The Gap

We’ve been talking in Bridges about this concept so I wanted to share it here. For those of us who’ve come through trauma, our experiences can make it difficult at times to connect with people who haven’t. I call this the Gap. Let me explain.

A few years ago I was undertaking one of my ill-fated attempts to get through university, and was keen to make some new friends. I joined the local French society, being in love with French movies and culture myself. One day myself and the group went out to see a French movie and caught up for coffee afterwards. As the group was chatting, the talk turned to nightmares. I quietly dropped out of the conversation.

I have Post Traumatic Stress Disorder, which was diagnosed at 15. The reality is I’ve suffered from severe nightmares for all of my life. This is a common symptom of this disorder, and it can be difficult to explain just how distressing and crippling it can be to people who don’t experience it. So, none of my experiences in this area are the stuff of coffee table conversation with new friends.

One young woman was sharing how she enjoyed her nightmares, that to her they were like horror movies, scary in a fun kind of way. She said that if she ever became too scared, she’d discovered that all she had to do was die in the dream to end it and wake up immediately. So she’d jump out of a window or in front of a car and the nightmare would be over.

The Gap that opened between me and the rest of that group at this point was so big I couldn’t bridge it. I felt sick to my stomach and had to leave early. I crept home and went to bed feeling badly shaken.

Why?

Because people like me often get through our day by pretending that we’re basically the same as all the people around us. In fact we may put a lot of effort into blending in and trying to look normal. We don’t want people to know we have a terrible history that has left marks on us. We don’t want to be different. You can do this by pretending that the things that make you different – trauma history or mental illness, aren’t real. Or, by forgetting that they aren’t universal, that not everyone has experienced these things. I tend to lean to the latter. I muddle through my days in an imaginary brotherhood where we’ve all come through what I have.

So, for this young woman to tell us that she has a had a life where she has been so secure and so stable, that even in her nightmares she retains control, shatters my illusions. It forces me to confront that my experiences aren’t universal. And that brings me face to face with the rage and anguish I work so hard to bury, about what has been done to me. About the monstrous unfairness. About the things other people can take so for granted, like feeling safe, like feeling in control. I become instantly and painfully aware of everything that I have lost.

The Gap opens between me and the rest of this laughing group. In my mouth burn stories of my nightmares, of experiences where I have screamed for hours in my dreams, trying to wake and unable to. Of the sense of being tortured that re-experiencing the worst moments of my life night after night creates. I felt like I was suddenly watching these laughing people from a very long distance away. I felt that they lived in an entirely different world to mine. I felt profoundly alone.

There are many ways this Gap opens up. It can create deep and complex feelings of grief, fury, and alienation. It’s often set off not just by an awareness of difference, but by the way the un-traumatised misunderstand and misrepresent the challenges we face. I feel it whenever someone asks in a dismissive way “Why don’t abused women just leave?”. I feel it when I sit in a pub hearing a loud conversation from another table about how “those schizophrenics” are a danger to society and should be locked up. I feel it when a television program comes on getting hostile about all the dole bludgers on disability support and how we shouldn’t have a welfare system at all. For me, part of the Gap is an awareness of how hard I work just to break even in my life. Just to stay alive, let alone to make progress. And how painful it is when the progress I make is measured against people who haven’t come from where I have, through what I have. Context is everything.

From a trauma perspective, part of this Gap is living in a society that is often hung up on the superficial, chasing happiness, and reluctant to talk about big issues. Silence and being silenced opens the Gap. It becomes difficult to be patient with friends complaining about utterly trivial matters, painful when you try to share your thoughts or feelings about a traumatic experience only to be told to move on and get over it, humiliating to feel judged if you let slip some sign of your wounded-ness like have a panic attack in a crowd.

Some of the work in healing from trauma is becoming aware of this Gap and learning how to live with it. Part of this is forming relationships with people who are on your side of it, who live in your world. Part of this is learning how to bridge this Gap and connect with people on the other side of it. That involves a certain amount of translation, learning how to present yourself and your experiences in a way that can be accepted and understood by people who don’t share them. For trauma, this means learning how to talk a little about experiences and reactions that are visceral in nature. This isn’t easy. Other people who have come through similar trauma will usually instantly understand what you don’t like about that crowded lift. People who haven’t, need you to explain. Trauma reactions are not intuitive if you haven’t personally experienced them. Many people on the other side of the Gap are good folks, some are brilliant even, incredibly sensitive and thoughtful and wonderfully safe people. Some, of course, are awful. The same goes for your side of the Gap for that matter. You can become an ambassador, helping to make that Gap smaller for other people like yourself by educating and raising awareness in general society.

Having said all that, Gaps are tricky things. You can see them even when they’re not there, just because you become used to having them there. It’s easy for us to take each other at face value and conclude that we are the only ones who are struggling, who are anxious, overwhelmed, deeply conflicted, or grief stricken. There is much common ground despite Gaps. Try not to get so focused on the differences that you lose the ability to notice the similarities, that which unites us as human beings. It is often these things that help us to bridge Gaps.

A last important point. There is more than one Gap.

There are many Gaps. People in wheelchairs feel the Gap when the only disabled toilet at the train station is out of order for six months. People who’ve experienced poverty feel it when they hear middle class people sneer at the ‘white trash’ who live in caravan parks. Gay teenagers feel it when they’re forbidden to take their partners to prom. Gaps make us feel alone, irrelevant, unvalued. Gaps make us feel like we don’t count, like we’re not even people. And the thing that nearly everyone craves is to feel human. To have a sense of belonging and value. And for the differences between us not to define us to the exclusion of all else.

So, Shane has a mental illness. Did you know he loves to fish? Jess has cystic fibrosis. Did you know she’s passionate about children’s charities? Damien survived severe burns from a car accident that killed his brother. He loves comics, is an avid football fan, has read all the Harry Potter books six times, and his favourite food is Mexican. Gaps define us by a single characteristic. Reclaiming our humanity is about seeing ourselves and being seen by others, as human beings.

 

Using Public Transport

Is something a number of people who have a mental illness find challenging. Unfortunately, we often have to rely upon it to get around, either because we’re not well enough to drive, or simply lack the finances to run a car. If we find using public transport impossible, this can contribute to serious problems such as social isolation and lack of contact with our support people such as GP’s. I am fortunate to now own a car and have a license, but I still find myself in situations where public transport is the best option – whether it’s because the trip is a really long one, such as an interstate train trip, or because there’s no parking available at my destination. I’ve been working on being able to cope with public transport better so that these trips are less stressful for me. So, here are a few tips I’ve found helpful.

1. Take it slowly
If you also find public transport a challenge, you need to build up to it with small steps. I’d advise against an interstate train trip if you have panic attacks on trains! Work up to it in small stages. I started by taking a short bus trip to a friend’s house who would drive me home afterwards. I’d only do this in daylight and in good weather, the trip was pretty short, and I had something nice to reward myself with straight afterwards – catching up with a friend. I also knew I was going to be dropped home afterwards, so I wasn’t stressed during the visit. Small successes build up your confidence to manage bigger challenges. Whereas biting off more than you can chew and throwing yourself into a huge challenge where you crash and burn will leave you feeling humiliated and deeply discouraged. Don’t be embarrassed if you have to start small. Slow and steady wins the race here. It’s also okay if you need to just take the bus one or two stops away and then walk home.

2. Reward yourself
Try to create a positive association with public transport by rewarding all your efforts and taking yourself to fun and exciting places. If you are really stressed about it and the only places you ever go on it are to the doctor or dentist – that spells trouble! Go to the local park, visit a friend, go to a cafe for an icecream, down the art gallery or museum, whatever you like. The more enjoyable, the better. You may even find yourself looking forward to the destination more than worrying about the process. I used to take myself to the movies.

3. Trauma Issues
One of the reasons many people find public transport difficult is the closeness to strangers. This has been a big one for me. There’s a couple of ways around this – for starters, try using public transport during the quiet times of the day. Avoid getting on a bus at peak hour! Take a bag with you that you can put onto the seat beside you to discourage company. (obviously, this isn’t fair if the bus is full) Sit near to the door so that you don’t feel trapped by people in the passageway. Use grounding techniques to manage your anxiety. Move away from anyone who intimidates you – go and sit close to the driver if you need to. Try to make eye contact with anyone you find non-threatening and focus on their presence. I often wave to small children or chat to Mum’s with prams. I smile at elderly folks and help people with trolleys on and off the bus. This makes me feel useful and gives me something else to think about instead of focusing on my anxiety. It also helps to remind me that most of the other people on public transport are just regular folk like me, not scary or threatening. I was on the bus the other day and a man was standing in the aisle next to me, when I noticed that he had a big mop of long fluffy white cat fur stuck to his nice dark pants! I suspect he has a lovely white persian cat at home that had been sleeping next to him on the couch. It suddenly flipped how I saw him – from being a threatening man standing too close to me, to just a regular guy with a cat and not someone to feel afraid of.

Night is also an additional stress. Waiting at a bus stop in the dark adds another level of stress to the experience. I’ve been creeping up on this one. Initially I wouldn’t catch any kind of public transport when it was close to dark. Then I moved onto being able to cope if I arrived home when it was a little dark, as long as it had been light when I first got on the bus. Then I started to catch the bus home after dark provided it was from a good stop – lots of light and plenty of other people waiting. The bus stop outside the TAFE is a good one for this. I always have my mobile phone with me, and if I feel scared, I call someone to talk, or I pretend to call someone and talk into the phone anyway. This helps me to feel safer and generally stops anyone else approaching me.

4. Voice Hearers
May also find public transport a big challenge. If you find you sometimes need to talk to your voices out loud, something that may make you more comfortable on public transport is to turn your phone off or to silent, and pretend to be speaking to someone on it. (it’s important to turn it to silent while you do this – it’s pretty embarrassing otherwise if it suddenly rings!) An MP3 player can also provide something else to focus on and may make things easier. If your voices get so loud you can’t hear what other people say to you, you might want to try learning some basic lip reading. One way to start this is to watch daytime soapies on mute. The overacting and lots of face close ups can help get you started. I don’t find this easy but I’ve heard of others who say it takes the edge off a bit. 🙂

5. Dissociation
If you’re prone to dissociation then the combination of a stressful environment plus the rhythmic motion of the vehicle may really have you zoning out. I miss a lot of stops! I leave books, jumpers, and handbags on trains. If you have a phone or digital watch, set it to go off a minute or two before your timed stop to alert you. Then, set it to snooze or to go off again every 30 seconds! If you have to put down belongings, put them on the seat by the aisle so you have to pass them to get out of your seat. Better yet, put them on your lap, or into a bag. Never put things on the floor by your feet. Ladies, use a handbag with a long shoulder strap and put it in your lap with the strap still around you. This makes it a lot harder to leave behind! Guys, use pockets or a student satchel. You can also tie belongings to one wrist with a piece of string or ribbon, esp if they are too big or awkward to put on your lap – eg a guitar. Don’t feel silly – the most important thing is not to donate your precious shopping or other belongings to the transport association!

6. Take a friend
If you have a lovely helpful person with some time on their hands, try taking along a friend while you get used to using public transport again. I was really surprised how much difference this made to me. It can help you create some more positive memories and experiences.

7. Distraction
I love my MP3 player for this. I put in one ear bud so I can hear my music, but I’m still aware of what’s happening around me. This is pretty important when you’re near traffic and roads, your sense of hearing plays a huge part in warning you about traffic and keeping you safe. But trips which felt excruciatingly long seemed to shrink to nothing when I have some of my favourite music to listen to.

8. Weather
This can certainly make a big difference to your travels. There’s not much more miserable in life than being stuck at a bus stop in the rain or in 40C heat. So, check the weather before you go out. Invest in a small fold up umbrella. Always take a jumper even if there’s only a small chance it will get chilly. I’ve found that catching a bus in the evening on hot days can be very cold because the air conditioner is still running even though its now mild outside. Try to avoid long waits for transfers during heatwaves. Take a frozen water bottle with you if you have to go out. This might all sound really silly, but if your stress level is already high things like getting wet or being really hot can be the difference between being uncomfortable and having a meltdown.

9. Smart phones
One of the things that I really struggle with is reading the guides! I have a minor learning disability that means I tend to scramble numbers and have difficulty with some kinds of maths. Bus timetables are basically my worst nightmare, and I frequently end up in the wrong place at the wrong time waiting forever for a bus that isn’t coming. This is incredibly frustrating! I also end up carrying a lot of timetables around so that I can get home. Knowing that I may read them wrong, I always go home a few buses before the last ones of the night even if I was at a function I was really enjoying. I’ve just upgraded to this entry level smart phone, which means I can pay for a small amount of internet and access google maps. In fact some internet data is included on my phone plan, I’ve just never been able to use it before. So, no more carrying around wads of timetables, and it’s much easier for me to be flexible and change plans last minute when I can just google map a new route home. I’ve spent the last couple of days bussing about the place getting used to using the phone to work out my next step. This wont be an option for everyone, but now that basic smart phone prices are down to $50, it is becoming more achievable.

10. Control issues
One of the things that can make public transport more stressful than other forms of transport is the awareness that you are not in control of the vehicle. It requires a certain degree of trust to get on board! If this is an issue for you, stay near the door, try sitting on the left aisle, away from the other traffic, and never forget – if you really need to, get off at any stop, catch your breath, take a small walk perhaps, and then get on the next bus that comes. You may feel trapped, but the reality is you can get off at any stop you need to, and very few bus drivers would prefer to keep on board someone who’s having a panic attack. For longer trips this is more challenging. Using creative visualisation may help you feel less trapped – in simple terms, try going away to your happy place and stay there until the trip is up if you need! If you can read or watch a movie that may help to distance you from your surroundings. Alternatively, mindfulness techniques may help you to adopt a more detached and curious perspective about your circumstances. If at all possible, try to get off public transport before you become overwhelmingly distressed. This will help you feel more in control of your condition. If you hang on until you have panic attacks or meltdowns, public transport will become more associated with these really upsetting experiences, which will only make it harder to use in the future.

11. Use alternatives
On bad days when you know you wont cope – and hey we all have them! – don’t set yourself a task you know can’t achieve. Go for a walk instead, or have a ride on your bide. Get a second hand pair of roller blades. Hitch a ride with a friend or family member. Don’t curl up in a small ball at home and brood forever!

Constriction and isolation are bad for your mental health, and you can easily get stuck in a downward spiral where the more miserable you feel, the less you’re able to cope with public transport, so the more you’re stuck at home, and the more miserable you feel. You deserve the freedom to explore your world. Feeling familiar with and safe in your space can help expand your world and reconnect you to outside events. Having a local park you can walk to if you need some space or to get out of the house for a while is a good thing. I go hop on the swings when I need a breath of fresh air. Check your local messenger for free events such as gallery openings. Find a local pub and make it yours. Make sure your world is bigger than your bedroom.

This article can be found in pdf form here for easy printing or downloading. Feel welcome to share using the buttons below. To read similar articles, click on a label below. To see my copyright policy, go to my About this Blog page.

Hearing Voices

I’ve been attending, and lately, co-facilitating, a group called Sound Minds for over a year now. This group was started by MIFSA, based on the principles of the Hearing Voices network. I initially went along to support a friend, but found it so helpful for myself I stayed on. I feel very fortunate to have a group like this in my life, it has made a huge difference for me.

Hearing voices is actually a fairly common human experience, but one that has become linked to serious mental illness and major stigma. A lot of people who do hear voices keep this a secret and fear being found out and thought of as mad. Technically, a diagnosis such as schizophrenia require a number of criteria to be met, not just an experience such as hearing voices. But in my experience, if you tell a doctor you hear voices you will likely receive a diagnosis like this whether you have any other symptoms or not.

The standard medical approach to voice hearing goes something like this:

  1. You hear voices because your brain isn’t working properly. You have a mental illness. Your voices are auditory hallucinations.
  2. The cure for this is medication, which addresses the chemical imbalance presumed to be the basis of this illness.
  3. If medication isn’t working, increase the dosage, add more meds, and possibly ECT.
  4. If this still doesn’t work, you are a chronic case, likely to experience lifelong disability.
  5. Talk therapies don’t help, and you should never talk to or about your voices as this will only make them worse. There is no context or meaning to your voices, and hearing voices can never be a neutral or positive experience.

The problem is that for many people, this approach isn’t particularly effective. The Hearing Voices network is a grass roots movement that started in the Netherlands in the 80’s. There’s an interesting article in The Times about how Hearing Voices groups work for people. Some very interesting findings have come out of research into voice hearing, such as-

  • Many people who hear voices do not meet any of the other criteria for a mental illness
  • Many people hear positive or encouraging voices and are not distressed by their experiences
  • Most people who hear voices do so after a particularly emotional or traumatic event
  • Some people only hear voices for a short period of time, then they go away.
  • Some people find that ignoring their voices and constantly trying to distract themselves actually makes their voices worse.

So, the idea behind Sound Minds is having a group that doesn’t use the medical approach to hearing voices. We don’t presume to tell each other what their voices mean or how to manage them best. We each share our journey, our understanding of our own voices, what helps us and listen to each other and borrow strategies to help us manage our experiences. All newcomers to the group are given this printout, and told that it’s been written by other voice hearers, not by ‘experts’. We encourage them to notice if there’s anything listed they’ve already tried, and if it was a helpful approach or not.

The emphasis is upon individuality – how each person understands their voices is legitimate, and what works for each person is often different. Group members are encouraged to be accepting of a diversity of experiences and approaches to voices, and to share ideas without pressuring each other to see things their way. Some people find the biochemical model most helpful and have found medication and/or ECT to be lifesaving, but wish also to be able to talk about their experiences with people who understand. Others have a spiritual framework for their experiences, or link hearing voices to trauma. Some people find telling the voices to be quiet can restore a sense of control, while others find it escalates them. Some people find that the right approach leads to their voices going away, others find it helps them learn to live with them.

I’ve just been listening to a presentation from an International Conference about Recovery from Psychosis. The talk was called “The Personal is Political” by Jacqui Dillon. This would have been an incredible conference, the talks are available quite cheaply (compared to the cost of attending the conference!) on DVD here. Jacqui’s understanding of her own voice hearing experience is closer to DID than schizophrenia, she considers her voices to be parts of herself. This approach has clearly worked well for her and she presents about her experiences in an articulate and deeply moving way. You can hear a different interview with her here.

So, if you hear voices, or know someone who does, take heart. It is still possible to lead a wonderful meaningful life, even if your experience is one of those around learning to live with, rather than being cured of. If what you’ve tried or been told to try so far hasn’t worked, perhaps there’s some suggestions in these links that may help you to look at your situation from another perspective, and find a new approach. It’s important to keep in mind that even your best strategies may not work all the time in all situations, so don’t give up, keep looking, learning, and discovering those keys that help to give you back a sense of hope.

The Australian Hearing Voices network have a website here, with some of the groups listed. They don’t update it very regularly and so far we haven’t been able to coax them into including Sound Minds in their listings, but we’re working on it! If you’re in SA and you’d like to come to Sound Minds, the details are all here. The group runs every week but there’s no pressure to attend, people come as often or as little as they wish. You are also welcome to bring along a friend for support if you wish. If you’d like to print a flyer to keep or share, there’s a pdf here – and that’s my artwork designed in consultation with the group and donated for the flyers. 🙂

For more support, see the community I founded: The Hearing Voices Network of South Australia: www.hvnsa.org.au

Surfacing from dissociation

In Bridges last week we shared the incredible experience of surfacing from chronic sensory dissociation. Sometimes people experience short episodes of dissociation, lasting hours to days. Some of us experience chronic dissociation that can last for years, sometimes punctuated by little episodes of reconnecting. When this happens, it is a very precious experience and important to make time to treasure. I’ve experienced chronic dissociation where for months my sight has been dim, colours seem dark and dull to me, my hearing is poor, my taste and smell are dulled, and my skin doesn’t perceive touch clearly. Everything is dulled, far away, darkened. It feels like being a zombie, alive but dead.

Coming back to life, even if it’s only brief, is glorious. To taste, smell, or feel things clearly, sharply, is intense. Being numbed by dissociation can be like walking about muffled in a huge overcoat. Taking this off and feeling the breeze on your skin, the sunlight, the smell of gum trees or grass, is an intense and sensual experience. Chronic dissociation can leave you raw, like feet kept in shoes all winter long, they are tender when you first walk barefoot in the spring. If you experience chronic dissociation, treasure any moments it subsides. Take time to touch life, to breathe it in, to remind yourself what it feels like to be alive. These are the memories that keep us going when our world goes dark again. This is what we are fighting for.

After the weeks made dim
By fear and stress,
incessant storms,
bloody foam
on the black water

A day like today
is so strange and welcome
To wake, and find the devils gone
No shades at my bed – misery,
loneliness, hopelessness, and bleak 
despair
All mysteriously called away
And instead the day is mine, to fill with my own things
Bliss.

The anxiety and the wrenching pain
Drive me before them,
bound and bruised,
Resentful and unable to escape
Burning with black dreams
Enslaved to brutal masters
On whom I wish evil ends.

To be free of them – is to fly!
I enjoy everything, the sunlight through the windows
Bare feet on carpet, the colour of my dress,
Smell of my skin
My mind is clear, clean as snow melt
My fingers are alive; I perceive and create
I soak it all up
To get me through
When the haunting starts again.

Recovering from Trauma – Object Constancy

At Bridges this week we talked about ways people recover from trauma, beginning with the area of Object Constancy. Simply put, object constancy is something children generally develop as they grow. It is about attachment, and means that – when Mum is out of the room, the child understands that she still exists, and is able to be comforted by the thought of her. Children who do not have object constancy have an ‘out of sight – out of mind’ kind of experience, where if Mum isn’t in sight, she ceases to exist entirely, which is frightening and upsetting. A lack of object constancy in adulthood can be a painful part of a number of different mental illnesses. Many people with dissociative disorders have difficulties in this area.I’m no exception. I’ve discovered that managing chronic dissociation is often about finding creative ways to help information cross dissociative divides. So, I have learned that I need reminders of my important relationships around me, such as photographs. I wear perfumes that have links to people that are special to me, such as my Grandma, or my lovely neighbour Marie when I was a child. I have had to write the names of my friends on paper and pin them somewhere I can read them regularly, or when I am stressed, I forget that these people exist and care about me.

That sounds cosy and simple. The reality is more complex. Sometimes there are no relationships to draw comfort from. Sometimes there are relationships, but they are cold, or distant, or abusive. None of these qualities inspire attachment. There’s no point in trying to overcome dissociation to be more connected to an existence that is painful and destructive. There’s often a reason it’s there in the first place. Sometimes relationships can look and seem close, but be missing essential qualities that create connection. Sometimes, feeling lonely in a relationship can be indicative not of attachment problems, but of a relationship that is disconnected on some fundamental level. I once had a close relationship with someone like an aunt in my life. Increasingly discontented and confused by my sense of distance I tried to rebuild a closeness between us, sending gifts and cards and calling by. Eventually when confronted she told me that she had stopped loving me years before, but still maintained the semblance of a friendship so that I would not make a fuss. Having attachment issues does not mean that all your relationships are good and any problems are always you.

But, when there are good caring people around you, having them cease to exist on an emotional level the moment they leave your side is a horrible and frustrating experience. So, carry pictures of your children with you. Keep tokens that remind you of your loved one. I have a candle I burn at Christmas in memory of my Grandma. She’s still with us every Christmas. I wear jewellery given to me by people special to me. I keep cards on display for months. This is the place I’m trying to stay out of:

I can’t feel you

or see you
everything is dark here
and you are
only a story told to me
so alien and lovely
I try to believe
That the world is not empty
That other hearts beat in the dark
But it is difficult
On the edge of my vision, you blur into the night
Becoming only shadows and whispers
The wind speaks cruel things to me
And I wonder
If there is any love left in the world.

Introducing DID

In our group Bridges this week, I gave a talk introducing DID (Dissociative Identity Disorder). We are planning to present a forum on the topic in about 2 months time. It’s a very big topic and there’s a lot of misinformation and confusion out there about it. This talk is by no means comprehensive, but it is I hope a good introduction and overview of the condition.

What is Dissociation?

I’m going to start with a quote by a psychiatrist, Judith Herman:

The psychological distress symptoms of traumatised people simultaneously call attention to the existence of an unspeakable secret and deflect attention from it. This is most apparent in the way traumatised people alternate between feeling numb and reliving the event. The dialectic of trauma gives rise to complicated, sometimes uncanny alterations of consciousness… which mental health professionals, searching for a calm, precise language, call “dissociation.”

What does that mean? Dis-association is the disconnection between things that are normally associated. In simple terms, dissociation is to be unplugged in some way. 

Most of us have experienced a small degree of dissociation. One common example is called highway hypnosis, which is where you may drive say, home from work, and arrive not able to recall any details of the trip. You’ve been driving on autopilot probably thinking about other things. Another example is daydreaming, or getting ‘lost’ in a good book. These are common experiences, and do not indicate a problem of any kind. Dissociation only becomes a disorder when it is severe, distressing or disabling. It can be difficult to imagine what severe dissociation might feel like, but if you have ever stayed awake for a night or two, perhaps studying, then you have some idea. You may have felt confused, foggy, your sense of time might have been different, perhaps the room appeared fuzzy or spun around you, you may not have felt your feet upon the floor. Remembering this experience can help you imagine what someone who experiences severe dissociation may feel like.

Dissociation and Mental Illness

Dissociation is a symptom of a number of different mental illnesses, such as Post Traumatic Stress Disorder, and Borderline Personality Disorder. There is also an entire category of disorders where dissociation is the primary issue, just like the category of anxiety disorders groups different mental illnesses where anxiety is the underlying feature.

Dissociation can happen in may different areas. It depends which area has been ‘unplugged’ as to which symptoms a person experiences. People who suffer from chronic dissociation may struggle with symptoms such as:

  • Emotional numbing – where someone cannot connect to their own feelings, feeling flat, empty or numb instead.
  • Amnesia – ‘zoning out’/blackouts/lost time, when dissociation occurs in the area of memory, for example suddenly discovering that it is Thursday, and having no memory of Wednesday.
  • Time speeding up or slowing down – if you have ever been in an accident you may have experienced this common dissociative symptom.
  • Losing sensations – not being able to feel your own body, or feel sensations such as heat, cold, pain, hunger. Dissociation can unplug someone from their own senses, dulling or even removing altogether their sight or sense of hearing or ability to feel pain for example.
  • De-realisation – this describes someone’s experience when they are unplugged from the world around them, it may feel like being in a dream, or that they are living in a film. Nothing feels ‘real’. This may not sound so bad but it can be very distressing to experience.
  • Depersonalisation – describes being unplugged from yourself, where someone may feel unreal, like being a robot or living in a dream. They may not recognise their own reflection in a mirror, and may have out of body experiences where they seem to be watching themselves.

Many people experience one or more of these without having a mental illness. And people who do have a dissociative disorder may experience only one or all of these. Some people struggle with chronic symptoms, while others experience episodes and then recover.

What is DID?

DID is one of the Dissociative Disorders. In DID, Dissociation occurs primarily in the areas of memory and identity. DID used to be called Multiple Personality Disorder. The name was changed in the DSM to reflect a different understand of the condition. DID is not someone having more than one personality, it is one personality that is divided into parts through dissociation.

Dr Warwick Middleton, an Australian psychiatrist who is the Director of the Trauma and Dissociation Unit at Belmont Hospital in Queensland wrote “It is inaccurate to conceptualise a patient with DID as having ‘multiple personalities’. A more helpful conceptualisation is that such individuals have access to less than one personality.” (at any one time)

We all have parts

We all show different sides of ourselves with our workmates, children, and friends. We play different roles in our lives. We know what it feels like to be “in two minds”, we say things like “part of me wants to go out tonight, and part of me wants to stay  in”. For a person with DID, these things are true in a literal way. 

Parts Divided

For someone with DID these parts are separated from each other by dissociative barriers. As a result, they develop separately and can be very different from each other. For example, they may have different ages, gender, skills, interests and beliefs.

There are some common terms associated with DID it may helpful to know the meaning of.

  • Part or Alter – commonly used to describe the different personalities in a person with DID.
  • System – this describes the group of personalities that make up the whole person with DID. Many people prefer other terms such as family, tribe, or community.
  • Switching – one part going ‘inside’ or away, and another one coming ‘out’ and inhabiting the body. This may be slow or quick, obvious or very subtle.
  • Trigger – is anything that makes a switch between parts happen.
  • Coming out/Going in – used by people with DID to describe times where they are in control of their body and times where another part of their system is.
  • Kids/Littles – refers to any parts that are children or young teens. It is quite common for people with DID to have younger parts, but not everyone does. A person with DID may talk about their ‘kids’ to mean not biological children but their children parts.
  • Multiple – a shorthand way of describing someone who has separate parts. People without dissociated parts may be called Singletons.
  • Co-consciousness – means that more than one part is aware of what is happening at the same time.

Why does it happen?

The development of DID has a very high association with childhood trauma. In childhood the identity is still forming, and trauma during this time can result in dissociation in this area. It’s important not to make assumptions here, trauma may involve abuse, but there are many other ways children may be traumatized. For example a very ill child who must undergo many painful medical procedures may develop DID. Not everyone who has DID has come through childhood trauma, and certainly many people who are traumatized as children do not develop DID. It is also important to note that while some people with DID have come through extreme abuse, others’ experience was less severe yet they have still developed DID. 

Whilst DID is considered a mental illness, it can also be thought of as a defence mechanism, a way to survive. Psychologist Deborah Haddock writes “Many people with DID baulk at the use of the term disorder. When every ounce of your being comes together to fight for survival, having it termed a disorder can feel discounting to say the least.”

How do people survive trauma?

1. Containment

There are, among many others, two key abilities that all  people may draw upon to get through a traumatic situation. One of these is containment. This is about being able to compartmentalise experiences. If you have ever put aside your feelings to assist at an accident, then after everyone was safe, gone home and shaken and cried, you have used to containment. You have contained your overwhelming feelings to do what needed to be done, and then felt them later on.

Someone with DID uses containment in an even stronger way, where different parts contain different skills, memories, or emotions. One of the advantages of this is that damage is contained, and healthy areas of functioning are preserved rather than the whole person being overwhelmed and unable to function. An analogy is the way a flock of geese flies. The goose at the front encounters the most air resistance, it has the hardest job while the rest of the flock rest in the slipstream. When the front goose tires, it drops back and another goose takes the lead position. The parts in a DID system may do this, where one part is out, then goes away inside to rest while another comes out.

2.Adaptation

Another way people get through trauma is through our ability to react and adapt to new situations and environments. We’re all capable of drawing on different strengths and skills in different environments. For someone with DID, this ability to adapt can be life saving. For example, a child may develop a part that copes with physical pain by numbing and not feeling anything. They may have another part who goes to school, has none of the bad memories, and is able to behave normally. They may also have another part tucked away inside who keeps fragile characteristics safe from being destroyed by a harsh environment, for example hope, self esteem, or optimism.

Theories

There are two main frameworks used to describe the way separate parts form in a person with DID.

The Smashed Vase theory is that every part of a system is a piece that together makes up the whole person. This explains the way systems can divide up basic characteristics such as emotions, one part manages anger, another expresses joy.

The Alternate Selves theory is that every part is one possible version of who the person could be, given their experiences and history. This explains the way DID systems can continue to split and form new parts, there seems to be no upper limit of how many parts can form. Also the way parts can un-form, meld into each other, and disappear.

The reality for a person with DID may be an overlap of both processes.

Challenges

There are some huge challenges facing a person with DID. Deborah Haddock writes “Most DID patients see several therapists and have an average of seven diagnosis before finally finding someone who understands the dissociative aspect of their behaviour… Confirming the diagnosis of DID is not easy, however. One of the difficulties lies in the nature of dissociation, which compartmentalises behaviours and experience that would normally be connected. Also, the dissociative personality system is usually set up to avoid detection.” In a nutshell, DID generally only works as a defence mechanism if it is hidden and secret. Otherwise, being divided may make someone more vulnerable to abuse.

Dr Middleton writes “For dissociation to be an effective mechanism in protecting individuals from being overwhelmed… it is necessary for the individual to a fairly large degree to dissociate the fact that they dissociate. If they are fully aware of the extent of their dissociation, they they are very close to being overwhelmed by the underlying reasons for it.” DID can be extremely confusing to experience, and even finding the words to express what is happening can be extremely difficult. It is not a very common diagnosis, and not many professionals specialise in the area of dissociative disorders. Even once diagnosed, finding a competent and caring professional to work with may be difficult. 

People with DID are not all the same

We tend to think in absolutes, something is black or white, someone is crazy or sane. The reality is less concrete. Dissociation is more a continuum, with normal, healthy experiences at one end, and severe mental illness at the other. Likewise, within the realm of multiplicity, there are a number of continuums, and the result is that there is a lot of variation between one person with DID and another. For example, the degree of amnesia varies considerably. Some people with DID have total amnesia for the times when other parts are out. Others are aware of what is happening, which is called co-consciousness. Some multiples don’t experience the level of amnesia needed to fit in the category of DID, and they may receive a diagnosis of DDNOS (Dissociative Disorder Not Otherwise Specified) instead. Some other differences between people with DID are

  • Obviousness of switching – for some people it is obvious when they switch, for others it is so subtle that only someone who knew them very well might be able to tell.
  • Number of parts – this can range from just one, to hundreds.
  • Switching – some multiples switch all through the day, others only very occasionally, and some people never switch, but they talk to their parts and hear them in their mind.
  • Degree of internal control over triggers – some multiples can chose which part is out, others have no control over this.
  • Degree of fluidity – some multiples have fixed systems with, say, 5 members who have been there for years. Others are more chaotic, they are difficult to learn about as they are constantly changing with new parts forming and old ones going away.
  • Other diagnosis – people with DID may have other physical or mental illnesses which will change how they experience life.
  • Degree of disability – some people with DID are extremely unwell and struggle to function, perhaps spending a lot of time as inpatients, while others live and work unnoticed in the community, perhaps with no one around them aware of their condition.
  • Polyfragmentation – some people with DID have mini systems within their system, or have parts who have themselves split to form parts of their own.

DID is about identity – it is therefore extremely individual in the way it presents and is experienced.

How can I help a friend with DID?

One of the most important things a person with DID needs is acceptance. It can be very stressful and discouraging to have a condition that is uncommon and often misunderstood. Media representations of DID are often dramatic and frightening. It is also important not to be invasive. Some people with DID are comfortable sharing details about their systems, others are not. Asking questions like “who is out now?” or “what are all your names?” can be confronting. It helps if you are willing to cope with inconsistency. Someone with DID may one day love apples and the next hate them, may tell you on different occasions about a film they saw and give you completely different impressions of it. Often, this is misunderstood as lying, when it is just parts with different tastes.

It will also help if you are willing to cope with confusion. Dissociation is extremely confusing by its nature. It may take a long time to work out what is happening. It may take a long time even to determine if the symptoms are dissociation rather than something else. Try not to pressure the person to know more about what is going on for them they can. Learning about this is a process, and the diagnosis of DID often carries a lot of stress and fear for people. Being safe is very important, if you have a friend with DID it is vital that you never take advantage of their multiplicity. If they have child parts, treat them as you would treat children for example. And lastly, although you may have a strong friendship or relationship with one part, do your best to embrace and welcome their whole system, and recognise that your friend is part of a community.

Is there hope?

Yes!

Connections that have been broken can be rebuilt. Trauma can be healed. It is important to find good caring support people, friends or family or professionals. As much as possible, work on learning about your system, increasing communication, self awareness, and self acceptance. Reducing denial, and learning how to ground yourself can also make a big difference. The goal is to come together to function as a team, all protecting and looking out for each other instead of fighting and pulling in different directions. This goal can be reached through cooperation, and/or through integration, which is where the dissociative barriers between parts dissolve, so every part is out all the time.

People with DID can be very vulnerable, but they are also incredibly resilient!

Cameron West, who has DID, writes:

I desperately want to feel like I’m part of this world and somehow connected to the people in it. I guess that’s why I’m here today. I’m hoping that somebody will look into my eyes and tell me they see somebody there, tell me they see Cameron West there. And if they see other people in there, well that’s okay too. It has to be okay. I’m through being disconnected from me. I am who we are, and it’s got to be okay, or I’ve got no chance of a better life.

For more information see articles listed on Multiplicity Links, scroll through posts in the category of Multiplicity, or explore my Network The Dissociative Initiative.

Managing Triggers

I led the discussion in our group Bridges yesterday, on the topic of managing triggers. I thought I’d share it here for the benefit of a wider audience. 🙂 Just brushing the surface of what can be a very big topic – What are triggers? Anything in our environment that ‘triggers’ a reaction so quick or so strong it bypasses our conscious control is a trigger. On a simple level, touching something hot and recoiling without thinking about it is an example of a trigger. When we use the term in mental health, we’re usually talking about things that trigger strong emotions, strong memories or flashbacks, dissociation, or for those with DID/DDNOS (Dissociative Identity Disorder or Dissociative Disorder not otherwise specified), perhaps alters. Really, anything can be a trigger. Some of my triggers are certain smells, such as a particular brand of cologne associated with bad memories for me, sounds such as certain songs or music, places – such as my old school ground, and situations such as encountering someone aggressive or violent.

Everyone has some things that trigger a reaction in them, and triggers are not necessarily a bad thing. It isn’t just strong bad memories or strong negative emotions that can be triggered. Positive memories and emotions can also be triggered by things in our environment. Hearing ‘our song’ on the radio, being present at a birth, smelling something that we associate with a loved one – great grandma’s perfume. All these things can trigger a strong, even overwhelming reaction in us, and this is a good thing. To be moved by things is part of what it means to be human. So for those of us who find triggers difficult to cope with, it can help to remember that the goal is bringing them back to something manageable, not getting rid of them altogether.

I’ve pulled out of my journals this poem I wrote about being triggered in a positive way. At this time in my life I was suffering from severe dissociation. Most of my senses were dulled severely, I could not taste, my sight was limited and colours were dull. My sense of touch was reduced, a hand on my arm felt faint and far away, I couldn’t feel my feet touching the ground. It was a very bad time and very distressing. On that evening I was coming back from an event, being driven through the city. As I came along King William Street, the bells of St Peter’s Cathedral rang out. And the sound triggered me, I surfaced through the dissociation and suddenly felt alive again, for a brief moment.

The Fire
Yesterday I woke with a fire in my chest.
All the leaves of autumn burned.
My thoughts were sharp and clear
The night was sharp and clear
I awoke
From where I had been lost
In dream-haze, in exhausted slumber.
I reached out
To the sound of bells that rang
Through the city.
I tasted the air and felt my mind inhabited
I turned and looked with eyes that turned and looked with me.
Like a vault opened to the light
Like a moth from a cocoon I awoke
The fire stirred me.
And beneath the clarity like diamond-fire
Was the little tightness
The knowledge that fatigue, like wolves
Would return when the flame was ash.
This respite from the haze that is my life
Was brief. For a glorious moment I touched the night.
I knew myself familiar.
Stranger! I cried
I had missed you
Lost you
Loved you
And I know you will not stay.

However, triggers can make life very difficult! If, like me, you find that you are very reactive and struggling to manage many triggers, here are some starting points on ways to try and calm things down.

One of the first options most of us try is to avoid. It’s worth mentioning because it is a legitimate option! If the trigger is something easy to avoid, like a particular location you don’t need to go near – for me, my old school, then avoid it! Easy. This option falls apart a bit if you have lots of triggers or triggers that are really common in your everyday life. Then you end up not being able to get out of bed. But there’s no prizes for stressing yourself out trying to make yourself cope with a bad trigger you don’t need to confront.

Desensitisation is another approach. This comes from treatments for anxiety and phobias. The idea is that you gradually build up your ability to cope with a trigger, until it gets to the point where it no longer affects you. For example, for awhile there the smell of rosemary was a trigger for me. It would immediately make me feel extremely nauseous. So, I used to occasionally put an oil blend containing a tiny amount of rosemary in an oil burner on days I was having a good time, friends over, feeling good. It would bother me a little bit but not much. Over time I increased the amount slowly, and kept linking the smell to good, fun experiences. Now, it doesn’t bother me at all and own a rosemary plant I cook with all the time. This concept of association is what gives triggers their power to affect us – they have been associated with a strong feeling or memory. Sometimes you can in time break down that association and create a new one.

I often cope by trying to overpower triggers. Smell is one of the most potent memory triggers for all people, and I use my perfumes to help me cope with other triggers in my environment. I find the smell of strangers upsetting, so in situations like public transport I can become very distressed. If I am wearing my own perfume, a smell that is comforting and familiar, I can breathe this in and literally overpower the other triggers. But it can also work on other levels – for example, I have a ring that reminds me of my sister, which is a comforting thing to me. I wear it to work on days I know will be stressful, and I touch it and look at it to ground myself and remind me I am safe and loved. I use it to overpower those things in my environment that are triggering fear and threat in me. Another way of putting this is that I use the strength of a positive trigger to help me deal with a negative one. I call this anchoring and I’ve explored the idea more in

If you find yourself jumping at shadows and reacting to everything, then going through each trigger one at a time is probably going to be time consuming and frustrating. In that case it may be a better idea to work on lowering your reactivity. If your baseline stress levels are really high, you are much more sensitive to triggers. What do I mean by that? Your baseline is what you return to after stress. So, in this picture, those red spikes are periods of massive stress, while the green zone done the bottom is you feeling all chilled out and okay with the world.

As you can see, for some of us, when we go through major stresses, we don’t ever quite get back to as chilled out as we used to be. Each episode leaves us more stressed and anxious and highly strung than the last. Our baseline – how we feel when nothing is actually happening to stress us out, gets so high that we feel permanently stressed out. When we’re in this space, we are highly reactive. Nearly everything is a trigger. The idea is try and recover better from stressful events, so our baseline looks more like this:

When we’re getting good time cruising along in that green space, we’re less reactive and will find triggers easier to manage. For more ideas about how to get back to the green space see:

Something else to bear in mind if you’re having troubles in this area, is that you may find taking some time to process your stuff can help. If, like me, you get through the day by burying a lot of what you’re feeling and thinking – this can come back to bite you. Sometimes triggers are the price you pay for using suppression to cope. It can be like trying to hold a beach ball under water – at some point it will get away from you and come hurtling up! If you have grief or trauma to work through, making some space for that in your life can help to reduce your reactivity to triggers. This doesn’t necessarily have to be intense, anguished and time consuming. It can be as simple as starting a journal where you write about some of those feelings, going to a counsellor to talk about grief, or putting up a photo in memory of someone you’ve lost. Sometimes very small things that signify to yourself that you are listening and paying attention to your own needs can make a big difference with how well you cope in other areas of your life. For an example of this see

And lastly, for the multiples, if the big issue you’re having is trying to prevent things that trigger alters, then you can try everything listed above – and it may indicate you have some system work to do. If you’re functioning by suppressing everyone else in your system – some of them are going to fight you. And they can gang up on you, be very persistent and wear you down. Working to make some safe time and space for everyone to get a little of what they need – which sometimes is just to be acknowledged that they exist – can make a big difference in coping with triggers. If your team are working together instead of fighting each other, then things that trigger switches aren’t such a big deal. You can also learn about how to use triggers to generate useful switching, see

I continue talking about the management of triggers and the risks and benefits of the way we think about them in Mental Health needs better PR.