APS talk.

This is pretty informative. Though I found quite a bit of it too hard to understand.

PS I was charlieab but lost my password and couldnt reset it!

6 Replies

  • Great new name, thanks for putting this on, will watch it later. MaryF

  • Thank you! I will repost in LUpus Patients Understanding & Support (LUPUS) as many people with systemic lupus also have APS/Hughes.

    With good wishes,


  • Ros,

    do those people know about this site?youve probably mentioned us. Probably, but maybe not, Cindy

  • Thanks Charlie again! Can relate to some of this very well!

  • Just watched through completion, thank you, Cindy in NJ

  • Watched this with great interest over several hours is a lot to take in

    Thanks for posting

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