Donald Thomas’ Post

Uniting Lupus Groups Around the World https://lnkd.in/gcjiiMAz It's estimated that at least 5 million people worldwide have some form of lupus. On average, it can take nearly six years to be diagnosed with lupus. So the numbers are probably higher. Use the link above to see if there is a lupus group in your country. If there is one not listed please feel free to post a link to the group here. #arizonalupus #lupusawareness #lupuswarrior #menhavelupus

Today, on #WorldLupusDay, we shine a spotlight on lupus, a complex #autoimmunedisease affecting millions worldwide. Together, we can advocate for better research, treatments, and support systems. 💜 #LupusAwareness

WORLD LUPUS DAY: The time is now to pursue remission as a key care goal in lupus.    Aligned with the latest clinical recommendations, we can aim to reduce reliance on oral corticosteroids and work to build a future where remission is possible for more people living with lupus.     This World Lupus Day, learn more about how we’re following the science to help make remission a reality: https://bit.ly/3Wt2QkT    #WorldLupusDay #MakeLupusVisible 

On World Lupus Day, we stand together to champion the cause of lupus warriors worldwide. As we raise awareness and shed light on this complex illness, let's also emphasize the critical role of clinical research in driving progress. By supporting and advancing research efforts, we pave the way for better understanding, more effective treatments, and ultimately, improved outcomes for those living with lupus. Together, let's unite our voices and efforts to make a meaningful difference in the lives of millions affected by lupus. #kvcr #lupusawareness

Here's what's unfolding this week in honor of Arthritis and Lupus Awareness Month! Don't forget to tag your friends, share your thoughts in the comments, and repost to join us in strengthening our research efforts! #StrengthInEveryStep

“People don’t realize it’s painful”, said Maria, diagnosed at age 20. Beyond managing physical symptoms, lupus impacts individuals' mental and emotional well-being. That’s the reality for millions battling this chronic autoimmune condition. In recognition of Lupus Awareness Month, we’re amplifying the voices of those living with this disease, helping to create bridges of understanding and support. Lupus can be a complex and frustrating illness for both patients and providers. According to the Lupus Foundation of America, symptoms can be wide-ranging and unpredictable, making diagnosis and treatment challenging. Watch their video to hear directly from patients about what it’s like to live with lupus, then let’s work together to raise awareness. Here’s how you can help: • Share this post with your network and help break the stigma surrounding this invisible illness. • Advocate for patients by supporting policies and research initiatives that benefit those living with lupus. • Learn more about lupus and access valuable resources from reputable organizations like the Lupus Foundation of America or the Lupus Research Alliance. These organizations tirelessly educate, advocate, and provide resources and support for millions affected by Lupus. Together, let’s amplify awareness and support for the lupus community. https://bit.ly/3wtq1B2 #LupusAwarenessMonth #SupportLupusWarriors #HealthcareAdvocacy #AutoimmuneDisease

⭐️ On World Lupus Day, let's shed light on the complexities of this challenging disease. Lupus, an autoimmune condition, can affect multiple tissues and organs, from skin to brain. 🩸🦵🏼🧠 Its invisible symptoms often make diagnosis a long journey, taking an average of 7.5 years. Let's raise awareness, advocate for faster diagnosis, and support those battling lupus every day. Please share this post to help raise awareness of this condition. You can learn more at: www.lupusuk.org.uk #worldlupusday #lupusawareness #supportandserve #medical #pharma #medcomms #lupusresearch https://lnkd.in/eqycYQrf

The results are in! From our Facebook and Instagram poll, we determined your biggest inquiry is, "Where can I find more information about lupus?" Thankfully, we have THE lupus expert Dr. Don Thomas here to help! He will be joining us in September to respond to each of the most asked questions. More details to come!!!

LUPUS EUROPE is conducting a survey to gather insights into the experiences of individuals living with #lupus across Europe. 🌍 In 2020, Lupus Europe launched a large “Living with lupus survey”. Thanks to the huge participation from patients around Europe, the insights from this survey are largely used. Time has now come for a new survey, with different topics, to add to our knowledge of what it means to live with lupus in 2024. The survey is anonymous and should take approximately 10 minutes to complete. It is available in 19 different languages. Click the following link to complete the survey: https://lnkd.in/eA8A57sh 🔗 Thank you for sharing your views! #LupusAwareness #LupusResearch #SLE #LupusCommunity #LupusEurope

Spotlight on Lupus: Illuminating the Path to Understanding and Support Our latest infographic is a deep dive into the world of lupus, a complex autoimmune condition. Join us on a journey of awareness and advocacy as we navigate the unique challenges faced by those living with lupus. Lupus is more than a medical diagnosis; it's a story of resilience, strength, and courage. Share this visual narrative to shed light on the experiences of individuals touched by lupus and to foster a community that stands with them. Dive into the details of lupus—its symptoms, impact, and the daily battles faced by those living with this autoimmune disorder. Through knowledge, we can break down misconceptions and build a foundation of support. Your share is more than a click; it's a gesture of solidarity. Let's amplify the voices of those living with lupus, creating a chorus of understanding, empathy, and support. Knowledge transforms perceptions. Share this infographic to educate others about lupus, fostering a compassionate environment that embraces diversity in health experiences. Tag friends, colleagues, and advocates who can join us in spreading awareness about lupus. Together, let's build a network that uplifts and empowers those facing lupus with strength and compassion. In the tapestry of health, let lupus find its place among the stories of resilience. Join us as we champion the cause of understanding and support. #LupusAwareness #SupportInUnity #StrengthAgainstLupus