Little Traveling Dress | Mesa Arizona Family Photographer

A couple of months ago, I was trying to come up with some fun projects for myself. I saw that there are many people who are doing traveling dress projects—essentially, sisterhood of the traveling pants but dresses and for photographers. Then I thought, how about doing a traveling dress but for little sisters?! I bounced the idea of a Little Traveling Dress Project to a few friends of mine and many of them jumped on board quickly! How exciting!

On August 27th 2018, I ordered a dress and our Little Traveling Dress Project began.

One little dress, two countries, six states/provinces, eight photographers.

We all had the same dress for a week to create. We will not reveal the work we have created until everyone had a chance to finish their journey. This is where magic happens. And the whole project was finished just before Christmas.

For the past few months, we have all been anxiously waiting to see what the other people had created and today is the day! It’s our reveal party today! Please follow along and find out how creativity works magic with each individual in an amazingly different way.

I’m so excited to share my part of the journey and you will be able to link to the other 7 photographers’ work as well!

---

Originally, when I started the project, knowing that I would be the last person to play with the dress, I was planning a BIG EPIC vision in my mind. I was going to have my girl wear the dress. I was going to make her all gorgeous. I was going to take her to all these epic places around the valley in Arizona.

HOWEVER, when time went by, my vision changed.

I had been digging into my soul a little bit about why I am doing all these photos. I realized that ever since I have started my business, I have felt more insecure and more inadequate than ever. I look at other people’s photos and think—I want a house like that with a big window and pure white walls so I can take better photos with better widow lights; I want to go to those epic places because dang those locations are so cool; I want to have darker dinning table so it looks better as a background when I take photos of my kids make cookies…The list goes on and on. I realized that, I ALWAYS have a vision and what I am trying to do is to create something out of my norm to fit into my vision. So instead of trying to make epic lifestyle like our normal way of living a life, I want to find the beauty in our seemingly normal life.

SO, instead of taking road trips in this pretty dress and makeups and flower crowns, we just lived a good normal life, but wearing a pretty dress.

It’s close to Christmas. My family doesn’t really have Christmas traditions as we never grow up celebrating it. But it would be nice to help my kids to get into the holiday feels. So we went to a Christmas Tree Lot. The owners there were super nice and let my kids run through the trees. They even pointed out that they have colored trees in the back.

My kids were beyond excited to just run free there.

I’ll have to say, I’ve never seen a happier face in a tree lot.

Our Church, the Church of Jesus Christ of Latter-day Saints, set up a Giving Machine in downtown Gilbert this year to make it easy for people to give in the holiday seasons. It gives you such a good warm feeling when you know that you can give because you have been given much. For my kids who are still very young, it can be challenging to find service opportunities for them so we took advantage of the giving machine and stopped by after we ran in the tree lot for a good while.

We explained to the kids that we get to give something to people and children who are in need and they get to choose what they want to give. Both of my kids took it pretty seriously and looked at the menu/list of possible items for donation for quite a while. My boy, who loves balls more than anything, decided to donate soccer balls. My girl actually decided to donate some building-block toys and also funds for after school program so other little friends can go to school like her and play with blocks too! They were literally shouting with joy when they see the items they chose was donated through the giving machine.

There is no place better than home.

I mean, seriously. This should be the case. If you are like me before drooling over other people’s home, you got change. Not saying that we should use it as an excuse to never clean dishes or vacuum your carpet just because you love your home no matter what. But seriously, this is our life now and we should love it no matter what.

Dance in the street in front of the house even on a super overcast and cold day. Walking through irrigation rivers at home and pick up flowers and dirt. Who cares if people driving by think that we are crazy. We are home and we are happy.

One of the awesome perks about living in Arizona is that we get super amazing citrus in the winter time.

And, lucky us, we LOVE citrus.

When we found out that a few of our own citrus trees have gotten sick and we are not going to have many good fruits this year of our own, we were really sad. Good news is that we have a great citrus orchard close by and every year they host citrus picking events. Just before all the oranges and grapefruits got picked this year, we went in the orchard to enjoy the view of an approaching harvest.

Of course, when there is food to look at but not allowed to pick any, all her energy goes into a goofy ball and shows up in every single photo I attempt to take.

It is Christmas season after all. With little ones at home, we tend to decorate the house a little later so all the ornaments can stay on the tree for a little bit and all the lights can stay on for a while. It took about 5 days for our tree to become bare on the bottom 2/3 and our lights on the tree to totally go out. But while it lasted, we had fun having a festive house.

When there is a little “devil” tearing everything down at home, you gotta balance it out with a little angel.

---

So yeah, these are what I’ve done with the Little Traveling Dress. These are no where near what I had envisioned at first. They are not epic. They are not that artistic. They are not the ones that stir up the darkest dust in your soul and make you think.

HOWEVER, each one of these photos

MADE ME SMILE.

Yes, for that week, I was almost constantly taking photos for my girl. I was always thinking what fun stuff we could do. I gave my kids so much more attention than before. I was not on social media. I was not comparing myself with other moms. I was not comparing how my kids are with other kids.

While these photos might not mean anything to other people, they mean the world to me. These reminded me of the pure joy of being a child. These reminded me of the pure joy of being a mom. These reminded me of the joy of simply being alive and enjoying life to the fullest.

My girl’s name means Life. She is full of life. Her simple brightness is epic enough to light the world—at least my world.

Like I said, even the eight of us who had the chance to create using the same object, had different perspectives and angles. My journey with this little dress helped me to confirm my why—Life is crazy, but life is good. And I’m loving it.

I surely hope all of you can feel the joy of this little girl and be inspired to find and focus on the simple, small, seemingly insignificant joyful moments in your life AND document them! When life gets hard, which is almost every other minute especially if you have a few little munchkins in your house, look back at those small moments that bring smiles onto your face.

Hope you all had a wonderful 2018 and wish you a happy new year in 2019!

---

To follow along our reveal party with our Instagram Loop starting here: @amydangerfieldphotography

To check some of the other 7 photographers’ work on their blogs starting here:

Sabrina: https://forever22photography.com/2018/12/30/the-little-traveling-dress-project

Tracy: https://www.tracydawnphotography.com/blog/

Susan: https://www.susan-rice-photography.com/blog/2018/12/29/the-little-traveling-dress

Erica: https://woodsywondersphotography.com/uncategorized/a-little-traveling-dress-project/

Life with Spina Bifida| Spina Bifida Awareness Day 2018

It is Spina Bifida Awareness Day today on October 25th. October seems to be the month of awareness, but to me, it is a special month to remember what life is like with Spina Bifida.

I don’t really talk about this with people other than close family or friends so many people probably are not aware that my daughter has a birth defect called Spina Bifida. There is a great article on “What is SB?“ on the Spina Bifida Association Website explaining the ins and outs of Spina Bifida you can check out if you have a few minutes.

I was 24 weeks pregnant and we were living in China. I just remember me being alone in the examine room while my husband was waiting outside in the lobby, hoping to poke the technician a little bit to find out if we are having a boy or a girl (it is actually illegal in China to reveal gender during pregnancy) and then was notified that I should wait in the hall way to get a second scan by another expert because there might be something going on. Ever since that morning, all I know is that we’ve read so many documents, seen so many different doctors and done all the possible tests during a pregnancy.

The Chinese doctor said that it did not look good. Our baby might not be able to ever stand up, or walk, or read, or live a normal life. “You guys are still young and you should try again.” the doctors recommended.”Oh and remember to take folic acid next time.”

They mean well. However, they just don’t have enough experience with cases like this. The good thing was that we have access to doctors from other areas in the world. We went to an Australian doctor in the city where we were and she helped us and referred us to multiple neurosurgeons around the world to get a further diagnosis and an action plan for us. And one of the neurosurgeons actually became my daughter’s actual doctor now, which is really cool to me.

What is Spina Bifida to us? My girl’s official diagnosis is Lipomyelomeningocele, a word I still can’t remember how to spell. It means that her spine was not closed during the initial forming stage and has an opening on her spinal tube. And because of the opening, her spinal cord instead of being dangling in the spinal tube, it was stuck on the inside lump of her back and was pulled out of the spinal tube. She has a bump on her back. Because of the spinal cord being attached to a fat lump and pulled, some nerves are damaged. She had surgery when she was 6 months old. We didn’t know what nerves were damaged exactly and we still don’t know how some of her nerve-functions will be(including being potty trained and being able to walk on super sharp rocks).

I don’t usually talk about her condition mostly because when you look at her, you would not have guessed that she has Spina Bifida. Quoting her grandpa: “ The only thing that’s not really normal with her is that she started speaking way too early.” I as a parent, don’t really want to make it a big deal. I don’t think she is disabled enough for me to go around and say that I’m a special need parent. I don’t think we’ve really suffered as much as some of my friends who have real challenging special needs children. At the same time, I don’t want people to always say, oh I’m so sorry that this happened to her after knowing about it. I don’t want people to ask me “did you take folic acid last time?“ because I surely did. I don’t want people to treat her differently because now they know she is actually sort of different.

However, I think it’s a good time to actually bring it up. Mostly for me. But also for my daughter. And probably for people who might not know about some of the special conditions that come with life.

For me, I just want to say to myself—you are a good mom. You did all you could have done and you made the right decision to bring her to this world. You were not selfish because you were afraid of the pain of abortion and it is always good to respect life.

For my girl, I just want to say to her—you are different, but we are all different, one way or another. Go live your life the way you want and don’t let others dictate your life. And go make friends with people who are different from you.

For other people who might be hearing about this for the first time—please don’t feel sorry for us and don’t put a tag on special need children. See beyond their disabilities and focus on what amazing things they could achieve.

I’ve tried to channel my inner sorrow and the dark little spot associated with this. (Oh, believe me, I’m not saying that it was not hard. ) But every time when I focus on the fact that I went through the craziest pregnancy as a first time mom and there are so many uncertainties ahead of us, I just feel really down. And I simply don’t like it. When I spend too much time worrying if she will ever be totally normal or if I am doing all I can to protect her future siblings from having the same trials in life, I see myself buried in doubt and fear. I simply don’t like it.

While it’s healthy to express feelings, which I’m definitely not very good at and am working on, I think it can also be a good idea to just focus on the good, the bright, the positive.

During that pregnancy, time seemed to be frozen at times and to be flying by at other times. The crazy pregnancy definitely prepared me for any possible pregnancy tests—blood test, MRI, amniotic fluid test—come what may and I will deal with it. It also brought me ever closer to God. It was a good lesson to learn to stop asking why and instead to ask how I can do this thing. It was awesome to be able to get closer to family as well. It definitely helped my little family to hold together because it was seemingly us against world at some point. It was also really heart warming to really see how much my family cared about me even though their way of saying love at first was slightly different from how I wanted.

I’ll have to say that it was really cool when my girl beat all the odds and started crawling before her surgery. And then see her stood up by herself. Then see her running through rock piles. Then see her getting potty trained(mostly). And of course, it is just cool to hear her talk like a champion in both Chinese and English. I try not to be too prideful and brag too much but it is really the best thing to see your baby grow and be strong. It is also a great confirmation to me that I made the right decision back then to keep going.

Having a kid who needs special medical attention is also a very humbling experience for me. It reminds me that we all have weaknesses and how little we know. I have to trust her medical team. It’s also a great opportunity for me to practice my patience. I can remind myself that she might never be able to do certain things as fast even though she could speak faster than I could sometimes. It has also helped me to not taken things for granted and also to not over think. Not saying that I absolutely don’t actively parent all her behaviors, but I sometimes do look at her and say, hey, this might be just a three years old being a three years old, or there might be actually something going on developmentally in her brain and we will figure it out in its due time.

So, if you are friends of mine. Yup, that happened. And we are glad to have our perfect little girl in our lives.

If you are pregnant and are struggling with a diagnosis of a birth defect—you are not alone! There are amazing communities out there. Talk to other people who have gone through similar situations. No matter which country you are in, there is help and hope. And I’m here if you ever need someone to talk to :)

If you are a new mom or a woman who is thinking about getting pregnant but is scared of things going wrong during pregnancy—It’s totally normal. I had this gut feeling before I found out about it actually and I sometimes think if I actually jinxed it. But it’s also ok to just let go and go for it. Things happen and that is just part of life. Embrace the uncertainty and it can be an empowering experience if you let it to be that way.

If you are someone who just learned a new word today. Yay! You are better than I was. I didn’t know until I saw it on my ultrasound paper. Good for you!

There are so much I could say about life with Spina Bifida but I don’t think there is any better way of showing what life is like than living it!

So here is my little girl who has Spina Bifida and also someone who is extremely talented with language, who is absolutely creative, who is definitely full of life. And now, hopefully, you are aware that there is a birth defect called Spina Bifida and it does not define the capacity of someone’s life!

Thank you for reading! <3

A Glamorized Childhood | Payson Arizona Childhood Photography| Mesa Family Photographer

There has been some big controversy in the photography world lately. This whole situation with childhood made me think really hard. 

As adults, we look back to our childhood and all kinds of memories come up-- the sweet ones and the nightmares. It's healthy to face both and to recognize both. Growth comes after pain and acknowledging pain is half of the work to success. Don't deny your past. Don't try and hide your childhood. 

With that being said though, when it's our time to teach our children, it's our responsibility as adults to choose which part of childhood to focus on. 

I always feel that there is enough sadness and negativity in this world so I would prefer to focus on the bright side. Have those bright little joyful moments be my light. To remind me that there is goodness in the world. There is hope. 

As an artist or public figure, we have the blessing to be in front of so many people each day, including so many children. We can create something to speak to people's hearts. However, with great blessing comes great responsibility. We need to choose wisely. What we create. What we focus on. What we glamorize.

"Train up a child in the way he should go: and when he is old, he will not depart from it." Proverbs 22:6

If I ever get to glamorize childhood, I would love to glamorize the simple joy we feel as little children. That magic of being a child. Childhood needs to be celebrated instead of being rushed through. 

My kids don't usually dress up even though they may very well be the cutest kids when they do dress up. I don't want to go through the hassle of cleaning their nice outfits. I don't want them to focus on their appearance too much. I don't need to spend too much money on things that don't really matter. However, this week, I decided to have my girl in this really nice brand new outfit and went on our trip up north to Payson into the woods. Why? Just because. 

Just because I want to show that dancing in the woods is cool. Kicking dirt and jumping off a little tree trunk is fun. Finding a huge pinecone the size of your face is absolutely amazing. These are the things kids should be doing. And this is what we need to celebrate and glamorize. These are appropriate for little children. 

I may not be the most experienced photographer. I may not be someone who can stir the whole industry. However, I do hope that I can make tiny waves in little girls' hearts when they look back at the photos and think to themselves look, that was me. I was beautiful and I had fun as a kid. That, is enough to me. That, is glamorous to me. 

As always, thank you for reading. Enjoy our little girl having fun in the woods for the very first time.