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Frequently Asked Questions
What is GLAD doing to strive for equality, diversity, and inclusion?
What is the Genetic Links to Anxiety and Depression (GLAD) Study?
What is the NIHR BioResource?
Should I still send back my saliva sample if I am feeling unwell?
What should I do if I feel distressed?
Can I still take part if I haven’t received a diagnosis or treatment?
How will you use the survey, biological and genetic information data I give you?
How is the information I give you kept confidential?
Will commercial companies be accessing my data?
Why do you need access to my medical records?
How will you access my medical records?
What sections of my medical records will you access?
What will you do with my medical records?
What other studies might I be invited to take part in?
How do I sign up to the GLAD Study?
Need any help?