This article was published by the Cystic Fibrosis Foundation and is a personal account of a young woman with CF and trying to come to terms with the limitations that loss of lung function has placed on her young life. There is a grief for her lost life, the one where she was fitter and stronger and could do so much more,
Grieving the life I once had
Just like any grief, it has a process that we all go through, and has a new life at the other end. The article is well worth a read.
NB Aspergillosis Support Groups run by the National Aspergillosis Centre in the UK can be found on Facebook.
Also, see NHS advice for the grieving.
Share this post
Latest News posts
Aspergillus in a well-loved pillow written by Caroline Hawkridge
January 23, 2019
Patients meeting November 2018
January 11, 2019
Patients meeting August 2018
January 11, 2019
Patients meeting July 2018
January 11, 2019
Patients meeting May 2018
January 11, 2019
Patients meeting April 2018
January 11, 2019
Patients meeting March 2018
January 11, 2019
Patients meeting 8th AAA, Lisbon February 2018
January 11, 2019
Patients & Carers meeting December 2017
January 11, 2019
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