Sunday, August 7, 2011

Happy Birthday Hazel!

Hazel in her Belle dress ready for her Belle Birthday Party
I can't believe my beautiful girl is 4 years old.  She talks more like she is 10....  She is a sweet, special little girl and we love her very  much!

She had a wonderful birthday party yesterday along with all of our other festivities.  I have about 500 pictures (not kidding) from this weekend to sort through and then I will post photos and updates. 

I wish I had time to catch up right now but I have to leave in exactly 12 hours for New York!  I have to pack what I will need for 2 weeks, do laundry, go to church, say goodbye to all my family that came to town for the weekend, clean the house, tie up loose ends, pay bills, etc.! 

It has been a crazy few days but we survived and had a great time being together as a family. 

Talk to you soon!

Thursday, August 4, 2011

Am I Insane?

I think we all know the answer to that question by now, however I seem to get even crazier by the day.  That being said, I like it this way.  The times in my life when I had nothing to do, nothing going on and no challenges were the most boring, depressing and unfulfilling times in my life.  I am not AT ALL saying that is like that for anyone else!  Because of my personality I like to stay very busy and I tend to take on WAY more than anyone should.  However, I seem to just function better that way.  I do more, I accomplish more and I am happier.  Backwards huh?

So - that being said, let's look at the schedule for the next 4 days shall we?

Tomorrow:  Leaving by 10 to drive 5 hours to arrive just in time for my baby sister's bridal shower!  My whole family will be there and I am so excited! Go to sleep and then....

Friday:  Leave by 7 a.m. to drive 5 hours back home to prepare for my baby sister's second bridal shower at my home!  My whole family arrives hours later as well as a few family member's from Bo's side!  We will have 22 people staying in our house!

Saturday:  Hazel's Birthday party is at 10!
                 Brody's Birthday Party is at 12! (He missed having one with while we were gone)
                 Brody's baptism is at 5!
                 Dinner following baptism is at 7!

Sunday:  Hang out with family and then take the red eye to NYC where I will stay for TWO WHOLE WEEKS!  I will be attending the Brain Balance training and I am so excited.  I will be learning so much more than I already have.  I can't wait to be able to learn what I need to know to effectively treat children and help them and their families!

So - What do I have to do in between these above listed items over the next 4 days? 

  • Pack for Bridal Shower
  • Finish reading training manuals and books! 
  • Clean my house and get ready for another shower!
  • Shopping to get food for shower, parties and baptism dinner
  • Preparing food for shower and doing a few decorations
  • Figure out what we are even doing at the birthday parties!
  • Get balloons/decor for birthday parties and figure out what to do since they can't have cake!
  • Pack to live in New York for 2 weeks!
  • Work on getting our Lease signed for our center space
  • Work on the floor plan layout to get it finalized
  • Spend time with my family!
  • Sleep! (ha!)
  • Go even more insane!
  • There are hundreds more but I won't bore you with my "to do"list.. :)
I am going to post as much as I can over the next 2 weeks and I am excited to share things I learn at training.  

Center update:  We are hoping to sign our lease this week and start construction very soon!  After that will be hiring, training, marketing and then opening!  Sounds easy right? :)

Goodnight!

Sunday, July 31, 2011

Sweet Rewards

Well, I am not going to lie to you it is really hard to be a mom. (Not a shocker to all of you moms out there)  It is even harder to be a mom of kids with special needs or disabilities.  Its even harder to try to still be a wife, a sister, a friend, a homemaker, a daughter, and a business owner.  But this is not a gripe session.  Life is hard for everyone and we all have trials that we are given and they are all at different times in our lives. 

The last couple of days have been a bit hard for me and I have been COMPLETELY overwhelmed (way more than usual).   It seems as though whenever this happens, I am given "sweet rewards" to remind me of why I do what I do and that it is all worth it.  :)

These things may be little to you, but they are big to me!
  • Brody is awesome. I can't even begin to describe how different he is.  Over the last few days I have noticed even more growth and maturity.  I ask him to do something, he does it right away.  Not only is a good boy for not whining or complaining, but he actually immediately does the task and doesn't get off track.  I can even send him up the stairs to do something and he actually comes back!  He used to go upstairs, get distracted, and I would find him an hour later playing Legos.   
  • I also observed him in school and watched him do an entire math worksheet without moving, wiggling or needing his teacher to cover all the problems on the page besides the one he was working on.. 
  • He LOVES to read and it is so cute to see him reading and reading and reading.  He reads in the car, during meals, in bed and everything in between.  Don't worry - he still does plenty of other things. :)
  • He uses his words.  Rather than just yelling or screaming when a problem arises with his sister, he comes to me and talks to me about it. 
  • This morning something happened that just amazed me.  I was still mostly asleep but I heard Brody and Hazel come into the room and talk to Bo.  Then I heard Brody say "Sorry Papa".  And Bo said "for what?" Brody then said "I stepped on your clothes that were on the floor - I didn't see them there".  Bo told him that was okay and he walked out of the room.  I was SHOCKED!  Before Brain Balance if there was ANYTHING on the floor in Brody's road he just stepped right on it.  A book, a puzzle, clothes, toys, my foot, etc.  Most of the time he didn't even notice it.  It was as if it was just part of the floor.  I don't know how many times I had told him not to step or stand on things that were not the floor.  And now all of the sudden he didn't only notice that he stepped on clothes but he stopped and apologized for it.  This truly is amazing and made my whole day. 

There are probably more things, but that is all I can think of right now.

Oh wait - this one is HUGE!  Today we were outside and the kids were riding bikes and scooters.  Brody was on his Razor scooter and had a little crash.  I was preparing myself for the crying and freaking out over the tiniest little scratch.  But instead, Brody said he had an owie and ran in the house.  He wasn't crying or too upset and Bo and I were discussing something outside, so I didn't follow him in.  When I went in a little bit later I found Brody with a band aid on his leg.  I asked him what happened and he said that there was blood running a bit down his leg from his owie.  I told him I could clean it off and he said he already had washed it off, put antibiotic ointment on it and a band aid!  I could NOT believe that he was so self sufficient and just took care of himself like that! That has NEVER happened before.  What was even more amazing was that he wasn't crying, screaming and freaking out over a a scratch and some blood.  The band aid was actually already bloody and he had blood on his shorts so I know it wasn't just a tiny cut.  However, he handled himself so well and just took care of it. 

  • Wyatt is communicating so much!  The best part is that he is using words or phrases that were NOT previously taught during ABA therapy.  He had learned to say a ton of words, but NEVER used them.  Now he is using them so much AS WELL as talking and using words that we have never heard him say.  He also puts phrases together that were never taught.  That tells me that he is thinking for himself!  He is taking the knowledge in his head and the things he has been taught or has been observing and using them all on his own!
  • Yesterday he came to me and said "piggy back" so he got on my back and we started walking.  He then said "couch, lay down".  I LOVED it!  I love that he can tell me what he wants to do and where he wants to go and that I didn't teach him to do it.  He is learning it on his own. 
  • Today he was in my room and I kept trying to get him to go out.  He kept saying "train" so I told him we would go find his train.  He wouldn't come out and kept looking around the room and under the bed.  I asked Bo if he had seen a train and he said no.  Wyatt then said "white train".  It is so great that he is just putting words together and describing things like that!  So sure enough I kept looking and found a gray and white train under the bed.  That is all he wanted so he grabbed it and was on his way!
  • He also says things like "blue shirt", etc.  :)
  • He is understanding body language/non-verbal communication more.  He sees me move towards him like I am going to chase him and he smiles and turns and runs (even with his cast on!)
  • When asking for bacon he now says things like " one two bacon" or "three bacon".  It is so cute that he is telling us how many he wants!
  • Yesterday, I gave Wyatt a muffin which he calls "toast".  He always wants us to cut it up and won't just take bites of it (yet...)  This time I put it on his plate and tried to get him to take a bite of it and he wouldn't.  I was doing the dishes or something so I just left it there and walked away.  The next thing I knew, Wyatt had gotten a knife out of the drawer and went to sit back down.  Then he proceeded to cut his own muffin!  He used to just say "knife" or "cutting" so that we could cut it (which was also amazing!) But this is even better!  
Isn't he cute?!
  • Overall he just is at a higher cognitive level.  He understands what we say, he follows directions and he communicates back with us.  
Wyatt still has a long way to go, but seeing these kinds of things on a daily basis gives me the strength to continue on this journey for as long as it takes!

And then there is Hazel... What to say about Hazel?  :)  She is growing up so fast and will be 4 in ONE week!  I can't believe that my "baby" is that old.  She is doing so well overall.  However, she has been having a few tantrums here and there.  We have been working on using our words..  We are also working on cleaning up her own toys and things which she does NOT really like.  However, she is getting better.  Today the "toy monster" took some of her things which she will have to earn back. 

The other day she disappeared upstairs for awhile.  When she came downstairs it was obvious what she had been doing..

Eyes, lips hair combed and necklace and I didn't teach her any of it.  We are in trouble... :)
So much to tell you but so little time!  This is the latest I have been up probably since I moved home.  I have been so much more tired here and I can't figure out why.  I used to stay up until 3 am and get up at 6 or 7 and just keep on going.  But now I go to bed at 9:30 and get up at 6 and I am dragging all day.  What is going on?  My mother in law says I am just catching up on the last 5 years of sleep that I missed out on :) 

Goodnight!

Thursday, July 28, 2011

COULD YOUR CHILD BENEFIT FROM BRAIN BALANCE?

 Does your child exhibit signs of a Right Brain Delay?

Please read this and pass it along.  Even if you think your child is perfect :) There may be something that you have missed.  I did for awhile and many other parents do.  When a child is more severe and non-verbal it is easy to see there is a problem.  But when they appear to be a typical child, often times we miss the fact that there may actually be something going on that we didn't realize.  I was actually SO relieved when I realized WHY Brody acted the way he did.  I had always known he was smart, but why did he still dart in front of cars or avoid homework like the plague?  Why couldn't he ride a bike?  Why did he have emotional outbursts as if he were 3 years old?  It changed the way I viewed and dealt with everything when it came to him. 

Note:  The majority of children suffering from a Functional Disconnection are right brain delayed.  Right brain delays are typically characterized as:  ADD, ADHD, Autism, Asperger's, OCD, non verbal learning disorder, and Pervasive developmental disorder.  There are still many children with left brain delays and I will try to go over those symptoms in another post.  However, because the majority of children, including my own, suffer from right brain delays, that is what this post will be focused on.

At Brain Balance, they don't use labels.  The typical labels out there like Autism, ADHD, etc. are just lists of symptoms.  These symptoms are better described as a right hemispheric delay.  In fact, there are many, many children out there that don't come near to meeting the typical criteria for Autism,  Aspergers or ADHD.  These labels create a situation where so many kids fall through the cracks just because they may not have all the symptoms of one of these disorders.  In fact, these children may have many of the symptoms and have significant issues or deficits in some areas but are not getting the help they need.  Sometimes this is because parents don't even realize what is going on and why their child is acting the way they are, why they are struggling in school or socially, etc.  On the other hand, if a parent does see that their child needs help, if they don't have an official diagnosis, they are not able to get services through the school or state. 

The very best thing to do is to get Disconnected Kids and read it!  Go through the checklists and see if things sound familiar when it comes to your child.  *The information and symptoms below came directly from the book.*

After reading this and/or the book if you are concerned about your child and even think they might benefit from the Brain Balance Program, take them to the nearest center and have them assessed.  It is totally worth the small price you pay for the VERY comprehensive assessment.  You will then sit down with the Center Director and they will explain to you exactly where your child is at developmentally, cognitively, etc.  They will tell you their strengths and their weaknesses and exactly what they can do to PERMANENTLY address those problems.  If any investment is worth it, this one is.  Especially where it can help you address problems before they get worse and/or may find problems that you didn't know existed yet - i.e. visual processing, auditory processing, sensory issues, etc.  For example:  Brody was a good reader, but he HATED to read.  He never read for fun.  However, he tested at a 7th grade reading level BEFORE entering Brain Balance.  They found that he had visual processing issues and other problems with eye muscles and with his eyes working together which made reading VERY laborious and not fun at all.  Now, he will NOT stop reading.  He reads during meals, in the car and in bed.  At summer school his teacher told me that he will ask "how many more math problems do I need to do before I can read".  I LOVE it!  It is so amazing to see him completely turn around like that. 

Okay, so here is the list of symptoms/red flags, warning signs or whatever you want to call them.   If you notice that your child has even some of these issues, it is worth looking into it.  The longer problems are left untreated the harder they are to correct.  Also, the heartache, stress, financial strain, etc. that goes along with trying to correct these issues in ways - that only make a dent - in treating the symptoms could be shortened or avoided.  I am so extremely grateful that there is a real solution to these problems and that it is safe, permanent and SO fast.  Even though some children with more severe imbalances could need multiple sessions, it is still SO much faster than the years and years or maybe lifetime of therapies that they would need and still never achieve these results.  Why? Because no other program actually CHANGES and "rewires" the brain.  

I tried to put these in categories, but it is a bit scattered.  There are also some things that are repeated...  I decided it was better to get it posted for you to read rather than worry about how organized it was :)

Final note:  This list applies to children of ALL ages.  In fact, I find things on this list that apply to me :)  Also, your child does not (and WILL not) have to have ALL of these symptoms.  You will read it and see many that don't apply to your child.  But, if you notice they do have some of them, or a lot of them, there is cause for concern.

Here we go!


the brain is not developing properly some symptoms are:
  • Inappropriate laughing and giggling
  • lack of fear, especially in the face of danger
  • risk taking
  • an aversion to being cuddled or held
  • sustained unusual or repetitive play
  • avoiding eye contact
  • a preference to play alone
  • difficulty in expressing needs
  • making wild gestures
  • insistence on everything being the same
  • difficulty interacting with others
  • difficulty setting goals and prioritizing
  • difficulty controlling emotions
  • difficulty learning, remembering and paying attention
  • poor motor control
  • inability to monitor own actions
POOR BODY AWARENESS
  • They have a poor sense of gravity and are not very good with balance. 
  • They are clumsy and walk into things
PROPRIOCEPTION
  • They can be physically awkward
  • walk oddly,
  • be unusually clumsy. 
  • lean to one side or 
  • be unable to ride a bike. 
POOR GROSS AND FIND MOTOR SKILLS
  • Bad posture
  • Awkward gait 
  • Uncoordinated and have no sense of timing or rhythm 
  • May have crawled or walked late or crawled strange like scooting.  
  • They may have skipped crawling altogether and start walking earlier than usual. 
  • Clumsiness and odd posture
  • Poor coordination
  • Not athletically inclined and has no interests in popular childhood participation sports
  • Poor gross motor skills such as difficulty learning to ride a bike and/or runs and walks oddly
  • Repetitive stereotyped motor mannerisms
  • Fidgets excessively
  • Poor eye contact
  • Walks or walked on toes
  • They have a hard time manipulating their hands, fingers, toes and feet.  Often displayed later as poor handwriting
* Some kids have motor problems very subtle like a head or body tilt in one direction, a foot that turns in and legs that appear knock-kneed are other signs of improper postural muscle growth.

POOR SOCIAL SKILLS

Very common and a significant problem.  Most of these kids are very friendly and motivated to have social relationships but they don’t know how to go about it and do it all wrong.

Normal development of social skills is dependent on the normal development of the area of the brain that controls nonverbal communication.  That is the ability to read body language and understand people’s emotions and intentions by observing their facial expression, tone of voice, etc.  This is not a skill that can be taught, it develops naturally.

ABNORMAL EMOTIONAL REACTIONS
  • Spontaneously cries and/or laughs and has sudden outbursts of anger or fear
  • Worries a lot and has several phobias
  • Holds on to past “hurts”
  • Has sudden emotional outbursts that appear over reactive and inappropriate to the situation
  • Experiences panic and/or anxiety attacks
  • Sometimes displays dark or violent thoughts
  • Face lacks expressions; doesn’t exhibit much body language
  • Too uptight; can’t seem to loosen up
  • Lacks empathy and feeling for others
  • Lacks emotional reciprocity
  • Often seems fearless and is a risk taker
SENSORY PROCESSING SYMPTOMS
  • Fussy eaters due to an under sensitive (or oversensitive) sense of taste and smell.  
  • Some children cover their ears because they cant stand a noise that sounds normal to everyone else.  
  • Some don’t like to be hugged. 
  • Poor spacial orientation, bumps into things often
  • Sensitivity to sound
  • Confusion when asked to point to different body parts
  • Poor sense of balance
  • High threshold for pain - doesn’t cry when gets cut
  • Likes to spin, go on rides, swing, etc. anything with motion
  • Touches things compulsively
  • A girl uninterested in makeup or jewelry
  • Does not like the feel of clothing on arms and legs, pulls off clothes
  • Doesn’t like being touched and doesn’t like to touch things
  • Incessantly smells everything
  • Prefers bland foods
  • Does not notice strong smells, such as burning wood, popcorn, or cookies
  • Avoids food because of the way it looks
  • Hates having to eat and is not even interested in sweets
  • Extremely picky eater
COMMON ACADEMIC PROBLEMS
  • Poor oral and written expression
  • Poor reading and written comprehension
  • Poor writing skills
  • Inability to organize
  • Lack of focus
  • Reading and spelling problems
  • Inability to follow directions
  • Lack of concentration
  • Difficulty understanding cause and effect
  • Poor sequencing ability
  • Confusion when presented with multiple bits of information
  • Poor social skills
  • Cognitive symptoms
BEHAVIORAL CHARACTERISTICS OF A RIGHT BRAIN DELAY
  • Logical thinker
  • Often misses the gist of a story
  • Always the last to get a joke
  • Gets stuck in set behavior; can’t let it go
  • Lacks social tact and or is antisocial and or/socially isolated
  • Poor time management; is always late
  • Disorganized
  • Has a problem paying attention
  • Is hyperactive and/or impulsive
  • Has obsessive thoughts or behaviors
  • Argues all the time and is generally uncooperative
  • Exhibits signs of an eating disorder
  • Failed to thrive as an infant
  • Mimics sounds or words repeatedly without really understanding the meaning
  • Appears bored, aloof, and abrupt
  • Considered strange by other children
  • Inability to form friendships
  • Has difficulty sharing enjoyment, interests, or achievements with other people
  • Inappropriately giddy or silly
  • Acts inappropriately in social situations
  • Talks incessantly and asks the same question repetitively
  • Has no or little joint attention, such as the need to point to an object to get our attention
  • Didn’t look at self in mirror as a toddler
ACADEMIC PROBLEMS OF A RIGHT BRAIN DELAY
  • Poor math reasoning (word problems, geometry, algebra)
  • Poor reading comprehension and pragmatic skills
  • Misses the big pictures
  • Very analytical
  • Likes slapstick or obvious physical humor
  • Is very good at finding mistakes (spelling)
  • Takes everything literally
  • Doesn’t always reach a conclusion when speaking
  • Started speaking early
  • Has tested for a high IQ or is above normal in verbal ability and below average in performance abilities
  • Was an early word reader
  • Is interested in unusual topics
  • Learns in a rote (memorizing) manner
  • Learns extraordinary amounts of specific facts about a subject
  • Is impatient
  • Speaks in a monotone; has little voice inflection
  • Is a poor nonverbal communicator
  • Doesn’t like loud noises like fireworks
  • Speaks out loud regarding what he or she is thinking
  • Talks “in your face” - is a space invader
  • Good reader but does not enjoy reading
  • Analytical; led by logic
  • Follows rules without questioning them
  • Good at keeping track of time
  • Easily memorizes spelling and mathematical formulas
  • Enjoys observing rather than participating
  • Would rather read an instruction manual before trying something new
  • Math was often the first academic subject that became a problem
IMMUNE CHARACTERISTICS OF A RIGHT BRAIN DELAY
  • Has lots of allergies
  • Rarely gets colds and infections
  • Has or had eczema or asthma
  • Skin has little white bumps, especially on the back of the arms
  • Displays erratic behavior - good one day, bad the next
  • Craves certain foods, especially dairy and wheat products
AUTONOMIC CHARACTERISTICS OF A RIGHT BRAIN DELAY
  • Problems with bowels such as constipation or diarrhea
  • Has rapid heart rate and /or high blood pressure for age
  • Appears bloated, especially after meals, and often complains of stomach pains
  • Has body odor
  • Sweats a lot
  • Hands are always moist and clammy
I think that is it!

It is SO important that we are all aware of these symptoms for our own children, and for our friends and family.  The numbers of these disorders are rising at an incredibly terrible rate and those are only the ones that are diagnosed.  There are many, many children out there struggling and many parents who are trying to find answers.  For those of you looking, Brain Balance IS the answer.  I promise.

Goodnight!

Monday, July 25, 2011

Still Improving!


The kids are doing so well and they are continuing to progress (even though we aren't actually attending a "real" session of BB) We are doing as much as we can at home and it is working amazingly! The kids have started summer school and are doing great. They all love getting out of the house and interacting with other kids. Wyatt especially loves it he wakes up every morning saying SCHOOL!

The school is great and just what they need.... mostly right brain learning...Yahoo! They all do very well and are adapting to the school environment. They can't wait for the school year to start!

*Note* Today we got home from school and Wyatt ran in the door and I said "Wyatt" he replied with an "oh hi!!" Then I said did you have fun at school? Wyatt said NO! Little punk.....It's amazing that he is initiating the communication! 

Here are a couple pictures of them at school.....(I don't have any of Brody cause he is in the older class!)  Enjoy!






 
 


Must See!

I have a great post in the works, but it is not done yet -(It is quite time consuming...) 

But in the meantime, I realized that I hadn't posted Dr. Melillo's latest interviews.  These are great!  They are short, but VERY informational and all based on great science and recent studies. 

Please take the time to watch them and then share them with anyone you think could use the information - which is everyone!   We should all be educating ourselves and exercising our own brains too.  :)

Again, Dr. Melillo is the amazing man who founded the Brain Balance Centers and is also the author of "Disconnected Kids" and Reconnected Kids" which are both amazing books!  I truly think that EVERY parent should read them regardless if they feel their child has any issues at all.  It is so informative and can even help parents with things to help prevent a brain imbalance (or a worse imbalance) in their child. 

Goodnight!








Saturday, July 23, 2011

We Are Going Green!

*Note:  Life is SO crazy and I will continue to post on this blog, but if you don't see one for a day or two, don't give up on me! :)

We have already taken a lot of steps to "Go Green" over the years, but here are a few recent ones just to make the blog fun :)

We have replaced these.....

Plastic (even BPA free) has other toxins that can leach into your food...
 With these....

Glass containers - Costco has great sets for a great price!
 And these.......

Not only are these not biodegradable, they also are still made of plastic!

With these.....

A good friend of mine is making these washable, reusable snack bags!  They have a Velcro closure and a great liner that is not made from plastic!  I will Put more information up later of how to order from her.  Her prices are great and way less than Etsy and other sites.  Also, some bags out there still use plastic liners... Email me or make a comment if you would like some info on how to contact her to make an order!
We also replaced this....

Our backyard has been dirt for almost 3 years!   My amazing husband was trying to surprise us with having at least part of the backyard landscaped when we got home.  We came home early and ruined his surprise :)


With this!

Our beautiful green grass!! Now the kids have somewhere to run and play complete with a bike path around it!  Thanks Papa!  Now only if it wasn't 110 degrees outside... :)

We also replaced this....  (not Wyatt!! - the cast!)


 With this new GREEN one..... :(


Yes, that is correct.  Wyatt got a new cast.  That was actually what I had really hoped to avoid and didn't think would happen.   So why did it?  Well let me tell you.  Wyatt had worn a hole in the bottom of his cast from dragging it around the first 2 weeks, but we had taped that up and it had been fine.  But then he overflowed the toilet during his new fun game of "unroll the entire roll of toilet paper into the toilet and try to flush it".   Most of the time I had caught it before it actually overflowed, but this time I found him standing in a pool of water...  After that the cast smelled worse and you could tell the structure was compromised so I had to take him in.  

I was hoping and really thought they would just tell me that it had been 4 1/2 weeks and that they could just take it off now and be done, but that was not so.  They said that either way it had to come off because of the water so they brought in their big saw and started cutting.  Wyatt actually did really well considering... They said that removing a cast is traumatic for ANY child because of the loud saw, the pressure it puts on your leg and the fact that you are watching a saw and hoping it doesn't cut you!  Wyatt was very scared and was crying pretty bad.   Here are a few videos of him getting the cast off.  Still so sad!



 

 



Trying to split open the VERY thick and hard cast.  The Dr. said it was HUGE when he saw it. 

The first moments without his cast on...

You can kind of see how red his leg is.  There were also a few little bleeding sores and so much dead skin.  We washed it as good as we could in the sink but it was still not looking great.  It was very interesting because he only had his cast off for a total of about 10 minutes, but he didn't even try to stand up, move, run around or anything.  When I picked him up to take him in for his X-ray, he grabbed onto his leg the way he used to before he got his cast as if to support it.  It seemed as though he still thought that it was broken or going to hurt him? 

Here is a picture of the X-ray.  As you can see, there is still a break in the bone... He said that it was healing up, but hadn't all the way.  He said that if I could ensure that Wyatt wouldn't run or jump, we could leave the cast off and just be careful.  Ha!  Obviously, the cast went back on!  He said that just jumping could re-break the leg and we were NOT going to risk that!


I tried to explain to Wyatt that we had to put his cast back on.  I know he understood me.  He started getting teary and his lip quivered a bit.  He was sad and scared.  When the doctor asked him if he wanted red or green, Wyatt said "car".  That was his way of saying, "I want neither, can we please leave now?!"

He was a very good boy as they put his cast back on.  He whined and whimpered, but sat still so they could do it.  The doctor said he could go ahead and walk on it now (which he was already doing!) but they put the cast on kind of strange and the poor guy is stuck in a "tip toe" position!  He is trying to walk all over like that and it is hard for him and looks so uncomfortable!  If taking the cast off wasn't so traumatic, I would go get a new one put on him.  But since he only has to wear this one for 2 weeks (we hope!) then we will just have to live with it the way it is.

Poor Little boy!
This little boy has been through just about everything in his life.  It seems like if something is going to happen, it happens to him.   However, he has always been so brave and does very well even considering his circumstances.  I truly wish I knew what was going on in his head during all of these trials he has had. 

He always has such a good attitude though.  We got home with his new cast and he adjusted to it quickly learning how to walk and run even with the strange shape of the cast.  He has also been playing games with everyone!  He initiates play with Hazel to tickle him, and with Brody to build pillow forts and then they destroy them.  He also comes running in the room and says "Mama - Potty!" and runs to the bathroom.  I follow him as he laughs all the way.  He sits on the potty and says "bye bye" and so I leave.  Then he comes and gets me again and wants me to chase him back there and he laughs so hard.  It is so cute to see him initiating play with all of us and calling us by name.  He is communicating SO well and telling us what he wants and it is amazing.  He is continually improving and  I know this is just the beginning.  This sweet little boy will someday be whatever he wants to be - something amazing - I am sure of it.
Happy Saturday!
Tammy