Chris X
Chris had years of AF attacks on medication that did not suit him. Two years ago, helped by the Atrial Fibrillation Association, he got referred to a specialist hospital and had an ablation. He now feels well. He takes flecainide and aspirin daily.
Looking back, Chris remembers having attacks of a very fast heartbeat as a teenager, but it was in his late thirties that he really started to notice symptoms, particularly after exercise. In his late forties, Chris saw his GP and was referred to a local hospital for tests, but nothing was found and he was told that his symptoms were probably caused by stress. He now realises that family members may have had similar symptoms, and made his own DIY ECG machine to prove to the doctors that he had an irregular heartbeat. Chris says for him, an
episode of AF is like having something alive in your chest, banging and thumping.
Initially, the local cardiologist put him on amiodarone. Chris says that no alternatives were offered and that there was no discussion of other options. He experienced lots of side effects, such as problems with his sight, his skin went greyish in colour, he became sensitive to sunlight and his thyroid gland was affected. The side effects got him down. A cardiologist in a different hospital reviewed his case and changed his medication, but the new medication was not effective. Chris says he lost all confidence in the doctors at his local hospital, and when he was 55 he decided to retire due to the effects of work pressures and his health.
Chris then found the Atrial Fibrillation Association (AFA) online. He attended a conference and met an arrhythmia nurse there. She advised him to get referred to the hospital that she worked at, and Chris asked his GP to refer him under ‘choose and book,’ although his GP was not really aware that the system was available to use. The arrhythmia clinic changed his medication to flecainide, which worked far better for Chris, and he was offered an ablation (although he was initially worried about this). However, Chris says he later reached a ‘tipping point’ when he felt so unwell that he decided to have the ablation. Chris needed several cardioversions during the ablation as he kept going into AF during the procedure. After the ablation, Chris had a couple of AF episodes, missed heartbeats and sometimes a rapid pulse in the following six months, but 18 months on he now has few symptoms and is feeling much better. He now goes to the gym regularly, and has just started running again.
Chris feels so much better that he now wishes he had never retired. Chris says he is still very unhappy with the way he was dealt with at first at his local hospital. He feels that if he had been properly treated straight away, like he has been at the most recent hospital, he could have carried on working. Chris says he realises now that he may have been at risk of a stroke for probably ten years, but that this was overlooked.
Chris finds that certain foods can trigger AF and other arrhythmias. For him, these include caffeine, chocolate, cheese, and MSG in Chinese food. He currently takes a small dose of flecainide plus 75mg aspirin daily, and a beta blocker called bisoprolol to take in the event of a very fast heartbeat. Chris believes that, since he has had a successful ablation, his stroke risk is not as high as it was before. He does not take warfarin as he is unhappy with the risks of bleeding and the blood test monitoring required. He says he would not want to take the new alternatives to warfarin, as he feels such drugs have not been in use long enough yet to know the problems that they can cause, and it concerns him that, unlike warfarin, there is no antidote. Chris regularly visits the AFA online he says he used to find it an excellent source of reassurance, but is now more likely to offer support to others.
Chris thinks that family doctors and the primary care system should focus much more on detecting AF, and feels that AF is not taken as seriously as some other heart conditions, even though it is known to increase the risk of having a serious stroke. He feels that not only would early diagnosis be more cost effective for the NHS (in terms of the potential consequences of treating strokes), but also better in terms of people’s quality of life. Chris says that his delayed diagnosis, the uncertainty of AF, and feeling unwell really got him down. He has much more confidence now as he believes his AF is virtually cured. He has found the arrhythmia nurses at his hospital to be very supportive, and he can still contact them even though he has been discharged from the clinic. Chris advises people with AF not to despair, as AF can be successfully treated. He urges people to find out information from
an organisation such as the AFA, and to discuss the condition and treatment options with a specialist, preferably an electrophysiologist who specialises in heart rhythms. Chris advises people to be informed and aware patients and never be afraid to ask questions. He reminds family members, friends and employers to be understanding, and to appreciate that just because someone with AF looks fine on the outside, it does not mean that they are not feeling terrible and having difficulty coping on the inside.
Interview held 15.12.11