APLS Hemotologist in NY: My wonderful... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,397 members10,601 posts

APLS Hemotologist in NY

nyctapdancer profile image
2 Replies

My wonderful hemotoligist, Dr Sanford Kempin, retired several years ago and I have yet to find a hemo who has clue one about APLS.

Does anyone see a hemo in NYC who understands the syndrome? By chance is there one at Weill Cornell or NYU?

The Dr who replaced Dr Hughes, Dr Cromwell, didn't come close to his caring, informed, always learning approach.

Recommendations are welcome.

Written by
nyctapdancer profile image
nyctapdancer
To view profiles and participate in discussions please or .
2 Replies
MaryF profile image
MaryFAdministrator

I am sure you will get some recommendations soon, as many from the USA on here, as you know. Keep well. MaryF

KellyInTexas profile image
KellyInTexasAdministrator

I’m also looking for a hematologist in NYC. ( preferably in the financial district for now - near 22nd Dutch street as this is my hub when I’m in the city.

Will be setting myself up with a GP/ internist within walking distance - I can’t remember his name. ( He’s the GP listed on the Swiss consulate general website- by happenstance).

If you find a good one- do let us know. Weil is associated with Dr Erkan so I’m sure there will be a good hematology department associated with Weil Cornell. That might be closer to where you are located.

Not what you're looking for?

You may also like...

Should I go for 2nd opinion?

I had a recent MRA done and it shows I have a partial clot in my transverse sinus vein and a small...

DVT AGAIN

WE don't want to hear the DVT thing - I was sent to the ER last night for pain and weakness left...

Lecithin and APLS

Hi, Does anybody know if it's ok (or even beneficial) for a Hughes Syndrome sufferer to take...

Arvind says APLS experts on every continent

Arvind in a chat session said there is an APLS expert on every continent. Who is it in Australia...

Leaches and bleeding

My latest blood work came back today and confirm I "still" have APS. My hemo Doc was a bit...