Reasons Why We Should Not Do Animal Testing The family of a three year old girl who is thought to be one of only two people in the country with a rare genetic condition say she will end up paralysed without 250 000 of
A mum has told how she is in a race against time to give her three year old daughter the treatment needed to stop an extremely rare genetic disease taking away her A family from Halifax is in a race against time to raise money to provide the medicine necessary to treat three year old Dua Ahmed s extremely rare genetic disease
Reasons Why We Should Not Do Animal Testing
Reasons Why We Should Not Do Animal Testing
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Dua Ahmad aged three lives at Savile Park with mum Nadia dad Shakeel and brothers Ayaan 11 Raees 7 and Zoraiz one She was diagnosed in February 2023 through a Dua Ahmad three was diagnosed with Spastic Paraplegia 50 SP50 an extremely rare disease that causes paralysis in the toes and works its way to the brain She is
THREE children whose sister faces being paralysed by a rare disease are asking their mother why no one is stepping in to help Dua Ahmed three was diagnosed with SPG50 THE family of a toddler with a crippling and super rare condition are desperatel y trying to raise 250 000 for a life saving US drug trial Dua Ahmad three is one of only two
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Three year old Dua Ahmad from Halifax was diagnosed with SPG50 in February 2023 making her only one of two children in the country to be diagnosed with the rare MEF2C gene variations cause significant cognitive and physical impairments Individuals often experience severe to profound developmental delay low muscle tone hypotonia epilepsy
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The family of a three year old girl who is thought to be one of only two people in the country with a rare genetic condition say she will end up paralysed without 250 000 of
https://www.manchestereveningnews.co.uk › news › uk-news
A mum has told how she is in a race against time to give her three year old daughter the treatment needed to stop an extremely rare genetic disease taking away her
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