This is something I read a long time ago that I have shared with friends and it seemed to help some understand this illness. I don’t know who wrote it, I wish I did, I’d love to thank her or him. (I recently found out…see comments, 9-5-2012….that Tina McDonald is the author of this essay….Thank you Tina for speaking for us!)
Please Don’t Judge Me
Life with Meniere’s Disease : Before you judge me on one of my good days, you need to understand what one of my bad days is like.
Tinnitus – imagine having a headache caused by a fire alarm ringing or a bee buzzing in your ear continually for a long period of time. You can’t hear anything but that fire alarm or bee – It drowns everything else out.
Vertigo – Now imagine yourself as really drunk or with the flu at the same time as the fire alarm is going off. Now imagine that with these two things, you’d be dumb enough to get on one of the super roller coasters that does loop-de-loops or the amusement park rides that spin in two different directions at the same time. I’m not that dumb, but unfortunately I have no choice in feeling these sensations.
During one of these vertigo attacks that can last from several minutes to several hours if not days. I can’t keep food or water down, I can’t walk, and in order to get out of bed to go to the bathroom, I have to crawl like a baby on my hands and knees. The movement makes me so ill, if I’m able to crawl back to bed, I’m covered in sweat from exhaustion. Otherwise, I keep a pillow and a blanket at the bottom of a linen closet in the bathroom so that I can pass out lying across the bathroom floor. I end up sleeping for days after one of these attacks, only getting out of bed to go to the bathroom or to get something to drink, if I think I can keep it down. I have to call my family to see what day it is when I wake up. That is, if I can hear.
You see, this disease while playing havoc with your balance and equilibrium, also reeks havoc with your hearing. It wouldn’t be so bad if the hearing loss was constant and predictable. But no, one day I can hear conversation fairly OK, and the next I can be virtually deaf, then the next day I can hear again. The hearing loss can fluctuate, but is usually progressive, and many with the disease end up severely hard-of-hearing or deaf.
Even on a daily basis, your mind is so confused by the signals it’s getting from your ears that your balance sucks. You run into things constantly because you can’t balance well enough to avoid walking into things, or your mind is telling you the object is a couple of inches from where it really is. I don’t know whether to laugh or cry when someone teases me about being such a klutz. I could make the Keystone Cops look graceful.
I also have days that my coordination just doesn’t seem to be together. I’m carrying something, and all of a sudden I drop it because my brain seems confused as to whether my hand is really attached to my body. I sometimes miss a step and fall because of the feeling that my legs are not quite part of me and I have to focus on them to realize they are there. Apparently this happens because the part of your brain that recognizes parts of your body as belonging to you is the parietal brain lobe and it sits right above your ear, so if the nerves around your ear are inflamed, it can press on this part of the brain, or send the wrong signals to it (I’m not quite sure which), and you can lose coordination.
Ironically, the few high frequencies I don’t seem to have a hearing loss in can sound extremely loud, unbearably so. When a baby cries, an alarm goes off, or a microphone gives off feedback, I’d be willing to climb up a wall to get away if I thought I could make it. This symptom is called recruitment.
The disease also plays tricks on your vision. For some strange reason, the nerve that goes from your inner ear to your brain also controls some of your eye movement. Your eyes can twitch or bounce constantly, making focusing on objects, much less print, extremely difficult at times. Your eyes tend not to be able to “track” movement at the same speed, giving you double vision, and a bad headache.
You can get confused easily and your memory and concentration aren’t reliable. It’s what some people with the disease refer to as “brain fog”. Many of them originally were afraid that they may have a brain tumor or Alzheimer’s because it can sometimes gets so bad. Finally they find either a doctor whose very knowledgeable regarding the symptoms, or they happen to ask someone else with the disease, and find that this too is a symptom of this blasted disease.
Now try to imagine living with this disease never knowing when one of these periods of tinnitus, vertigo, hearing loss, double vision, lack of coordination, recruitment, disequilibrium, or “brain fog” is going to hit, or how bad it will be. At least with being drunk or riding an amusement park ride, you know what’s causing it, and you can make the choice not to do it again. With this disease, there’s very little warning if any for these attacks, you don’t know what’s causing it, and there’s no cure – only devices, surgeries, and some medications that can somewhat help alleviate the symptoms. And some of the surgeries are so radical, you think they came from a horror movie about a mad doctor. My ENT surgeon won’t even perform any more surgery on my left side, since I have the disease in both ears. He’s concerned about what would happen if my right side became worse than what my left side is now.
Understandably, anxiety and depression seem to go hand-in-hand with Meniere’s for many sufferers. We often ask how much worse can this disease get? For some strange reason, doctors aren’t very willing to give out worst case scenarios.
Now decide if you think I’d be able to do the same things you do on as punctual and regular schedule. For me, there’s no way. I’m being up front about my limitations. I try the best I can at living up to my full potential. Could you if you were in my shoes? They think now that Van Gogh suffered from this disease, and he cut off his own ear trying to escape it.
Yet on my not-so-bad days I may look like a totally healthy, able-bodied person. You ask me “why can’t you bend down – pick it up – lift it – drive – get a job – walk without a cane” It’s because I know these things can either bring on an attack – I couldn’t do them on a regular schedule because of the symptoms – or if I did do them, I could put myself and others in jeopardy if I should have an attack. You have to realize that with my friendship, love, dedication, and loyalty comes the fact that I can’t decide when I’m going to have a bad day, and the more stress I’m under, the more likely I will have a bad day.
So, please don’t judge me unless you’ve been in my shoes.”
(Of course, part of this is personal to this person’s situation, but it hits pretty darn close to mine. I don’t walk with a cane, because I don’t feel like it helps. I do find that a walker helps when I get dizzy. It stays steady. A cane just falls with me. And of course, you all know that I do have some hope that things are going to get better because of fixing the CSF imbalance. However, It doesn’t look as if my right ear will regain it’s hearing and it looks like I will always have tinnitus in that ear too. I’ll be very lucky if that’s the only symptoms that remain.)
I hope this little essay helps you in some way. If you are a friend or family member of mine, perhaps it will help you understand me a little more. If you are a fellow sufferer, perhaps it will help you in explaining things to others.
6 thoughts on “Please Don’t Judge Me”
I absolutely love this. I don’t fit everything, either, but oh, man. I may be borrowing this tomorrow!
What a wonderfully articulate way to describe what happens and how the disease affects people.
Definitely something to pass along so that others may understand a little better the various things that can happen to us.
I really like this story about having Menieres. I have shared it with friends and family because it tells alot about how life can be. I just read about “The Spoon Theory” linked on http://fleetlydreaming.wordpress.com/. This also tells about having an invisible illness. I will link that story, too, to my family and friends and whoever asks “How is it?” It´s hard to describe in words.
I am the author. I would appreciate if you gave me credit. I gave permission to Dr. Alec Salt to publish it, which he did so without my name due to HIPPA laws and the University’s lawyers. Although He wouldn’t post my name, I do have the original email as well as his personal private acknowledgement.
Sorry about the curt comment before. The Social Security disability recertification clerk found it ALL over the web and thought I’d lied. Had to show the not from Dr. Salt before they’d believe me. Apparently a lot of people are acting like they wrote it.
Tina, No problems. I said when I first published it that I didn’t know who wrote it, and would love to give them credit. Thank you for speaking out for us. good luck in your future. wendy