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The long term reality of religious abuse

In my book (It’s Life Jim…) I cover the subject of mental health openly but fairly lightly.

Although these days I help many work through the debilitating trauma of religious abuse and it’s impact on LGBT people, I realise I haven’t actually shared much of my own struggles – only snippets really. I was wondering why I’ve avoided it, and I realise it’s because of the stigma. I’m afraid that it will invalidate me – that if I share too much, I will have no credibility in my work with Silent Gays and just be relegated to the rubbish heap of nutters!  But life is about facing our fears, so here is my day to day reality… (pull up a comfy chair, it’s going to be a long one)

The first layer of fear was from very young, realising I didn’t fit the expectations of family and society (although I couldn’t express it as that at the time). I was ADHD but it wasn’t a “thing” back in the 60s so I was constantly being judged for being a space case and a dreamer. I couldn’t focus for long on anything, always wanting something new and getting bored far to quick and most of the other classic “symptoms”.

The next layer was hitting puberty and finding that I had zero attraction to girls and it was the boys who would send my hormones on a rampage. But it was taboo to even talk about it. So I lived a conflicted dual life in my most formative years.

The next layer was the impact of religion, enforcing the stigma that anything outside of “normal” heterosexuality was living a dreadful sin. This drove me ever onwards to find a “solution”, get healed/cured/changed/whatever – anything but live in the excruciating pain of guilt and shame caused by the religious beliefs. This became the most damaging part of my life, as I pursued every imaginable way of becoming straight.

During all this time, through two marriages, numerous different church denominations, doctrines and theologies, and endless counselling, I fell deeper into depression and suicide ideation. But I couldn’t even let anyone know that either! I was already a “loser”, if not to those around me, most certainly in my own mind – I was a failure.

Finally, I embraced the “gay conversion therapy” practices of Living Waters for 15 years, clinging to the hope that this was going to finally change me and bring the freedom I was so desperate for. But of course, it didn’t. The depression became worse and I would become crippled with anxiety, but still I had to hide it and use every ounce of strength I had to live day by day. My marriage was an absolute sham, and my wife constantly shamed me. So often I felt like I would “explode” – what exactly that meant I’m not sure, but that was the feeling.

My wife died, and I collapsed. I had lost all my reference points, I didn’t know how to process what was happening and depression and anxiety left me needing “real” counselling (not Christian pseudo counselling) and medication. Thus began the slow climb out of the pit.

Here’s the reality though that so many of us who have been through something like this suffer. We “walk with a limp”. I don’t mean that in some nice wise sounding metaphor. I mean it as a limp with a bloody open wound that although it doesn’t stop us from getting involved in, and enjoying life, does mean we are always walking in the pain and effects of our injury. We do our best, and yes, it’s unbelievable better than what we lived through, but the wounds never seem to heal.

To put that into my daily practical affairs, here’s what my own “wound” is like.

I have ADHD, so my ability to focus is limited, unless I lock on to something that absolutely captivates me and then I can’t leave it. I am impulsive, get bored quickly, forget stuff, remember the wrong things at the wrong times, and all the classic ADHD stuff. But after the meltdown when Min died, these symptoms became heaps worse. I could pretty much work around them in the past, but now they are extreme. I have regular bouts of depression still, although not crippling like they used to be, and I’m sooo thankful for that! I get anxiety attacks too. At first they were pretty bad – things like freaking out in the supermarket and bursting into tears. But I still get them. I’ll start to get nervous and tense for no reason and keep thinking I’ve forgotten something really important.

I used to be pretty good with complex technical information and did well as a technical writer and instructional designer, but another aspect of my meltdown was that as the ADHD and anxiety had increased, I lost the ability to comprehend that sort of information any more. This has been a source of incredible frustration and sadness, especially as I was a bit of a wiz with electronic music and computers. I’m also a qualified trainer/facilitator but the thought of teaching IT or Health and Safety Systems (as I used to) sends me into a panic!

As a result, I couldn’t hold a job any more. I’m pretty much a liability, never knowing one day, or even one hour to the next, what my mental state will be. Pressure, expectations, deadlines etc cause my mind to go blank, which sets off anxiety because I can’t function, and become fearful that I’ll let people down. So I went on the sickness benefit (thank you New Zealand for your wonderful social welfare system – even if it does have it’s problems).

About a year ago I decided to try getting work again and coming off the benefit and the meds. It’s been one crazy year! I ended up doing security work, simply because its pretty chilled with low expectations, but there was constant pressure for long hours at crappy pay to cover the bills. 12 hour night shifts, brain numbing day shifts standing around, which for an ADHD person is living hell! I finally had to quit a couple of months ago because I could feel my brain falling back to the point of breakdown again.

This is my life – I never know from day to day how my mind will be. I’m really good at putting on a happy face, and I’m always the funny guy, but I’m broken. I’m happy, in fact life has never been better, but my wounds are deep and I simply can’t function in life as we are supposed to.

What happens is that the mind is deeply scared from having to adopt unhealthy coping mechanisms all its life. A life of shame and guilt creates patterns of thoughts and reactions that simply don’t suddenly leave, especially as you get older and the responses are so ingrained. Things that may appear “normal” life to others trigger me into confusion and anxiety. I can start the day with the best of intentions and find that suddenly my brain has totally lost the plot and I can’t complete a single thing I’ve planned.

I can however, communicate! I can write with passion about religion and being gay. I can talk to a crowd for hours about it! I can take people on roads of self discovery. I can run workshops and seminars, and feel incredible compassion and empathy for the broken like myself. But ask me to sort out technical stuff like my website, and accounts and running a proper organisation and I grind to a halt – despite the fact that in my past life I was very capable and even had small business management qualifications.

These days I’m trying to find part time work that I can actually handle, that pays enough to cover the bills while I try to build some online work to finance my passion of helping others.

Anyway, I’ve rambled somewhat, but only in the hope that I’ve created a picture of the ongoing effects of mental illness. I’m at peace in many ways with it all however, as long as I allow myself to roll with it. If it’s a “bad” day, I try to just chill out in the knowledge that tomorrow will be different. Not always easy of course when I’m often faced with daily simple tasks, but I’m getting there, despite the niggling shame that persists for not being “normal”. Things like mindfulness meditation have been the biggest help, as well as long walks on the beach.

That’s my “limp”. That’s my life. It’s a good life, but only if I let it be a good life in the full acceptance of my limitations, embracing all that I am right now, with all its mess and unpredictability. I love who I am now. I have no regrets. I don’t live in constant shame and guilt any more. I want to live, and live that life to its fullest, which is amazing considering most of my life was spent figuring out ways to kill myself and spiralling through chronic depression and fear.

Yep, this is me, warts and all!

Meds

After Min died I had something of a breakdown and ended up on Escitalopram. Just the minimum dose, but it was all I needed. It lifted the dark heavy blanket of depression and eased the anxiety attacks. It made life bearable and gave me the freedom to move forward. "If you're happy and you know it, thank your meds" LMAO, Maxine!

Over the years I tried stopping or cutting down but it soon became evident that it was too soon. Over the last few months I began to reduce the dose again, just too see what would happen. I had a visit to the doc a couple of months ago and he asked how the side effects were going, although he didn’t know I had reduced the dose at this stage. I said they were fine and I’d never noticed anything significant… until he asked more specific question. Damn… I hadn’t realised that many small but annoying things were actually side effects.
Sooo anyway, I reduced and finally stopped them a few weeks back and the changes are very noticeable. Some areas are coming right faster than others (sex has never been better, lol) and so far, depression and anxiety are still at workable levels.

One of the interesting things is my emotional reactions. Before the meds, I used to become teary at the strangest things, especially things that expressed passionate emotion, but that faded on the meds. Now it’s returning, much to my annoyance but paradoxically, I’m also pleased. In the past I had worked through why this would happen and I think it was centred around having to repress so much all my life, and emotional triggers would crack open all the repressed stuff. As it faded I became less concerned as I thought I’d processed all that stuff and I was now “normal” (lol).

But it’s coming back, so here I am, looking at these teary moments with a new interest in what they mean, and how to process them and hopefully control them in a healthy way.

Just thought I’d share this, because meds are a hot topic these days and it’s good to share our experiences, especially with our emotional journeys.

Onward and upward 😉