Anybody know a good Rheumy in Leicest... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,356 members10,544 posts

Anybody know a good Rheumy in Leicester area?

traceylou profile image
7 Replies

Any recommendations much appreciated many thanks

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

Hi there, I am sure at some point, your peers in the Midlands will come on and advise, better than myself! They will have better expertise than myself. Best wishes, Mary F x

jessielou profile image
jessielou

Hi Tracey,

I live in Leicestershire, but haven't been to a rheumy in this Leicester. I have heard that dr sue Pavord who's a haematologist, is very good, she works privately out of Spire's Hospital and NHS at the Leicester Royal Infirmary. She is knowledgable on Aps and associated conditions.

Will have a search around see if we can find rheumy that's helpful!

Hope you feels ok today,

Take care gentle hugs love Sheena xxxxx :-) :-) :-)

Hilda_G profile image
Hilda_G in reply to jessielou

It sounds like Dr Pavord has been getting herself educated. About eight years ago she told me to come off the warfarin, and could show me no back up information/research articles to support her suggestion.

Suzypawz profile image
Suzypawz

Hi I live close to that area too, I am trying to get back into the Burton hospital, as I had 'complications' in the beginning with mine! now I have to go to London!!!.....so not sure of any good rhumies in Leicestershire....but good luck, wish I could help more....just wanted to say hi & if I do another Staffordshire / Derby meeting would you like to join us? :) xx

traceylou profile image
traceylou

Absolutely keep me posted thank youxxx

traceylou profile image
traceylou

Hi Suzy just read your details and yep all the same things as me, could you tell me have you had a positive test for aps and the others, if so it would be interesting to know what they are as I am very simular.....many thanks traceylouxx Are you close to the Market Harbrough maybe we could meet and catch up talk to you soon. PS I remeber listening to your corby interview well done.

Suzypawz profile image
Suzypawz in reply to traceylou

Aaahh really? thank you :)

I am positive for APS, Menieres & Raynauds......so far nothing else apart from degenerative disc disorder & migraines!

Hi not that close really? I dont have transport & have to rely on hubby :(

Do you ever come to Burton On Trent at all to our shopping malls at all? or would like to?!

I could meet you if you have transport to get here & spend the day showing you around.....& drinking coffee!!!! :)

we could even go & visit our Sheena at her pub :) x

You may also like...

back from rheumy , good things

every thing, when i talked he listened, is very much , as far as i am concerned, formiller ? with my

I am moving to the Woodlands in Texas anybody know a Doctor Who is good with Hughes syndrome

Does anybody know about Sneddons syndrome secondary to aps?

not write this in any letters to my GP I do not know what to think, not getting any clear answers...

Looking for practitioners in Chicago area

Chicago area. We are located in the western suburbs Thanks!

Anybody suffer from alopecia?