Friday, August 29, 2008

August update

Life has been so crazy this month. I don't know why I thought it would calm down with school starting but it definitely didn't. The update on Tia's school situation is good. She got a new aide who I really, really like! She is young and has a 14 y.o. sister with DS so she loves children with DS. HOORAY!! Tia seems to really like school. I went and talked to her class last week about her having Down syndrome and what that meant. It went well I think. She showed them some sign language and we talked a lot about how everyone is different but we can all be friends. Tia loved showing off and telling them about the things she loves to do. It was really cute.

Now for the update on Max. He is cruising furniture!!!! We were a bit unsure how long it would take because he seems to have very unstable ankles but he holds on and walks from one end of the couch to the other without a problem. It is so exciting to watch. Now for the not fun part. He is teething and has a cold so he is crying a lot and having a hard time sleeping. It has been a bit stressful at times but we are hanging in there.

Tyler likes school too and I really like his teacher. He pretty much only tells me about snack but I hear him singing all the songs and he is talking a lot more. He never wants to go to school because he thinks life as a couch potato is much more appealing but once the bus comes, he is ready! Too funny.

Tonight on Dateline was a look into institutions/orphanages in Serbia. It was SO heartbreaking. Max came from a Children's Home that was NOT like that. We are so glad that he had good care and that he was put up for adoption there. The other institutions do not offer children for adoption and so the overcrowding is terrible and the staffing is low and the neglect is high. My life is busy. Sometimes my life feels very stressful but I am so thankful for Max in our family and for those who helped bring him to us. Thanks.

Wednesday, August 13, 2008

Saturday, August 9, 2008

First week of first grade

Tia's first day of first grade!!! How cute!! Can you guess what her favorite color is? =-)


So how was the first week of school, you ask? STRESSFUL!!! Tia's teacher and aide did not have any information on her. I had written a 3 page "All about Tia" for them and I was really glad I did. One thing they did not know is that Tia will not poop in the potty so she is still in Pull-Ups at school and needs to be changed and taken to the bathroom on a schedule to pee. The aide is less than thrilled about this and has asked for a different student assignment. So, we will see how long it takes to get a different aide. I can't blame her, I don't love it either but have no idea how to get her to "go".

There was NO aide for lunch like there was supposed to be so I played lunch aide all week and had to find a sitter for Ty and Max during lunch. Now she is going to eat with a Special Needs class so she can have some help opening things and making sure she gets to the right places and has time to eat. She eats 3 things. Pasta squares (by Gerber), mac-n-cheese, and Vienna Sausages. That is what she will eat every week, all year. YUCK!!! I really hope I can convince her to broaden her horizons a bit. Hot lunch has a lot of choices but I am worried she will ask for something she doesn't like and won't eat. She does that a lot. She will ask for pizza or PB&J and I know from years of wasting food, that she won't eat it. I'm not sure if she is just asking for what she knows other kids eat (like Tyler) or what?! Sigh.

I just wish I could enroll my kids in school and that was it. But, it is so much more work, effort and stress with a child with special needs. After 4 days, the Resource teacher offered us a Skills Class (self-contained classroom) as an option for Tia instead of the regular ed. class she is in. That was frustrating. Could they give her a chance to adjust??? I am not anti special education at all but, I know that research shows children with DS are better off in a typical class with modifications. Tia is bright, she does not have behavior issues, she tries hard and there is no reason they cannot help her succeed in a regular classroom. I don't know what the next few years will bring but for now we feel strongly that Tia is in the right place. I pray, cry, stress and read as much as I can before her IEP meetings to place her in the right setting. It is hard to have someone tell you they don't think you made the best decision. I don't tell other people that they made the wrong decisions for their children! I can't imagine telling someone, "So, I noticed your son is immature for his age" or "most kids his age can jump better than that" or whatever. If I said that to a typical parent they would hit me! I don't know why people think they can point out our children's short comings. They have Down syndrome. They are not going to be age appropriate in everything. This is why Special Education services are in place to help them. OK, so to sum up, this week was hard! =-) Sorry for ranting and raving. Hopefully, this week will go better and Tia will get a new aide.

Thursday, July 31, 2008

It's almost August

My 3 cuties in Utah. Yes, I was standing on the right of them. And yes, this is the best shot we got.

This is Tia with her cousin Elisabeth getting ready for "camping". They slept in the tent in the backyard and Tia was SOOOO excited!!! Daddy will have to take her camping now. (Notice I didn't say mommy. =-))

You have to click on the picture to blow it up and see the true love of ice cream this boy possesses. And how cute is he sitting in the wagon?

Fish face? Kisses? I don't know but super cute!!!

We are back from a long vacation to Utah and Idaho. I think it will be a while before Max wants to sit in his car seat for any length of time. It was a long drive. We had such a fun time at my brother Dave's house as you can see. Getting out of the AZ heat was wonderful!!! We did all get the stomach flu (except Kevin and my brother, go figure) but what could be more bonding than throwing up together?! Ha ha. No, only a few got it while we were actually there. The rest saved it for this week.

School starts here on Monday. Tia will be in first grade and it will be the first time she is going to school ALL day. I am a ball of nerves. I got sick to my stomach as I shopped for lunch box foods yesterday. I really have NO idea if she will eat anything. She is a super picky eater and only eats warmed up foods like raviolis, mac and cheese, etc. So, what to pack in a lunch box??? I don't know! She won't eat bread or meat or cheese or pretty much anything packable. I am just planning on heating stuff before she goes to school and hope she eats it 4 hours later. She is in a regular ed. classroom but will have an aide with her so she won't be able to just eat the cookies and go play. But, I am sad. I will really miss her. She will have therapy 4 days a week right after school, then do homework, eat dinner and go to bed. She is losing her playtime and that makes me sad. It also makes me worry about her behavior getting crazy. I hope it all goes well and I have worried all summer for no reason. =-)

Ty goes to preschool and has a new teacher this year. He is pretty easy going and I think he will be fine. Max may be confused to have such a quiet house for a few hours a day. I'm SURE he will enjoy his one-on-one time with mommy. He is a mama's boy. Poor guy got the stomach flu on vacation and now has a cold. He has been really cranky and I think he is teething as well. It makes the days really long this week. But, I still have to say whenever anyone asks about him I have to just say he is wonderful. Because he really is such a joy!

Friday, July 11, 2008

July fun

Our little Serbian-American celebrating the 4th of July! How cute is that?! We didn't get to see any fireworks but we went to a parade and had tons of fun in Flagstaff at my sister's house. We went to Mormon Lake and saw team roping, buffalo, goats, chickens, cows, etc. The kids were all excited to see "real cowboys."


Now that Max weighs 21 lbs., 9 oz (9780 grams) he gets a forward facing car seat!!! Yes, that is over 4 lbs of weight gain in 6 weeks! We are officially off Pediasure and onto whole milk. Well, as soon as we can wean him off the flavorful Pediasure. We are at about a 30/70 mix right now in favor of milk.


This is Tia and Tyler playing hide-and-seek. Can you find them??? Too funny!!! If I say, "Where are Tia and Tyler, I can't find them. Tia will stay hidden but yell out, "Over here. Look over here." Kids are awesome!

Max has his first word!! He is clapping his hands now and with it says, "EEEAA" otherwise known as, "YEAH." He is such a joy. He loves balls and is really starting to love playing with Tia and Tyler. Tia is not fond of sharing her tea parties with the party wrecker but she loves him. I can't believe we have had him for almost 2 months now. In some ways it feels like he has been here forever and in other ways it feels like he just got here. He is changing everyday and picking up new skills left and right. It is so much fun to be part of showing him new things and watching him succeed and learn. He is funny and silly and fits right in. He is such a blessing to our home!

Saturday, June 21, 2008

Look at Max now!!!

He pulled himself up!!!! I walked into the room and there he was standing. Awesome, huh?!
Is this my child??? He wouldn't even take a bath a month ago and now he LOVES the pool! Click on the picture to see it bigger. His face is so cute!!


This is what Tyler did one morning before waking us up. He lined up all the matching containers on the counter and stacked up the soup. He could be VERY instrumental later in helping mommy organize my life. He loves to count and line stuff up. Too cute!

Life is good. Max is probably 20 lbs by now. We are on a waiting list for a feeding therapist (there are 20 people on the list!!!) so we'll see how long it takes. In the meantime, he is eating very thick foods and doing well. He has a fever today thanks to his vaccinations but it will pass. He is only taking one bottle a day now. Everything else is spoon fed. Way to go Max!!! I keep him on the bottle on purpose and will probably do that for a while. It is a good bonding activity and comforts him at bedtime. Being laid down for bed is not his favorite thing. He would much rather be held but rarely falls asleep in my arms. He will fight sleep forever and just get more and more cranky if I hold him. I don't let him cry to sleep though. So, if he cries for more than 10 seconds, I pick him up, rock him longer and try again. I wouldn't suggest this technique unless your child is adopted. :-) It makes for a long evening sometimes. But, he is getting more trust that I will be here tomorrow and he can go to sleep.

We put our papers in yesterday to change Max's name and re-adopt him in the US. This just helps build a paper trail here and give him a US birth certificate, SS # etc. I can't wait for his name to be Max officially, so doctor's offices quit calling to confirm appts for my daughter!! The attorney said it could be a few weeks until court, or several months. Strange, huh? We get the attorney FREE through my husband's work which is very nice. So, hopefully it won't take too long to get the court date. I'll keep you posted.

Wednesday, June 11, 2008

I love you through "Thick or Thin"

We had Max's Upper GI swallow test yesterday. He was not thrilled drinking barium but he drank enough to get results (and to poop white!) Basically, he aspirates anything thinner than pudding consistency! Not great news, but... the great news is that it is NOT structural. Meaning, it is just because of his lack oral motor control. So, the therapist recommended 2-3 months of feeding therapy and then come back to check it again. I was relieved to hear that! We are not supposed to give him any liquids. I don't know how that is possible. I meet with the pediatrician tomorrow to figure it all out. We are also upping his Prevacid for reflux.

Oh, I talked to an elderly lady while waiting in the hospital for the test. She asked me what Max's "condition" was called. I told her Down syndrome. She said, "Some of the people with Down syndrome are really pretty advanced." I agreed, of course. She told me she had seen "So You Think You Can Dance" when the young man with DS was on there. She said, "He was a bright boy. He spoke well and seemed to have a good life." I was SO thrilled that the boy on that show had been given air time. He truly did what he set out to do...change people's opinions. Way to go!!