Showing posts with label Eye and Facial Twitching. Show all posts
Showing posts with label Eye and Facial Twitching. Show all posts

Sunday, October 26, 2008

What does twitching look like? Video Clip

Twitching!  What does it look like?

Curious about what Amanda's NAS (Non-Auditory Stimulation) or twitching as we call it, looks like...here is a video clip.  It is just under 8 minutes long (7 min. and 58 sec. to be exact.)


In it, her dad is videotaping while I am testing her on all three programs with the 6 Ling Sound Test (Ah, Oo, Ee, Mm, Ss, Sh) as well as listening for Goldy's dog tags and clapping.  She wanted me to test her with the volume all the way up.  She doesn't typically keep the volume this high, but from time to time she does turn it up like this.


When the volume is lower, most of the twitching is not there, but the sound is quieter except for Ss and Sh which she seems to be able to consistently hear.


For you who have cochlear implants or are involved in those who do and want details about her programing, her current mapping is as follows:


Advanced Bionics 90K Harmony

Hi Res-S w/Fidelity 120

P1 (09/12/08)  T-Mic only IDR 70

P2 (10/10/08) T-Mic only IDR 80 (newer program with wider pulse width and increased IDR)

P3 (09/12/08) Mic/Aux 50/50  IDR 70


Although all electrodes are inserted into her cochlea, she currently only has 4 of the 16 electrodes active due to trying to control the twitching.


 We are still awaiting an xray of her implant to see if there is anything internal that is causing this twitching and we have an appointment with her audiologist and an AB audiologist on Nov. 14th.


Amanda likes hearing whatever it is she's getting and can distinguish some words based on the high frequency sounds she is hearing.  If this wretched twitching could be eliminated...

 

Monday, October 20, 2008

Jennifer's son, Trevor visits


Here we are at Disney's California Adventure where we had a few hours to play in the park with my son, Trevor.  He will be on the Disney Cruise Line on the Magic for  6 months.  So if you happen to be going on a cruise and end up on the Magic look for Trevor as Entertainment Host.

Behind us is Hollywood Tower of Terror as Amanda poses with Trevor.   In the next photo is Amanda's brother, Joseph, her dad, Gonzálo, me, Trevor and Amanda in front.

It was Amanda's first visit to Disneyland and California Adventure since her CI was activated 2 months ago.  She still can't identify any sounds but knows she hears "something."  If it's turned up a little too loud, she gets twitching.  If it's turned down to avoid the twitching, she hears soft sounds.  Sigh.  

Her next mapping is November 14th and an Advanced Bionics audiologist will again be in attendance to see if she can help figure out why the twitching is still present, why Amanda can't hear her own voice and to assist in finding an appropriate map. 
Amanda's surgeon has authorized an xray of her head to see what's going on in there (smile)  so as soon as we hear from radiology we'll get that scheduled.

Amanda continues to enjoy hearing whatever it is that she's hearing, wears her processor faithfully and has a positive attitude about the whole thing.

Saturday, August 23, 2008

Amanda's Second Mapping Update


Dear readers and followers of Amanda's Cochlear Implant Journey,

Review
If you've been following my blog, you know that on Wednesday, August 13, 2008, I posted regarding Amanda's Tuesday, August 12th activation.   You also know that we were surprised, unprepared and disappointed to say the least.  

We were not at all prepared for Amanda to only feel her right eye twitching and getting no sound whatsoever.  If you viewed all 6 video clips you would even have witnessed this twitching for yourself.

Fran, her audiologist, set the volumes very low since Amanda said the twitching was bothering her.  That afternoon and the next day,  Amanda was experiencing music on her iPod with the direct connect earpiece and cable via the twitching. 

What?  No twitch?  No nothing?
Two days after activation, half way through the day on Thursday, August 14th, Amanda reported she didn't feel a twitch anymore, which meant she wasn't sensing sound anymore.  She had worked up through the softest to loudest programs: Program 1 (P1), Program 2 (P2) and Program 3 (P3).  We thought that maybe after her auditory nerve rested perhaps she'd feel the twitch again.  But the morning of Friday, August 15th, after a night of rest brought no twitching when Amanda put on her processor.  So her brain had acclimated and she was ready for more volume.

On Friday, August 15th we put a call in to Fran.  She had a small window of time and agreed to increase the volume since Amanda still had another week before her second mapping.  Fran upped the volume in the computer and then when we arrived, took Amanda's processor and downloaded the new program.  Amanda was back to twitching again and we felt somewhat relieved that she was getting something again.  This time, Fran set the volume levels with a larger range since Amanda had adapted quickly through the smaller range of volumes.

Amanda took it remarkably well that instead of going to Long Beach Aquarium of the Pacific that we had started out for,  that we instead drove the hour and a half to Los Angeles to fiddle with her processor.  She has been such a trooper throughout this whole process and wants to have as much success as possible with her CI.

What?  Increased twitching?
So again we started the process of starting on P1 and working her way up through the volume levels of each program 'til we got to P3.  THEN....we were alarmed on Sunday, August 17th, five days after activation, when Amanda displayed severe facial twitching in her jaw in response to loud sounds at the increased volumes.  We hadn't realized she had any facial twitching from the first day, until with the extended viewing during the editing and captioning process of the activation video clips, it was evident that the minor twitching had been there all along.  Now, with the increased volume this facial twitching was major and quite alarming.

We again called Fran and who said to keep the volumes low to keep the twitching minimal if it bothered her.  So Amanda adjusted her programs and volume where she could find the balance between keeping the eye twitching but not the facial twitching.  It was a trial and error process which wasn't always successful.  But even so, sometimes Amanda would adjust it so that she'd twitch wildly to the music in her iPod or PSP, or she'd ask us to clap or speak loudly so we could witness it.  So it obviously wasn't painful, but something that took getting used to.  

We likened it to electronic stimulation technology like a TENS machine or a High-Dow, which Gonzálo and I had purchased recently to ease aching muscles in our shoulders and back. The feeling is weird and a bit alarming at first, but you get used to it.  So Amanda dealt with this odd twitching for 5 days, knowing that her second mapping was scheduled for Friday, August 22.

Amanda's second mapping:  Friday, August 22, 2008
Amanda had her second mapping yesterday.  Fran stimulated each electrode separately and isolated four channels where Amanda could sense something in her head in response to auditory stimulation.  This was the first time Amanda felt anything inside her head.  AND....no twitching was present!

When Fran found the first channel, Amanda excitedly exclaimed in ASL, "I feel something inside my head!"  She described it as a pulsing or whooshing.  We, of course, were ecstatic that there was something new there!  The no twitching was a pleasant bonus!

Fran consulted the implant manufacturer, Advanced Bionics, by phone for assistance in setting a map for Amanda.  The AB audiologist guided Fran in planning the mapping for this week.  So, Amanda ended up with two 4 channel maps; one at a soft level (P1) and one at a louder level (P3.)  The third map (P2) is a 14 channel map set at minimal facial stimulation level.

In addition, Fran programmed Amanda's second processor similarly except at a louder level for P1 and the loudest level for P3.  P2 is also a 14 channel map, set slightly louder. Depending on how this week and Friday's next activation goes, an AB audiologist may be present at Amanda's September 5th mapping.

We have seen progress these last two days in that her auditory nerve stimulation seems to be habituating so that louder volumes are necessary to achieve the same "inside the head" feelings, pulses, whooshing, whatever it is that she is getting.   She is already on her second processor and is experimenting between at P1 with higher volumes and P3 with lower volumes. 

She just tried the P2 setting on the first processor.  Even on the lowest volume there was facial twitching and no "inside the head" feeling.  We'll try again later in the week.  

We had a family get together today and Amanda's goal had been to be able to shock people by having them say her name and she would nonchalantly turn around to see what they wanted.

Needless to say, it didn't happen.  It was noisy and lots of sounds were coming at her at one. She doesn't have the discrimination to determine if it is a voice talking to her or a door slam or people yelling and splashing in the pool.  Plus she herself was in and out of the pool and spent a good part of the time waiting for her hair to dry enough to put her processor back on.

So, all in all we feel as though we are on a positive track.  We had Fran initially leave Amanda's green processor light flashing in response to sound, and red light on if the headpiece magnet wasn't in place so we could have a visual cue.  With her new found "inside the head" sensation, we may ask Fran to disable it at her next mapping.  

School starts Monday, August 25, 2008 and that will be just one more thing kids find to be "curious" about.  We've coached and practiced... and we'll see.  Amanda is very excited to start the new school year as an 8th grader and be with her friends and favorite teachers.

Here is a photo of a gift she received from two of her young cousins who couldn't make it to the BBQ yesterday.  It is a barrette from Olvera Street in Los Angeles, along with a note to say that they couldn't wait to see her, talk to her, hear her hear and were praying she'd do well.  Sweet girls.