Sweet Memories

Some of my most precious memoriesas a child are of sitting with my Grandaddy and watching football!  I learned to love football because of him and all of the time we spent watching the Dallas Cowboys together.


Tonight we were able to capture a precious moment like that with Miss P and her Pa.  I hope she creates many more special memories like this.

Miss P watching football with Pa!

Then she moved in to watch the Amazing Race with Mimi & Pa.

Such sweet memories! 

                                                                                                                                           

Miss P did very well on the plane yesterday!  We were in the bulkhead and so she got to sit on the floor and play!!

She thought she was such a big girl!

 

Then she ate lunch in my lap!!

You can see she was having fun and Mommy was exhuasted!!

She loved looking out the window!!!

This is a girl after her Daddy's Own Heart (lovin' planes as much as she does)!!!

 

 

Then it was time to take a nap, but it's sure hard to get comfortable on a plane!

So, I'll stand in Daddy's lap and wave at everyone behind me!

She met a sweet friend from Canada and tried to snuggle with her, too. 

Miss P tried so hard to sleep on the plane, but just couldn't get comfortable.  Within about two minutes of us pulling out of the parking lot at the airport, she was asleep in her car seat and slept almost the entire way to B's parents house!!!  Please pray for her to adapt well to a schedule while here.  She has a great schedule at home that she does so well with...however, she is very thrown off with the time difference.

B's Nana is having a heart catheterization tomorrow.  So, please send up some extra special prayers for her protection and the doctor's wisdom! 

A picture is worth...

There really aren't adequate words for what we experienced last night!

Yesterday was B's birthday!  His favorite spot is Pappasito's.  So, Mom took us all for dinner.

B loves their salsa.  He goes through so many bowls it's amazing!  They never quite believe him that he'll go through it as quickly as he does.  Well, we called ahead  last night and they believed us!  His spot was ready, tons of bowls of salsa waiting to be devoured by him.  However, what we weren't expecting was....

Yes, you are seeing our 21 month old eat just about as much salsa as her Daddy!  She could have cared less about the chips, she just wanted the salsa.  She was grabbing huge scoops and eating them off the chip.  Then, we pulled out her fork so that she could eat her meat.  She could have cared less about the meat.  She scooped up the salsa with her fork!!!!

Did I mention that the bites that I took had my mouth burning?  It was spicy salsa.  My Mom coughed/choked with a few of her bites it was so spicy.  However, our little angel LOVED IT!!!

Not being able to get out and drive, I was worried that the gifts I found for B weren't exactly what he would have wanted for his b-day!  If you had seen the smile on his face and the pride beaming from this father, you would have seen that this was the greatest gift ever for him...his very own salsa eating buddy!!!!!

Really?  chicken?  That's it?

Here!  Dip it in this and it's worth it!!!

How about some more?

She never really touched her milk at dinner.  Ummmm...this is spicy, the milk should help.  Would you like your milk, Miss P?

"No thank you!  Salsa will be fine!!!"

I think she almost finished two bowls of salsa!!!

Finally, his b-day dessert arrived.  He's coaching her on how to help him blow out the candle.  Can you see the pride and astonishment in his eyes, though?  He's still overwhelmed with joy that his little girl loves salsa as much as he does!!!!

Happy Birthday, B!  We love you!!!

FOUR MORE YEARS

Well, it is almost election day...Praise God!  But this time it is different.  Four years ago today Princess went into SURGERY.  While America had an important decision at hand we here at the Foxhole had an additional weighty decision on hand.  I still remember the day very well.  We had just slept off a fun night with friends and family as we did a hair cutting party and Princess and I both shaved our heads in preparation for this day while at Memorial Hermann Hospital. 

We weren't expecting her surgery to be until a little later but very early we were awoken as the staff came to take Meredith back to surgery... Here is the post from this time...

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Wednesday, November 5, 2008

Surgery

Well it was quite a wake-up today. About 5:30 this morning, we heard from the surgeon's resident that surgery would be at 9:30. However, we we whisked away at 6:30 and headed in to the surgical unit. Please pray over these next four to five hours as M is undergoing surgery. We will continue to post and update as events unfold. Also, I will be posting pictures later this morning of our "Buzzfest" to benefit Children With Hair Loss.

PS- Two friends that were with us last night at the Buzzfest are about to deliver their first kiddo. Please lift A and L up in your prayers. She was not due till Nov 16. Ironically, it was M's nurse Mary that told them to get to the hospital immediately to see about delivering. So...they have been at the hospital since last night. I know M will be very excited to hear of the days events when she is back with us later today.

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So today, is eerily similar.  This time we are facing an important decision for America and tomorrow we will learn what direction America has chosen to follow again.  Additionally, while we are not waking with Physicians coming into our room, we do have luggage packed and we are on our way to Pennsylvania to determine if we can move forward with surgery again, but this time going further trying to eliminate Princess' seizures. 

So please be prayerful for our trip that our time in the hospital will be fruitful.  That the new team of doctors and physicians we will be meeting will be able to bring this 6.5 year journey to a close.  As some of you have been following, just in the last two months, Princess has experienced a dramatic increase in her seizures is upwardly approaching an average of 5 to 6 seizures per day.  Additionally, we are beginning to see even more some of the seizures devastating effects.  

Be looking for more in the coming days!

Au Pair

Webster defines au pair as:
 
a usually young foreign person who cares for children and does domestic work for a family in return for room and board and the opportunity to learn the family's language 

We define an au pair as:

A BLESSING!!!!

As most of you know, our community stepped up after Miss P was born and took two shifts each day to help care for her.  It has always been risky for me to be left alone with her due to the seizures and her crying was always a huge seizure trigger.  Well, many of you prayed and the Lord answered your prayer that her crying does not seem to be too much of a trigger anymore.  Many sounds are triggers, but the Lord has allowed me to hold my sweet angel when she needs her Mommy.  Thank you, Jesus!

So, we had so many amazing people come and take shifts the first six plus months of P's life and love on our sweet girl and help me care for her.  Then, after the Foxhole Relief weekend, we were able to bring in a few nanny/babysitters that were wonderful!!!  We loved them so much.  However, if they worked 9-5, B couldn't go to work until they arrived and had to be home before they left (since, again, we couldn't risk me being alone with her).  This allowed B more of an opportunity to work, but he wasn't able to do much of what was needed for the business.

So, in walks my cousin.  She tells me that we have to consider an au pair.  They had one for their family and loved her.  However, I just made the assumption that there was no way that we could afford such an option.  We were struggling to afford a nanny/babysitter and so how could we afford something that had a french name?  Doesn't that make it more expensive?  Surely we can't afford that...As well, they live with you.  So, now I have to buy more food, utilities increase, etc.  It just didn't seem feasible.  Then, she pushed some more for us to consider it.

Once we did the math, we found, among many things, that we would actually pay less to have an au pair than we would for a nanny and she could work longer hours.  We started to truly see the benefits.  My cousin continued to tell me amazing stories that kept softening our hearts to the idea.

Then, came our trip to the Mayo Clinic in February.  It was a rough trip, but while we were there, we had the opportunity to have a Skype interview with a possible candidate from Brazil.  To keep the story short, we loved her and now that she's been living with us, in America, for seven months, we still love her!  She is an amazing blessing!!!  Miss P is crazy about her and so are we!!!

So, without further ado, meet Ms. C...a gift FROM the Lord THROUGH each of you that participated in the Foxhole Relief Project. 

Ms. C with J & her kiddos.  J is one of the two that created the Foxhole Relief Project.

Again, Ms. C is such a blessing and we love having her as a member of our family!!!

 

Critter Update

For those who have been following and faithfully praying, you will recall Critter was diagnosed back in June with Juvenile Arthritis.  We have been blessed to work with Scottish Rite hospital for her diagnosis and treatments.  Today was our third visit and all signs point to continued improvement and progress in her toes!  The inflammation and swelling have gone down and her toes still seem to be doing exactly what the doc wants them to do.  Great news!  We will still continue her medicine, thus putting off chemo.  So we'll keep with our current follow-up schedule to be evaluated very 3-4 months.

PS-please lift Princess up in prayer.  Her seizures have continued to increase over the last two months and we have no answers.  We are still making plans to be at Jefferson Hospital soon for evaluation, but would obviously would like to see a decrease in her seizures.

Thank you!

We've received a few e-mails requesting that we share some quick updates.

First, thank you all for your prayers!!

Second, thank you each so much for your sweet birthday wishes!  Wow!  My inbox is going crazy with blessings from each of you!  What a precious gift!

Finally, the update:

We came home from the hospital that Thursday evening (two weeks ago).  I had two decent days.  Then, they started up again....That Sunday was incredibly rough.  We had home health out to do some IVs and I have no real recollection of the nurse being here.  That was the beginning of four rough days where I averaged close to three seizures per day.  So, needless to say I was exhausted!!!  Then, I had a bit of a break for a day or so, only having one each day.

Then, came Saturday.  I had two seizures within 20 minutes of each other and another one a few hours later.  So, I had to take the "rescue med" before 6am.  I didn't have any more seizures Saturday or Sunday, but most of the days were "erased" and I was asleep.

Then, came Monday.  The day that so many of you remembered, my birthday!!!!  Thank you!!  I only had one on Monday and one on Tuesday.  So, the break was great.  Thank you, Lord!

Wednesday hit with a bang, literally.  I already had too many by 7am and had to take a rescue med which only lasted about five hours.  A dear friend from college was coming over to "play" that day.  She has two little ones.  This was our first ever playdate.  I had no idea what to do.  No seizures while the kids were here!  Thank you, Lord!  However, soon after they left, chaos.  I had four seizures in less than eight hours.  So, B had me take another rescue med.

Here we are, today, Thursday.  I've had four seizures today.  So, more rescue meds and pleas for prayers for some days with rest included!  Our pup also had a seizure tonight.  Thus, it's been a bit crazy around here.  Thank you all for your prayers!!

Here are some cute pics of P with the Halloween present she received from her grandmother tonight:

She absolutely loved it and walked all over the place with it...it's a little pumpkin bag with a pumpkin flashlight that she can shine all over the walls!!! ; )

Nate

We received this update on Monday in regard to Nate:

Nate and I just landed in Los Angeles and are on our way to the hospital for several days full of scans and tests. Nate is feeling great and very spunky. Please pray for great scan results. His MRIs are this afternoon. Last scans six weeks ago were horrible and the doctors thought he didn't have much time left, but he looks and feels great. Our God is awesome and we know HE is watching over us and HIS mercies have been great toward Nate. Thanks for all the prayers.

  

We received this update this evening in regard to Nate: 

Well, the scans show the brain to be much improved with the tumors greatly reduced and the spine clear now of tumor. Praise God and thank you for all the prayers. The doctors are very pleased with the results and are developing plans right now on the next steps. This is truly amazing and we are very grateful. With God nothing is impossible. Heading back home with a plan and renewed spirit in the morning. Thanks again everyone.

 

Post Hospital Update and What's Next

Howdy to all!  First, many and many thanks goes out to you for your constant prayers and emails.  We had an extremely difficult week (see previous post) and are relieved to be back at home.  Princess was discharged from the hospital on Thursday evening as the seizures had for the moment calmed.  There are, and were not, any answers for what happened over the weekend or at the start of the week other than maybe a possible reaction to a new medication that was added to our regimen.  That said, we were able to determine that particular medication is not an option for Princess. 

Other than that it is back home and rely SOLELY on GOD for His strength that is becoming so evident in Princess' life each day.  Truly, she is the most incredible woman in the world to get up each day and take care of our family.  Her strength to endure and yet even just be part of life is amazing.  While along this 6.5 year journey so far, God has continually blessed Princess with an amazing attitude and life.  We truly don't know what today has...will Princess have no seizures?  will she only have one? or could today be a day like we just experienced and will she have 15 seizures in a day?  We don't know...As frustrating as the unpredicatablity can be we are still learning how to balance.

Balance...

While our balancing act can be somewhat challenging, both Princess and myself will first and foremost tell you that it is not anything we can do.  But first things first, it is because of our foundation in Christ Jesus!  We do, and have to start each and everyday with Him.  He is the source of our strength.  He is the Master Architect of our days.  Princess and I do constantly tell ourselves that it is not a surprise to God about what we are enduring.  And in addition, it is truly awe inspiring to witness Princess daily and see God's provision in her life. 

But there's more.  God is unfolding His plan to do great and mighty things in Princess' life and in yours and mine. While our trip to the hospital this week may not have been eye opening in providing  a cure, it more or less confirmed the direction we are heading.  This week our Neuro mapped out a plan of action that would lead us down a path to Philadelphia to start the initial steps for brain surgery.  While surgery is not a desirable option, it appears that it is the only option that man can provide.  What does this mean? 

Next month we will be headed to Philadelphia to one of the leading Epilepsy Surgery centers in the nation.  We will be somewhat starting from scratch with new sets of eyes, different EEG recording devices, different MRI scanners, and much more.  We will have the advantage of bringing in all previously collected data and comparing it to what will be collected in this trip.  Depending upon the results obtained, the physicians and specialist will make a recommendation to move forward or not with brain surgery.  Should they want to go further with surgery, we'll most likely return in January of 2013 to begin again Princess' surgery we did in November of 2008 with the hopes of placing electrodes deeper in the brain and more of them covering the surface to potentially locate the seizures.  Thereafter, assuming the seizures are located, our team would then "map" Princess' brain and determine how to remove the tissue where the seizure(s) is/are located.  If January were to happen, we will have much more praying to do and will really have to weigh our options due to the potential cognitive, and who knows what else, impact this will certainly have. 

Bottom line, God is and will be the hero.  Princess has for years now said that God is the hero in this story.  The stage is set again that as doctor's have said there really is nothing more that can be done.  Our own Neuro reminded us again that we have to stop the seizures.  The impact they are having is detrimental and there is grave concern for what Princess will be like should these continue for 5 or 10 more years. 

So pray.  Prayer comes first.  God is Holy. God is God and He is the only answer for all of us.  In Him, eternal life is found.  He provides the strength for today and our time here on earth.  We turn to Him and ask for healing and peace for Princess.  We ask for wisdom and peace in the midst of this storm.  We ask for guidance as we venture on this journey.  We pray for the doctors in the path ahead.  AND MOST IMPORTANTLY- that Christ would be communicated in ALL that we do.  May God be glorified!

Thanks for sticking with us! 

The day that would not end...

After Princess' trip to the hospital through the ER, we were finally on the floor of the hospital around midnight.  Followed by another hour of getting settled in with the staff and getting Princess hooked up to her EEG.  Soon it was 2 AM and we were just now able to think about falling asleep.  Then around 3 AM we were moved to the EMU (Epilepsy Monitoring Unit) where we had to do more adjustments and introductions and it was now close to 4 AM and time for us to get some much needed rest. 

Thereafter, Princess, by far, had one of her worst days in the last six years and actually had 15 seizures before going to bed last night.  So, it was a rough day altogether.  We are not really sure of what happeed yesterday with seizures but we were very thankful that the day was eventually over. 

 As for Princess, the talk most of yesterday was to figure out what was going on that got us into the hospital and what was going on that she was having more seizures.  It was later in the afternoon that most of our conversation, now with Princess' Nuero, centered on adding another medication and getting ourselves to Philadelphia to Jefferson Hospital's Epilepsy Center.  The thought with Jefferson is to eventually look toward another surgery....our most likely answer to getting Princess better, next to a miraculous healing from the Lord. 

So as it is already late, we wanted to provide just a brief update and will be sure to post more very soon!

ER, PRAYERS- JEHOVAH RAPHA

THE LORD THAT HEALS YOU...

Lord, I pray for healing today!  Please take away this awful illness from Princess.  Lord, it is my heart, mind and soul's desire to trust you and yet at times the journey is so difficult.  You know all our fears, all our concerns, our frustrations, and our desires...Please bring healing into Princess' life right now.  She is tired.  She is weak.  She is frustrated.  Lord, I don't ask as in a request hoping you can heal her....What I know is that you are ABLE.  YOU ARE ABLE!  Father, You alone have sustained Princess for the last 6.5 years.  You have protected her when docs have no answers.  Lord, in continued and steadfast faithfulness we continue to seek You for your guidance, provision, and healing.  Please Lord...let today be the day that you end this chapter.  Father, I trust You.  You have told me....You have told us...that you know our plans, our days... YOU, who has ordered the stars to their places and knows us so personally....our lives are held in the cup of your hands.  So today, as long as it is called today, we turn to You and GLORIFY your HOLY name.  Please Lord, bring rest and restoration to Princess today.  Take away this illness.  Thank you for providing Your strength.  Please bring some calm and rest today. 

Selah.

Amen.

Update:  For a second weekend, Princess has not felt well.  We have recently made some changes with our physician in hopes that we can stop these seizures.  And what all of the changes have turned into is something very wrong for Princess.  After another very difficult weekend we were finally able to reach our Neuro and Princess has been ADMITTED back into the hospital through the Pysician Referral ER.  While not desired, the situation at hand warranted and necisitated the visit.  Princess' mom graciously was able to be on call to start the process and I myself will be reunited with Princess shortly.  At this present time we don't understand nor really know exactly what Princess is experiencing.  All we can say is that something is not right...We hope that we can have answers soon.  These recent events are all trailing our most recent doctor visit where our Nuero is presently trying to get Princess to Jefferson Hospital in Philadelphia to be monitored eventually for surgery in January of 2013.  So we are prayerful today about all that has been laid before us and even what new medications we should consider, if we were to venture down that road, too. 

Please pray for Princess.

Snuggles

Hopefully, there will be time to catch up on the overdue updates.  However, I had to share that I just received precious snuggles from my beautiful little girl!  Wow!  She usually gives a quick hug to Mommy and is off to Daddy's arms.  Tonight was different, she wrapped her sweet arms around my neck, laid her head down, and even played with my pony tail.  What a difference!!  Wow!!  What a precious gift!  This Mommy loved it and is still swallowing the lumps in her throat!!!!

Update on My Man

Hey Prayer Warriors!

We went to the doc yesterday for B & Me and received some updates.

In regard to B, he is a Rockstar!!!   When we left his test the doc that performed it said that he is "brilliant!"   Our neuro yesterday said the same thing!  They said he is truly above average and performed off the charts.  That's my man!

The doc performing the test & the neuro also stated that they did see "deficits" that made him normal!  Thus, he didn't score as high on certain areas of the test.  Those areas are indicative of the damage that they are seeing on the MRI.  However, they said that his "low" scores were actually normal!  Meaning that he scored in those areas what most "smart" people would score.  That was considered a deficit since he's brilliant!!!

So, the end result is that our neuro wants to run a few labs, looking for other things, and she wants to do an EEG (the test that I have done all the time with the electrodes attached to your head).  Otherwise, we have a follow-up appt next week with the doc that performed the test.  At that appt. she will be able to give us the entire report and then some "exercises."

Exercises-as we understand it, he will meet with this doc frequently to do mental exercises to help strengthen what has started to atrophy.  So, call it brain rehab maybe...Imagine if you broke your finger and had to do exercises to get it back in shape.  Then, imagine if you had to have your finger amputated and learn to use the other four to do what five were doing.  As I understand it, this is as if he lost a finger.  So, we're having to let the other four learn how to do the work of five. 

We'll tell you more once we understand it.  However, those are the basics as we understand them!

What Makes Today Special?

Many look back on this day eleven years ago and remember so many innocent lives lost.
In our family, there is a secondary reminder, one of life!  Yes, on this day, September 11th, 2006 (the five year anniversary of lives lost), a special man that I love, went in to surgery.  While he was still waking up from his anesthetic, his doctor told me that he had cancer.  To most of us, that is a bad word and it means death because we've lost someone to the yucky disease.  A few minutes later, my amazing husband woke up from his anesthetic and wanted to know about his surgery.  The doctor had not made it back in to the room and so I had to tell my hubby that he had cancer.  September 11th no longer meant death or fear.  The first words out of B's mouth were, "Cool, that means I get to be a cancer survivor!"  Yes, you can blame it on the anesthetic, but I blame it on a man that is completely sold out to his Savior, Jesus Christ.  He trusted and still trusts fully in the Lord and HIS healing power over B's life.

You can read more about that day here: Survivor
You can read more about the journey here: Psalm112-survivor.blogspot.com.

In the meantime, we both head to the doctor on Thursday.  The neurologist has told us to expect a long appointment.  We will be getting a preliminary update on B's test from last week.  That doc told us (what his wife already knew) that he is brilliant, but she can also see in the test scores the areas of weakness where the scans pointed to damage to the brain.  So, in the next few weeks, we will begin to learn what type of "rehab" will be required to strengthen those areas. 

We will also learn the next step that they want to take with me.  Last we were told, the next choice was chemo, but there was one other option that she was trying to look into...So, please say some extra prayers for wisdom for all docs involved and for us.  Please pray for P's protection amidst all of this chaos.  Please pray for B's job that he is able to continue working and serving others while still taking care of himself and the rest of us!  We love him SO MUCH and PRAISE THE LORD that HE chose to make September 11th a celebration of life for our family!!!

We love you, B & Daddy!!!

Psalm 112

¹ Praise the Lord.^[b]

Blessed are those who fear the Lord,
    who find great delight in his commands.

⁷ They will have no fear of bad news;
    their hearts are steadfast, trusting in the Lord.
⁸ Their hearts are secure, they will have no fear;
    in the end they will look in triumph on their foes.

Thanks and Update

Many, many thanks to all of you for praying for M yesterday.  These last few days have truly been difficult as it seems the seizures just won't stop.  We did have home health come in and do IV medication yesterday morning as we will sometimes see good results administering M's anti-seizure medicine this way.  While not a sure thing in stopping the seizures, we can usually get some reprieve.

M was able to get some rest throughout the day and some much needed reprieve for most of the day after getting the IV.  PRAISE THE LORD! While the day did progress better than it started, the seizures unfortunately returned by bedtime with M having a few around going to bed and during the night.

Pleas be in continued prayer and, in addition, pray for our Neuro, Dr. S.  We have an appointment later this week to go over some additional thoughts and possible future treatment.  We too are very much prayerful about our upcoming appointment.

Thoughts:  Since we were not able to get out to church yesterday due to the chaos that ensued, we had our own little church last night.  Our time had us in a familiar passage, James 1:2-8.

Consider it all joy when you face trials of of many kinds....

A very good point that I don't think we really considered is that JOY does not necessarily mean happiness.  Unfortunately, circumstances that are not always in our favor do happen.  BUT God can make good from our trials.  Our focus should not be on the trial or tribulations, but rather we are to look through the circumstance.

Your thoughts?  For more insight we would encourage you to also listen in to the message we listened to.  Look through the trial and trust : Message by Pastor Brian Fisher, Grace Bible Church, College Station, TX 09/02/2012

Emergency Prayers

Prayer Warriors!  Please continue to pray for M.  It is just the early morning here today, but already M is at 4 seizures since midnight and 5 in just the last 12 hours.  Please pray for her healing and rest as she is incredibly tired and we all are just floored by how bad the seizures have become this month alone.  M is averaging nearly 4 seizures per day right now.

Since this morning has been crazy, we will be doing medicine with home health and trying to make sense of things and hopefully get in contact with her doc.

Thank you for your continued prayers!

Quick Update/Prayer

We've held off on posting about this for a while. 

Many of you know what an amazing and "soft" heart B has...

We found out a few weeks ago that his brain seems to be softening, too.  He was starting to behave a bit differently and I just told myself it was my seizures and I was seeing something wrong.  Well, Mom finally asked one night at dinner what was different about him.

I brought it up to him that night.  He had noticed some minor things.  He then became a patient with me at my next neuro appt.  She ordered an MRI.  The MRI showed a really big word that means softening/atrophy of the brain usually following an NFL concussion.  We're still waiting on the NFL disability payout!!!  Right?

Anyway, doc has ordered a test that looks at overall brain performance.  It is an all day test.  So, we are down in the hospital world today.  As far as we know, we won't have any real results until next week.  We just wanted to get those prayers headed to the Lord for B's healing!

B with his girl!!

FIRST Day of Preschool

It's so hard to imagine that our little angel is growing up so quickly.  Today was her first day of preschool!

Sitting down to pose as soon as I saw the camera!!!

Showing off the dress that Gamma bought for the first day of school!

Snuggling with Daddy before school!

Daddy made Mommy pose even though she didn't have on any make-up!!!

Getting out of the car to go meet my friends at school!

Good Morning to the squirrel!

Already starting to play!

 Pray that it's a great day!  She seemed to enjoy it when she arrived!!!  We hope she loves the entire day!

Important Business with Winnie the Pooh

We would love ideas from all of you experienced parents on the next car seat for our girl!!

P is about to need to get out of the infant car seat...what is the best seat that could be forward or backward facing?  She's still a skinny little thing and so she's supposed to be backward facing for now.  However, she's getting a bit too tall for the infant carrier.

This is serious business, folks!  I have to sit in this seat while I take care of important phone calls with Pooh!!!

 

Just kidding!!!!  Will you come sit with me, too?  We could have fun playing with my Pooh phone!

Mommy and Daddy sure would love help on picking the right car seat, though!!!!  We had great advice on the infant carrier and have loved it.  Now we need to find something new for our growing girl!!!

Y'all were incredible with the advice on the diapers at bedtime.  We switched to night time diapers and we've only had one morning that required new sheets!!  Thank you!!!