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@hopeful2023

My sincere thanks for reaching out. It's hard for me to write about my son, so I can only imagine how difficult it is to write about yourself. Curious, do you have APS as a primary or secondary diagnosis? Per my son's hematologist, they will do more tests to look for sign of Lupus, but at this time he does not suspect that he has it. Of course from what I've read that could change with time, but at this point they are focused on just the APS. Hence the initial direction toward Hematology, but I'm wondering if we should also be pursuing consults in Rheumatology?

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Replies to "My sincere thanks for reaching out. It's hard for me to write about my son, so..."

I have APS as a primary diagnosis. But i believe they will conduct more experiments for lupus just like your son. I have a very simular condition with your son, as i am a man with just a few years elder than your son, Active also, I used to play soccer every Sunday.
I am not sure Pradaxa is the best medicine for me as I have CVST as the first Symptoms I have.
The doctor says they prefer this as they could have reverse medicine for Pradaxa.
I have booked for a consultation of Rheumatology in March and I hope everything will get more clear.