Balance issues/Ménières?
Posted , 6 users are following.
Several years ago I was told I had labyrinthitis twice. The first time I had it, it took 6-8 weeks for my balance to return to normal. The second time it never really returned to normal and has been at a level where I’ve had to put up with it as medication and balance therapy have not helped. I have constant tinnitus in the form of ringing in my left ear and some hearing loss at lower tones. More recently I’ve experienced sinus/head/cheek pain on the side where the tinnitus is and my balance feels worse. I also have an enlarged lymph node on that side of my face that has been like that for 2 years (scan confirmed nothing sinister). The doctor said it is Eustachian tube dysfunction and I’m being referred to a specialist. I don’t think I have M.D. although it has been suggested as a possibility a couple of times, but my symptoms aren’t as disabling as many of you describe. It’s enough however to have an effect on my daily life and has caused me to have issues with anxiety. I guess my question is whether M.D. is always severe or can it be present in a more moderate form? I get spaced out/fogginess quite regularly and I’m sensitive to light, both bright sunlight and artificial lighting. Certain environments seem to make the symptoms worse - busy places with a lot of movement, patterned carpets etc. I also suffer with terrible travel sickness.
0 likes, 10 replies
ruth17826 klwpvfc
Posted
Mine is currently severe - off work for months, at one point daily vertigo attacks lasting 10 hours, now down to 3-4 attacks a week lasting 4-6 hours. All these attacks really do affect you balance, and the best thing to do to restore it is to walk about - even if you have to build up very slowly.
And no it's not always this bad, I can have months or even years where I feel perfectly fine. The month before it became bad I'd been on holiday in France, and had 2 short breaks in the UK. I'd been on trains, planes and buses, and walked miles some days. Without warning it exponentially got worse, and at some points I've been totally unable to leave the house.
I was diagnosed about 10 years ago, and this is the only time it's been like it is now. I'm having steroid injections but no lasting improvement yet
klwpvfc ruth17826
Posted
john02577 klwpvfc
Posted
klwpvfc john02577
Posted
I guess I thought it couldn’t be that as I don’t experience the symptoms to the degree a lot of people are describing. I’m due at ENT at the end of the month so I’ll see. Sorry to hear that yours is so awful, it must be difficult to deal with that on a regular basis.
judy2018 john02577
Posted
christine_35821 klwpvfc
Posted
klwpvfc christine_35821
Posted
I had a couple of attacks like that but it was several years ago and I was told it was labyrinthitis. Ordinarily it’s more of a disorientation/imbalance which affects how I go about day to day life - walking next to a wall to feel secure, needing something to hold onto if I’m standing still in one place, struggling with busy public places etc. I have some hearing loss at lower tones.
Freezeframe klwpvfc
Posted
Hi! I am in a somewhat similar situation as you. I am not suffering as badly as some of our other MD sufferers, but my life has been substantially impacted. Uncertainty of attacks, limited driving, days of little productivity.
I have tinnitus in both ears, suffer an occasional to regular vertigo attack ( my external environment becomes quite unstable, and objects move a little) and spend most of my time in between vertigo attacks recovering (feeling light headed, dizzy and unsteady gait). It takes me a few weeks to recover from the Vertigo attack. I don't get nausea, or fullness in the ear.
I have been tested by Neurologists, Dizzy Clinic, ENT and they wont diagnose Meniere's with any certainty. There appear to be some common patterns in both diagnosis and management of Meniere's ie: tinnitus, vertigo are commonly occurring symptoms and low salt diet is deemed to be universally helpful. However, I think Meniere's tends to be variable, individual, and its effects on a person in a spectrum from mild to severe Just as its management is as individual as the person experiencing it.
At the end of the day, I have taken the perspective that it is all academic and I work on managing my day to day experience. I am currently not taking any medications, but manage my diet, stress, exercise and tiredness I'm not sure I've got it right as yet, but keep on trying to find what helps until the silver bullet arrives.
It would be a good idea to get a couple of specialist opinions as a baseline and then work out a management approach.
All the best
Freeze Frame
klwpvfc Freezeframe
Posted
judy2018 Freezeframe
Posted