RE Train announcement and other things 
Monday, May 7, 2007, 12:13 PM
We went to London over the weekend and for the first time in my life I heard a part of the train annoucnement.

It said Ladies and Gentleman blurgh baaa blurg blurg!

Even so I was shocked that I head the start of an announcment in a busy noisy area. Who knows, one day I might even hear the full announcment!

Birds and purring also seem loud and rich sounding these days. As does a rather large cat falling of the fence :eek: It actually sounded rather painful...

I now hear the hands free phone in the car depending on who is speaking (ie not my brother who mumbles - but any one else seems fine)

RE it just gets easier 
Saturday, April 28, 2007, 11:22 AM
I am still using the phone at work. I have noticed that I am able to hear my voice a bit more now. I think itís because I have got use to the difference in the phones and I just pick up the sound of my voice a bit better now.

I still have trouble with names of people and places - but this is getting much easier - the more I practice the easier it gets. I have got people to spell things out - which sometimes works and sometimes makes it harder - I really need to be more honest with people from the start of the call and explain that I am hearing impaired - but I find this really difficult as most of the time I am speaking to people who have never met me.

Batteries going in the middle of convos are also an ongoing problem! Due to the amount of batteries I get thru in a week I worry about losing the dead ones and a child swallowing them :eek: so regularly clearing out my bag is a big thing.

As I am still new in my job people do not know how to cater for my needs. They see me speaking on the phone, answering things without lip-reading and assume that my hearing is very good.

The other day a women asked me a question with her back to me and normally I would hear her but she was standing in a funny position where she was pointed away from my processor side - and I was not able to position myself so that the processor side could be pointed at her - so I kept missing what she was saying. She was also talking with her hand over her mouth which made everything muffled. I had to take her a side and explain the difficulty and why I was not hearing her as well as normal. She was very embarrassed and I was a little too because we both know that she had not meant to be insensitive in anyway - more that she just did not realise that I am still moderately hearing impaired even if I am able to use the phone.

I also had a funny situation where one person introduced me to another person who did not know me. As I turned away to say hello I missed the name that was said so it got repeated. The new person said "you donít have to repeat yourself" and got told " well ZoŽ is deaf" she said "ah, well I am well known for putting my foot in it - nice to meet you!" made me laugh sometimes it seems politer to say "I am deaf" before "Hi I'm ZoŽ!" when I was younger I used to think that my name should have been "I'm deaf" as that was all I ever seemed to say when I met new people!!! Itís a bit of a mouth fall to say Hi I'm ZoŽ and just so that you are aware I am deaf." When you first meet someone.

I was readly Ivan's blog and he really hit the nail on the head when he described "{not hearing ] new sounds anymore, but what I do get is a greater 'roundness' and fullness of sound"

For some time now I have noticed the same thing - but could not put it in to words how to describe that I am hearing things in a way that is different to how I first heard them. Some how they now sound more like the sound than they used too. Everything has a richness to it and the mechanical edge that used to be there has gone.

I hope he finds the info about the cam shell mobile useful - I find using this type of mobile is much better and clearer than any other mobile. Some mobiles are terrible for interference and these should be avoided - I am able to use my cam shell both with the T and without which goes to show there is no need to suffer the interference - just change the mobile!

I know its stupid but I find myself saying the words " how did I get by/ cope with out the telephone with my job" I know I did - and at the time I thought it was easy to do. But now I look back and think Jeeze " how on earth did I do it?" and to be honest I dont know, I must have been more out of the loop than I fully realised - maybe I made the most of Email/ fax and depended on others to make calls for me. My confidence is really growing as I feel less dependant on others and more able to do my job. I can keep up in meetings much better.

The only down side - is I am shattered after big meetings or if I have been to more than four interviews in a day. The effort of listening is still very draining on my brain and sometimes I feel so tired that I have to go to bed early to get some sleep so I can be fresh for the next day. I am sure as my brain gets use to working this hard, I will start to feel less tired.

RE Info about Microphone protectors 
Thursday, April 19, 2007, 11:32 AM
I wondered what the Microphone protectors were for as they did not seem to need replacing like any other part of the processor.

Someone told me that you could change the colour of them - to give it an individual feel - but I felt that this was not really the main purpose.

SO! I went and asked on of the hospital staff - they did not know!! Eventually I found someone who did know - apparently it is exactly what it said on the box - it projects the microphone. If you work in dusty places then you might need to change it more often. The paper in it goes from white to dark grey/ black. If you work in an office then you might need to only change it once every 6 to 12 months.

Of course I had to then have a look at mine because itís never been changed - so I took the dish off and unclipped the protector and it looked fine. Only then did I realise that as I took the dish off the pin had not come off with it and this was still in the processor. I thought it had come off to easily! Normally I find the dish fine to put on but a bugger to remove. *sigh*

The only thing I am a bit surprised about is no one ever said anything about checking that the micophone protector is clear as it can affect the quality of the sound if it gets dusty.

Luckily I have a spare dish and I had to request another.

Sometimes I donít know why I just donít leave things well alone!

RE I started a new job 
Tuesday, March 13, 2007, 04:32 PM
I started a new job on Monday, my new office has a large number of people in it. So many names to remember! :uh:

One of the things I noticed was the very newish posh looking internet phones they have. I decided that I should at least test one out before asking if my own (beloved) BT land line phone could be plugged in somewhere.

I went down to the reception to explain what I was doing and that I needed to test it out. So when they got an odd call it would be me! :lol:

Lucky that I did warn them as they would have thought they had a dirty heavy breather down the line :eek: as for the first few min's of the call I was pushing the volume as I could not hear a thing. Then I head a faint worried "hello?" The phone was very cool as I can get it to go a lot louder than I need to.

Must remember to turn this down eventually though when I leave the position or it will burst someone's ear drum! :ooer:

The only draw back is I canít hear myself very well. With the BT phone I can hear both. With this phone I can hear the speaker very well indeed.

I have been making calls all day. The only thing I have found is that I lack confidence to know if I have heard correctly ie names and addresses. As I do not have a log in code for the computer yet I have to check the post code etc on the map for most part I get it correct or close to correct - :clap:

So itís worth persevering with as it will mean I can answer any phone in the office which is a rare luxury in deed :cool:

Although I am hearing very well I still like to be able to see everyone who is talking. So in a large group if a person is standing between two other people blocking my view I do not hear as well. (this normally tends to happen when I am not actually part of the conversation but I have heard something that has triggered my interest and made me look up and attempt to join in - this is not something that ever used to happen so as a consequence I would be quite isolated or behind slightly on current topics or office news) My new team are very deaf aware as I have observed them gradually moving themselves in to a position so that they are no longer blocking my view and I can see everyone, without being asked or making it a big issue. It is a big issue for me as they are so discreet about it that I always make sure I give them my biggest and best smile of :thanx:

I have already been asked to join the night out with the team and I have only been here two days! I think I am going to like it hereÖÖ

I have also noticed the different way people pronounce things and I am starting to ask if the way I say things are wrong or if its just a dialect thing ie

status = "stayus" or "stat us"

is one that I am hearing a lot on TV right now.

re private health insurance 
Monday, March 12, 2007, 04:50 PM
I have collected my letter from my gp and just need to send it off to my private health insurance wish me lots of :luck: as I think I am going to need it.

Plan B is that we have friends who play the lottery - they have promised me that if they win big time they will pay for my second implant :ooh: awwww

Plan C is that I start playing the lottery myself! :lol:

RE Rice Crispies 
Friday, March 9, 2007, 02:04 AM
Today I asked my partner if rice crispies really made a sound like the advert claimed. He nodded and held the spoon full of crispies up to my ear

I heard :eek: pop crackle and snap :clap:

How cool is that!

My other half continues to fluffle and fart to his heart content, so even if I dont smell it :eek: I do hear it... very clearly there is even such a thing as a *whisper* wet sounding fart... ewwwwwwwwww :ooer:

RE Hi ya Dawn 
Tuesday, March 6, 2007, 04:26 PM
Hi ya Dawn

I decided to post this in a new entry as you asked so many questions :eek::lol::ahh:

1) The type of phone I use

I use the BT Converse for all my landline calls as its hearing aid friendly and has a volume thingy. I have two, one which I leave at work.

Some people find that they dont have any problems - but I find most other phones give me nasty feedback and I can hardly make out the sounds of the person speaking.

2) The difficulties with Typetalk
I used to get that problem with people saying that they were too busy. If it was work related I would say ok before you hang up I would like to remind you of the Disability Discrimination Act 1995 and not taking my call is discrimination so can I have your full name, the name of your manager/ supervisor and their number please as I would like to make a complaint.

For some strange reason they always made time to take my calls from then on. The ones that made me cross was the ones that hung up on me before I could reply. I always made sure I got a name so I could call them back to give them my rant....

Even worst were the ones who would say oh I will transfer you to our disability team and I would say NOOOOOOOooo itís YOU I need to talk too!! Grrr!

I have not used typetalk since the implant has been switched on. My mobile which was typetalk compat died and T-mobile had stopped doing it. I would have to buy a new mobile with Vodaphone and the nokia is just to expensive (they only last me three years max)

3) not posting on the blog much

Sorry for not posting enough for you! I only post when I have something implant related to say and sometimes there is not a lot to say!!

4) Rechargeable batteries

I have been told I can buy these if I want to use them - but the NHS are not supplying them just yet. (jeeze)

I have a feeling that if the maps are like mine (ie take a lot of power) rechargeable batteries might not be the best thing as I change my batteries every other day.

But it still would be better than carrying dead batteries around with me. I am scared that one day I will drop one or something and a small child will eat it :eek: So I like to only throw mine away at home. My local hospital have a strange policy where they like the hearing aid batteries back but donít care about the implant batteries. So I throw mine in our bin. I donít think I am meant to tho....

5)Second implant

I have not met anyone who has had a second implant. I have heard of a number of people who have had a second implant and recommend it. They were the lucky bug*ers who were invited to take part in a pilot study to see the effect of a second implant.

I have tried to encourage the Manchester programme to do this pilot study again but they have flatly refused to do so - which I think is plain selfish!

The research states that a second implant will not be as effective as the first one - well durh.

I mean a consultant does not say to a person who needs laser treatment on their eyes - "Right research has shown us that the second eye is not as effective as the first so we now only do one."

I mean can you imagine people accepting that and saying "oh yes I can see your point totally" DOH! No one is going to agree to only have one eye done - "itís bloody cost cutting con they would scream!"

Research will say what the NHS wants people to believe when money comes into play.

I believe that while it may be true that people who have one implant at the time done - may find the first one enabled them to hear much better in terms of what they could hear with hearinga aids. The quality of the sounds they hear with a second one would be able to provide, should not be ignored.

I believe that if people are implanted with two at the same time - which some countries do. Then this research is shot to bits.

I strongly believe that I am at a disadvantage only having one implant.

Oh gosh that reminds me I went to the GP last week and forgot to go back and collect my letter to give the private health care place!:eek:

Must do that tomorrow!!! :thanx: for reminding me :cheers:

RE Improvements 
Sunday, March 4, 2007, 04:50 PM
My sweetie is working away at the moment :waah: itís kinda boring without him here. It's also kinda spooky. Now I can hear things quite well if an unexpected sound occurs it makes me jump :uh: Sometimes I can't figure out where it is... Sometimes itís outside ie arguments or kids throwing things and fighting! :uh: I've taken to leaving the light on in the hall when I feel scared :ooer: coz it makes me feel better :uh: when I am off to sleep :zzz: Hopefully potential burglars will think oh she is still up I wont break in....

I have noticed these days when I am shopping - sometimes I can really hear the music and almost get the lyrics. I canít quite make out what is being said but it's so close.... I am starting to think that eventually I will be able to make it out. I really should step up a bit and start turning on the radio for further practice as it really does make a difference.

I have watched a few documentaries on the TV that have not been subtitled and found that I am not doing to badly. I have also noticed that when something is really poorly subtitled I tend to notice as I am hearing what is said - and its nothing like the subtitles!


I am starting to hear the land line much better than the mobile now - I am not sure why this is - and can't decide if I need my maps relooked at.....

RE Referal 
Tuesday, February 27, 2007, 04:33 AM
I have been to the GP today to request a private health care referral for consideration to be made for a second cochlear implant. The GP was very nice and has arranged for me to have a copy of the letter to give my insurance within the next two days.:yay:

Just have to see what happens from there....:wiggle:

I requested information about the new mini processor and was told in very blunt terms if you want the mini you can buy it yourself.

I donít really understand this attitude as surely it would be better for the NHS if I only used two batteries in said of three?

How would I get repairs/ insurance/ updated maps on a private processor Ė the NHS would refuse to touch it. They already refuse to touch hearing aids provided by other NHS Trusts Ė so I dread to think of the problems that I just know would occur.

But there you have it - it looks as though the mini is not going to be available on the NHS.:waah:

RE Ear Mould 
Sunday, February 25, 2007, 05:21 AM
Ok, it does not fit well! :uh::sad: it squeeks a lot and worst it hurts! :sad: So I am back with my old ear mould and off to the hospital to get it redone. *sigh*

On a more postive note depending on your point of view!:

I can answer my partner's belly grumbling :eek:

I can (ew) now hear him actually make a nasty fart

I used to stand outside the door and talk to my partner when he was in the loo (coz he always rushes in there when I have something I just HAVE to know!) Not any more

I can hear people taking a tinkle if I stand to close to the door! :eek:


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