Covid-19 Impact on Wellbeing in Families of Children with Rare Neurogenetic Disorders (CoIN Study)
29 July 2020
![](/images/made/images/common/picsea-EQlTyDZRx7U-unsplash2000x700_800_600_s_c1.jpg)
Are you the parent of a child aged 0-16 with a rare genetic and/or neurodevelopmental disorder?
You can help to better understand the impact of Covid19 on the wellbeing of families of children with rare genetic and neurodevelopmental disorders. If you fit the criteria, Kings College London and a UK-wide team of researchers (CoIN Study) would like to invite you to take part in a regular online survey.
The CoIN Study will track changes in wellbeing during and after the pandemic in order to understand the specific challenges facing families of children with rare disorders. Your responses will be rapidly fed back and used to identify and provide better ways of supporting you both now and in the future.
The survey will take up to 40 minutes to complete the first time you do it and about 15 minutes to complete thereafter. We will ask you to complete the survey once per month until children are back in their usual education.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Sarah-Page-Preview-800-x-500-px_800_600_s_c1.png)
Sarah’s Story
Sarah has NF1 and works full time for the NHS check out her intriguing story here
Read More![](https://nervetumours.org.uk/images/made/images/common/laura-2Desktop-1600-x-900-px-copy_800_600_s_c1.png)
Laura’s Story
Read about Laura's experience of undergoing surgery to remove a tumour from her spine here:
Read More![](https://nervetumours.org.uk/images/made/images/common/durhamPage-Preview-800-x-500-px_800_600_s_c1.png)
Visible Difference Equality Law Research: summary of findings
Find out more about the results here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Galloway-Page-Preview-800-x-500-px_800_600_s_c1.png)
The Galloway Family and their “amazing” four year old Ruby
Have a read about the incredibly brave young Ruby Galloway (NF1) and check out their previous and future fundraiers.
Read More![](https://nervetumours.org.uk/images/made/images/common/James-blog-3Page-Preview-800-x-500-px_800_600_s_c1.png)
“Framing the face: History, Emotion, Transplantation” a blog from James Partridge
Find out more about the blog and what is concerns here:
Read More![](https://nervetumours.org.uk/images/made/images/common/halloween-Page-Preview-800-x-500-px_800_600_s_c1.png)
A Spooktacular Halloween day for NTUK
Find out more about the wonderful fundraising event here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Nick-and-elidihDesktop-1600-x-900-px-copy_800_600_s_c1.png)
Nicks Triathlon in Support of his daughter Eilidh
Find out more about Nick's Triathlon and his daughter's experiences with NF1 here:
Read More![](https://nervetumours.org.uk/images/made/images/common/TOM-GK-MusicalPage-Preview-800-x-500-px_800_600_s_c1.png)
Tom GK- Hearing Loss: The Musical
Find out more about the musical and how you can secure your ticket here
Read More