APS Foundation of America
@apsfaorg.bsky.social
APS Foundation of America (#APSFA) is the only US org spreading #Antiphospholipid Syndrome #APS & #Lupus #Awareness! #DVT #PE #Stroke #APS #miscarriage
Pinned
Credit to @apsfa APS Magnet
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
July 26, 2025 at 10:25 PM
Credit to @apsfa APS Magnet
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
Reposted by APS Foundation of America
✨ August Issue✨| Comment article on the risks and benefits of immunosuppressant withdrawal in systemic lupus erythematosus
bit.ly/45kkdIK
#Rheumsky #Medsky
bit.ly/45kkdIK
#Rheumsky #Medsky
Risks and benefits of immunosuppressant withdrawal in systemic lupus erythematosus - Nature Reviews Rheumatology
Withdrawing immunosuppressive treatment in systemic lupus erythematosus offers reduced toxicity and improved quality of life for patients in remission but carries a risk of disease reactivation. Emerg...
bit.ly
July 25, 2025 at 8:53 AM
✨ August Issue✨| Comment article on the risks and benefits of immunosuppressant withdrawal in systemic lupus erythematosus
bit.ly/45kkdIK
#Rheumsky #Medsky
bit.ly/45kkdIK
#Rheumsky #Medsky
APS Magnet
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
July 17, 2025 at 7:30 PM
APS Magnet
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
Yes, FB cropped the picture.
100% of the proceeds go to the APSFA. Only 100 in stock. They will ship by USPS without tracking.
They fit in my palm.
To order: www.paypal.com/ncp/payment/...
The end of the month is here!
Today's the day when we take a moment to say THANK YOU to everyone who has liked, commented on, and especially to those who shared our graphics all month long! Awareness begins with YOU. Get your story out there! Share your experiences! We can
Today's the day when we take a moment to say THANK YOU to everyone who has liked, commented on, and especially to those who shared our graphics all month long! Awareness begins with YOU. Get your story out there! Share your experiences! We can
July 1, 2025 at 11:11 AM
The end of the month is here!
Today's the day when we take a moment to say THANK YOU to everyone who has liked, commented on, and especially to those who shared our graphics all month long! Awareness begins with YOU. Get your story out there! Share your experiences! We can
Today's the day when we take a moment to say THANK YOU to everyone who has liked, commented on, and especially to those who shared our graphics all month long! Awareness begins with YOU. Get your story out there! Share your experiences! We can
Whose got a similar collection? Raise your hand.
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June 30, 2025 at 3:47 PM
Whose got a similar collection? Raise your hand.
✋️
✋️
Today, we bring you some tips on coping with #APS.
How do you #cope with APS?
Do you see a #therapist?
Do you #journal?
Share with others how you cope with APS. In the end, remember you are not alone, and you can join our private support group here on Facebook if you need to vent.
How do you #cope with APS?
Do you see a #therapist?
Do you #journal?
Share with others how you cope with APS. In the end, remember you are not alone, and you can join our private support group here on Facebook if you need to vent.
June 29, 2025 at 7:29 PM
Today, we bring you some tips on coping with #APS.
How do you #cope with APS?
Do you see a #therapist?
Do you #journal?
Share with others how you cope with APS. In the end, remember you are not alone, and you can join our private support group here on Facebook if you need to vent.
How do you #cope with APS?
Do you see a #therapist?
Do you #journal?
Share with others how you cope with APS. In the end, remember you are not alone, and you can join our private support group here on Facebook if you need to vent.
Getting a diagnosis of Antiphospholipid Syndrome (#APS) can feel overwhelming, but take a deep breath. You are not alone, and there are resources, support, and treatments to help you live well.
Find a Knowledgeable Doctor
Ideally, a rheumatologist or hematologist with APS experience.
Find a Knowledgeable Doctor
Ideally, a rheumatologist or hematologist with APS experience.
June 29, 2025 at 1:45 PM
Getting a diagnosis of Antiphospholipid Syndrome (#APS) can feel overwhelming, but take a deep breath. You are not alone, and there are resources, support, and treatments to help you live well.
Find a Knowledgeable Doctor
Ideally, a rheumatologist or hematologist with APS experience.
Find a Knowledgeable Doctor
Ideally, a rheumatologist or hematologist with APS experience.
Reposted by APS Foundation of America
Clinicians — are you looking for a trusted place to stay sharp on anticoagulation care? Expert anticoagulation education awaits at AC University!
New:National Conference Bundles (7.25 CE), Boot Camp (14.5 CE), & CARE AF/VTE.
Plus, free modules, resources, recaps & tools.
Join us: www.acforum.org
New:National Conference Bundles (7.25 CE), Boot Camp (14.5 CE), & CARE AF/VTE.
Plus, free modules, resources, recaps & tools.
Join us: www.acforum.org
June 27, 2025 at 3:01 PM
Clinicians — are you looking for a trusted place to stay sharp on anticoagulation care? Expert anticoagulation education awaits at AC University!
New:National Conference Bundles (7.25 CE), Boot Camp (14.5 CE), & CARE AF/VTE.
Plus, free modules, resources, recaps & tools.
Join us: www.acforum.org
New:National Conference Bundles (7.25 CE), Boot Camp (14.5 CE), & CARE AF/VTE.
Plus, free modules, resources, recaps & tools.
Join us: www.acforum.org
Living with Antiphospholipid Syndrome (APS) can bring fatigue, joint pain, swelling, and a higher risk of blood clots. While intense workouts may feel out of reach, gentle, simple exercises can play a powerful role in maintaining your health and well-being.
June 29, 2025 at 1:16 AM
Living with Antiphospholipid Syndrome (APS) can bring fatigue, joint pain, swelling, and a higher risk of blood clots. While intense workouts may feel out of reach, gentle, simple exercises can play a powerful role in maintaining your health and well-being.
#Swelling and #pain can be common and serious symptoms in people with Antiphospholipid Syndrome (APS). These symptoms often result from blood clots, #inflammation, or related complications.
If you are not doing better in a timely fashion or it is an emergency, please consult your doctor
If you are not doing better in a timely fashion or it is an emergency, please consult your doctor
June 28, 2025 at 6:44 PM
#Swelling and #pain can be common and serious symptoms in people with Antiphospholipid Syndrome (APS). These symptoms often result from blood clots, #inflammation, or related complications.
If you are not doing better in a timely fashion or it is an emergency, please consult your doctor
If you are not doing better in a timely fashion or it is an emergency, please consult your doctor
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
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
June 28, 2025 at 12:35 PM
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
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
Myth: Only older or sick people get blood clots
Fact: Anyone can get a blood clot, even if they are young - that includes children and healthy people.
When did you first start clotting?
#AntiphospholipidSyndrome #APSAwareness #apsawarenessmonth #apsresearch #WTD25 #raredisease #APS
Fact: Anyone can get a blood clot, even if they are young - that includes children and healthy people.
When did you first start clotting?
#AntiphospholipidSyndrome #APSAwareness #apsawarenessmonth #apsresearch #WTD25 #raredisease #APS
June 27, 2025 at 7:54 PM
Myth: Only older or sick people get blood clots
Fact: Anyone can get a blood clot, even if they are young - that includes children and healthy people.
When did you first start clotting?
#AntiphospholipidSyndrome #APSAwareness #apsawarenessmonth #apsresearch #WTD25 #raredisease #APS
Fact: Anyone can get a blood clot, even if they are young - that includes children and healthy people.
When did you first start clotting?
#AntiphospholipidSyndrome #APSAwareness #apsawarenessmonth #apsresearch #WTD25 #raredisease #APS
Reposted by APS Foundation of America
Just a few days left to register! Don’t miss this important conversation on a shift in Medicare policy.
Join us June 27 for a webinar on how Medicare’s new drug pricing power will impact access to heart meds. Hear from national experts on what prescribers need to know.
🔗 Register: bit.ly/444KZTs
Join us June 27 for a webinar on how Medicare’s new drug pricing power will impact access to heart meds. Hear from national experts on what prescribers need to know.
🔗 Register: bit.ly/444KZTs
June 25, 2025 at 3:01 PM
Just a few days left to register! Don’t miss this important conversation on a shift in Medicare policy.
Join us June 27 for a webinar on how Medicare’s new drug pricing power will impact access to heart meds. Hear from national experts on what prescribers need to know.
🔗 Register: bit.ly/444KZTs
Join us June 27 for a webinar on how Medicare’s new drug pricing power will impact access to heart meds. Hear from national experts on what prescribers need to know.
🔗 Register: bit.ly/444KZTs
#Lupus (Systemic Lupus Erythematosus, or #SLE) is an #autoimmune disease that often doesn't appear alone. It can "cluster" with other autoimmune diseases or symptoms in the same person, family, or community. This is known as #disease #clustering.
June 26, 2025 at 6:42 PM
#Lupus (Systemic Lupus Erythematosus, or #SLE) is an #autoimmune disease that often doesn't appear alone. It can "cluster" with other autoimmune diseases or symptoms in the same person, family, or community. This is known as #disease #clustering.
Catastrophic #Antiphospholipid Syndrome or #CAPS is a complication of #APS.
CAPS is very rare, and in about half of the cases, the APS patient does not survive.
Has anyone survived CAPS?
Have you lost a loved one due to #CAPS?
CAPS is very rare, and in about half of the cases, the APS patient does not survive.
Has anyone survived CAPS?
Have you lost a loved one due to #CAPS?
June 25, 2025 at 6:15 PM
Catastrophic #Antiphospholipid Syndrome or #CAPS is a complication of #APS.
CAPS is very rare, and in about half of the cases, the APS patient does not survive.
Has anyone survived CAPS?
Have you lost a loved one due to #CAPS?
CAPS is very rare, and in about half of the cases, the APS patient does not survive.
Has anyone survived CAPS?
Have you lost a loved one due to #CAPS?
Formerly known as Seronegative APS or #SNAPS.
Basically, it's having symptoms of APS without the numbers. It can be challenging to get a positive APS diagnosis and, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because
Basically, it's having symptoms of APS without the numbers. It can be challenging to get a positive APS diagnosis and, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because
June 25, 2025 at 1:50 PM
Formerly known as Seronegative APS or #SNAPS.
Basically, it's having symptoms of APS without the numbers. It can be challenging to get a positive APS diagnosis and, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because
Basically, it's having symptoms of APS without the numbers. It can be challenging to get a positive APS diagnosis and, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because
Reposted by APS Foundation of America
Autoimmune disease may almost double risk of mental ill health, study suggests
Autoimmune disease may almost double risk of mental ill health, study suggests
Chronic exposure to inflammation may explain link to conditions including depression, anxiety and bipolar disorder, researchers say
Living with an autoimmune disease may almost double the risk of mental health conditions including depression, anxiety and bipolar disorder, a study suggests.
The link may be explained by the chronic exposure to systemic inflammation that the autoimmune disease causes, researchers at the University of Edinburgh said. Continue reading...
www.theguardian.com
June 24, 2025 at 10:32 PM
Autoimmune disease may almost double risk of mental ill health, study suggests
Formerly known as Seronegative APS or #SNAPS.
Basically, it's having symptoms of APS w/o the numbers. It can be challenging to get a positive APS diagnosis &, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because it is not widely recognized.
Basically, it's having symptoms of APS w/o the numbers. It can be challenging to get a positive APS diagnosis &, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because it is not widely recognized.
June 25, 2025 at 1:38 PM
Formerly known as Seronegative APS or #SNAPS.
Basically, it's having symptoms of APS w/o the numbers. It can be challenging to get a positive APS diagnosis &, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because it is not widely recognized.
Basically, it's having symptoms of APS w/o the numbers. It can be challenging to get a positive APS diagnosis &, therefore, difficult to receive necessary treatment.
Being diagnosed with SNAPS can be frustrating because it is not widely recognized.
Leg cramps are a common occurrence that most of us have felt before. Regular muscle cramps will go away pretty quickly by stretching or walking. Crampy feelings in the legs that won't go away or worsen over time are symptoms of DVT.
June 24, 2025 at 6:24 PM
Leg cramps are a common occurrence that most of us have felt before. Regular muscle cramps will go away pretty quickly by stretching or walking. Crampy feelings in the legs that won't go away or worsen over time are symptoms of DVT.