Cystic fibrosis information leaflet updated and published in digital format
The PHE Screening information for parents of babies suspected of having cystic fibrosis (CF) has been updated and published in accessible digital HTML format.
Jamili Miah
Jamili Miah joined Public Health England in September 2013. Jamili worked for the Diabetic Eye Screening Programme in Birmingham for three years as a screener and disease grader. She then moved to London to join the NHS Newborn Blood Spot Screening Programme Team as Project Support. Her work has included supporting the national roll out of expanded screening and, implementing the new blood spot quality guidelines across all English newborn screening laboratories. In addition Jamili has recently also joined the Sickle Cell and Thalassaemia Screening Programme.
Newborn blood spot sampling quick reference guide published
We have published an updated HTML version of the newborn blood spot sampling quick reference guide.
SCT screening programme offering free study days
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Jamili Miah, Posted on:
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NHS Sickle Cell and Thalassaemia Screening Programme
Register now for an SCT screening programme update or specialist counsellor update.
Bursary applications now open for genetic risk assessment and counselling course
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Jamili Miah, Posted on:
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Categories:
NHS Sickle Cell and Thalassaemia Screening Programme
The NHS Sickle Cell and Thalassaemia (SCT) Screening Programme is offering 25 funded places on this year’s course at King’s College London.
PHE says goodbye to Cathy Coppinger
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Jamili Miah and Robyn O’Loughlin, Posted on:
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NHS Sickle Cell and Thalassaemia Screening Programme
Cathy Coppinger recently stepped down as manager of the NHS sickle cell and thalassaemia (SCT) screening programme to enjoy a well-deserved retirement. Her former colleagues pay tribute to her hard work.
Sickle cell disease in childhood: standards and recommendations for clinical care — consultation now open
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Jamili Miah, Posted on:
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NHS Sickle Cell and Thalassaemia Screening Programme
We are working with the Sickle Cell Society to update the Sickle Cell Disease in Childhood: Standards and guidelines for clinical care. We want you to tell us your views.
Sharing best practice to improve early access to sickle cell and thalassaemia screening
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Jamili Miah, Posted on:
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NHS Sickle Cell and Thalassaemia Screening Programme
Early access to sickle cell and thalassaemia screening is important in giving time to women and couples to consider their options. Performance varies across the country, so we are sharing some best practice tips and a new checklist tool.
We’re updating the clinical care standards for children with sickle cell disease and want your views
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Jamili Miah, Posted on:
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Categories:
NHS Sickle Cell and Thalassaemia Screening Programme
We are working with the Sickle Cell Society to update the Sickle Cell Disease in Childhood: Standards and guidelines for clinical care 2nd edition. Please let us know what you think of the clinical care standards.
Application for funded place on genetic risk assessment and counselling course is now open!
Posted by:
Jamili Miah, Posted on:
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Categories:
NHS Sickle Cell and Thalassaemia Screening Programme
The NHS Sickle Cell and Thalassaemia Screening Programme is excited to offer 25 funded places on the King’s College London Genetic Risk Assessment and Counselling course. This year the 4-day course takes place on 9 May, 10 May, 13 June and 14 June 2019.
We’ve made changes to the family origin questionnaire (FOQ)
Posted by:
Jamili Miah, Posted on:
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Categories:
NHS Sickle Cell and Thalassaemia Screening Programme
Details of the February 2019 changes and improvements to the sickle cell and thalassaemia screening family origin questionnaire.