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.
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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, #lupus, #lupusresearch
Instagram
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
#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
Supporting @LupusResearchAlliance through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures. 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
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: 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.
#ManyOneCan learn more about @LupusResearchAlliance and how to educate your community about lupus by visiting: https://bit.ly/ManyOneCan2025
Facebook
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
#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
Supporting @LupusResearchAlliance through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures. 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
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: 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.
#ManyOneCan learn more about @LupusResearchAlliance and how to educate your community about lupus by visiting: https://bit.ly/ManyOneCan2025
X (Twitter)
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!
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.
Learn how to get involved with @LupusResearch by visiting https://bit.ly/ManyOneCan2025
Supporting @LupusResearch through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures.
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
#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
Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus.
#ManyOneCan learn more about how to get involved with @LupusResearch and educate your community. https://bit.ly/ManyOneCan2025
LinkedIn
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
#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
Supporting @LupusResearchAlliance through a gift is an empowering way to help fund the science of tomorrow’s treatments and cures. 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
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: 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.
#ManyOneCan learn more about @LupusResearchAlliance and how to educate your community about lupus: https://bit.ly/ManyOneCan2025
