Just secured an appointment with this rheumatologist in LA. Apparently he is good friends with Professor Hughes and I think they have similar platforms of treatment.
I had to "apply" to get an appointment by sending over my records, but they accepted me which lends me to think that maybe there is hope.
Anyone here a patient of Dr Wallace and can offer insight?
Diagnosed Aug 2014, mild APS, no known clotting events. Just feel crummy all of the time.