The replies to my "Two year" post a couple of days ago were really
fabulous, a big howdy to you all. If you're new to this group and
you've never come across these names, they're some of the most caring
people you'll ever have to privilege to meet. The huge thing about it
is that none of them need to be participating on this group, not
anymore that is, as they've all overcome what you as a newcomer are
trying to work out for yourselves right now. They are, however, here.
Maybe not always active and out in front, but they're here
nevertheless and many of them have big & strong shoulders available
for you to lean on.
The moral of the story is: they, like many others before them, have
found a way to overcome it. It's your turn to bat right now and as
utterly impossible as it may seem right now for some of you, you too
really will find a way to work it out and to come to terms with it.
The big thing for you to realize is that you are not alone, you are
not weird, you simply hear sounds others do not. I remember all too
well that it isn't easy at times. In fact, sometimes it was so totally
crummy that well... - no doubt you can finish this sentence for
yourself.
The weird thing is that some day down the road you won't even care
whether them nutty sounds are still around or not. By all means, you
should travel the medical path because who knows, there may be reason
for you to experience all this. If so, it may even be fixable and you
wouldn't want to rob yourself of that opportunity. In the mean time
though, keep living your life the way you're used to. Don't start
robbing yourself of the pleasures of life and stressing yourself out
in the process. Impossible, even ludicrous? In 1996 I would have
agreed with you...
Keep trusting yourself and don't loose sight of common sense,
Bart.
-
Check my most up to date email address at:
www.haruteq.com/contact.htm
awesome banjo bridges, tabs, stained glass:
www.haruteq.com
**may your moments of need be met by moments of compassion**
Skycloud - 04 Jul 2005 13:26 GMT
> The replies to my "Two year" post a couple of days ago were really
> fabulous, a big howdy to you all. If you're new to this group and
[quoted text clipped - 35 lines]
>
> **may your moments of need be met by moments of compassion**
Nice post. I'm a relative newbie (2rs+ now with T) but I back up every
word. What once seemed a sudden and shocking end to all value in my life 2
yrs ago proved to be nothing of the sort. I learned to evolve my own ways
to deal with the T. Today (unbelievably) it's become almost an old friend.
Either I've got so used to it I hardly notice it, or it really has
moderated.
This group too has been an interesting diversion for me, with its quirky
characters (I count myself among them!) and their unique personal
preferences on how to deal with tinnitus. The main thing is, you all mean
well. And that's what support is all about. Thanks for helping me.
Steve
RainyDaze - 11 Jul 2005 05:13 GMT
Bart V, it really is good that you took the time to post this message.
My Tinnitus started 4 months ago. I read everything I could get my
hands on. For the first two months I was so depressed that I didn't go
out except for work - stayed home on weekends and did nothing. I've
read what other people have written about the destruction of lives and
it really is extremely difficult to appreciate what these people are
talking about unless it happens to you.
Long story short I've seen an ENT, had an ear test which included a
sincere talk about welcome aboard to the 40 million people with
Tinnitus. Funny thing is, my Tinnitus rages (high pitched tones) and
If 40 million people have what I have, I can't imagine there isn't a
public uproar regarding Tinnitus research/potential cure. I surmise
that some people have it much worse than I have it, and for some it is
less in "volume."
And so now in the fourth month I was coming along well and then a week
ago I woke up to the T kicked up a notch. Same deal, more depression,
staying home again even though I have a million things I need to do,
and want to do. Very strange to want to do something, but feeling you
just can't deal with it - why bother. It really is difficult to shake
it off, but your words give hope.
Thank you.
tory is: they, like many others before them, have
> > found a way to overcome it. It's your turn to bat right now and as
> > utterly impossible as it may seem right now for some of you, you too
[quoted text clipped - 38 lines]
>
> Steve
Murray Grossan - 11 Jul 2005 05:21 GMT
On 7/10/05 9:13 PM, in article
1121055203.056255.4670@g47g2000cwa.googlegroups.com, "RainyDaze"
<myrainydaze@verizon.net> wrote:
> Bart V, it really is good that you took the time to post this message.
> My Tinnitus started 4 months ago. I read everything I could get my
[quoted text clipped - 64 lines]
>>
>> Steve
Patients with recent onset Tinnitus that increases often have cochlear
hydrops - a condition of increased fluid pressure in the inner ear. This may
respond to a diuretic such as methazolamide. You might ask your doctor about
this.
RainyDaze - 11 Jul 2005 06:28 GMT
Murray,
Thank you very much for taking the time to provide this information. I
will inquire about this.
Thank you.
> Patients with recent onset Tinnitus that increases often have cochlear
> hydrops - a condition of increased fluid pressure in the inner ear. This may
> respond to a diuretic such as methazolamide. You might ask your doctor about
> this.
Elly Byrne - 11 Jul 2005 21:20 GMT
http://eebee.net/TinnitusIsaPainintheNeck.shtml
Elly's Tinnitus Resources
http://eebee.net/
>Bart V, it really is good that you took the time to post this message.
>My Tinnitus started 4 months ago. I read everything I could get my
[quoted text clipped - 64 lines]
>>
>> Steve