayed. Sigh.

Sex and sexuality, expectation and reality. Not being honest, not communicating about what you like, and how before you marry or commit to a relationship with someone who may not really be on the same page or need as you are in the sex department.

I know that my partner and I were very very lucky but we did work very hard at communicating and not judging. When he became ill with his cancer, he told me it would be OK if I had sex with someone else I told him how touched and appreciated I was by his very kind words. I told him it meant a lot to me but he meant more and I knew at this point in his life if I did that even with his blessing it would hurt him. I also told him that I was quite happy if I needed to to masturbate, something he quite enjoyed being present for. lol he found it fascinating.

I feel sex is one thing but a sexual relationship and a commitment to being a couple goes deeper than sex. Many women find masturbation satisfies them better than sex with their partner. Have they shared it with their partner maybe not.

I am a very open and willing person in relationships within reason and my being in charge of my situation(not sure that makes sense) So if any person I was in a relationship with say went off and had sex with say a paid sex worker or an affair. I would much prefer that it was a safe hygiene where the sex worker was not taken advantage off, but a ‘professional’ than if the person had an affair. Firstly I would want to know why my partner had done this, and what I was not willing to do to satisfy the need. If I was nt willing but the person told me and still needed that to help then it would be to me no different to other therapies that help people cope. It is a business transaction, not emotional. If it was an affair, why? would I want the person still to be in my life if they did not want to be with me, I dont think so. As I age Sex is important but it is such a transient thing dependent on so many things. Both parties feeling like it at the same moment, weariness, children, stress, work, finances, body image, making noise and disturbing neighbours, having different desires (consenting adults ones) comfort levels, education regarding sex. some people seeing it as a necessity but not enjoyable, other loving it. Not feeling satisfied by it. feeling inadequate.

It is really a tragedy that so much is put upon sex in a relationship. If you are really having such incredible issues in regard to your partners sexual needs (as long as they are in regard to consensual adults) than perhaps love is not what you have but a dream of what you thought it would be.

I believe you have to be honest before committing to live with someone. Be honest with yourself too. If you can not communicate about sex, openly with the person that might be a red flag.

I have never been married as I see it as a institution by the religious organisations to keep woman powerless and certainly in our history as chattels and owned by their spouses. Even now many religious services continue to have obey for the woman to say to the man but not the other way.

When in fact what you enter into is a a business of sorts. You are supposed to be today a partnership equal(cough cough choke choke)

Relationships like any business takes a lot of work, communication and give and take. Understanding of differences, and respect from both parties. No one owns the other person and or control anyone else. No one is better or worse. But sadly that is not what seems to be reality.

Marriages /relationships evolve over time, change heaps from the early days. My parent who did divorce, told us their children when we were all still a family, that imagine the person you think you are in love with is throwing up or has diarrhea and you have to help them. That they have an injury and can no longer have sex. Or their looks are disfigured would you stop loving them.

My way is not going to be anyone else’s way. We had trust, openness, respect, honesty,

We fought, we would work through the reasons we fought after wards, and we both learnt we were not mind readers. Accepting our minds thinking process, expectations understanding, cultural, age, gender and family upbringing along with our ideology of what our relationship would be was one of unconditional love. along with lots of laughter and communication and not the sort of we need to have a chat. Neither of us were uptight about sex.

Now my partner is dead (10 Years ) his legacy is I doubt I will have another relationship of live in, I know what I need and sex is not the most important thing in any real relationship as time goes bye. The thing I miss most is touch, the little touches that a couple have just in the day to day life, and laughter.

My partner and I were together 11 years, our actual time together was different to most couples in that I worked two nights a week, and stayed in Hobart to sleep on the day in between. Apart from that we were together five days a week. So we spent a lot more time together in our 11 years than most couples do who work five or more days/nights a week.

With exceptions of our personal activities. We never were concerned if one of us went to something with out the other. In fact we encouraged each other as enjoying our own time and hobbies social support friends and community involvement in my mind made us more appreciative of all we had as a couple. As we had very different interests and did not necessarily enjoy the social aspects that the other did.

I was not HIS and he was not MINE. We were two adults and our commitment was strong, yet we both knew having had relationships in the past they evolve, things happen and feelings can change. We committed that we were free to leave our relationship as long as we were honest and not angry. We both knew from past experiences there are feelings and changes we had known that indicate it might not be the best relationship to be in. My partner had been physically abused in one marriage, and his wife in his second had an affair with his best friend. In other relationships for both of us there was far more of us giving to the other party, and receiving very little from the other them.

You can not CHANGE ANYONE except yourself. If you are in a relationship and feel you can or are with someone and feel I can make her/him different. You can not. This would be an alarm to me.

I know there are people who manipulate others out there, by being someone very different in the beginning of a relationship and then once the other party has committed to she/he they change completely. DING DING DING, would be in my head. Yet I know for some people out there hope, love, and desire for the person they fell in love with abound to keep them in the relationship.
He /she is only like this when they drink, or take drugs. This will all impact on how you the other party feel and act, how sexual and sensual relationships are between you. How you work through the issues. If you can even bring up the issues. You can not change them, though they will change you by all sorts of ways. GET OUT TALK to someone and leave this person.

I do not have children, but my parents divorced and it took tooo long for them to do it. They waited until the youngest was in their mind old enough 15. I nannied children of divorce who were 4 & 5 and another family 7, 9, 3 It impacts us kids no matter what age it occurs. For me at 15 it seemed just as hard even though I understood the reasons they were divorcing, I had also witnessed the fights, the not coming home, heard the tears, and had the words of anger and betrayal about one party from the other. Yet these were both my parents whom I loved. It would have been better as a child not to have had to endure the years of all the pain and suffering both parties put on the other and us.
(added) Fear is often what is stopping us leaving a relationship. How will I manage, how will the kids be, what might my partner do. As hard as it is to leave surely it is so much harder to remain in a place that has little or no happiness, joy, respect, unconditional love. Pain violence, threats intimidation, abuse, being controlled in any manner are not a loving partnership relationship.

If you can not tell your boy/girl friend, partner/spouse that you are not happy with how they touch you during sex, or what you enjoy, that you love them and having sex with them is wonderful but if they can not bring you to orgasm and masturbation can especially self. This should not be a bad thing where any partner feels embarrassed or shamed. For some of us out there it is the way it is sexually and it is OKay.

It does not mean the other party is a failure or incompetent. It can be a time for sharing how to help each other receive the pleasure.

Some people do not enjoy sex, but enjoy the intimacy holding hugs and kissing. Having sex should not be seen in my view as a given in any situation.
If you are forced by your girl/boy friend to do something that makes you uncomfortable that is wrong. Very wrong against the law in fact. If you believe you are in love no one who loved you in return would treat you in this manner.

If you can never see yourself as being OK with any activity between consenting adults in your relationship than the person you believe yourself to be in love with will assuredly go in search of this from some other source.
Sex is part of life, and we must all be able to say what we enjoy, want and need without fear or any other form of emotional, physical, financial abuse.
As long as it is with consenting adults. (any other form is NOT NEVER OK) !

I would like to add to this, that it is perfectly OK to not want to be in a sexual relationship or any. No one has to live with anyone or marry anyone today. Happy ever afters take huge amounts of effort giving and taking by both parties, and understanding honest, open, discussions about your sexual likes dislikes.

This was my response to the post on Marty’s https://ptsdawayout.com/ See below Martys blog C PSTD A mindful way to heal.
https://ptsdawayout.com/2020/09/18/how-betrayal-trauma-manifests-itself/ How Betrayal Trauma Manifests Itself.
Marty’s ” blog is designed for daily support of complex PTSD. Our attitudes and daily effort will determine our misery or happiness going forward.” as this is also my mantra for my own healing from CPSTD (complex post traumatic Stress Disorder) I find his blog so encouraging and informative with other people who are on the way to managing positively and healing from CPTSD.

Blesssings to You, Tazzie

Frustration, helplessness and mental health. (may be triggering)

Hi everyone it seems to never rain but hail when computer/internet issues occur. My internet account was suspended and now I am dealing with our countries Technology Ombudsmans office and they are dealing with my service provider. I am Back now fingers crossed.

I find off shore call centers really difficult to deal with, this is partly due to my mental illness, (CPTSD) and a feeling of no control at all over a service that I pay for. I have been dealing with my provider for 8 weeks now, and my benefit payment went in two days late which meant I missed paying my provider. (It used to be done by automatic payment each month). Of course you have to add that my provider has you paying two weeks ahead and two weeks behind. (this I really do not understand) It also seems suddenly for know reason my date due to pay has altered.

It is not the date the missed payment went through, as they did not inform me until the next payment was due that it had not been credited to the right invoice? How is that my fault? I paid it to the invoice they sent me demanding payment for.

I then found that I was now 2 months behind according to my internet provider, (this was on the 8th of April) even though the next invoice was not due to be paid until the 12th of April? I had the money and was going to Bpay as they no longer were able to do a direct payment that had been set up. According to the call centre. I said I would be paying this invoice on the 12 when it was due. But no that was not OK. So in the middle of all this I check with my bank as to why the direct payment to my internet provider was not able to continue. My bank said they had no issue in continuing it as I had not authorised it to be stopped from this end.

So if my service provider had just processed the payment it would have all gone through. I rang my service provider and informed them of this. That they could take the money as per normal as the authority was in place.

So I believe that my service provider is taking the money out as normal.

Instead I get messages telling me my service would be suspended from the the 14th if the outstanding money was not paid for the two invoices. This all happened on Monday the 13th of April. Which here is Easter weekend we have a four day holiday Good Friday through to and including Easter Monday.

I tried to explain to the lovely lady on the phone that in Tasmania it is another holiday for the Banks, financial and Government organisations and businesses. So I would not be able to go to my bank UNTIL the Wednesday. I also advised her that for some reason I was not able to get into my toolbox, the access to my account from the service provider. Even though I knew my password and id were correct. She said she would note all of that.

Wednesday morning finds me and the dogs, in town at our bank. I was a little early and they were not open at the time. I tied the dogs up and sat and waited.

The wonderful staff at my community bank, helped me and I decided to pay the two months that I ‘was overdue’ plus the May June payment which would mean I was in fact ahead. Relief.

Dogs and I went for a walk, headed home and found my internet down! WTF!

I spent the next four hours attempting to get someone to understand what had been going on, getting cut off! Being told it would all be OK. When it wasnt. I requested to speak to supervisor and refused! I hung up and tried again, I ended up going to a sales number. Realising that the person in sales during business hours might be an Aussie. It was YEAH!!! I cried. Yes I did.

This wonderful woman heard me as I explained my problem with my account, she was very supportive when I shared with her that all this was impacting my mental illness, and sometimes just dealing with call centres can be triggering to me. She apologised that she could not help me personally and unfortunately there was ‘no one’ in Australia who could? What the heck! She assured me the person she would put me on to would be able to assist me.

What else could I do but trust her. The chap I spoke to was helpful, he listened to me, as I tried to explain. He assured me my internet would be reinstated. He also seemed to understand my not answering any phone calls without numbers or people not leaveing a direct phone number for me to call. I got his details and requested copies of our converstaion, he sent them to me. I had also

It was great I felt like some order was restored, as my internet was back on.

For the next two weeks it was all good.

Then I began to get text messages telling me my service was going to be disconnected for not being paid. I had people ringing me all the time, I did not know the numbers I was not picking up, any messages left were weird noises, or just nothing. I sent emails, advising that all invoices had been paid, that I had actually paid the following month as well. I also included that I could not access my toolbox.

They acknowledge receipt of emails. Two days later I received a response, saying if did not pay the outstanding invoices my account would be disconnected, and to go into my toolbox, and see. That I could also chat to someone whilst in the toolbox! ARRGGH !

I lost it. I sent an email back saying how horrendous this company was, and the fact was proven that no body had actually read my email properly as PART OF MY PROBLEM IS I CANNOT GET INTO MY TOOLBOX!

I keep getting how did we do handling your issue emails, and you most likely can imagine how I replied.
I was also getting several messages a day on my phone telling me my accounts were overdue. My account would be disconnected.

Again the hours trying to get someone to actually understand that I had paid my account. Again the call centre people were varied in abilities, and some just hung up on me, (I was not yelling or swearing), others tried but could not find any invoice paid. I would ask for supervisors, and then be told they would call me back. I answered unknown numbers but the person could not resolve the issue.

This went of for two more weeks! We are now into May. My bank said that the money had gone on the 15/04/2020 to the BPay account (which is my service providers) Sigh…

I tried again with the call centre. It was over an hours wait to get to talk to anyone. I waited. Again I was on the phone, I hung up in frustration when someone said that my account would be disconnected on Friday if the invoices were not paid. Even though I had just told him I paid them on the 15/04 (US 04/15). It was now the 04/05 (US 05/04). I had asked to speak to a supervisor there is no one available! I asked to have one call me, No one did!

The next morning I tried again and spoke with a lovely woman who I said I really just need to speak to a supervisor. She said could she have someone call me. I explained how I waited all afternoon and evening for someone to call me yesterday. She explained that she could not transfer me as they are all working from home. I said oh OK she assured me she would contact someone and they would ring me today.

They did two hours later I received a message on my phone saying …. would be ringing me very shortly. She did. She listened, and tried to see if the invoices had been paid. They still hadn’t. I just burst into tears and hung up.

The next day my internet went off. I could not check emails. I had had enough! I called the Ombudsmans office. The first person I talked to told me it was not an issue for their office? I said it is. No I have to deal with the company first???? He was really helpful and actually seemed to be bullish!. I rang again and got someone else. I said how I had rung before and I was very upset with how I was spoken to and treated. That I was told this was not an issue for this office. The person I spoke to listened to my tale, and said no it is an issue we can look into for You. Relief. I stated that my internet had been disconnected for not paying my bills. She said she would get onto it right away for me.

Sigh I thanked her and than had not expectations. She had also said to me that whilst there was ongoing issues between me and the Obusdmans office was involved I can not be disconnected. Three days later I am back online.

I sank down a lot, during this time. I did not go back wards, and I am proud of myself that I did not get to the trigger point I may have where I was screaming and swearing as in the past. I felt so drained and flat. I was not going to let this get on top of me. Unfortunately my ‘old’ normal responses have rared their ugly heads. I have stayed up too late, (but am working on it again) I have not been eating as well and sugar was high, (condensed milk can not be in this house). I am not proud of the two cans I consumed over four days but it could have been two days. Progress..lol up until yesterday Saturday I had been walking, but have not over these two days. Writing here is my accountability. I have been doing some pottering outside so not just sitting on the lounge, and I did take the dogs for a play with the neighbour across the roads dogs. So I have communicated with someone. Along with leaving the house.

Tonight I made a delicous Korma, rice and salad with greens from my garden. I have eaten sugar only in some fruit. I will be in bed lights out by 22:30.

I am determined to not stay slumped down, I have not gone backwards, I am still moving forward.

I saw that I had had emails from my service provider saying they wanted a copy of my payment, this was from the day my internet went down? The next day they sent me another email saying they were wiping the debt? It was a one off. A sign of their goodwill? (Remember I have paid them)?

I rang the Ombudsman’s office as I was still missing $209.97.

It took a bit of getting the person on the other end of the phone to understand, that by crediting the account as good will, means that they are still saying they have not received my money.

This means my $209.97 has vanished, and I might have internet service but I am out of pocket this amount. She asked me what I wanted, I said originally I just wanted to pay the account which I have done, but now as they have credited my account as goodwill, I want my money back!.

Seems a totally ridiculous situation, and as I said to the woman at the Ombudsman’s office my mental health has suffered a lot over this. I never tried to not pay my bill/s..

Such a ludicrous circus. This is why no company should be allowed to operate within another country without having people working in that country at a level who can actually help. Or the call centres should be able to have someone from financial management ring you when the situation goes on and on. Yet I have no real leg to stand on. I have had my internet off for ten days in the five weeks.

What rights do we the consumer have when using companies that operate outside of our National laws? It is something I am thinking more and more about whilst safe at home. You want Australians to get back to work than make more companies pay for Australians to work for them, so the services we pay for are traceable!

I am thankful for this place to off load. I am thankful for the wonderful world that the internet opens up to me. Being an introvert and someone who may have the potential for agoraphobia if I dont push myself I am so very thankful that this surreal time has seen me get on the whole fitter, healthier, mentally stronger. Thankful to know my rights, thankful to know processes to ensure my rights are taken care of. Thankful for the people who are working from their homes. I am thankful to the lovely helpful and pleasant (generally woman I have to say) in the call centres who do really try to help but the situation is not in their handbooks.
I am thankful for the lovely food I have access to. I am thankful for the clean water I have to drink. I am thankful for the fresh air I breathe. I am thankful for my dogs. I am thankful for the birds, and critters in my garden. I am thankful for the rain that is falling. I am thankful for having wood for my fire. I am thankful that I have no debt, that I am so very very fortunate to own my home outright. I am thankful for You.

blessings to You Tazzie

Dogs and Isolation.

Off we went for our walk this morning. It was wet but warm and the rain had stopped. Busby and Miss Treacle took off, up the drive to our small country road. Miss Treacle just races out my breath catches every time. Busby is incredible every single time we leave he looks to the right (direction in Australia cars would be heading towards him closest side).

It was muggy and I hate humidity I did not imagine Tasmania would have such humidity as it has in recent times.
Busby had gone and said hi to Chubbs and Toby at their gate across from us. They looked forlornly on as he raced up the road without even looking back.

We had not gone to far further up when we met Ruby and her owner. Do not mistake Ruby for a brown sheep. She is a sweet labradoodle. (her big brother is Basil he is a tenacious elderly pug who can no longer handle big walks).
We left Ruby and her owner and continued up the hill on our walk. Busby saw Toby (yes 2 Tobys, and when my third dog was alive there were 3 tobys on our small rural road). It did not look like Toby would be coming out to play as he sat by the fence. Then the gate was open, and WOWEee , it was playtime.

Miss Treacle was incredibly disappointed when she realised it was not her man but his wife who was with Toby today. She ignored her with disdain. The bros had a ball and stirred up the ducks by running straight towards them, not even really seeing them as they were playing. The ducks took flight.

The warmth and humidity rising and the evaporating water was forming clouds across the river and the clouds thinned. As we walked past Chubbs and Toby were still hopefully waiting by their gate wanting to play. It was not to be so the three of us headed for home.

I had to wheel my bin down to the road where the truck picks it up in the morning. As I was bringing it to the top of my driveway, I was almost flattened by three big dogs coming straight at me, the black ones tail wagging so much it nearly was ahead of his head. The boys had been released. They were thrilled.

Busby, Chubbs and Toby ended up playing ball in the paddock as I talked with their mum, and two teenager neighbours (all social distancing actually much more than the suggested space. The kids were earning their some money by bringing other neighbours bins down. Love their ingenuity. They ride their bikes down hill towing the bins. No fear these guys.

It has been another wonderful day spent in isolation? My routine continues in bed by 22:30 lights out, eating more healthily, walking every day, and showering every second day.

I do have to say, I feel so much better following this routine, I see how I really knew what was best for my own needs and am now working to ensure I follow this as best as I can. If I don’t make it to bed or eat healthy for a day, it is not a a failure in my eyes, it is just normal. I will just pick it up the next day. That is my plan.

I am thankful for the rain. I am so thankful for my dogs. I am thankful for having such great dogs living about us. I am thankful for my neighbours and the greater sense of community we have now. I am thankful for my garden. I am thankful for my warm comfortable bed. My doona, and electric blanket. I am thankful to have a roof over my head. I am thankful to have food and fresh water. I am so thankful for all that I have.

blessings Tazzie

Blog at WordPress.com.

Up ↑

%d bloggers like this: