Top Tweets for #APSAM22
The cause of #APS is not yet known. We know that it stems from an over-activity of the #immunesystem that may be triggered by genes, infections, medication or hormones.
Much research is still needed.
Find out more: https://t.co/XRqBzZ6BCg
#APSMatters #APSAM22
#APSAwarenessMonth
Thank you for reading and sharing our Awareness Month posts! Keep in touch with our latest news here: https://t.co/TPfJB0f5u8 or become a Friend of the Charity here: https://t.co/N6F1OLSBOt
Thank you from everyone at APS Support UK.
#APSMatters #APSAM22 #APSAwarenessMonth
As #APS can present with so many symptoms, people can sometimes initially be misdiagnosed. Common misdiagnoses can include #multiplesclerosis, #rheumatoidarthritis and Bell’s palsy.
Find out more: https://t.co/Nv7VsS9AnN
#APSMatters #APSAM22 #APSAwarenessMonth
Is #APS hereditary? We simply don’t know. However, there is certainly anecdotal evidence supporting links in some families, & research is starting to look at the possible genetic links now.
Find out more: https://t.co/XGUpXDTfVD
#APSMatters #APSAM22 #APSAwarenessMonth
It can be isolating & frightening when you’re diagnosed with #APS, but plenty of online support groups can help you learn more about your condition from other people’s shared experiences.
Find out more: https://t.co/fokpm1QvHa
#APSMatters #APSAM22 #APSAwarenessMonth
The eyes can often be affected in people with #APS. In addition to #migraine aurae such as flashing lights & patterns, visual loss can result from clots on the brain or optic nerve.
Find out more on our website: https://t.co/EJ8PGzccvB
#APSMatters #APSAM22 #APSAwarenessMonth
Around 20% of #APS patients have a skin condition called #livedoreticularis. Livedo reticularis is caused by tiny clots that develop inside the blood vessels of the skin that reduce the blood flow.
Find out more: https://t.co/Os64bNl9AE
#APSMatters #APSAM22 #APSAwarenessMonth
Most people with #APS will find they suffer from fatigue; this is because they have an #autoimmunedisease. Learning how to manage your fatigue is vital, so you’re not always exhausted.
Find out more on our website: https://t.co/DfAhchf0JR
#APSMatters #APSAM22 #APSAwarenessMonth
It is now known that due to clots, #kidneydisease is not uncommon in #APS & can be the first & only sign of the condition. Early detection of kidney problems often improves the outlook of patients.
Find out more: https://t.co/Q7OZKlmcAB
#APSMatters #APSAM22 #APSAwarenessMonth
Our charity maintains a comprehensive and up-to-date #APS specialist directory which has been compiled thanks to patients sharing information with us & recommending doctors who have treated them.
Find out more: https://t.co/E83nyJMl0J
#APSMatters #APSAM22 #APSAwarenessMonth
According to @rcgp, APS is significantly underdiagnosed. We developed the first-ever Royal College online APS training course for GPs, visit: https://t.co/vASipNgxhO
#APSMatters #APSAM22 #APSAwarenessMonth
Lucy tragically lost her daughter, Isabelle, at 29 weeks. Isabelle was born weighing 880 grams & was classified as a low-weight baby. We are very grateful to Lucy for sharing her story. Read it here: https://t.co/VNHuUc6idT
#Stillbirth #APSMatters #APSAM22 #APSAwarenessMonth
On average, APS patients will spend ten days in hospital prior to diagnosis.
Find out more here: https://t.co/Ih7q923QD8
#APSMatters #APSAM22 #APSAwarenessMonth
Around 30% of #APS patients will experience some form of #heartvalvedisease. In most cases, the condition is mild, but it can lead to heart failure in severe cases, and patients may require surgery.
Find out more: https://t.co/3STbc6pBgX
#APSMatters #APSAM22 #APSAwarenessMonth
#APS is diagnosed with blood tests that detect #antiphospholipidantibodies (aPL). The lupus anticoagulant (LA) test is a confusing name: if you are + for the LA, you do NOT have #lupus but have aPL.
Find out more: https://t.co/IDLABsEeIZ
#APSMatters #APSAM22 #APSAwarenessMonth
For every 7 women affected by #APS, there are 2 men affected. Women are likely diagnosed earlier due to #pregnancy problems. Sadly, men tend to only be diagnosed after a serious clotting event.
Find out more: https://t.co/RVrRYeFilg
#APSMatters #APSAM22 #APSAwarenessMonth
June is not just #APSAM22 but is also @SandsUK awareness month. Many women with #APS sadly know that losing a baby later in pregnancy can be shattering. Sands, the #stillbirth & neonatal death charity, supports anyone affected by this tragedy.
#WeAreSands #BabyLoss
Today is the first day of our new campaign Together, we are Sands 💙🧡
Everyone in the Sands community has an important role to play in helping bereaved families and #SavingBabiesLives
Together, #WeAreSands
➡️ https://t.co/WhWaumoxTr
#BabyLoss #PregnancyLoss
In addition to recurrent #miscarriage, women with #APS are 5x more likely to suffer a stillbirth. Women must receive correct treatment & regular monitoring during these high-risk pregnancies.
Find out more: https://t.co/sjfWTYUXhb
#APSMatters #APSAM22 #APSAwarenessMonth
After suffering a #TIA, Vicky was diagnosed with #APS. Since then, she has had to battle with a whole host of related conditions & symptoms. We are very grateful to Vicky for sharing her story. Read it here: https://t.co/LPQWhw5PAG
#APSMatters #APSAM22 #APSAwarenessMonth
Some people with #APS will also have other #autoimmune conditions, as may other members of their family. Between 30-40% of people with #lupus will have #antiphospholipid antibodies.
Find out more: https://t.co/QyOBSyVcsw
#APSMatters #APSAM22 #APSAwarenessMonth
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