A mother has shared the "heartbreaking" reality of watching her young daughter's health decline daily - as she loses her ability to walk and speak. Maria Rushaid Algaradi is now battling to raise funds for essential medication to halt her daughter's deterioration ahead of a planned transplant operation.

Three-year-old Mylah Algaradi received a diagnosis at birth of a rare and debilitating condition called Arginase deficiency, which forms part of the urea cycle disorders.

This severe metabolic disorder is now ruthlessly attacking Mylah's health, causing her mobility to worsen with each passing day.

Whilst Mylah has been living with this condition since birth, she had been progressing well and was achieving all her crucial milestones having adhered to a strict low protein diet under the

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