Top Tweets for #apsawareness
🌍🩸 World APS Day
🩷 Awareness saves lives. Today we stand with everyone affected by Antiphospholipid Syndrome (APS), supporting awareness, research, and hope for a healthier future. Together, we are stronger. 🤝🌎✨
#WorldAPSDay #Support #APSAwareness #Sağlık #AntiphospholipidSyndrome #HealthAwareness #GlobalHealth #Araştırma #MedicalResearch #RareDisease #Hope #DünyaAPSGünü #Farkındalık #BirlikteGüçlüyüz 🩸💜🌎🤝
189 days without treatment
Waiting in the dark for my weekly INR blood test
I could have gotten treatment many months ago, living my life, but unfortunately I live in #Sweden
#CSFleak #InfratentorialSuperficialSiderosis #APSAwareness #livingwithss
📰 Our Autumn 2025 Newsletter is out now! 🍂 Packed with #APS related updates, involvement opportunities & charity news.
Not subscribed yet?
👉 Join APS Support UK: https://t.co/VEifcZKKG1
👉 Free e-news sign up: https://t.co/6cX2QRQ3Ef
#APSSupportUK #APSawareness #APSNewsletter
Tammy Talon had two strokes before 45. The cause? #AntiphospholipidSyndrome.
⚠️ Her early warning signs were easy to ignore. Now she’s sharing her story to raise awareness.
🔗 Learn more: https://t.co/1cwSsaxweP
#APSAwareness #Stroke #Autoimmune #Thrombosis #InvisibleIllness
Today is #WorldSjögrensDay 💜
Many with #APS also live with Sjögren’s – an autoimmune condition causing dry eyes, dry mouth, fatigue & joint pain.
We stand with everyone navigating both.
🔗 https://t.co/dCYGlNYBNh
🔗 https://t.co/W1OZz24fvO
#Sjögrens #APSawareness #Autoimmune
Today is #WorldSjögrensDay
A message from our Chair:
"Let’s make a difference however we can. Tell someone how it really feels, share what this disease means to you."
What are you proud of today?
Share your moment with #ProudWithSjögrens & tag us so we can celebrate with you!
Did you know there was such a thing? Do you get them?
Today, we bring you the symptoms of an #APS Flare!
For those who have #Lupus, you'll notice that these are very similar to a Lupus #flare.
#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA
globally to bring awareness to APS!
#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #WTD25 #raredisease #charity #donate #sle
preventing dangerous clots — but they must be taken carefully to avoid serious bleeding. Knowing the risks helps you stay safe and prepared.
#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #WTD25 #raredisease #charity
Kerri & her sister have completed the 96-mile West Highland Way in support of a friend with #AntiphospholipidSyndrome, raising awareness of this rare clotting disorder. They've raised £410 so far. Support their journey: https://t.co/oOLmqVjSC9
#APS #RareDisease #APSawareness
June is #APSAwareness Month! Check out the latest APS Program Update, featuring our investigators in a special article with @APSFA, add'l news & achievements, a patient's story about living with APS & What I’m Reading in APS Research by Dr. Ajay Tambralli.
https://t.co/A5JiP4u3Zt
donate: https://t.co/JfyAUdmkoo
We also have a button on our Facebook page that you can use.
#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #WTD25 #raredisease #charity #donate
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 #GoBurgundy #APSMatters #APSFA
stillbirth. It is also associated with other complications such as pre-eclampsia, low birth weight babies, and premature births.
Join our friends around the world in raising awareness of antiphospholipid syndrome.
#APSAwareness #apsawarenessmonth #collaboration #teamwork
We thank you for supporting us for 20 wonderful years!
#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #twentyyearanniversary
not alone. We offer a closed support group here on Facebook.
The link is https://t.co/Xbanro27nw Please join us for your support needs!!
#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #support #mentalhealth
from clots in the brain or optic nerve.
Find out more here about APS & the eyes: https://t.co/K7bFoLu4S6
#AntiphospholipidSyndrome #APSAwareness #GoBurgundy #APSMatters #APSFA #apsawarenessmonth #apsresearch #visualloss #eyes #MigraineAwareness
Migraines! UGH! Who gets them?? Raise your hand! 🙋
Yep...us too! #Migraines are a common feature of #APS.
How do you cope with them? Any pointers or tips you'd like to share?
#AntiphospholipidSyndrome #APSAwareness #APSMatters #apsawarenessmonth #headache #MigraineRelief
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 is APS Awareness Month: June is #APS AWARENESS MONTH!!! We will bring you graphics each day of the month to help educate & raise awareness about #antiphospholipid syndrome, its symptoms, and related issues.
#AntiphospholipidSyndrome #APSAwareness #APSMatters #apsawareness
📢 We’re looking for APS patient stories to feature during #APSAwarenessMonth in June.
Want to share your journey? Email us at [email protected] – and feel free to include a photo if you're happy to. 💜
#APS #APSAwareness #PatientVoices #APSAM25
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