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473 total results
Comments (415)
It looks most like 'mixed cryogobulinemia' with non-hepititis SLE and APS. The cure is plasmapharesis. Where...
https://connect.mayoclinic.org/comment/212946/
cryogobulinemia' with non-hepititis SLE and APS
I also have APS and would like to be part of this study to learn more...
https://connect.mayoclinic.org/comment/996020/
I also have APS and would like to be
Hello to all, i was wondering if having a bad reaction to a childhood shot, i...
https://connect.mayoclinic.org/comment/104551/
cough, could be a trigger to develop APS ... possible correlation in developing APS
Hi I am new here does anyone have a high beta 2 igm and aps syndrome
https://connect.mayoclinic.org/comment/853917/
anyone have a high beta 2 igm and aps
I was diagnosed with APS 30 years ago and advised to take a baby aspirin everyday....
https://connect.mayoclinic.org/comment/847941/
I was diagnosed with APS 30 years ago ... a fine print advisory stating that APS
I was diagnosed with APS right after Covid. I was told that in my particular case,...
https://connect.mayoclinic.org/comment/1286164/
I was diagnosed with APS right after ... had tested me in recent times for APS ... or lupus, I might have had APS without
I was diagnosed with APS/Hughes syndrome 33 years ago when I tested false positive for syphillis...
https://connect.mayoclinic.org/comment/801801/
I was diagnosed with APS/Hughes syndrome ... Anyone else with APS have a Mom who
No. I decided not to get it on my own. I also have APS, which causes...
https://connect.mayoclinic.org/comment/657666/
I also have APS, which causes my blood
APS is a diagnosis not to be taken likely I’m in my 5th year and it’s...
https://connect.mayoclinic.org/comment/847240/
APS is a diagnosis not to be taken likely ... .The only medication I know of for APS ... all speak up to your doctors about APS
I know Eliquis is a blood thinner but strongly believed not to treat APS Talk to...
https://connect.mayoclinic.org/comment/847433/
but strongly believed not to treat APS
APS/Autoimmune thyroid disease diagnosis! Struggling with pain fatigue and weight issues ! Glad to finally have...
https://connect.mayoclinic.org/comment/815013/
APS/Autoimmune thyroid disease diagnosis
@dancing1 I might need to get a tilt table test. I have small fiber neuropathy (SFN)...
https://connect.mayoclinic.org/comment/1067551/
possibility for anti phospholipid syndrome (APS ... APS is a higher risk for clotting.
Have u or do you know anyone who has suffered a catastrophic event w APS? aka...
https://connect.mayoclinic.org/comment/872335/
has suffered a catastrophic event w APS
I was told by a hematologist that Coumadin is the best blood thinner for APS. I’m...
https://connect.mayoclinic.org/comment/1129640/
Coumadin is the best blood thinner for APS
@scottham777 I am a 55 year old female and had APS autoantibodies detected in 2 different...
https://connect.mayoclinic.org/comment/1114418/
I am a 55 year old female and had APS ... but never officially diagnosed with APS ... diagnosed with sleep apnea since your APS ... your doctor considered adjusting your APS
Diethylstilbestrol (DES) is a synthetic form of the female hormone estrogen. It was prescribed to pregnant...
https://connect.mayoclinic.org/comment/870919/
able to tell me how I might’ve gotten APS ... there was a correlation between the APS
Hi! I’m a DES daughter also. My mother was prescribed the drug while pregnant with me...
https://connect.mayoclinic.org/comment/814271/
In 1990, I was informed that I had APS ... wondering whether anyone else has APS
I have Primary APS. In addition to that, I have the following...Factor V Leiden, Elevated Factor...
https://connect.mayoclinic.org/comment/185860/
I have Primary APS.
@wig How were you diagnosed with APS? How are you being treated and monitored (what types...
https://connect.mayoclinic.org/comment/1066406/
@wig
How were you diagnosed with APS ... not been formally diagnosed but had APS ... me away as “ok” even though I had APS
My APS was diagnosed after I had a CRVO in my right eye. This occurred two...
https://connect.mayoclinic.org/comment/1068183/
My APS was diagnosed after I had a CRVO ... vaccine or Covid didn't cause APS
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