Here at the National Aspergillosis Centre, we understand how difficult it is living with a rare disease. Add in a global pandemic, increased social isolation and the fear of contracting Covid-19, and you have a perfect recipe for anxiety, stress and loneliness.
That is one reason why every Thursday at 10am (UTC) we run virtual support meetings via Zoom. They are free, everyone is welcome, and it is a fantastic opportunity to chat with other patients, carers and NAC staff.
Peer support is an invaluable tool when you are diagnosed with a rare disease like aspergillosis. It can help you realise you are not alone and provides an understanding environment to express feelings and concerns. Many patients attend our meetings who have been living with the disease for a long time, and they often share their experiences and personal tips for living with aspergillosis.
Why not come along and join us via the link below:
https://us02web.zoom.us/j/405765043
The passcode is 784131.
Share this post
Latest News posts
Thinking about joining a clinical trial? What are your concerns?
December 12, 2024
Biologics & ABPA – what are they and what can they do?
October 19, 2024
UK National RSV vaccination program launched
July 26, 2024
English prescription charge to rise 1st May 2024
April 26, 2024
The Role of Speech & Language Therapy (SALT)
April 16, 2024
Understanding How Our Lungs Fight Fungus
April 15, 2024
Chronic illness diagnosis and guilt
April 12, 2024
News archive
- Antifungals in development
- COVID-19
- Events
- Fundraising
- General interest
- How do I...?
- Information and Learning
- Latest research news
- Lifestyle and Coping Skills
- Living with Aspergillosis
- NAC announcements
- News archive
- Patient and Carer Blog
- Patient stories
- Recordings
- Supplements and complementary therapies
- Types of aspergillosis
- Video