Let’s make our voices heard! This month, encourage your friends and family to educate the world about lupus, inspire others to get involved with the Lupus Research Alliance (LRA), and connect with those who are either new to the journey or have been lupus champions for decades.
Below are easy-to-use social media text and graphics that can be posted before and during Lupus Awareness Month. There’s also special content for you to use on World Lupus Day, which is May 10.
Click on the plus signs below to expand, and simply copy and paste the content to post through your own preferred social media channels, or download all the text and graphics at once.
Let’s show the world our commitment to lupus research. No one individual can do it alone, but together, #ManyOneCan!
Engage with LRA!
Be sure to follow the LRA on social media and tag us in your posts!
: @LupusResearchAlliance
: @LupusResearch
: @LupusResearchAlliance
: @LupusResearchAlliance
However you share your social media post, be sure to use the hashtags #ManyOneCan, #LupusAwarenessMonth, #lupus, #lupusresearch, #WorldLupusDay
Instagram
May is #LupusAwarenessMonth, a time to celebrate all #lupus champions and raise awareness about #lupus. Millions of people worldwide are affected by lupus, and each of us can make a difference. We can’t do it alone, but together, #ManyOneCan!
Get tips and resources from @LupusResearchAlliance and learn about the many ways to get involved here: https://bit.ly/ManyOneCan2025
May is #LupusAwarenessMonth, a time to spotlight the millions affected by #lupus. #Lupus can be hard to diagnose and treat since symptoms vary from person to person. Your voice can help drive progress in treatments, and ultimately, a cure.
Learn how you can get involved with @LupusResearchAlliance by visiting https://bit.ly/ManyOneCan2025 #ManyOneCan
Today is #WorldLupusDay! Let’s shine a light on #lupus, honor all lupus champions, and celebrate those driving change. No one is alone in this fight. #ManyOneCan make a difference.
Learn how you can get involved with @LupusResearchAlliance by visiting https://bit.ly/ManyOneCan2025. #LupusAwarenessMonth
Supporting @LupusResearchAlliance through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures. This #LupusAwarenessMonth, consider donating in honor of a loved one. 100% goes to support #lupusresearch programs.
Click here for more information: https://bit.ly/ManyOneCanDonate
When our community joins together and speaks up, our elected officials listen. #ManyOneCan advocate for the #lupusresearch funding needed to bring us closer to a cure.
Learn about @LupusResearchAlliance advocacy efforts and how you can help by visiting https://bit.ly/ManyOneCanAdvocate #LupusAwarenessMonth
Ninety percent of people with #lupus are women, with Black, Latinx, Indigenous, Asian and Pacific Islander people disproportionately affected, both in prevalence and severity.
Since lupus affects each person differently and symptoms can change over time, continued research that includes adequate representation of women and people of color in lupus clinical research is essential to the development of effective new therapies.
Learn more this #LupusAwarenessMonth: https://bit.ly/ManyOneCan2025
Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed.
This #LupusAwarenessMonth, #ManyOneCan learn more about @LupusResearchAlliance and how to educate your community about lupus by visiting: https://bit.ly/ManyOneCan2025
Facebook
May is #LupusAwarenessMonth, a time to celebrate all #lupus champions and raise awareness about #lupus. Millions of people worldwide are affected by lupus, and each of us can make a difference. We can’t do it alone, but together, #ManyOneCan!
Get tips and resources from @LupusResearchAlliance and learn about the many ways to get involved here: https://bit.ly/ManyOneCan2025
May is #LupusAwarenessMonth, a time to spotlight the millions affected by #lupus. #Lupus can be hard to diagnose and treat since symptoms vary from person to person. Your voice can help drive progress in treatments, and ultimately, a cure.
Learn how you can get involved with @LupusResearchAlliance by visiting https://bit.ly/ManyOneCan2025 #ManyOneCan
Today is #WorldLupusDay! Let’s shine a light on #lupus, honor all lupus champions, and celebrate those driving change. No one is alone in this fight. #ManyOneCan make a difference.
Learn how you can get involved with @LupusResearchAlliance by visiting https://bit.ly/ManyOneCan2025. #LupusAwarenessMonth
Supporting @LupusResearchAlliance through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures. This #LupusAwarenessMonth, consider donating in honor of a loved one. 100% goes to support #lupusresearch programs.
Click here for more information: https://bit.ly/ManyOneCanDonate
When our community joins together and speaks up, our elected officials listen. #ManyOneCan advocate for the #lupusresearch funding needed to bring us closer to a cure.
Learn about @LupusResearchAlliance advocacy efforts and how you can help by visiting https://bit.ly/ManyOneCanAdvocate #LupusAwarenessMonth
Ninety percent of people with #lupus are women, with Black, Latinx, Indigenous, Asian and Pacific Islander people disproportionately affected, both in prevalence and severity.
Since lupus affects each person differently and symptoms can change over time, continued research that includes adequate representation of women and people of color in lupus clinical research is essential to the development of effective new therapies.
Learn more this #LupusAwarenessMonth: https://bit.ly/ManyOneCan2025
Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed.
This #LupusAwarenessMonth, #ManyOneCan learn more about @LupusResearchAlliance and how to educate your community about lupus by visiting: https://bit.ly/ManyOneCan2025
X (Twitter)
May is #LupusAwarenessMonth, a time to celebrate all #lupus champions and raise awareness about #lupus. We can’t do it alone, but together, #ManyOneCan!
Learn the many ways you can get involved with @LupusResearch by visiting https://bit.ly/ManyOneCan2025
#Lupus can be hard to diagnose and treat since symptoms vary from person to person. Your voice can help drive progress in treatments, and ultimately, a cure.
This #LupusAwarenessMonth, learn how to get involved with @LupusResearch by visiting https://bit.ly/ManyOneCan2025
Today is #WorldLupusDay! Let’s shine a light on #lupus, honor all lupus champions and celebrate those driving change. No one is alone in this fight. #ManyOneCan make a difference.
Learn how you can get involved with @LupusResearch and visit https://bit.ly/ManyOneCan2025
Supporting @LupusResearch through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures.
This #LupusAwarenessMonth, consider donating in honor of a loved one. 100% goes to support #lupusresearch programs: https://bit.ly/ManyOneCanDonate
When our community joins together and speaks up, our elected officials listen. #ManyOneCan advocate for the #lupusresearch funding needed to bring us closer to a cure.
Learn about @LupusResearch advocacy efforts and how you can help by visiting https://bit.ly/ManyOneCanAdvocate
#LupusAwarenessMonth
#Lupus affects each person differently, and adequate representation of women and people of color in lupus clinical research is essential to the development of effective new therapies.
Get involved with @LupusResearch and visit: https://bit.ly/ManyOneCan2025 #LupusAwarenessMonth
Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus.
This #LupusAwarenessMonth, #ManyOneCan learn more about how to get involved with @LupusResearch and educate your community. https://bit.ly/ManyOneCan2025
LinkedIn
May is #LupusAwarenessMonth, a time to celebrate all #lupus champions and raise awareness about #lupus. Millions of people worldwide are affected by lupus, and each of us can make a difference. We can’t do it alone, but together, #ManyOneCan!
Get tips and resources from @LupusResearchAlliance and learn about the many ways to get involved here: https://bit.ly/ManyOneCan2025
May is #LupusAwarenessMonth, a time to spotlight the millions affected by #lupus. #Lupus can be hard to diagnose and treat since symptoms vary from person to person. Your voice can help drive progress in treatments, and ultimately, a cure.
Learn how you can get involved with @LupusResearchAlliance by visiting https://bit.ly/ManyOneCan2025 #ManyOneCan
Today is #WorldLupusDay! Let’s shine a light on #lupus, honor all lupus champions, and celebrate those driving change. No one is alone in this fight. #ManyOneCan make a difference.
Learn how you can get involved with @LupusResearchAlliance by visiting https://bit.ly/ManyOneCan2025 #LupusAwarenessMonth
Supporting @LupusResearchAlliance through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures. This #LupusAwarenessMonth, consider donating in honor of a loved one. 100% goes to support #lupusresearch programs.
Click here for more information: https://bit.ly/ManyOneCanDonate
When our community joins together and speaks up, our elected officials listen. #ManyOneCan advocate for the #lupusresearch funding needed to bring us closer to a cure.
Learn about @LupusResearchAlliance advocacy efforts and how you can help by visiting https://bit.ly/ManyOneCanAdvocate #LupusAwarenessMonth
Ninety percent of people with #lupus are women, with Black, Latinx, Indigenous, Asian and Pacific Islander people disproportionately affected, both in prevalence and severity.
Since lupus affects each person differently and symptoms can change over time, continued research that includes adequate representation of women and people of color in lupus clinical research is essential to the development of effective new therapies.
Learn more this #LupusAwarenessMonth: https://bit.ly/ManyOneCan2025
Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed.
This #LupusAwarenessMonth, #ManyOneCan learn more about @LupusResearchAlliance and how to educate your community about lupus: https://bit.ly/ManyOneCan2025
