It’s the last day of #LupusAwarenessMonth
Please spread the word to help improve the lives of patients
You can also grab a copy of our book explaining how lupus develops in the body in an interpretable and accessible way: The Zombie Invasion
All profits go to lupus charities
amzn.eu/d/5qdGIOe
Today marks the final day of #LupusAwarenessMonth
Thank you to everyone who took part, whether by learning about #lupus, fundraising, resharing content or showing support, your involvement has made a real difference. 💜
As we near the end of #LupusAwarenessMonth, I hope this video with @royalfreecharity.org helps highlight why research is so important to help improve the lives of patients, particularly those with younger onset disease. Thank you for this support and please raise awareness!
youtu.be/bXHFWIwRWE0?...
For Lupus Awareness Month, we’re spotlighting George Robinson’s work on personalised therapies for lupus - research funded by your support. He’s studying treatments that could reduce symptoms.
Watch the full interview via the link in our bio.
#LupusAwarenessMonth #Research #NHS
#weekend ready ✌🏾🙏🏾 #London #indoor #outdoor #autumn #active www.gelliottservices.com Lupusfit™️ #freelance #mind #body #yoga #fitness #health #wellbeing #muscle #tone #strength #stretch #heart #exercise #goals #Motivation General & #Lupus #raynauds #CKD #advocate #awareness #LupusAwarenessMonth ✋🏿🐺💜
Did you know that 35% of people with #lupus report symptoms of hairloss?
For more information on symptoms of lupus, visit www.lupusuk.org.uk/the-symptoms/
Do you experience hairloss?
#LupusAwarenessMonth #KnowLupus #MakeLupusVisible #SLE #Hairloss
Please consider giving what you can this #LupusAwarenessMonth and donate to our JustGiving page, or make a donation through our website.
We are grateful for your support! 🫶
JustGiving: http://bit.ly/4ok2yHR
Online Donation Form:
Did you know that 50% of people with #lupus report symptoms of headaches or migraines?
For more information on symptoms of lupus, visit www.lupusuk.org.uk/the-symptoms/
Do you experience headaches or migraines?
#LupusAwarenessMonth #KnowLupus #MakeLupusVisible #SLE
#Headaches #Migraines
Catherine Sutherland at her desk working.
Lupus is a complex autoimmune condition that affects thousands of people globally 🌍
This #LupusAwarenessMonth, learn how our scientists are advancing understanding through genetics and immune research 🧬
sangerinstitute.blog/2025/10/07/five-question...
Did you know that 77% of people with #lupus report symptoms of joint pain?
For more information on the symptoms of lupus, visit www.lupusuk.org.uk/the-symptoms/
Do you experience joint pain?
#LupusAwarenessMonth #KnowLupus #JointPain #Autoimmune #SLE #LupusUK
It's Lupus Awareness Month! A case study highlights the risks faced by those with lupus. Read more in the Open Access journal ACMI: doi.org/10.1099/acmi... #AccessMicro #LupusAwarenessMonth
We’re proud to share our official #LupusAwarenessMonth poster for 2025! 🎉
Lupus can affect anyone regardless of age, gender, or ethnicity. However, it disproportionately impacts women and people of African, Caribbean, and Asian heritage.
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October is Lupus Awareness Month in the UK, which plays a crucial role in increasing knowledge & awareness of lupus.💜
Help us raise awareness by ordering free awareness supplies here: http://bit.ly/4nludI6 🔗
#LupusAwarenessMonth #LupusUK #LupusAwareness #Autoimmune #ChronicIllness
In a meaningful moment for Institute policy fellow Roshawn Neal, Rep Summers and other members of the Black Legislative Caucus passed a resolution designating May as #LupusAwarenessMonth, bringing light to the experiences of those with chronic conditions & bringing hope to a new advocate.
🎗️ Lupus may be invisible—but your voice is not.
Let’s lift every voice and empower every story each month.
👉 Start here: info.nmqf.org/beyond-lupus
#BeyondLupus #LupusAwarenessMonth #LupusWarrior #LiftEveryVoice #HealthEquity #ChronicIllnessAwareness #WomensHealth
Thank you for ending #LupusAwarenessMonth with us by making our Lansing Walk for Lupus a success! Thank you to all participants, volunteers, supporters & our event sponsors. We raised critical awareness of #lupus & strengthened the sense of community & hope for those living with the disease. 💜
Join us in 30 minutes, Facebook Live with me and
@LupusMore
LINK: facebook.com/morethanlupus
We will end #lupusawarenessmonth by my proclaiming the monumental leaps forward in treating lupus
#SLE #lupus
We will also have a live Q and A
We’re grateful to our corporate partners for standing with us this #LupusAwarenessMonth and beyond. 💜 Your support helps power research, education, and support for people with #lupus.
If you have a company that wants to get involved, learn more here: buff.ly/KsQKuWV
Today's Mantra I AM growing into a more loving, empowered, abundant and liberated version of myself. Person meditating in Burmese position on colored grass assumingly representing chakra awakening - yellow/orange (sacral and solar plexus chakras) and purple (crown or third eye chakra).
Day 84.
#LupusAwarenessMonth
As #LupusAwarenessMonth comes to a close, our commitment to raising awareness continues! 💜 A huge thank you to all the #lupus warriors, families, friends, and supporters who helped make lupus visible this month. Your voices, advocacy, and support make a difference every day.
We're closing out #LupusAwarenessMonth w/our final 2025 #GameOntoEndLupus livestream, playing the winning pair from our fundraising poll (Ducktales+Rescue Rangers on the #NES) + other games by request. Head over to twitch.tv/2uptogether for family retro game night in support of @lupusorg! #gotel2025
💜 Lupus Awareness Month | Representation. Trust. Access.
🩺 Learn how SHC is driving equitable lupus care through data, resources, and provider training:
🔗 shcdrive.org/lupus-module/
#LupusAwarenessMonth #SHCDrive #BeyondLupus #HealthEquity #ClinicalTrials #RepresentationMatters #NMQF
May is #LupusAwarenessMonth! Meet Dennisse Bonilla, Clinical Research Manager, #Lupus Program @schroeder-uhn.bsky.social. "I am deeply inspired by our patients, whose resilience and strength in facing daily challenges fuel my commitment to finding innovative solutions that enhance their well-being."
Join us tomorrow with More Than Lupus: Live Facebook event to celebrate better care for #SLE #lupus #lupusawarenessmonth
www.facebook.com/morethanlupu...
Today's Mantra I see through fear and past illusion to the divine power that lives within me. I AM remembering. Person meditating in Burmese position on colored grass assumingly representing chakra awakening - yellow/orange (sacral and solar plexus chakras) and purple (crown or third eye chakra).
Day 83.
#LupusAwarenessMonth
#FactFriday 💜 Diagnosing #lupus is like piecing together a puzzle. Symptoms, lab tests, medical and family history all play a role. That’s what makes awareness so important.
🔗 During #LupusAwarenessMonth, learn how lupus is diagnosed: buff.ly/ohy5eql
#Lupus is considered a disease of unmet medical need because of the lack of efficient diagnostic tools, effective therapies, and well-designed clinical trials. #LupusAwarenessMonth #LupusAwareness
#Lupus is considered a disease of unmet medical need because of the lack of efficient diagnostic tools, effective therapies, and well-designed clinical trials.
#LupusAwarenessMonth #LupusAwareness
@lupuschat.bsky.social @caringforlupus.bsky.social @michiganlupus.bsky.social @ghlforg.bsky.social
A fat light skinned feminine person with glasses wearing noise cancelling headphones. They are wearing light blue shorts, beige compression stockings and a red, white and blue sleeveless top. They are also in a disability shopping cart
It's Lupus awareness month day 29
Lupus fact of the day
Over 1.5 million folks suffer from Lupus. I am one of these folks.
Here's A picture of me from memorial Day 2 years ago.
#lupusawarenessmonth #lupusfactoftheday
Today's Mantra I AM trusting my journey. Person meditating in Burmese position on colored grass assumingly representing chakra awakening - yellow/orange (sacral and solar plexus chakras) and purple (crown or third eye chakra).
Day 82.
#LupusAwarenessMonth
Lupus and vertigo - is there a connection? v1st.co/lupus to read a free blog on autoimmune vertigo. Let's support our patients with autoimmune issues, to reduce dizziness and imbalance related to vestibular issues this month and all year round! #lupusawarenessmonth #vestibularrehabilitation #bppv