Hi, can anyone recommend which Doctor at London Bridge Hospital would be good for helping to get a diagnosis of APS/ Hughes Syndrome? This is for another person that has contacted me for help. She needs to see a specialist that will do the necessary blood tests and listen carefully to her symptoms and look at her history of clotting episodes. She is not getting this help from her current Doctor and is prepared to travel to London Bridge Hospital.
I was lucky enough to get my diagnosis some years ago by Prof Hughes 😀
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AvsG
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I am sure members on here will tell you who they see, I see Prof Hughes but he is not taking on new patients, some of my friends seen Dr Kaul and have been very pleased, but there are quite a few doctors there, I am sure you will get some good ideas, having asked the question. MaryF
I see Dr Kaul and he would be my recommendation going by the excellent treatment I have received from him. I’m sure the other doctors at London Bridge Hospital are good too but speaking from experience I highly recommend Dr Kaul. Especially for a first time diagnosis from the start.
I see dr Natasha Jordan simply because she not only has the APS additional training, but has the “tag on” expertise in vasculitis also. That’s why I chose her- my veins were having so much trouble.
I was diagnosed in 2008 by Prof Hughes himself after being told to take 2 Aspirin a day for the rest of my life by a consultant t my local hospital.!! Decided to write to Prof Hughes as I was not happy with this and so glad I did as I would not be here to tell you this otherwise. Prof Hughes put me onto Prof Khamashta who is now in Dubai working who was a fantastic Professor . Since he left I see Prof D'Cruz who is to the point but very good indeed. Kim is a Lupus Nurse who will help with questions and concerns - she is a very caring and informative person and answered all of my concerns. Extremely helpful indeed to know.
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