In my research and journey in finding sources to use in my annotated bibliography, and eventually my research paper, I've found three different articles in scientific journals that greatly help in the quest of learning more about my topic.
The first article is titled "Perceptions of Supportive Behavior By Young Adults With Bipolar Disorder". In the article the authors mention that one in every 22 people are effected by Bipolar Disorder and of those 22 people, roughly one fifth of them will commit suicide. I learned more statistic facts like the suicide rate of people with Bipolar Disorder is 28 times higher than the rest of the population. But more importantly, I learned that there are huge changes in quality of life when those who have been diagnosed perceive themselves to have a solid support system. The authors intentions were to examine support methods and track what the sufferers found to be beneficial. I was surprised to learn that a huge part of coping is simply how one perceives themselves and their relative support groups.
In the second article titled, "Effects, Experiences, And Impact of Stigma on Patients with Bipolar Disorder", the authors give surveys to those effected with Bipolar Disorder in an attempt to find out what they thought about how social stigma effects their lives and how they assume society perceives them. I learned that over 50% of those with Bipolar Disorder think that society looks upon them in a negative light. The authors found that sufferers assumed the stigma to be so apparent that it affected their self esteem and figured it made it harder for them to live in a normal world. The only thing I wish I had in regards to this article is a higher amount of people in the test. But in retrospect, I was happy to see that tests were done in two separate countries, Argentina and Canada, and then compared to one another. This shows that Bipolar Disorder has stigma that reaches beyond the shores of our own country.
The third article came from the
Iranian Journal of Psychiatry and is titled "Family Care Giving in Bipolar Disorder: Experiences of Stigma". In this article, the authors delved into the lives of those who care for people with Bipolar Disorder. I was surprised to find that most care givers, which mainly consisted of family members, were effected by stigma just as much, if not more, than the people they were caring for. Many care givers spoke about the fear they had in speaking about Bipolar Disorder and assumed people would think they were crazy or unfit for society. It was interesting to learn about how families are effected by their loved one's disorder and how it can actually have a negative effect on their lives as well.
I believe there are a few holes in my research up to this point in the areas specific to how these negative stigmas are effecting diagnosis and whether or not people are willing to seek a diagnosis, and therefore a treatment to their illness. I believe the stigma is apparent enough to effect peoples decisions and thoughts of Bipolar Disorder but I've yet to find an article about the exact correlation. I expect to find more information in articles of scientific journals provided by our library. I just have to narrow my search terms and dig deeper into the database.