Eve
Eve, age 54, was diagnosed with asthma at age 36. She is white and originally from the United States but has lived in the UK for many years. She lives with her husband, and has one adult child, and also lost a child to cancer several years ago. Eve lost her sight as a very young child through a rare form of cancer. Eve experiences symptoms intermittently, but generally has her asthma well controlled using preventer and reliever inhalers. Triggers can include getting a cold, weather conditions, pollen, over exertion, and smoke or fumes.
Eve was 36 when she was diagnosed with asthma. During a day out walking in the countryside with friends one day she found herself feeling very breathless and unable to manage the walk. On that occasion she dropped out of the walk, which was unusual for her as she had never had problems like that before. Prior to this she remembers that she had become more sensitive to being around dogs and people who smoked on several occasions she had found herself coughing. She visited the GP and asked whether it could be asthma, and the GP thought that was probably the case and gave her an inhaler to use, which worked the next time she went walking with friends after using the inhaler she was able to go all the way. Looking back Eve thinks she may have had mild asthma as a child. She grew up in the states and went to a school in Los Angeles which at the time was heavily polluted, and she remembers that on some days her mother wouldn’t let her go to school because her chest was feeling tight. She also recalls an occasion when she was staying with a relative who smoked where she couldn’t stop coughing and wheezing and realises now that she had an asthma attack at that time, but this was a few years before she was diagnosed with asthma.
Initially she was given a preventer inhaler to use and this seemed to work to alleviate symptoms. About a year later when she saw another GP her peak flow reading was quite low and she was then given a reliever inhaler to use in addition to the preventer at times when she was struggling with her breathing. Typically she became breathless when she walked to the shops or took any form of exercise, so she began to use the reliever before leaving the house and sometimes she would also use it when she was out. Symptoms would be worse in summer as she has hay fever and this exacerbates her asthmatic symptoms. Over the years Eve says she has become allergic to more things which trigger her asthma.
It wasn’t until sometime after her diagnosis that she was given her own peak flow meter to enable her to monitor her own condition. As Eve is visually impaired, it was a problem to be able to read the peak flow meter but her husband made some markings on the side using clear nail varnish to enable her to be able to use it for herself.
Normally Eve’s asthma symptoms are coughing, a tight chest and feels breathless, and she only gets wheezy in hot steamy conditions for example in a hot steamy shower or if the heater in the car is on high. She also finds that her asthma symptoms will flare up if she has a cold, or if someone she is in close contact has one.
Eve recalls when her son was about 11 that he wanted to have a pet and she agreed he could have a guinea pig and a rabbit, however being close to the pets exacerbated her asthma and she needed to take steroid tablets to help overcome the symptoms. She was also given a long acting bronchodilator to use in addition to her two inhalers, however eventually the pets had to be given away as they were clearly making her feel very unwell. Eve herself doesn’t have a guide dog and never wanted one as she manages very well with her cane, however she does find that she is allergic to friends guide dogs.
A few years ago Eve’s symptoms were particularly bad during the summer. She kept having asthma attacks, and her regular medication wasn’t working to alleviate things. She was prescribed a tablet called Singulair, to take in addition to her other medication (Singulair is a leukotriene receptor antagonist). That year she had been due to go to Italy for her silver wedding anniversary but had to cancel the trip because her asthma was so bad, and she was advised that flying was not a good idea due to the lower oxygen levels in the air cabin. She recalls that year was one of the worst she has experienced she was taking antibiotics, steroid tablets, the Singulair tablets and using inhalers but she kept having bad asthma attacks nonetheless.
Eve sometimes gets acid reflux which can exacerbate a coughing spell, so she takes medication to help with that. It took a while to get the dosage right but now it is under control.
Eve has kept her symptoms well managed over the years but this year she had a particularly bad attack and had to be taken to hospital where her conditioned was monitored and stabilised, and she was then discharged back home. Generally though, Eve says that she can go for several months sometimes without having any symptoms of asthma, so it doesn’t always impact on her life, however it can be difficult to predict when her symptoms will flare up so there is an element of uncertainly involved in not knowing when she will feel well or being able to plan to do certain things.
Eve says that asthma doesn’t prevent her doing most things. There are some activities that she would like to be able to participate in, such as singing in a choir, or cycling but she has come to terms with the fact that she can’t do that, mainly because she would feel she could be unreliable and have to stop when it might be inconvenient for other participants.
Eve has been blind since she was born and so is accustomed to running her life without sight. In terms of her asthma she says that generally she manages very well and her visual impairment doesn’t make a lot of difference in the way she can manage things. She doesn’t have a written care plan for managing her asthma, but has had discussions with her asthma nurse about what to do when her peak flow measurement is low, and she says she keeps that in her head remembering it rather than having it written down. She is able to recognise her different inhalers because the turbo inhalers that she uses have braille numbers on them. She keeps them in certain places around the house so that she can find them easily.
Eve sees her asthma nurse about every 6 months and finds it useful to have somebody else helping her to evaluate her progress in self managing her asthma. She has occasionally been referred to see the hospital consultant if her asthma is very bad, and she has also recently been seeing another respiratory specialist who is looking into the possibility that she may have sleep apnoea (where the airways close up when you are sleeping).
Eve says she has no qualms about using her inhalers when other people are around and she thinks it’s important not to hide away and do it in private. She thinks that generally people can be unaware of the symptoms and triggers of asthma and she works with Asthma UK as a volunteer giving talks to groups of people about asthma to raise awareness.