Type 1 Diabetes & the day our lives changed forever (Copy)

It’s been a little over a year since I’ve written for my blog. It’s something I wish I had more time to do, but between balancing motherhood, my career and life it’s been hard to keep up. With the challenges life has thrown our way over the past couple of months, blog posts might be very few and far between for a long time. This isn’t the end of a chapter for my blog, but I did want to update on my life since I’ve been absent. If you’re reading this, you’re either family, a friend, a follower of my instagram/facebook or blog. Or you’ve stumbled here because we unfortunately share something in common in our lives. Type 1 Diabetes.

I entered motherhood with the same eagerness, joy and worry every mother has. I became a mother and thought I would teach my child about the world, and while that still may be true, never in a million years did I imagine I would be here.. hoping to teach the world about my child. But that is exactly why I’m here, writing this for the world to see. So the people in our lives and the people who enter my sons life in the future, have more insight into this disease that has taken over my family. I’m not here for pity, or sympathy. I’m here so others are informed, and educated. If it’s one thing we’ve learned so far, absolutely no one understands this disease unless they have gone through it themselves.

In May of 2022, my husband and I took a last minute trip to Vegas just the two of us. It was our first time flying out of state and leaving our son behind! We had a great time, and little did I know that would most likely be the last trip we took just the two of us for the foreseeable future. When we returned home I planned to start potty training our son. He would be 2 in July, and I was hoping to have him potty trained by his birthday. Things were going pretty well, he seemed to understand the potty, and would even get excited about it. He made it to the potty more times than he had accidents, but what I first noticed was how often he peed. He would go every 15 minutes on the dot, and it wasn’t ever just a small amount. I found it strange, but I continued potty training thinking maybe he just needs to learn to hold his pee. I thought to myself, well he does drink A LOT of water too. Maybe thats why. It is summer in Texas after all, I’m sure he’s just hot. I gave it 11 days until I made an appointment to bring him into the pediatrician. The day before I brought him in, I remember looking at him and thinking he looks skinnier. But again, I thought maybe he was just growing and getting taller. Later that night, I had put his diaper on and within about 30 minutes the diaper fell off because it was filled with so much urine. We did just get bigger size in diapers maybe these don’t fit, I thought to myself, still I was in complete denial that anything could be wrong with my kid.

We woke up the next day and had a normal morning, and I drove to take him to the pediatrician. I truly thought we would leave and go about the rest of our day. I even had plans to go home and garden with my mom after. We got the the doctor and a successfully got him to pee in a cup, I was so proud of him! Little did I know the news we were about to get and getting him to pee in a cup would be the last of my struggles. We waited in the room with our doctor while she asked us questions about his symptoms. The word diabetes hadn’t been mentioned yet. It looks like he’s lost 2 pounds, the doctor said. Then I proceeded to tell her the other symptoms. “well he was peeing every 15-20 minutes when I was potty training, and I noticed he was drinking about 48 ounces of water a day.” “Yes he does pee the bed sometimes.” “No, no other symptoms, he’s always been a bad sleeper, but other than that he seems fine. Still calm, I was waiting for her to say oh yea! he seems fine, probably just growing. I’ll see you guys at his next visit! But, I saw it on her face as soon as the nurse come in to deliver the urine test results. She immediately turned to me and said, “I am so sorry….” In that moment the world went black. my heart sank to my butt. I don’t even remember what she said, all I heard was “Nathan has type 1 diabetes, this is going to be so hard, it’s going to be so so hard. but you can do this. I know you can because you brought him in here SO early mama, you knew and you trusted your gut that something wasn’t right and you did it. Most kids are not sitting there like he is right now, most kids don’t come to me first. Usually they are sent straight into the ER.” I cried so hard and she hugged me, then gently said “you got this. But you guys need to go to Dell Childrens now.” Wait, what? I thought to myself. We’re going to the hospital? I thought she would tell me what to do when we got home and that would be that. I had no idea how much our lives were about to change. I knew it was going to be different and hard but it wasn’t until we got to the hospital that it really sank in. I was so naive to this disease, like so many are, I had no idea what the next 3 days would entail.

(For those that don’t know, type 1 diabetes is a lifelong, chronic disease where your pancreas can no longer produce insulin. It can not be prevented, cured and is not caused by diet. Type 1 can be fatal if not caught, or managed properly. Type 2 diabetes is a completely different disease. They are not comparable diseases)

My son, my sweet happy baby boy was diagnosed with a life threatening disease that is incurable. 2 weeks before his second birthday.

The next several days were a blur of emotions, shock, anger, denial, and sadness. All while taking educational classes in the hospital about his disease and trying to stay strong for a 2 year old. Diagnoses day and the weeks to follow was much like going through grief. We are mourning the lives we had before, the life that would never be again. As we were leaving the hospital I was SO nervous. How can I do this on my own without the nurses and doctors? I’m going to kill my child. I cried the whole first night home, and the days and weeks to follow. I remember the first day I finally said to my husband, “hey I don’t think I cried today” what an accomplishment. I will never forget those first few fragile weeks and the people who made it easier for us during the hardest time in our lives. I’ll never forget my sister driving down and getting us set up with a new phone for our son to track his new CGM, and getting me set up with an apple watch so his numbers are always easily in sight because I could barley think straight to do it myself. The first 2 weeks back at work were absolutely the hardest and I’ll never forget the clients and coworkers who made those days more bearable.

The months to follow have looked like this: wake up, check blood sugar, listen to podcast about diabetes, check blood sugar, treat a low, over-treat a a low, oops-give him more insulin, count carbs, check sugar, treat a high, treat a low, read books about diabetes, go to bed and hope for the best.

I quickly learned that this disease is a full time job, that is never fully taught. It’s been trail and error every day. There are no breaks whatsoever. It is around the clock care, its life or death. Every day is an obstacle. Every decision is crucial. We’ve absolutely had good days and when we do I feel like supermom. But good days usually come with some bad to follow. It seems like once you get it figured out, things change and start back over on the roller coaster of blood sugar control.

Being a mother to a type 1 child, especially a two year old means I don’t know what it’s like to fully fall asleep at night without checking blood sugars through the night. I do know what it’s Iike to sleep with one eye open, with my phone clenched to my hand in fear of missing an alert that could end my child life. I don’t prepare a meal without a calculator, measuring cups, or the proper timing of insulin delivery before a meal. I don’t know what it’s going to be like to drop my child off at school fearing he is in good hands of someone who will know how to take care of him. I do no what it’s like to feed my child sugar through the day and night- knowing that I am sacrificing his teeth to save his life. I do know what it’s like to give insulin late at night and pray I’m not too tired to make a fatal error. I do know the absolutely gut wrenching feeling of hearing my tiny 2 year old have a bad dream and say “no boo boo” in the middle of his sleep. I know what it’s like to hold him while he says “no mama” as I’m injecting his already bruised arm with insulin. I know what it’s like to pick up my next round of 200 needles, when it seemed like it not long ago we just picked up the first set. I do know what it’s like to know my husband and I can no longer take our annual anniversary trip to Fredricksburg because I couldn’t imagine leaving him through the night. I know what it’s like to fear my son being jealous of his future siblings, cousins, classmates and friends. The last thing you ever want is your child to feel different or less than. I now know what its like to see notifications all day long of high blood sugar alerts wondering which long term complications he can get from these high sugars. I know what it’s like for someone to offer him a sucker and I have to say no. I know what it’s like to one day fear a teenager driving or experimenting with alcohol- then add diabetes in the picture. I know what its like to hold a 2 year old down with my husband to inject what feels like a staple gun into his lower back every 10 days while he screams. I could go on forever.

I quickly learned that if I blame myself for this I will drive myself crazy, although I still carry that guilt with me every day. I think as a mother I will always wonder if there is something I could have done to prevent this. I’m still not sure why I was chosen for this. I’m not sure why I went through pregnancy during a world wide pandemic/lockdown, or had a traumatic birth experience, and then to be given the biggest fear of all everyday: the fear of losing my child. It just doesn’t seem fair. But I do know this has absolutely changed me. I am brave, and some days I am strong. I have become more fearless, and I hope that continues to progress. I know I will carry the weight of this for my child for as long as I possibly can, so he can be a kid for as long as he can. I will wear the fanny pack with his supplies, I will do the research. I will talk to pharmacies and doctors and I will keep fighting when I’m tired and weak and had enough. I hope to never let him see how hard this all is, so I will carry that for him until it’s time for him to branch out on his own. And when he does, I hope that I have set a good example of bravery and strength to fight this, confidence to control blood sugars. I hope he hears my firm, but gentle voice when dealing with pharmacies and insurance. I hope he never feels less than or lets this disease stop him from anything he wants to accomplish. I hope I can show him that.

Type 1 Diabetes & the day our lives changed forever

It’s been a little over a year since I’ve written for my blog. It’s something I wish I had more time to do, but between balancing motherhood, my career and life it’s been hard to keep up. With the challenges life has thrown our way over the past couple of months, blog posts might be very few and far between for a long time. This isn’t the end of a chapter for my blog, but I did want to update on my life since I’ve been absent. If you’re reading this, you’re either family, a friend, a follower of my instagram/facebook or blog. Or you’ve stumbled here because we unfortunately share something in common in our lives. Type 1 Diabetes.

I entered motherhood with the same eagerness, joy and worry every mother has. I became a mother and thought I would teach my child about the world, and while that still may be true, never in a million years did I imagine I would be here.. hoping to teach the world about my child. But that is exactly why I’m here, writing this for the world to see. So the people in our lives and the people who enter my sons life in the future, have more insight into this disease that has taken over my family. I’m not here for pity, or sympathy. I’m here so others are informed, and educated. If it’s one thing we’ve learned so far, absolutely no one understands this disease unless they have gone through it themselves.

In May of 2022, my husband and I took a last minute trip to Vegas just the two of us. It was our first time flying out of state and leaving our son behind! We had a great time, and little did I know that would most likely be the last trip we took just the two of us for the foreseeable future. When we returned home I planned to start potty training our son. He would be 2 in July, and I was hoping to have him potty trained by his birthday. Things were going pretty well, he seemed to understand the potty, and would even get excited about it. He made it to the potty more times than he had accidents, but what I first noticed was how often he peed. He would go every 15 minutes on the dot, and it wasn’t ever just a small amount. I found it strange, but I continued potty training thinking maybe he just needs to learn to hold his pee. I thought to myself, well he does drink A LOT of water too. Maybe thats why. It is summer in Texas after all, I’m sure he’s just hot. I gave it 11 days until I made an appointment to bring him into the pediatrician. The day before I brought him in, I remember looking at him and thinking he looks skinnier. But again, I thought maybe he was just growing and getting taller. Later that night, I had put his diaper on and within about 30 minutes the diaper fell off because it was filled with so much urine. We did just get bigger size in diapers maybe these don’t fit, I thought to myself, still I was in complete denial that anything could be wrong with my kid.

We woke up the next day and had a normal morning, and I drove to take him to the pediatrician. I truly thought we would leave and go about the rest of our day. I even had plans to go home and garden with my mom after. We got the the doctor and a successfully got him to pee in a cup, I was so proud of him! Little did I know the news we were about to get and getting him to pee in a cup would be the last of my struggles. We waited in the room with our doctor while she asked us questions about his symptoms. The word diabetes hadn’t been mentioned yet. It looks like he’s lost 2 pounds, the doctor said. Then I proceeded to tell her the other symptoms. “well he was peeing every 15-20 minutes when I was potty training, and I noticed he was drinking about 48 ounces of water a day.” “Yes he does pee the bed sometimes.” “No, no other symptoms, he’s always been a bad sleeper, but other than that he seems fine. Still calm, I was waiting for her to say oh yea! he seems fine, probably just growing. I’ll see you guys at his next visit! But, I saw it on her face as soon as the nurse come in to deliver the urine test results. She immediately turned to me and said, “I am so sorry….” In that moment the world went black. my heart sank to my butt. I don’t even remember what she said, all I heard was “Nathan has type 1 diabetes, this is going to be so hard, it’s going to be so so hard. but you can do this. I know you can because you brought him in here SO early mama, you knew and you trusted your gut that something wasn’t right and you did it. Most kids are not sitting there like he is right now, most kids don’t come to me first. Usually they are sent straight into the ER.” I cried so hard and she hugged me, then gently said “you got this. But you guys need to go to Dell Childrens now.” Wait, what? I thought to myself. We’re going to the hospital? I thought she would tell me what to do when we got home and that would be that. I had no idea how much our lives were about to change. I knew it was going to be different and hard but it wasn’t until we got to the hospital that it really sank in. I was so naive to this disease, like so many are, I had no idea what the next 3 days would entail.

(For those that don’t know, type 1 diabetes is a lifelong, chronic disease where your pancreas can no longer produce insulin. It can not be prevented, cured and is not caused by diet. Type 1 can be fatal if not caught, or managed properly. Type 2 diabetes is a completely different disease. They are not comparable diseases)

My son, my sweet happy baby boy was diagnosed with a life threatening disease that is incurable. 2 weeks before his second birthday.

The next several days were a blur of emotions, shock, anger, denial, and sadness. All while taking educational classes in the hospital about his disease and trying to stay strong for a 2 year old. Diagnoses day and the weeks to follow was much like going through grief. We are mourning the lives we had before, the life that would never be again. As we were leaving the hospital I was SO nervous. How can I do this on my own without the nurses and doctors? I’m going to kill my child. I cried the whole first night home, and the days and weeks to follow. I remember the first day I finally said to my husband, “hey I don’t think I cried today” what an accomplishment. I will never forget those first few fragile weeks and the people who made it easier for us during the hardest time in our lives. I’ll never forget my sister driving down and getting us set up with a new phone for our son to track his new CGM, and getting me set up with an apple watch so his numbers are always easily in sight because I could barley think straight to do it myself. The first 2 weeks back at work were absolutely the hardest and I’ll never forget the clients and coworkers who made those days more bearable.

The months to follow have looked like this: wake up, check blood sugar, listen to podcast about diabetes, check blood sugar, treat a low, over-treat a a low, oops-give him more insulin, count carbs, check sugar, treat a high, treat a low, read books about diabetes, go to bed and hope for the best.

I quickly learned that this disease is a full time job, that is never fully taught. It’s been trail and error every day. There are no breaks whatsoever. It is around the clock care, its life or death. Every day is an obstacle. Every decision is crucial. We’ve absolutely had good days and when we do I feel like supermom. But good days usually come with some bad to follow. It seems like once you get it figured out, things change and start back over on the roller coaster of blood sugar control.

Being a mother to a type 1 child, especially a two year old means I don’t know what it’s like to fully fall asleep at night without checking blood sugars through the night. I do know what it’s Iike to sleep with one eye open, with my phone clenched to my hand in fear of missing an alert that could end my child life. I don’t prepare a meal without a calculator, measuring cups, or the proper timing of insulin delivery before a meal. I don’t know what it’s going to be like to drop my child off at school fearing he is in good hands of someone who will know how to take care of him. I do no what it’s like to feed my child sugar through the day and night- knowing that I am sacrificing his teeth to save his life. I do know what it’s like to give insulin late at night and pray I’m not too tired to make a fatal error. I do know the absolutely gut wrenching feeling of hearing my tiny 2 year old have a bad dream and say “no boo boo” in the middle of his sleep. I know what it’s like to hold him while he says “no mama” as I’m injecting his already bruised arm with insulin. I know what it’s like to pick up my next round of 200 needles, when it seemed like it not long ago we just picked up the first set. I do know what it’s like to know my husband and I can no longer take our annual anniversary trip to Fredricksburg because I couldn’t imagine leaving him through the night. I know what it’s like to fear my son being jealous of his future siblings, cousins, classmates and friends. The last thing you ever want is your child to feel different or less than. I now know what its like to see notifications all day long of high blood sugar alerts wondering which long term complications he can get from these high sugars. I know what it’s like for someone to offer him a sucker and I have to say no. I know what it’s like to one day fear a teenager driving or experimenting with alcohol- then add diabetes in the picture. I know what its like to hold a 2 year old down with my husband to inject what feels like a staple gun into his lower back every 10 days while he screams. I could go on forever.

I quickly learned that if I blame myself for this I will drive myself crazy, although I still carry that guilt with me every day. I think as a mother I will always wonder if there is something I could have done to prevent this. I’m still not sure why I was chosen for this. I’m not sure why I went through pregnancy during a world wide pandemic/lockdown, or had a traumatic birth experience, and then to be given the biggest fear of all everyday: the fear of losing my child. It just doesn’t seem fair. But I do know this has absolutely changed me. I am brave, and some days I am strong. I have become more fearless, and I hope that continues to progress. I know I will carry the weight of this for my child for as long as I possibly can, so he can be a kid for as long as he can. I will wear the fanny pack with his supplies, I will do the research. I will talk to pharmacies and doctors and I will keep fighting when I’m tired and weak and had enough. I hope to never let him see how hard this all is, so I will carry that for him until it’s time for him to branch out on his own. And when he does, I hope that I have set a good example of bravery and strength to fight this, confidence to control blood sugars. I hope he hears my firm, but gentle voice when dealing with pharmacies and insurance. I hope he never feels less than or lets this disease stop him from anything he wants to accomplish. I hope I can show him that.

Best of Austin Beauty

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I’ve been wanting to do this blog post for a while & I’m so excited to put this list together for y’all! So many clients ask my recommendations for beauty services around Austin and I thought it would be fun to put together some of my personal favorites! I also did polls on instagram for all of my followers to leave me their favorite places too!

Below you’ll find a list of MY personal favorites along with the TOP recommendations from ladies around Austin! If I haven’t personally been to the place that was recommended, I looked up reviews and photos before adding them to this list! I think this is a great list because if several different people unknowingly recommended the same place- thats such a great testimony AND I know my clients personally, which means they expect the same type of quality service I give them in the salon! Meaning- these places should not disappoint! ;)

I am not working with any of the following businesses (other than Blonde Faith of course) and these recommendations are 100% just recommendations based on trusted resources or myself! I am not a blogger posting for trade or getting paid in anyway for these reviews.

** = places I have personally been
(others are top recommendations from y’all!)

All things hair:

AKA best hair extensions, best blonde highlights, best overall color, best cuts, best blow outs etc etc etc…..
BLONDE FAITH SALON

Best Nail Salon:
**CAESARS IN THE DOMAIN
This is my personal favorite place! It is upscale, affordable, clean and I’ve never left disappointed. I normally get pedicures and if I do my nails I get shellac/gel

E’shee Nails in the Arboretum
This was the top recommended nail salon. I’ve walked past it but never been in, looks nice! It’s also next to a home goods, target and michaels…what more do you need in one day?!

Bliss Nail Bar

Best Botox:
**
Dana Kirk with Rejuvenate Austin
I’ve seen Dana for YEARS and her botox seems to have the most longevity and overall best results! She’s also the sweetest human. I’ve been a few different places over the years since Dana moved a little further from me, but I just love her and always find my way back to Dana! It’s worth the drive to me for longer lasting results!

The next top recommended Botox Injector was Alicia Long with Synergy I have been to Synergy but didn’t see Alicia! I’ve heard great things from several followers, coworkers, and clients. She has been highly recommended from trusted sources as well!

Best Massage:
**
Oak Haven Massage
I go here frequently for massages! It not a spa, but I’ve always had great results and its a great place for affordable, routine massage services.

**Viva Day Spa
also a great place for massages, they are a little more expensive but has more of the spa atmosphere. I’ve gone to the one in the Domain!

Best Spa Day:
Top responses for sure are:
Lake Austin Spa
Miraval Austin

Ok so I’ve never been to either but definitely want to try both. After mostly everyone said these as their top answers I started really looking into it!

I have my eye on Miraval Austin right now because they have a 25% off for an entire spa day if you go Monday-Thursday! Even without a discount it is reasonably priced! See what all it includes here. I’m going to try it and let y’all know what I think.

Lake Austin Spa also has a half day away which looks pretty cool and affordable! View what their half day away includes here. I’d love to go overnight or for a full day sometime too but everyone said great things about both places!! Miraval seems like a better deal in my opinion because it’s about the same price (and way cheaper if you go during the week) for an entire day VS a half day at Lake Austin Spa. I’ll eventually try both and let you guys know which place I liked better!!

Best Lash extensions:
Pink Lady Lash
I don’t get lash extensions so I’ve personally never been but they have been highly recommended through the years and if I did get them this is for sure where I would go!
ATX Volume and Lash

Best Facial:
Lindsay at Skin Spirit
-Going here in April and I’m so excited! I’ve been following her for a while and she also gives great skin care tips on her instagram here
Mint & Thyme
Rejuvenate Austin
Skin Savvy - ok this place looks adorbs
Hydrafacial at Maui Med Spa (most affordable price in Austin)

Best Spray Tan:
Airbrush-360 Tans
Went here for all my wedding custom airbrush tans and always had great results!!

Also recommended- Organic Bronze Domain

When I don’t get Airbrush I get the Versa Spa at any tanning salon. I ONLY use the Versa because it gives natural results and you can pick your color. I usually do a “clear 4” it’s very natural looking!

Best Couples Massage:
**
Spa Sway in the Domain
**Viva Day Spa
Of course either Lake Austin Spa or Miraval would be a great option too but at the higher price point.

Best Lip Injections-
Cece, @derm_nurse at Skin Spirit OMG I’m going soon and I’m PUMPED!!! Her work speaks for itself.

Alicia Long at Synergy Plastic Surgery
Top Recommendation from y’all again!!

Best Plastic Surgery
Not a ton of answers for this one but these were recommended
Synergy Plastic Surgery
Jennifer Walden

Best Teeth whitening/Veeners
Cosmetic Dentists of Austin

Best Waxing
**
Soooo many recommendations for European Wax Center
Also, The Pretty Kitty Domain

Best Microblading:

I’ve been eyeing lovemybrowsby_m foreverrrr and want to go see her someday! Her work is incredible and she books out several months in advance. If she is booked she trains all of her employees I believe and she can recommend someone else!

Other Recommendations are:
Resshape Microblading Studio
Kara Sanchez

Prenatal Massage:
Honestly never had a great prenatal massage in Austin, the best one was of course the last trip we took over a year ago when I was pregnant at a spa in Charleston :( Maybe prenatal massages aren’t meant to be comfy haha. But the best results I had was when I was laying on my side VS the donut pillow. I went to all of the following places even towards the end of my pregnancy.
**Spa sway
**Milk and Honey Spa
**Oak Haven Massage
Viva Day Spa
Lake Austin Spa for Mothers to be Day Away



Our favorite toys for an 8 month old

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Hey guys! I know it’s been a while since I’ve done a blog post. Mom life has been so busy and trying to balance being a mom, wife, dog mom, blogger and stylist definitely hasn’t been easy! I thought it would be fun to share some of the toys Nathan has been loving, here are some of his favorites!

Panda Crate
I’m adding this one first because I seriously LOVE the panda crate toys! I’m suppperrr picky about toys and like for them to be aesthetically pleasing. These toys are not only super cute but we have loved every single thing we’ve received and actually use the toys that comes in the kit! I think it is delivered every 3 months and is super affordable for the amount of toys you receive and the quality is great.

Finger Puppets

Bubbles

Music Set
He specifically loves the tamborine in the music set. I bring it with me everywhere and can get him to stop crying in a second by shaking it around!

Activity Center

Water Play mat

Stacking Teethers

Teething Blocks

Crawl along toy

Jolly Jumper
(we have the one that attaches to the door but would recommend the one that can travel around your house!)

Playmat
(ours is out of stock but this one is beautiful, under $100 and the same company!)

Balloons
This helium tank comes with balloons but is super fun! I’ve tied them to Nathans legs and arms for a fun kick and play activity. Obviously this one needs adult supervision.

Popsicles
I know this isnt a “toy” but it keeps him entertained so I’m adding it haha. I add yogurt mixed with pureed fruits to create popsicles and he is OBSESSED!

I also love getting books from Target! They have a great selection and are super affordable. Also get a cheap mirror from target or walmart and lay it horizontal against the wall by the babies tummy time mat! Nathan could stare at himself all day in his mirror.

How to make a kids christmas eve box!

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I’ve already had a lot of questions about how we did our Christmas Eve box so I wanted to share how we did it! It’s SO easy and such a fun tradition to start!

When I was younger I always remember Christmas eve being so fun and exciting because my siblings and I were always allowed to open one gift on Christmas Eve. It was so fun as a kid because we were not only excited about Christmas but Christmas eve too! I wanted to carry on the tradition but in another way. Each year we will gift Nathan a Christmas eve box filled with candy, pajamas, a toy, book, and a letter from Santa, etc. We might use it as our elf on the shelfs farewell too!

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Heres how to make the box! You can click on the photos to purchase the items!
First I started with this box below! I found it at Michales and it was super easy because the back already had this decal on it and was already painted white. You could also just paint any white crate!

Then I bought these decals from etsy to apply to the blank side of the box! Super Easy. Hoping to get a cricut for Christmas so I can do this myself…. ;)

I made my own letter from Santa on Canva. Here’s what ours looks like and says for reference. You can also buy one on etsy! I’ll link those here!

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Then I stuffed it with the following items, this year we just did books, and pajamas and the little moose! It will change as he gets older of course! Here are some of our favorite books and pjs!

Updated Nursery Tour with a 5 month old!

I wanted to update our nursery tour video to show you guys what we use and how we have things set up now that we are 5 months postpartum! Everything is linked below.

Click here for a link to the nursery tour from before we had Nathan!

Baby Boy Outfit Guide

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Lots of questions where we get this cuties outfits so I’ve put together a little blog post full of some of our favorite places to shop, and our favorite outfits. I’ve even put together a little mommy and me outfit guide too! Some of our favorite places to shop are Lou Lou and Company for the easiest tie gowns, H&M, Zara, Etsy and Amazon! Nathans style is mostly neutrals and classic pieces he can wear with several different outfits! We like to dress him in an edgy and trendy style and I don’t really like dressing him in much color other than neutrals, and some greens and blue. And I LOVE matching him so I’m excited to share a few of our favorite outfits.

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HATS
We get hats from Amazon, Binky Bros, Etsy, and H&M! Here are a few of our favorites linked below!

ONESIES
I’m linking our favorite onesies below. He has a couple white ones, but I wanted something “different” than the basic white onesies so we got some black ones and ended up tie dying white oneses instead! Linking our favorite black onesies (good quality) and the tie dye kit we used too!

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Pants
We have a few packs of these h&m pants that Nathan mixes with so many cute shirts!

Outfits
Here are all of the cute baby boy outfits!!

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mommyandmeoutfit.png