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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




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

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