British Columbia
Borderline Personality Disorder, OCD, Anxiety



My name is Mikayla.
I deal with O.C.D., B.P.D., which is Borderline Personality Disorder, and occasionally bouts of social anxiety.

I’ve been dealing with it for about eight years. I think what brought on my mental health problems would probably be genetic and environmental.

I guess in terms of coping strategies, I would use stuff like anything from that I’d learned in terms of mindfulness, pleasure activities like drawing, but also bigger things like exercise and eating properly. And building those goals like going to work more and just taking it one step at a time. A lot of it is just focusing on yourself, focusing on how to get through the situations. I take the skills that I have been taught and I work it into my life. And with that it’s like when you kind of get little snippets throughout your days or months or weeks or years, you bring that, those little ideas in, and you just work with them. It’s a work in progress. I mean there’s no magical wand that is just going to cure you.

B.P.D. is a personality disorder so a lot of it is action based. So it’s a very, very, self-destructive illness. It’s very personal; it’s very all about you kind of thing. It’s the way you act out, the way you think and it’s personal with everything. Everyone’s different, but my own experience with B.P.D. is that I have challenges with self-harm and that was my biggest addiction. It’s masking your emotions or it’s a release. I mean it can be. I use to do it anywhere, any reason from being bored, to being angry, to being sad, or even happy. And sometimes I did it to feel emotion and sometimes I did it to suppress emotion. Sometimes I just did it because I was punishing myself for punishing someone else and I took it out of my body and then sometimes it was just plainly the release.

The thing with B.P.D is it is a very dramatic illness, and I mean there definitely were a lot of traumatic events based on the drama that went on in my environment. A lot of it I’ve learned, you know, that I have hurt people with my illness but it’s learning that it is not me that hurt them, but it is my illness that hurt them. It’s coming to that understanding that you know you’re not doing it to hurt people, it’s your illness, it’s inside you and sometimes it controls your brain, it controls your operating system. I give a big shout out to my family because I know they went through a lot and it made us stronger, it did, and it gave us a lot of really good moments too. And you know, it goes with any family who has a child who is very sick.

If we band together and we help each other, we’re going to spread that knowledge of what helps each other and what works and what doesn’t work and how we can fight back to get us, to get our voice heard. You know, you’re all worth it. We’re all worth it. We’re all pieces of a puzzle that connect the world.

I believe I can live positively. As much as it’s a negative atmosphere, it’s definitely is, I wouldn’t have had so many awesome attributes about myself. Some days I’m like I wish I never had to go through what I went through; I wish I’m not going through what I’m going through now. But when I am in a positive frame of mind, I wouldn’t take back those years. I wouldn’t change them because it’s taught me so much and it’s given me so much insight and so much wisdom and so much empathy and it’s really just kind of brought me to where I’m supposed to be in life and what I’m supposed to do. It showed me the path of what I’m supposed to do in life. I mean it can be a real pain, a pain in the bum, but it’s really, there are moments where, I mean even laughter even just having a bout of laughter and you cherish it so much more than most people. You don’t take things for granted. You don’t take those happy moments for granted. And so yeah I think I can live positively. You know maybe not all the time, as this is a lifelong process. But if I live in the moment and if I live through the skills and helping myself then yeah there are going to be a lot more moments that are really worth living for.



British Columbia
Dissociative Identity Disorder, Depression, PTSD, Anxiety



My name is Suzanne.
I deal with dissociative identity disorder, depression, complex P.T.S.D., and anxiety.

I was correctly diagnosed with dissociative identity disorder in May of 2003, but I’ve been dealing with it all my life, as well as the depression, anxiety, and complex P.T.S.D. So yeah, all my life.

D.I.D. is created in early childhood usually before the age of seven and it’s a result of overwhelming circumstances, in my case it was severe neglect and abuse, and it can also happen if a young child has had multiple surgeries or medical procedures. It also happens with kids, young kids, which have grown up in refugee camps and live in a civil war area. What it basically is is the child has nowhere to go when the overwhelmed circumstances happen. So what I did was, if the perpetrator came into the room, me the typical Suzy that you see here, would kind of go into the background and I created this persona that would deal with the event in the situation and they would hold all the memories and everything of that event. When the event was over and the perpetrator was gone, that persona would kind of go back into my subconscious and the apparent normal self, me, would come out just kind of carry on and try to carry on the best I could.

Beforehand my disassociation was my coping. Whenever life got too bad I would dissociate. In D.I.D. you create at a young age these personas to deal with stuff and so I would just kind of basically check out of life and another persona would come and deal with life. But then I would have no memory of what I had done. I’d have people come up to me on the street talk to me and they know who I am but I have no flipping idea who the hell they are because I don’t remember talking to them. Being aware when I need to pull out of things, I’m fairly busy and fairly active, but being aware when I know when things are getting too much and there’s personal stuff that I need to work on. Being able to be in an environment and the activities that I do, that I can say I need to back off, I’m going to stop for a couple weeks but I’ll be back. Like my dragon boat team, I’ve been dragon boating for ten years, and I’ve been in the hospital. I called the psychiatric unit in the hospital the St Joseph Spa and Treatment Centre and I’ve been there many times. But each time I come out, the dragon boat team, I still got a seat. So there’s nothing, I’m not going to lose any seat or anything like that.

When I was in the psych unit one time on my birthday – the hospital is up on the hill – they paddled during practice, they paddled underneath to sing me Happy Birthday. I remember sitting outside and my nurse came up to me and said what are you doing, you know conversation sitting at the picnic table. I said “Oh waiting for my dragon boat team to sing Happy Birthday.” Well she couldn’t see the dragon boat team because the hospital is on the cliff. So she’s looking at me like thinking is Suzy hallucinating again, what is she talking about? I said no, no it’s dragon boat practice and the team did paddle by, we couldn’t see them but we could hear them and they were singing Happy Birthday. They’ve been there from the very beginning and they have been an awesome phenomenal support system all in their own way.

I guess mainly knowing what I need to do, lots of self care, lots of knowing what my limitations are. For years I have, while I still have years of blank memories. I don’t remember Christmases, birthdays, any major events. Grade One, Two, Three, Four, I remember little snippets of it. I went to college for two years when I was thirty; I can pull up little bits of memory of that but not a whole. I don’t have access to those memories. I’ve obviously got them because I’m the one that was doing everything. But being able to pull up those memories, whether I’ll ever be able to, I don’t know.

I’ve got three/four, maybe five, major personas. One is Stanley. Stanley was created when I was six years old. I had an older brother who was one of my protectors, and when he was sixteen he joined the army, so I no longer have the protector when crap happened. I created Stanley and Stanley’s job was to find really small places for me to hide in when stuff happened.

I would like to get out more and be able to do more public speaking, talk to more students, talk to more classrooms. Actually I would love to do a conference, a mental health conference. But because I don’t have the PhD and all the letters behind my name, it’s kind of hard to get into it. But it will come. Whatever’s meant to come, will come. I never thought I’d be talking to youth and at risk groups and stuff like that. I never thought I would ever be doing that but that’s what I want to do. So I just want to keep doing what I’m doing. I have done presentations, given talks to nursing staff or nursing students from the college. I’ve also done talks with a couple at risk youth groups and then the girl’s group at the local transition society here. And then this last June, I went back to my old school, my old high school and presented to three psychology classes there. That was a little surreal. Each class is a bit different but yes; I just go in there and talk about the D.I.D. and what it really is and what it isn’t. I discuss how it’s affected my life and talk about the depression and the complex P.T.S.D., mental health in general and why we need to start talking about it. What’s really interesting is once I start talking about mental health issues, other people start opening up and it just blows my mind. Could be teachers, it could be people I sing with, could be people in the dragon boat team, people I golf with. Because mental health touches everybody, whether you have it or family member have it, you know somebody who’s got it, so it touches everybody. It’s very interesting that people come up to me and talk to me about their issues or their struggles with it.