A Rainbow of Words

A Crazy Fun Life With 3 Kids

Friday, March 27, 2009

Michael went back to Afghanistan

So the last 2 weeks went by so fast but they were so fun. Michael came home on the 14th and he had to leave on the 25th. We had a lot fun getting to see him. The kids were a little shy when they first walked over to him but in a few minutes the shyness was gone and they were all over Daddy. The loved playing with Daddy and having him put them to bed. Broc was so happy I thought he might just keel over from being so happy that Daddy was home. While Michael was here his brother Sam got married and he was the best man and Peyton was yet again a flower girl. This was the 4th wedding she was the flower girl for. I think I should start renting her out to be a flower girl for weddings cause she has so much experience now. It was also Broc's 2nd Birthday while Michael was here we threw him a big Cars themed party and I made him a really cool cars cake. He got lots of.....Cars for his birthday. It was also Michael and my 5 year wedding anniversary I can't believe its been that long already. We upgraded our wedding rings and Michael got a Swiss Army Watch. Michael also got to bless Katie son Ace while he was home he thought it was a very enjoyable experience. Peyton was given a definitive diagnosis on having PDD-NOS which means Pervasvise Developmental Disorder Not Otherwise Specified. A big word which means she doesnt fall into just one category she falls into multiple things but not enough of one of them to be that one thing. They say that she will be in special ed for almost all of school. But they say as an adult she should be able to live on her own get married and have her own kids. They say its very rare for a child with PDD-NOS to grow out of there delays and problems. So she will always have it she will just have to learn and adjust around it. So she will start taking more Speech Therapy and Occupational Therapy along with seeing a regular therapist to help her with coping and keeping her at a balance level. They are excited with the progress she has been able to make so far. They said they dont see any of the traits in our boys though which is good that means they won't have the same problem as Peyton. In other news Hunter is a crawling maniac now. We weren't suppose to let him learn but he figured it out and does a sort of Army crawl. He still favors is bad arm he doesnt put much weight on it with the funny crawl he does. He is also sleeping by his self almost. He is getting a little better about sleeping he can almost sleep for 4 hrs in his own bed before he comes into bed with me and bugs me all the rest of the night.

Slid down the rainbow at 2:12 PM 1 comments

Thursday, March 5, 2009

Meeting of the Minds

Michael is finally on his way home. He will get to be home for 2 weeks then he will have to go back to Afghanistan for another 2 months then he will come back for good. Then we will move back to TX where all are stuff is. I am excited I can't wait for him to be back for good. I miss having my own space.

Ace has been coming up to hang out and Hunter and Ace love to stare at each other they are going to be good friends when they get older. Peyton has some more testing to pinpoint where her delays are and how severe they are and how to help her with them. Broc 2nd bday is coming up and he is having a car themed party. He will also start getting all his shots now that he is 2. After Peyton started showing signs of delay we choose to forgo immunizing the boys till they were 2. In that short time things have changed. There used to be so many more shots when Peyton was the boys age but they cut out like 7 shots. So I think that regardless of the bull they push on immunizations not leading to autism or be harmful they must of not bought it themselves and cut back and changed the age on some immunizations.

Michael and I 5 year anniversary is this month as well. I still can't believe its been 5 years. It has gone by so fast. We are going to do sealing for the dead at the SLC Temple for our anniversary. I would tell you what I got him but he reads my blogs so then he would know so you will just have to wait till after the 20th.

It's been 3 months since my my car accident where I was rear ended when I was stopped at a red light. I am still fighting with the insurance company of the person who hit me. They are being cheap skates on paying me a fair value for my minivan. Also my attempts at finding a 2000 or higher in Land Rover Discovery II SE7 are still in vain. I looked at many who have problems with the shift differentals or engine problems. Then I looked at 2 worth buying but one guy just stopped answering my calls and the other family want more then it is worth. I am waiting cause I think the lady will cave cause no one else has made offers and with the economy no one is willing to shell out 6 grand. So I am hoping her desperation for the money will make her come down to what I am willing to offer her. I shall keep you updated on my process of finding a Land Rover. Thankfully the medical portion of my thing will finally settle. I have to have surgery to screw my muscles into my shoulder to fix my problem they also think there is tear in there that they wont be able to see till they cut my arm open. So needless to say my payout I have been told will be substantal due to the pain and the surgery. I havent been able to take anything to help with the pain the last 3 months due to breastfeeding Hunter. So my pain and sufferage will be high. I am hoping it high enough to payoff the loan on our 2007 Suzuki Forenza it is such a bad luck car. It has already had its tranmission and alternator replaced and still the radio doesnt work. There are also a few areas that still need to get painted because of accidents and stuff. I hate the car personally and I think it hates me too so I avoid driving it at all costs.

Slid down the rainbow at 5:18 PM 0 comments

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