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/comedians_cover_photo_370x280_800_600_s_c1.jpg)
RAISING THE ROOF COMEDY NIGHT
First night on the NTUK 40 years Comedy Circuit 2022 at London's Backyard Comedy Club
Read More![](https://nervetumours.org.uk/images/made/images/common/Chloe_1_370x280_800_600_s_c1.jpg)
Chloe’s NF1 story
Chloe gives an honest assessment about coming to terms with having NF1 and how it has made her determined & strong
Read More![](https://nervetumours.org.uk/images/made/images/common/KarennArtboard-1_500_572_s_c1_370x280_800_600_s_c1.jpg)
“Happy Easter”
A message from Karen, our Charity Director, wishing you a very Happy Easter!
Read More![](https://nervetumours.org.uk/images/made/images/common/image0_(2)370x280_800_600_s_c1.jpg)
Lisa helps Shine a Light on Neurofibromatosis in Belfast
Lisa has NF1, & lobbied the Belfast Lord Mayor to get Belfast City Hall lit up blue on Neurofibromatosis Day, 17th May
Read More![](https://nervetumours.org.uk/images/made/images/common/20170430_104321_370x280_800_600_s_c1.jpg)
Alex’s NF1 story
Alex describes her life with NF1, growing up in care, doing adaptive boxing & gym classes & getting NCFE Care qualifications
Read More![](https://nervetumours.org.uk/images/made/images/common/874A4A6E-C1C4-4F33-88A7-7BBF8ABBF870_370x280_800_600_s_c1.jpg)
Sumeeth’s Schwannoma story
Sumeeth, thought nothing of a muscle twitch after a hangover - it was the first symptom that led to a Schwannoma diagnosis
Read More![](https://nervetumours.org.uk/images/made/images/common/quino-al-rK_nz3DswX4-unsplash_370x280_800_600_s_c1.jpg)
Laura’s NF1 story
Laura is doing a skydive fundraiser to raise awareness & funds for NTUK, after her daughter was diagnosed with NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/queen-mary-logo_370x280_800_600_s_c1.jpg)
Disfigurement equality at work - research
This research study by Queen Mary University, London, aims to improve workplace equality for people with disfigurements
Read More![](https://nervetumours.org.uk/images/made/images/common/Comedy_night_370x280_800_600_s_c1.jpg)
RAISING THE ROOF: CHARITY COMEDY NIGHT IN AID OF NERVE TUMOURS UK
Join us in London on our first comedy night to celebrate 40 years of Nerve Tumours UK
Read More