Here is an update about what I have been working on the past couple of weeks. My mentor gave me the task of ‘coding’ three individual on-one-one interviews. For those who don’t know what ‘coding’ is, it is the process of reading and analyzing information and recognizing common trends among the information and organizing the ideas accordingly. These interviews were with women who have HIV and cervical cancer and the purpose was to discover what barriers, if any were keeping them from their doctor’s appointments and from getting their pap smears. To say the least, there were so many different answers and feedback from these questions and each one was similar, yet specific to each individual patient.
After reviewing the interviews, I have come up with a list of trends among the three interviews that strike me as important to look further into. This list includes, but is not limited to lack of knowledge, lack of empathy/understanding, lack of trust with health care provider, common misconceptions, and fear. Each individual had their own experiences that shaped their reasons for feeling the way they do about physicians or being diagnosed.
One topic that cut me to the core was fear and lack of trust. One of the common responses I read was the fact that they felt isolated when they went to their appointments and because they have HIV, they are treated differently than the other patients in the clinic. They also responded that the physicians were very insensitive to the fact that they had this diagnoses and aren’t always honest about possible treatment options or social support.
During my presentation, I would like to present the patients with the facts, possible solution options for their concerns, and also resources around their community that they can use to help cope with their diagnoses. It is important for the patients to know about the disease, but you should also inform them as much as possible about the entire spectrum. As I’ve learned in nursing school, we want our patients to receive holistic care. While I was shocked to hear some of the responses, it was what I needed to become aware of the real issues that lie within the system and the patients. The research team did an awesome job on the interviews, they were able to gain the trust of the patient/participant and answer questions necessary to make a difference.
Overall, this was a great learning experience and I look forward to attending the focus groups, giving my presentation, and making a difference in the community!