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Purveyor of all things lovely...
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Facts/Myths Busted!⠀
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1. Brain surgery -  An internal implant is placed under the skin behind the ear and an electrode inserted into the cochlea. No part of the brain is touched. ⠀
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2. Evaluation - Healthcare providers PROVIDE and recommend options. You could even go as far as scheduling the surgery date and change your mind that  it's not for you. ⠀
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3. You will not wake up from surgery and be able to hear. You will not activate and everything is crystal clear. Time and adjustments will still be needed. Aural Rehabilitation is highly recommended. ⠀
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4. A CI is not a natural device that replaces your ear. It is a medical device that serves to help/assist. It is surgically implanted and bypasses the outer and middle ears to directly stimulate the hearing nerve and communicates with your brain.⠀
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5. Your doctor knows when - Unfortunately audiology is still super specialized. Most PCPs know a little bit about a lot of topics. If you feel like your hearing aids aren't giving you enough, take initiative to investigate further and schedule an evaluation to find out if you are a candidate.⠀
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6. Last Resort - With recent advances in technology, cochlear implant candidacy criteria has changed.  It is no longer only for those who are profoundly deaf bilaterally but are now beneficial for those with moderate/severe hearing losses, single sided deafness and high frequency only hearing losses.⠀
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7. Not only for kids/babies! Many think that older brains cannot adapt or benefit from new technology but it absolutely is possible!⠀
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8. Not for everyone! Criteria is still specific and evaluations are considered on case by case basis. The choice to undergo surgery is not one to be hastily made!⠀
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9. MRI - again, advances in technology have made it possible for MRIs to be completed on CI recipients. Each manufacturer has different levels of MRI tolerance and some implants have the option to remove/replace the magnet. ⠀
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Leave a 👋🏼 in comments if you ever pondered these questions! Hope this helped ease some of your concerns!
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Do you know someone with hearing loss? Do you get frustrated when trying to communicate with them? Have your intentions been good but tactics didn’t work? ⠀
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Here's some helpful Do's and Don'ts!

Leave a 👂🏼if you plan to try something new from this!
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Have you ever been frustrated with your hearing aid or CI program but didn't know how to communicate the problem to your audiologist? Here's a tip sheet created by popular request! ⠀
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Know that we are here to help you - but sometimes we need to work together to reach that goal! ⠀
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If you've ever been a parent you know that each and every child has their own preferences, personalities, likes/dislikes - this is similar for hearing perspective! One person might like a certain filter or frequency while another absolutely hates it. ⠀
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We are constantly learning about new technology and programming strategies so let us worry about what tools to use. ⠀
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The more that you tell us about what you like or dislike about a certain sound/situation, the better we can help you! ⠀
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Save this post for future reference! Would you like me to make it into a PDF available to print?
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This question is often asked by parents and relatives of patients and the curiosity is real! ⠀
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Anyone can listen to a CI processor's microphone but because a cochlear implant is a surgically placed device, ONLY the recipient can understand and experience what the delivered sound is like.⠀
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Hearing aids are miniature sound amplifiers. Sound comes into a microphone and out of a speaker for anyone (with at least some hearing) to hear.⠀
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A cochlear implant on the other hand - doesn't actually amplify anything. The cochlea's job is to convert acoustic information into electrical and hand it off to the auditory nerve. ⠀
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The CI external processor takes the place of the outer and middle ear with its microphones and computer chip. Then the internal device/electrode delivers the electrical signal directly to the nerve. ⠀
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It's common to see patients in awe of or annoyed by the new squeaky and fricative sounds they now have access to due to two reasons: ⠀
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1.  New recipients likely haven't heard or had access to high frequency sounds ever or in a while. ⠀
2. Because of something called tonotopic organization, the CI electrode covers the high frequencies first. ⠀
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These are some responses that I've heard from recipients regarding the sound at the beginning of their post implantation journey. ⠀
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My own initial experience isn't on there because I can't think of a specific word for it. For me it sounded like the the stretchy graphics on the television screen when a character goes into or comes out of a dream in an 80s sitcom. 🤷🏻‍♀️🤣⠀
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Because every cochlea, nerve and brain is different - there's no way of knowing how things will sound for a recipient. It's simultaneously nerve-wracking and exciting. I've seen so many different emotions ranging from fear, dislike, overwhelm, exhaustion, relief, joy, gratitude, wonder and exhilaration!⠀
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Hope this gives CI users some words to help describe sounds - and non recipients a little bit of insight into our hearing world! ⠀
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Would it help if I created something/dialogue for CI users make the most of their programming appointments?
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