Over the weekend, I was sitting outside by the campfire with my husband Bill. It was still daylight. We were waiting for a couple of our friends to arrive. Bill had his iPod connected to speakers that were hanging on the house about 20-25 ft away (I hope I'm not exaggerating the distance. Bill's not here so I'll ask him when he gets home.) The music was not loud and we were talking to each other without any problems. I could hear the music but wasn’t really paying attention. All of a sudden a song came in very clearly. I started singing along. Bill did a double take and said ‘You can hear that?’ I nodded and kept singing bits of the song until it ended. Bill said ‘You were even on key!’ And a new Rock Star is born!
The campfire after dark with 4 people around it was a less than exciting hearing experience. Maybe with time it will improve.
After the friends left, I used the direct connect to hook my Harmony up to a book on CD. I had been reading the book all week and when I went to the library, I found it on CD. I decided I’d finish it by listening and reading along. I turned my left ear off. First I was disappointed because the book on CD was an abridged version so I could not follow along word for word. After a few minutes I started getting excited because I could hear the CD version well enough to know where it was skipping sentences and paragraphs in the book version. I stayed up until midnight and finished the book listening and searching for where it was in the book version. Not exactly a relaxing read, but fun to be able to do it less than three weeks after activation!
The next day we were riding in the car. The radio was playing a hunting show. The guy was talking about dogs. He said “I like dogs.” After about 4 times and finally I said, “Ok, the guy likes dogs!” Bill was surprised again that I was hearing it and I just kept repeating what the radio guy was saying. “It can be very challenging but it’s also very rewarding to train your own dogs.” I’m finding that I love showing off how good I am hearing!
Sometimes I am still frustrated and I am clueless about what is being said around me. Hearing encounters of the successful kind like I describe above (my second CI has been activate for less than three weeks) gives me lots of hope that it is going to be awesome in a few more months! I try to remember it is still early in my foray into hearing in stereo and to not get too upset when I don’t hear all that I’d like to.
It is still as if I am hearing two different things. I can just go with the flow and listen to both or I can focus on one ear or the other to hear what is coming out of it. Actually “what is coming into it” might be the correct way to refer to the sound, but at least with the new CI, if feels more like the ear is outputting sound than inputting it. I’m sure that doesn’t make much sense to anyone except maybe another new CI recipient. I’m wondering if the focusing on one ear over the other is how people can determine direction, but it’s not automatic for me. I have to think about which ear to listen to and sometimes I can’t really get the focus on the individual ear. It’s just been too long for me to remember how having two ears felt and then I probably didn’t pay attention to how they worked together anyway.
Tuesday, August 26, 2008
Monday, August 18, 2008
Sounds in Paradise (and elsewhere)
Last Thursday, I used the phone at work using both 'ears'. It rang so I had to answer! It was a co-worker needing support on the claims system that I work with. She was talking really fast. I explained that I was HOH and could she please slow down a bit. I understood what she needed me to fix but asked her to send me the details in an email so I'd know I had the right policy number, claim number, unit number, etc. That was just too much to try to get over the phone and in that situation; a guess was not good enough. We emailed back & forth a bit and once I had the fix finished I started to email her to let her know. My hands paused over the keyboard. Good opportunity for some phone practice, I thought. Not much I need to understand except her confirmation that the problem has been corrected. I quick grabbed the phone and dialed before the little doubting phone devil forever sitting on my shoulder could stop me.
Friday, I had my one week checkup. I was re-mapped and then tried S and P again. I felt I could hear equally well with either. I commented that P had an echo or hollow sound and my audiologist said ' Why make your brain get used to that if it doesn't have to.' Good question! I agreed to just go with S this time. Program one is T-mic only. Program two is 50/50 T-mic and internal mic. Program three is 50/50 with T-coil activated. Guess what I discovered! I don't have a phone that works with a T-coil! At home and at work, I have always used direct connect to my BWP and my cell I just put up to my CI microphone.
We spent another weekend at the lake, this one much dryer and warmer than last weekend. It was beautiful. Caseville, otherwise known as Key North (and sometimes Margaritaville) was having their "Cheeseburger in Paradise" festival. The bay we are on is called Wildfowl Bay but goes as Flamingo Bay during Cheeseburger. This is a wacky, tacky festival that is all about music - Jimmy Buffet music in particular. Hence the name. Cheeseburger stands line the main drag all week long. Activities abound! Cardboard boat races, lots of music & dancing on the beach and everyone makes crazy hats to wear. Flamingos and parrots rule the land. We went to a concert at the marina around the corner and it was so nice to enjoy the music bilaterally! I didn't hear all the words but I heard the words on the songs I was most familiar with.
During the weekend, I found one situation where the body processor is safer than the ear level processor: Speeding across the lake in a boat with the wind streaming through your hair. I held on to the ear level processor for dear life. Finally deciding there wasn't enough to listen to during that activity to justify the worry, I pulled it off, slipped the battery out, put it all in my shorts pocket, stuck my face to the wind and enjoyed the ride. No more visions of my precious Harmony processor flying off my head, landing in the bay never to be seen again.
Today, I spent a couple of hours in the car and took the opportunity to listen to some CD’s that I’d had trouble hearing before being bilateral. Bread, James Taylor and Cat Stevens came alive in my car like never before! ( Well, it’s been at least 20 years since I heard them as well!) Bread was still a bit of a struggle. I’m sure they will all improve with time. That reminds me, I had a Rod Stewart CD that I couldn’t hear. I love the song Maggie May. I’m going to go hunt that one down to try it! Til next time…
Friday, I had my one week checkup. I was re-mapped and then tried S and P again. I felt I could hear equally well with either. I commented that P had an echo or hollow sound and my audiologist said ' Why make your brain get used to that if it doesn't have to.' Good question! I agreed to just go with S this time. Program one is T-mic only. Program two is 50/50 T-mic and internal mic. Program three is 50/50 with T-coil activated. Guess what I discovered! I don't have a phone that works with a T-coil! At home and at work, I have always used direct connect to my BWP and my cell I just put up to my CI microphone.
We spent another weekend at the lake, this one much dryer and warmer than last weekend. It was beautiful. Caseville, otherwise known as Key North (and sometimes Margaritaville) was having their "Cheeseburger in Paradise" festival. The bay we are on is called Wildfowl Bay but goes as Flamingo Bay during Cheeseburger. This is a wacky, tacky festival that is all about music - Jimmy Buffet music in particular. Hence the name. Cheeseburger stands line the main drag all week long. Activities abound! Cardboard boat races, lots of music & dancing on the beach and everyone makes crazy hats to wear. Flamingos and parrots rule the land. We went to a concert at the marina around the corner and it was so nice to enjoy the music bilaterally! I didn't hear all the words but I heard the words on the songs I was most familiar with.
During the weekend, I found one situation where the body processor is safer than the ear level processor: Speeding across the lake in a boat with the wind streaming through your hair. I held on to the ear level processor for dear life. Finally deciding there wasn't enough to listen to during that activity to justify the worry, I pulled it off, slipped the battery out, put it all in my shorts pocket, stuck my face to the wind and enjoyed the ride. No more visions of my precious Harmony processor flying off my head, landing in the bay never to be seen again.
Today, I spent a couple of hours in the car and took the opportunity to listen to some CD’s that I’d had trouble hearing before being bilateral. Bread, James Taylor and Cat Stevens came alive in my car like never before! ( Well, it’s been at least 20 years since I heard them as well!) Bread was still a bit of a struggle. I’m sure they will all improve with time. That reminds me, I had a Rod Stewart CD that I couldn’t hear. I love the song Maggie May. I’m going to go hunt that one down to try it! Til next time…
Tuesday, August 12, 2008
Another day in the life of a Bilateral CI'er
I had my first meeting at work (post CI bilateralism) and I didn’t use my FM. It was in a smaller room than usual with the usual 11 people attending. I did just fine. I even heard a lady at the end of the table whisper to the lady next to her “What’s Friday’s date?” as she took notes. At least I was sure I heard her when it happened. Now I’m wondering if I lip read it. I just take in all the clues there are and don’t always realize where the actual understanding comes from.
Ok, I admit I chickened out on using the phone at work today. I looked at it but I just couldn’t do it and it didn’t ring so I didn’t have to pick it up. As Scarlet would say “Tomorrow is another day!”
However, I just spoke to my mom on the phone here at home. It’s often very hard for me to understand my mom. I plugged my left side BWP in directly and held the handset to my right ear. It was much better. I’d hold the handset away from my right ear and it was hard to hear, put it back and the sound was just so much louder and fuller. Bravely unplugged the BWP, yikes didn’t sound like I was getting much out of the right side at all. No understanding of what she was saying. Quickly plugged the BWP back in and there was that rich full sound again. This is very odd and yet it seems to be what most people report when they have gotten two implants at different times.
I’ve been watching TV with the captions off. Not great results there. Oh, well, I’ll keep trying! Tomorrow marks a full week with the new CI!
PS. Check out the free classic audio books for listening practice - the link is on the right with the Rehab Links.
Ok, I admit I chickened out on using the phone at work today. I looked at it but I just couldn’t do it and it didn’t ring so I didn’t have to pick it up. As Scarlet would say “Tomorrow is another day!”
However, I just spoke to my mom on the phone here at home. It’s often very hard for me to understand my mom. I plugged my left side BWP in directly and held the handset to my right ear. It was much better. I’d hold the handset away from my right ear and it was hard to hear, put it back and the sound was just so much louder and fuller. Bravely unplugged the BWP, yikes didn’t sound like I was getting much out of the right side at all. No understanding of what she was saying. Quickly plugged the BWP back in and there was that rich full sound again. This is very odd and yet it seems to be what most people report when they have gotten two implants at different times.
I’ve been watching TV with the captions off. Not great results there. Oh, well, I’ll keep trying! Tomorrow marks a full week with the new CI!
PS. Check out the free classic audio books for listening practice - the link is on the right with the Rehab Links.
Monday, August 11, 2008
Weekend one after Activation, August 9-11, 2008
My ear is quite sore, but I remember that from hearing aid days so I pretty much expected it. I know my ear will toughen up after a while. I don’t have any moleskin so I used a band-aid and cotton ball and stuck it right to my ear. It's helping.
It's easy to change the programs on the Harmony without taking the processor off my ear. I do use two hands, one to hold the processor steady, and the other to switch the program. If I forget which program it's on I just go back to the first one and count up to the number I want. Volume is what is harder to change. It's difficult to know how much you've turned it up or down. I find I have to take the processor off to be sure of where I am with the volume dial.
We had a houseful at the lake this weekend. My sister, her husband, two sons, daughter, Bill, me, our two boys and one of their friends spent the two days talking, eating and watching it rain! The boat was in the shop anyway – bummer - and it poured for two days straight. Lake Huron has been low for the last 10 years and it seemed like our dear God finally decided to fill it back up over the weekend! The sun would come out for maybe 5 minutes and then it would be raining buckets again, coming down so hard and fast that anyone to venture out was soaked to the skin in minutes.
I had a nice conversation with my niece. I talked to my son’s friend about his recent trip to Ecuador and had conversations with everyone there. I think the whole weekend was less stressful than usual for me because I was hearing so much more.
I got up this morning (Monday) and worked on rehabbing my ear for an hour or so, using a headset and the English site listed on my links section. I could hear some parts and other parts not so well. I’m using P today after switching back and forth all weekend.
Our cottage is part of a subdivision that is just around the corner from a marina. The rain finally stopped and our company all had gone home Sunday night. Bill and I went over to the marina on our bikes. We stopped to talk to some folks. Usually, I mostly tune out because I can never follow conversations outside with the wind howling like it was this morning. This time I listened to stories about boating, boats that almost sank and other mishaps. I laughed along with them. I even contributed to the conversation. I spoke instead of just nodding my head and smiling!
We also met up with the brother of one of our friends who was in town with his wife. We decided to ride our bikes around with them to show them the good places to ride since they’d be there for a few more days. I actually heard her talking with my new CI and I could not hear her with my old CI. As little as a week ago, I would have shied away from this bike ride because I would not have been able to hear. In fact, I almost avoided it today because I didn’t know the people we rode with very well. I couldn’t really see a way out that wouldn’t be rude though so I went. I’m so glad I did!
The best is yet to come! I had most everything packed up when Bill said he wanted to mow before we left. “Go for it” I said. Having some time to while away, I sat down at the computer. I found a site for internet radio called www.pandora.com and started listening to music. This site is neat because you are able to create your own radio stations. I picked The Beatles for one station and Carole King for the other. The site created two radio stations that had songs by these artists and some similar songs by other artists. The only problem was the windows and doors were open and the mower was so loud I was having trouble hearing. Then as I’ve been doing all weekend, testing what I’m hearing with each CI, I turned the older one off. The mower sound was gone and in its place was music. I could follow the lyrics of the songs I knew really well! I was thrilled! It still didn’t sound natural to me, but following the beat and understanding the lyrics at this point (5 days after activation!) has been very exciting! The new CI seems to filter out much more of the background noise than my older CI does.
Tonight, the hospital anesthesia department called me to ask me some questions about my surgical experience. I had volunteered to be part of a study on the day of my surgery. When I’m home, I use a patch cord to plug my BWP directly into the phone. This is how I took the call but I also placed the phone to my right ear so I could also hear using the T-mic. Sure seemed like using both ears really helped and I’d like to try this out at work. I will be going to work tomorrow for the first time with my new CI. Wish me luck in being brave and trying the phone with both ears. Generally, I avoid the phone like the plague at work.
I am so impressed with the technology of the Harmony! Each day and each new listening experience impresses me more. I'm very grateful to be bilateral!
It's easy to change the programs on the Harmony without taking the processor off my ear. I do use two hands, one to hold the processor steady, and the other to switch the program. If I forget which program it's on I just go back to the first one and count up to the number I want. Volume is what is harder to change. It's difficult to know how much you've turned it up or down. I find I have to take the processor off to be sure of where I am with the volume dial.
We had a houseful at the lake this weekend. My sister, her husband, two sons, daughter, Bill, me, our two boys and one of their friends spent the two days talking, eating and watching it rain! The boat was in the shop anyway – bummer - and it poured for two days straight. Lake Huron has been low for the last 10 years and it seemed like our dear God finally decided to fill it back up over the weekend! The sun would come out for maybe 5 minutes and then it would be raining buckets again, coming down so hard and fast that anyone to venture out was soaked to the skin in minutes.
I had a nice conversation with my niece. I talked to my son’s friend about his recent trip to Ecuador and had conversations with everyone there. I think the whole weekend was less stressful than usual for me because I was hearing so much more.
I got up this morning (Monday) and worked on rehabbing my ear for an hour or so, using a headset and the English site listed on my links section. I could hear some parts and other parts not so well. I’m using P today after switching back and forth all weekend.
Our cottage is part of a subdivision that is just around the corner from a marina. The rain finally stopped and our company all had gone home Sunday night. Bill and I went over to the marina on our bikes. We stopped to talk to some folks. Usually, I mostly tune out because I can never follow conversations outside with the wind howling like it was this morning. This time I listened to stories about boating, boats that almost sank and other mishaps. I laughed along with them. I even contributed to the conversation. I spoke instead of just nodding my head and smiling!
We also met up with the brother of one of our friends who was in town with his wife. We decided to ride our bikes around with them to show them the good places to ride since they’d be there for a few more days. I actually heard her talking with my new CI and I could not hear her with my old CI. As little as a week ago, I would have shied away from this bike ride because I would not have been able to hear. In fact, I almost avoided it today because I didn’t know the people we rode with very well. I couldn’t really see a way out that wouldn’t be rude though so I went. I’m so glad I did!
The best is yet to come! I had most everything packed up when Bill said he wanted to mow before we left. “Go for it” I said. Having some time to while away, I sat down at the computer. I found a site for internet radio called www.pandora.com and started listening to music. This site is neat because you are able to create your own radio stations. I picked The Beatles for one station and Carole King for the other. The site created two radio stations that had songs by these artists and some similar songs by other artists. The only problem was the windows and doors were open and the mower was so loud I was having trouble hearing. Then as I’ve been doing all weekend, testing what I’m hearing with each CI, I turned the older one off. The mower sound was gone and in its place was music. I could follow the lyrics of the songs I knew really well! I was thrilled! It still didn’t sound natural to me, but following the beat and understanding the lyrics at this point (5 days after activation!) has been very exciting! The new CI seems to filter out much more of the background noise than my older CI does.
Tonight, the hospital anesthesia department called me to ask me some questions about my surgical experience. I had volunteered to be part of a study on the day of my surgery. When I’m home, I use a patch cord to plug my BWP directly into the phone. This is how I took the call but I also placed the phone to my right ear so I could also hear using the T-mic. Sure seemed like using both ears really helped and I’d like to try this out at work. I will be going to work tomorrow for the first time with my new CI. Wish me luck in being brave and trying the phone with both ears. Generally, I avoid the phone like the plague at work.
I am so impressed with the technology of the Harmony! Each day and each new listening experience impresses me more. I'm very grateful to be bilateral!
Sunday, August 10, 2008
Activation Day
Activation Day, August 7, 2008:
The waiting was pure torture, but finally my right CI has been activated! I was practically dancing with anticipation all day Wednesday and Thursday morning. We were a whole hour early for my appointment! First we stopped in just to see if there was a cancellation: Both because I was so eager to get it going and also because we’ve had that happen before. But no cancellation occurred, so we went to a nearby mall to walk around and while away the last hour.
Programming the new Advanced Bionics Harmony and 90K is much easier and goes much faster than my older C1 CI. My audiologist had me turn the left platinum processor off for the mapping of the new Harmony on the right side. First we set loudness on 4 electrodes at a time, and then we went back through them individually to make sure they all sounded like they were at the same level of loudness. It was not extremely loud sounding but I was a bit reluctant to raise the loudness too much after not hearing in that ear for so long. Then the big moment came! She turned it on so I was hearing whatever was going on in the room. I couldn’t really hear speech very well but I could tell someone was talking.
My audiologist explained that she would just start me out on the Fidelity 120S. She didn’t think I’d be able to tell the difference between the S and P at that time. At my follow-up the next day we'd try the P option and compare the two. She did some very basic testing, covering her mouth and saying colors and then numbers. I got them all right except one number! I felt like it was probably 40% what I heard and 30% that I knew it had to be a color or number and 30% guess. When she asked me a question, I couldn't get that at all, but I was pretty sure what she was saying was more than one word and it was not a color. Everything sounded very computer like, high pitched and kind of squeaky. I knew that's normal at first so I wasn’t concerned. She gave me three maps of varying volume for the first day.
My audiologist explained that she started me out on the Fidelity 120S. She didn’t think I’d be able to tell the difference between the S and P at that time. At my follow-up the next day we'd try the P option and compare the two. She told me to go ahead and wear them both most of the time because our goal is to get them to feel normal together. But she also said it was ok to take the older one off if I wanted to just practice on the new one. We went over everything in the box and she explained the parts that were included and about the volume dial and program switch on the BTE processor. Then I was ready to go out in the real world and see how it sounded! First stop is to get an X-ray of my head which will show the exact position of both of my CI’s and the coils in my cochleae.
After my appointment, Bill and I checked into the hotel. We were staying overnight since I had a follow-up with my surgeon and another mapping appointment in the afternoon the next day. It was my son’s birthday and we needed to do some shopping so we went to Best Buy, Meijers and ate at Real Seafood again. (This could get to be a habit!). I switched up to program three, the loudest at some point during the shopping and eating, already adjusting and needing more volume. Then, after dinner, Bill said he wanted to go see “Dark Knight”. Gulp! After a moment’s hesitation, I said “Ok, I’m game”. I’m not afraid of a little sound right? Wow, that is one loud movie! I switched back down to program two for most of the movie, not so much because it was uncomfortable exactly, but I didn’t want to completely traumatize my ear and brain! I would not necessarily recommend going to a movie to someone who has just gotten their CI (s) turned on for the first time if it’s your first CI experience. Unless you are very adventuresome! Having one CI that I’ve been wearing for 10 years, I thought I could handle it and let’s face it, how much speech do you really need to hear in a batman movie?
Day two after activation, August 8, 2008:
I am wearing the body worn processor (BWP) on my left ear and the BTE on my right. It's not strange at all to have the BTE, because wore hearing aids for almost 20 years before getting a CI.
My follow-up with my surgeon is at 9:45, which gives us plenty of time to lounge and listen to TV in the morning. I put on my new Harmony and leave the platinum BWP off for awhile. I’m watching TV when a commercial comes on. The fellow has a mustache and beard and there is no captioning. I’m listening and not getting much, then all of a sudden I hear ‘Now that’s real insurance!’. I blink and sit up straight. Wow, I heard that! What a way to start the day!!
We head out to the hospital for my follow-up. Dr Telian looks in both ears and reviews the x-ray that I had done the day before. He tells me the older CI has not moved at all and they both are positioned perfectly. The good news just keeps coming and I’m all smiles! I promise to send him a Christmas card to let him know how I’m doing in a few months. There will be a follow-up appointment next August. That’s all there is to that. Bill and I are off for some more shopping and lunch before my mapping appointment at one pm.
The sounds coming from each ear are so different that it is a bit distracting at times. The left ear sounds so natural and why wouldn’t it after ten years? The new CI on my right still sounds like someone is playing a sound clip that has been altered to be much more high pitched and tinny sounding that the left. I keep turning the old one off just to see what I’m getting from the new one. I know this is not an instant process though! My hope is for small progress every day.
While driving around we try several CD’s. They don’t sound bad. I start realizing that I’m hearing things with the new CI that I don’t hear with the old. I can hear the guitars strumming with the new CI. I don’t hear that as a distinct sound with the old one. I’m so excited about what I’m hearing!
It’s time for my next mapping. My audiologist and I go through the process of setting volume levels. I’m braver today and ready for more volume. It doesn’t look like they are going up very much to me. After we have the levels set, my audiologist tells me we turned them way up, from 70 to 110 of whatever measure they use (I can’t remember what she called it). We tried the 120 S and it sounds good as far as volume. Then she switches me to P. That sounds very loud! The volume goes down a little. We chat a bit so I can see if I like P, then she switches me back to S. I can no longer hear the S map we just did! It’s very faint after listening to P. But I’m not sure at this point which one I like better. I’m sure I don’t need a T-coil setting yet and I'm also sure I want to use the T-mic. We decide to put on an S map and a P map both with 100% T-mic and on the third one I have a P map with 50/50 on the mics. This means that the top mic will pick up 50% and the t-mic will pick up 50%. We did this so that if the t-mic stops working it will revert to the top mic and I will still have sound. Not that we expect the t-mic to stop, she said they are very reliable now. So then I’m done and Bill & I are ready to head home. Bill and I go outside and get in the car. I realize it’s really loud and I have half a mind to run back in and get the volumes turned down. However, I know it’s going to be a whole week before I’m back so I decide to use the volume button to turn it down and see if I need the extra volume s the week goes on.
I keep it on P most of the day. On the way home I’m switching the old one off every so often to test myself. With only the Harmony going, I’m actually able to hear some of my CD’s enough to sing along! I’m so happy that I’m crying. I’m not a crier at all, but this is just too exciting! It is sometimes difficult to know which ear I’m actually hearing things out of. I think this is a good sign that they are already trying to working together. I continue to turn one or the other off periodically just to see which ear is actually giving me what sound. Sometimes I realize it’s actually coming from both but as different sounds. Soon I hope my brain will begin to recognize these as the same.
The waiting was pure torture, but finally my right CI has been activated! I was practically dancing with anticipation all day Wednesday and Thursday morning. We were a whole hour early for my appointment! First we stopped in just to see if there was a cancellation: Both because I was so eager to get it going and also because we’ve had that happen before. But no cancellation occurred, so we went to a nearby mall to walk around and while away the last hour.
Programming the new Advanced Bionics Harmony and 90K is much easier and goes much faster than my older C1 CI. My audiologist had me turn the left platinum processor off for the mapping of the new Harmony on the right side. First we set loudness on 4 electrodes at a time, and then we went back through them individually to make sure they all sounded like they were at the same level of loudness. It was not extremely loud sounding but I was a bit reluctant to raise the loudness too much after not hearing in that ear for so long. Then the big moment came! She turned it on so I was hearing whatever was going on in the room. I couldn’t really hear speech very well but I could tell someone was talking.
My audiologist explained that she would just start me out on the Fidelity 120S. She didn’t think I’d be able to tell the difference between the S and P at that time. At my follow-up the next day we'd try the P option and compare the two. She did some very basic testing, covering her mouth and saying colors and then numbers. I got them all right except one number! I felt like it was probably 40% what I heard and 30% that I knew it had to be a color or number and 30% guess. When she asked me a question, I couldn't get that at all, but I was pretty sure what she was saying was more than one word and it was not a color. Everything sounded very computer like, high pitched and kind of squeaky. I knew that's normal at first so I wasn’t concerned. She gave me three maps of varying volume for the first day.
My audiologist explained that she started me out on the Fidelity 120S. She didn’t think I’d be able to tell the difference between the S and P at that time. At my follow-up the next day we'd try the P option and compare the two. She told me to go ahead and wear them both most of the time because our goal is to get them to feel normal together. But she also said it was ok to take the older one off if I wanted to just practice on the new one. We went over everything in the box and she explained the parts that were included and about the volume dial and program switch on the BTE processor. Then I was ready to go out in the real world and see how it sounded! First stop is to get an X-ray of my head which will show the exact position of both of my CI’s and the coils in my cochleae.
After my appointment, Bill and I checked into the hotel. We were staying overnight since I had a follow-up with my surgeon and another mapping appointment in the afternoon the next day. It was my son’s birthday and we needed to do some shopping so we went to Best Buy, Meijers and ate at Real Seafood again. (This could get to be a habit!). I switched up to program three, the loudest at some point during the shopping and eating, already adjusting and needing more volume. Then, after dinner, Bill said he wanted to go see “Dark Knight”. Gulp! After a moment’s hesitation, I said “Ok, I’m game”. I’m not afraid of a little sound right? Wow, that is one loud movie! I switched back down to program two for most of the movie, not so much because it was uncomfortable exactly, but I didn’t want to completely traumatize my ear and brain! I would not necessarily recommend going to a movie to someone who has just gotten their CI (s) turned on for the first time if it’s your first CI experience. Unless you are very adventuresome! Having one CI that I’ve been wearing for 10 years, I thought I could handle it and let’s face it, how much speech do you really need to hear in a batman movie?
Day two after activation, August 8, 2008:
I am wearing the body worn processor (BWP) on my left ear and the BTE on my right. It's not strange at all to have the BTE, because wore hearing aids for almost 20 years before getting a CI.
My follow-up with my surgeon is at 9:45, which gives us plenty of time to lounge and listen to TV in the morning. I put on my new Harmony and leave the platinum BWP off for awhile. I’m watching TV when a commercial comes on. The fellow has a mustache and beard and there is no captioning. I’m listening and not getting much, then all of a sudden I hear ‘Now that’s real insurance!’. I blink and sit up straight. Wow, I heard that! What a way to start the day!!
We head out to the hospital for my follow-up. Dr Telian looks in both ears and reviews the x-ray that I had done the day before. He tells me the older CI has not moved at all and they both are positioned perfectly. The good news just keeps coming and I’m all smiles! I promise to send him a Christmas card to let him know how I’m doing in a few months. There will be a follow-up appointment next August. That’s all there is to that. Bill and I are off for some more shopping and lunch before my mapping appointment at one pm.
The sounds coming from each ear are so different that it is a bit distracting at times. The left ear sounds so natural and why wouldn’t it after ten years? The new CI on my right still sounds like someone is playing a sound clip that has been altered to be much more high pitched and tinny sounding that the left. I keep turning the old one off just to see what I’m getting from the new one. I know this is not an instant process though! My hope is for small progress every day.
While driving around we try several CD’s. They don’t sound bad. I start realizing that I’m hearing things with the new CI that I don’t hear with the old. I can hear the guitars strumming with the new CI. I don’t hear that as a distinct sound with the old one. I’m so excited about what I’m hearing!
It’s time for my next mapping. My audiologist and I go through the process of setting volume levels. I’m braver today and ready for more volume. It doesn’t look like they are going up very much to me. After we have the levels set, my audiologist tells me we turned them way up, from 70 to 110 of whatever measure they use (I can’t remember what she called it). We tried the 120 S and it sounds good as far as volume. Then she switches me to P. That sounds very loud! The volume goes down a little. We chat a bit so I can see if I like P, then she switches me back to S. I can no longer hear the S map we just did! It’s very faint after listening to P. But I’m not sure at this point which one I like better. I’m sure I don’t need a T-coil setting yet and I'm also sure I want to use the T-mic. We decide to put on an S map and a P map both with 100% T-mic and on the third one I have a P map with 50/50 on the mics. This means that the top mic will pick up 50% and the t-mic will pick up 50%. We did this so that if the t-mic stops working it will revert to the top mic and I will still have sound. Not that we expect the t-mic to stop, she said they are very reliable now. So then I’m done and Bill & I are ready to head home. Bill and I go outside and get in the car. I realize it’s really loud and I have half a mind to run back in and get the volumes turned down. However, I know it’s going to be a whole week before I’m back so I decide to use the volume button to turn it down and see if I need the extra volume s the week goes on.
I keep it on P most of the day. On the way home I’m switching the old one off every so often to test myself. With only the Harmony going, I’m actually able to hear some of my CD’s enough to sing along! I’m so happy that I’m crying. I’m not a crier at all, but this is just too exciting! It is sometimes difficult to know which ear I’m actually hearing things out of. I think this is a good sign that they are already trying to working together. I continue to turn one or the other off periodically just to see which ear is actually giving me what sound. Sometimes I realize it’s actually coming from both but as different sounds. Soon I hope my brain will begin to recognize these as the same.
Wednesday, August 6, 2008
Less than 24 hours until Activation!
I'm am super excited about my CI activation day tomorrow and getting my new Harmony! This week it has been hard to wait, but now it's getting very close to the BIG A DAY. Today I received a reminder call from the CI center. I didn't need that, no way I'll forget this appointment.
I found my journal from ten years ago. Comparing then and now will be interesting. I don't have to read it to remember that my initial activation with my first CI was not great as far as understanding what I was hearing. I had to work at it. I'm fully prepared to do the same this time around. At work employees in my department can now listen to music with ear buds. I plan to connect my new CI to music while at work and not connect the older CI. Doing so will allow me to exercise the new one on my right ear almost all day at work and still hear out of left CI. Might be distracting, but I'll give it a try.
The too salty, too sweet taste thing has gone away. It only lasted a week or so. Good thing because I lost 8 pounds the first week after surgery. That's not necessarily a bad thing, but it did leave me feeling pretty washed out.
There hasn't been much tinnitus but I do notice a high pitched sound now and then. I don't really have anything it reminds me of. Just ringing in the ear. I do sometimes notice a faint thunder or drumming but it's not loud. Makes me curious about what is going on in there rather than annoyed. Mostly both my ears are pretty quiet.
I'm peeking in my journal and four days after I was activated ten years ago I wrote:
"Hey, I can pick out some words on Kenny Rogers' greatest hits without any printed words to follow along with! The Gambler & Lucille are the best! Thank you Kenny!"
We thought this was funny back then because I wasn't a really big fan of country music, although I did like this particular CD. I remember it when everywhere with me. I do believe I will take this CD with me tomorrow! I'll post soon about my activation very soon!
I found my journal from ten years ago. Comparing then and now will be interesting. I don't have to read it to remember that my initial activation with my first CI was not great as far as understanding what I was hearing. I had to work at it. I'm fully prepared to do the same this time around. At work employees in my department can now listen to music with ear buds. I plan to connect my new CI to music while at work and not connect the older CI. Doing so will allow me to exercise the new one on my right ear almost all day at work and still hear out of left CI. Might be distracting, but I'll give it a try.
The too salty, too sweet taste thing has gone away. It only lasted a week or so. Good thing because I lost 8 pounds the first week after surgery. That's not necessarily a bad thing, but it did leave me feeling pretty washed out.
There hasn't been much tinnitus but I do notice a high pitched sound now and then. I don't really have anything it reminds me of. Just ringing in the ear. I do sometimes notice a faint thunder or drumming but it's not loud. Makes me curious about what is going on in there rather than annoyed. Mostly both my ears are pretty quiet.
I'm peeking in my journal and four days after I was activated ten years ago I wrote:
"Hey, I can pick out some words on Kenny Rogers' greatest hits without any printed words to follow along with! The Gambler & Lucille are the best! Thank you Kenny!"
We thought this was funny back then because I wasn't a really big fan of country music, although I did like this particular CD. I remember it when everywhere with me. I do believe I will take this CD with me tomorrow! I'll post soon about my activation very soon!
Tuesday, August 5, 2008
Surgery Day!
Day before surgery: Tuesday, July 8, 2008
I scheduled my pre-op appointment for the day before surgery since my implant center is one and a half to two hours away depending on traffic. We were hoping for an early morning surgery so we didn’t want to get up before the crack of dawn to drive down so we stayed the night in Ann Arbor.
At my pre-op appointment, I saw a physician’s assistant, a nurse and my surgeon, Dr Telian. They each asked various questions of me and answered questions that I had. My blood pressure, pulse and weight were checked. I had some blood drawn for tests. I received the news that I would be the first CI surgery of the day! I was to report to the hospital at 6 am with surgery to start at 7:30 am. I could eat up until 12 midnight, only water after midnight and nothing after 4 am. That wasn’t hard at all. Once I received instructions for surgery the next day, my husband, Bill, and I were free to explore the Ann Arbor area. Bill treated me to ‘Real Seafood’ and then we explored a bit before heading back to the hotel to use the pool and try to relax. Relax, right! Didn’t really happen! I didn’t sleep very well either.
Surgery Day: Wednesday, July 9, 2008
5 am – Per instructions I showered at the hotel using antibiotic soap. Dressed in loose clothing, making sure my top was button down so I could not be trying to pull something over my head after surgery. Worst part of this was no morning coffee!
5:45-7:30 am – Bill and I reported to the hospital about 5:45. Yes I was eager! I pretended to watch TV while waiting for them to call me. After a short wait, my name was called. Bill & I proceeded to the pre-op area. Here I was asked to put on a hospital gown and given some nice fuzzy socks to put on.
I must have had a ‘visitor’ every five or ten minutes! The pre-op nurse put my IV in. The anesthesia team of three each stopped by at least once to introduce themselves and ask me a few questions. My surgical nurse stopped by to introduce herself and to tell me that she would be with me through the whole thing. She advised me to think of something happy when they started to put me under so that I would think of this happy thing all through the surgery. She told me my current CI would stay on until I was asleep, then she would take it off and put it into the bag that had my clothes which was under the bed. After surgery, she would put it back on, slipping it under the pressure bandage, and turn it on for me. I would not need to be without my CI at all. Awesome! She also explained that she wanted me to say my name and what I was having done and that they would also ask me to do this once I was in the operating room and just before surgery started.
I had a visit from another young lady asking me if I’d like to participate in a study of a new anesthesia monitor that would be used in addition to what they were currently using. I agreed to participate so she stuck some funny looking monitor things to my forehead. The pre-op nurse was in and out taking my blood pressure, pulse, and generally getting me ready.
My surgeon, Dr Telian, stopped by to say hi and to answer any questions I might have before the surgery. He explained that they would mark my right ear just to reassure everyone and me that the correct ear was being worked on. It was really nice to meet all the people who would be there at the surgery doing various jobs. Very reassuring! Bill stayed with me throughout this time.
7:30-8:30 am - Promptly at 7:30, the team came to take me to the operating room (OR). Bill gave me a good luck kiss and left for the waiting room. Once in the OR, I was asked to slide over to the operating table which I did without incident. Sorry, no funny thoughts about the table and whether I could make the slide without incident. I just did what I was told. I’m sure I looked terrified. Considering that the only time I have ever fainted is when I say my own blood running out of one of my fingers after a cut, you can imagine how I felt. Not that I wasn’t sure I wanted to do it or that I wasn’t confident in Dr Telian and the surgical team. I was sure!
They began positioning me, padding my left arm which I’d be lying on while they operated on my right ear. The oxygen mask was put over my face and I started trying to think of sitting out on the bay with the water stretched almost as far as you can see and a warm breeze… I was out!
8:30-10:30 am – Surgery actually started at 8:30 and was finished up at 10:30. Dr Telian talked with Bill after and let him know that everything went really well with implanting the Advanced Bionics HiRes 90K cochlear implant.
10:30 am - ?? – I have no idea what time I woke up! I have this feeling it was after noon but I don’t really remember now. What I do remember is that I was in this beautiful meadow and didn’t want to leave but someone (the post-op nurse) was saying ‘Janet’, ‘Janet’… So I opened my eyes. Back to reality, I was in a hospital bed and my head really hurt, except it’s not my ear, it’s my forehead! The pressure bandage has a knot in it and that is what hurt. I told the nurse that it hurt and she pushed it up a bit. Then everyone that walked by gets shown my red bump from the pressure bandage. I noticed my ear was roaring and it lasted for about 5-10 minutes then quieted down. I did wonder who was whispering in my ear about a meadow when I was trying to think about the bay. LOL
I was offered a beverage. Only a soda, no wine, yet! So I sipped a Sprite and boy did that taste sweet and so very good. I was offered crackers so I nibbled one but it was very hard to get it down because my throat was so dry and sore feeling from the tubes. Then I had a sudden feeling that it was coming up! The nurse jumped and got me the barf bucket in time. She gave me something in my IV for nausea. After a while, I was moved to another post-op area and had a different nurse – who actually was my pre-op nurse too. This is unusual to have the same nurse both pre and post op. It was at this point that Bill joined me again.
1:30? –3:30 pm – Bill explained that Dr Telian could not wait for me to wake up because he had to be over at the new surgery center to do the next two CI’s of the day. The nurse continues to be in and out checking on me. I received the post op instructions. Bill got the honor of taking the pressure bandage off after 24 hours which will be just before we leave the hotel the next day. I can’t shower or bathe for 24 hours. After 24 hours I was to still keep the incision dry by holding plastic over it when I wash my hair. Bill goes to get my prescriptions filled. There are two prescriptions, one for pain medication and one for an antibiotic.
The nurse offered me a wheel chair to go to the bathroom, but since I know I am going home, I wanted to walk so I’d know if I was going to be dizzy. The nurse assisted me in getting up and walking to the bathroom, still with my IV pole. I did fine on that little. I was asked if I’m ready to go and I’m sure they wanted me out sooner than I actually left. I was told by the nurse at my pre-op appointment the day before to make sure I was ready before I left. I took her advice and stayed until I was sure I felt ok. My IV was removed just before I left. I took a pain pill to ward of any possible pain on the trip back to the hotel. Bill and the nurse helped me into a wheelchair. Bill took me up to the car which was parked in the parking ramp and we’re on our way!
3:30 – 9:30 pm – I tried to eat a bit of chicken soup, crackers and applesauce when we got back to the hotel. I started vomiting though and couldn’t keep anything down. A pain pill every four hours but every time I took one, I vomited shortly after and it was getting worse over time. Bill called the clinic to get a prescription for anti-nausea medicine, and then went out to a nearby pharmacy to pick it up. While he was gone, I huddled on a towel on the hotel bathroom floor thinking it was probably one of the worst places to be right after surgery (germ wise). Thank goodness I would be taking an antibiotic! Once Bill returned, I took one anti-nausea tablet and within minutes my stomach was settled (magic stuff!) and I was able to take my antibiotic. It stayed down. I tried to eat a little more. Everything tasted too salty or too sweet though so I didn’t eat very much. This time I had no metalic taste and no numbness in my tongue, just everything tasted over-seasoned. I propped myself up with pillows and did a pretty good job of sleeping that night. I’m sure the pain medication helped!
Day after Surgery: Thursday, July 10th
When I woke up I felt pretty good. Bill went down to the hotel breakfast bar for coffee. I felt good enough that I switched to extra-strength Tylenol and eliminated the anti-nausea medicine. Bill took a picture of my bandaged head and wild hair with my phone because I forgot the camera. I didn’t bother looking too close at the picture to see how it turned out because the pressure bandage simply had to come off. It was really hurting my forehead where the knot was. I kept trying to move it around but by that time it hurt no matter where it was. Bill cut the bandage off and, whew, what a relief that was! He declared that the incision looked good.
We hung around until it was time to check out and then I took some more extra strength Tylenol just before leaving. I used a neck pillow to help on the ride home so my head would be supported a little bit more. It was an uneventful drive home. I was feeling very alert on the ride home. When we got home I felt strangely energetic and yet sort of shaky from the surgery. I’m sure this was in part because the anesthesia had not worn off completely. I took it easy the rest of the day.
Day two after surgery: Friday, July 11th
At about midnight I woke up with a horrible migraine-like headache (the hang over? LOL). I took more extra strength Tylenol, but the headache kept getting worse. By the time Bill got up at 8 am I was in a lot of pain. He called the clinic and the nurse directed me to take two pain pills, which I took with one of the anti-nausea pills. I went back to bed with the room darkened. I spent the entire day taking a pain pill every 4 hours and an anti-nausea pill every 6 hours. By 6 pm I was beginning to feel better and was moving around a little bit. By the next day I was no longer taking any pain medication.
After that, every day, I felt a little stronger. My stitches came out on Thursday morning a week after surgery. I went back to work on that same Thursday, but it really was too soon. I only worked 4 hours on Thursday and 4 hours on Friday. Monday was a day off, so by the time I went back on the next Tuesday, July 22, I felt good. If I ever do this again, I will plan on taking two weeks off.
Less than 48 hours to hook up on August 7th! I'm looking forward to getting started on rehabing my ear and being bilaterally bionic!
I scheduled my pre-op appointment for the day before surgery since my implant center is one and a half to two hours away depending on traffic. We were hoping for an early morning surgery so we didn’t want to get up before the crack of dawn to drive down so we stayed the night in Ann Arbor.
At my pre-op appointment, I saw a physician’s assistant, a nurse and my surgeon, Dr Telian. They each asked various questions of me and answered questions that I had. My blood pressure, pulse and weight were checked. I had some blood drawn for tests. I received the news that I would be the first CI surgery of the day! I was to report to the hospital at 6 am with surgery to start at 7:30 am. I could eat up until 12 midnight, only water after midnight and nothing after 4 am. That wasn’t hard at all. Once I received instructions for surgery the next day, my husband, Bill, and I were free to explore the Ann Arbor area. Bill treated me to ‘Real Seafood’ and then we explored a bit before heading back to the hotel to use the pool and try to relax. Relax, right! Didn’t really happen! I didn’t sleep very well either.
Surgery Day: Wednesday, July 9, 2008
5 am – Per instructions I showered at the hotel using antibiotic soap. Dressed in loose clothing, making sure my top was button down so I could not be trying to pull something over my head after surgery. Worst part of this was no morning coffee!
5:45-7:30 am – Bill and I reported to the hospital about 5:45. Yes I was eager! I pretended to watch TV while waiting for them to call me. After a short wait, my name was called. Bill & I proceeded to the pre-op area. Here I was asked to put on a hospital gown and given some nice fuzzy socks to put on.
I must have had a ‘visitor’ every five or ten minutes! The pre-op nurse put my IV in. The anesthesia team of three each stopped by at least once to introduce themselves and ask me a few questions. My surgical nurse stopped by to introduce herself and to tell me that she would be with me through the whole thing. She advised me to think of something happy when they started to put me under so that I would think of this happy thing all through the surgery. She told me my current CI would stay on until I was asleep, then she would take it off and put it into the bag that had my clothes which was under the bed. After surgery, she would put it back on, slipping it under the pressure bandage, and turn it on for me. I would not need to be without my CI at all. Awesome! She also explained that she wanted me to say my name and what I was having done and that they would also ask me to do this once I was in the operating room and just before surgery started.
I had a visit from another young lady asking me if I’d like to participate in a study of a new anesthesia monitor that would be used in addition to what they were currently using. I agreed to participate so she stuck some funny looking monitor things to my forehead. The pre-op nurse was in and out taking my blood pressure, pulse, and generally getting me ready.
My surgeon, Dr Telian, stopped by to say hi and to answer any questions I might have before the surgery. He explained that they would mark my right ear just to reassure everyone and me that the correct ear was being worked on. It was really nice to meet all the people who would be there at the surgery doing various jobs. Very reassuring! Bill stayed with me throughout this time.
7:30-8:30 am - Promptly at 7:30, the team came to take me to the operating room (OR). Bill gave me a good luck kiss and left for the waiting room. Once in the OR, I was asked to slide over to the operating table which I did without incident. Sorry, no funny thoughts about the table and whether I could make the slide without incident. I just did what I was told. I’m sure I looked terrified. Considering that the only time I have ever fainted is when I say my own blood running out of one of my fingers after a cut, you can imagine how I felt. Not that I wasn’t sure I wanted to do it or that I wasn’t confident in Dr Telian and the surgical team. I was sure!
They began positioning me, padding my left arm which I’d be lying on while they operated on my right ear. The oxygen mask was put over my face and I started trying to think of sitting out on the bay with the water stretched almost as far as you can see and a warm breeze… I was out!
8:30-10:30 am – Surgery actually started at 8:30 and was finished up at 10:30. Dr Telian talked with Bill after and let him know that everything went really well with implanting the Advanced Bionics HiRes 90K cochlear implant.
10:30 am - ?? – I have no idea what time I woke up! I have this feeling it was after noon but I don’t really remember now. What I do remember is that I was in this beautiful meadow and didn’t want to leave but someone (the post-op nurse) was saying ‘Janet’, ‘Janet’… So I opened my eyes. Back to reality, I was in a hospital bed and my head really hurt, except it’s not my ear, it’s my forehead! The pressure bandage has a knot in it and that is what hurt. I told the nurse that it hurt and she pushed it up a bit. Then everyone that walked by gets shown my red bump from the pressure bandage. I noticed my ear was roaring and it lasted for about 5-10 minutes then quieted down. I did wonder who was whispering in my ear about a meadow when I was trying to think about the bay. LOL
I was offered a beverage. Only a soda, no wine, yet! So I sipped a Sprite and boy did that taste sweet and so very good. I was offered crackers so I nibbled one but it was very hard to get it down because my throat was so dry and sore feeling from the tubes. Then I had a sudden feeling that it was coming up! The nurse jumped and got me the barf bucket in time. She gave me something in my IV for nausea. After a while, I was moved to another post-op area and had a different nurse – who actually was my pre-op nurse too. This is unusual to have the same nurse both pre and post op. It was at this point that Bill joined me again.
1:30? –3:30 pm – Bill explained that Dr Telian could not wait for me to wake up because he had to be over at the new surgery center to do the next two CI’s of the day. The nurse continues to be in and out checking on me. I received the post op instructions. Bill got the honor of taking the pressure bandage off after 24 hours which will be just before we leave the hotel the next day. I can’t shower or bathe for 24 hours. After 24 hours I was to still keep the incision dry by holding plastic over it when I wash my hair. Bill goes to get my prescriptions filled. There are two prescriptions, one for pain medication and one for an antibiotic.
The nurse offered me a wheel chair to go to the bathroom, but since I know I am going home, I wanted to walk so I’d know if I was going to be dizzy. The nurse assisted me in getting up and walking to the bathroom, still with my IV pole. I did fine on that little. I was asked if I’m ready to go and I’m sure they wanted me out sooner than I actually left. I was told by the nurse at my pre-op appointment the day before to make sure I was ready before I left. I took her advice and stayed until I was sure I felt ok. My IV was removed just before I left. I took a pain pill to ward of any possible pain on the trip back to the hotel. Bill and the nurse helped me into a wheelchair. Bill took me up to the car which was parked in the parking ramp and we’re on our way!
3:30 – 9:30 pm – I tried to eat a bit of chicken soup, crackers and applesauce when we got back to the hotel. I started vomiting though and couldn’t keep anything down. A pain pill every four hours but every time I took one, I vomited shortly after and it was getting worse over time. Bill called the clinic to get a prescription for anti-nausea medicine, and then went out to a nearby pharmacy to pick it up. While he was gone, I huddled on a towel on the hotel bathroom floor thinking it was probably one of the worst places to be right after surgery (germ wise). Thank goodness I would be taking an antibiotic! Once Bill returned, I took one anti-nausea tablet and within minutes my stomach was settled (magic stuff!) and I was able to take my antibiotic. It stayed down. I tried to eat a little more. Everything tasted too salty or too sweet though so I didn’t eat very much. This time I had no metalic taste and no numbness in my tongue, just everything tasted over-seasoned. I propped myself up with pillows and did a pretty good job of sleeping that night. I’m sure the pain medication helped!
Day after Surgery: Thursday, July 10th
When I woke up I felt pretty good. Bill went down to the hotel breakfast bar for coffee. I felt good enough that I switched to extra-strength Tylenol and eliminated the anti-nausea medicine. Bill took a picture of my bandaged head and wild hair with my phone because I forgot the camera. I didn’t bother looking too close at the picture to see how it turned out because the pressure bandage simply had to come off. It was really hurting my forehead where the knot was. I kept trying to move it around but by that time it hurt no matter where it was. Bill cut the bandage off and, whew, what a relief that was! He declared that the incision looked good.
We hung around until it was time to check out and then I took some more extra strength Tylenol just before leaving. I used a neck pillow to help on the ride home so my head would be supported a little bit more. It was an uneventful drive home. I was feeling very alert on the ride home. When we got home I felt strangely energetic and yet sort of shaky from the surgery. I’m sure this was in part because the anesthesia had not worn off completely. I took it easy the rest of the day.
Day two after surgery: Friday, July 11th
At about midnight I woke up with a horrible migraine-like headache (the hang over? LOL). I took more extra strength Tylenol, but the headache kept getting worse. By the time Bill got up at 8 am I was in a lot of pain. He called the clinic and the nurse directed me to take two pain pills, which I took with one of the anti-nausea pills. I went back to bed with the room darkened. I spent the entire day taking a pain pill every 4 hours and an anti-nausea pill every 6 hours. By 6 pm I was beginning to feel better and was moving around a little bit. By the next day I was no longer taking any pain medication.
After that, every day, I felt a little stronger. My stitches came out on Thursday morning a week after surgery. I went back to work on that same Thursday, but it really was too soon. I only worked 4 hours on Thursday and 4 hours on Friday. Monday was a day off, so by the time I went back on the next Tuesday, July 22, I felt good. If I ever do this again, I will plan on taking two weeks off.
Less than 48 hours to hook up on August 7th! I'm looking forward to getting started on rehabing my ear and being bilaterally bionic!
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