APS and ear problems: Hi, I was... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,401 members10,612 posts

APS and ear problems

Christine7 profile image
6 Replies

Hi, I was diagnosed with APS about 18 months ago after a venous sinus thrombosis. Since this I have been told I have sjogrens although I tested negative I have very dry mouth and eyes which is easily treated with drops. About a week ago I started having problems with my ear. This feels like trapped water but instead of being deaf I have ultra sensitive hearing. All searches lead to meniers disease but this has lasted a week and not cleared up in between. I haven't been sick I'm in no pain and my balance is ok. My head feels a bit fuzzy at times. Any ideas would be good. Going to see my GP next week. 

Written by
Christine7 profile image
Christine7
To view profiles and participate in discussions please or .
6 Replies
Manofmendip profile image
Manofmendip

Hi Christine

Ear problems are common in APS.  I saw, at Prof Hughes' recommendation, Peter Savundra at The Portland Hospital in London.  Peter is a Consultant Audiovestibular Physician.  A lovely man, he as a good knowledge of APS related ear problems.

I don't know if you can see him on the NHS but it was very well worth paying to see him, in my case.

Dave

Christine7 profile image
Christine7 in reply toManofmendip

Thanks, I do have insurance so might ask my GP for referral and see if I can get an appointment. 

MaryF profile image
MaryFAdministrator

HI there, I am going to let Dave answer this one, as he has very very good advice on ears.    MaryF

Manofmendip profile image
Manofmendip in reply toMaryF

I do indeed Mary.  My advice on ears is, yes you need them. lol. :)

Manofmendip profile image
Manofmendip in reply toManofmendip

Seriously though, Peter Savundra is the best in the business.  He is one of only 10 of this type of consultant in the country and he has worked on APS with Prof H.

Manofmendip profile image
Manofmendip

Great.  He's a fantastic guy, his clinics always run late because he spends so much time with each patient. 

Not what you're looking for?

You may also like...

APS AND EYESIGHT PROBLEMS

Hi my neurologist recently told me that Hughes Syndrome and MS are extremely rare to have together....
Stereolover profile image

APS and balance

Hi, I have suspected APS as I have had high Igg Cardiolipin for 12 months now, 2 previous...
Crose86 profile image

Heart problems and APS

I never thought much about how Sticky Blood can affect the heart. Without a family history of heart...
orygun66 profile image

Aps and gynea problems

Hi again Just wondering if anyone can help here with some general advice was diagnosed with...
bevjane74 profile image

APS

I was diagnosed with APS about 20 years ago and have been on Warfarin for 25 years now. I have had...
ledlegs profile image

Moderation team

See all
HollyHeski profile image
HollyHeskiAdministrator
lupus-support1 profile image
lupus-support1Administrator
KellyInTexas profile image
KellyInTexasAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.