twitter.com/bre48431150/status/1105510016545628161

oh you don’t look deaf, er … how am I suppose to look!!!
You can’t see my stomach on spin cycle either! Or that I cannot see probably or balance… or speak properly… I may ignore you in the street as I cannot communicate!
That makes me ignorant… but no that makes you ignorant and uneducated about invisible illness and disability!!!
Rant over!
We go through this all the time that’s why the 🌻 lanyard is so important to be rolled out world 🌍 wide!!! It will make people think before they judge !!! HOPEFULLY 🌻🌻🌻🌻🌻
Published by Ménières Suicide or Survivor
Loving passionate Mother of two trying navigate my way through a new kind of life I find myself in through no fault of my own.
I suffer with bilateral Ménières, on many medications and tried skull surgery to no good outcome. It’s a living hell. I am a retired primary teacher who had a fantastic career.
How do people we Ménières live with this horrific sentence? That is what my site is about... me, my journeys before...during ... now! My coping strategies and not coping...
It’s a rollercoaster, but that’s my life, I never know from one minute I the next how my day will be. Spinny, dizzy, sick, ear pain pressure yes pretty much always, attacks or non. Can I maintain the “I’m ok” face or not.
What I will say, I want to help and support anyone, it’s a lonely and horrible journey. Nobody really understands. Unless you have been there. If I can help one person I will be happy and raise awareness of this debilitating life changing and obliterating condition that is Ménières.
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