clair

The non-profit organisation ClAIR which groups lupus, arthritis and scleroderma associations (among them our French-speaking Belgian member) is organising a virtual congress from tomorrow, 30th March 2018, to 13th April included.

LUPUS EUROPE will have a virtual stand in the congress. 

For more information, please see the press release: virtual congress CLAIR

The congress is held in French. To connect please click here.

To know more ?

  • CLAIR, Asbl : www.clair.be; info@clair.be
  • Arthrites, Asbl : www.arthrites.be; 0800/90 356 ; contact@arthrites.be
  • Association des Patients Sclérodermiques de Belgique, Asbl : www.sclerodermie.be; 069/777 019; info@sclerodermie.be
  • Association Lupus Erythémateux, Asbl :lupus.be; 0487/266 664 ; contact@lupus.be
  • PPP : patient-partners.be; info@patient-partners.be

If you would like to know more about the association ? Please visit CLAIR.be.

 

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2 weeks ago
LUPUS EUROPE

As much as we love hearing from you all and appreciate the time you take to share how you #kicklupus and inspire others, we cannot allow any content specifically about healing products for lupus.

We would greatly appreciate if you followed this rule when posting on the page.
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2 weeks ago
LUPUS EUROPE

#WorldLupusDay finishes today, but #lupusawareness does not. There is so much more we can do to make life with #lupus better. Watch our vice chair, Anne Charlet, talk about her journey of becoming a Board Member.
You can also join us and become a volunteer
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Wauvvvv SO good looking :-)

LUPUS EUROPE Uniting people with Lupus throughout Europe
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