I wonder if you would mind explaining what you base that on? Do you mean that - as an alternative - some kind of oral medication would (possibly) be safer? Or something else?
hi there.
by all means... as i said: it´s me and the needles when it comes to
tinnitus. Here we have guys with some weeks of T. what is that? well.... nothing. How can they even know what´s going on and yet they are rushing for some trial treatments. Understandable but also worth mentioning that it´s good to calm down a bit...
Should there be the "C" (cure) with some ear injections, yes i would take it if it´s
101% certain. Before that i wouldnt bother. All the others are free to inject anything they like into themselves.
One doctor recommended gentamycin injections for me.
http://www.dizziness-and-balance.com/treatment/ttg.html
Mr. Meniere likes to spin me around for hours sometimes.
and
in many cases those shots actually do some tricks to vertigo attacks, yes indeed. but I am not going to take them. Again, its me and the needles. A needle into my head is like a phobia to me. I´d rather suffer some vertigo attacks every now and then.
Trial pills? that depends on adverse effects.
I take betahistine for Meniere´s but it seems totally harmless and i find it hard to see if it´s helping at all.
And again: all the others can do whatever they like. It´s great that some are willing to volunteer. Respect and hat tip to that.
So it seems to me that enlisting in the trial would in the worst case scenario end up with a status quo result; best case, an improved result. Would you agree?
I wouldnt agree.
again, that´s just me. worst case scenario? T gets worse or some other, new problems appear. I have just enough ear-related problems for me. T is just one of them. In many ways i am in the wrong forum but i see Tinnitus as my main tormentor.
I have lived with tinnitus with some 20 years soon. It was the new T2.0 which was summoned with Meniere´s that got the best of me last year. Had someone told me years ago what is ahead with this disease of mine.... i wouldnt have understood.
my T is sometimes like a fog horn or a jet engine with a dog whistle flavour in it. It´s so loud sometimes it´s hard to actually
see with my very own eyes what´s in front of me since the brainfog hits and i get tired too easily. It´s like a curtain of smoke pulled down i have to try see through. The longest phase with this lasted some 10+ weeks. I started hearing noises. I became angry and felt hopeless to the point of suicidal thoughts. I was "done". MD gives these kinda periods... the duration is unknown when it starts. Could be a day or could be months.
Finally it calmed down to what i like to call my base camp. Not symptomless, T there as always, pressure in the ear with some mild feeling of pain in the inner ear or somewhere there, but i can manage this somehow. During those hellish week the best is to lie down on a sofa and try to gather some energy to move on. cant lie down for weeks so it makes life a bit "interesting" sometimes. But that´s another story.
Took myself some years to get used to that normal, basic T back in the days. People do habituate to it. I did, too.
The first weeks are the worse, naturally. That´s why it´s good to try stay calm.
To my new T i cant get used to anymore. i know my limits and capabilities with T and Meniere´s all too well.
i just try to get by somehow day by day. What has helped me the most with MD is time, talking and perhaps the AD-pills called buprobion hydrochloride. MD has been a total game changer for me.
All the best and a happy new year.