The lovely Petra Balážová from Slovakia has a wonderful blog called Petronela’s Journey, where she talks about healthy eating, life with lupus and so many other very interesting topics. Petra has kindly allowed us to republish one of her video interviews with rheumatologist Dr. Alessia Alunno here, on a very interesting topic; lupus fatigue. Here it is: 

Understanding fatigue in lupus can make your life easier. For the longest time I have been asking myself… What is fatigue? What is the cause of it? Do I have some other medical condition that is making me so overly tired? Why am I also emotionally tired? What I can do about it? If you are asking the same questions, this video is for you. I interviewed a rheumatologist, Dr. Alessia Alunno, who shed some light on this topic for us. Share this video with your friends who could benefit from it.

https://www.youtube.com/watch?fbclid=IwAR388wPisZjsdYleurbEnmLW6oBR7dKxbmuoEjijXNpcTRdyQQrNQW6YNI0&v=o53GNtVk58A&feature=youtu.be

Many thanks to Petra for allowing us to share her video about such an important topic!

Her blog can be found at: https://www.petronelas.com/en/

The blog’s Facebook page can be found at: https://www.facebook.com/petronelasjourney[/vc_column_text][/vc_column][/vc_row]

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🤩 May 10 is the #WorldLupusDay! And our Youth Group is commemorating it with a 𝐬𝐩𝐞𝐜𝐢𝐚𝐥 𝐰𝐞𝐛𝐢𝐧𝐚𝐫 focused on one of the most important and often overlooked topics for young people living with lupus: 𝐟𝐞𝐫𝐭𝐢𝐥𝐢𝐭𝐲 𝐚𝐧𝐝 𝐟𝐚𝐦𝐢𝐥𝐲 𝐩𝐥𝐚𝐧𝐧𝐢𝐧𝐠.

👩‍⚕️ How does lupus affect fertility?
💊 What should you consider before planning a pregnancy?
🧠 How can healthcare professionals better support young patients in these decisions?

This session brings together clinical expertise and real patient perspectives to provide clear, practical insights.

📅 𝐌𝐚𝐲 𝟏𝟎
⏰ 7 pm CET (i. e. Paris time)

🎙️ Speaker: Prof. Laura Andreoli
🗣️ Moderated by our Chair, Jeanette Andersen
👥 Organised with the Lupus Europe Youth Group

📌 Whether you are living with lupus, supporting someone who is, or working in healthcare, this webinar is for you.

👉 Don't wait any longer and register now! Send an email to secretariat@lupus-europe.org
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🤩 May 10 is the #

🌈 Beyond what you’ve experienced, something awaits.

🌟 A new way to approach your consultation is coming.

Make your consultation count.

💥 Stay tuned

#MakeItCount
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🆘 𝗦𝗸𝗶𝗻 𝗺𝗮𝘁𝘁𝗲𝗿𝘀 𝗶𝗻 𝗹𝘂𝗽𝘂𝘀.

🌍 The World Health Organisation has opened a public consultation on the draft Global Action Plan on Skin Diseases, a strategic framework that will guide governments in developing national plans on skin diseases.

🟣 Why is this important for the #lupus community?

👉 75–80% of people with SLE experience skin involvement. Skin lupus, including ACLE, SCLE and CDLE, has seen no new treatment options for over 80 years.

💬 This is an important opportunity to make sure that the voices of people living with lupus and the wider civil society community are heard.

📅 Deadline: 10 May- #WorldLupusDay
🔗 Add your voice and share with your community: www.who.int/news-room/articles-detail/public-consultation--draft-global-action-plan-on-skin-disea...
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🆘 𝗦𝗸𝗶�

❤️‍🔥 Something big is coming...

... this #WorldLupusDay 🌍.

#makeitcount
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LUPUS EUROPE Uniting people with Lupus throughout Europe
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