Meniere's Disease - First drop attack
Posted , 16 users are following.
I've been diagnosed Meniere's for about 3 years, the usual hearing loss, tinnitus and dizzy spells but recently experienced what I think was my first 'drop attack'.
I was lucky to be sitting down watching TV when it felt like the room had been turned upside down. I yelped and grabbed at the sofa for support. Very quickly I felt OK, but then slowly went into a dizzy spell and vomited.
The dizzy spells I'm used to, but the sudden rush of movement was terrifying. I think I've previously been lucky as my spells of vertigo have been infrequent.
My initial treatment for Menieres was to be prescribed serc-16 betahistine dihydrochloride tablets and then later I entered a medical trial for a new drug called OTO-104 containing dexamethasone.
My main concern is driving. I haven't driven since the attack and am concerned that I will never be able to drive again. I have read that drop attacks come in bouts in later stages of Meniere' disease so I'm waiting to see what happens next. I have not always been careful about salt intake and prior to the attack had eaten salty pork and drunk quiet a lot of red wine, probably a big mistake. I'm now being more careful about my diet and hoping for the best.
I am waiting for an appointment with my ENT consultant to discuss the drop attack, but having found this forum wondered what other Meniere's sufferers experiences of drop attacks had been like.
1 like, 30 replies
adam50210 david24820
Posted
Hi
Although I a man currently going through a bad spell of Menieres I've had mine about 5 years now, touch wood I've never had a drop attack and I've been put on 32mg of Betahistine 3 times a day since Friday, although this seems to have had little affect.
How often to do you generally get attacks of vertigo and did the OTO trail have any benefits as I was supposed to be on this but couldn't attend the appointment
Thank you in advance
david24820 adam50210
Posted
Full attacks which I would describe as room spinning and feeling nauseous have been rare since the trial. I hadn't had a lot before the trial, but was hoping for some improvement in the tinnitus and hearing loss in my left ear.
The problem with the trial was that they would not let you know if you'd had four injections of the drug or two as some people on the trial were getting a placebo. I was offered a further two injections that were the drug, so I either had four or six doses.
The last of the injections were at the beginning of the year and until the drop attack a couple of weeks back I had not had any full on vertigo this year. I had had some mild spells of dizziness but not like a full on attack. My hearing and tinnitus have got worse if anything. I was told others on the trial had felt much better after, this might of been because they were having more attacks before. My lack of attacks this year might of been down to the trial, I don't know.
I'm currently not taking any medication and waiting to see what comes next.
Questor david24820
Posted
David, I can't tell from your post where you live. I had thse episodes when I was first diagnoised 10 years ago. The Betahistine, (SERC) stopped that completely. I continue to have what I call wonkeness along with all the other symptoms. I do drive and can actually drive well even when feel dizzy. Please look up Dr Michael Burcon on Facebook and/or utube and watch his videos. I see an Upper Cervical Chiropractor on a regular basis and am convined I wll have this care for the rest of my life! Good luck these symptoms do suck!!
david24820 Questor
Posted
I'm in Gloucestershire. I have driven while a dizzy spell was starting because I was stuck in traffic and not able to pull over. The drop attack was a totally different thing as it was a sudden rush as if I had been shoved. I think had I been on a busy road I would of suddenly swerved to a halt possibly causing an accident.
I've printed off the dvla form and it asks if you would have sufficient time to stop your vehicle safely - I would have to enter no and I'm sure this would mean they would take my license away.
My hope is that this was a one off attack and I can prove that over time.
What benefits are there from seeing the Chiropractor and what's the link to Menieres?
david24820 Questor
Posted
Questor david24820
Posted
Thats why I suggested you see DR Burcons indormation. After treating hundreds od Meneir's patients he and other Upper cervical chiropractors have concluded Meniers is the result of an whip-lash injury...something that probable happed to up many years ago and maybe you have even forgot about.The head now does not sit on its Axis correctly and after years with the body while trying despartely to over compensate thes symptoms emerge.Just watch and listen to what he says. People are coming from around the world to seek treatment. He statement is "Every parient I have seen has had some kindof an injury, probably 20,30, or even 40 years ago and then Menier's symptoms happen." Not everyon with an injury develops Menier's but every patient I have treated has had an injury." I encourage everyone to at least read his studies they are all online and he has traveled all over in an attemp to educated not only ENTs but other practioners who remain so ignorant. Please read its free and convenient!!!
marilyn74554 Questor
Posted
I have had Menieres off and on since I was 18 but in the last 5 years attacks have got a lot more regular and intense with significant hearing loss and tinnitus. I am now 63 and have been on betahistine for 2 years. I have sort of resigned myself to having this disabling disease.
However your post has given me hope! I had a bad car accident when I was 18 resulting in 6 weeks physio for severe whiplash. The same happened in 2006 and in 2013. The last accident was the worst and despite the physio, I have had neck pain almost continuously since. This does seem to relate to my menieres activity so I am going to seek out a chiropractor locally. I will let you know how I get on.
Questor marilyn74554
Posted
Good luck!
Lizzie1453 david24820
Posted
david24820 Lizzie1453
Posted
That sounds like what happened to me. I'm assuming that if I had been standing I would of fallen over. I think we were lucky to be seated.
tanney david24820
Posted
adam50210 tanney
Posted
That is one of the most informative posts that I have seen on all of the websites I've searched looking for answers.
At least there are options and although a terrible condition to live with, there is possibilities to improve things
Thank you
david24820 tanney
Posted
Thanks for the information. I've had the steroid injections and am nervous about going any further with the destruction of the balance function, but am desperate to drive again.
sharon17905 david24820
Posted
Lizzie1453 sharon17905
Posted
I have never sweated like that in my life. I went to the front door for fresh air thinking it would help and the street & cars were moving up sideways . I crawled upstairs....
Lizzie1453 sharon17905
Posted
Ps Sharon, if it's hot we have takeaway or microwave as a hot kitchen makes me ill.
catherine_8 sharon17905
Posted
So appreciate the fact there are others who deal with these horrid symptoms. The profuse sweating is my clue I had better take my Antivert and Ativan tablets ASAP, a head to bed. This crazy disease rules my life. I can actually control the vertigo and drop attacks by staring at an object, not closing my eyes. It is hard as my eyes want to keep moving. If I let my eyes move a full blow attack will take over. So I hold onto that object with my eyes. This technique helps to stabilize my brain and calm things down. It works! Try it sometimes to see if it helps you. Unless you have experienced these crazy symptoms, no one can really grasp what you go through. Hang in there. You are not alone.