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Hughes Syndrome APS Forum

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Someone knows a Hughes Syndrome specialist in Johannesburg?

Joana_Doutor profile image
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Joana_Doutor profile image
Joana_Doutor
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MaryF profile image
MaryFAdministrator

Hi there, the best I can do is give you some leads to follow up.

1. prodder.org.za/civicrm/cont...

2. gauteng.co.za/antiphospholi...

and

3. Also a paper with medical names to track down in the hospitals: biomedcentral.com/1756-0500...

please let us know how you get on. Mary F x

Joana_Doutor profile image
Joana_Doutor

Hello! Thanks for your help. Regards. Joana

MaryF profile image
MaryFAdministrator in reply to Joana_Doutor

I hope it helps you in some way. Mary F x

Jade profile image
Jade in reply to MaryF

You do work hard Mary :)

MaryF profile image
MaryFAdministrator in reply to Jade

I think we all do it together on here.. I have found this before, somewhere in my foggy memory banks! Mary F xx

fourstar profile image
fourstar

Prof Barry Jacobson at the Charlotte Maxeke hospital. Do not go to Dr Karen Gunthet at Floro clinic.

eltrl profile image
eltrl

I am in Botswana & have seen an excellent rheumatologist in Johannesburg who follows the work of Prof Hughes et al v closely, attends all conferences etc and is willing to consider seronegative APS. Her name is Dr Du Plooy and she can be found at the Wits University Faculty Practices/Donald Gordon Medical Center where they have a group of great specialists who are all engaged in research as well as seeing patients. The APS Foundation of South Africa apssafoundation.co.za is also an excellent resource.

Dr du Plooy saved my sanity and quite possibly my future health. As she put it - what if the next attack is a stroke? You shouldn't have to wait to have a stroke before getting treatment.

Hope I'm not too late with this, do let us know how you get on

Eleanor x

MaryF profile image
MaryFAdministrator in reply to eltrl

Thank you for this valuable feedback! Mary F x

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