Still looking for specialist - Hughes Syndrome A...

Hughes Syndrome APS Forum

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Still looking for specialist

SoulRebel-APS profile image
4 Replies

Im just checking in thought I would ask again if anybody know of an APS specialists in New Mexico. Thank u for your time!

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SoulRebel-APS profile image
SoulRebel-APS
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4 Replies
MaryF profile image
MaryFAdministrator

I hope somebody can help you, did you try contacting these to see if they knew of anybody in the area? hss.edu/clinical-trials_ant... If not it is of course the usual route, with members on here in the USA helping, plus a willingness to travel away for short break perhaps?

MaryF

SoulRebel-APS profile image
SoulRebel-APS in reply to MaryF

No I haven't but I will. Thank you Mary! Have a great day!

christylee profile image
christylee

In Albuquerque, there are some hematologists - mostly I think they specialize in either hemophilia, or oncology, but will treat other conditions. I just go to a coumadin clinic. I don't think the pharmacists are too knowledgeable about aps, nor is my primary care doc. When I was in the hospital though (i had an ulcer and they were saying - just take her off the coumadin - the PE was a year ago), I said I had asked for copies of blood test and thought I might have aps. I think an intern researched it, so they knew what I had, and that is where they gave me the 2nd test for APS where I proved positive

APsnotFab, I would love to know the name of the specialist you know in LA.

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