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473 total results
Comments (415)
Hello everyone, my 14 year daughter has just been diagnosed with APS (likely Lupus as well)...
https://connect.mayoclinic.org/comment/823932/
daughter has just been diagnosed with APS
Yes, I am worried to start warfarin. With the diet restrictions and vit k level adjustments....
https://connect.mayoclinic.org/comment/778934/
another type of anticoagulant for APS
Again, very thorough and helpful. Thanks for really taking the time to help me through this...
https://connect.mayoclinic.org/comment/1119786/
this too, be related somehow to my APS ... my wild imagination, I think of my APS
I just don't know if I can take this. The last decade or so has been...
https://connect.mayoclinic.org/comment/1445529/
passing away, mental health diagnosis, a APS ... health meds as well as my warfarin for APS
@teddyz Have you had bloodwork to see if you have autoimmune Antiphospholipid Syndrome (APS)? I have...
https://connect.mayoclinic.org/comment/1075497/
autoimmune Antiphospholipid Syndrome (APS
I also was diagnosed back in 1986 with Chronic Epstein Barr Syndrome while in the military....
https://connect.mayoclinic.org/comment/1263490/
range from Lupus, MCTD, Sjrogrens, APS ... overall diagnosis from other blood work, APS
Hi @elaine1809, Welcome to Connect. While we wait to see if other members are able to...
https://connect.mayoclinic.org/comment/104552/
Antiphospholipid Antibody Syndrome (APS
Hello I don’t understand why your doctors is treating you with aspirin and Eliquis .My advice...
https://connect.mayoclinic.org/comment/785336/
Eliquis is not the medication for APS.Want ... to do more research on APS .Amazon
You are one of the first ppl Ive seen here with APS. I too have that,...
https://connect.mayoclinic.org/comment/1121189/
of the first ppl Ive seen here with APS
Welcome to Mayo Clinic Connect @jkrobertson ! I’m so glad you found us! On MCC people...
https://connect.mayoclinic.org/comment/963572/
they will share their journey with APS
I have been on hydroxychloroquine for 20 years, and I have never had any kind of...
https://connect.mayoclinic.org/comment/1260817/
It has worked wonders with APS, and
@elizabeth513, I'm afraid that this is a medical question that we cannot answer. It's really important...
https://connect.mayoclinic.org/comment/665412/
to get medical guidance regarding APS
Hello all my APS friends .Hope everyone are doing well I would like to know whether...
https://connect.mayoclinic.org/comment/817497/
Hello all my APS friends .Hope everyone
I was worried to let my daughter start Warfarin (she's only 14), and she was on...
https://connect.mayoclinic.org/comment/854719/
months, for a PE, now Triple Positive APS ... better protection for anyone with APS
After having bloodwork done recently, I tested negative for the first time in 33 years for...
https://connect.mayoclinic.org/comment/801805/
years for the autoimmune disorder APS
You have APS which ‘’breeds’’ clots. Why are you NOT on an anticoagulant? I’d be worried...
https://connect.mayoclinic.org/comment/784750/
You have APS which ‘’breeds’’ clots
I had lymes disease twice with the “bullseye”and was treated both times, had OPS(open heart surgery)...
https://connect.mayoclinic.org/comment/104550/
correlation: Articles and people say APS
The symptoms of TIF-1 feel and look very familiar. I had a persistent skin rash from...
https://connect.mayoclinic.org/comment/1420652/
was your husband ever checked for APS
Following SARS-CoV-2 infection, I developed petechiae, suggesting possible vascular or hematologic involvement. Subsequent administration of the...
https://connect.mayoclinic.org/comment/1407505/
SJS) and Antiphospholipid Syndrome (APS
@rebaba I wish you the best getting answers. I have a new rheumatologist appointment early July...
https://connect.mayoclinic.org/comment/1082255/
SLE and Antiphospolipin Syndrome (APS ... very concerned about my untreated APS ... My APS plus COVID makes me think I am
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