Category : Search result: genetic screening


Jesy Nelson's Petition for Newborn SMA Screening

Former Little Mix star Jesy Nelson is launching a petition to add SMA to the NHS newborn heel prick test after her twin daughters were diagnosed with the 'horrible' disease. Learn about her fight for change.

Jesy Nelson's twins diagnosed with severe SMA Type 1

Little Mix star Jesy Nelson reveals her baby twins have Spinal Muscular Atrophy. Early treatment is vital, but NHS screening is not routine. Learn about private testing options and the campaign for change.

HPV and Cervical Cancer: Expert Busts Common Myths

Consultant gynaecological oncologist Miss Adeola Olaitan explains the nuanced link between HPV and cervical cancer, debunks stigma, and highlights the importance of vaccination and NHS screening.

GMB: Kate Garraway comforts guest after mum's kidney death

Good Morning Britain's Kate Garraway offered heartfelt support to guest Genieva Owens, who lost her mum to kidney failure linked to a genetic risk. The interview highlights urgent calls for APOL1 gene screening in Black communities. Read the full story.

UK rejects prostate cancer screening for all men

The UK National Screening Committee has decided against a national prostate cancer screening programme, sparking disappointment from public figures and highlighting higher risks for black men.

NHS rejects wider prostate cancer screening

The UK National Screening Committee is expected to reject calls for routine PSA tests for Black men and those with a family history, prioritising caution over unnecessary treatment.

UK Prostate Cancer Screening Review: Key Update

The UK National Screening Committee is set to issue new recommendations on prostate cancer screening today. Discover how a £42m trial could transform diagnosis and save lives.

90% Demand Prostate Cancer Screening Programme

A major poll reveals 90% of Brits want a national prostate cancer screening programme as the UK National Screening Committee prepares its crucial decision. Join the call to save lives.

Sisters, 27, diagnosed with breast cancer months apart

Two North Carolina sisters in their 20s, both carrying the CHEK2 gene mutation, were diagnosed with breast cancer within months of each other, prompting urgent double mastectomies. Their story underscores the critical need for early genetic screening.

UK toddler first in world with unique genetic condition

In an extraordinary medical breakthrough, 19-month-old Oscar Sparrow from West Midlands has been identified as the only person worldwide living with a never-before-seen genetic mutation, offering new hope for rare disease research.

Daughter's rare condition breaks hearts daily

Exclusive: The heartbreaking story of a family coping with their daughter's rare Cri Du Chat syndrome, revealing the daily challenges and emotional toll of caring for a child with complex needs.

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