2010 July 4th Wittick/Warren Family Reunion

Over July 4th weekend this year we headed to Buffalo, Wyoming for a family reunion. Eric's grandma has wanted to get all of her family together for a really long time, so they tried to make it happen for her. There were so many pictures to choose from, but I just picked a few highlights and threw them into a slide show!

It's great to see family that you haven't seen for a long time, and meet new family members you didn't know you had. :-)

My kids had a blast with their cousins!!

Ward Camp-out 2010

Just a few weeks after moving in to the ward we were able to go to our ward camp out. We had a really good time, and it was fun getting to know more people in the ward.

Kids loved playing around.

Bubblegum blowing contest.

Peek-a-boo!

Trying to get "cleaned up" for the day.

Heading to breakfast.

Pancakes!

A friendly little mouse we found hiding in the rocks.

Learning to cook with an apple box oven. Pretty cool!

Overall a really fun time. Can't wait for next year! :-)

Cade's 3rd Birthday!

Cade turned 3 on May 25th, and things were so crazy we waited to celebrate his birthday. We were finishing up school, and moving, so we thought we would wait until we were all the way in our house before we celebrated.

Not sure of the cake. He doesn't really like it anyway.

Happy Birthday Cade!

Opening presents.

A couple more.

His favorite!

Love the facial expression.

New jammies!

Showing off his new jammies, and scooter!
(Don't mind the long hair, dad hasn't had time to give him a haircut yet.)

We love you buddy! Happy Birthday!

Relay for Life

This year I decided to support a good friend of mine, and join her team for the Relay for Life! Something fun that I have never done before, and also for a good cause. Can't beat that! The relay is being held from June 11th - June 12th at Mountain View High School in Orem. For those of you who don't know about this event, here is some general information:

The American Cancer Society Relay For Life is a life-changing event that gives people in communities across the globe a chance to celebrate the lives of people who have battled cancer, remember loved ones lost, and fight back against the disease. At Relay, teams of people camp out at a local high school, park, or fairground and take turns walking or running around a track or path. Each team is asked to have a representative on the track at all times during the event. Because cancer never sleeps, Relays are overnight events up to 24 hours in length.

Part of participating means collecting donations, and offering any type of fundraiser. Each participant is asked to raise $100. If you are interested in helping me reach this goal, you can make donations straight to the American Cancer Society in my name from the website below.

http://main.acsevents.org/site/TR/RelayForLife/RFLFY10National?px=16073983&pg=personal&fr_id=25094

I also decided to put my business to good use as well and have set up an Eshow Fundraiser for this event as well. I will be donating my commission from any and all books ordered from this eShow. Here is the link to the eShow:

www.ubah.com/HOS174302

I would love your support! Thank you so much!

My poor hubby's feet...

Almost 3 years ago, Eric's feet started bothering him. They would be tingly, numb, and sore all off and on. He played around with different things, and it got better for a while, then went bad again. Not really painful, just enough to be annoying.

About 6 months ago, I seemed to notice that it was getting worse. He seemed to tough it out daily, but I could tell his feet were bothering him. When I finally convinced him to go see a Dr. he didn't fight be as bad as I thought he would, so it must have been bad enough.

First he went to our family doctor. They took blood, ran some tests, one of which was for diabetes. They did come back with the diagnosis that his blood sugar was a tad bit high, but that couldn't have had anything to do with the fact that he was drinking Mtn. Dew by the gallon. LOL
So, he quit drinking Mtn. Dew and they put him on metformin, so of course between the 2 his blood sugar is normal. So now no more metformin, and not near as much Mtn. Dew either.
But still, after those changes, nothing had helped his feet, so we decided to keep digging.

The next step was to see a nerve doctor. He went and got his feet poked and prodded to check to see if he has neuropathy. That was a no go, so they next sent him to a podiatrist.

This doctor put him on Lyrica, which is a nerve medication to help replenish the nerves or something. After a couple weeks of that and no relief, we kept digging on the internet trying to find our own answers.

The tingling and numbness had since turned too quite a bit of pain, and was making it hard to walk and move around. This hasn't been easy what with us trying to move and all.

Anyway, finally the other night we were reading on the internet and came across the most perfect description of what Eric was going through. We printed it out so he could take it to the doctor with him and show him what we thought. At his appointment yesterday the doctor had come up with the same diagnosis in his notes. It is called Morton's Neuroma.

Morton's neuroma begins when the outer coating of a nerve in your foot thickens, or becomes enlarged. We are not sure what caused this, but we do know it is very painful now and something had to be done.

While at the Dr. he was given a cortisone shot in each foot. I think this was more painful than the neuroma itself. However, in the long run hopefully it will help!
After 6 weeks, if things haven't changed, we will try foot orthotics, if that doesn't work we move to surgery as a last resort.

Please pray for the cortisone shots to work! He has suffered enough!

New House!

Here is a picture of our NEW HOUSE!!!!!!!!!! I just snapped one of the outside for now because we haven't moved all the way. Once we get all moved in and settled I will post more updates!

Easter 2010

Easter was pretty simple at our house this year. We just hid a few eggs in the yard and let them go looking. They had fun! Here is Cade doing a little collecting!

Preston grabbing a few for his basket!

Jaida looking intently at what she just got in her egg.

Alyssa grabbing one of the last eggs.

Here they all are after they found all the eggs. They got a few other fun things like kites, flashcards, candy, and other odds and end toys.

Happy Easter!!!

Happy 9th Birthday Jaida!!!

Nine years ago on April 9th my sweet little Jaida snuck in to this world a tad too early. Born at 27 weeks, weighing just 2 lbs. 12 oz., and measuring 15 inches long. She scared us all half to death by coming that early, and we didn't know what the next few hours, days, weeks, or months would mean for us.

Needless to say, here she is 9 years later, a perfectly happy, healthy little girl. She is our little miracle baby! We love her and are so proud of the big girl she is becoming!!

We went shopping and she was determined to have these blendy pens!!

She also chose Pixos!

Mom decided it was time for a new jacket!

And a girl can always use a new pair of pajamas!

Her little brother played photographer for the night and captured a close-up of her new piggy bank! (This year Target had the cutest banks, so I made it a goal to get each of my kids one for their birthday.)

She also got money from Grandma & Grandpa Saul, and Great Grandma Wittick, and a sewing machine from Grandpa & Grandpa Robison!

We love you Jaida! We hope you had a really fun birthday!