Bronchiectasis

Bronchiectasis Patient Conference 2024

Join us on Saturday 23 March 2024 from 10:00-16.00 CET for our free, online annual bronchiectasis patient conference.

Online
23/03/2024

Programme


Join us on Saturday 23 March 2024 from 10:00-16.00 CET for our free, online annual bronchiectasis patient conference.

There will be a mix of live talks and videos from both bronchiectasis patients and medical experts on:

  • Basic overview for those recently diagnosed or those who need more general information
  • Resources and information to help you live your life well
  • Bronchiectasis and the future – exciting updates on treatment, research and what lies ahead
  • How to live with bronchiectasis and another airway disease like asthma or COPD
  • Living with the additional challenges of bronchiectasis (sinus, gut, wellbeing etc)
  • Airway clearance – making decisions about the devices and methods that are best for you
  • Inspiring stories of what has helped people with bronchiectasis

There will be lots of opportunities to ask questions to the speakers.

Download the full schedule of the bronchiectasis patient conference

Language options


The bronchiectasis patient conference will be held in English. We will be providing a live transcription service that will allow participants to generate captions in over 50 languages.

Speakers, chairs and contributors


The following is a list of the confirmed speakers, session chairs and video contributors.

Professor James Chalmers  - profile image
Professor James Chalmers
United Kingdom

Professor James Chalmers is the British Lung Foundation Chair of Respiratory Research at the University of Dundee, UK, and a consultant respiratory physician.

He is an expert in lung infections and has been involved in a number of projects during the COVID19 pandemic, including leading the ERS Guidelines Task Force for COVID19, being chief investigator for several trials of new COVID19 treatments and answering many of the questions received for the ELF Q&A.

He works closely with ELF to involve patients in respiratory infection research through projects such as EMBARC, and is an advocate for involving patients in guidelines, clinical research, and clinical trials.


Tan Chin Kong - profile image
Tan Chin Kong
Singapore

Chin Kong is celebrating his 70th birthday in March this year. He has had bronchiectasis for more than 20 years but only learnt about his condition in July 2022 when he had to be admitted to the hospital’s emergency ward for breathlessness. Chin Kong is managing his bronchiectasis condition by staying active with daily meditation, exercises and birding. He is also maintaining a daily regimen to clear his phlegm twice a day.


Sanjay H Chotirmall - profile image
Sanjay H Chotirmall
Singapore

Associate Professor Chotirmall is an internationally recognised clinician-scientist with an established translational respiratory research group at the Lee Kong Chian School of Medicine, NTU Singapore. To date, he has performed key work on endo-phenotyping pulmonary infection, including the use of next generation sequencing approaches, in the context of chronic inflammatory respiratory diseases that have led to publications in Nature Medicine, the New England Journal of Medicine (NEJM), the Lancet Respiratory Medicine, the American Journal of Respiratory and Critical Care Medicine and Cell Host and Microbe. He has been appointed Provost’s Chair in Molecular Medicine at NTU Singapore since 2019 and currently serves as Vice Dean (Research) at the Lee Kong Chian School of Medicine and as Deputy Editor at the American Journal of Respiratory and Critical Care Medicine (AJRCCM).


Barbara Crossley - profile image
Barbara Crossley
United Kingdom

Barbara Crossley has been a member of the ELF Bronchiectasis Patient Advisory Group since 2017.

She has helped organise four Bronchiectasis Patient Conferences, collaborated with EMBARC researchers on ongoing projects, helped formulate patient surveys and patient-friendly information for the European Lung Foundation website, including a patient self-care guide.

She has lifelong bronchiectasis and is a writer who lives in the Peak District in Derbyshire, UK.


Bridget Harris - profile image
Bridget Harris
United Kingdom

Member of ELF Bronchiectasis Patient Advisory Group.


Donna Heilweil - profile image
Donna Heilweil
Switzerland

Member of the ELF Bronchiectasis Patient Advisory Group


Nancy Ho - profile image
Nancy Ho
Singapore

Nancy is a retired teaching assistant who has lived with bronchiectasis for over 12 years and hopes to do more to support other patients with bronchiectasis as this is a condition that few are familiar with. She also hopes to contribute to respiratory medicine research.


Fran Husson - profile image
Fran Husson
United Kingdom

80-year-old patient advocate with a portfolio of activities. My various health and social care interests (lung diseases, problematic polypharmacy, antimicrobial resistance and antimicrobial stewardship) have merged into a dominant activity to promote the use of Personal Health Records (PHR) in the UK and internationally. I currently serve as PHR public partner with the UK Health Security Agency’s English Surveillance Programme for Antimicrobial Utilisation and Resistance and often present at conferences and webinars on my own PHR use to cope with aspergilloma and bronchiectasis, as well as other co-morbidities.


Eliza Kompatsiari - profile image
Eliza Kompatsiari
Greece

Eliza holds a PhD in Criminal Law and works as a barrister in Greece.

She has been a member of the ELF Bronchiectasis Patient Advisory Group since 2021 and has engaged with its activities and represented it in different projects and working groups over these years.


Paul McCallion - profile image
Paul McCallion
United Kingdom

I am an Advanced Respiratory Medicine Physiotherapist with a specialist interest in Bronchiectasis and research. I lead the Newcastle upon Tyne Hospitals NHS Foundation Trust Physiotherapy Bronchiectasis service. I graduated from Queen Margaret University, Edinburgh, UK in 2011. I completed rotations in Northumbria Foundation Trust before moving to a Senior and then Advanced Respiratory post in Newcastle upon Tyne Hospitals, UK. I am passionate about research, completing my MSc in Public Health and Health Services Research in Newcastle University in 2022. I am a current National Institute of Health and Care Research (NIHR) Clinical Doctoral Research Fellow. My PhD is looking into the use of Shared Decision Making to support patients with their Airway Clearance Techniques for Bronchiectasis. I hold the Long Term Conditions role for the Association of Chartered Physiotherapists in Respiratory Care in the UK (www.acprc.org.uk).


Rachael McGill - profile image
Rachael McGill
United Kingdom/Portugal

Rachael is a theatre and fiction writer and literary translator who lives between the UK and Portugal. Rachael is a member of the ELF bronchiectasis patient advisory group.


Professor Lucy Morgan - profile image
Professor Lucy Morgan
Australia

Lucy is a lung specialist working in Sydney. She was the foundation chair of the Australasian Bronchiectasis Consortium and the Australian Bronchiectasis Registry and is now Chair of Lung Foundation Australia. She is passionate about empowering patients to have equity of access to great clinical care and great clinical trials, wherever they live.


Dr Fiona Mosgrove - profile image
Dr Fiona Mosgrove
United Kingdom

Dr Fiona Mosgrove is a GP with special interest in respiratory medicine. Fiona has been a GP since 2012 and works in a large practice in Aberdeen city. She began to develop a respiratory special interest in 2018, studying for a postgraduate diploma and then a masters in respiratory medicine, with a project focused on the microbiology of bronchiectasis exacerbations. She sits on the primary care respiratory society education committee, the ACT on COPD working group for Scotland and is part of the international primary care group sentinel network question and answer group.


Joyce Norwell - profile image
Joyce Norwell
United Kingdom

Member of ELF Bronchiectasis Patient Advisory Group


Eva Polverino - profile image
Eva Polverino
Spain

Annette Posthumus - profile image
Annette Posthumus
The Netherlands

Member of the ELF Bronchiectasis Patient Advisory Group


Ed Powell - profile image
Ed Powell
England

I was diagnosed with bronchiectasis of the middle right lobe when I was 8 years old having suffered from chronic cough and wheezing since I was five months old.

I am currently 16 studying for A levels in Biology, Chemistry and Maths and I am also doing my gold Duke Of Edinburgh’s award.

In autumn 2023 I joined the ELF council.

I play the trumpet and sing in a variety of bands, ensembles and choirs in school and with a music school on a Saturday. I also enjoy cycling and hiking in the local countryside.


Prof. Michal Shteinberg - profile image
Prof. Michal Shteinberg
Israel

Michal Shteinberg received her MD and a PhD in biochemistry from the Technion-Israel institute of technology. She trained in internal medicine and pulmonology, with a Fellowship in bronchiectasis and adult CF.

Prof. Shteinberg is heading the bronchiectasis and adult CF unit in the Pulmonology institute and CF center, Carmel medical center, Haifa, Israel.
She is a Clinical Associate Professor in the Faculty of medicine at the Technion, Israel Institute of Technology, and a member of the executive committee of the Israeli Society for Tuberculosis and mycobacterial diseases.

Her main research interests are bronchiectasis and its overlap with other airway diseases, mainly rhinosinusitis, and connective tissue diseases, as well as adult CF.

Prof. Shteinberg is a member of EMBARC management and heading Patient Activities Work package.


Partners


This event has been developed with and supported by EMBARC, a pan-European network and the ELF Bronchiectasis Patient Advisory Group.

Previous events


This is the fourth instalment of our annual bronchiectasis patient conference. Find out more about the previous events:

Support ELF events


ELF does not charge for its events and materials. We want to make sure they are available to anybody who wishes to join or use them. To ensure we can keep doing this we ask that those who can afford to pay to make a donation. We are grateful to everyone who supports us in this way and helps lung health patients to understand more about their condition and have their voices heard.

Donate

European Lung Foundation

ELF is a patient-led organisation that works internationally to bring patients and the public together with healthcare professionals to improve lung health and advance diagnosis, treatment and care.

EMBARC

EMBARC is a European Respirtory Society (ERS) CLinical Research Collaboration (CRC) in the field of bronchiectasis. Clinicians from EMBARC have been involved in the planning of this event. ELF received funding from EMBARC to hold this event.

European Respiratory Society

ERN-LUNG

ERN-LUNG is the European Reference Network for rare respiratory diseases. It is a network of European patients and healthcare providers dedicated to ensuring and promoting excellence in care and research to the benefit of patients affected by rare respiratory diseases.