← Return to What can I expect with Antiphospholipid Syndrome (APS)?

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Anyone with APS on here ?

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Replies to "Anyone with APS on here ?"

Welcome, @mskeith. I moved your message about treatment options to this existing discussion:
– What can I expect with Antiphospholipid Syndrome (APS)?: https://connect.mayoclinic.org/discussion/aps/

I did this so you can easily connect with members like @nicholas94 @perematharanseridaran and @sunshine71. You may also be interested in these related discussions:
– Anyone have experience with Antiphospholipid syndrome (APS)? https://connect.mayoclinic.org/discussion/antiphospholipid-syndrome-hughes/
– Antiphospholipid: Weird symptoms, don't understand what’s going on: https://connect.mayoclinic.org/discussion/weird-symptoms-no-clear-understanding-of-whats-going-on/

What is your experience with APS? Is this a new diagnosis for you?

I am! but I’m a newbie, so not much to add at this point except that I’m taking Pradaxa because I’ve also had two strokes, and am so far..5 years..very happy with that. Eloquis should be outlawed and is a non discussion!