Anne Zablotowicz
annezab.bsky.social
Anne Zablotowicz
@annezab.bsky.social
I'm a Forever Friend, Native Queens Girl = Mets Fan 💙🧡 (also Knicks & Jets). I am a Lupus Warrior and Advocate for the wellbeing of persons with lupus and a proud LADA Board Member.
Reposted by Anne Zablotowicz
Kudos to @zahitouma.bsky.social and the #LUPUS2025 organizers for hosting a wonderful Gala event last evening while the #LADAOrg team enjoyed the food, music and networking. #Lupus

@lupuschat.bsky.social @caringforlupus.bsky.social @annezab.bsky.social @alhkim.bsky.social
May 24, 2025 at 6:36 AM
Reposted by Anne Zablotowicz
#LADAOrg is honored to sponsor #LUPUS2025 & bring our mighty team to learn, engage, & share insights.
@lupuschat.bsky.social @caringforlupus.bsky.social @annezab.bsky.social @tiffanyandlupus.bsky.social
Kathleen Arntsen,
Dina Thachet, Kaamilah Gilyard, Whiney Carter, David Arntsen,
Autumn Austin
May 23, 2025 at 7:42 PM
Reposted by Anne Zablotowicz
The Lupus Walk webpage is live! Join us on May 17th by walking or running to benefit lupus research sponsored by @masonicresearch.bsky.social and #LADAorg while also promoting #LupusAwareness during Lupus Awareness Month.

www.mmri.edu/ways-to-give...
Lupus Walk Utica, NY | MMRI Research
Join us for the Lupus Walk, co-sponsored by MMRI & the Lupus and Allied Diseases Association, Inc. to support lupus research by MMRI.
www.mmri.edu
March 7, 2025 at 2:43 AM
Reposted by Anne Zablotowicz
Are you ready to show your support for those affected by #lupus on May 10th by sharing facts about lupus and proudly wearing your purple for #WorldLupusDay #MakeLupusVisible WorldLupusDay.org/tool-kit @lupus.org @lupuschat.bsky.social @michiganlupus.bsky.social @caringforlupus.bsky.social
April 15, 2025 at 10:27 PM
Reposted by Anne Zablotowicz
A Truly Amazing DOCTOR is hard to find
Difficult to part with
AND Impossible to Forget
Thank You Doctor Moorthy 💜🦋🥼
#LupusChat
#LupusAwareness

@lupuschat.bsky.social
@ladaorg.bsky.social
@lupusresearch.bsky.social
April 17, 2025 at 3:15 AM
Reposted by Anne Zablotowicz
Our next #LupusChat will be on Sunday, May 4 at 3PM Eastern Time! Stay tuned for our upcoming topic announcement and remember to mark your calendars to save the date!
March 23, 2025 at 7:59 PM
Reposted by Anne Zablotowicz
Lupus is often life altering, dream stealing, career ending and physically, emotionally and financially devastating, but you can have a full life by becoming educated and empowered. With only 2 days to go ‘til Lupus Awareness Month, please read and share our daily Lupus facts. @lupuschat.bsky.social
April 29, 2025 at 10:00 PM
Reposted by Anne Zablotowicz
#Lupus is a complex chronic inflammatory #autoimmune disease in which a triggering agent causes the immune system to dysregulate and attack the patient’s tissue in any organ system of the body; including the skin, joints, kidney, brain, heart, lungs, blood & blood vessel. @lupuschat.bsky.social
May 1, 2025 at 7:15 AM
Reposted by Anne Zablotowicz
A person with #lupus takes between 8 and 12 medications a day, requiring careful attention to drug interactions and unique allergies and sensitivities and a team approach. #LupusAwarenessMonth #LupusAwareness @lupuschat.bsky.social @caringforlupus.bsky.social @ghlforg.bsky.social
May 2, 2025 at 7:35 AM
Reposted by Anne Zablotowicz
#Lupus clinical research has been problematic due to the lack of basic understanding of the disease, reliable biomarkers, and uniform control groups, clinical outcome measure limitations and the heterogeneity of the patient population. #LupusAwarenessMonth #LupusAwareness @lupuschat.bsky.social
May 3, 2025 at 7:43 AM
Reposted by Anne Zablotowicz
We were thrilled to sponsor the 40th Annual Health Policy Ball to support #healthpolicy fellows. Loved networking with passionate stakeholders like #SequoiaRagland from the House Health Committee.
#HealthProm25 #patientvoice #KathleenArntsen @annezab.bsky.social
@infusionaccessfoundation.org
March 2, 2025 at 8:20 AM
Reposted by Anne Zablotowicz
The #LADAorg Board was honored to attend the @masonicresearch.bsky.social 1958 Gala to represent the #PatientVoice and support #Lupus, Autoimmune, Cardiovascular, and Autism research. Kudos to Maria Kontaridis and her staff for hosting such an amazing event! @annezab.bsky.social
April 1, 2025 at 4:37 PM
Reposted by Anne Zablotowicz
#LADAorg thanks our patient experts @annezab.bsky.social Kaamilah Gilyard and Whitney LaBar for attending #CARRA2025 to provide valuable #patient insights and interact with the amazing CARRA research community!

carrainc research community!
April 7, 2025 at 1:34 AM
Reposted by Anne Zablotowicz
#FluSeason is here, and if you have #lupus, protecting yourself from infection is essential. With a higher risk due to lupus and treatments, proactive steps like flu shots and managing exposure can help.

Learn more tips: buff.ly/41jQ9eI
Protecting yourself from infections
When you have lupus, you are at increased risk for all kinds of infections. There are two main reasons for this higher risk: lupus disease and treatments.
buff.ly
December 6, 2024 at 3:22 PM
Reposted by Anne Zablotowicz
We’re at the finish line! @speakerjohnson.bsky.social help us make history by including the #MCEDAct in the end of year package. This legislation will revolutionize #cancer detection, improve survivorship, and save lives. Cancer doesn’t wait, and neither should we. #MCED @acscan.bsky.social
December 11, 2024 at 3:41 AM
Reposted by Anne Zablotowicz
Investing in #HealthForAll means protecting people, especially the most vulnerable among us, from impoverishing health costs and financial hardship caused by illness.

It’s on the government to adopt laws and budgets that guarantee the right to health for everyone, everywhere.
December 12, 2024 at 2:44 AM
Reposted by Anne Zablotowicz
@govkathyhochul.bsky.social please prioritize passing step therapy reform & sign #A901AS1267A. NYers shouldn't have to suffer through ineffective treatments before receiving the medication they truly need. It's time to prioritize patient well-being over unreasonable cost-cutting measures.
December 12, 2024 at 9:38 PM
Reposted by Anne Zablotowicz
Patients, families and communities across NY cannot wait any longer for access to #MCED technologies. The time for Congress to act is NOW – we urge Congress to pass the #MCEDAct this year @schumer.senate.gov
#HakeemJeffers
@ghlforg.bsky.social @acscan.bsky.social @infusioncenter.bsky.social
December 12, 2024 at 9:47 PM