Helping you through these tough times
Covid-19 has created numerous challenges for everyone affected by genetic, rare and undiagnosed conditions – both the people directly affected and the organisations who support them. Watch our video to hear from our CEO, Jayne Spink, about how the hub can help.
Genetic Alliance UK is hosting a weekly virtual meeting every Tuesday between 10-11am for any organisations supporting communities affected by genetic or rare conditions.
Our weekly virtual community check-ins are a safe space to raise concerns or issues, share information and work together as a community to meet the challenges of Covid-19. You do not need to be a member organisation of Genetic Alliance UK to attend, just get in touch via the contact page for joining instructions.
If you are an individual looking for support please check out the resources page for online communities run by Genetic Alliance UK or our member organisations for condition specific support.
About Genetic Alliance UK
We are the national charity working to improve the lives of patients and families affected by genetic, rare and undiagnosed conditions. We are an alliance of over 200 patient organisations.
We are home to Rare Disease UK– the national campaign for people with rare diseases and all who support them – and SWAN UK (syndromes without a name), the only dedicated support network available for families of children and young adults with undiagnosed genetic conditions in the UK.