#APSMatters
2️⃣ Second session "Beyond the clot: challenges in obstetric antiphospholipid syndrome", chaired by Nathalie Costedoat-Chalumeau and Karoline Mayer-Pickel!
#RheumaPreg25 #APS #APSmatters #oAPS
May 9, 2025 at 10:38 AM
June 13, 2025 at 12:52 PM
June 12, 2025 at 10:43 AM
June 9, 2025 at 10:24 AM
Today is #WorldAPSDay! 🩸

Join us in raising awareness of antiphospholipid syndrome and the people living with it every day.

💬 Share your story using:
#WorldAPSDay #APSAM26 #APSMatters #APSAwarenessMonth

🔗 Sign up for updates: cutt.ly/enews
June 9, 2026 at 5:00 AM
Raise your hand if you will raise money for the APSFA in June.

Fifty percent (50%) of the money raised goes towards research! 

#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #WTD26 #raredisease #charity #donate #APS #APSAM26
May 31, 2026 at 5:03 PM
Raise Your Hand: Raise your hand if you will raise money for the APSFA in June. Fifty percent (50%) of the money raised goes towards research!

#APS #AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters
#apsresearch #apsawarenessmonth #antiphospholipidsyndrome #APS
May 31, 2025 at 11:41 PM
during pregnancy and plan your pregnancy ahead of time.

Any words of wisdom to share, ladies?

#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #WTD25 #raredisease #charity #donate #APS
June 11, 2025 at 8:48 PM
the stage is yours....... Please, also share in the comments below.

We may even publish yours in our #newsletter.

#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #storytime #apsawarenessmonth #apsresearch #WTD25 #personalstory #mystory
June 10, 2025 at 12:25 PM
Clinical Features of APS: APS Awareness Month - Day 1:

Today we bring you the clinical features of #APS. Have you experienced any of the symptoms listed?

#GoBurgundy #APSMatters #apsresearch #APSFA #antiphospholipidsyndrome #apsawarenessmonth
June 1, 2025 at 6:09 PM
#APSAwarenessMonth is here! 🩸
Join us throughout June as we share daily facts, stories & insights about #AntiphospholipidSyndrome — a rare autoimmune clotting disorder.
Follow, share & help raise awareness.
🔗 aps-support.org.uk
#APSAM26 #APSMatters #RareDisease #Autoimmune
June 1, 2026 at 12:10 PM
There are some #statistics you can say out loud. How rare is #APS? Not so rare anymore. It really was misdiagnosed & underdiagnosed.

However, there is now the problem of overdiagnosing.

#AntiphospholipidSyndrome #APSAwareness #APSMatters #APSFA #apsawareness #apsresearch
June 2, 2025 at 6:50 PM
Learn More
Visit apsfa.org for trusted information, patient resources, and ways to connect with others who understand.

#WTD25 #raredisease #charity #donate #newdiagnosis #newlydiagnosed #AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch
APS Foundation of America, Inc. | Antiphospholipid Syndrome - APS
apsfa.org
June 29, 2025 at 1:45 PM
If you're diagnosed with Antiphospholipid Syndrome (APS), it's essential to take all possible steps to reduce your risk of developing blood clots.

What other ideas do you have to add to this list?

#AntiphospholipidSyndrome #APSAwareness #APSMatters #APSFA #apsawarenessmonth #mentalhealth
June 13, 2025 at 6:38 PM
How is APS Diagnosed? APS Awareness Month - Day 2:

Three blood tests are used to diagnose #APS.

Do you know what they are? You do now! How many do you have?

#APS #AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawareness #apsawarenessmonth
June 2, 2025 at 1:35 PM
APS can’t be cured, but it can be treated.
Most patients manage #APS with anticoagulants or antiplatelet meds like aspirin, warfarin, or heparin. Rivaroxaban may be an option for some.
🔗 cutt.ly/how-is-it-tr...
#APSAM25 #APSMatters #RareDisease #APSAwarenessMonth #Thrombosis
June 4, 2026 at 10:37 AM