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A Life of Trauma and Tragedy (Possibly Triggering Content)

A Life of Trauma and Tragedy (Possibly Triggering Content)

As a young child and into my teens, I have vivid memories of a violent and abusive father. Dad was essentially a good man and worked hard to provide the necessities for his young family. He was also a very proud man, and it was hard to make ends meet as a lowly paid manual worker. He was by nature a quiet, shy and gentle man with a lovely dry sense of humour. But alcohol turned him into a violent abusive drunk, with a quick and volatile temper. Mum would tell me and my siblings to go to our room whenever this happened. I know she tried her best to shield us from the violence as much as she could. But it's hard to miss the shouting and the smashing of items as arguments raged. Our tiny 4-roomed home allowed no escape from what was going on. We all knew not to comment afterwards on Mum's frequent and obvious injuries.

As a pre-teen, I experienced the heartbreak of losing a much loved uncle via a tragic shooting accident. Soon after, I lost a school friend to drowning in a farm dam, and a fellow classmate to an accident in a grain silo.

In my senior high school years, my best friend died in a car accident, 2 additional classmates died in separate car accidents the following year. All this while still at school.

When I started going out on dates (as a young and naive 19yo) the first boy I ever went out with was critically injured in a random attack in a hotel. The second man I dated, died in a work accident while carting hay. My next boyfriend lasted a little longer, I dated him for a year before he too died - in another car accident. I was devastated.

When I was in my late 20's, my Mums youngest brother died at the hands of his then girlfriend. When in my early 30's, my Dads youngest brother (and my favourite uncle), committed suicide.

It was in Feb 1996, when in my mid 30's, that I was beaten and sexually assaulted in my own home, by a former friend and someone I had once trusted. This caused major trauma and it took a very long time for me to recover from, both physically and emotionally. I could not escape the fear of it happening again, nor the horror of it all. Feeling vulnerable and unsafe, I desperately needed to escape to hide, so I sold my home a few months later and moved. Still trying to escape I sold and moved again, this time to another state. I could not allow this person to find me again. The mental trauma of this violent rape continues to affect me badly every year.

A couple of years after the assault, I entered into what turned out to be an abusive and highly volatile relationship. I married someone just like my Dad. My husband is essentially a good man, but has a traumatic past himself, and is an alcoholic and a narcissist. I guess that old saying, that you end up marrying someone just like your Dad, is true.

In my early 40's my remaining best friend from high school died on the operating table during what should have been a very simple routine minor procedure. I'm godmother to her children. She had fled a violent marriage when her kids were young, and had essentially been in hiding since that time.

Around the same time, the husband of a workmate of mine died in a freakish workplace accident. My 24yo nephew was seriously injured in a mining accident which resulted in permanent injuries to both legs which will limit him for life.

Our neighbour from the adjoining farm to ours, committed suicide during the hardship of a prolonged drought in the mid 2000's. Our two families had been quite close, and this hit the very small rural community very hard.

I was in my 50's when my youngest brother was seriously injured in a fatal car accident. He was very lucky to survive and, five years on, he continues to have serious ongoing physical and mental health challenges. Tragically his young daughter died in the accident. This major loss affected my whole family very badly, and marked the rapid decline of my Mums health. The loss of her only granddaughter, whom she was very close to, broke her heart. My beloved Mum died just over 12 months ago.

After so many of my friends and family died or were permanently injured in freakish circumstances, I started isolating myself to a large degree - cutting myself off from any remaining friends. In my 20's and 30's I never went on dates - no more boyfriends for me. Therefore no more losses? I never permitted myself to get close to any new friends. I figured I was cursed somehow and caused all these tragic things to happen to so many around me. It seemed I wasn't safe to be around. As tragedies continued to happen throughout my life, it served to reinforce that thinking.

Working life ... I experienced a workplace accident when in my late 30's which resulted in permanent physical impairment and ongoing chronic pain. In my 50's I was targeted by my workplace manager after calling out a case of workplace bullying against a fellow worker. I became the target of sustained harassment and bullying as a result. It became more than I could handle, so I resigned.

Given my physical limitations and ongoing pain levels, I sought and found part time work. I worked with a lovely bunch of people and thoroughly enjoyed the work for about 6 years in total. Unfortunately I was forced to leave work a few years ago due to carer responsibilities. Leaving work and being stuck at home every day was a major adjustment for me. I miss the mental stimulation of work and the interaction with former workmates. As I do not have friends, my workmates was all I really had.

My husband suffered permanent brain damage as a result of life saving medical treatment he received two years ago. He has Stage IV terminal cancer, a degenerative neurological disorder, a serious auto immune disorder and several MH disorders. Caring for him is now my full time job.

Last summer's bushfires raged all around us, and we were on evacuation alert numerous times. In the end, we were one of the lucky ones. But tragically, 4 lives were lost in our local area.

And now of course, we are all living through the COVID situation. I have been unable to visit elderly and frail family members due to border closures and travel restrictions. With restrictions and impositions on our normal everyday life changing seemingly every day, life is such a rollercoaster. COVID is making us change our lives every single day, and I do not adjust well to major change.

I know I should switch off the news and not look at sad and traumatic news, but I seem drawn to it like a moth to a flame. I feel I need to know what's happening at all times. And yet I find myself more and more upset by the growing death tolls, lost livelihoods and global virus tallies. I do not think life will ever be the same again. How can it?

I don't know if you become immune to trauma and tragedy, or if trauma builds until it eventually breaks you. There's been times in the past that I've felt almost numb to it all. But more recently, I seem to be breaking and feeling even more alone and without hope of things ever turning around for the better. I just feel that I have no hope left in me.

Emelia 🌸

4997 replies

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In response to: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

@Faith-and-Hope 💕 The picture finally came through last night. Its lovely .. thank you.

@Former-Member 🙏 Thanks so much. Zero cost for cancer treatments etc? I didnt know that. I have always heard about all the out-of-pocket and extras involved in cancer treatment for people. With hubby and his 3 cancer treatments (kidney 10 years ago, melanoma 4 years ago, metastatic cancer in lungs 3 years ago, and all the other side issues he's had as a result) he is DVA Gold Card, so everything is just automatically picked up. He has no idea how lucky he is in that regard. But for the rest of us, I have always thought there were so many excessive hidden costs involved in any medical treatment. So thats reassuring at least. I may have more questions of you about the radiation therapy when the time comes. I dont even know where it will be done. I believe closest facility is an hours drive away, so thats probably what will have to happen. How long does a typical radiation therapy session last? I think its done 5 days a week for 6 weeks, or thats what I've been told. I'm also told that it causes a lot of fatigue, so that will be a difficulty in itself. With needing to drive there each week day and receive the treatment and then drive home again. I'm already exhausted. 😵

@Lee82 ... thank you beautiful lady for your well wishes and support. I can see that I am going to need that over coming months. Its nice to know that members here are so supportive and caring.

@Bunniekins ... thank you beautiful Pea. I will definitely keep that in mind, and will tag you in those early morning hours if I need company and reassurance any time. Please know that you can do the same to me.

@Anastasia ... thanks so much. As I mentioned to others here ... its really comforting to know you are all here for me. I will definitely be needing a lot of support over coming months. You mentioned that when your Dad was diagnosed with cancer, the was spurred on to attend to his affairs. A cancer diagnosis is definitely very daunting, and brings to the fore our mortality. Incidentally I attended to my legal affairs about 2 years ago. When my husband was in hospital completely off his head with encephalitis as a result of cancer treatment. He was not capable of walking, talking, thinking, eating, or anything for about 3 weeks. He was completely bedridden for a month. And the hospital were constantly needing signatures to authorise procedures etc. I would sign, but they would ask if I had power or attorney, enduring guardianship, etc. Which I didnt. So that was really hard. They accepted my signature and instructions because it was what they were advising, and what would have happened if there was no proper authority anyway. But all I was .. was 'next of kin', which essentially holds no legal authority. Anyway, once he finally recovered his senses (albeit with some brain damage) enough to be considered of sound mind, we both did Wills, POAs and Enduring Guardianships. So that is all in place already thankfully. How are things going with your Boy since his return last night @Anastasia ?

@Schitzo ... thank you so much. I love seeing you around the forums, offering your support and love to so many.

@eth ... hi there, how's things going for you? I know you've had a couple of very busy weeks, which is mostly a good thing. Yes you're right .. everyone here has been very supportive and lovely. I appreciate it so very much. My husband has been caring and quite kind, as much as he is capable of. I too hope the road ahead is as smooth as possible, because its going to be tough in so many respects. Thanks for tagging @Exoplanet ... Exo .. I do not know much about your story, but I would like to know more if you'd like to tell me. Otherwise, please tag me to your thread next time you're there perhaps?

@Former-Member ... thanks sweet friend. Yes I have gone through all that ... life is just not fair! Getting through that now though, the angry bit. Yes a long road ahead unfortunately. I will definitely keep a diary of everything I need to do, and have actually bought a 2021 diary only yesterday. I saw the interview with ONJ a day or two ago actually. She is quite inspiring isnt she? Thanks for the links you posted, I will definitely go and check them out.

As for the Staging of cancer, I do not know yet what Stage I am in. They havent done the required tests to determine if the cancer has spread yet. I think that will all happen once I get to see a surgeon, and prior to surgery. More tests still to come in other words, before they can determine a Stage. Yes I am very much aware of what Stage 4 cancer is ... my husband became Stage 4, after his melanoma spread to his lungs. But he is in remission currently (6 monthly scans due early next month), so it can be beaten. When I say that I am GRADE 3, that is not the same as STAGE 3. The Grading rate is more an indication of the actual cancer cells and how different they are from normal healthy cells and how fast they are growing. There are 3 grades, with Grade 3 being the agressive one and the one most likely to spread quickly. So thats why they need to perform more tests to see just where its gone, if at all. Only after that is determined, will they be in a position to give me a Stage rating. I'm hoping and praying that it will be Stage 1 (not yet spread to lymph nodes) or Stage 2 (spread to only a few lymph nodes) at worst. But I just have to wait and see. Its all a big waiting game it seems.

@Eve7 ... I just noticed you online. How are you going gorgeous? Are the weekends tough for you, or do they provide you with a much needed break from normal routine? Are any groups run over the weekends?

Emelia 🌺

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

@Emelia8 as a PUBLIC patient the only expenses we have had with Mr D's treatment have been some scripts (perhaps 5 which he paid 6.60 for being on DSP). We did get reimbursement for travel to the big smoke ("PATs" travel assistance for regional patients) as we stayed with my sister there was no accommodation needed but there is discounted Cancer Council accommodation and the Social worker (and radiation team) will fill you in on this and the expected PATs rebate if applicable. Mr D did not have radiotherapy in the end so I am not so versed in that.

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Going ok here thanks @Emelia8 . Had a much quieter week than I have for a while, which was really good for me. I needed to put the brakes on as I was getting quite accelerated.

I'm so impressed with how staunch and practical you are being about your new diagnosis. And glad to see you have informed people supporting you here and giving you helpful information.

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Thinking of you today @Emelia8 I hope you can relax a bit today and enjoy some sunshine.

❤️💙❤️

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Thinking of you today @Emelia8 and hoping you can get some answers you need.

Lots of love and hugs hun 💖💖💖

In response to: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

@Emelia8 💖💞

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Thank you @Emelia8 xxx

My boys doing ok x 💙

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Thanks @Former-Member, I will look into the TAPS travel subsidies. In NSW I think its called IPTAAS ... I just looked it up. So if I have to travel for surgery or other treatment, it will be helpful.

Hi @eth ... good to hear that you have given yourself permission this past week to have a quieter week. It sounds as though its been worthwhile. Glad to hear.

Thank you beautiful @Eve7 ... I have made a point yesterday to get out into the sunshine and enjoy it while I can. Its a stunningly beautiful morning here again today too, so I will do the same again today. Not doing much, just wandering aimlessly around the garden and block. We live on 3 acres here, which is nice. I know you are finding things difficult right now, and being sedated during the medication transition. I hope things start to improve for you soon. Kindest thoughts and much love to you Eve.

@Snowie ... thank you, I really appreciate your continued support and kind thoughts. Its important to me.

Awwww @Former-Member ... how beautiful. Thank you so very much.

@Anastasia ... very happy to hear that your boy is doing okay so far. Fingers and toes crossed that it continues, and that he does not experience another dip. Thinking of you gorgeous.

Emelia 🌺

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

You are such a lovely person @Emelia8

You say such kind words, thank you for your kindness.

I really hope today has some sunshine and roses in it for you. You deserve that ♥️

Love and hugs to you and all here

In response to: Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Re: A Life of Trauma and Tragedy (Possibly Triggering Content)

Hello @Emelia8

It's been about a year since I had cancer removed, my experience was a bit different to yours, but then I think everybodies experience is different. My little town doesn't have a doctor anymore, I went to one in the next town over. I'd noticed a dimple many months before I went, I made a conscious decision not to do anything about it - I tell you that to give you an idea of my personal thought & emotional process. It was not until the dimple became more like a hole & the nipple changed shape, becoming inverted & 'crispy' & tingles of pain occurred, that I went. From go whoa, before any biopsy's, starting with my GP it was referred to as advanced; I also was honest from the very beginning that I had no interested in chemo or radiation therapy - I didn't even really want the surgery. I'm in my 50's closer to 60 & I live very solo. I have my own beliefs & opinions about life, some of them include that in my mind we live too long, we survive too many ailments & injuries, that we are supposed to end but we defy that & it has unbalanced everything, making us the greatest threat on this planet. At the first appointment with my GP it was the doctor trying to rush the surgery, I told her I needed time to think & I took 6 weeks. I do not have a good relationship with my only offspring, my daughter; this has changed in recent years, I used to believe we had a strong, close bond & it was devastating to learn otherwise. But when she found out she began talking to me for a short while & it was for her that I had the surgery, she had accused me of committing suicide by not consenting to it. Though even for her I could not consent to a unilateral, I had E cup breasts, quite large, they took 3kgs off my chest, if they had only taken 1 I would have been left with a kilo & a half hanging off of one side. I remember a lovely breast nurse cooing to me that it would be alright, I would be given a prosetic, it would be weighted . . . the last thing I wanted was to put the weight back on! After several appointments with the breast surgeon, each time stating that I wanted a bilateral mastectomy, each time having him say they didn't like to do that, each time ending with my telling him I needed time to think - I feel the surgeon accepted that I would not consent to a unilateral & perhaps I found the right words, you see I'm the 4th member of my family to develop cancer, the 3rd consecutive generation to develop it in the breast; I told him I believed due to these facts I had a higher percentage chance of developing it in the other breast, he agreed with & supported me. All of a sudden I had nothing left to think about, no reason to continue delaying it & the appointment was made. I went through the public system, my initial appointment for radiology with made with a private organization, I think my GP wanted to speed up the process, but the fee was shocking; the first scan was free but they immediately made an appointment for me to have biopsies {fine needle & core}, that appointment was $600! When I told my GP of my shock from that fee, she put me into the public system. I have been, not just impressed but in awe of the public system; of the caring manner I have been treated, of the medical treatment I have been given, of the understanding or at least acceptance of my will over my health, my body, my life. There has been exceptions of course, but the doctors, nurses & staff of the public system . . . & the private one, are all only human. After the scan I was told {though I think the wording should have been more professional} they had found something really nasty approximately 4-5cm in size, after the biopsies {I found the fine needle one was much worse the the core one} I was told the cancer had spread into the nodes, after surgery I was told that all of the nodes had been affected & removed. After the doctor told me that it was not a good prognosis & was going to continue explaining in more detail, I was honest again; I did not want to know, I don't want that knowledge. I believe the people involved have done their best to honour my wishes. I was required to attend a oncologists appointment, though he had been pre-told of my views & he did not push; he recommended the
maximum treatment, a year of chemo followed by a year of radiation, but accepted my choice. I did try the hormone pills for a short time {a matter of weeks} but my individual reaction was a change of emotions, anger doesn't cover it, even the word I use to describe it doesn't, rage; so I stopped taking them. The surgery, though this may seem a strange way of describing it, was amazing! I felt no pain what-so-ever! My surgery was 4-5 hours as it was a bi-lateral, I woke up feeling fantastic - the medication I was given was incredible! Not long after waking I got out of bed & went to the toilet, the only difficulty was juggling the tubes & bags {I had 2 drains, 1 on each side} whilst trying to hold the hospital gown together at the back & shuffle to the bathroom; then a short moment of 'what to I do with these drains so I can get to the undies? 😄 Perhaps I got up a little sooner than expected, the nurses soon attached little hooks to the bags which made them easier to carry. I stayed overnight & walked out the next morning, they gave me little cotton handbags to put the drains in -
those drains where the only difficulty I had with the surgery & recovery, they did have to stay in for a
couple of weeks; I also wasn't allowed to drive for about a month, I spent a fortnight at my Sisters & the next fortnight I was home bound. The only appointments I chose to attend have been the physio ones, I want to keep my ability to move independently 😉 I have had no problems related to the surgery with movement {I have a specific arthritis}. It's no surprise to me that we have different thought & emotional processes, my experience is not going to be like your experience. My only advice to you would be to think very carefully & deeply about the very important decisions you are about to make concerning your body, your health, your life.
Love to you Emilia

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