I was diagnosed with Hughes Syndrome after several recurrent miscarriages between 10-12 weeks and the only time I have taken medication has been during (failed) pregnancies.
I have lots of symptoms which seem to fit the APS diagnosis but do not see any specialists or take medication.
I am not currently ttc or thinking about it in the future but am worried about the long term implications of the APS diagnosis, blood clots, tia's etc.
If there is anyone who also has APS who would be willing to talk about how they are/or not treated I would be very grateful.
I am planning to go and speak to my GP at some point and would like to be aware of any facts/risks.
With Thanks