After a stroke 8 years ago and several years of feeling increasingly I'll I've finally had SLE with secondary APS and Reynaulds confirmed. Bloods done in June and repeated in September showed increasing evidence.
Finally got to see a haematologist last Friday (still waiting for appt at St Thomas') and they are starting me on heparin and warfarin tomorrow.
Bit swept away by it all. What can I expect at my appointment and will the treatment make me feel anything different? Also has conflicting advice about how often I need to go back to get levels checked.
I'm on a range of meds already including amitryptaline for pain. Will the be a problem?