Thursday, February 4, 2010

What's Going On....

Things have been pretty crazy at our Home! January 15th we picked up Molly, well it seems like since they things have just been out of control. It's like having twins I swear except one of them walks around just trying to eat everything in site (that would be Molly not Tate).
Tate is great, he is getting so big. He has had quite the time with a cough and stuffy nose, but I think part of it is because he is teething. His first tooth has finally made its appearance. I cannot believe it! My little baby boy is growing too fast! Here are some pictures of our hectic life lately! I had Josh get a picture of Tate and I, we spend a lot of time doing this and yes I am holding his bottle, he knows how to hold it, but when I feed him he lets me hold it for him. He wont hold it for me at all! I hate it! (but love it at the same time).
Playing with those toes! Tate Loves the Cowboys already! Maybe next year we'll get our superbowl ring!


Molly and Gunner
Molly and Tate, she loves him. Look how cute, this was one sunday when we were going to Steve and Chelese's house.

this just shows you how much she loves Tate.


Libby and Tate
Berlyn, Tate and Libby

Eva had Devyn and I over for dinner tonight, it was so fun! The babies played so well together! Tate was obsessed with Berlyn's head and Libby wanted Tate and Berlyns binki's and Berlyn wanted Tate's binki, it was a blast!

Libby


Berlyn

Wednesday, January 20, 2010

Help expert Mommy's

Tate has a had a bad cough and stuffy nose for a while, on and off. It's been on this time for almost 2 weeks. He is breathing fine (except when he eats), and he has had no fever. a little fussy but for the most part seems okay except when a coughing spur comes.
WHAT CAN I DO....
the pediatrician said motrin, but on the package, it says after 2 days stop giving it to him.
the pediatrician also said there is nothing you can do, just watch his breathing. well its fine but there has got to be something.
He has a cool mist humidifier, I suck the boogies out at every chance.
I tried baby vicks on the feet for 2 nights, no change really.
Any miracle cure out there that you all might know of?
Please share if you have a cure for a nasty cough and bad stuff nose.
thanks!

Tuesday, January 19, 2010

Meet MOLLY

This is Molly our New Mastiff Puppy! This is what I got for Christmas, definatley a surprise. I have been wanting a Mastiff for quite some time and Josh found a good deal and a good breeder and here she is. She is 7 weeks old today. She is Apricot color and a TANk! She is the biggest of litter weighing in at 11 pounds last week, when all the other pups were 8.
Here are some pictures of our little girl. She Loves Tate and tries to take his toys, its really funny. He likes her, just not when she chews on his feet.
She will just sit with Tate, its so cute.






I will keep pictures coming so you can watch with me how fast she will grow.

7 MonThs

Tate turned 7 months last week (yes I am behind). I cannot believe how fast that last month went! He is growing so fast and He is so much fun! Here are a few pictures of our little chunk!
Some fun things about Tate:
He LOVES Veggies: peas and sweet potatoes are his favorite
also Enjoys Bananas & Peaches
So far he is not a fan of Juice
He enjoys watching the animals, he gets so excited when Meeka gets close.
He definately knows how to get a rise out of people, he is the smiliest baby! Every where we go he is smiling at someone.
Enjoys his blocks, stuffed animal from Ang, and his Keys
and well his Hair is out of control, I don't know what to do with it! Its so Curly!!
We love you Tater!











Friday, January 15, 2010

missing you

I miss posting weekly! I am at work...tee hee....so I thought I would say that my GOAL this weekend, is to update my blog! Tate is so big and I need to introduce our newest member of the family!

Thursday, January 7, 2010

Maurice

they sent this article to us at work, i tried to get the picture uploaded so you could see this mans face but it didnt' work. I am sure you could find it online through the Standard Examiner.
I thought you might like to hear this feel good story. It touches my heart so deeply. I want to cry for this man who has had to have such trials in his life but as you read the story you see that he has not had trials but has been blessed in his perspective. It is so wonderful to know that in a world of selfishness there are people out there that still want to give back, no matter the cost. I hope this year brings us all many blessings of Love and Happiness. enjoy...



A new hope for Washington Terrace husband, father and youth coach. He will have surgery to remove facial tumors today
By JaNae Francis (Standard-Examiner staff)

WASHINGTON TERRACE -- Maurice Simpson knows all too well that he has a face people don't forget.
Simpson, 33, is afflicted with neurofibromatosis, a rare genetic condition that causes tumors to grow on the right side of his face and head. The tumors get bigger over time.
He is disfigured by elongated tubular lesions hanging most noticeably from his eye socket and nose, leaving him with only one eye. His mouth slants at about a 45-degree angle, causing him to slur his words.
While a number of folks carry the genes for the disease, his family knows of only one other case as severe as his. But despite all that, Simpson's self-image couldn't be higher.
"I don't shy away from social interactions," said Simpson, the general manager of the Bountiful Arby's who has worked continuously in the food service industry. "I enjoy people and I want to interact."
But today, much of the continual reminder of his condition and barriers to such interactions could start to change for Simpson. Starting early this morning, he will undergo surgery at University of Utah Medical Center that could last as long as 12 hours and involve a dozen doctors. At least four specialists will contribute, he said.
The surgery, Simpson said, will not only change the shape of his face but could save his life as well. One of the tumors is encroaching on his brain.
"It makes me a little nervous, but the excitement is overshadowing my nervousness," Simpson said. "It's been so long (17 years) since I had surgery."
It's just one of a series of operations he'll undergo in the next few months to reconstruct his nose and maybe even his eye socket.
He said doctors are considering giving him a glass eye to give him a more regular appearance.
It's all been made possible by a generous donation from an area businessman who would like to remain anonymous.
"It's a touching gesture," said Simpson's dad, Willey Simpson, of Flint, Mich., who is visiting during the surgery and part of the recovery. "He is our angel."
Maurice Simpson's wife, Charity, said the philanthropist first saw her husband 10 years ago and was haunted by the image of his face and thoughts about how he could help him.
"He thought about it a long time," Charity said.
Then last spring, Simpson saw the man again when he was delivering 10 pizzas to his office complex.
Simpson remembers the meeting.
"I was trying to get the pizzas in and he said, 'Here, let me help you.' And he was the owner of the company."
Weeks later, Simpson's supervisor at the Roy Pizza Hut told him a man wanted to pay for him to have surgery and she'd already checked out the philanthropist to make sure he was legitimate.
Simpson doesn't remember ever having a normal-looking face. His mother, Brenda Simpson, said she discovered a problem with her child's eye when he was just 2 months old.
By the time she found the right specialists who could operate on her son, unusually large growths already had begun to jut out from his face.
Even after dozens of surgeries from that time until he was 15, mostly to remove the bulky parts of the tumors, Simpson said his appearance never changed all that much.
But despite his looks, Simpson said his parents raised him to feel good about himself.
"My self-esteem is pretty much out the roof because of my upbringing," Simpson said, recalling his parents telling him to be proud of who he was and putting him in special schools with kids who were worse off than him, who could be his friends.
"Don't be ashamed of who you are," Brenda still tells her son today. "Jesus Christ, people talk about him. No matter who you are, people talk about you."
But Simpson said doctors and surgeries in the past have taken away from his sense of self as specialists gave him false hope that the tumors would stop growing when he reached puberty or adulthood.
"I felt like there was a lot of broken promises from the doctors," Simpson said, explaining his decision as he approached adulthood to give up on surgeries and get on with his life.
Back then, the family had insurance that would pay for the work.
"We had insurance through General Motors," said Willey. "It was good insurance."
But despite that, the parents decided to listen to their son when he didn't want any more surgery 17 years ago.
"The tumors just kept coming back, coming back," Willey said. "When he decided he'd had enough, we decided he was old enough to decide for himself."
But Brenda said she has renewed hope in today's technology.
"The things they can do with medicine now, they can make it a lot more presentable," she said.
Today's surgery is largely cosmetic and not covered by insurance.
The family has not been involved in the finances behind the procedure and can only imagine the astronomical costs involved.
But they also understand the personal benefits of charitable service to be received by the donor, who they've met and have promised not to disclose.
"You can imagine how people would go to him once they find out he has money," Willey said.
In like fashion, Simpson has given his share of service by coaching boys and girls recreation and competition basketball teams in the city for the past 12 years.
He and his wife also have four children of their own
Simpson said his condition opens doors for him to be a positive influence on those he coaches.
"I find it makes it easier," he said. "I bond with them a little easier and I love it. ... I don't get any complaints."
Simpson recognizes the positive influence he has on others who don't share his challenges, as he holds his head up high every day and focuses on the abilities he has and not those he doesn't.
"I play in different basketball leagues," he said. "Adults know that I am playing and they'll bring their kids. Their kids will be saying 'Dad, he is so cool.'"
Simpson said a coach at a three-on-three basketball tournament paid him the highest compliment.
"He said, 'My kids are just sitting there amazed by your confidence,' " Simpson said.
It's those experiences that keep a smile on the left side of Simpson's face and the words of his father in his heart whenever he gets a negative reaction from those he meets.
"Sometimes the world can be cruel, but you gotta face it," Willey said.
And that's all Simpson wants to do, tumors or not

Saturday, January 2, 2010

A look Back at 2009

2009 What a Year!! Here is our Review, it's a long one, for we had a LOT of things going on this year! It was a great year, We had some trials but when Ilook back I see all the blessings we have recieved this year! We ended 2008 and rang in the new Year by finding out we would be having a Baby Boy!
JaN: Josh played church ball

Angie's baby shower



Jamie & Haylee visited


Feb: painted our upstairs
March: Josh turned 26


Had a Great Easter

April: 28 weeks went into pre term labor and got to spend the night in the hospital, luckily they stopped Tate from coming and I was able to make it to my baby shower. Ended up going on best rest for 6 six weeks.
May: another baby shower in Tooele!

Had our Maternity pictures done at 32 weeks.

Josh worked very hard on Tate's room!


Bought a New Car so we had a vehicle to fit our family
June: Just before we went to the Hospital 10th, at 10pm

332 pm on the 11th Tate arrived: 6 pounds 11 oz. 19 1/2 inches
Adjusting to parenthood
July: visited the new Oquirrh Mountain Temple

Tate's first trip to the Lake: Willard Bay

Went to Washington DC, went to a Nationals games, vs Atlanta Braves
Tate first Airplane ride: he did great!
Uncle Kenny's baptism
spent the 4th of July in DC
August: Tate's baby blessing

Josh and I went on a ride out at Antelope Island

Some did a hit and run on our truck!

September: Labor Day hike, in the Unitas
Made salsa and Jam with my Grammy!
Josh broke his hand playing soccer. Celebrated 3 years of Marriage!
October: Jaquie got married
Went to Days Farm with Tate's preschool and Eva and Libby came along to get pumpkins with us!
Tates first Halloween, the soccer family. November: I turned 27! Tate's first Thanksgiving: at Josh's parents
December: Tate ate Peas and Loved them
Had fun at all the Christmas parties!
And we had a great Christmas (pictures to come later).