Guide for schools Sierra Leonean approach

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Content Author:
Professor Simon Dyson

Level:
Healthcare professionals, teachers, policy makers, families

OER Features:

SCOOTEROER114b_Simon Dyson Guide for Schools_11April17 (PDF)

SCOOTEROER114a_Simon Dyson Guide for Schools_11April17 (Word doc)

OER Description:

On this page you can find a Sierra Leonean version of Professor Simon Dyson’s ‘Guide to school policy for young people with sickle cell disease‘, the second version of which was released in 2016.

More details to the background of the work in Sierra Leone can be found on a second blog post here. The SCOOTER project would like to reflect here our thanks to all of those mentioned in the guide who helped produced this vital adaptation.

We would like to thank the following for their work in producing this adaptation of the Guide to School Policy:

Parents, caregivers and young people with sickle cell, Sierra Leone Sickle Cell Disease Society Amelia Eva Gabba, Sierra Leone Sickle Cell Disease Society
Tamba P. Kellie, Sierra Leone Grammar School
Benson A. Sesay, Freetown Secondary School for Girls

Samuel O. Macauley, Milton Margai College of Education and Technology Samuel I. Bangura, Helen Keller International, Freetown
Osman Kamara, Helen Keller International, Freetown
Annie Sesay, Sierra Leone Sickle Cell Disease Society

Cassandra Leigh, Sierra Leone Sickle Cell Disease Society
Iyamide Thomas, GT Consultancy and UK Sickle Cell Society
Maria Berghs, De Montfort University, UK
Students and staff at Sierra Leone Grammar School, Freetown Secondary School for Girls, and the Methodist Girls High School

A blog post by Simon Dyson explaining the production of this guide can be read here.

Version 2 Guide to school policy for young people with sickle cell disease

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Guide for Schools Cover V2

Content Author:
Professor Simon Dyson (and research team)

Level:
Healthcare professionals, teachers, policy makers, researchers

OER Features:

Guide for schools V2 Word Document: SCOOTEROER112a_Simon Dyson Guide for Schools_V2_June 2016

Guide for Schools V2 PDF: SCOOTEROER112b_Simon Dyson Guide for Schools_V2_June 2016

 

OER Description:

The most popular resource by far on this website is Professor Dyson’s ‘Guide for Schools’, and this page provides an updated version of this.  Details of the earlier version can be found here – http://sicklecellanaemia.org/teaching-resources/resources/scooter24-29/scooter25.html – and this resource has been translated into several other languages.

The reason for this second edition is change to UK law with the introduction of the Children and Families Act of 2014. This requires schools to make provision for young people with conditions such as sickle cell disease, and the guide further supports this.

We hope this guide is useful and it continues to lead improvements in the way that young people with SCD are integrated into school.

This second blog post provides more background details of the second version of this guide.

 

Sickle cell disorders guide for schools

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Content Author:
Professor Simon Dyson

Level:
Healthcare professionals, school professionals, policy makers

OER Features:
Video – YouTube

PDF – SCED_HAUSA_2014 Slideshare

Slides via SlideShare – Sickle cell disease a guide for schools

OER Description:

The ‘Schools Guide‘ was the result of research by Professor Simon Dyson and colleagues, and assists teachers and policy makers in supporting children with sickle cell anaemia and thalassaemia in schools. The guide is one of this projects most popular open educational resources (OER), and through Simon’s hard work has been translated into several Nigerian languages, with others planned.

This is a lovely video outlining the work, and the bundle of resources contains downloadable slides and documents to support further understanding of this area.

Guide for schools to help learners with sickle cell

Guide for schools

 

 

 

 

 

 

Image: School Health and Safety Guide by Professor Simon Dyson
Creative Commons BY-SA

Author:
Professor Simon Dyson

Level:
Undergraduate social sciences and healthcare, postgraduate, education and healthcare professionals.

OER Features:

Funding report: Education of young people with sickle cell disease
http://sicklecellanaemia.org/resources/resources/scooter24-29/scooter24.html

Editable guide for schools
http://sicklecellanaemia.org/resources/resources/scooter24-29/scooter25.html 

OER Description:

These open educational resources are perhaps some of our most important. They are the result of a research project funded by the UK Economic & Social Research Council and conducted between De Montfort University, University of York and Loughborough University. The first report provides some essential background information to sickle cell disease, which is a complex condition with symptoms ranging from stroke, silent stroke, chronic pain and acute painful crises.

This research project explored how young people are treated in schools, and as a result, a help guide has been produced which many schools are now using and have adapted to provide support and better care of sickle suffers in their education setting.

Lecture series discussing ethnicity and screening

S Dyson Research

Image: Ethnicity and screening lecture series by Professor Simon Dyson
Creative Commons BY-SA.

Author:
Professor Simon Dyson

Level:
Undergraduate social sciences and healthcare, postgraduate, healthcare professionals.

OER Features:

Narrated presentation: Ethnicity questions and antenatal screening for sickle cell and thalassaemia.
http://sicklecellanaemia.org/resources/resources/scooter24-29/scooter26.html

Narrated presentation: Research study.
http://sicklecellanaemia.org/resources/resources/scooter24-29/scooter27.html

Narrated presentation:
http://sicklecellanaemia.org/resources/resources/scooter24-29/scooter28.html

Narrated presentation: white carriers of the sickle cell gene.
http://sicklecellanaemia.org/resources/resources/scooter24-29/scooter29.html


OER Description:

These open educational resources incorporate a series of 4 narrated presentations, presented by Professor Simon Dyson of De Montfort University. They describe research exploring ethnicity questions and antenatal screening for sickle cell disease and thalassaemia. These are superb resources for any medical and healthcare students and professionals.

 

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