I don't have anything against people with a disability. Why would I? Being disabled means nothing about the individual, it simply indicates their situation. It would be like being against people with siblings. It would just be silly. Nevertheless, when considering my own bipolar disorder, I bristled against the word "disability." I know; this is hypocritical of me and a double standard. It's OK for someone else to be disabled but not me? I'm embarrassed to even think it. But bristle I have and think it I (mostly subconsciously) did. The truth is, though, I'm a person with a disability.

The solutions to ending verbal, mental, emotional and physical abuse are disheartening. We tell families of abuse victims: "There's nothing you can do until s/he's ready to accept what is happening." We tell abuse victims: "The solution to your problem is inside of you. No one else can solve this problem for you." The "solutions" seem mystical, magical...untouchable. The solutions leave abuse victims, already reality-impaired, with the sense that all they can do is wait and hope that someone or God will eventually flip the switch and life will become sweet. The solutions feed into the theory of co-dependency which in part states that at some level, co-dependents wait for rescue instead of using their innate powers to change their situation.

It was 3 a.m., January 1, 2012. I had been struggling to sleep for hours. All had did though was constantly shift around in my hospital bed and throw covers on and off, as my head throbbed and waves of heat flushed my face. It left me hot and then freezing cold. It was the last night of my hospital stay and I had gotten progressively sicker in the past few days. The nurses simply told me I must have the flu or something since I had a slight fever and struggled to eat — not a good thing for a recovering anorexic. I pushed the call button for the night nurse, hoping for some relief but knowing I had just taken a pain killer a few hours before and, therefore, there was nothing anyone could do. He brought me a box of tissues as I started crying and tossing around, saying "I guess this is what they call hitting rock bottom, huh?" He told me to go ahead and cry. I had been in the hospital since December 26. It has been both the hardest and most rewarding thing I have ever done.

The good news is there is hope. BPD is treatable. However, it is useful to know if you fall into a subtype in order to better communicate with your mental health professional. You may not know where you fall, and you may not fall into one of those categories--that's okay. What's important is that you understand your diagnosis, in order to improve the outcome of treatment.

This afternoon, I submitted Bob's draft 504 plan to the school counselor (who serves as their IEP/special ed coordinator). Now, I suppose we sit back and see what comes next.

My wife recently left a note by the bed that hit me right between the eyes. And it hurt. “I’m not sure what is going to make you better, maybe nothing,” she wrote. “I’m not sure what else there is out there to try. Right now, I feel like we are back in a bad place, and I am finding myself exhausted and apathetic.” It got worse.

Bipolar disorder is an affective disorder, in other words it affects your emotions (among other things). Bipolar disorder symptoms are often about feelings. Well, they're about FEELINGS. I feel HAPPY. I feel SAD. I feel IRRITATED. I feel ENERGETIC. But one thing that's rarely recognized is that sometimes bipolar disorder is about feeling nothing at all.

I’m a good goal setter. I see it as a way to challenge myself and keep things interesting. A bit like playing a game and figuring out which hoops I need to jump through to get to the prize. Sometimes I stick to these new resolutions…too often I don’t. I always have the best intentions, but I confess I haven’t always gone past this initial phase into taking the steps needed for success. This year I made a promise that it would be different. This time, I’d reach the prize.

Communication in abusive relationships is like communicating with someone who cannot see or hear you and knows no word that describes the idea of someone who isn't me. When your abuser talks at you, they are talking to themselves. Communication in abusive relationships is an all or nothing fight to the finish. Whether you're discussing the shade of towels for the guest bathroom or what elderly care facility Aunt Polly needs, the abuser expects you to say what s/he would say. Nothing more, nothing less, and definitely nothing different. The only one who will ever attempt real communication in abusive relationships is you.

The diagnosis of mental illness is akin to being hit by a bulldozer. But you survive and work to carry on--to recover. It can be hard, while in the midst of things, to forget the people who have stood by our side. The people who we might have hurt when we were sick. My Experience I enjoy reading posts that mention the authors personal experience--it makes it real. It makes the person real. So, let me summarize twenty-six years: Diagnosed at 12, I have been blessed with a family who never left my side, despite mental health professionals telling them to put me 'in a home.' I am their child and they could not fathom doing this. As I grew up and addiction engulfed my life, they pulled away out of necessity, quite literally waiting for me to die. I have two siblings and they needed my parents just as much as I did. They could have given up. Many parent's do...but they waited. Waited for me to hit bottom, and bottom I did, before reclaiming my life. When I was sick, I did not understand the sacrifices they made. I did not recognize the effect my illness had on their lives, my siblings--the family dynamic. I felt angry. Alone. Unloved. Like the black sheep. As I became better, I realized that I owe much of my life, the fact my heart is beating as I write these words, to them. I am able to express my feelings to them now, but not without guilt. Working Through the Guilt and Embracing Those Who Love You