How do you explain a micro preemie to a 5 year old…

As we approach the holidays, we drag out old ornaments and art projects that the kids completed and reminisce about those times. This always brings a little bit of a struggle for Noelle. She LOVES to put up the tree, help wrap presents and get everything ready. She knows that Santa comes, but she also knows the reason for the season and how important it is to celebrate “Jesus’ birthday!”

However, she had a lot of questions this year about her birthday. Wanting to know why her baby pictures were so “scary” and told me that they make her sad. I’ve heard of other preemie parents keeping the baby pictures away from the child until they are old enough to handle it. However, that’s Noelle’s history, that’s her past. Quite frankly, she still has oxygen and a feeding tube and I always thought her baby pictures were so cute. I was so used to seeing the tubes, lights, wires, IV poles….I didn’t even think about how she might portray these pictures in her curious mind. She has had baby pictures hanging on her wall since she came home…and I don’t intend to take them down. I decided it was time to explain….

Way easier said than done. She had tons of questions. She wanted to know why she didn’t have baby pictures without oxygen and she wanted to know where Andons baby pictures WITH oxygen were. I explained that babies are suppose to grow and cook in a mommys tummy for a long period of time. Andon stayed in for the full cooking time. However, Noelle was just so excited to see us that she came a bit too early. I told her that this was the coolest thing because mommy, daddy and Andon were able to watch her grow on the outside of my tummy instead of inside. I told her we were able to hold her, play with her, sing to her much sooner than most other babies. Her smile and amazement told me I was doing an okay job. I asked her if she wanted to see more and she said yes!

I have boxes of every little paper, every form signed, each and every blood pressure cuff as they got bigger, the bilirubin “sunglasses”, pictures upon pictures, every diaper size she went through (clean of course), each binky size, sweeties containers, outfits, hats, blankets, anything homemade by volunteers or nurses, surgery pager papers, “Drama Queen” pillows still in the same plastic bags, I even kept her first g-tube! I pulled all this stuff out and showed it to her. Patiently waiting to see if I had made the right choice to share at age 5. I did! She was amazed and astonished at everything. She wanted to look through every little thing and asked for explanations.

The outfits were a hit, the diapers were a hit, everything she looked at was filled with big eyes and “awww’s!” Almost as if something had clicked. She understood. She asked a few more questions…. For instance, why do her lungs need oxygen? My answer of her lungs being so small when she was born finally clicked. I hope a lot of things clicked. I explained the scary pictures. Even though, it looked like she was tiny with a lot of tubes….look at mom’s face!

That picture was the day I got to hold you for the first time.

Oh, look! That was your first bath!

That was the day you got to try out peanut (she knows peanut as her bipap machine…it just looks a little different on a tiny baby).

Look, this was the day we got to say goodbye to your warming bed (isolette) and you got to be in a big girl crib!

Look! This was your first Thanksgiving, Christmas and New Year! All in the hospital surrounded by people who love you.

We have pictures with each nurse, doctor and therapist. So, she wanted to know who they were….name by name…picture by picture. So we did. It’s been five years and I still know every name and face. I still know the smells, I still can hear the machines beeping … I’m glad she won’t know that part. Then, I was able to match faces and names to things she knew. For instance, Nurse Megan and Nurse Tonya made a lot of Noelle’s signs. Nurse Emily made her night night CD that she STILL listens to every night. It went on and on….

She just knew that each person holding her was smiling and happy to be with her. I explained that she spent so much time with these doctors and nurses…that they loved her like family.

It was a bittersweet evening with Noelle and I. We went through so much together and I felt like I finally got to share it with her. She needs to know how special she is, how loved she is, and how much people generally enjoy being around her and with her. She needs to understand what a true miracle she is!

As we approach Christmas next week, I’m reminded of all those babies, doctors, nurses, therapist and staff who will be at the hospital on Christmas. All the parents that will visit their sweet babies in the hospital on Christmas Day. Say an extra prayer for those. It’s hard to visit your child in the hospital on Christmas. However, the people that are there make it so special. I’ll never forget that. Say a prayer for the people working in the hospital on Christmas. They are leaving their families to take care of others. I hope they know how appreciated and thankful the parents are…even if they seem sad. It’s been 5 years….and I’m not sure if I’ve ever said thank you to those people. So… THANK YOU! Thank you not only for making Christmas special for those in a cruddy situation….but thanks for making such wonderful memories that I was able to share with my gal 5 years later. I’m so thankful that her baby pictures are no longer scary. The reason being because I was able to express the memories behind those pictures.

Merry Christmas from the Mikels!

Xoxo,

Stacie πŸ™‚

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Mother of the Year!

I really deserve a mother of the year award. I would love a super mom cape just like Wonder Woman….

Last night, this conversation really happened in my house!

Noelle: drops her book on the floor and says, “aw crap!”
Me: “don’t say crap, that’s a bad word!”
Noelle: “you just said crap!”
Me: “well, yeah I guess I did… But it’s a bad word! Who’d you hear that from?”
Noelle: “you, mommy!”
Me: “well, crap!”
Andon: “mom, you just said crap again! I thought it was a bad word.”
Me: “well, it is… We shouldn’t say crap! But since I’ve already screwed that up, let’s just spend the next five minutes before dad gets home saying crap nonstop to get it out of our systems!”

So, all three of us walk around saying “crap, crap, crap, crap!” I told them that crap was officially a bad word again once Ross walked through the door! They knew not to say crap ever again!

Ross walks through the door and asks “How was your day? What have you been up to?”

How does Noelle respond? She says, “not much dad…. Just saying crap!”

#parentingfail

Oh well… Happy Friday!

Xoxo,

Stacie πŸ™‚

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New Beginnings…

The first day of school always brings so much excitement, anxiety, new friends and best of all new beginnings.

My kiddos started school today. Andon started the second grade and Noelle started kindergarten.

When Andon started kindergarten, I cried before I even woke him up on the first day. Held my tears while I dressed him, fed him and made sure he brushed his teeth. Held it together until the bus pulled away….then cried my eyes out. I quickly realized that my babies were growing up and didn’t need me as much. I followed the school bus to school, stalked….uh….I mean watched as he walked into school. Then, I called to make sure he made it into his classroom. I worried about what kind of day he was having and prepared his favorite snack for when he finally came home.

This morning with Noelle was different. I was so proud of her. I didn’t cry at all getting her ready, feeding her breakfast, brushing teeth together and doing her hair. She was so excited and I was so excited for her. We put Andon on the bus and then I took her to school (she can’t ride a bus, they wanted to transport her in an SUV….so I just decided to take her myself.) As I was driving to school a song by Switchfoot called “This is Home” came on. This is the song that Emily (one of Noelle’s NICU nurses) gave us on a CD when we left the NICU. Enter tears….BIG ONES! I know how blessed I am. But on that ride to school….I thought about all those NICU parents who didn’t get to take home their kiddos…let alone take them to the first day of kindergarten. I remembered the moments that I was unsure if Noelle would leave the NICU or start kindergarten. Those memories just came flooding back and once again realized how incredibly blessed we are!

I get a lot of reminders about how blessed we are…but today was a big one! That little miracle girl has come a long way from her 1 lb 11oz preemie! My biggest fear today was that the kids would look at her differently and not want to be her friend. Seems like the opposite happened!

Noelle has AMAZING teachers and therapists! Her teacher said that some of the kids were even correcting other kids about stepping on her tubing!! (Enter tears now!) One of the little girls even gave her a “Nice to meet you” card! I teared up this evening again as she was making a card for that kid! She did it on her own without even telling me what she was doing. It says, “I love you, Kaylee!”

These kids of mine have HUGE hearts!! Sometimes, I hate the fact that summer is over and I have to share them with school (but other times, I’m so thankful that summer is over!) Watching them blossom over a school year and make friends is priceless! I am really looking forward to a great year…. This year is going to be one of the best, I feel it!!

Cheers for new beginnings!

Xoxo,

Stacie πŸ™‚

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5 years later…

Noelle's Birthday!

Noelle’s Birthday!

Happy 5th Birthday!

Happy 5th Birthday!

It’s been 5 years!! Noelle turned 5 today and I can’t help but look back to the day she was born. By far the absolute worst day of my life, yet still holds as one of the best days too. It’s an odd feeling looking back. Having a 24 weeker comes with huge responsibility and a lot of chaos. Yet, huge blessings. As I’m typing this, Noelle is in her room singing “Happy Birthday” to herself!

This 5 th birthday holds a lot of weight on my mind. I remember when I first got to see my girl. I was hesitant to name her, couldn’t hold her and without the help of doctors, nurses, machines and tons of medicine…she wouldn’t be here. I was told everything: Noelle would never walk, probably wouldn’t talk, she might be a vegetable for the rest of her life, she could be trached and vented forever. I had a little bit of hope and a lot of prayer…

i remember being by her bedside when she was about 2 weeks old. She wasn’t even 2lbs and she was getting ready to have heart surgery. I just wanted to fast forward to her 5th birthday and get a preview of what her life might look like on her fifth birthday. I kept having dreams about her fifth birthday. Would I be celebrating with a normal kid, a wheelchair bound kid, a trached kid….or would I be celebrating at her grave? I just wanted a preview so for 2 seconds….I could stop worrying.

In my wildest dreams, I couldn’t imagine a better, stronger and more beautiful 5 year old. She still on oxygen, still has meds, still has a feeding tube….but who cares?! She’s gorgeous, smart, and has a sparkling personality that will charm anyone that meets her. Most important, she has more love tucked into that tiny body than most adults. I was teasing her tonight and told her we weren’t able to pick up birthday presents (even though she asked about them all morning), her response was “that’s okay mommy! Do I still get cake?”

i used to have feelings of jealousy towards parents with “normal” kids. Screw that…I’m beyond blessed and so thankful for both my kids. What’s true is they complete me, I can’t imagine my life any different way. Having a special needs kiddo has given me so much! Patience, perspective, patience, education, patience, perseverance…. Did I mention patience?

I just got back from Cub Scout camp today with Andon. It was such a welcome change just being me and him! We both enjoyed it and have made a pack to do more things one on one together. It was an absolute blast!

My grandmother always told me that the older I got, the faster life would pass me by. She’s right. These past 5 years have flown by….it feels like yesterday when it felt like INOVA Fairfax was home! I need life to slow down a bit. These kids are getting too big…way too fast! I only hope I can continue to stop and remember all the small and insignificant moments in order to savor all the big milestones.Β 

Xoxo,

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Stacie:)

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Things we are THANKFUL for….

The kids and I have been playing a game lately. I ask them what they are thankful for and we list several things each morning. The first day, as expected, it was toys and material things. However, I have been playing the game too and have listed some things such as family, health, roof over our heads, ability to create memories as a family, doctors, etc….

So, the kids have caught on. They are listing bigger and better things…not so many “things.” Today, they were thankful for Ross helping to make a blanket fort in the family room so they could read and be quiet so daddy could rest. They were thankful for me coming home (I had a planned visit with several out of town friends and we were either expecting Ross’ treatment to start long ago or in a few more weeks.)!! Lastly, they were thankful for ice cream (baby steps…. lol).

So, I gave Ross his first shot on Thursday evening. By Friday, he had a few bloody noses….but virtually NO OTHER SIDE EFFECTS!! We were both pretty blown away and SO THANKFUL!!! On Friday, I had a planned weekend away. Honestly, my thought was that I had to cancel it. However, when Ross was feeling great…I decided to go!! It was a wonderful get away after all the stress from the week. On Friday night, I literally crashed. Between Pittsburgh and doctors appointments all week for Noelle and Ross…my schedule for the week was to just “get through the day!” When I had nothing scheduled other than fun….I was a little lost and I think I started to really process my week. We had Pulmonology and GI appts in Pittsburgh Children’s on Monday and Tuesday, Noelle had a Neurology appt at Children’s back home on Wednesday morning and then Ross’ appointment to train and start treatment on Thursday.

I felt like I didn’t sleep at all Thursday night. Everytime Ross moved, I just imagined him puking all over me. So, I hopped up everytime the poor guy twitched in his sleep to make sure he was okay. He was fine. By Friday evening, I was exhausted. I was with my girlfriends in a nail salon and kept hearing the Casting Crows song, “I Will Praise You In This Storm.” I am so utterly thankful that I’m healthy and able to take care of everyone. I also kept hearing the Laura Story song, “Blessings.” Because even though things are crazy and chaotic….we are so blessed! Just because life isn’t going as planned….doesn’t mean its going badly. Sometimes it takes a few trials in life to make sure you know whats truly important. I’m thankful for my trials.

By Saturday night, Ross was having fevers and chills. He’s a bit achey all over and is just tired. Luckily, the kids were amazing, went to bed early and were perfect for quiet time to allow for his naps. He barely told me anything and really wanted me to enjoy the time with my girlies. He is amazing…. and I enjoyed my time. Now that I’m back…he’s moving slower, is more tired and is admitting that without small doses of tylenol, the chills and aches are pretty bad. But…if thats as bad as it gets….We are thankful!!

Ross is planning on going to work tomorrow. So, we’ll see! Overall, I’d say that his first few days on the Interferon treatment were not that bad. He is a tough guy.

We are keeping the faith that his side effects will remain minimal and that treatment is being effective! During Week 5, he will have to add another drug, which by our research will be the hardest part of the treatment. Any side effects that he is having will apparently be multiplied. So, we pray that he will continue the minimal side effects throughout the course of treatment.

We are expert prayers and waiters!! πŸ™‚ There is a plan…..we pray, we wait….we hope! πŸ™‚ Thanks again for the continued prayers! We feel them and you have no idea how much they are appreciated!

xoxo,

Stacie πŸ™‚

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Things that should be easy…

You would think it would be easy for me to give Ross his first treatment shot today. I’ve watched needles go in and out of him and Noelle what feels like thousands of times! To give a shot… Knowing the side effects that the shot may cause… was sad for me today!

The shots and pills are in… So for now, we wait, we pray and we hope!!

Ross is in a great mood and even decided to do a video blog about his journey through treatment! This is crazy because he is usually such an introvert! I think he has kept this secret for so long (because even doctors have been quick to judge how he got the Hep C… Until they hear the story)… I think it feels good to let it out!!! I’m proud of him! Check it out:

Our marriage hasn’t been roses and chocolates everyday! We have had to work to keep our relationship and marriage strong. It hasn’t been easy. Tonight, it’s easy! He has always worked so hard to provide for us and love us unconditionally. I’m proud of him for taking this with such ease so far……

So, again… We wait, we pray, we hope… Thanks for joining us!

Xoxo,

Stacie πŸ™‚

These are the days of our lives….

So, I’ve been super quiet lately. Partly because I’ve just been too busy to sit down and write. Partly, because maybe I’m still in a little bit of denial. Also, partly because I’ve taken on a new job at my work that I love…but it’s made me busy!

We had a magical trip to Disney. There really are no words to how much fun we all had. What you don’t know is the why! Why did we plan a last minute, bank breaking trip? Well, the hubby wanted to. You see, when Ross was a kiddo….he had cancer, twice. Just in case your mind goes there…he does NOT have cancer again! Whew!

However, during his cancer treatments…he received ONE blood transfusion. This was in 1989. They didn’t start to screen blood for bad things until 1992. So, unfortunately, the blood he received was tainted with Hepatitis C. He did treatment way back for it and it has remained a low risk disease for him for years!

During a routine visit with his doctor this fall, his liver enzymes were elevated. No big deal…they always are slightly elevated. However, these results were pretty high. They scheduled a liver biopsy around the holidays and the results were slightly worse than we were expecting. Ross was told he had some significant liver damage. This is basically borderline liver failure. So, the doctor gave him really no choice….he needed to start an Interferon treatment, or else he would need a liver transplant soon if we can’t get the Hep C under control. Treatment can last from 48-72 weeks…so basically the next year. We were told the treatment comes with some pretty serious side effects, but weren’t too concern because he has already been through it (and back then, it coincided with chemo).

So, knowing that he would be feeling kinda crummy for a year or so…we planned our Disney trip. Did I happen to mention it was magical?!

We got home from Disney and treatment has been delayed for one reason or another. The nurses were stressing that we read all the information that comes along with treatment. Quite frankly, I know they have to cover their butts….but the treatment paperwork is downright scary. “May cause heart attacks, strokes and even death.” The most common side effects include fatigue, flu like symptoms, hair loss, headaches, vomiting, etc….but the extreme side effect is death. No big deal, right?! ((Yikes!))

So, here we are. Tomorrow starts the first day of treatment for Ross. We know that God has a plan….a plan that we can’t see or even imagine. But we are asking for prayers….as many as you’ll send up! We pray that the side effects are minimal and that the treatment is effective. After about 6 weeks of treatment, he’ll have extensive bloodwork done to see how the Hep C is responding to treatment. If his numbers haven’t rapidly decreased….they will consider treatment a failure and he will stop. At that point, I guess we just wait around for his liver to get bad enough for a transplant.

I know for a long time, Ross didn’t want me to share this with anyone. But now, he doesn’t care. This is a guy who has never drank, smoked or done drugs. He has taken care of and protected his body well. So, we are just waiting and praying to see what Gods plan is for the Mikels family. If Noelle taught us anything, it’s that God has a plan….and sometimes you just have to be patient for it.

Noelle and I just returned from a doctors trip in Pittsburgh….I’ll save that blog for another day because there is really not much to tell. Noelle remains a mystery….just the way she likes it!

So for now, we wait….we pray! Feel free to join us!

Xoxo,

Stacie πŸ™‚

Old Times Revisited…

Ross and I just spent the last 45 minutes looking through old photos of the past 5 years. Most people look back on old photos and reminisce about how wonderful the times have been, how precious the memories are and how wonderful it is to look back!

Honestly, ours are painful. I cried… A lot! I look into all of our eyes in the pictures and see pain. Andon feeling so left out (yet, still smiling) and ignored. Ross having just blank stares. Noelle having pictures of barely surviving, hooked up to life support and in the hospital smiling. Then there’s me!

For the first probably 2 1/2 years after Noelle was born… My life was absolute chaos! I felt so GUILTY! Guilty that I couldn’t keep my baby inside and mad at my body for failing me and my daughter! Angry for not seeing the signs sooner that she was on her way! Mad that there was no turning back time to keep her in longer! Guilty describes me best. I felt like my body failed and was responsible for turning our lives upside down. Not to mention, I often felt guilty for waving my white flag and admitting that sometimes, it was easier to admit her into the hospital rather than be so sleep deprived that I screw up her meds (yup… That happened!).

Many of those pictures were from our first few weeks at home. Noelle spent 222 days in the NICU. Came home for 3 1/2 weeks and then went back into the hospital until a few days before her first birthday. I took a lot of pictures. The doctors told me that her getting sick would potentially be fatal… I felt like pictures had to be taken, just in case!

Because of this, I turned into the germs worst nightmare! I wouldn’t let anyone in our home without washing hands. I made Ross change his clothes after work before picking up Noelle. Andon and I stayed home with the exception of Noelle’s doctors appointments. I even fired our first home nurse because she was a smoker and just dirty and gross!

I had no friends! I didn’t let them in much, especially after having to quit my job! And realistically, who would want to be friends with me? I was a crazy fool.

Noelle needed nebs every 2-4 hours round the clock. Ross had to sleep at night so he could work and function during the day. Which meant I slept about 1 1/2 hours at a time, every few hours only at night. I had to potty train and somewhat pay attention to Andon during the day. I was a sleep deprived zombie! Most of the time, Noelle also needed meds round the clock (She came home on 16 medications)!

There was one day after staying home for a few weeks by myself… Andon was acting out (heck, I would have been screaming for attention if I were him) and Noelle was screaming and desatting like she did everyday! I was overwhelmed, sleep deprived and had a to do list of too many things. We were in the process of trying to find ways to save our home and avoiding bankruptcy. I lost it… Andon was in his room screaming, Noelle was downstairs crying and beeping and I locked myself in my bedroom bathroom and cried… For what felt like hours. Crying didn’t help me face reality. I pulled myself together, said a prayer and found the strength to carry on with the day. I always tried to put on a front when people called or came by… But I was miserable.

Honestly, I didn’t realize how miserable I was until I started to look back at pictures. It does give me a sense of sadness still today. How our lives were turned upside down in an instant…

Thankfully, the guilt and anger are gone. Replaced by a little bit of sadness. Our little family has been through a lot and much of our experiences have changed us. I’d like to think changed for the better. I’m a far more patient person now than I ever pretended to be before. Andon doesn’t seem to be too phased and can’t remember “BN… Before Noelle!” Ross still gives me that blank state occasionally when I talk too much about the medical stuff. Me? I’m a far better understander of people, life, death, hard times and how everyone (at one point or another) just needs a break!

Just putting it out there… There are a LOT of feelings that come with having a preemie and a special needs kiddo. It has taken me almost 5 years to admit this! Typically, when we say we are fine… We are not! Usually, when we have a super upbeat attitude about something medical or developmental… It’s because (partly) we are still convincing ourselves! We are far from super human… But would rather have a sleepless night researching a cure or cause than sleep not knowing what’s going on. I’ve heard a special needs momma does better research than the FBI… I’m almost positive this is accurate!

I guess my point is that, yes! I smiled and put on a happy face while my world crumbled around me. But really… What choice did I have? Pretty sure if I had acted the way I felt back then… I would have been put in the looney bin! Realistically, I didn’t (and still don’t) have a choice! This is our life! Sometimes it’s still miserable! Sometimes it’s absolutely awesome! Thats why its called LIFE! Just like any normal family… We have our ups and downs.

I had a doctor tell me in the NICU that Noelle’s life would be a bit of a roller coaster for a while. I figured that. However, I failed to realize that our whole family would be on this “ride.” Obviously, our “ride” isn’t over yet. I’m not sure what (if anything) I would change at this point. This is our life… It’s normal to us now! Looking back is hard… Looking forward is sometimes hard!

One day at a time is perfection!

Xoxo,

Stacie πŸ™‚

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Disney Bound!

In about one week, Ross and I are picking up and taking the kids to Disney World. I’m pretty excited (and now pretty poor!) and literally can’t stop planning! I want to make sure this experience is once and a lifetime for my family! My mom bought the kids new Ear Hats (well, Noelle wanted to pink sparkly Minnie Ears headband…but whatever) and autograph books for all the character spots!

We are renting a mini van (in order to pack all of Noelle’s equipment with us) to drive from Virginia to Flordia and getting to see some friends along the way!! Believe me when I say…there won’t be room for anything extra in our van.

So, I’m reaching out to those who have been to Disney World with kids (ours are 4 & 6) before! What are some of the activities that you would place at the top of your to do Disney list? What are some things you wished you had skipped?

Noelle will be in her wheelchair, so I’m not too worried about lines. She would never make it from the parking lot to the gate…let alone around the park! We are planning to go to the parks in the morning, come back mid afternoon for a nap (Noelle will never make it for a full day…after 5 hours at school she takes a 2-3 hour nap as it is) and then be back at the park for dinner and evening activities.

Also, we purchased a dining package. What places to you recommend? I need recommendations for reservation and quick dine places!

I recently downloaded the My Disney Experience App on my iPhone. I also downloaded the Disney Maps app. Are there any other apps to download before we go?

Thanks for the advice ahead of time! We are super excited!!!

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Somedays….we do the best we can….

Let’s face it….sometimes….I simply suck as a mom! There are moments (even days) that I feel like I’m absolutely super mom. Today does not happen to be one of those days! Today was one of those days I ran around like a chicken with my head cut off! This is the brutal honesty about being a parent and parenting…

Anyone ever thought that they were a much better mom, BEFORE they had kids? I had all these rules and things I would never do with my kids. For instance, I said my kids would hardly ever watch TV. TV rots kids brains and I was determined not to use it as a babysitter. I also was NEVER going to give my kids fast food. I wasn’t going to let them play video games for more than 15 minutes per day. I was going to have them potty trained by the age of 2. They were going to be dressed and looking cute everyday with hair in place and teeth brushed.

Currently,Β Andon is watching a movie on the iPad while Noelle plays video games (lets just say its been longer than a half hour) and I’m so thankful to have some peace and quiet. Oh, and we stopped and got Happy Meals on the way home today….yup….after they already had lunches at school. What can I say…maybe its a growth spurt, right?! And I can’t forget that I’m pretty sure Andon went to school this morning without brushing his teeth….and we were running so late that he ate breakfast in the car!

I pride myself on giving my kiddos lots of fresh, wholesome and healthy meals…and then bomb occasionally! I know other parents can relate…but this really is not how its suppose to be. I imagined a perfect mom in myself…doing everything right. Yet, as soon as I get stressed or have too much to do…I immediately go to TV, Video games or movies.

I wish things were like they were when I grew up. From the moment I got our of school, we ran outside to play in the neighborhood and my mom wouldn’t see us until dinner. Alas, the world has changed. Don’t I wish I could just ship the kids outside and not worry! Maybe then…their little brains wouldn’t rot with TV!

Oh well! Somedays we just do the best we can! Today will have to be good enough… πŸ™‚ Let’s face it….I’m not the only one, right?!

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xoxo,

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Stacie πŸ™‚