Fourteen female partners were interviewed in two focus groups (n = 14; group 1 = 7, group 2 = 7; non-Hispanic white = 12, Black = 1, unknown = 1, married = 13). The length of diagnosis of prostate cancer ranged from 1 to 18 months. The average age of participants was 61.6 years (range 47-77). All of the male partners had received surgical prostate cancer treatment prior to the focus group. Each group lasted 1.5 hours including the consenting process. None of the participants reported distress as part of the study process so no referrals to the psychologist were required.
Three distinct themes emerged from the focus groups including 1) support needs, 2) role of primary care and urologist and 3) changes to the couple's relationship.
Theme 1: Support Issues and Needs
The participants identified two main areas of support needs: emotional and informational. Support came from a variety of sources including friends, primary care physicians, urologists, and support groups. Participants emphasized the need for additional support for themselves as well as their spouses. One woman said, "why isn't there a group for me to go to?" There was consistency in the fact that the women thought the male patients were reluctant to attend a support group and might benefit from mandatory or prescribed support groups to encourage greater buy-in and help validate some of their concerns. As one participant noted, "He won't ask for help, but he might accept it...there's been a great deal of denial."
The primary need identified by the participants was the need for more information. All of the participants believed that they did not receive enough information and were thrown into an unfamiliar role as a caregiver instead of a companion. This was highlighted by the fact that two woman mentioned that "The wife in something like this is very much involved," and "This diagnosis affects the wife as well." Some of the women said that "most of their questions were answered" but they also noted that they did not know what questions to ask which left them unprepared. They relied on the primary care physician and urologist to tell them what they needed to know, both the good and the bad. One woman said, "Maybe they don't tell us these {bad} things because they don't want us...to put ideas in our head." Another participant continued, "I think the men need to be told upfront...they need to come out and say...this can be a real problem. This is what's going to happen." Another said, "Is he {husband} the unusual one, or is he not the usual one?" One participant mentioned that she was interested in knowing as much as she could about the diagnosis and available resources while her husband didn't want to "face the reality." Some of the women suggested that they needed doctors, both the urologist and primary care physician, to be honest and give "more practical information" about how difficult and long the recovery is going to be. It was said "It's all trial and error...if you could share that information that would be helpful."
In addition to more information, the female partners identified a strong need for emotional support from family, friends, and others going through the same diagnosis. One participant said, ''When you find this out {diagnosis} you need to talk to somebody and that somebody's just not there.'' Discussion of shared experiences through support groups was mentioned by many of the women as important for both the patient and their partner to feel like what they were going through was normal. One of the women suggested the need for a public figure to serve as an advocate for prostate cancer and discuss the ''long road after treatment''.
Theme 2: Role of Physicians (primary care and urologist)
Some of the participants said that the doctors ''were very respectful'' in regards to any questions that they would have but ''not really worried about me {emotionally} at all.'' A number of participants agreed with this statement and added:
" He {primary care doctor} would ask 'how are you doing' and you would say 'fine' and that's it. They don't ask anymore questions....I am not saying he doesn't take the time to talk to me, but he talks about the issue that I'm in there for."
Many of the women said that they tried to seek comfort from their own primary care providers but were disappointed with the lack of information and support they received. One woman said, "I have never talk with my family physician...I was never asked how I felt." Interestingly when asked whether the women received support from their husband's doctors, one women noted:
"...they {treating doctors}were not really worried about me at all. And I guess I wasn't surprised with that. I think actually... now that you've asked that question, I think I would have been very surprised if they had been worried about me. I just didn't...I mean, that never occurred to me. So that's an interesting question."
One woman noted that she was frustrated by the lack of ongoing support for her husband after surgery from his primary care physician and urologist. She said that she would bring her husband into the clinic with numerous symptoms and was told to wait and see what happens. A few participants, however, noted that they received more information and support from the primary care doctor then the urologist.
"He'll sit there with you...ask you about the family, everything. He'll say 'well, and how are you' and I have a bit of a habit of saying 'I'm OK' {Doctor says,} 'What do you mean by OK? Why don't you tell me what...why it isn't fine."'
".... He answered all the questions that we both asked, and we both had our list of questions and he would get them from both of us. You know, both of us would come at him with different types of questions, and we both felt very confident with the doctor."
"...we went in and we saw the primary care physician at that point and talked with him about the various options. So he was very helpful, very supportive. Obviously has some opinions but talked through all of the options, pros and cons, before we actually made the decision."
One woman noted that her partner was disappointed that his primary care physician did not visit him in the hospital after surgery. She noted, "His primary care just never came by to see him...he didn't stop by because he couldn't bill me."
General discussion emerged during the focus groups regarding inconsistencies in who should be providing follow-up, whether the urologist or primary care physician. One woman suggested that a team approach to the treatment and follow-up of prostate cancer could ease some of the burden on the patient and their family members. Several women mentioned
"...they were on their own until the next appointment."
"...once you're done seeing the urologist, you're still going back to your primary doctor. And if there are problems with one, the primary doctor needs to know about that. For further treatment down the line".
"If I have a question I would call the {urologist}. Those would be the first ones I would pick to phone and call".
Two participants suggested the addition of a visiting nurse to help "relieve a little stress" by answering questions and assisting with care-giving duties.
Theme 3: Relationship changes
During the course of the diagnosis and treatment many of the female partners said they felt as if they had taken on the role of the primary caregiver and were the sole emotional support for their partner. One woman said, "The wife in something like this is very much involved. It changes your life afterwards, not only the husband's, but yours." Another participant noted, "I can be there to listen, but I don't have any answers".
Many of the women emphasized that, at times, they had to communicate the emotional and physical struggles for their partner because he shut down. The lack of information and increased time serving as a caregiver rather than a couple caused increased stress for the female partner and at times took a significant toll on the couples relationship causing increasing tension and even arguing. One woman said that a high level of stress due to the diagnosis and treatment caused her to become physically ill with shingles and high blood pressure. She said,
"You just don't know where they're going to be from day to day. 'Cause one day they're one way, and the next day they're in a different mood and the next day...this is bothering them and that was where I wasn't prepared. I just...I knew we had to get through but I think you go through that big trauma period and then you hit a point where you go, 'okay, now we've got that sort of under control. We're not sure where we're going with it yet but it's kind of under control,' and that's when things sometimes get out of control. And you're their back at home, and they're going through all these different things emotionally. Well you're sucked into all that stuff. I mean, you don't know from day to day how they're going to handle it."
Another participant said, "We are still trying to figure it all out. It was a big change for both of us."
The couple's relationship during the diagnosis and treatment seemed to shift from the male patient attending doctor's appointments alone to the couples attending appointments together. One of the women lamented this relationship change when describing her partner's use of the words "we" and "us" to describe his illness. However, she noted a difference in classification when faced with her own illness. "When I had breast cancer, it wasn't 'our breast cancer. It was my breast cancer." A number of women expanded on this statement.
"From the very beginning of the process, we always did it together and I think it was just assumed... the two of us assumed that we would do it together."
"I didn't really get involved in going along on the visits until...you know, we got the point of the cancer diagnosis."
"I didn't have anything to do with the primary doctor and then when he had the diagnosis...after the biopsy then I went to the appointments with him."
Several women noted that physical changes during treatment and recovery caused changes to their relationship.
"{My husband} was never sick a day in their life...got a cold that would only last a day....there's been a great deal of denial."
"he had no symptoms...and you go to the doctor and all of a sudden, you're in the hospital and you come out feeling like hell, and you have incontinence and all of this, and ....you didn't feel like there was anything wrong with you".
"But everything's still not quite the same because now you're told you'll heal up, but when you have major surgery, your whole body goes through a change. And he seemed to like... he got moody and, you know, crabby, and so I just kind of went 'OK' cause you know... I don't know what to do".
"After two weeks my husband couldn't even get out of bed because of the pain...the discomfort...I mean I wasn't prepared for that".
One of the women said that her husband felt a "loss of manhood" due to a decrease of sexual function as well as the innate instinct to provide for his family during this time. Also, the physical effects of the diagnosis decreased the men's activity levels leaving the wife to take on more duties around the house.
"There's so much that's affecting their masculinity...."
"This is sixteen months later, we only go places where he can be near a restroom because he always feels like he has to go".
"I feel like a baby!...then you kinda feel like a women, you know, with a pad on".
"a women can't know what it's like mentally to a man not to be able to have sex and still have the desire".
" A man in his fifties...ending your sex life as you knew it, it's a big step. Especially with my husband, it was a big...a big blow to his ego and our sex life stopped as we knew it".
On another level, one of the women noted that her partner puts on his "social face" when around other people, including family, because he doesn't want them to know how sick he is.