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473 total results
Comments (415)
Talk to your dr. Warfarin is standard for APS
https://connect.mayoclinic.org/comment/847998/
Warfarin is standard for APS
Hello, is anyone caring for APS syndrome? For young teenagers?
https://connect.mayoclinic.org/comment/598011/
Hello, is anyone caring for APS syndrome
Thank you, Ginger. Is APS a state ....and national organization?
https://connect.mayoclinic.org/comment/216871/
Is APS a state ....and national organization
My son has APS since 2007. He has been on warfarin since 2007 with exception of...
https://connect.mayoclinic.org/comment/1064962/
My son has APS since 2007. ... drug current or since diagnosis for APS ... Learning a lot about APS. ... do hv a question, does anyone with APS ... Thanks and prays for all with APS!
Hello @lindzchic24 and welcome to Mayo Clinic Connect. I found an existing discussion on the topic...
https://connect.mayoclinic.org/comment/802604/
expect with Antiphospholipid Syndrome (APS ... /connect.mayoclinic.org/discussion/aps
Has anyone else with APS had eye problems?
https://connect.mayoclinic.org/comment/872832/
Has anyone else with APS had eye problems
Welcome, @cthomp77. I moved your question to the Autoimmune Disease support group https://connect.mayoclinic.org/group/autoimmune-diseases/ where you will...
https://connect.mayoclinic.org/comment/1462294/
discussions about Antiphospholipid Syndrome (APS ... search=APS
Several members have talked
I would strongly encourage you to open a dialogue with your doctor regarding this, do you...
https://connect.mayoclinic.org/comment/1294427/
regarding this, do you have primary APS ... have lupus, or do you have secondary APS ... of Care since 2023 for those with APS ... The majority diagnosed with APS who
It’s my understanding that the DOAC blood thinners aren’t gold standard of treatment for APS. Didn’t...
https://connect.mayoclinic.org/comment/1115274/
aren’t gold standard of treatment for APS ... don’t understand why everyone with APS ... Primary APS is pretty rare though I
Bienvenidos, @encarni. I moved your message to this existing discussion: – What can I expect with...
https://connect.mayoclinic.org/comment/844491/
expect with Antiphospholipid Syndrome (APS ... /connect.mayoclinic.org/discussion/aps ... experience with antiphospholipid syndrome (APS
I have APS and so far I’m on warfarin and Plaquenil.Please check with your doctors because...
https://connect.mayoclinic.org/comment/868407/
I have APS and so far I’m on warfarin ... inflammation and joint pains when you have APS
Have APS and wondering how off does my blood have to be before medication is necessary?
https://connect.mayoclinic.org/comment/820830/
Have APS and wondering how off does
I’m just a tired wreck ! I want some relief from APS ! 🤷🏻♀️
https://connect.mayoclinic.org/comment/854517/
I want some relief from APS !
@meghanl, you may also be interested in this related discussion: - Anyone have experience with Antiphospholipid...
https://connect.mayoclinic.org/comment/955235/
experience with Antiphospholipid syndrome (APS ... antiphospholipid-syndrome-hughes/
Have you been diagnosed with APS
My hematologist prescribed Eloquis to me for long plane or car rides over 2 hours in...
https://connect.mayoclinic.org/comment/833848/
Eloquis commercial that warns of use by APS ... distrust my Doctor’s knowledge of APS
Welcome @renee12345. You might also be interested in this related discussion: – What can I expect...
https://connect.mayoclinic.org/comment/778728/
expect with Antiphospholipid Syndrome (APS ... /connect.mayoclinic.org/discussion/aps
D.E.S.???? Was anyone with APS born to a mother who took D.E.S. during their pregnancy? My...
https://connect.mayoclinic.org/comment/869767/
Was anyone with APS born to a mother ... definitive answer as to how they developed APS
Does anyone has APS and is on warfarin How do you cope with the monitoring .Please...
https://connect.mayoclinic.org/comment/776101/
Does anyone has APS and is on warfarin
Just wanted to mention, my hematologist is a specialist with this disorder and tells me Warfarin...
https://connect.mayoclinic.org/comment/1068998/
is the only effective treatment for APS
I am on eloquis, but that seems rare, because everybody else I’ve heard from with APS...
https://connect.mayoclinic.org/comment/847270/
everybody else I’ve heard from with APS
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