The above picture is the best glimpse that I can give you as to what schizophrenia is like for me. My son and his girlfriend had to move in with us for a short time until they can get an apartment they like. So they are living in my basement which is difficult because she is like a stranger to me. And that sets off my positive and negative symptoms. When she touches my things or rearranges stuff then I can see voices and there are so many it is like a crowd of people around me all clamoring for attention. Hopefully, they will only be here for a few more days instead of the month that they asked for earlier.
Category: schizophrenia
Cognitive Behavioral Therapy (CBT)
This will be my last week of cognitive behavioral therapy. I only tried it because my family pleaded but due to time and expense it is no longer an option. Plus I don’t think that I’m in that category of those whom it helps the most. CBT is a common adjunct to meds when the person with schizophrenia is stabilized but continues to have a baseline of functional disturbances. It is commonly done with exercises out of a workbook given to the client by the psychotherapist. CBT has both behavioral and cognitive aspects.
Regarding behavior, CBT is supposed to weaken the mental connection to troublesome situations and thereby altering the reactions (fear, depression or anger). The cognitive component of CBT targets thought patterns and seeks to alter the emotional state and corresponding behaviors. My psychotherapist worked with me to make me aware of my irrational beliefs and alter them through cognitive restructuring (behavior modification). I did cognitive rehearsal and practiced different responses to different situations that I encountered. Not only did I have workbook exercises but I also was required to journal which this blogging assisted with over the time I tried out CBT. Overall the positive reinforcement and systematic desensitization helped me learn new tactics to handle my illness.
Magnetic Resonance Imaging
At my request, my doctor set me up for an MRI (magnetic resonance imaging). I wanted to know more about the course of my illness and the prognosis. So he set me up for the MRI to determine a baseline point and then monitor how it changes down the line.
My doctor said the above image shows a schizophrenic brain on the right as compared to a normal brain on the left. The gray matter (neuronal cells) and the white matter (fibrous connections) are shown. Volume is a major difference. With schizophrenia there are enlarged ventricles and reduced gray matter. There is also reduced volume in the temporal lobes and hippocampus which affect auditory processing, language and memory. I’m glad we chose to do the MRI because I want to know the structural and functional findings so it helps them consider what the possible outcome might be.
Course of Illness (Schizophrenia)
My psychiatrist can’t confirm any possible course of my illness; but he does think that due to my later onset and of my being female that it will be milder. At this point on my vigorous medication regimen, I’m having essentially no positive or negative symptoms. He doesn’t think that there will be any deterioration in behavior or cognition. However, potential short-term working memory problems may arise and he also thinks that I may continue to have subtle peculiarities in my language (negative symptom).
Although, I’d have been the first to say that I never got depressed just anxious, it has been determined that I have suffered from depression and may continue to do so. My depression is an anxious case not the sad states. Fertility and fecundity are a non-issue for me as I’ve already raised my four kids. And my doctor doesn’t think that life span will be decreased but I am at risk for diabetes and high blood pressure due to the medication side effects.
As for the meds, I have to be symptom free for a year before he will cut back on any one or better yet discontinue all. He worries about the statistic of 90% recurrence within five years of stopping meds. So, that was the extent of my discussion with my doctor today.
Psychosocial Treatment
I’ve been receiving psychotherapy since I was twelve plus in and out of group therapy from the age of fifteen. So why is it now that I’m being prompted to add other psychosocial treatments to the mix. I know the response: to improve socialization. However, doesn’t class work count towards psychosocial therapy?
Psychosocial treatments include cognitive behavioral therapy (changing negative thought patterns), family education, occupational therapy, group and family psychotherapy, and cognitive remediation. They are thought to help lessen schizophrenia symptoms, learn new skills, help in coping with the illness, prevent relapse, and achieve a connection with others.I already learn new skills from all the classes that I take. Regarding the compensatory learning strategies, I think the classes I’m in also aid in memory, planning, organizing, and concentration. I think this blogging helps, too. It allows me an outlet to journal experiences each day. In that way, it will aid in preventing relapse by getting feedback from my family members in order to stay focused on being mentally healthy.
My Phases of Schizophrenia
During my acute phase, my family practice doctor sent me to the emergency room which resulted in a diagnosis of psychosis and schizophrenia. My general practitioner thought that I was in danger of harming myself or my family. I couldn’t control my own behavior, primarily my emotions, and I had limited functioning. Fortunately for me, my family was a strong support structure. In addition to the treatment, I also had a strong connection with my community aftercare team; they called twice daily to make certain that the anti-psychotics were working well.
Now that I’m in my stabilization phase, I’ve returned to the community and work (architectural drafter). I’m an avid reader and perpetual student; there is always something that I want to learn or try. I’m not a real risk taker though, so there are still obstacles in my way. I continue on my path to symptom reduction and have every intent of remission and even more improved functioning, particularly socially.
Positive vs. Negative Symptoms for Me
The positive symptoms (in addition to reality) of schizophrenia are: hallucinations (see and hear things), delusions (false beliefs that defy reasoning), paranoia, disorganized thinking,and grandiosity (believing that I have supernatural powers),
And the negative symptoms (lacking from normally considered behavior) are: lack of emotion, slow speaking, poor hygiene, impaired memory, poor concentration or decision making skills, limited social functioning, lacking motivation, and inability to experience enjoyment in things I once found pleasurable.
I’ve highlighted the ones that I experienced. In addition to those, I experienced sleeplessness, OCD, depression, and high anxiety. All of my symptoms have been treatable. I do still experience hallucinations when the stresses in my life are too great. Things haven’t gotten easier for me; instead, with the aid of medication, psychotherapy and my support structure, I’ve learned what is and isn’t real. I can control my emotions but I still have trouble relating to other people because I fear that my symptoms may arise in their presence. But the key is that I am in control and feel empowered.
Contrary to myths, as a person with schizophrenia, I don’t have developmental disabilities, violent tendencies, or a split personality. Not being in contact with my birth family, I don’t if genetic susceptibility or environmental factors (nature or nurture) played a role. I was diagnosed with PTSD years back due to physical and emotional trauma as a child; but I believe those are irrelevant at this point in my life as I’ve gotten over and forgiven all responsible. I truly hope they are as happy as they can be in their own part of this world.
At this point, the medication works but isn’t without side effects. The worst of all is the tremors. However, restlessness comes in a close second. All in all, I prognosticate that I will be in full remission (symptom free), with the aid of medication, within six months time.
Suicidal Tendencies
Hi, my name is Angie Grey and I attempted suicide at the age of seventeen while I was pregnant. It was within six months after being released from the psychiatric ward. I jumped off a train bridge in Bismarck, North Dakota and was rescued by a boater in the water beneath me. I didn’t realize how lucky I was for him to be there that late at night because I didn’t know how to swim and was sure to die. For a long while, I was okay with living up until May of 2009. At that point, I had a suicide date in mind. Fortunately for me, I found Pathways Health Crisis Center in Minneapolis. At that time, my next door neighbor, Angela had committed suicide and I was in full blown delusion. For years, the dead woman living in my home urged me to take my life just as she did my neighbor. My grandiosity was that I could see through walls to the adjacent townhome. I saw my neighbor laying in her bathtub, with pill bottles and a bottle of wine in hand. All the while, the dead woman who lives inside my home was telling me that life wasn’t worth living. Most recently, during my psychotic break, the dead woman said my new neighbor is planning on taking his life too; but this time it will be with a gun and due to the constant hip pain he is experiencing. She (the dead woman) continued to tell me and show me how obvious it is that life isn’t worth living. Look at all the suffering. Thanks to my medicine, I see this isn’t real. Fortunately for me, I have a strong support network and Pathways as well. I feel bad for the others that don’t!







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