Social Media Toolkit

Let’s Make Our Voices Heard!

Encourage your friends and family to educate the world about lupus, inspire others to get involved with the Lupus Research Alliance, and connect with those who are either new to the journey or have been lupus champions for decades. You can showcase what hope looks like in action!

Below are easy-to-use social media text and graphics that can be used anytime.

Expand the sections below and simply copy and paste the content to post through your own preferred social media channels. You can also download all the text and graphics at once.

Be sure to tag the Lupus Research Alliance in your posts!

: @LupusResearchAlliance
: @LupusResearch
: @LupusResearchAlliance
: @LupusResearchAlliance

Instagram

Millions of people worldwide are affected by lupus, but there is hope. This #LupusAwarenessMonth, join @LupusResearchAlliance as we turn hope into action. Get tips and resources and learn about how to get involved here: https://bit.ly/LAM2026IG

#Lupus #LupusResearch #LupusAwareness #HopeInActionTheFutureOfLupus

#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/LAM2026IG

#LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

Supporting @LupusResearchAlliance through a gift is an empowering way to help turn hope into action. Your gift helps 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/LAM2026IG

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #LupusFundraising #HopeInActionTheFutureOfLupus

When our community joins together and speaks up, our elected officials listen. This #LupusAwarenessMonth, help advocate for the research funding needed to bring us closer to a cure. Together, we can turn hope into action.

Learn about @LupusResearchAlliance advocacy efforts and how you can help by visiting https://bit.ly/LAM2026IG

#Lupus #LupusResearch #LupusAwareness #LupusAdvocacy #HopeInActionTheFutureOfLupus

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/LAM2026IG

#LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed.

Learn more about @LupusResearchAlliance and how to educate your community about lupus by visiting: https://bit.ly/LAM2026IG

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus
Facebook

This #LupusAwarenessMonth, join the Lupus Research Alliance as we turn hope into action and work toward a future without lupus.

Get tips and resources from @LupusResearchAlliance and learn about the many ways to get involved here: https://bit.ly/LAM2026FB

#Lupus #LupusResearch #LupusAwareness #HopeInActionTheFutureOfLupus

#Lupus can be hard to diagnose and treat since symptoms vary from person to person. But progress is happening and you can be a part of it. 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/LAM2026FB

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

Supporting @LupusResearchAlliance is a powerful way to turn hope into action. Your 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/LAM2026FB

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #LupusFundraising #HopeInActionTheFutureOfLupus

When our community joins together and speaks up, our elected officials listen. Help advocate for #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/LAM2026FB

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #LupusAdvocacy #HopeInActionTheFutureOfLupus

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/LAM2026FB

#LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed.

Learn more about @LupusResearchAlliance and how to educate your community about lupus by visiting: https://bit.ly/LAM2026FB

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus
X (Twitter)

Millions of people worldwide are affected by #lupus – but there is hope. This #LupusAwarenessMonth, turn hope into action with @LupusResearch and help shape the future of lupus. Learn more: https://bit.ly/LAM2026X

#LupusResearch #LupusAwareness #HopeInActionTheFutureOfLupus

#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/LAM2026X

#LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

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/LAM2026X

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #LupusFundraising #HopeInActionTheFutureOfLupus

When our community joins together and speaks up, our elected officials listen. Help 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/LAM2026X

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #LupusAdvocacy #HopeInActionTheFutureOfLupus

#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/LAM2026X

Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus.

Learn more at @LupusResearch and educate your community.
LinkedIn

Millions of people worldwide are affected by lupus, but there is hope.

This Lupus Awareness Month, the @LupusResearchAlliance invites you to turn hope into action and help shape the future of lupus.

Learn how to get involved: https://bit.ly/LAM2026LI

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

#Lupus can be hard to diagnose and treat since symptoms vary from person to person. Your voice can help turn hope into action and drive progress in treatments, and ultimately, a cure.

Learn how you can get involved with @LupusResearchAlliance by visiting https://bit.ly/LAM2026LI

#LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

Supporting @LupusResearchAlliance is a meaningful way to help turn hope into action. Your 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/LAM2026LI

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #LupusFundraising #HopeInActionTheFutureOfLupus

When our community joins together and speaks up, our elected officials listen. By raising your voice, you help ensure that policymakers prioritize funding for life-changing research.

Learn about @LupusResearchAlliance advocacy efforts and how you can help by visiting https://bit.ly/LAM2026LI

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #LupusAdvocacy #HopeInActionTheFutureOfLupus

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/LAM2026LI

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus

Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed.

You can more about @LupusResearchAlliance and how to educate your community about lupus: https://bit.ly/LAM2026LI

#Lupus #LupusResearch #LupusAwareness #LupusAwarenessMonth #HopeInActionTheFutureOfLupus
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Michael Niggel April 21, 2025

Social Media Toolkit

Instagram

Facebook

X (Twitter)

LinkedIn

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