A new diagnosis of aspergillosis can make you feel scared and isolated. You probably have a million questions and not enough time with your consultant to have them all answered. As time goes on you might find it comforting to talk to other patients who ‘get it’ rather than relying only on partners, friends and family.
We organise peer support groups in different formats to suit people with different needs:
An area for patients and carers to submit blog posts and interact with others in the aspergillosis community.
A collection of stories, mainly told by patients themselves or their carers.
Help and advice for carers of aspergillosis patients.
A Q&A forum for patients to ask questions and interact with each other.
Information and advice on UK disability benefits entitlements.
Information about the monthly NAC Patient and Carer meeting.
Information about local support meetings around the UK, and in other countries.
Support and advice on making end of life plans.