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Gateshead boy's rare genetic condition means he is constantly smiling and laughing

Gateshead boy s rare genetic condition means he is constantly smiling and laughing Paige Abigail found it hard to come to terms with son Oliver s diagnosis of Angelman syndrome, but now says she wouldn t change a thing about her amazing little boy Get the latest North East news and updates delivered straight to your inbox Invalid EmailSomething went wrong, please try again later. Subscribe When you subscribe we will use the information you provide to send you these newsletters. Sometimes they’ll include recommendations for other related newsletters or services we offer. OurPrivacy Noticeexplains more about how we use your data, and your rights. You can unsubscribe at any time.

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Grieving Blyth mum opens about the agony of facing Christmas without her daughter

Grieving Blyth mum opens about the agony of facing Christmas without her daughter Karon Adkins, lost her 13-year-old daughter Leonie King last year and can t thank True Colours Theatre charity enough for helping to keep her memory alive Get the latest North East news and updates delivered straight to your inbox Invalid EmailSomething went wrong, please try again later. Subscribe When you subscribe we will use the information you provide to send you these newsletters. Sometimes they’ll include recommendations for other related newsletters or services we offer. OurPrivacy Noticeexplains more about how we use your data, and your rights. You can unsubscribe at any time.

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