A call from the European Patients’ Forum:

In order to gain some more insight on “direct” experiences of patients, EPF would like to get in touch with patients who have accessed treatment across borders (whether under the regulation or the directive), who have tried to access cross-border healthcare, who have tried to find out information about cross-border healthcare, whether they were successful or not.

Know someone in that position? Please share our call!

Deadline 15th March. For more information.

 

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4 days 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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1 week 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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