Thursday, February 18, 2016

Again! Again!

I theorize special needs parents have more theories about kids shows, ideas for spoofs no one else would understand, and time to think about the enormous holes in premises or plots because our kids fixate on a few shows or movies for a longer period of time. Maybe this is just my kid, but we have been watching "Wonder Pets", "Cars", and "Oswald" FOREVER.


I will admit a crazy amount of joy in discovering "Robot Chicken" took the time to visit with Linny, Tuck and Ming Ming.  It is off color, it makes me laugh. You can choose for yourself if you click on it.  If over years you have seen every episode of "Wonder Pets" at least twice and some favorites more than 50 times that makes it funnier, just sayin'.


How are the characters in "Cars" born? Who taught McQueen to race? How old is he? How did he not know anyone until Radiator Springs? Does he have parents? Did he grow up rich and sheltered? Do they live forever? Can a mechanic / doctor replace every part? If so, what gives each vehicle identity or soul? Is it a post apocalyptical world where the people created the vehicles and then the vehicles took over and killed all the people off?

 Is Daisy a cannibal when she eats a salad? Why does Flippy live in the water, but Oswald lives in the air? What makes Weenie a pet? How did they decide how many roller skates Oswald would need? Why doesn't Johnny melt? Is he selling his offspring?  Peppa has similar, though less surreal, questions. How do they have pets? What decides if you see Dr. Hamster (a vet) or Dr. Brown Bear (a doctor)?

There was a period where she loved "Penguins" and currently she can not get enough of "Home". I think she would watch "Home" multiple times every day if we would let her. I love this "Home" trend as she acts out many parts of this movie, including lots of hugs, and has a line up toys she needs, including a hello kitty heart that helps her find "my mom" when they use the map. I am excited when she is willing to give something new a chance, as she is usually resistant. The excitement fades quickly as we watch the same thing over and over and over.

I  found an About Me project from three years ago and her favorites were... drum roll please... "Wonder Pets", "Cars", and "Oswald".  

What are favorites in your house? Any theories you have been searching for a venue to explore? Any answers to the questions above?

Wednesday, February 17, 2016

Not Feeling Well

Clues of Illness
1) Would not put Abby Cadabby down
2) Took Abby instead of Talker when we left the house
3) Refused ice cream
4) Little appetite in general

How She Threw Me Off
1) Didn't stop jumping for joy
2) Look at that smile
3) Chatty as can be
4) We were on vacation from school and PJs and lounging were the norm

Results
1) Fever
2) Fades out in the evening
3) More days off school
4) Snuggles


AAC Specialist

About six months ago we started seeing an SLP that specializes in AAC, alternative and augmentative communication, devices. He is a MAN! We once had a teenage boy teach swimming, every other professional has been female.  Really, that is not important, but it is nice for her to interact with man in this type of environment.  

She is awesome at communicating her needs and wants. We want to know what she is thinking, have her be able to ask us things, and use her device for more than answering questions from the outside.

He is focused on her using her talker (AAC device) more conversationally. They have been working on "where" as the first question word to master. Every week she chooses a toys box, usually the baby, and then he hides things she needs to play with.  She has to ask on her talker "Where is the baby?" or "Baby is hungry. Where is the bottle?" He coaches her when she defaults to "I want baby." or "I want bottle.". 

They struggle, some days she wants to work with him and some days she doesn't. We drive an hour each way for her 30 minute appointment. Recently she just cried for 27 minutes because she didn't want to work with him. This center has an observation room where I watch the sessions and can hear everything they do. I am so thankful for this to see their progress and learn strategies, but also to know she had not mistreated her and not have to worry too much about her crying for a week. 

One cool thing that has developed recently with her talker is describing things she sees, when we don't ask. If "Wonder Pets" are headed to save an animal then she says the name of the animal on her talker. If she sees a baby, or a snack, or a ____. She tells us on her talker. This new spontaneous talking is not in complete sentences, and sometimes makes context difficult, but it is spontaneous! 

Rufus Kisses

It is nice having the love of a girl (and her mom) when you are an old dog.

Saturday, July 4, 2015

So, yeah, I abandoned the blog for 18 months. These things happen. We have been busy.


 There was a sixth birthday....



                                           ...and a seventh.



A deep love of Hello Kitty was discovered, and we now feature her on every surface of the house. 



 We are sadly now a one dog house.  


We listed our house, accepted an offer, and have found a new house. 
We hope to move to before the summer is over.  

Of course there was more. Maybe there are stories to tell. We will see. 



I WANT TALKING

Yesterday, after spending a long time searching her device for what she wanted to say. She finally gave up and with a pout used it to say "I want talking".  I think my heart actually broke.  I know it is motivating she is frustrated. I know it is awesome her device gives her a way to express it.  I just wish it wasn't so hard for her.

Tuesday, December 31, 2013

Saturday, December 21, 2013

The Mayo Clinic Adventure

C, Granny, and I hopped in the car this past Monday morning for the 9.5 hour drive to Mayo Clinic.

We decided to stay at a "family resort" outside of Chicago because (a) it was going to snow (b) it was less than 2 miles from the path we would be traveling and (c) there was pool and bowling alley in the hotel.  The first leg of the drive was a piece of cake and as we checked into the hotel the snow began to fall.  It snowed steadily that evening and we were glad we decided to take the extra travel day.  We came to discover the pool and bowling alley were in a different building on the campus and due to the snow decided we didn't want to go back outside with wet hair.  So, we drove into the town of Itasca.  We grabbed a coffee and found America's Best Train, Toy, and Hobby Shop.  They had more Geotrax and Cars stuff than we have ever seen in one location.  We picked a treasure or two after about an hour of browsing and were off to a local pizza place for yummy dinner.

Tuesday morning we had breakfast and jumped back in the car to Madison for lunch and a visit to the Children's Museum.  We had so much fun running around and playing.   This museum has building toys, an art area with lots of projects, and a huge area to run ramps, climb stairs, slide down slides and more.  It was a great stop and everyone had fun.  Back in the car we went for the final leg of our trip.  The little one had a nap in the back.  Granny and I were excited to cross the Mississippi and enjoyed the landscape changes.  We arrived in Rochester after dark, stopped for a bite to eat and were off to get settled in to our home for the week.

We decided to rent "4 Private bedrooms in Rochester, Minnesota".  For a fair rate we rented the downstairs from someone's private residence.  I had hemmed and hawed about this decision for quite some time as I was nervous about staying with a stranger; but just a hotel room for the three of us for the week sounded tight.  We were to have 4 bedrooms, a living room, and bathroom.  We found the house and met our host and her beautiful baby.  She only had two beds made up for us (which is all we really needed) and we were surprised to find space heaters in every room, outlets with no plate covers, open vents, and a few other minor issues.  When I asked how we were supposed to come and go, there was no key available for us "yet". And the wi-fi was down.  We unpacked and got settled in, ready to make the best of it.  As the night progressed it became frigid.  It was the kind of camping cold where you can not move under your enormous pile of blankets because it might break the seal and the air could enter.  As I lay in the cold not sleeping I concluded we would leave in the morning, this was completely unreasonable.

At 4 am I awoke to C waking abruptly coughing, and throwing up all over our bed.  There was no bath tub, no paper towels, no extra sheets, and we had to leave the bed in the cold to clean it up.  I pulled out the wipes, threw the sheets in the wash (benefit of staying in someone's basement), got C settled in with blankets and her iPad and packed up all our stuff.  I called and made a reservation at the hotel I had been considering while hemming and hawing.  We could check in at noon.  I should mention she was not sick on the way there or again after we left, I think it was related to the cold.  Also, our hosts apologized, there is usually heat and it was supposed to be fixed before our arrival, but they did not think it was important to tell us before our arrival or during our stay.

C had an appointment at 7:30 and then one at 10:30.  We drove to the Mayo Clinic complex, Granny dropped us off at what we thought was the right building, and went to park the car.  We were a few buildings off, but everything is connected by tunnels and we made it to the first appointment tired, but on time.   C doesn't like medical environments, the more medical it seems the less she likes it.  When I say she doesn't like it I mean: "if someone comes near her in a medical environment she screams like you are peeling off her toenails." We have never had a successful blood pressure reading as she will not calm down enough for it if someone is near her.  After much screaming they had checked her height and weight.  We saw a neurologist who is the gatekeeper to get into the speech and language department we were really there to see.  We had time for breakfast in the cafeteria before headed to see Dr. Strand, a leading apraxia researcher who is part of the team I heard present at the national conference last year.  At this point we had been up since 4 am and C was holding it together, but was not at her best to meet someone new for an evaluation.

Corinne was semi-cooperative for the first day of the evaluation.  The office had a sofa and a kid size table and chairs.  This made C much more comfortable than a room with an exam table.  They did a receptive language test, we discussed her skills and challenges, and discussed the intensive program they have for a select few appropriate candidates.  This first day, she told us she did not believe C was ready for the type of therapy that is most effective in treating Childhood Apraxia of Speech.  The therapy in their intensives use no games or pictures.  The focus is getting as many repetitions as possible by the child watching the therapists face and mimicking what the therapist does.  When we completed that first appointment we grabbed lunch and were able to check into the hotel.

Oh, the luxury!  There was heat!  There was a pool in the building!  It is connected to the Mayo system through the indoor tunnels!  We had keys!  It was lovely.  Joy and relief were felt in our very nice mini-suite with a half wall between the sitting room and beds and everyone laid down for a much needed nap.  It was an excellent decision to move to the hotel.  The pool was 3 feet deep all the way around, Corinne could touch all the time and loved it.

The following days, we had additional appointments with Dr. Strand and she was surprised how different C behaved from that first meeting.  We learned and practiced some new strategies and are stepping back to focus on empowering C to know she has control.  We are doing large and small, tight and loose, and fast and slow motions to learn what they feel like on our big muscle groups and then moving to our smaller muscles in our hands and face.  We are also using physical and spatial cues to elongate or shorten (control) sounds.  Her ability to maintain focus, ability to control her body, and language (not speech) are the suggested focuses for the time being.

The ability to walk from the hotel to our appointments, stores, restaurants, and more without stepping foot outside was fantastic.  There is a grand piano on the subway floor of the building our appointments were in.  Most times, someone was playing the piano or choirs were singing, and crowds were gathered to enjoy.  There are volunteers around every corner waiting to direct you as you find yourself lost (again) in the maze of tunnels.  Mayo was efficient and well planned.  It was an unusual feeling looking around any room or hall and trying to imagine each person's story and what brought them there.  We only left the enclosed tunnels of Mayo once more to visit Costco, and a blow up jumping place.  The Costco was empty. There were no lines or crowds the week before Christmas and this was busy for them. Minnesota is strange land.

Out last appointment wrapped up at noon yesterday.  We were able to conference Kevin in for the recommendations, questions, and observation summary.  We were on the road by 1 pm and drove straight through to arrive home at 1:45 am this morning.  C changed into PJs in Chicago, read a story, and went right to bed.  I can not thank my mom enough for joining us on this adventure.  I am not sure what we would have done without her.  She was a great driving companion well into the night when we were getting sleepy and silly.  It is so nice to be home.  We missed Kevin and the hounds like crazy.




Tuesday, November 12, 2013

S-U-G-A-R Jump Into Your racing Car

It is time we talk about something important over here.  I am so excited the favorite movie of the moment is "Wreck It Ralph".  I love this movie, she loves this movie, he likes this movie, we love this movie.  Let's take a moment to overanalyze this great movie and it's life lessons.
1.)  Believe in yourself.
2.)  Get outside of your box.
3.)  You can do anything you put your mind to.
4.)  Don't ever let others tell you what you can do or who you are.
5.)  Princesses and heroes don't always look like princesses and heroes.
6.)  People that do bad things are not always bad guys.
7.)  Watch out for double stripes.
8.)  Closing credits = dance party
9.)  Stop playing the same old games and whole new world is waiting for you.
10.)  Your dump could be a whole new life for someone down on their luck.
11.)  Friends are worth fighting for.
12.)  Whatever people say about you they can not change who you are.
13.)  You are not defined by how others perceive you.
14.)  Always sign your masterpieces.
15.)  Watching someone get hit (but not injured) is funny.
16.)  Beauty is in the eye of the beholder.
17.)  You find the best friends (or the someone who gives you the honey glow) in the most unlikely places.
18.)  Funny nicknames are always fun.
19.)  You can't reprogram the world and pretend you are someone else.  It will blow up in your face.
20.)  Memories can not be locked away.  They get out.

Saturday, September 21, 2013

Messy Party

 We had a messy party this summer.  It was my dream.  

We started with every kid grabbing a huge sheet of paper and toe painting.

Once everyone arrived we opened all the activities.  This is a water table full of cornstarch and water with kool-aid coloring droppers to squeeze in.  


 Fun included shaving cream covered slides that landed on the mat or slip and slide.


We filled our sandbox with 20 packages of spaghetti.  It was my favorite.  Awesome!

Toward the end we filled the pool with bubble solution.  I used the glycerin, dawn, water recipe to make 10 gallons of bubbles.  At the very end we turned on the hose and cleaned them all up.  I had everyone bring a towel, but also had a box of extra towels just in case.

Of course, no summer party is complete with out ice cream sundaes and popsicles.

A Break and A New Start

It has been a while (again) since I posted.  I do not think I am a born blogger.  It was a very fun summer.  A week in Denver, a week in DC, a trip to Michigan Adventure, lots of swimming, playing, parties, and fun.  We had an awesome messy party in the backyard (she stayed clean) and fun times with friends and family.  

C took August off of all therapies and just had fun and started karate.  She is going twice a week and seems to love it.  She has a very hard time following directions and trying new novel motor movements.  She is a great jumper and kicker, but struggles with the concept of punching, or making a fist.  We practice all the opening stretches at home and she is getting better at those.  The place she has class is awesome and there are helpers that help the whole class, but spend a lot of time with my kid.  She has made tons of progress.  I worry other parents don't like how much attention she takes, but they have all been very supportive and keep telling me it just takes time to get the hang of it.  Some of the other kids are frustrated she doesn't do everything they do.  I love that her teacher punishes her for talking or not following directions just like she punishes the other kids.  I hope this is good for her, I think it is.  

Once we started to get the hang of karate it was time to go back to school.  This year back to school meant a whole new school and schedule.  I am the proud mama of a kindergartener.  She has two classes.  One with 8 kids and 4 adults with lots of support and help and one with 22 kids and 2 adults where she is expected to participate in the standard curriculum.  The first day of school Kevin and I both dropped her off and picked her up.  When we dropped her off she cried a bit and was just apprehensive about the whole thing.  She was seriously glowing when we picked her up.  She was up early the rest of the week thrilled to go to school.  Her team seems amazing.  

It is so hard for other kids to include her and realize she is different.  I am volunteering in art class with her big class.  The kids didn't know who I was and some of them were explaining to me what C can or can't do.  It was such a weird moment.  I need to get used to these moments where other kids complain C doesn't have to do what they are doing, or find her hard to get to know.  I have not mastered handling these moments at all.  I explain things she enjoys and things that are challenging and how everyone is different.  It is hard to understand when you are 5.  

I just hope they are nice to her, and she makes friends and learns and has fun and loves school.  I know every one will not be nice forever and hope she has the self confidence to not worry about what other people think or say, but I want everyone to be nice for a few more years.  I know problems create problem solving and I don't want to keep her in a bubble.  It is just that so many things are so hard for her I want some things to be easy.  

She chose her Halloween costume this morning.  You can look forward to adorable rainbow fairy pictures in the future.  She is so excited she wants to wear her wings everywhere.  She is studying herself in the mirror in her wings as I type.  I better go play.