Lupus Foundation of America
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lupus.org
Lupus Foundation of America
@lupus.org
Lupus Foundation of America is the only national force devoted to solving the mystery of lupus while giving support to those who suffer from its brutal impact. 💜
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Have you ever thought of joining a support group? They offer a place to build community in an understanding environment where people with #lupus come together to share & help each other. Find out more about our support group network: buff.ly/LTFhDUC
🚨 Medicare Part D Open Enrollment Ends Soon! This year, new benefits include a $2,100 out-of-pocket and the Medicare Prescription Payment Plan (MPPP) for monthly installment options.

Read our Open Enrollment Guides and make your selections before 12/7: buff.ly/t24oPL9
November 26, 2025 at 8:00 PM
Through LFA’s Gina M. Finzi Fellowship, Dr. Carlucci deepened his interest in #lupus and found his path to rheumatology.

LFA grants support researchers across basic, translational, & clinical studies — supporting breakthroughs. Apply today: buff.ly/oU1OM5R

#Medsky #Rheumsky #LupusResearch
November 26, 2025 at 6:01 PM
For #NativeAmericanHeritageMonth, we’re highlighting the experiences of Native American communities affected by #lupus.

💜 This playlist shares insights on how lupus shows up in Native American communities, barriers to care and the need for support: buff.ly/tCRxzFY
November 25, 2025 at 8:30 PM
#GivingTuesday is just a week away, and your gift can go twice as far. 💜 When you donate by 12/2, every dollar will be matched—supporting research, resources, caregivers, & community programs for people with #lupus.

Give today & double your impact: buff.ly/hqJKDau
November 25, 2025 at 1:00 PM
Navigating health insurance can be overwhelming for caregivers, but understanding your loved one’s coverage can make a difference. 💜 Knowing what services and networks are included helps you plan ahead.

Learn tips here: buff.ly/I06CY5p

#NationalFamilyCaregiverMonth
November 24, 2025 at 1:00 PM
Great news! Lupus Science & Medicine’s 2024 Journal Impact Factor has risen to 4.0 (up from 3.5), ranking #14 of 58 rheumatology journals. A strong reflection of the progress and impact of lupus research worldwide.

Read the latest studies: buff.ly/1LAkQYq
November 23, 2025 at 2:00 PM
We want to hear from you! 💜 How has LFA community made a difference in your life?

Share your feedback, a quick quote or reflection & help other #lupus warriors discover programs, resources & support that make a difference: buff.ly/rKuaUcB

#LupusAwareness #LupusWarrior
November 21, 2025 at 9:03 PM
ICYMI: New research has found that Epstein-Barr Virus may be a trigger in the development of #SLE.

Read more here: buff.ly/BafdloI
New study finds link between Epstein-Barr virus and the development of Systemic Lupus Erythematosus
A new groundbreaking study has recently identified the link between the long-standing mystery in autoimmune disease: Epstein-Barr Virus (EBV) and how it contributes towards the development of…
www.lupus.org
November 20, 2025 at 8:07 PM
For #WorldChildrensDay, we’re sharing snapshots of Amélie’s journey to shine a light on children with #lupus. She faced a new diagnosis—but with her family and care team, she pushed through. Her story reminds us to recognize the signs and support kids facing this disease.
November 20, 2025 at 1:00 PM
We're excited to announce the Be Fierce. Take Control. Mini Grant Program to raise #lupus awareness among Black/African American and Hispanic/Latina women ages 18-25.

HBCU and HSI faculty, staff, students, and organizations can apply by December 31, 2025: buff.ly/UOqFM2i
November 19, 2025 at 9:00 PM
Now that the government has reopened, Congress must finalize the Fiscal Year 2026 budget & increase funding for #lupus programs. Without a full-year budget, critical lupus programs could be cut or eliminated.

Take action today: buff.ly/pBkubQV

#LupusAdvocacy
November 19, 2025 at 6:27 PM
On this #InternationalMensDay, we’re raising awareness of the men who face #lupus—often quietly. 💜 Meet Paul, diagnosed at 45. He finds comfort in the same infusion chair each visit, passing time with conversation or Netflix.

👉 Learn about lupus in men: buff.ly/PJWKhw5
November 19, 2025 at 1:01 PM
Thank you to all the #lupus warriors, families, friends, and partners who joined us for this year’s #WalktoEndLupusNow.

Check out some of our favorite moments from this year’s walks, and let’s keep moving forward, together.
November 18, 2025 at 9:30 PM
Thank you to all the incredible streamers and their communities who joined #TwitchTogetherForGood in support of LFA! 💜 Your dedication helps raise awareness and supports #lupusresearch. 🎮 #GameOntoEndLupus 2026 is just around the corner! Stay tuned for details!
November 18, 2025 at 5:02 PM
🚨 A $50,000 Matching Gift for #GivingTuesday is available early! Donate early for Giving Tuesday and help fuel research, expand support, and bring hope. Every donation is doubled to reach twice as many families.

💜 Make your matched gift: buff.ly/QyDcKCr
November 18, 2025 at 1:01 PM
Today, #TwitchTogetherForGood kicks off! Tune in as content creators go live to support causes they’re passionate about, including the Lupus Foundation of America. Join in 11/17-12/2 to make a difference and help end #lupus! 💜 🎮
November 17, 2025 at 5:04 PM
#Lupus affects Native American and Alaska Native communities at higher rates than other ethnic groups. 💜 Our new fact sheet highlights information to help raise awareness & support early detection.

Download the fact sheet: buff.ly/4uCsWao

#NativeAmericanHeritageMonth
November 16, 2025 at 2:02 PM
If your company has an employee matching gift program, you can maximize your support for the #lupus community throughout the year by doubling or even tripling your next donation to the Lupus Foundation of America!

Visit our site to learn if your company has a similar program: buff.ly/ZmANjOI
November 15, 2025 at 2:01 PM
Early detection matters in #lupus. 💜 This #NativeAmericanHeritageMonth, learn the symptoms and retweet this to raise awareness.

American Indians and Alaska Natives face higher lupus rates than other ethnic groups—talk to a doctor if you notice signs.
November 14, 2025 at 9:17 PM
November is #NationalHospiceandPalliativeCareMonth 💜 — raising awareness of the care and support available to people living with #lupus.

Discover the types of palliative care that can support you: buff.ly/bvtOCU7

💜 Repost this graphic to raise awareness!
November 14, 2025 at 1:01 PM
💜 Join #lupus warriors nationwide for the 2026 National Lupus Advocacy Summit, April 19–21! Help advance the fight on Capitol Hill, increase research funding, and improve access to care.

✨ Save the date and learn more about the event: buff.ly/CjCpiYW

#LupusAdvocacy
November 13, 2025 at 4:02 PM
The Lupus Foundation of America’s 2026 grant opportunities help researchers at every stage of their careers—advancing basic, translational, & clinical research & fostering mentorship & discovery in #lupus.

Apply now & shape the future of #lupusresearch: buff.ly/7NP6P0d

#Medsky #Rheumsky
November 11, 2025 at 6:02 PM
This #VeteransDay, we’re spotlighting #lupus warriors and Army veterans Sharlinda and Tameka, who turned their experiences into purpose by launching the Military Lupus Support Group. 💜

Their strength shows the power of unity, read their inspiring stories: buff.ly/ijvtzq7
November 11, 2025 at 1:01 PM
Looking to make an impact this holiday season? Host your own charity stream! 🎮 #TwitchTogetherForGood kicks off 11/17-12/2, with an amazing team of content creators streaming in support of the Lupus Foundation of America.

💜 Learn how to get involved: buff.ly/c2tylyb
November 10, 2025 at 8:00 PM
Caring for someone with #lupus takes strength, empathy and balance. 💜 From offering support and helping with daily tasks to managing stress and finding time to rest.

Learn how to care for your loved one and yourself: buff.ly/Di0CDvy

#NationalFamilyCaregiversMonth
November 10, 2025 at 1:01 PM