We are very proud to announce that LUPUS EUROPE has been recognized by the EMA (European Medicine Agency) as “eligible entity”, the select network of patient organizations that work with the EMA to ensure that the needs and concerns of a wide range of patients are represented via direct contact with the Agency. This status is granted after an extensive evaluation and confirmation that we fulfill all eligibility criterions for working with EMA.

As an eligible organization, we will now receive targeted EMA communications and consultations and assist in the identification of experts for product-specific matters. Today already, 3 members of our Patient Advisory Network are assisting the EMA on specific requests raised to us.

This is a great development in our continued progress towards our Strategic Objective #1 : “that people with lupus in Europe participate in, and benefit from, lupus research”. Thanks to this new step, we will be in an even better position to bring the voice of people with lupus in clinical trials design, patient relevant outcome measurements, pharmaco-vigilance, drug authorization or other topics relevant to EMA.

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13 hours ago

🌍 This #WorldLupusDay, take part in a unique event specially tailored for young people living with lupus:

😃 "Lupus and Youth: A Dialogue between the Lupus Europe Youth Group and a Young Rheumatologist".

📆 May 10th.
🕖 19:00 CET (i. e. Paris time).

‼️ This is not just any webinar for the youth. It is a webinar made by youth for youth.

👀 So expect anything! This is why you cannot miss this date, whether you are young or not: understanding the worries and needs of young people with lupus is key to addressing their needs.

📧 Join us! Send an e-mail to secretariat@lupus-europe.org and secure your spot now.

www.lupus-europe.org/lupus-europe-youth-webinar/
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🌍 This #WorldLupusDay, take part in a unique event specially tailored for young people living with lupus:

😃 Lupus and Youth: A Dialogue between the Lupus Europe Youth Group and a Young Rheumatologist.

📆 May 10th.
🕖 19:00 CET (i. e. Paris time).

‼️ This is not just any webinar for the youth. It is a webinar made by youth for youth.

👀 So expect anything! This is why you cannot miss this date, whether you are young or not: understanding the worries and needs of young people with lupus is key to addressing their needs.

📧 Join us! Send an e-mail to secretariat@lupus-europe.org and secure your spot now.

https://www.lupus-europe.org/lupus-europe-youth-webinar/
2 days ago

✅ While it's true that 9 out of 10 individuals diagnosed with #lupus are women, it's crucial to also reflect on the significant impact this disease has on men. Lupus does not discriminate, and understanding its effects on all genders is vital.

🌍 𝗠𝗲𝗻 𝗺𝗮𝘆 𝗳𝗮𝗰𝗲 𝘂𝗻𝗶𝗾𝘂𝗲 𝗰𝗵𝗮𝗹𝗹𝗲𝗻𝗴𝗲𝘀 𝗮𝗻𝗱 𝘀𝘆𝗺𝗽𝘁𝗼𝗺𝘀 that can differ from those typically reported by women and that is why we have included a specific section for men with lupus that has been created by men with lupus.

🇪🇺 If you are a 𝗺𝗮𝗻 𝗹𝗶𝘃𝗶𝗻𝗴 𝘄𝗶𝘁𝗵 𝗹𝘂𝗽𝘂𝘀 𝗶𝗻 𝗘𝘂𝗿𝗼𝗽𝗲, your participation in this survey is essential to help us better understand how lupus affects men.

Your insights can lead to better support and more effective interventions for all men affected by lupus.

🔊 Remember! This anonymous survey is available in 21 languages and will take no more than 10 minutes to complete.

buff.ly/3UMZkAQ
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2 days ago

♦️ Few days left to fill the Living With Lupus in 2024 survey!

✍🏻Weź udział w ankiecie.

🔊Udostępnij w swojej społeczności.

🙏 Help us and Lupus Poland achieve more answers to ensure that the Polish population is represented in the results

s.surveylegend.com/-Nr1vl1sxwISBcDaeOzP
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5 days ago

♦️ Few days left to fill the survey!

✍🏻 Realiza la encuesta.

🔊 Comparte con tu comunidad.

🙏 Help us and Felupus ensure the Spanish population is represented

s.surveylegend.com/-Nudx9pGv-1XtZ6OnYWs
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LUPUS EUROPE Uniting people with Lupus throughout Europe
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