The last post (for a while anyway)

I’ve decided to take a bit of a break from blogging.  When I started More Than A Bit Deaf in February 2016 I thought I’d keep going for six months, or perhaps a year.  It’s been longer than that and I’ve reached the point (54 posts later) where I feel in need of a blogging vacation.  Rather than a long list of topics jostling for attention in my “ideas” folder it’s more “hmmm, long overdue for a post – what can I say that I haven’t said before?”  So time to stop for a while.  I don’t want to bore you.

I am keeping the site, in the expectation of returning at some stage, so please don’t unsubscribe if you might want to hear from me again.  I’m also planning to still occasionally write for other deafness/hearing loss media and (with a bit of luck) they might sometimes publish things – so keep an eye out.

THANK YOU for reading.  Thank you for the feedback; whether that’s comments on the blog, or e mails, or talking about it when you see me.

To people who can hear – the best thing has been people telling me they understand a little more about what hearing loss is like.

To people who can’t – those of you who’ve said I’ve managed to capture some of the things that YOU experience and feel have given ME a big boost.

Au revoir then.  See you again.

Here I am, heading off down the lane for a walk with Izzy



Ratchet up the bravery setting

One of the best things I’ve read about deafness recently is on the SayWhatClub website.  Michele Linder and Chelle Wyatt (Michele and Chelle) write posts about lip reading but, as they rightly point out, you can’t lip read unless people are looking at you, speaking at a reasonable speed, standing in a good light (and so on) and THAT doesn’t happen, more often than not, unless we take charge of the situation and ask for what we need.  So their latest post is less about the mechanics of lip reading and more about how comfortable we are (or are not) with our hearing loss and making other people aware of it.

That’s a big topic.  Continue reading

Eating whilst deaf

Copyright: bbbar / 123RF Stock Photo

I probably wouldn’t be big on eating out even if my hearing was good (I love to cook) but meals out when you can’t hear certainly have their challenges.

Problem one – Busy, noisy pubs, restaurants and cafes with lots of hard surfaces for the sound to bounce off (tiled floors, tables without table cloths, windows without curtains).  It’s hard to believe the difference that soft furnishings make to speech comprehension if you have hearing loss, but it’s true.  They absorb a lot of the clatter and make speech much easier to understand.  Open plan restaurant kitchens are a particular disaster – all that rattling of pots and pans and the shriek of the coffee machines.  I’m picturing Pizza Express as I write this.  I like Pizza Express, but the acoustics can be terrible.  Continue reading

Bing bong

One minor casualty of our building works is that the doorbell stopped working.  It was at least twenty five years old so it didn’t owe us anything, but it had an excellent sound for me – a deep, long, loud buzzing – and it was a shame to lose it.  I resolved to look up what was available in the Action on Hearing Loss catalogue but before I got round to that a couple of minor problems occurred.  Nigel left his keys at home one day and had to resort to ferocious banging on the front door to get my attention (scarred by previous experiences, he knows there is no point knocking politely).  Continue reading

Deaf at the dentist, and other random things that have been going on

Copyright: maximillion / 123RF Stock Photo

Recently I had a check-up at the dentist.  Dentists’ surgeries are not hearing-loss-friendly environments.  The main problem is the dentist’s mask.  Lip reading?  Impossible.  Then there are all those hygienic hard surfaces, perfect for creating a noisy, echoing environment and disastrous, therefore, for making sense of speech.  Also presenting a challenge are the plastic goggles they give you when water-spray equipment is being used in your mouth. Continue reading

Tips for hospital waiting rooms

Copyright: neyro2008 / 123RF Stock Photo

Last week I had my follow up appointment at the Ear Nose and Throat Department, after my blocked ears saga.  The outcome of the visit was that I was referred for another cochlear impact assessment, of which more in another post some other time. Today’s post is about the process of waiting and queuing,

I arrived at the hospital incredibly early because parking is a nightmare.  Public transport isn’t an option.  From where I live it would mean taking two buses and one train, with a probable journey time of about two and a half hours each way.  That’s if you ever got there at all. Continue reading

My thoughts on Parliament’s adjournment debate about NICE’s cochlear implant rules

Whoah – what a long title.  Today’s blog comes to you courtesy of the Limping Chicken – the world’s most popular deaf blog, laying eggs every weekday.  Last Friday they published my post on the above (thank you Limping Chicken).  Here’s what I said…..

It’s not often that Parliament debates deafness, so Friday 24 March was important; an adjournment debate* discussed whether the current rules set by NICE, the National Institute for Health and Care Excellence, are preventing some adults who would benefit from a cochlear implant from receiving one. Continue reading