THE PARENTS of a little girl whose condition is so rare even a cough or cold could prove fatal say they feel constantly on edge.
Ivy Reed was diagnosed with a genetic condition called propionic acidemia when she was just two weeks old.
The inherited disorder leaves the body unable to process certain parts of proteins and fats properly.
The condition means little Ivy, who lives in Bolton, has to be tube fed every few hours through the day and night and needs several different types of medication.
It also leaves the tot very vulnerable to illnesses meaning the smallest sicknesses including a cough or a cold could tragically prove fatal.
While there is no cure for propionic acidemia, Ivy, who attends a special needs school, underwent a liver transplant back in February in a bid to improve her condition and reduce the need for hospitalisations.
And while the transplant was a success, Ivy's parents Carl and Phillipa still live in constant fear that their only child could become poorly with a common illness.
この記事は Manchester Evening News の June 13, 2024 版に掲載されています。
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この記事は Manchester Evening News の June 13, 2024 版に掲載されています。
7 日間の Magzter GOLD 無料トライアルを開始して、何千もの厳選されたプレミアム ストーリー、9,000 以上の雑誌や新聞にアクセスしてください。
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