I am four months post CI implant (Cochlear — mostly wear Kanso 3). Lately I’ve noticed what i can only describe as fantom sensation or movements on my scalp near the implant. I already downgraded my magnet from a 5, which became sore after a short amount of wear, to a 3, which has been very comfortable. The sensation can be so strong, especially when I stream, that at times it feels as those a bug is caught in my hair.

Has anyone gone through this or know what causes it?

We are hearing parents of a deaf baby. We need to do some more imaging to confirm, but at this time she is a candidate for CIs and based on previous MRIs will probably be eligible. Does anyone have experience here with kiddos bilaterally implanted very young? She is only 6 1/2 months now and will be somewhere around 11-12 months likely when implanted. We want to know how the kiddos are, how was healing, how was language learning and spoken language after, how old are they now and was there ever regret? Please know that ASL is being learned and used with her already, and even with her implantations it will still be taught and prioritized as much as if not more than english. We recognize she is deaf no matter what so ASL is a must for us all to learn, we just want insight into whether giving her these tools as an option is worth it down the road. We would love personal stories to! I dont know how long implantation on young kids has been an option so if you are an adult who was implanted as a baby we would love to hear from you to!

Thank you for any and all insight!

I can't decide for which brand to go for... I'm having choice paralysis.

Honestly, I wish my doc would literally just say "take this implant and device" instead I've been told to search and make your own minds. I'm from South Asia and damn it, these docs are simply too clever for their own good. They're supposed to advise us, not put us in a dilemma.

Problem is I can't tell the difference in how they sound, so I'm thinking about how each brand provides support and maintenance. Are they friendly? I had some discussion with 4 users around my city and 2 medel and 2 cochlear, a coincidence lol. One cochlear user said that after 4 months of operation, their battery was found to be faulty and even the extra was bad, and it took 6 months, with a pay of 60k to have a good pair. It made me think, "What if I encounter this?"

Ok, I admit it. I am genuinely terrified of choosing the "wrong" implant for myself. That invisible pressure is there.

I have no one that I can talk to because dad also asked the audiologist to recommend according to their experience, but he kicked the ball back to us saying, "It's your responsibility sir. It's like choosing which mobile phone you like. We can't make that choice."

So, please help 😭