Hello Everyone! Hoping Today has been... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,388 members10,585 posts

Hello Everyone! Hoping Today has been a Good One!

GirlfromTennessee profile image

It is Post 8 months since I was diagnosed with APS. I'm currently taking 3.5 mg of Warfin, 200mg Plaquinel, Cardio-Tex Vitamin, Liptor 20mg & Synthroid. I manage pretty good & have more good days than bad. I work full time & own a small business. I have never let this illness overcome me. The questions I have are sometimes when I get stress my head feels full & sometimes my ears ring. Does anyone else have this happen? I've made mental notes of when my head feels this way & always it seems it happens when I get stressed? Any logic reasoning for this? Because once whatever the 'stress' dissolves so does this 'Fullness'

Written by
GirlfromTennessee profile image
GirlfromTennessee
To view profiles and participate in discussions please or .
Read more about...
4 Replies
MaryF profile image
MaryFAdministrator

All I can say, is at least you notice the connection, I think stress worsens any illness, although sometimes it is the other way round, ie you feel stressed due to perhaps being ill, or a flare coming on. It sounds like you are doing really well. Keep well. MaryF

GirlfromTennessee profile image
GirlfromTennessee in reply to MaryF

Thank You! Mary F, I'm trying to keep this illness stable!!

GinaD profile image
GinaD

As has been mentioned here, the capillaries that serve the ear are among the tiniest in the body, so tinnitus is quite common among APS patients.

And, as Mary pointed out, stress and autoimmune symptoms is a chicken or the egg question.

Lesley61 profile image
Lesley61

Yes I have been so stressed for the last mouth and mad head been fit to bust and the ring as well just glad of not got blood pressure or I would dried to think iv had APS for over a year I think put all sorts down to it good luck x

Not what you're looking for?

You may also like...

What a month!

Don't worry about reading if too long and boring.............. After a year that was pretty much...

IV Therapy safe with APS?

I am having trouble getting help with the next phase of my disease. I have been in a 5 month funk...

Azathioprine dose

First a little background: I have been on 200mg of Azathioprine, for a number of years. All that...

Might be diagnosed with Antiphospholipid Syndrome (APS)

Hi I previously in January 2023 was diagnosed with PE, the past year has been difficult and long...

A new discovery for potential treatment!

Light at the end of the blood thinner treatment tunnel? Just read this today:...