So my family has started referring to my cochlear implant as my coc. Not entirely sure how to feel about that.
I've never had a cock before.

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So my family has started referring to my cochlear implant as my coc. Not entirely sure how to feel about that.
I've never had a cock before.
I’m thinking of getting a cochlear. 
Its truly amazing to see people with DIFFabilities compete in the Paralympics!
Their courage, their determination! The way they keep moving forward in life, not letting their differences hold them back.
Go Paralympians !!!
🤟☺️👍🇺🇲👨🦽👩🦽👨🦯👩🦯
Are you watching?
We are!
There’s always a strange sense of camaraderie when I’m in a group of hearing people and there’s one other deaf/HoH person and I can just tell when they’re pretending to understand the conversation and they can probably tell that I can’t understand the conversation either.
How I do my job and accommodate my disabilities.
So, I have the best job in the world. I'm a fossil tour guide and basically walk around the beach with people talking incessantly about my special interest and they are actually interested and pay (extremely good) money for it. I'm living the dream guys!
As awesome as my job is, there are a few challenges due to my disabilities. Luckily, I have found ways to accommodate myself so both me and the customers all have a great time. I've decided to split this list up by disability rather than by different aspects of the job so if you have one of the disabilities that I mention you can just look at the bit that is relavent to you to see if any of the things that are helpful to me are helpful to you. If you have any other suggestions of different things to try, please put it in the comments!
Autism:
To be honest, the palaeontology field is full of autistic people so I really don't stand out. When people book a fossil tour, they expect the tour guide to be a little quirky, so I do have a bit of leeway for seeming socially awkward without too much judgement.
I don't really pick up the hint that someone isn't having fun any more, so when the weather is bad I make sure to tell people at the beginning of the tour "I know it's really (insert unpleasant weather situation here) today, so if at any time this stops being fun for you, we can always head back early, just please directly tell me 'I'm not having fun any more, can we go?' because I'm not great at picking up hints." If the family are from the UK, I sometimes make a joke about them not being my hostages, but I avoid this with foreign families because that kind of humour doesn't always land well with other cultures.
I have visual materials to help keep my talks on track and to better explain the points that I'm trying to make. I also keep my initial talk pretty similar every time so I don't have to think of the words off the top of my head every time.
I make sure I give clear factual answers to questions that give both the technical terms and a simplification to all age groups e.g."That is a fossil echinoid which is the scientific name for a sea urchin." This avoids having to guess the person's level of prior knowledge and avoids me being overly technical or coming across patronising.
I try to limit my work to around 3 hours per day to avoid getting overstimulated.
Deafness:
I always make sure to tell people about my deafness right at the start of the tour and tell them how to accommodate me. I try to make it lighthearted I'll say it like "Just so you know I'm Deaf which means I can't hear well. If I look like I'm ignoring you, I'm not, I just can't hear you. Please tap me or wave at me to get my attention and make sure to look at me when you're speaking so I can understand you." Some people just ignore the instructions, but at least then they know what they're supposed to be doing, and it normally works out okay.
I have a cochlear implant which helps me a lot, but is vulnerable to wet and windy weather. I use EarGear covers on my processor to block out the wind noise and to protect it from moisture. It works pretty well, but isn't perfect.
I probably would benefit from an interpreter, however my work schedule is pretty flexible and often there are last minute bookings, also there aren't many interpreters near where I live so it would be virtually impossible to find one, so I make do without and it seems to be working okay for me.
Balance and Mobility (HSD and balance disorder):
Luckily my hypermobility is pretty mild so I'm able to weight bear fully on both legs and climb stairs etc.
If I'm going to be walking/standing for over 1 hour, I use knee supports to help prevent knee pain. I use the ones that are thin and elasticated tubes (kind of like a sock) rather than the velcro ones because they look more sleek and I find them more comfortable, also I only need fairly light support. I recommend using the lightest support that is reasonable for you to avoid weakening your joints. If you're not sure, speak to a professional.
I use an ergonomic backpack with padded straps and try and keep my kit as light as possible. I always make sure to carry it over both shoulders to avoid an uneven load on my body. I used to just use any old backpack and cram it full of examples of every single fossil you could ever find. Don't do that. You're not on SAS who dares wins.
Trekking poles. (In my opinion) The most underrated mobility/balance aid out there. Does it make me look like I think I'm scaling Everest? Yes. Does that fact make me feel ridiculous? Yes. Am I very grateful for them when I lose my footing on a pebble bank? Also yes. Most of the time I use one pole just for balance so I can keep a hand free, but I do have two, just in case. It also allows me to point at things without bending down so much which helps with my vertigo issues. If you are considering whether you could benefit from a mobility aid for your balance, especially if you're often on uneven surfaces, I would urge you to try trekking poles. You can use two at a time for extra support, they're gentler on your wrists than a crutch or cane and they come with the option of rubber or metal tips depending on the surface you're on.
Here is my relatively comprehensive guide to how I do my awesome job. If you have any questions or you would like to suggest something that you've found helpful, please leave a comment.
Cochlear implants aren’t evil.
Cochlear implants don’t replace sign language. I am a proud BSL user alongside my cochlear implant.
Cochlear implants aren’t brain surgery. Cochlear implant surgery is generally safe (or as safe as any invasive surgery can be) and does not involve the brain.
No I can’t just use hearing aids instead. Hearing aids do almost nothing for me because I have almost no residual hearing. Hearing aids only allow me to hear some vague low pitched sounds, my cochlear implant allows me to be able to comprehend (with effort) 70% of speech in quiet.
Interpreters are a limited resource and my cochlear implant is the only coping mechanism I have when interpreters are not available. Also my family don’t sign (yes they should learn, but I can’t force them) so I need my implant to communicate with them.
Nobody forced me to get an implant. I chose to get it myself as an adult. The ethical considerations of implanting babies and young children is a little more complicated but that is not my situation so I don’t speak on that.
My lip reading skills are pretty mediocre and using my implant makes lip reading much easier as opposed to having absolutely no sound whatsoever. Also lip reading isn’t a viable stand alone communication method for most deaf people.
Cochlear implants aren’t perfect. In a perfect world where everyone knew sign language, I probably wouldn’t have bothered with an implant, but as it stands, it’s the right decision for my lifestyle and that’s okay. Cochlear implants aren’t for everyone and that’s more than okay, but it works for me.
Cochlear implants for babies are now FDA-approved from 7 months, offering earlier access to hearing and major developmental benefits.
Cochlear implants for babies are now #FDA-approved from 7 months, offering earlier access to hearing and major developmental benefits.
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