#APSAM26
The 3 key blood tests for diagnosing #Antiphospholipid Syndrome (#APS) include the lupus anticoagulant, anticardiolipin antibody & anti-beta2 glycoprotein I antibody tests. #Awareness is crucial for better understanding and support! Let’s keep spreading the word together!

#APSFA #WTD26 #APSAM26
April 9, 2026 at 3:05 PM
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
#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
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
#AntiphospholipidSyndrome can mimic many other conditions—like #MultipleSclerosis, #RheumatoidArthritis, or Bell’s palsy—so misdiagnosis is common. If your symptoms don’t add up, ask about #APS.

🔗 cutt.ly/how-is-aps-d...

#APSAM26 #APSMatters #RareDisease
June 29, 2026 at 5:00 AM
#AntiphospholipidSyndrome can affect your eyes—causing migraine aura (flashing lights or patterns) or, rarely, sudden vision loss in one eye due to clots. Any vision changes should be checked by your doctor.

🔗 cutt.ly/aps-and-the-...

#APSAM26 #APSMatters #APSAwarenessMonth
June 26, 2026 at 7:14 AM
Thank you for joining us for #APSAwarenessMonth! Your support helps raise the profile of APS across the UK.

What would you like to see for #APSAM27?

Stay in touch: aps-support.org.uk/get-involved...

From all at APS Support UK—thank you! #APSMatters #APSAM26
June 30, 2026 at 5:00 AM
APS is diagnosed through blood tests:

🩸 Lupus anticoagulant (LA)
🩸 Anticardiolipin
🩸 Anti-beta2-glycoprotein1

LA doesn’t mean you have lupus — it detects antiphospholipid antibodies.

🔗 cutt.ly/blood-tests

#APSAM26 #APSMatters #Diagnosis #APSAwarenessMonth
June 17, 2026 at 5:00 AM
APS often overlaps with other #autoimmune conditions. Lupus, RA, Sjögren’s & autoimmune thyroid disease are common in APS patients/family members. 30–40% of people with lupus also have antiphospholipid antibodies.

🔗 cutt.ly/related_cond...

#APSAM26 #APSMatters #APSAwarenessMonth
June 14, 2026 at 5:00 AM
APS isn’t just a clotting disorder.

As an autoimmune condition, it can cause “low-grade” but debilitating symptoms like fatigue, joint pain, migraines, memory loss & brain fog.

🔗 cutt.ly/what-are-the...

#APSAM26 #APSMatters #BrainFog #Fatigue #Autoimmune #APSAwarenessMonth
June 13, 2026 at 5:00 AM
#CatastrophicAPS is rare but life-threatening.

It causes rapid, widespread clotting in vital organs — usually triggered by infection, surgery or trauma.

It affects <1% of APS patients but has a 39% mortality rate.

🔗 cutt.ly/catastrophic...

#APSAM26 #APSMatters #APSAwarenessMonth
June 8, 2026 at 5:01 AM
🩺 Need an APS specialist?

We’ve got a UK-wide directory built from patient recommendations — covering haematology, rheumatology, neurology & obstetrics.

🔗 cutt.ly/specialists-...

#APSAM26 #APSMatters #RareDisease #APSAwarenessMonth
June 22, 2026 at 5:00 AM
Women with APS are 5x more likely to suffer stillbirth.

With the right treatment & monitoring, many can have successful pregnancies — early diagnosis is key.

🔗 cutt.ly/aps-and-preg...

#APSAM26 #APSMatters #PregnancyLoss #ReproductiveHealth #APSAwarenessMonth
June 15, 2026 at 5:00 AM
#APS is the most common treatable cause of recurrent miscarriage. Yet UK testing for #antiphospholipid antibodies usually only happens after 3 miscarriages.
We believe earlier testing could save lives.

🔗 cutt.ly/aps-and-preg...

#APSAM26 #APSMatters #MiscarriageAwareness
June 5, 2026 at 5:10 AM
A new #APS diagnosis can feel overwhelming, but you’re not alone.

Learn more and connect with support groups & others who understand: aps-support.org.uk/self-help/ne...

#APSMatters #APSAM26 #RareDisease #APSAwarenessMonth #NewlyDiagnosed
June 27, 2026 at 5:00 AM
🥱 Fatigue affects many people with APS. It can fluctuate between good and bad days, but managing fatigue helps improve daily life.

🔗 cutt.ly/coping-with-...

#APSAM26 #APSMatters #Fatigue #AutoimmuneDisease #APSAwarenessMonth
June 24, 2026 at 5:00 AM
#APS can affect the heart valves too. ~30% of patients develop #HeartValveDisease, causing fatigue, breathlessness & fainting. In severe cases, it can lead to heart failure or surgery. Early monitoring is vital.

🔗 cutt.ly/aps-and-the-...

#APSAM26 #APSMatters #APSAwarenessMonth
June 18, 2026 at 5:00 AM
APS affects men too.

For every 7 women, 2 men are diagnosed — often after serious events like stroke or heart attack. Early testing is key.

🔗 cutt.ly/how-common-i...

#APSAM26 #APSMatters #RareDisease #APSAwarenessMonth
June 16, 2026 at 4:45 AM
Is #APS hereditary? Right now, there’s no single gene for APS, but some families are affected. More research is underway to find out if there’s a genetic link.

🔗 cutt.ly/aps-faqs

#APSAM26 #APSMatters #APSAwarenessMonth
June 28, 2026 at 5:00 AM
What causes APS? We’re still working it out.

It’s linked to immune system overactivity, possibly triggered by genes, infections, hormones or medication — but research is ongoing.

🔗 cutt.ly/what-causes-it

#APSAM26 #APSMatters #Autoimmune #RareDisease #APSAwarenessMonth
June 7, 2026 at 5:00 AM
APS can affect the kidneys — sometimes it’s the only sign.

Clots may cause high blood pressure or back/abdominal pain. Early detection is crucial.

🔗 cutt.ly/aps-and-the-...

#APSAM26 #APSMatters #KidneyHealth #AutoimmuneDisease #RareDisease #APSAwarenessMonth
June 23, 2026 at 5:00 AM
APS can cause more than miscarriage.

It’s also linked to pre-eclampsia and low birth weight.
Careful monitoring in pregnancy is vital for those with APS.

🔗 cutt.ly/aps-and-preg...

#APSAM26 #APSMatters #PregnancyHealth #HighRiskPregnancy #APSAwarenessMonth
June 20, 2026 at 5:00 AM
Some #APS cases don’t meet full criteria.

🩸 #Seronegative APS = symptoms, no antibodies
🧠 #NonCriteria APS = antibodies, no clots

Rare but real — and still being researched.

🔗 cutt.ly/non-criteria...

#APSAM26 #APSMatters #APSResearch #AntiphospholipidSyndrome
June 19, 2026 at 5:00 AM
APS was first defined in the 1980s—but signs go back centuries. Queen Anne’s repeated pregnancy losses may mirror #APS. Today, we know aPL antibodies can cause serious clotting & obstetric issues. A long road to recognition.

🔗 cutt.ly/blood-tests

#APSAM26 #APSMatters
June 21, 2026 at 5:00 AM