Mum of boy with PPFIBP1 gene says finding others gave her ‘strength’


When Amanda and Nick learnt their son had a life-limiting condition, they had no-one in the same situation to turn to.

Jack is only 11 months old but is one of only 16 children in the world with a genetic condition that is so rare it doesn’t have a name.

“We are going to outlive our child, and knowing that his brothers and his sister may one day have to say goodbye to him… I can’t even begin to explain how difficult that is to process each day,” said Amanda.

But the mum said finding a woman in Georgia, USA, whose daughter had the same condition as Jack had been an source of “strength” for them, but added it was “very bittersweet” because unfortunately her daughter did pass away.

  • Related Posts

    Can AI ease Pakistan’s growing health burden?

    A representational image of a hospital ward. — AFP/File KARACHI: Chronic illnesses affect nearly half of all households in the country, The News reported citing an opinion poll conducted by…

    Jillian Sackler, Philanthropist Who Defended Husband’s Legacy, Dies at 84

    Though the Sackler name was tarnished over Purdue Pharma’s role in the opioid crisis, Arthur Sackler’s should not be, she insisted; a company founder, he died well before the trouble…

    Leave a Reply

    Your email address will not be published. Required fields are marked *