Saturday, January 23, 2010

Halle turns 9 - by mom

Where does the time go?  Seriously.  I can not believe that Halle is 9.  It all goes so fast!  I feel like everytime I blink she is bigger.  I love every age with her, however I have to admit that I really loved it when she wanted to spend all her time with mom. :-) 



What I have learned about Halle so far...
  • She has a huge heart
  • She is always concerned about others' feelings
  • She is a caretaker
  • She is very expressive
  • She is very dramatic
  • She is great at imitating other voices and accents
  • She is a performer
  • She loves to be on a stage
  • She is a great dancer
  • Her favorite sports are soccer and cheerleading
  • She is a loyal Iowa Hawkeye fan!
  • She works at her own pace
  • She is smart and good at school
  • Her favorite things to do are cheer, make up dances, sing, be goofy, play on Webkinz, and watch movies.
  • She knows what her sister wants before I can even figure it out.
  • She loves animals and has a special place in her heart for all of her pets
  • She is always on the GO!
  • Her favorite food is crab legs
  • Her favorite drink.....because mom rarely lets her have it....is Mt. Dew.
  • She is a worrier, but likes to take risks all the same.
  • She prefers to play at home.
  • She is great at imitating scenes from movies
  • She is super funny
  • Her favorite color is green
  • She is 9 going on 16
  • She makes me smile
I love her










Friday, January 22, 2010

My Birthday Party - by Halle



Hi my name is Halle and I am Landri's sister.My birthday is January 16 i tearnd 9 years old my mom tells me to stop growing and stop getting smarter than her. We all thought Landri was going to be born in January and she was supposed to be born on my birthday but she was born 2 months early she was born on November26 instead of January16.





She came with us and my birthday was at Grandharbor water park I got to invite 5 people counting me 6 there is a really big water park we spent the night there for 1 night .I brought Macey, Jilliann, Chloe,zoey and another Chloe.for my birthday and what I got from Macey is make up a whole bag of it. from Jilliann I got a catapilller webkinz and Alivin and the Chipmunks the Squeakles cd from Chloe I got UNO sparkel and from the other Chloe I got dot'zas and Zoey did not spend the night cause she had a cheer compation and so she did not have time to get me a present. At the water park there are 3 slides. 2 were body slides where you do not need a tube and the other 1 you need a tube.  The one that you need a tube goes outside. It is a tunnel tube though so it is not cold and the other 2 slides are not tunnels.





It was really fun I am glad all my friends could go. Thanks mom for letting me go. It was in Dubuque if you want to go google Grandharbor water park.




There was this scabenger hunt and if you found all the peices you got to make your own reindeer and keep it and they would also give you 2 free tokens for this really big arcade.  There is this Deal or No Deal game and I won 400 tickets only on 1 turn and there is this chair you can sit in and it buzzes.




Monday, January 18, 2010

Landri's Listening update! 7 weeks of hearing!



Things have been so hectic lately that I haven't had a chance to get updates on the blog about Landri's progress and reactions since her sound was turned on.  I have so much to share!  Whew!  What a rollercoaster this journey has already been!  Up and down, up and down!! Since Landri's activation 7 weeks ago we have been back to the University of Iowa 4 times for MAPing appointments, electrophysiology, speech, and an appointment with her surgeon about a game plan for finishing the implant surgery on her right ear.  Sprinkle in a blood draw for genetic testing on her heart condition that took 15 years off of my life, interviewing private speech therapists, jumping thru insurance hoops, concentrating on pumping in the language Landri needs daily, creating good listening environments, trying to evaluate what sounds we feel Landri responds to, understands and replicates and I think that the next appointment needs to be for a psychiatrist for ME! :-)  Thank goodness I have other rockstar CI mommies as role models that work full time, have older children with a 1001 activities, are fabulous advocates for their children and get it all done while remaining sane.


The highlights!!!


  • CI appointments and MAPings - Landri has received 18 MAPs..I think....since she was first activated.  Each one is gradually louder.  She had one set of 8 that she really struggled with and pulled her CI off every second.....every half a second......much like right after she received her processor  It really was a challenge and a battle of the wills.  But, we worked thru it and in her most recent appointment they sent us home with only 2 maps!  One loud and one soft for different listening environments.  I am thrilled to say that Landri loves her latest map!  We turn the volume down a bit in the morning and after naps, but have her up to her optimal volume within 45 minutes.....so much easier!  A huge thanks to her Audis at the University of Iowa for this great map!  At her next appointment in 3 weeks they will put Landri in the sound booth for the first time since her activation to hopefully get an audiogram out of her which will give us a better indication of what she is really hearing.  I can't wait!
  • New sound moments for Landri - Landri's two favorite sounds are "ahhhh" and "mmmmm".  Everyday is soooo different. Some days she only says "ahhhhhh" all day....like to the point that she is hoarse at night and I wonder if she is every listening to me.  Other days it is all "mmmmm" and other days she is sooooo quiet I keep checking to make sure her CI is on and working.  At first all the drastic changes from day to day concerned me, but when I step back and think about it she has never heard her own voice before. How strange would that be?  No wonder she wants to hear it all the time.  And just like a typical one year old it becomes old news at some point and then the other sounds she is hearing become exciting and those are likely her listening days when she is so quiet.  Her TOD was at the house the other night for her therapy session and found that Landri consistently dances when music is played and then just listens when it is speech so we know that she is hearing!  We also have started testing Landri with the 6 Ling Sounds that represent different sounds across the speech banana on the audiogram.  Landri responds to all of them with no visual cues.  What we are waiting for is for her to turn to her name.  We have never seen her do this and we must use her name about 1000 times a day to reinforce it. I am anxiously awaiting this moment!!  We do see Landri react to many environmental sounds and I love to see those moments when I can tell something new has clicked for her.  I still struggle to try to assess her receptive language, but I need to remind myself....she has only heard sound for 7 weeks!!  Crazy!!
  • Landri's Therapy and resources - As a parent of a deaf child you have many decisions to make - hearing aides vs. cochlear implants, bilateral or unilateral, simultaneous or sequential implants, brand choice, surgeon selection, age of surgery, etc.  Honestly the decisions never end nor do the opportunities....responsibility....to advocate for your child.  One of the decisions that needs to be made is a communication method.  After much research we chose an Auditory Verbal approach for Landri.  This means that our goal for Landri is to be completely oral and mainstreamed in our neighborhood school by Kindergarten.  We want to challenge her to listen and speak and develop her auditory nerve and listening skills.  We have chosen to pur our time, energy, and a bit of faith in this approach vs. teaching Landri sign language.  Unfortunately our state has not one licensed AV Therapist....not one.  Any AVTs out there looking to make a real difference in the lives of deaf children and make many moms smile and sleep easier at night....please move to Iowa!  :-)  Since Landri was diagnosed as profoundly deaf we have been very blessed to receive a Teacher of the Deaf for her 30 minutes a week.  Since Landri was activated we held a new meeting and were fortunate to increase her TOD services to 45 minutes a week and also add an SLP to her team for 30 minutes two times a month.   The U of I recommends private speech services in addition to the ones provided to us thru the state.  Since we have chosen an AV approach for Landri we have researched extensively a new way of doing therapy.  Some well respected therapists and Oral schools across the country are now offering distance learning programs via SKYPE and other web based services.  This is a new approach developed by therapists that love our kids and realize the children that don't live in a community with an Oral Deaf school also deserve to have the resources available to learn to listen and speak.  We have visited with 4 programs that offer this service and hope to have a decision made this week. We are also in the process of jumping thru insurance hoops to see if we can get some of Landri's private speech services covered.  Distance Learning programs are so new that we have some convincing to do with BC/BS.
  • Finishing Landri's right ear - After much research once we determined Landri was a cochlear implant candidate we made the decision that we wanted Landri to be bilateral...have CIs in both ears.  Studies have shown that these kids do better in noisy environments and in localizing sound.  Since Landri's first surgery could not be completed due to fluid in her ear we still need to have this ear completed.  We saw her surgeon at the beginning of the month and he said that her ear looks GOOD and that he would like to complete the surgery in the Spring.  Yeah!!!
  • Landri's heart condition - In Landri's last CI surgery they found that she has a heart condition called Long QT disorder.  It involves her electrical system and how her heart beats.  Within hours of that surgery they started her on medication to slow down her heart rate. She has been on this medication 3 times a day ever since.  She has had another EKG to confirm the condition.  The disorder is genetic and we need to figure out which strain of the disorder she has to determine best how to treat her as she grows.  We are awaiting the results of genetic testing.  It is a miracle when you think of it. Because of her we found out that I have the same heart condition as well.  Thank God Halle does not. 
Information overload!  This is just a snippit of all that has happened.  It is so hard to include every single thing!  To anyone that is still reading this crazy long post I wanted to share a cute story about Landri.  She found her belly button the other day.  She kept pointing at it...then she would point at her nose...then to me.  She did these three steps over and over again.  I am for sure she was saying " Look Mom! I found a nose growing out of my tummy!"  :-)  We also got to see her CI buddy Evan this weekend when we met in Des Moines. I can't wait to watch them grow together in their new world of sound.  Miracles do happen. Blessings to all! 

Wednesday, December 23, 2009

Our busy bee!

Halle has been so busy lately!  I am so proud of how hard she works at school and balances all of her outside activities.  She always has funny things to say.  She made up a new joke...."What did the pickle say to the hamburger?"  "You're HAM-larious!".  :-)  Makes me giggle!!  She has been making up new dances to songs, working on her back handsprings, doing a lot of crafts, planning her birthday party, and bonding with her sister.  She had a decaf mocha the other day (like mother like daughter) and she said "I think this mocha is making me overreact!" because she was in a chatty mood. Then she said, "mom, I think your mocha is making you under-react."  :-)  So funny!  She is so dramatic and I wouldn't have it any other way. The other day she got dressed for school and looked in the mirror and said, "I'm smokin' hot!".  She keeps us all sane and everything in perspective.  I love her.



                                                                      SNOW DAY!!! 





Playing a clown fish in the school musical!!! The forced smile is the humiliation of mom taking a picture of her in her class room in front of her friends. :-)


National Qualifying Cheer Competition in Des Moines!  Placed 3rd and received a bid to Nationals!


Greg and Landri have maybe seen enough cheer this year. :-)

Peace to all for a safe and happy holiday!

Tuesday, December 22, 2009

Oh Christmas Tree Oh Christmas Tree!

We went to a Christmas Tree Farm this year to get our tree.  We had a great time searching for the perfect tree.  Here's how it went!!


Halle's first choice


Halle's second choice


The tree that we fell in love with, but it had a funky trunk that they said wouldn't fit in our stand. So we had to say good bye to it.



Putting the winner on top of the truck!



The finished product decorated by Halle and her neighborhood friends!  We are ready for Santa!!

Keeping Landri's CI on - Goal Number 1!

Keeping Landri's CI on her head has been quite the journey!  The first 5 or 6 days were......brutal. :-)  Every 15 seconds Landri took her CI off.  The first night we got home the only way she would keep it on was if we kept her hands busy. 

We first tried pickles then we tried to get her out of the high chair and play with her but she pulled the CI off in 20 seconds.


Sooooooo.....she got more pickles! Then we tried to play and she took her CI off in 20 seconds!


Soooo....she went back in her high chair before bed and got a cookie......and then mom and dad decided it was time for bed.



The next couple of days Landri got to eat mashed potatoes in Aunt Paula's lap to keep her hands off her CI.....


She got to chew on things too small for her that she could choke on to keep her hands off her CI...


We tried little hats that her friend Lily sent her (thanks guys! - your support is amazing and we can't thank you enough!!).  Landri was less than thrilled to have an extra thing on her head - although they work fab when we are outside with her!!



And then finally we tried the Lite Wear option that Cochlear provided us with.  Part of the processor that used to be behind her ear is now clipped to the bottom of her shirt and connected with a cord to the piece with the microphones that are still behind her ear.....and we love it!!!  I think that when we had the whole processor behind her ear it was just too heavy.  We finally found a groove!! What a relief!!



And the whole time I am sure that she is thinking....."what are they fussing so much about? what's the big deal?"  :-)

Friday, December 18, 2009

Landri's first "word"

We have exciting news!  First word may be stretching it.....just a tad.... :-) BUT Landri made what I would call her first step toward speaking!  One of our tasks given to us from Landri's Teacher of the Deaf (TOD) was to give Landri a little airplane and keep one for ourselves and wave it in the air making the "ahhhhhhh" sound at different pitches.  We do it all the time, all different ways, with all different games and she would just smile at us so sweet or sit there and hum.  Then she started to "dance" by swaying her head back and forth everytime we did it so we knew she was hearing it because she was bopping to the beat.  Then Greg and I are sitting on the floor talking one night and out of the blue Landri picks up her little airplane and waves it in the air and goes "aaaaaaaa".  It wasn't "ahhhhh" like in awesome like we have been practicing, but "aaaaa" like in cat - but we will take it!  We practically fell over and Greg was scrambling for the camera.  She has done it like 5 or 6 times since - never on cue of course when we prompt her to do it.  Typical girl - everything on her own terms. ;-)  So whenever she wants to get our attention she pulls out all the stops and waves her airplane saying her first "word" and she knows everyone will stop what they are doing, praise praise praise her and then she is back to being the center of attention.  The perfect life. :-)