Showing posts with label Labyrinth. Show all posts
Showing posts with label Labyrinth. Show all posts

Wednesday, June 1, 2016

She Chose Down

A couple of months ago, whenever anyone asked me how I was, I sent them this video.


I think most people were just confused by this, but at the time I felt it was the best explanation I could give for what I was feeling. Labyrinth is one of my favourite movies, and I've written before about some of the meaning I think can be drawn from re-watching Labyrinth as an adult. As a child I never realised that in this scene, Sarah actually answers the riddle correctly. Yet she still falls through the floor a moment later.

I screwed things up this year. I made a choice - seemingly the right choice - but things went badly. Then I made another choice, although this time it really was the wrong one, and I ended up in a massive dark hole. This is the unfortunate reality with chronic illness. You can do your research, listen to expert advice, weigh up your options… but there are still no guarantees.


A few months ago, after my sleep study provided a whole bunch of inconclusive results, I decided to trial a drug-free treatment option to help with my sleep problems. It seemed like a safe option - it's been shown in clinical trials to be more effective than medication at treating insomnia, and it was recommended by my specialist. Sounds like the right choice, yes? Unfortunately no. Not only did it not help with my parasomnia, it actually increased it, and the resulting lack of sleep caused a significant flare of my autoimmune disorders. So I made another choice, medication this time, and while it did improve the parasomnia symptoms a little, it also had a significantly detrimental effect on my physical and mental wellbeing. I ended up in more pain than I've been in since... well, probably since I very first got ill. I went from doing weekly dance classes to struggling to walk to the bathroom, and I experienced far darker places with anxiety and depression than I care to revisit. Luckily my doctor was on to it, and recognised that the medication had become dangerous for me. I couldn’t stop it immediately, but she gave me instructions on how to taper it off safely. In the middle of all this, my blood work also revealed an unrelated medical condition, which fortunately was treatable but caused some neurological symptoms and added to the depression in the meantime.


So with all that going on, you would have thought I’d have stopped the drug-free treatment as well right? Well… no.


The choices I’d made had gone so horribly wrong, I found myself stuck in a decision paralysis. Everyone – my doctor, my family, my friends, even my own body were telling me I needed to stop the treatment programme, and just do whatever I could to get sleep and recover, but I was so terrified of making yet another bad choice, I kept going with it. I also knew I needed steroids to get the autoimmune stuff under control, but weighing up the positives vs the likely side-effect of insomnia seemed too hard a decision to make. 


My doctor was on sudden and indefinite leave, which meant there wasn’t anyone there to step in and tell me what to do. So I did nothing. I sat back and watched myself get sicker, because it seemed safer than making yet another bad decision. This of course ignored the fact that avoiding making a decision is a decision in and of itself. 


Sticking my head in the sand was not my most grown-up response, and after a few weeks of freaking out and crying lots I had to push my fear aside, make some choices and try get my life back on track. I was lucky this time. Stopping the treatment programme helped immensely, and in a bizarre turn of events, the steroids actually made me sleep for nine hours straight instead of the more common side effect of insomnia. 

I went through cycles of guilt, regret, blame and anger over what happened. Was it stupid of me to continue with treatments that were clearly making me sicker? Yes. Do I wish I'd never made the choices I did? Yes. Is that going to change anything…? No. It was incredibly frustrating and sad to find myself in the position of watching my health decline, but I learnt something from this. I've always been afraid of what would happen if my joint pain was to become really active again, or if my teenage depression and anxiety were to return. And well... I've discovered that the answer is that it's pretty awful. But I’m not the person I was as a teenager, nor am I the person I was 12 years ago when my physical health problems first got bad. 

I found reserves of strength within myself that I didn't know I had. As utterly horrible as things were, I found ways to keep going even when giving up felt like a much preferable option. When I wasn't sure if I could keep going, I reached out for help and my incredible friends and family reached back. They were there, supporting me - in person, with texts and phone calls, or messages from the other side of the world – through even the worst moments. 


I've read that when Jim Henson, creator of Labyrinth was asked why Sarah falls through the floor after getting the riddle correct, he admitted he didn't know. Before falling, Sarah does say "It's a piece of cake" and there’s a pattern of bad things happening in the Labyrinth whenever someone says this, but other than that there’s no logic to it and it's not fair. I don't know why treatments that were supposed to be safe went so badly wrong for me. When you have multiple medical conditions there's more chance for negative interactions, but other than there's not really a reason. To quote Sarah again "It's not fair, but that's just the way it is."

My doctor is now back and I have a sleep specialist appointment coming up, so I will likely have to make some decisions about treatments soon. At the moment I’m still in the stage of wanting to reject everything, hoping to avoid making the wrong choice again, but I'm aware that didn’t exactly work out that well for me last time. Not seeking further treatment could be as detrimental as this whole episode has been, and these are things that I'm going to have to weigh up, all the while knowing that it's entirely possible that I may again make the wrong choice. 


I've come to realise that fear of what's happened in the past is not worth ruminating on, because I’m not the same me, and it will never be the same set of circumstances again. I'm still not be back to where I was before all this happened but I’ve learnt things along the way and I’m hopeful that my health will continue to improve. It's not fair that I have to make these kinds of choices, but I can either fixate on resenting that and the bad of what's happened, or I can hope for the best, and know that I will most likely survive the worst. 


You never know, maybe this time I'll choose up.


Thanks for reading,
Little Miss Autoimmune

Wednesday, September 21, 2011

Happiness is...


So, for a while I've been posting my articles for work up here. This one doesn't have all that much to do with autoimmune disorders, but is more about depression and anxiety, but since these often go hand in hand with physical illness, I thought I'd still post it.

Recently I was having a conversation with my friend about what constitutes a hobby, and on a more abstract level – what makes us happy.


We came to the conclusion that there were many things that we enjoy, that don’t quite constitute “hobbies” but that didn’t mean they made us any less happy. For example, I really like reading children’s books, painting my nails and drawing pictures with felt pens. I think most people would think I was quite strange if I called those things hobbies, but having things like these, that I find both relaxing and enjoyable, is essential to my well being.

A few years ago, when I was really unwell, I watched the film ‘Labyrinth’ just about every day. I think most people thought I was a bit weird for doing this, but I really felt it helped my emotional recovery. For a lot of the time, I felt too sick to get out of bed but if I wanted to watch the film – which I did – I had to at least make it to the living room.

If you’ve never seen that film, or if you haven’t seen it since you were a child, I would really recommend rewatching it. In particular the last scenes.

I’m guessing most people reading this won’t know the film word for word by heart, so I’ll summarise here. Spoiler alert – if you haven’t seen the film and don’t want me to ruin the end for you STOP READING NOW :-)

In the last scenes there are some lines which as a child I completely missed the significance of. Now as an adult, I see them not only as significant in the film, but as a comment on life in general.

“You have cowered before me. I was frightening.” The dialogue then goes on to explain that Jareth, the main character is living up to her expectations – therefore, she wasn’t cowering because he was frightening: he was frightening, because she was cowering. I realised this line, “You have cowered before me. I was frightening” could easily be talking about anxiety, depression or any number of other things associated with mental illness. Often a situation does not become frightening until we have anxiety about it – not that we are anxious because of the situation. We are anxious because we are anxious in effect. Similarly, I know if I’m feeling sad I will be upset by situations that I wouldn’t normally be. Essentially, I’m sad because... I’m sad. Not because of whatever is happening.
So this is all very well, but it doesn’t change the fact that the end result is feeling anxious or sad whatever the cause.

I think one of the final lines in the film addresses this: “You have no power over me.” Sarah, the protagonist of the film, realises that even though Jareth is frightening, he is only living up to her expectations. In reality he has no power over her.

The other night, I couldn’t sleep, and since I only get two TV channels, my choice of viewing was motorsport racing, or the Grudge 3 – neither of which is quite my cup tea. So – on went Labyrinth. I could have sat there, feeling sad and lonely, unable to sleep. Instead, I chose to do something that made me happy. I still couldn’t sleep... but that had no power of me.


Thanks for reading, 
Little Miss Autoimmune