Tuesday, December 22, 2009
Words don't describe...
Wednesday, December 16, 2009
SEWING PROJECTS
Now as you may note in the title this post is called "sewing projects" (plural). I am giving you all fair warning the other project...not as cute!
Wednesday, December 9, 2009
Who wouldn't love to be two forever!
Look how good of friends these two little kids are!Friday, December 4, 2009
I am one whole half of one whole year old!
Saturday, October 31, 2009
"I need more candy"
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Klinton's work gets big into the costume party, so that is how he went to work on Friday (guitar in tote). It went over well! And no I did not dress up this year...I know let me hear it, I am lame...some things you just have to cut out.
In Other exciting news:
I am so excited today because after just eight months of living here the carpet that was put in the house before we moved here has already started to wear on the stairs...and for what I thought was going to be expensive (and definitely can be) we were able to cover all of our stairs for very little! It makes me so HAPPY...(For the past while I have been trying to walk up the edge of our stairs to preserve the life of the carpet.)
Thursday, October 29, 2009
Wednesday, October 14, 2009
Rainy Days...
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After appointment #3 up at Primary's I was advised to try to fatten Krieg up as much as possible (beyond what is healthy for a normal baby) in order to develop a cushion for when he inevitable becomes a picky 2 year old and lives on air and goldfish crackers. This is my 4 month old eating chicken baby food (we can't waste eating time with empty calories like green beans or rice cereal, we need to load up on meats...these baby food have 4 grams fat, 60 grams sodium, and 9 grams protein) What a different perspective...I am still having a hard time wrapping my head around this!Saturday, October 10, 2009
Yea for the zoo!

Tuesday, September 29, 2009
All I want for Christmas...
"I want a track hoe mommy!"We are getting our backyard started and little did I know when I wrote the check that I was also hiring a permanent babysitter. Ever minute they are here working Max is out on the deck watching them...even after they left last night it was hard to pull him away from the "pushing dirt" and "Blowing smoke" (when the dirt blows up he thinks it is smoke in the air).
Saturday, September 26, 2009
Elephant Parade and more Scar Stories (the two incidents are not related)
This is max yelling to the Elephants

Friday afternoon Klinton went into surgery to remove something growing inside his wrist...even though it was a small operation they had to put him under a general because of the major vessels nerves and what not that were running through the area. That is always fun. Here are the pictures of the scar. If you notice, you can see were the doctor came in to write "yes" on his hand to make sure they cut open the right wrist.
Max Pollock Starr at work...and His Buddha belly.
Tuesday, September 22, 2009
Doug Robinson on CF
The following column is a shameless, blatant, anything-but-objective solicitation for votes.
I just thought you should know.
The votes aren't for me; they're for Mandie. You and I are going to help pay for her education, but more on that later.
Look, every now and then we journalists do a story about someone who wins our heart. Like Burgon Jensen, the blind and deaf girl I wrote about on Monday. Like Chad Lewis, the big, gentle former NFL tight end.
Like Mandie Rudd.
Mandie was born was cystic fibrosis, although you wouldn't know it to look at her or talk to her. She's blonde, green-eyed, smiling and energetic. But beneath the pleasant exterior there's trouble. CF causes the body to produce a thick mucus that, among other things, clogs the lungs and leads to potentially lethal lung infections. Breathing can be arduous.
Mandie takes pills to enable her to digest food. She adds salt to everything she ingests, even Gatorade. At least once a day she straps on a special vest that uses pulsating air to pound her back and ribs to knock loose the mucus that collects in her lungs, which she then spits out. She can spit like a farmer.
When Mandie was born, the average life expectancy for CF patients was 18; she's 19. She hasn't exactly sat around waiting for trouble.
At Hillcrest High, she was an A student, a member of the National Honor Society and a three-sport athlete. She once competed in a track meet while wearing a PICC (peripherally inserted central catheter) line — a tube inserted into her arm to deliver medicine. She still competes in basketball and soccer in city and intramural leagues. She rises every morning at 6 for 90 minutes of exercise, which helps keep her lungs clearer.
"CF is part of my life, but it runs alongside me and does not stand in my way," she likes to say.
CF patients usually are hospitalized several times a year for what Mandie terms "a cleanout" — the lungs are cleared of the mucus that gradually collects there. By taking care of herself and exercising regularly, Mandie has been hospitalized only three times, including a 10-day stay last month. Every three months she takes a special medication to kill nasty bacteria that tend to infect the lungs of CF patients.
Meanwhile, Mandie lives her life. She works as a nanny and attends classes at Salt Lake Community College. She plans to become a dental hygienist, if she can afford it. This is where things get tricky.
Go figure. Only 30,000 people in the U.S. have CF — and yet two of the Rudds' three children have it (but not the parents, Dave and Aimee). What are the odds?
"My parents should never gamble, because the odds are stacked against them," says Mandie.
The expense of paying for medication and treatment of two daughters with CF — Mandie and Natalie, a student at Hillcrest — leaves little to pay for a college education.
"The only way I can do it is a scholarship," she says.
Earlier this year, Mandie applied for the SolvayCares Scholarship, sponsored by the Solvay pharmaceutical firm. Out of the hundreds of applicants, she was selected as one of 40 winners, which means she will be awarded $2,500 and becomes a finalist for the company's grand prize — the Thriving Student Achiever award, which is worth $17,000. This scholarship is selected by popular vote.
Which is where you come in. You can go online and vote for her at Solvaycaresscholarship.com — click on her name ("AMANDA" not "Mandie"). You can learn more about Mandie, Utah's only finalist, by clicking on a video clip that shows her talking about her candidacy for the award while she signs it for the deaf.
You also can read her 250-word essay and peruse her achievements. She plays piano and does volunteer work, serving as a spokeswoman for the Make-A-Wish Foundation, participating in food drives, making hygiene kits for abused women and quilts for hurricane victims and so forth.
CF is still running alongside her, but it doesn't stand in her way.
Saturday, September 12, 2009
Klinton the Triathlete

Klinton hates this picture because it caught him in the wrong position of his stride, he didn't look like he was struggling in real life, he ran straight in. Sadly this is the only picture that captured him running in.Tuesday, September 8, 2009
Krieg's blessing day
Wednesday, September 2, 2009
Signs your kid had CF:
The doctor calls you and says your 3 month old baby has a staph infection (staphylococcus aureus, MSSA), E-coli, moraxella catarrhalis, and haemophilus influenzae, and doesn't seem extraordinarily concerned.
This just means more medicine..seriously though, everyone should research getting vaccinated and immunized - do what you can to protect yourself and those who can't protect themselves.
Sunday, August 30, 2009
Perfect summer nights
Max is so funny, he was so excited for these but the second he got it in his hands he didn't want it because it was sticky and he hates having sticky messy hands...you wouldn't know it by the way he eats his noodles and sauce, but it is true. After some real convincing he decided he loved it. As you can see, we took the easy way out with the Coleman stove...much easier and safer with a two little babies, right by a river.
Even though the picture doesn't show Krieg was happy.
If you notice these last two pictures are on the same blanket...yes they are from the same day and no it is not uncommon for completely different clothes (especially for Krieg) on the same day...let just say my washing machine is always saving us money.Wednesday, August 26, 2009
Terrific Two-dollar Tuesdays
Yesterday was the final two dollar Tuesday at Thanksgiving point. I don't know how this month slipped away but I had planned to attend ever since we went last year and I almost didn't make it. On Monday I asked Max if he wanted to go to the Dinosaur museum and of course anything with dinosaur he would think is awesome, whatever that weird museum word means. He was so excited but I had to explain that he had to take a nap then play some, then go to bed, then wake up in the morning eat some breakfast then go to volleyball, then come home and eat lunch then take another nap and then we would go. He repeat the whole sequence to me and was really excited. After that conversation I didn't bring it up again. Well before I knew it we were in the middle of nap time on Tuesday and I was trying to decide how I was going to fit in the museum the gardens and feeding Kreig and Max. I started getting ready only to find out the stroller was in the back of the car that Klinton took to work because of the rain (he usually drives the scooter). Because of that, and also because I was debating the dinosaurs altogether, I decided to skip the museum and just go to the gardens. Lately Max has been terrified of anything bigger than him that isn't Human, He loves to talk about Smokey Bear - the first thing that scared him - but hates to see him in person. And I lost half the skin on my arm when the Ute Hawk came by during the parade.
Max, being the brainiac that he is, remembered our conversation and immediately asked about the dinosaur museum when he woke up from his nap. So...change of plans again. I didn't know how I was going to do it, but I had to take Max to the dinosaur museum, with Krieg and no stroller. Then my mom saved the day by offering to take Krieg so Max and I could go to the Museum and then my mom would meet us there with Krieg and my dad would meet us as well so we could all enjoy the Gardens together. What a perfect day...OK it was a little hot, but other than that everything was perfect.
Max and I had the greatest time ever, it was just the two of us, no bags, no strollers, no worries. And most importantly he did great, he was a little anxious a couple of times but after he got used to it, he was basically in heaven running free, and having my full attention and seeing all the big dinosaurs.
One of these days I am going to break down and buy a real camera, but in the mean time...
Also, I hate to stop the fun to get a better picture (I am not into the photography like everyone else in the blogosphere), so these are cell phone camera action shots with poor lighting. It works well enough I suppose.
This is how comfortable he was, he ran around and loved everything!
This was me trying to lift him with one hand and take a picture with another hand to make it look like the shark was after him...too bad I am not 12 feet tall
Just before this picture there was a pterodactyl on the ceiling that Max recognized (thanks to Little Einsteins) and everyone was so impressed by the little guy saying the names of the dinosaurs.
Can you find the t-rex devouring the other dinosaur
One more example of morbidity...the Woolly Mammoth (another of Max's favorite animals) smashing the human
Krieg is such a great baby, he is generally happy or sleeping, and big thanks to mom for finding and bringing the little stroller, it made life super easy.

still a poser
Friday, August 14, 2009
Monday, August 10, 2009
What we've been up to...
Here are some fun pictures:
Here we are at the Alpine day's Parade, Krieg's sleeping lasted all the way until the first cannon that starts the parade
"I'm swimming mommy, I'm swimming"
And here Max is with another hat of Klinton'she wants to be just like him.
"Big Stick"..."Very cold"This is us at the Cedar Hills community pool
This was way too difficult to do by myself. Max kept running around, so I would have to chase after him, leaving Krieg behind. Luckily I live where I don't have to worry to much about it, but it was kind of crazy.

Thursday, July 23, 2009
The first day of the rest of my life...
CF is a genetic disorder where there is a mutation in your gene that will not allow the correct amount of sodium chloride to leave the cells and creates too much salt leaving through the skin causing a great risk of dehydration, and it doesn’t allow enough sodium chloride to leave the cells in internal organs like your lungs and your pancreas, which in turn creates too much mucus. That mucus builds up in the lungs and makes getting a normal sickness very dangerous, it is harder to fight off infection and much easier to get sick. It is very hard to breath, and we have to do twice daily treatments to break up the excess mucus. The mucus also blocks the enzymes in your pancreas making it virtually impossible to absorb any fats calories proteins or nutrients from foods.
So what does this all mean? On Monday the 20th we talked to the CF nutritionist, social worker, and Dr. Chatfield and Sue again. They answered all of our questions (that we had at the time, I of course think of new ones all the time) and got us started on a plan for Krieg. They also ran more tests and checked more things. We were at the hospital for four hours. When Krieg was born he weighed 7 lbs 15 oz. Six weeks later, to the day, we weighted him at the clinic and he was 8 lbs. 7 oz. (he had gained only 8 oz.) They gave us some pork enzymes that he eats with a bite of applesauce every time before I feed him so they can break down the food and be absorbed. From that day to now (less than 10 days) he has put on over a pound close to 1.5 pounds. At this point, Krieg is also taking vitamins (they stink horribly and stain everything they touch bright orange) also we have added an 1/8th of a teaspoon of salt to his diet every day. (We mix that in throughout the day with his applesauce and enzymes.) Also Krieg just finished a round of a z-pack to help clear up some of the mucus in his nose and eyes. Next month when we go back to the CF clinic they are going to teach us a chest therapy where we pound on his chest for thirty minutes every morning and night. Once he gets to be about two there is a vest they sit in that does the work for us.
What the future holds: Right now we have no clue, mostly it will be filled with many miscellaneous medications (50 a day would not be uncommon) He will be taking enzymes with everything he ever eats the rest of his life, And he will probably have annual two week stays in the hospital to clear out the mucus and run other tests.
All this being said, the future is very optimistic, just ten years ago the life expectancy for people with this disease was around 20 but now it is at 40ish and people that are getting diagnosed with it today are being told as long as we stay on top of his medication and treatments, as long as we stay involved he will be able to lead a long normal and relatively very healthy life. There are drug trials going on right now with gene replacements that tricks the mutated gene into exited the cell membrane correctly that are having great success. Of course it is a long ways away but it could definitely happen in Krieg’s lifetime where he will have to do nothing more than take enzymes and one pill and his body will function completely normal.
As long as we are very careful to keep Krieg healthy from infections and make him gain as much weight as possible (His diet will consist of what a person without cf can only dream of. To stay healthy he needs to eat every fat, protein, salt, sugar, anything he can get his hands on.) He will be able to go to normal school and play in sports with everyone else, in fact athletics are encouraged because they help clean out the lungs, and he will lead a completely normal life.
Wow, if you made it through all of that you are amazing, no one plans to read that much on a blog. But I decided it was better to put as much as I can think of down to begin with and I will work from there. Still I left out so much. I am sure I will keep you all updated as life changes (as I know it will, we are going up to primary’s every month). Below are some pictures my dad took of our trip up there last Monday. More than anything the success that people have with this disease is directly correlated to the care they receive from the hospital and the support they have from friends and family. I am so grateful to have all of you supporting us. Since this all came crashing down on us last Thursday I have not broken down once, and that is directly because of everyone’s support, I know that what ever is going to happen I am being watched after. I know that God is watching out for our family and I know he knows what Krieg is going to have to endure. I am grateful that he has entrusted me with both Max and Krieg, and I am so grateful to be their mom. That, I cannot stress too much!
Wednesday, July 22, 2009
Every mother with at least 2 kids...

I ran upstairs and finished getting ready. Five minutes later I came back downstairs to this:

The picture does not do justice to the amount of rubbing in of the "bum cream" that Max coated Krieg in. Luckily Krieg slept through the entire lotioning and cleaning process.

Sunday, July 19, 2009
HAPPY BIRTHDAY KLINTON
The list of cakes are:
Bright blue Iron Maiden Eddie cake
Crazy 5 layer every color and two flavor awesome cake (thanks in great part to Megan Judd)
Chocolate peanut butter reses peices cake
Rocket Ship doughnut cake (Max was 12 days old)
no cake :( we actually found out we had to move on his birthday three day before
And this years...GUITAR CAKE

Wednesday, July 8, 2009
This one is for missionary Tyler...
Tuesday, June 30, 2009
HAPPY BIRTHDAY MAX
Here are some pictures from his party...

Wednesday, June 10, 2009
Sunday, June 7, 2009
KRIEG JACKSON STARR











Wednesday, March 25, 2009
Big Boy Monkey Bed


Sunday, March 22, 2009
A tribute to my brother and sister
Max's interesting food selection keeps getting more interesting. Here he was making salt water:
Here he is trying it:
And here he is deciding he really liked it so he went back for more. But this time with a greater salt concentration. he kept on going for a bit and would have drank all the salt if we had not stopped him:
p.s. Adam's blog does show his true awesomeness if you wanna check it out here is the link: http://adambowenwood.blogspot.com/
Friday, February 27, 2009
And the winner is....
Friday, January 23, 2009
Ahh, to be in debt again...
P.S. We get to find out what color of baby we are having next Wednesday morning...any guesses??
Friday, January 2, 2009
playing catch up...
On Friday the 26th we got up (not as early as we wanted, because of the crazy snow storm) and drove to San Diego. We spent A week at the zoo and wild animal kingdom and the beaches and sea world. It was sunny and warm and fabulous. All except for the drunken crazy scary party in our "fun" (code for worst EVER) hotel. With a quick 1 mile and bit of extra money hotel change we were right back on track and better than ever.
Here are some fun pictures of the trip
Thursday, November 6, 2008
dadadadadadadadadadadada (that's a drum roll)
Tuesday, October 14, 2008
Real Salt Lake's Inaugural Game



We looked cold but i think everyone was sufficently wrapped and warm. 
p.s. The dreaded parking sittuation that everyone was rightfully talking about turned out to be a breeze for us, we ran into almost ZERO traffic and parked at Jordan high school took the shuttle in and had NO HANG UPS whatsoever. I can't wait to go again.
Then the following night Klinton and Max and I went to the E center for a free Grizzles Hockey scrimmage and right as we pulled up The Cousins family was jumping out of their car, small world?? I think so (only Stephanie is the one that told me about it so i knew they would be there). We had fun, no one was there, the team looks GREAT for a high school league maybe. And we didn't really take any pictures but this one of Stephanie's boys Garrett and Weston was funny.


Tuesday, October 7, 2008
The Elephant Parade



A couple of weeks ago our whole family went through the worst stomach flu ever. On this particular morning I went to get Max out of his crib only to find him covered in dry throw up the he rolled all over in. That apparently didn't wake him up, good thing he got it all out of his mouth. However, the diaper that was not stopping the leaking everywhere did wake him (I'm sorry this is so gross). Anyway after a big load of laundry and a wonderful bath I got him dressed with long thick sock and some sweats and was rocking him in the chair and he threw up over everything again. I dressed him down to his onesie and big socks. A bit later he brought me his sandals and after I put them on he headed for the door. The picture I took actually turned out much cuter than I thought, I took the picture because he looked so funny tromping around. He always make me laugh, even when he is sick.
p.s. he is all better now and he just went in for his 15 month check up. And the kid is still small he was 1/2 an inch short of 30 inches and 1 ounce shy of 20 pounds. Still sitting at about the 5%. At least he is growing though. So no need to be alarmed. He is however a VERY VERY VERY picky eater, which makes it hard because his food choice is limited to begin with. I recently bought Max some "Tuffutti" (made with tofu) cream cheese and ice cream sandwiches, he likes both. WAHOO!! Here's a weird one, they make plenty of of soy and rice based cheeses but they all have whey and/or casein proteins in them. I don't understand the logic behind that at all, why would anyone eat them, they are pointless for vegans, vegetarians, and allergy sufferers. It's a wonder?Sunday, September 14, 2008
STAYCATION


Max Morris and Matilda Mae



Thursday, August 21, 2008
Playing catch up
I think Max is going to be an Olympian because he finally got up enough courage to realize he can walk on his own during the open ceremonies. He has been able to do it for months but he finally took off for real on the lucky day of 08.08.08
This isn't a very good shot of Max walking but he is so cute, he loves that little pool.
At the begining of the month we went to the Living Planet Aquarium up in Sandy, which by the way is half price on the first monday evening of every month. That is pretty much the only time it is worth it, after all we are landlocked and you can see half the stuff in there at Cabela's for free and in much better lighting. But they do have some Nemo's and Dory's some sharks and seahorse and octupus and a place to pet the stingray's.
Max loved it becuase he is really into pointing and "oohing" and "aahing" and this gave him plenty of oppurtunities
We forgot a camera and took cellphone pictures and I forgot to turn my flash on so this is what you get. 
This is Max Pointing and ooh ooh ooh - ing
Max likes drawing a lot now, so our latest activity is saidewalk chalk fun.
Thursday, August 14, 2008
Friday, July 25, 2008
Update from the blood test results
For the peanuts he tested positive at 1.97 which apparently is pretty significant. but for every other tree nut he was completely negative. But we should avoid them in general because of the high likelihood they come in contact with peanuts.
And for Milk he only tested at a .15 which is low. In fact .35 and lower used to be considered a negative result but the raised the bar and now only .1 and lower is considered negative. But over all he is 99% allergy FREE with milk, so the doctor and I decided to SLOWLY introduce milk into is diet and see how he does.
Overall there are great results, of all the allergies the milk is the biggest pain to deal with.
Yesterday we celebrated with Max's first staple of food that every little kid loves. I bought his some "Sunbutter" (peanut butter made with sunflower seed instead of peanuts) and made him and sunbutter and jelly sandwich. And he LOVED LOVED LOVED it. He was so happy, it was so great. However, we also used his first piece of regular store bought bread with a little bit of Milk proteins. No big deal right? Well, this morning Max woke up with tiny red dots all over his face a back, from one tiny piece of bread.
Back to square one again. I will wait for this rash to clear up and then try something tiny again and see how he reacts. WAHOO!
We are learning :)
Saturday, July 19, 2008
TERRIBLE, HORRIBLE, NO GOOD, VERY BAD DAY
Max went into the pediatric allergist Wednesday to get rechecked up in Salt Lake City. The doctor was great and Max was brave but the nature of the appointment was no fun. He got to do the prick test again with beef, chicken, turkey, eggs, two kinds of milk, dogs, cats, bees, seafoods, different grains and more. That of course was no fun. Imagine being pricked 20 times in your back. By this time Max was tired and done but we needed to get blood drawn for some more accurate results on the major allergies. Luckily this office had a lab right? Wrong. I held Max tightly and tried to comfort him while three nurses put tourniquets on Max's arms back and forth trying to find a vein. After switching back and forth a bunch they went for it. But before poking him they of course wanted to clean the area. Because of Max's eczema in his elbow creases, they didn't use alcohol but chloro-prop so it wouldn't sting -- well, that ended up stinging him very bad so he was screaming before they even poked him. They stuck the needle in but no blood, the nurse turned and twisted inside trying to hit a vein but never could, and finally pulled out and bandaged him up. Nurse number two tried the other arm again and poked in, she found a vein but his blood wouldn't flow.
After all that effort we had nothing, and I was ready to take Max home and not feed him anything that he might be allergic to ever again. But we were tough and went up to Primary Children's Hospital to have them do the blood work up there. After finding our way to the hospital and the lab inside, we were joined with two new nurses and their fancy lighting equipment to show where Max's veins are. The nurse decide to poke his hand, to avoid the already punctured elbows and eczema, however, once she got the needle in she pulled in right back out (on accident) so back to the elbow they go. They tourniqueted both sides and again. After so much trial they finally found a vain in the middle of his forearm and toke plenty of blood so we wouldn't have to come back for more. Max was wrapped up and given a new little "Cars" toy to play with on the way home which he did for maybe one second before he fell asleep for the whole ride home. When we got home, Max was no worse for wear, and was his happy little self again. We get his results back on Tuesday, but for now we are still carefully avoiding Milk, Eggs, Peanuts, Dogs and all things related and made near these products. (not pictured are his three other bandages from puncture wounds and his hives on his back from the prick test and his big bruises in his elbows)
And, in honor of "The Dark Knight" here's: NA NA NA NA NA NA NA NA BATMAN
Monday, June 30, 2008
HAPPY BIRTHDAY MAX
Highlights from June






Highlights from May
Max really liked playing with Matilda and she was pretty brave around him, they had a good time.
Then later that month Max and I hopped on a plane again (Max by the way is an excellent flyer, he loved looking out the window and playing with all the flight attendants and old ladies that would talk to him) this time with Klinton joined us, and we headed to Arizona to fulfill a life long dream on Klinton's. We saw Iron Maiden in concert, oh man do they put on one crazy show, those guys are old and they rocked hard. It was the coolest thing ever. Max was great too, he was happy and playing then he fell asleep and slept through Maiden's entire set, the drunk guy next to me could not get over how cool it was that Max was sleeping through the noise. We had a blast. Lucky for us Klinton's sister Karena lives in Arizona so we crashed at her place and played with her. It was a great little trip.
These first two pictures are the concert. The middle picture is at the Mesa, AZ temple and the last pictures are in the "Colossal Cave"
Wednesday, May 7, 2008
Figuring things out
Later this evening, max was well into his usual favorite activity of pulling everything off the bookshelf and dropping it on and around his feet, at this point he was sitting back down and found a small terracotta pot that we keep pens in. He was attempting to drink out if it (which he also loves doing...he always lets me know quite vocally that I need to share my drink with him) and then started a new game where he picked up his "suckie" - or - "pacifiers" - or - "binki" and put it in the pot then pulled it out and put it in his mouth and then pull it out and back in the pot again, only to pick it out and stick it back in his mouth...only for a moment. He continued this game for a solid 3 minutes before he even thought of moving on to something new.
I can't wait until Max starts talking so I can start to find out what is going on in that crazy head of his!!! He cracks me up, always doing something new and funny.
ECZEMA question
on a less fun note, Max has the worst eczema ever, and everything I have tried has not worked...any suggestions would be awesome :)
Wednesday, April 30, 2008
Our house is for sale!!
Most importantly if you all could tell your firends that are looking for a place to check this out, if you want to post a link to this blog on your blog's I would appreciate it.
Finally, I am looking for suggestions. I am open to any great ideas, tips, experiance on selling a house. The place we are in is fabulous, but lets face it my Husband is a "project" kind of guy and he needs a garage...we need more space.
p.s. let me know what you think of the house blog :)
Sunday, April 20, 2008
The Moab
A note on the pictures...Max has figured out what to do with a camera in front of his face and pulls the same face every time we take a picture...that kid cracks me up!!
Sunday, April 6, 2008
"My back doesn't hurt at all right now"
Thursday, March 27, 2008
My Daddy, My Daddy and Me
Friday, March 21, 2008
Break me off a piece of that!
I Made brownies on St. Patrick's day and new I couldn't dye them green like I did the pancakes and eggs and milk that I made for breakfast so I decorated the top instead...green brownies would just come out blackies.
MAX UPDATE: Max is all better from getting Roseola he was really sick and that of course was sad. While he was sick, before we knew what was wrong he had a swollen throat and because of that choked on a piece of cracker he has never had a problem with before. That was the scariest moment ever and I am so glad Klinton was home from work, Max stopped breathing and was turning blue, I was ready to call 911 and drive to the hospital just as Klinton was finally able to dislodge the piece that got stuck. That was the scariest moment of my life!! His fourth tooth finally after 4 weeks of threatening to come in poked through. He is having no problem crawling hand and foot and he can get anywhere he wants. His favorite place to play is on the first two stairs...he hasn't pulled his body up a stair yet but he likes stand up there. In the last week he has become very independent and can do anything he wants now. We had to lower his crib because he pulls himself up on anything he likes "cruising" around our coffee table and the chair and couch. It is so fun to watch his little body and mind get ready for the jump from one object to the next. Max is the best!!! We love him.
Tuesday, March 4, 2008
How I did the letters...
- Buy wooden letters from craft store
- Paint the letter - couple of coats
- Rub on stickers
- Tie a bow in the ribbon and stick the ribbon to the back of the letters with two sided tape and a heavy duty stapler
- Center on the wall and hang ribbon on two nails each so they wouldn't slack to one side.
I didn't know what I was doing but just kept trying stuff that kind of worked.



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Here he is trying to be like daddy, he prefers to play the guitar with the strap on.
Yes he did somehow climb up there all by himself, with no supervision...oops















