Our lights shine in purple and red this evening in honor of the
@LupusResearch
and its Lupus Breaking Through Gala that celebrates the power of science!
Honorary Chair
@selenagomez
making sure you know that anyone, anywhere can join us for the Lupus Research Alliance
#BreakingThroughGala
on Monday 11/ 22 at 7PM EST!
The online broadcast is OPEN TO ALL so RSVP now at for your event link and access pin!
Drumroll announcement! Register for this year’s Lupus Research 2020 Gala at and join
@selenagomez
and other powerful
#lupus
advocates! You don't want to miss this year's celebration!
#LupusResearchAlliance2020
5 Questions with Selena Gomez
We sat down with
@selenagomez
to find out how she plans to
#LiftUpLupus
. As one of our most powerful voices, she continues to inspire and provide hope to the lupus community. Read the full Q&A at
#LupusAwarenessMonth
This
#LupusAwarenessMonth
, we are teaming up with
@selenagomez
on a quest to accelerate research. Visit to learn about the many ways you can make a difference. No one individual can do it alone but
#ManyOneCan
!
Thank you
@POTUS
and
@VP
for taking steps to make health care more affordable for
#lupus
patients and all Americans. We look forward to working with you to improve care and find cures!
To help elevate the conversation on
#lupus
and mental health for those who may be struggling, we got personal with
@selenagomez
as she shared her challenges and her success stories to
#LiftUpLupus
.
Read the full interview here:
On
#WorldLupusDay
, I’m teaming up with the
@LupusResearch
Alliance to empower lupus warriors and let you know...you are not alone.
Let’s elevate awareness and support lupus research -- because together, we can make a difference.
Just TWO DAYS until we all come together for our
#ManyOneCan
Walk with Us to Cure Lupus virtual event 5/22! This celebratory Walk experience will unite the entire lupus community to support research that changes the lives of people with
#lupus
.
Join us!
As
@POTUS
and
@VP
lead on advancing equity, LRA is working to defeat lupus which has a disparate impact on minority women AND support groundbreaking work by researchers of color.
In just 3 short days Walk Day will be upon us! We will applaud your fundraising success and commitment to uncovering better treatments and ultimately a cure for
#lupus
.
Join us Saturday at 12pm ET for our
#ManyOneCan
Virtual Walk Day Experience:
Don’t miss tonight’s
#BreakingThroughGala
for an unforgettable night!! Tune in ONLINE at 7pm EST to support the promising research that is breaking through the complexity of lupus to find the cure.
Today is
#WorldLupusDay
where we raise awareness for this complex autoimmune disease. ♥️ If you’re able to make a donation to the
@lupusresearch
Alliance, please click this link:
In 2 days, join us in coming together on a global scale for the
#ManyOneCan
Virtual Walk with Us to Cure Lupus! The program kicks off at 12pm EST, and you can live chat with fellow lupus champions, LRA/LT staff, and corporate supporters until 2pm EST:
Selena Gomez has teamed up with international sports brand
@PUMA
to design the “Phenom Lux” shoe with matching socks that will benefit the Lupus Research Alliance! Learn more:
Thank you
@SelenaGomez
for sharing your personal story and advocating for the lupus community. Congrats on the premiere of your new documentary “Selena Gomez:
#MyMindAndMe
”. We can’t wait to watch it! ️👀🍿🎞
Every breath, a breakthrough. In honor of
#WorldMentalHealthDay
I wanted to share the trailer for my documentary Selena Gomez: My Mind & Me. November 4 on
@AppleTVPlus
Thanks for being an amazing inspiration
@SelenaGomez
– and raising your voice about kidney-related lupus. Working together we’ve made great strides, but the LRA remains steadfast on finding new and better treatments for our community. We salute you & all
#lupusnephritis
warriors.
To the entire world,
@ladygaga
is a winner. But to the lupus community she’s a hero. At the 2019 Grammy’s she won an award for Best Pop Solo in honor of her aunt Joanne who lost her battle with lupus at 19. We’re so proud & thankful for her support of the lupus community!
#WCW
Calling all little monsters &
#lupuswarriors
! Join us for a very special tribute by
@ladygaga
to her aunt Joanne who battled lupus, only at the LRA Lupus Research 2020 Virtual Fundraising Event!
Join us 11/23
#LupusResearchAlliance2020
Honorary Chair
@SelenaGomez
making sure you know that anyone, anywhere can join us for the Lupus Research Alliance
#BreakingThroughGala
THIS MONDAY 11/21 at 7PM EST!
RSVP now for your event link and access pin.
Selena Gomez’s first design collaboration with
@PUMA
, is the highly anticipated Phenom Lux—a shoe that is made to stand out and help out. The Phenom Lux & socks will benefit the Lupus Research Alliance, the world’s leading private funder of lupus research.
Ready. Set. Selena. Shop early access to the new
#CoachxSelena
collection, including her pretty-in-pink Trail bag. Discover it, along with accessories and ready-to-wear:
#CoachNY
@MikeAdamOnAir
We're so honored to have Selena Gomez and Lady Gaga as Honorary Co-Chairs of the
#BreakingThroughGala
this year. Unfortunately, they will not be in attendance tonight.
With you beside us at this very exciting time in lupus research, the LRA is on the cusp of major breakthroughs. As Selena Gomez describes in this video, the answers lie within - within her, within you, within the lupus community. Join us:
"It's been really fun to work so closely with PUMA on the design of this shoe. I'm also proud to partner with them in helping to affect lives and bring attention to a cause that is very important to me personally." -
@selenagomez
#SelenaxPuma
Thank you
@selenagomez
for being a true inspiration by beautifully shining a light on
#lupusnephritis
, which affects up to 50% of people with
#lupus
. Visit to learn more about the many studies the LRA is doing to better treat this dangerous complication.
This
#WorldLupusDay
we’re partnering with
@SelenaGomez
to empower people around the world living with lupus. It’s also
#MentalHealthMonth
and we recognize the strength of our community who also face that challenge. You’re not alone.
Sneak Peek:
Joanne (Where Do You Think You’re Goin’?) Piano Version
#Joanne
#music
#video
The
@LupusResearch
Alliance is receiving a donation in honor of Joanne Stefani Germanotta. Please consider a donation to this tremendous organization.
The limited-edition Phenom Lux and matching sock designed by
@selenagomez
benefits the Lupus Research Alliance. Available NOW at
@PUMA
stores and . Get yours before it's too late!
#SelenaxPuma
The Lupus Research Alliance sends an enormous thank you to Lady Gaga for her incredible support of the lupus community and wishes her luck at the Grammy's tonight!
#Joanne
@halsey
@LLSusa
Thank you
@halsey
for bravely sharing your story. ✨ Sending our support and best wishes. Congrats on the release of your new album and single, "The End.” Your message is inspiring to us all. 💜
This
#LupusAwarenessMonth
we want to thank all our champions and lupus warriors. Special thanks to
@LadyGaga
and her father, LRA board member
@germanottajoe
, who give back so much to this community and continually advocate for advancements and progress in lupus research.
1of2
Join us tomorrow 11/21 for this year’s Lupus Research Alliance
#BreakingThroughGala
live online broadcast at 7pm ET! Featuring inspiring speakers and performances, and a chance to support promising research that is breaking through. RSVP now!
LRA is pleased to award the 2022 Lupus Insight Prize to
@VirusesImmunity
, PhD for discovering the link between endogenous retroviruses and systemic lupus erythematosus. Dr. Iwasaki received the award at the 2022
@FOCISimmunology
Meeting. Read more:
That’s a wrap! What an amazing night celebrating our honorees, Peggy Dowd, Steve Burke, & Selena Gomez, and the power of
#BreakingThrough
to drive a new scientific era of pioneering innovation. Thank you again to all of our supporters!
#LupusResearchGala
Join
@selenagomez
in supporting the LRA by making a gift. When you give to our Campaign for a Cure Matching Gift Challenge, you’ll help ensure the best and brightest scientists can get the resources they need to fund investigations into new treatments and the cure for
#lupus
.
Support promising research that is breaking through the complexity of lupus to find the cure. Join us tomorrow for the LRA
#BreakingThroughGala
that will unite the entire community as one!
Happy
#WorldLupusDay
!
#JoinUs
in celebrating the lupus community, as we all come together to recognize lupus warriors throughout the world. Visit our NEW community section! You’re not alone, we are your community and are here to support you.
Thank you so much for the support and for spreading awareness
@selenagomez
! We're so thankful for you, Dr. Wallace, and the incredible lupus community. We're in this together!
Lupus nephritis (kidney disease) is one of the most serious complications of lupus. We're supporting one researcher who is building on his existing discoveries to evaluate a potential new therapeutic target for lupus nephritis. Learn more:
#WorldKidneyDay
The Lupus Research Alliance is excited to share great news about the FDA approval of anifrolumab-fnia (Saphnelo™) as a first-in-class treatment for moderate to severe systemic lupus erythematosus (SLE) in adults.
We have invested over $200 million in 500+ studies to understand lupus, improve treatments & ultimately find a cure. This month, we will bring you videos from these 3 funded researchers about how their important discoveries are transforming lupus treatment. Here’s a sneak peek.
In honor of
#WorldLupusDay
, Lupus Research Alliance President & CEO Kenneth M. Farber shares his perspective on the future of lupus treatment. Mr. Farber is incredibly optimistic because “we are breaking through!”
#Breakingthrough
#LupusAwarenessMonth
Join our Walkers and team captains as they rally for our
#ManyOneCan
Walk with Us to Cure Lupus virtual event on 9/12! This celebratory experience will unite the entire lupus community to support funding research that changes the lives of people w/
#lupus
:
To add to the excitement of the night, the
@EmpireStateBldg
is lighting up the NYC skyline in purple and red in honor of our Lupus Research 2020 Gala and the need for lupus research!
#LupusResearchAlliance2020
Adding sparkle to the night, the
@EmpireStateBldg
is lighting up the NYC skyline in purple and red in honor of Lupus Research Alliance
#BreakingThroughGala
to support lupus research!
Join us! | Pin: LRA21
💜 Today is
#WorldLupusDay
! Let’s take time today to shine a light on
#lupus
, honor every lupus champion, and celebrate all who are making a difference. We stand together! You are not alone.
#ManyOneCan
get involved:
#LupusAwarenessMonth
“Meet” our four lupus superstars in the first of a series of short films celebrating how they transcend lupus: Meredith, Marla, Genevieve & Cheryl! Stay tuned to hear their full stories throughout the month!
#LupusAwarenessMonth
Watch the full version: