I was diagnosed APS 19 yrs ago. Since then have DVT's PE PVD Ms Angina type 2 diabetes frontal lobe damage, memory loss, arthritis, postural hypotension, right ventricular outflow tract tachycardia, bladder and bowel problems.
So not much going right.
Still work full time. Had to retire from nursing as could keep the pace in A&E or Stroke Unit.
Hope you're all having a peaceful weekend.
Welcome, you will find quite a few on here have a similar patient journey, I am not surprised you have had to slow down a little. We all learn off each other on here, reading our various posts etc. MaryF
Welcome - you have been through the wars. We all help each other on here by sharing our experiences.
Shame about the nursing, what work do you do now?
Are you in UK?
I see youve just joined may i ask if you are in the US?
Has anyone got damage to their legs due to DVT and how does it affect you ??
To whom it may concern
Hughes London Support Group
Dorset APS Support Group
Support group in Northamptonshire???
