Present the patients’ perspective – European Lupus Meeting

headtop

The European Lupus Meeting is taking place in Venice, Italy from 5th-9th October 2016.

This year will be a great opportunity to share the research work done by patient organisations and/or single or groups of patients. This is a unique opportunity to present our work in the same sessions as the doctors.

LUPUS EUROPE invites all patients and patient representatives to submit an abstract as described on the LUPUS EUROPE website.

To submit an abstract please fill in the form (link below) and send it with the abstract to Kirsten Lerstrøm, LUPUS EUROPE, Chair (kirsten@lerstrom.dk), Francesca Marchiori, LUPUS EUROPE Co-Opted Patient Partner in Research (f.marchiori@tiscali.it)  and LUPUS EUROPE Secretariat (secretariat@lupus-europe.org).

Please contact any of the above for further information. Link to LUPUS EUROPE website and the abstract submission form (attached document), please click here.  The deadline for submission is 29th February. 

If you have any further questions please don’t hestitate to get in touch with Kirsten Lerstrøm, LUPUS EUROPE, Chair, Francesca Marchiori, LUPUS EUROPE Co-Opted Patient Partner in Research or LUPUS EUROPE Secretariat.

headtop

facebookShare on Facebook
TwitterTweet
FollowFollow us

About the author

Alain Cornet

    Live Facebook Feed

    Comments Box SVG iconsUsed for the like, share, comment, and reaction icons
    Author Avatar
    LUPUS EUROPE
    2 weeks ago

    🌈 The right to health is a basic human right. Everyone must have access to the health services they need when & where they need them without 💶 hardship.

    😔 30% of the global population is not able to access essential health services.

    #StandWithScience #WorldHealthDay #WHD2026     ... See MoreSee Less

    🌈 The right to he
    View on Facebook
    · Share
    Share on Facebook Share on Twitter Share on Linked In Share by Email
    View Comments likes 0 Shares: 0 Comments: 0

    0 CommentsComment on Facebook

    Author Avatar
    LUPUS EUROPE
    2 weeks ago

    🚀 #LupusGPT & #EasyLupus are currently offline as we continue improving them.

    🛠️You thought they couldn’t get better? We know they can, & we’re making it happen.

    In the meantime, for reliable, multilingual lupus information👉 lupus100.org/

    💜Thanks for your support!     ... See MoreSee Less

    🚀 #LupusGPT & #Ea
    View on Facebook
    · Share
    Share on Facebook Share on Twitter Share on Linked In Share by Email
    View Comments likes 4 Shares: 4 Comments: 0

    0 CommentsComment on Facebook

    Author Avatar
    LUPUS EUROPE
    3 weeks ago

    🎥 Did you miss our ELM 2026 Recap Webinar?

    😃 Watch it now on our YouTube channel!

    👉 Our Patient Advisory Network (PAN) members and volunteers share their key takeaways from the European Lupus Meeting 2026.

    👉 Doctors and researchers explain, in a clear, short, and patient-friendly way, key messages from their talks.

    🎯 Click the link below and discover the latest advances in lupus, explained directly by experts:

    www.youtube.com/watch?v=Bw5Iptu-ZNc

    More insights from #elm2026 coming soon. Stay tuned!     ... See MoreSee Less

    🎥 Did you miss ou
    View on Facebook
    · Share
    Share on Facebook Share on Twitter Share on Linked In Share by Email
    View Comments likes 5 Shares: 3 Comments: 0

    0 CommentsComment on Facebook

    LUPUS EUROPE Uniting people with Lupus throughout Europe
    Send