Saturday, May 31, 2008

Aiden Pulled an All-Nighter

HE SLEPT ALL NIGHT LONG!!!!!!!!

He went to bed at 8:30 last night and without an argument (this is rare). Usually, he plays with his stuffed animals for at least an hour before falling asleep. He went right to sleep and slept all night. He did wake up for his customary 4am bottle. But there was no playing, no singing, no yelling to be let free.

He did wake up at 6:30 this morning, but I'll take that over midnight any day.

And this was on top of a 3 hour nap yesterday after we got back from shopping. Babies R Us has some really cute clothes on clearance. I got him a Kenneth Cole 3 piece outfit for his calendar shoot on Thursday. Regular price was $40, clearance price $19.99. And a really cute Baby Snoopy 2 piece shorts outfit for $9.99.

We then had to go to Wal-Mart for dog food. Wal-Mart was not our usual happy shopping experience. Some guy banged a few carts together scaring Aiden. So, Aiden was screaming through the store.

He finally calmed down in the toy department. We were looking at sprinklers. The have a really cute Elmo sprinkler for $10 or a baby Slip and Slide type sprinker ($15) that I'm tore between.

Friday, May 30, 2008

Answering the Aiden Questions

I often get questions about Aiden from various places over the World Wide Web, so I'm going to answer the questions here.

Where did I get Aiden's Tooth Chart?
That particular chart, I got from anbesol.com. I saved it as a JPEG and customized it. As Aiden gets a new tooth, I use an editing program to add the date.

How often do we have "Aiden Nights"?
Aiden Nights happen about once a week. It really depends on much he has played that day. The more we play, the more he wants to play. Last night's episode was the second night this week. Last Friday night, was an Aiden Night. However there have been times when Aiden will not sleep unless he is permanently attached to me.

Aiden's Diet
Aiden's primary source of nutrition comes from Pediasure. He loves the stuff. He also has no fear of table foods. If he thinks it might be edible, he's willing to try it. This is where I say my child is defective. He'll eat anything, and I mean anything. Aiden will eat things that most kids his age won't even begin to think about trying - grapefruit, pickled okra, pickles, spicy Buffalo wings.....

Aiden's Medications
Currently, Aiden is taking three medications: Sotalol (Betapace) for his arrythmias, Enalapril (Captopril) for hypertension, and Lasix. He will also always be on some sort of medication for his heart.

Aiden's Milestones
Aiden is crawling more and more every day. The other day, he ventured down the hall to his bedroom. And we are working hard on learning to stand up. He'll say "bye bye baby" and wave (then he claps, because that's what we do). Aiden is great at mimicking. It is now a game to "plbbttt" (sticking his tongue out); he'll do it and wait for you to do it back. And this will go on for a good 30 minutes. And he goes outside to play every day. However he thinks that grass is edible. And he will pick flowers and give them to me.

Aiden and the Dog
Aiden HATES the dog. But the dog is now bigger than Aiden is and very hyper. He isn't the typical hound. Hounds are supposed to lay around and do nothing. The dog wants to be right up in Aiden's face, which Aiden hates anything in his face.

How old is Aiden?
Aiden's birthday is August 30, 2006. Today, he is officially 21 months old.

Can I ask why we he always be on some sort of heart medication?
Due to Aiden's heart "subscriptions" with the tachycardia and the small right ventricle, Aiden does have problems that can not be surgically corrected, short of a transplant (in which he'll still be on medications). He still has a moderate mitrial valve leakage that will need to be corrected in the future.

I think I have answered the most commonly asked questions. If you have more, please leave a comment and I'll answer them here.

It's Just Another Aiden Night

I really didn't want to name the post title that, but remember that song by Eddie Rabbit Another Rainy Night? Well, that song is stuck on auto replay in my head; only with Aiden's name.

Yes, the little boy was up at 12:26am. I got him a bottle, which he repeatedly let me know he didn't want. I changed his diaper and took him potty. The diaper changing wasn't so bad, but he obviously didn't want to go potty. I took him to bed with me, he was still yawning, in hopes that he would fall back asleep.

Apparently NOT! Nope, the little boy did his "alligator death rolls" for an hour along with squeals of delight and patting my face. So since he obviously wants to play, I put him back in his crib. After about 2 hours of playing in his crib, he bonks his head and screams. So back to bed with us. Chris is playing with him to get him to calm down. I put him back in bed and he played some more (an hour) before he goes back to sleep.

At 6:00 this morning, Aiden is awake. And His Highness is requesting a bottle. So I get up and give him his "milkshake". We both went back to sleep. Chris's alarm clock goes off at 6:45. I hate alarm clocks, absolutely detest them. It's not fair that everyone else gets to sleep until theirs goes off. And Chris's will go off 4 or 5 times before he gets up. Stupid snooze button.



Thursday, May 29, 2008

REPRESENT!

If you don't watch So You Think You Can Dance, last night was a really good show. They were auditioning in Salt Lake City and a young man, Bret, auditioned.



Bret DID represent!

As someone who has trained in dance, IMO, Bret actually did better than a lot of the other dancers who auditioned. A lot of times, I watch this show (and others like it) during the auditions and wonder who on Earth tells these people that they have talent. I know for a fact that I can't carry a tune in a bucket, therefore I would never, ever audition for American Idol. Bret's style is known as "club" and yes I would love to see him in action.

5 Teeth and Counting!

Aiden is up to 5 teeth now. This month he has pushed through 3; this week alone, 2 teeth have emerged. And he's working on another. So far he has both upper first molars, both bottom front, and first molar on his bottom left side. The one that hasn't quite made an appearance is the first molar on his bottom right side.



Tyson's Gold Medal Mom



Tyson Foods is sponsoring a contest to send one mom to China to support the US Olympic Team this summer. Missy Mitchell, daughter of Marsha Mitchell, has nominated her mom.


Marsha Mitchell is the founder of Aiden's school, The Little LightHouse.

Please take time to visit this site and vote for Marsha!


Wednesday, May 28, 2008

A NAP!!!!!!!!!

Finally, after a week of refusing to take nap, Aiden is taking a nap. Granted it's 10am CST, but it's a nap.





He should be sleeping in his crib, but I'm desperate for more than a 5 minute shower and I'm not about to touch him.

He almost got a nap yesterday. I had to take Chelsea to the cell phone store. Her cell phone stopped working and it is under warranty. Well, she went up there late last week, but because she is a teenager, the sales rep basically blew her off. I was going to take Aiden with us, but Chris said to leave him here with Chris. Aiden always falls asleep in his car seat. Heck, I don't blame him! I think I could fall asleep in it. It's basically a big, plush recliner.

It's Tough Being Aiden



For more Wordless Wednesday, click here.


Tuesday, May 27, 2008

The "Atti-two-ds"

If you haven't heard of the "Atti-two-ds", let me enlighten you. The "Atti-two-ds" are what 2 year olds get when they decide things aren't going their way. The temper tantrums, screaming 'NO', and everything that goes along with thinking that they are their own boss.

Aiden has entered this phase in life.

He no longer thinks that he needs a nap during the day. Midnight has become the time to be fully awake and playing for hours on end. Bookcases have to be rearranged as fragile things are now play toys. Meanwhile the toys you have bought, are still in their toybox. DVD cases are laying in the middle of the living room floor waiting for someone to walk by, step on them, and slip as part of Aiden's amusement.

Aiden thinks that diapers are no longer necessary.

It used to take a minute to get the child undressed for a bath. It now takes 10 MINUTES!! Getting Aiden dressed used to be a breeze also. Not anymore. Nope, it now takes 4 hands to hold the child still long enough to attire him in shorts and a t-shirt.

I've heard other moms ask, "Will you ever understand the word 'No'?" when talking about their own child. The answer is oh yes. However it will not be when you tell them no. Aiden understands the word no and repeats it several times throughout the day. "NO" when he doesn't want to take a nap. "NO" when he doesn't want to play with that toy. "NO" when he doesn't want that food and throws it on the floor. "NO" when he doesn't want held. "NO" when he wants held and you're trying to do dishes or cook something to eat. "NO" when he doesn't want to work on crawling or standing up.

Until further notice, Tuesdays will now be known as "Tuesday's Terrible Twos".

Any suggestions?

Monday, May 26, 2008

Aiden's Trip to the Zoo

Saturday, some friends of ours came up from Oklahoma City for a visit. We met Mandi and Kati during Aiden's open heart surgery and Kati was admitted for RSV. Since then, we have remained good friends.

So we decided to take the kids to the Tulsa Zoo. However, due to renovations, not many animals were out.



I tried to get the lions roaring on flim, but everytime I took out the video camera, he would stop. And Aiden was really fascinated by the prehistoric pig (rhino).

It was a learning experience for all of us. While some people awwwed over the kids, most stared. We've never been in big crowds, other than for the BuddyWalk. And at a BuddyWalk, you would expect to see a child with Down syndrome. But for some reason, I don't guess the general public expects to anyone with Down syndrome in such a public spot.

Well, why not? Our kids are just like any other kids. Why shouldn't a child who just happens to have Down syndrome enjoy the zoo?

But we've decided that our next trip to the zoo, will be the OKC Zoo. It's biggger and nicer.

Blogoversary Give-a-Way Day Contest

First, let me start off by saying

Happy Memorial Day



As usual, the sky has opened up and we're having torrential rains. It never fails, it ALWAYS rains on Memorial Day.

And now on to business. Today is Day 1 of our very first give-a-way to celebrate our one year blogoversary. And the prize is this beautiful Down syndrome awareness bracelet



The focal point of the bracelet is a freshwater pearl surrounded by twenty Swarovski pearls or crystals. Individuals with Down Syndrome classified as Trisomy 21have an additional twenty-first chromosome. The freshwater pearl along with the twenty surrounding beads symbolizes this twenty-first chromosome. The unique shape of each freshwater pearl represents the special and unique qualities of each child with DS. The freshwater pearl is accented with the National Down Syndrome Society's colors of blue and yellow in Swarovski crystals and with Swarovski rhinestone rondelles. Hanging from the sterling lobster clasp is a sterling awareness ribbon charm.

This gorgeous piece of jewelry is designed by Peanut's aunt. Feel free to check out her online store at Bead*Dazzle! on eBay or her new store on Etsy.

To enter, simply comment on any post made this week Monday May 26 - Sunday June 1. On Monday, June 2nd (our blogoversary), Aiden will draw one lucky comment and the winner will be announced here.

So happy reading and comment away!

Sunday, May 25, 2008

New Etsy Shop

I'm passing on this information I got in an email

Hi Friends,

I've started a new venture making cloth tunnels for young children with gross motor delays. It's called the T-crawler© and is available through Etsy. Each one is a little different and uses very fun, colorful, recycled and vintage materials. The Etsy site shows how it looks and works.

Check it out here

Please pass this link along to any friends or family who may have children who should be crawling but aren't. Most children with Down syndrome have difficulty with this milestone, but there are many children with other types of delays who also may struggle with a four-point crawl. The T-crawler forces a child to crawl properly and maneuver through on hands and knees that reciprocate.

The T-crawler is also just plain old fun for normally developing kids to take turns crawling through, learning to take turns and work together as team. It makes a nice gift for preschool teachers too.


Thanks!
Liita Forsyth


Friday, May 23, 2008

Miss Margaret



One of Aiden's aides at school, sadly, passed away yesterday. Miss Margaret had been a volunteer at The Little Light House for many years. She was Aiden's aide on Wednesdays. We will miss her.

Thursday, May 22, 2008

Friday Funnies on Thursday

So we were watching the finals of American Idol last night. Actually, we DVRed it. The Guitar Hero commercial comes on and theme of the commercial is from Risky Business with David Cook portraying the Tom Cruise character.
Aiden loved the commercial



Wednesday, May 21, 2008

Orthotic Fitting

Aiden's PT, Karrie, brought a SureSteps rep to PT today. Aiden got fitted for his SureSteps without any problems and even helped (he held his foot out for the measurements).

So, before long, Aiden will be sporting his SureSteps. We went with the Baby Sports design

Tuesday, May 20, 2008

Aiden and Other Kids

Last night, I took Aiden to our Mended Little Hearts of Tulsa meeting.It was the first time Aiden got to go. Our previous meetings, the weather didn't cooperate; either it was too cold or raining.

For the first part of the meeting Aiden sat with me and ate cheese and crackers. Finally, once he got used to the new surroundings, I decided that I would let him play in the adjacent room where all the other kids are playing.

Kids scare the crap out of me! Aiden is little, the other kids are huge compared to him. Being little kids, they view Aiden as "the baby". They want to poke and pet him and they want hold Aiden's bottle. One little girl kept trying to "feed the baby".

After about 15 minutes, Aiden had enough and started to cry. I went into the other room to get him. And he spent the rest of the meeting with me.

Friday, May 16, 2008

Thank You Renee

In my rather hectic week, I forgot to mention how wonderful Renee, Kennedy's mom, is.

She had a giveaway for her 200th post back in April. And I posted a comment on how I really needed to do my own giveaway. Well, I won! The gift was anything from Renee's online store available on CafePress.

There are so many things I like from Renee's store, so I let her choose. And this is what I got. OMG! I love it!!!!!!!!


Down syndrome in Russia

Last night, Aiden and I attended our local Down sydrome support group meeting. I was tickled that I remembered how to get there, as it has been so long since we have gotten to go. With other meetings and illness, sometimes it isn't possible.

Anyhow, I digress. Back to the subject at hand. The key speaker for the night is a volunteer at Aiden's school. Frank is there every day to make sure that things are working properly and to receive hugs that the children shower upon him.

A little background on Frank...

Frank worked for British Petroleum, or BP. And he worked long hours that wasn't on a set schedule. One day, his friend was talking about doing missionary work in Russia. Frank thought this sounded like fun. And was asked to attend. Without asking his wife, he said "Yes". Frank had tried and tried to do volunteer work for churches, but due to not being able to give set times when he could volunteer, he never had the chance.

On one missionary trip to Russia, Frank was asked to step out of the room to speak to a woman. When he stepped out, there was a woman waiting there with her son, a child with Down syndrome. And she asked for help for her son. Frank, being an American, HAD to know something about Down syndrome. At this time, Frank didn't know ANYTHING about children with Down syndrome.

But he did know about the Little Light House, a school for special needs children in Tulsa. So, Frank returned home and went to the LLH. On a rare occassion, Marcia Mitchell, the founder of the LLH, was there. He explained the situation to Marcia and asked what he could do to help this woman and her son.

Children who have Down syndrome in Russia are not, sadly, treated as people. They do not have the right to attend school, as the belief is that children with Down syndrome are "unteachable". They do not have the right to obtain medical treatment. In fact, of all the millions of people in Russia, there are only 3 doctors who will treat a person with Down syndrome. People with Down syndrome are laughed at, not snickered at, but literally LAUGHED at in the streets. Many parents will only take their children outside after dark to avoid the ridicule. (Is your head spinning yet?)

Many children with Down syndrome are placed in orphanages left to die. Mothers give up their children for fear that their husbands will leave them and they will be without a place to live.

Frank returned to Russia with the needed supplies and information to help this mother and her son. He also began a school 400 miles from Moscow, in Voronezh for chldren with Down syndrome. The school is called Up with Down Center. Through this school, children and adults with Down syndrome are taught.

Frank told us about this little boy, who now 13 years later, is a gymnast. He received 8 gold medals in China. In competitions in Russia, this boy has never recieved a medal, because he has Down syndrome.

I am glad that I live somewhere that people with Down syndrome are becoming accepted. However it saddens me to think that 60 years ago, Aiden would have been treated the same way.


Thursday, May 15, 2008

The Down syndrome Caucus

Urge your Rep to join the Congressional Down Syndrome Caucus

DATE: May 12, 2008

Your Advocacy Works

On Friday, May 2, 2008, NDSC and NDSS sent an Action Alert urging members to call their Congressional Representative and ask them to join the Congressional Down Syndrome caucus (See Action Alert at the bottom of this News Line). On May 12, 2008, we received an e-mail from Kristin Garesche, legislative staff assistant to Congressman Cathy McMorris-Rogers (R.WA) with an impressive group of Representatives who have joined the caucus. The e-mail reads as follows:

“I just wanted to thank you again for your support for the Congressional Down Syndrome Caucus and help getting Members interested in it. I wanted to update you on our membership. Our co-chairs are
  • Rep. Pete Sessions (TX),
  • Rep. Patrick Kennedy (RI),
  • Rep. Eleanor Holmes Norton (DC) and
  • Rep. McMorris Rodgers (WA).

Our members are

  • Rep. Todd Akin (MO),
  • Rep. Joe Barton (TX), Rep. Steve Buyer (IN),
  • Rep. Dave Camp (MI),
  • Rep. Christopher Carney (PA),
  • Rep. Howard Coble (NC),
  • Rep. Ander Crenshaw (FL),
  • Rep. Lincoln Diaz-Balart (FL),
  • Rep. Charlie Dent (PA),
  • Rep. David Drier (CA),
  • Rep. Mary Fallin (OK),
  • Rep. Tom Feeney (FL),
  • Rep. Rodney Frelinghuysen (NJ),
  • Rep. Doc Hastings (WA),
  • Rep. Jeb Henserling (TX),
  • Rep. Sam Johnson (TX),
  • Rep. Ric Keller (FL),
  • Rep. Steve King (IW),
  • Rep. Mark Kirk (IL),
  • Rep. Doug Lamborn (CO),
  • Rep. Nick Lampson (TX),
  • Rep. Frank LoBiondo (NJ),
  • Rep. Thaddeus McCotter (MI),
  • Rep. John McHugh (NY),
  • Rep. Lynn Westmoreland (GA),
  • Rep. Tim Murphy (PA),
  • Rep. Todd Platts (PA),
  • Rep. George Radonovich (CA),
  • Rep. Tom Reynolds (NY),
  • Rep. Dave Reichert (WA),
  • Rep. Peter Roskam (IL),
  • Rep. Mike Rogers (MI),
  • Rep. Mike Simpson (ID),
  • Rep. Lamar Smith (TX),
  • Rep. John Sullivan (OK),
  • Rep. Pat Tiberi (OH),
  • Rep. Chris Van Hollen (MD),
  • Rep. Greg Walden (OR),
  • Rep. James Walsh (NY) and
  • Rep. Bill Young (FL).

In addition, my boss sent out a video release regarding the Caucus to her constituents last week and she wanted to share it with all of you.

If your Representative is not on this list, please call and ask him or her to join the caucus. He or she may contact either Emily Davis, in Congressman Pete Session’s office (202.225.2231) or Kristin Garesche (202.225.2006), in Congresswoman Cathy McMorris-Rogers office.

To find out the name of your Representative, click here and key in your zip code. The main switchboard of the Capitol (202) 224-3121 will connect you to your Representatives office.

Ask your member of the House of Representatives to join the Congressional Down Syndrome Caucus House of Representative members:

  • Pete Sessions (R.TX),
  • Cathy McMorris Rodgers (R.WA),
  • Patrick Kennedy (D.RI) and
  • Eleanor Holmes Norton (D.DC)

Each of these members have sent a Dear Colleague letter asking other House members to join the Congressional Down Syndrome Caucus (CDSC).

According to the letter,
“the caucus will serve as a valuable resource for increasing awareness of those efforts and identifying ways that Congress and relevant departments and agencies of the Federal government can help to meet the needs of individuals with Down syndrome and their value to society. The CDSC will promote public policies to enhance the quality of life of individuals with Down syndrome by:

  • (1) raising expectations and improving outcomes in education;
  • (2) eliminating barriers to economic opportunity in employment and in programs that promote savings and investment; and
  • (3) promoting and funding research that accelerates the development of effective treatments and therapies.

In 2008, some additional priorities of the caucus will be to:

Promote the translation of Down syndrome research into effective new treatments through interdisciplinary cooperation among the various NIH institutes, the FDA, the CDC and privately funded scientists and clinicians.

  • To promote inclusiveness for people with Down syndrome.
  • To help provide family support services and a community of care model.
  • To protect the rights of those with Down syndrome and make sure those rights are being enforced.


In addition, the Congressional Down Syndrome Caucus will be holding a briefing for Congressional staff on May 8 to discuss where we are in terms of Down syndrome research. A representative from the National Institutes of Health will be attending as well as Dr. Bill Mobley, the Director of the Neuroscience Institute from Stanford Medical School.

If you have questions about this Call to Action, please contact Susang1961@aol.com or Ricki Sabia at Rsabia@ndss.org. We would also appreciate you letting us know if you contact your Representative.


Sponsor Aiden!!!

DSAT (Down syndrome Association of Tulsa) is gearing up for our Annual Buddy Walk to be held October 19th. If you would like to sponsor Aiden in this year's Buddy Walk for Down syndrome Awareness click here




Wednesday, May 14, 2008

Brownie Bites





**Edited to add this by special request**




For more Wordless Wednesday, click here



Sunday, May 11, 2008

Mother's Day Pictures

It was a pretty good Mother's Day. Aiden decided that with his new teeth, he wanted to try calamari and crayons. Here are some of the pictures taken:



We went to my second favourite restaurant, Macaroni Grill, as the waiting line was shorter than at Zio's. Chris's mom and dad (Grandma Nise and Grandpa JC) went and they got to try new things, hopefully they liked it.

I got a new charm bracelet from Chris and Aiden. It has a heart charm with diamonds in it. And Grandma Nise got me two heart charms with my name and Chris's name on them. (For Aiden's birthday, she got me a heart charm with Aiden's name on it.)




To All the Mothers

Being a Mother


Somebody once said that it takes about six weeks to get back to normal after having a baby.

That Somebody doesn't know that once you are a Mother, "Normal" is history.

Somebody said being a Mother is boring.

That Somebody never rode in a car driven by a teenager with a driver's permit.

Somebody said if you're a "good" mother, your child will "turn out good"

That Somebody thinks a child comes with directions and a guarantee.

Somebody said "good" mothers never raise their voices.

That Somebody never came out the back door just in time to see her child hit a golf ball through the neighbour's kitchen window.

Somebody said you don't need an education to be a mother.

That Somebody never helped a fourth grader with her math.

Somebody said you can't love the fifth child as much as you love the first.

That Somebody doesn't have five children.

Somebody said a mother can find all the answers to her child-rearing questions in the books.

That Somebody never had a child stuff beans up his nose or his ears.

Somebody said the hardest part of being a mother is labour and delivery.

That Somebody never watched her "baby" get on the bus for the first day of kindergarten.

Or a plane headed for military boot camp.

Or seen her child through open heart surgery.

Or held her child through chemotherapy.

Somebody said a mother can do her job with her eyes closed and one hand tied behind her back.

That Somebody never organized four giggling Brownies to sell cookies.

Somebody said a mother can stop worrying after her child gets married.

That Somebody doesn't know that marriage adds a new son or daughter-in-law to a mother's heartstrings.

Somebody said a mother's job is done when her last child leaves home.

That somebody never had grandchildren.

Somebody said your mother knows you love her, so you don't need to tell her.

That Somebody isn't a mother.





Friday, May 9, 2008

For Your Video Viewing Pleasure





Help Rhett and Parker by Reading!!

Jessica, Joey's mom, has been thinking of ways how she can help out Parker's and Rhett's families with some of their medical expenses. So, she has decided to donate 50% of her online Usborne Books sales income to them both from now until June 10. That's 25% for each of Joey's and Aiden's buddies.

Please help spread the word!! Not only could you get awesome books for your kids but you will be helping these little guys to continue to get the help they need.

Jessica's Usborne Book Store

And if you just want to donate a book to either Rhett or Parker, email Jessica.

Keep Reading!

Get your own free Blogoversary button!


Our first blogoversary is in 24 days. And I am commemorating the event by having my first Bloggy Give-A-Way!

The contest will be held the week of May 26th - June 1, 2008. Aiden will pick the winner (and yes, there will be video footage to insure fairness) on June 2, 2008, our blogoversary. All entries will be from comments to posts made during that week only.

So keep reading and waiting for your chance to win this



The focal point of the bracelet is a freshwater pearl surrounded by twenty Swarovski pearls or crystals. Individuals with Down Syndrome classified as Trisomy 21 have an additional twenty-first chromosome. The freshwater pearl along with the twenty surrounding beads symbolizes this twenty-first chromosome. The unique shape of each freshwater pearl represents the special and unique qualities of each child with DS. The freshwater pearl is accented with the National Down Syndrome Society's colors of blue and yellow in Swarovski crystals and with Swarovski rhinestone rondelles. Hanging from the sterling lobster clasp is a sterling awareness ribbon charm.

This gorgeous piece of jewelry is being generously donated by the maker, Peanut's aunt. Feel free to check out her online store at Bead*Dazzle! on eBay or her new story on Etsy. This is the same bracelet that I am asking for my birthday (coughGrandmas,Chriscough).


More About Me

Mrs. Wibbs tagged Pam, Rhett's Momma for a Meme, who in turn tagged me. And obviously from the time, yes Aiden is awake.

What Was I Doing 10 Years Ago: That was 1998. I was 24 then. I was also working at Wal-Mart in the Electronics Department. I lived in a farmhouse and had two dogs, Chief (an Akita) and Sandy (a Basenji).

5 Things On My To Do List Today:
1. Laundry
2. play with Aiden (he has a musical duck and I'm trying desperately to get him make it quack on video)
3. buy a birthday gift for best friend's one year old
4. get old clothes ready to donate to charity
5. schedule service work on my Jeep (it has a recall).

Things I Would Do If I Were A Billionaire: Build a bigger house, donate to a few favourite charities, and if Aiden were healthy enough to fly, go to Scotland.

3 Bad Habits: Pepsi, letting things stress me out too much, not wanting to do the dishes (I hate, hate, hate the kitchen)

5 Places I have Lived:
1. Houston, TX
2. Claremore, OK
3. Tulsa, OK
4. Coweta, OK
5. Pasadena, TX

5 Jobs That I Have Had:
1. Wal-Mart
2. Customer Service for major insurance company
3. Financial Service for cell phone company
4. I worked in a dog kennel
5. Mommy and Nurse to Aiden

5 People I Want To Know More About:
Terry at Noah's Trek
Renee at My Special Ks
Debbie at Finding Normal
Shannon at Gabi's World
Debbie at 3 Weddings