Marcus is in the final stages of his senior year football season.
He starts Offensive Tackle. He has done well in his position and has been dubbed "MB Master Blocker". Our family has enjoyed watching him play through his Jr. High & High School years. Callie suprisingly is a MAJOR Cougar fan & steals the show when nearby fans catch her cheering right along with the cheerleaders & yelling out "go Show Low", "go Cougars" and putting her fingers to her mouth as she emits an exceptionally shrill sound that is a nearly perfect imitation of my whistling.
Conference games ended last week and last night was the first and thankfully not their last game in state playoffs. They played against Estrella Foothills and came away with a 34-10 win.
Next week they will be up against Winslow at Campo Verde High School. The game will be at 4pm for anyone interested in going. Playoffs are single elimination, so of course we are hoping to see a win there. The final state playoff game will be the Sat. after Thanksgiving! We hope to see the Cougars there, we shall see! One week at a time.
We also enjoyed watching Burke play this year and look forward to him playing in High School next year. He starts as center and they ended their 8th grade season undefeated. They were also undefeated their 7th grade year also. For those of you familiar with our region, yes, that means that they beat Blue Ridge, something we hope continues throughout their HS years! It is especially fun for me to watch their group. They have played school yard and neighborhood football together all their years, and I have had some of the other boys in cub scouts over the years.
We also enjoy attending concerts for Marcus, Elsie, Burke & Emma. They are all in choir and Burke & Emma play in the band.
Marcus & Elsie got to perform this past week at the State Fair. Fun! Fun!
It brought back the memory of leaving the hospital to go see Marcus perform there last year.
Feast of Carols practice will be starting soon, and we are looking forward to that. They are having a dessert night with much lower price & also have lowered the dinner tickets by $5 per person. Anyone interested in going, let me know. It's fun to go and sit together. We thoroughly enjoy it every year we attend.
May blessings attend you ALL!!!
Sunday, November 8, 2009
Thursday, October 29, 2009
from my metal art & creative writing classes
Metal Art Music
Tink tink tink
Pum pum pum
Tata tata tata tat
Ding ding ding ding ding
Rat a tat a tat
Buzz
Sizzle
Roar
Thunk thunk thunk
Hummm
Through my spongy electric green ear plugs, I hear music.
…the tink tink tink of Mr. Noble’s hammer as he pushes wrenched metal smooth.
… the pum pum pum of the rawhide mallet mashing steel.
… the tata tata tata tat of the ball peen on the rivet, James is working so hard to set.
…the ding ding ding ding ding ding of the planisher as Hillary stretches out the fine details of her wings.
… the rat a tat tat as I weild the rounding hammer to push out the edges of my bowl.
…the buzz of the grinder used to polish the metal’s surface fluid.
… the sizzling torch as Gary melds two halves into a whole.
… the roar of the fiery forge, who’s white hot flames temper black iron red.
... the thunk thunk thunk as James presses and shapes the red-hot iron.
… the hummm of the mighty furnace pushing out torrid heat to add to our steamy sweat.
Thursday, October 15, 2009
BIG NEWS!!!!!
WOW!!!
We are SOOOOOOO EXCITED!!!!
Recently Callie has been forming up to 3-4 word sentences
as regular conversation for her :) which is a BIG thing for her!
Then this morning she zipped up her pajamas after a diaper change!!! Yeah for her!
The BIGGEST news of the day has been over 1 year in coming. At the appt week before last, her Neurologist had not talked about the possibility of regaining the damaged nerve function, which we have previously thought was the 3rd & 7th nerve, and recently learned that she is also lacking 5th nerve function.
She has been to an Institute one time so far (Gifford Health Institute in Gilbert AZ run by Dr. Kevin Gifford), where they do therapy targeted to stimulate nerves that lack proper function. We have been doing some of the therapy here at home. We hope to get her back soon & frequent. She has also been receiving electrical facial stimulation to the left side of her face aimed to stimulate the damaged nerves, and hopefully "Wake up" the left side of her face! She pats her left cheek and says "Wake up Face!", she also says "tickle" when they apply the devises & sometimes clamps her little hand tight to her cheek & will NOT allow them to apply their "tickle tortuous" devices until bribed with a sucker! (the dum dum or tootsie variety :)
So, for the big news.... this morning she coughed, and her left eye squinched down tight every time she coughed and we have been noticing all morning how she is having general MOVEMENT on the left side of her face!!!!
It isn't in balance with the right side yet, but it is a very GREAT beginning!!!! and we are OH SOOOOO HAPPY about it!!!
We are SOOOOOOO EXCITED!!!!
Recently Callie has been forming up to 3-4 word sentences
as regular conversation for her :) which is a BIG thing for her!
Then this morning she zipped up her pajamas after a diaper change!!! Yeah for her!
The BIGGEST news of the day has been over 1 year in coming. At the appt week before last, her Neurologist had not talked about the possibility of regaining the damaged nerve function, which we have previously thought was the 3rd & 7th nerve, and recently learned that she is also lacking 5th nerve function.
She has been to an Institute one time so far (Gifford Health Institute in Gilbert AZ run by Dr. Kevin Gifford), where they do therapy targeted to stimulate nerves that lack proper function. We have been doing some of the therapy here at home. We hope to get her back soon & frequent. She has also been receiving electrical facial stimulation to the left side of her face aimed to stimulate the damaged nerves, and hopefully "Wake up" the left side of her face! She pats her left cheek and says "Wake up Face!", she also says "tickle" when they apply the devises & sometimes clamps her little hand tight to her cheek & will NOT allow them to apply their "tickle tortuous" devices until bribed with a sucker! (the dum dum or tootsie variety :)
So, for the big news.... this morning she coughed, and her left eye squinched down tight every time she coughed and we have been noticing all morning how she is having general MOVEMENT on the left side of her face!!!!
It isn't in balance with the right side yet, but it is a very GREAT beginning!!!! and we are OH SOOOOO HAPPY about it!!!
Monday, September 14, 2009
Na Na Na Na!
(Sorry the pictures are sideways, but I had to post them anyway!)This morning Callie was in her high chair eating breakfast! Jeff & I were talking about high school football, when she had all she wanted, she stood up & sang so clearly, "na na na na, na na na na, hey hey hey hey!" She cracks me up! That must be what she remebered from the football game on Friday!
I guess I'll take a minute to brag on the boys... Marcus & Burke are, both playing this year, Marcus as OT & kick off team & Burke plays center & defensive linebacker & kick off team. They also are both #56 (makes it easy on me :) & both of their teams are undefeated so far this season! I'm really enjoy football season :)
Anyway, Callie was just too cute this morning to not share!
Have a wonderful day!!!
Tuesday, September 8, 2009
Our Year of Miracles
Today marks One full year from the day of Callie's accident!
We have been sooooo blessed in so many ways & by so many people.
I feel that I have never adequately been able to show our thanks.
We have decided as a family that we would like to have a
Come & go Open House to honor this year with Callie
Sunday September 13, 2009
from Noon to Nine
in our home.
The invitation is to EVERYONE of you & anyone you feel would be interested to come!
We have been so AMAZED by the journey & feel that many have been touched
by the experience with Callie & ALL have been blessed that have been touched by it.
Please come & join us in our Joy for the year we have had with Callie.
If you would like to come & don't know where we live, please leave a comment & how you would like to be contacted & we will get directions to you.
We have been sooooo blessed in so many ways & by so many people.
I feel that I have never adequately been able to show our thanks.
We have decided as a family that we would like to have a
Come & go Open House to honor this year with Callie
Sunday September 13, 2009
from Noon to Nine
in our home.
The invitation is to EVERYONE of you & anyone you feel would be interested to come!
We have been so AMAZED by the journey & feel that many have been touched
by the experience with Callie & ALL have been blessed that have been touched by it.
Please come & join us in our Joy for the year we have had with Callie.
If you would like to come & don't know where we live, please leave a comment & how you would like to be contacted & we will get directions to you.
Tuesday, July 14, 2009
I know it has been such a long time since I have posted... We have been having a wonderful summer! Callie is doing so well & is making so much progress. Even though she still has challenges with her left eye, we continue to hold out hope for it one day to be a "thing of the past". We love you and continue to be blessed by each of you in our lives. Life is so precious! May you all have a wonderful summer and may your lives be blessed in every way!!!!
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