Mia's story: Living with multiple medicines

Find out about Mia and hear her speak about the value and challenges of taking multiple medicines.

Female
Age at interview: 30
Number of medicines: 12
Cultural background: Israeli-Australian

 

Background

Mia lives in a beachside suburb of Sydney on her own, although she often has family to stay and has other family living in the same street. She works full-time as a paramedic providing emergency medical care.

 

Current medicines and conditions

Some medicines are taken regularly; some are taken only as needed.

  • Azathioprine: Crohn’s disease
  • Mesalazine: Crohn’s disease
  • Sertraline: anxiety
  • Drosperidone/ethinylestradiol contraceptive pill: contraception
  • Probiotics: for gut health
  • Fish oil: to reduce inflammation
  • Prednisolone: Crohn’s disease flare-ups
  • Maxidex (dexamethasone) eye drops: uveitis
  • Hycor (hydrocortisone) eye ointment: uveitis
  • Ibuprofen: painful joints
  • Buscopan (hyoscine butylbromide): stomach cramps associated with Crohn’s disease
  • Dolasetron: nausea associated with Crohn’s disease.

 

About Mia

Most of the medicines Mia takes are for managing her Crohn’s disease. She takes mesalazine and azathioprine to prevent flare-ups, which has generally been successful as long as she takes her medicines as directed.

Mia finds it difficult to remember to take her medicines regularly as she works irregular shifts as a paramedic and has a very busy social life, which makes it hard for her to stick to a routine. She tends to forget her medicines more when her condition is stable and there is no trigger (such as painful symptoms) to remind her to take them. Mia is grateful that when she does take her medicines regularly her Crohn’s disease is well controlled.


More about Mia

Mia’s first significant medical issue was anxiety, which started around 10 years ago. She tried to manage her symptoms with relaxation techniques and counselling without much success. Within a week of starting sertraline in 2004, she felt she was back to her old self, and since then anxiety has not been an issue for her.

Most of the medicines Mia takes are for managing Crohn’s disease, which was diagnosed when she was 22. Immediately after her diagnosis, Mia took the oral steroid prednisone to help treat flare-ups in the hope that she would go into remission, which unfortunately did not occur. She was then started on mesalazine and azathioprine to try to prevent flare-ups, which has generally been successful provided she takes her medicines regularly.

Mia has had episodes of uveitis, inflammation of the eye, thought to be associated with Crohn’s disease, which she manages with steroid eye drops and ‘horrible’ ointment. On the advice of her gastroenterologist, Mia takes probiotics for her gut health, and fish oil to reduce inflammation.

One of the biggest issues Mia has in managing her Crohn’s disease is remembering to take her medication regularly. Her work as a paramedic involves irregular shifts, which makes it hard for Mia to develop and stick to a routine for taking her medicines. She has a very active social life so is often not at home at regular times, which makes taking multiple medicines difficult. Mia never consciously decides not to take her medicines; her life is so busy that she simply forgets to take them.

If she remembers to take one medicine, she generally remembers to take them all. Likewise, if she forgets to take one, she usually forgets them all. If she only misses her medicines for a few days, Mia is usually all right, but if she forgets them for a long time she can end up with symptoms and flare-ups of Crohn’s disease. Unfortunately Mia finds if she misses her medicines for a few days, she tends to forget them for the week, and then tends to forget to have prescriptions filled.

Mia finds it easier to remember to take her medicines when she starts a new medicine. Generally she only starts a new medicine if she is feeling sick, so is motivated to take her medicines so her symptoms improve. Her problem is more when her condition is stable and there is no trigger in her day to remind her to take them. She has tried leaving her medicines where she can see them and using phone app reminders, with little success. She intends to buy a decorative pill box off the internet to pack her tablets in, to see if that helps her to remember.

Mia dislikes knowing that she just can’t forget about her medicines hoping her Crohn’s disease will go away and is concerned about the long-term consequences of forgetting to take them. On the other hand, she is grateful that her medicines are available and, when takes them as she should, her Crohn’s disease is well managed.

 

Listen to Mia's story

Mia finds it easier to remember to take the contraceptive pill than medication for Crohn’s disease because there is an incentive with the pill that is more immediately meaningful.
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Mia was frustrated when her doctor did not accept that non-pharmaceutical methods to deal with her anxiety did not work and she needed prescription medication.
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Mia was relieved when a medicine that was not government-subsidised was ineffective, as the cost was too high for her. She just misses out on the PBS Safety Net most years and, although she can afford her medicines, it is money other people her age can spend on other things.
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Mia was relieved when a medicine that was not government-subsidised was ineffective, as the cost was too high for her. She just misses out on the PBS Safety Net most years and, although she can afford her medicines, it is money other people her age can spend on other things.
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One doctor Mia saw questioned her about taking one medicine ‘for the rest of her life’. Mia agreed to stop taking it for a while, but doing so made her feel unwell.
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Mia does shift work and consequently does not have a set routine. Her symptoms trigger her to take her medicines instead.
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Mia does shift work and consequently does not have a set routine. Her symptoms trigger her to take her medicines instead.
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People often learn about Mia’s condition by seeing her take medicines. She has found that others seem to identify her by her illness, which she does not want.
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The doses that Mia is on for her medicines mean that side effects are a rare and temporary occurrence.
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Mia is aware that, had she been born in an earlier time, she probably would not be alive today.
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People at work have seen Mia taking her medicines and have made jokes, especially about the eye drops which have to be taken often for a very obvious condition.
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If Mia remembers to take one medicine, she remembers to take all of them. She found this easier when she lived in the country and had less to do.
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The Living with multiple medicines project was developed in collaboration with

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