Meniere's stories

Each sufferer has a story and their story helps others understand life with Meniere's. 


Share these stories with  family and friends to help them understand 


Information for Family and Friends (Meniere’s Society UK)

https://www.menieres.org.uk/information-and-support/day-to-day/information-for-family-and-friends



Scroll down to read stories from  Dianne, Paul, June, Julieann, Esther, Mathew, Dizzy Anne and an unknown 


** Julieann has written a number of books profits of which will go to Meniere's Research 



Dianne

Dianne was a registered nurse who has bilateral Meniere’s.  Dianne was 58 when she was diagnosed with Meniere’s 13 years ago.  

 " .... It is a daily challenge for all of us whether unilateral or bilateral.  I deal with the symptoms as they happen and really try to give it as little of my day as possible.  When it all becomes too much, I have used behaviour therapy with some success."

Paul

" ...  At the time of my drop attacks it was suggested I have Gentamicin injections. This would have reduced or eliminated these attacks but I chose to ride it out as my balance was still very good and I knew it would have compromised my cycling and old age balance.  I had a total of 16 drop attacks from July 2013 to Sept 2016. "

June

"...   As a singer I was often concerned should I lose hearing in both ears. As singers are right ear dominant I was still able to pitch perfectly despite diminished hearing in the left ear. During my singing career of thirty years, approximately 500 performances and 60 productions I only missed one performance as a result of Ménière’s.  I often wonder if adrenaline has a part to play in the control of this condition."

Unknown Author - Unknown Date

"So, please don't judge me unless you've been in my shoes."   

This story has been shared on various websites and goes back more than 10 years. Author and date unknown.  

Share this with family and friends.  

Julieann

Julieann is an author who was diagnosed with Meniere's Disease in 1995.  She is an advocator of MD and has written books to raise awareness. The profits from the sale of her books are donated to medical research at MRFI. "For the future, I’ll keep on searching, researching, and writing. It’s time to find a cure"

Dizzy Anne

I have had Meneire's since 2015.  When I was first diagnosed I was relieved in a strange sort of way as I finally found out what was wrong with me.  I needed support and so did others so I started the Sydney Meniere's Support group.  Without their support, I would have managed as well as I have. 

Esther

  

Esther was diagnosed in 2000.  "I feel any relief from my chronic imbalance may only come from a balance device or implant to restore the equilibrium of both ears. I am therefore hoping that budding inventors, innovators, scientists, researchers etc. will take up the initiative and fast track a device in order to reduce or eliminate the chronic imbalance."

Mathew

Mathew noticed there was a problem in 1997.  His next episode was in 2006 and in 2007 he was diagnosed with Meniere’s. 

“Throughout my journey I have been very lucky with beautiful love and support from my partners and my son and daughters.  They have been my rock and not sure that I would have gotten through without them.  Work has been amazingly supportive but I feel like lately their patience has run out . “