Vera
Vera felt tired and breathless but put this down to another health condition. A routine blood pressure check and subsequent ECG showed that she had atrial fibrillation. She takes warfarin to reduce her risk of stroke.
Vera had a routine blood pressure check and was found to have a varying heart rate. She had an ECG and her doctor told her that she had atrial fibrillation. She recalls feeling tired and breathless, but had put these symptoms down to another medical condition. She says she would have gone to see her doctor if she had had more noticeable symptoms.
Vera had never heard of AF when she was diagnosed. Her doctor explained about AF and said she could take aspirin or warfarin to reduce her risk of stroke, and printed out information sheets for her to take away and read. Vera felt that her doctor explained the condition very well he was reassuring, and she appreciated having time to go away and think, as she feels it is often hard to take in all information given at once. Vera says it was completely up to her to decide which anticoagulant to take. She was not keen on taking aspirin as she had had a stomach ulcer in the past. She discussed the options with her family before telling the doctor that she wanted to take warfarin.
After starting on warfarin, Vera had blood tests for two weeks and was told to adjust her dose to try and reach the correct level for her. She then began having a finger prick blood test, weekly at first, then fortnightly, and currently monthly. Her finger prick testing and AF is managed by her GP and practice nurse, who she feels she can share any concerns with. She says the finger prick test is very quick, and she immediately gets a print out with which dosage of warfarin to take and her next appointment date. Vera currently takes 3.5mg/day and 5mg once a week, and tries to take her dose at 6pm (but always in the evening). She does feel that it could be easy to take the wrong dosage of tablet, as the print out sheet only says which colour tablets to take. Therefore she double checks the box and dosage before taking. Vera assumes she will need to keep on taking warfarin indefinitely, and already takes lots of medications, so says this is just another. She does not take any other medication for AF. Vera does have a yellow anticoagulant monitoring book which she carries with her at all times. It contains details such as her name, address and GP, and says that she is on warfarin. Her blood test results and dosage are recorded by the nurse in it. Vera says it would be useful and easily recognisable if she were in an accident. She was advised to avoid cutting herself if possible, as she could bleed easily. She does notice that she bruises easily. Vera says she still gets breathless and tired, but allows herself plenty of time to do things and to rest and recover. She was also advised to avoid grapefruit and cranberry whilst on warfarin.
Vera’s mother had heart problems, but did not share this information with Vera whilst she was alive. Vera is not sure whether family history has anything to do with her development of AF, but does feel it is important to share health issues with family members, as it could affect them in the future. Her family were surprised when she was diagnosed, but she was relieved to have an explanation for her tiredness and breathlessness. Vera says she does not dwell on her AF, and is not sure whether she is always in AF or just occasionally. Vera is trying to lose weight, but medication she takes for another condition increases her appetite, so she admits to finding it hard. She would like to visit her son in USA soon, and her doctor has said that her AF should not restrict her travelling.
Vera remembers when she was a child, her parents struggled to pay a healthcare bill for her (before the introduction of the NHS). She feels we are very fortunate to have the NHS, and has nothing but admiration’ for the supportive and positive staff she has encountered. She feels that medical professionals and family members should be encouraging of people with AF. She urges people diagnosed with AF to try not to worry and to take the medication that is prescribed. Vera says she would look on the internet if she wanted to find further information on AF, but feels her GP’s information was sufficient. Vera feels that decision-makers within the NHS should continue to focus on patients and staff, and not just finances. Vera noted that her friends and family had not heard of AF when she was diagnosed. However, she is unsure whether public education on AF would be effective, as she feels people are given so many health-related messages that they may not take it in, unless they have some personal experience or interest in the condition.
Interview held 28.7.12