#antiphospholipidsyndrome
#AntiphospholipidSyndrome (APS) in orthopaedic foot & ankle surgery. Findings suggest higher post-op clot risk for #APS vs matched controls, including higher #DVT at 90 days even with prophylaxis, and higher PE at 90 days without prophylaxis: journals.sagepub.com/doi/10.1177/...
February 17, 2026 at 3:57 PM
A light bump, pinch or punch can add a new bruise to the endless collection. I’m often surprised to find a new one hidden somewhere on my body"
🔗
www.achronicvoice.com/2021/07/14/b...

Via @achronicvoice.com

#AntiphospholipidSyndrome #PulmonaryEmbolism #ChronicPain #APS #MedTwitter
12 Visible Evidence of a Body Gone Rogue (Is Invisible Illness Truly Invisible?)
Here is some visible evidence of invisible illness — photos, signs and symptoms from my personal life with chronic illness.
www.achronicvoice.com
February 13, 2026 at 5:48 PM
Maja was just 16 when she developed blood clots (DVT & PE). After tests, she was diagnosed with May-Thurner syndrome and triple-positive #AntiphospholipidSyndrome. She’s sharing her story to help others. Read more: www.stoptheclot.org/patient-stor... @stoptheclot.bsky.social #APS #PatientStory
February 13, 2026 at 2:08 PM
"This is a common conundrum for those with #AntiphospholipidSyndrome, as so many beneficial foods need to be moderated due to #warfarin intake.": buff.ly/7Z0bOOn

#ChronicallyIll #spoonies #ChronicIllness
February 11, 2026 at 9:30 PM
New 2025 review highlights why early recognition of #AntiphospholipidSyndrome matters—incl. appropriate antibody testing (and repeat testing) and risks of delayed diagnosis. Encouraging to see wider clinician training: cutt.ly/RtnlpBl2 #APSresearch #Awareness #APS
February 10, 2026 at 6:56 PM
"The #emergency doctors at #TanTockSengHospital tried for more than 4 hours to transfer me to #SingaporeGeneralHospital for proper care, but they refused to accept me, citing that I was ‘unstable’.": buff.ly/zegXbCO

#healthcare #AntiphospholipidSyndrome #MondayBlogs #NEisVoid #singapore
February 9, 2026 at 7:30 AM
New review on obstetric APS (OAPS): why it happens, how risk may be better predicted, and therapies being explored for refractory cases (beyond aspirin + heparin), including HCQ, IVIG, statins & biologics. Read: cutt.ly/ztbgDgHY #AntiphospholipidSyndrome #APS #OAPS #PregnancyResearch #MaternalHealth
February 5, 2026 at 7:10 PM
"We invite u to attend this symposium, featuring leading #Hemostasis experts—Dr. Steven Pipe & Prof Katrien Devreese, along with 2 patient #advocates." — I am excited to be a speaker for #Werfen! Sign up to watch 🙂 buff.ly/vtjPjQI

#AntiphospholipidSyndrome #MedSky #ChronicIllness #rheumatology
Webinar: Shared Journeys in Hemostasis: Connecting Patient Voices with Hot Topics in the Hemostasis Laboratory | Werfen North America
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buff.ly
February 2, 2026 at 8:30 PM
Jagoda’s APS story is live 💛 Postpartum clots, loss, hope, and her rainbow baby. “It’s important to be proactive—if you see/feel something, don’t hesitate to get checked!” Read: cutt.ly/patient-stories #APS #AntiphospholipidSyndrome #PatientStory
February 2, 2026 at 6:35 PM
"I truly wish that I were seeing a #gynecologist for pregnancy reasons, but unfortunately, it’s because I’ve had two deadly #OvarianCyst ruptures, no thanks to the #medications I take for #AntiphospholipidSyndrome.": buff.ly/XCRWjd7

#MondayBlogs
February 1, 2026 at 9:30 PM
February 1, 2026 at 8:08 PM
"People do get surgeries done immediately to remove such massive #BloodClots, but because I was on #warfarin & have #AntiphospholipidSyndrome, no #surgery is ever straightforward..they put me in the high dependency ward..to 'see how it goes'.": buff.ly/Sqd3BIC

#MondayBlogs #BloodDisorder #spoonie
January 26, 2026 at 9:30 PM
Last week we shared Louise Rogers’ fundraiser — and Louise has now kindly shared her patient story too. 💙
“Unfortunately, the ‘highly unlikely’ was reality.”
Read Lou’s story: cutt.ly/patient-stories
#APS #AntiphospholipidSyndrome #PatientStory #RareDiseaseAwareness #BloodClotAwareness
January 26, 2026 at 7:17 PM
" #Researchers are still trying to understand the full role of β2GPI as well as #AntiphospholipidSyndrome. So whilst these #therapeutics sound exciting, it will probably still be many years before we see them in practice.": buff.ly/r5TlLCA

#MedSky #ChronicIllness
January 23, 2026 at 9:30 PM
#CaseReport: ischaemic stroke in a 34-year-old with no conventional vascular risk factors. Work-up found persistent antiphospholipid antibodies and a new HIV diagnosis. Authors highlight the value of broad aetiology work-up in young #Stroke patients: cutt.ly/EtzPWWrH #AntiphospholipidSyndrome #APS
January 22, 2026 at 9:14 PM
🏃‍♀️🏃‍♂️ Saucony LDN 10K 2026 (12 July) — we’ve got 7 charity places left for #TeamAPS Support UK!
Run/jog/walk, get fundraising support + an APS running vest 💙

Email: info@aps-support.org.uk

#London10k #LDN10K #CharityRun #APSSupportUK #APS #AntiphospholipidSyndrome #RunForCharity
January 20, 2026 at 6:31 PM
New research on non-criteria obstetric #APS suggests higher-risk aPL antibody profiles (type/level/combinations) are associated with a higher likelihood of pregnancy complications. Worth a read for clinicians & the APS community: link.springer.com/article/10.1... #AntiphospholipidSyndrome
January 20, 2026 at 6:28 PM
"As with any #AutoimmuneDisease, #genetics have a complex interplay in #AntiphospholipidSyndrome, where factors such as environment, trauma and comorbidities also need to be accounted for.": buff.ly/7Z0bOOn

#ChronicIllness #MondayBlogs
January 19, 2026 at 9:30 PM
“The Rise of “Tetra-Positivity”: #Patients positive for LAC, aCL, anti-β2GPI, and aPS/PT (anti-phosphatidylserine/ #prothrombin) represent a distinct, high-risk phenotype with persistent #antibody profiles.”: buff.ly/QkaHQA7

from hemostasistoday #AntiphospholipidSyndrome #MedSky
Danny Hsu and Nicola Pozzi on "Tetra-Positive" APS - Hemostasis Today
Danny Hsu and Nicola Pozzi on "Tetra-Positive" APS
buff.ly
January 18, 2026 at 4:30 PM
"I suffer from a number of #ChronicIllnesses whose names sound like tongue twisters. #AntiphospholipidSyndrome. Systemic #Lupus Erythomatosus. #SjögrensDisease. Paroxysmal Supraventricular Tachycardia... #epilepsy is the easiest, except that it isn’t.": buff.ly/yw0HHFX
January 17, 2026 at 9:30 PM
Cheering on Louise Rogers as she takes on #DogJog for APS Support UK 🐾💙 After her DVT diagnosis, she’s fundraising to support people affected by #AntiphospholipidSyndrome. Please donate/share: www.justgiving.com/page/louise-... #APS #TeamAPS #APSSupportUK
January 16, 2026 at 1:48 PM
"Soon, #clinical, #biochemical & structural evidence could provide a rationale for measuring #antiprothrombin #antibodies with the aPS/PT test or other tests we are developing for all suspected [ #AntiphospholipidSyndrome ] patients & other disorders.": buff.ly/cly1nuu

via @jthjournal.bsky.social
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January 14, 2026 at 9:30 AM
" #Hematoma [due to #AntiphospholipidSyndrome & #warfarin ] didn’t only make my #knees look more distorted physically, but all that internal pressure was painful..felt like my knees were oranges about to burst with their juices, but not in an appetising way.": buff.ly/lpavCiX

#ChronicPain
January 14, 2026 at 7:30 AM
"A light bump, pinch or punch can add a new bruise to the endless collection. I’m often surprised to find a new one hidden somewhere on my body"
🔗
www.achronicvoice.com/2021/07/14/b...

#AntiphospholipidSyndrome #PulmonaryEmbolism #ChronicPain #APS

Via @AChronicVoice
12 Visible Evidence of a Body Gone Rogue (Is Invisible Illness Truly Invisible?)
Here is some visible evidence of invisible illness — photos, signs and symptoms from my personal life with chronic illness.
www.achronicvoice.com
January 13, 2026 at 3:25 AM