Last week, I wrote a post stating that “Natasha Tracy” is my nom de plume – it is my writing name and not my legal name. Some people showed concern over this and felt it was inconsistent with my convictions regarding stigma and standing up for one’s rights. I would now like to respond to these concerns regarding my own choices, writing and reasons.

I don’t remember most Christmases; they tend to blur together in a sea of turkey, denial and wrapping paper. But the Christmas of 1998 was different. That Christmas was the one just before I began medication. That was the one I spent lying on the couch with bandaged arms. Looking back 1998 should have been a good year for me. I had completed an 8-month work term for my university degree, I had some money for the first time in a long time and I went backpacking across Europe. But unfortunately, 1998 was the year that bipolar decided to attack full-force. I spent the end of 1998 slicing and dicing and sobbing and begging for mercy. From what, exactly, I have never been able to say, but from whatever was causing the pain whatever made it impossible to move from my mother’s couch as the activities of Christmas went on around me. But in spite of this I had no intention of seeing a doctor and I most especially had no intention of seeing a psychiatrist. Those people were nothing but pill-pushers, nothing but drug dealers with letters after their name. And everyone knew that depression wasn’t a real disease and that anyone with real strength of character could overcome mental anguish on their own – not with the crutch of pharmaceuticals.

Last night I was feeding my cats and thinking suicidal thoughts - I like to call that a Wednesday night. And I was thinking to myself that no one (save others in my position) understands what that is like - to go from some sort of normal person in the daytime to a sobbing, suicidal headcase at night. I thought about the fact that I have spent eight years talking about this very disease, this very state, this very problem, and yet still, people don't get it. No matter how many words I use, no matter how I phrase it, people simply do not understand. So what do we do with the lack of understanding by others?

Recently someone who I consider a friend had some rather unfortunate things to say about me, including that I'm narcissistic. This, I do not believe to be true. Not even a little. Nevertheless, this particular insult echoed inside my brain over and over until I was sure it was stabbing the inside of my head with heated spikes. I couldn't let it go. I tried, really I did. I told myself it's not about me. It's just one person's opinion at one moment. It isn't true. And so on, and so forth. But my brain had a death-grip on the insult and refused to let it slip. So what do you do when you're obsessive, bipolar brain turns to thoughts of crazy?

Recently, someone who was new to the world of bipolar disorder asked me if there was a cure for bipolar disorder or if he had to live like this forever. I had to, of course, tell him there is no cure. I felt like I was telling him his dog was about to die. I felt like knowing this, he might give up.

If you follow me here, or particularly elsewhere, you might have noticed there are some very vocal people who hate me. Mental illness is contentious, and some people take it to a personal level. That’s people for you. Sometimes I talk about these people. I call them “the nasties.” But today is not about them. Today is about celebrating all the wonderful, amazing people who support me, Breaking Bipolar and the mental health community in general.

I write at HealthyPlace about the problems associated with living with bipolar disorder, and let’s face it, there are many. I also talk about the problems with the treatment of bipolar disorder, and yes, there are many of those too. But just because I recognize issues, discuss genuine, painful emotion and make loud an inner voice that among most people is strangled, doesn’t mean my treatment has been a failure. Just because I’m not “all better,” that doesn’t mean treatment doesn’t work.

Earlier this month, I wrote about how to stay on psych medication. I gave tips and tricks to help you stay on track. In today's video, I show you my own twist on psych medication reminders.

Normally I try to grab the reader's attention in the first few lines of the piece so that you'll want to read the rest. Something snappy, touching or pithy. Normally I try to make sure it's an interesting subject. Usually I try to provide some sort of universal appeal to the piece or at least a good quip. But today, quite frankly, I'm talking about me.

I had a VNS implanted about three years ago. The surgery involved two incisions, one under the left arm and one on the left lower front of my neck. My neurosurgeon promised a scar between 1-3 inches but it’s probably closer to four. Of course, I would much rather he get the surgery right and have a bigger scar than the other way around. Someone messes up your vagus nerve and you know about it, pretty much forever.