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Drug companies are putting a price on the lives of those with cystic fibrosis | Isabelle Jani-Friend | Opinion

Drug companies are putting a price on the lives of those with cystic fibrosis | Isabelle Jani-Friend | Opinion

Placing a life-changing drug beyond the reach of NHS Scotland is cruel, says recent graduate Isabelle Jani-Friend. At 7am, I wake up and, while most people are starting their days, having breakfast and making their way to work, I – like the 10,400 people in the UK with cystic fibrosis – am beginning my daily treatment regime. For me, this involves a concoction of 30 tablets to fuel my morning, each with their own variety of debilitating side-effects, from sickness to dizziness and fatigue. The morning calm is disturbed by my noisy inhalation machine as I breathe in medications, while a positive pressure machine helps me cough up thick, sticky mucus from my lungs, which takes another hour. All in all, it’s a glamorous way to start the day.

And it doesn’t stop there. Every time I eat, I have to take enzymes to help me digest my food, and I take a regular dose of painkillers to help me get through the aches and pains. It’s a constant reminder of my disability and all the limitations it has on me living a “normal” life. After a long and exhausting day, my medication routine is repeated in the evening, with...

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