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Disney's in the Desert

Taming The Tangles: Curls Edition

July 30, 2022

Managing my curly hair has taken up a good chunk of my life – for the longest time it seemed like the biggest inconvenience and chore. Now I have (not 1, but 2!) curly kids of my own, I’m determined to not let them have that experience too. For Cole, his hair is super short so keeping up with his isn’t really that much work, but for Colly, I know it’s only going to get to be more and more as she gets older. I really want her to embrace her curls and feel confident in taking care of them.

Tangles go hand in hand with curls, and Colly’s have been tough tangly since she was about 8 months old. We started detangling her hair every few days back then, and now it’s essential for her to have a daily detangle routine to combat them from building one giant knot.

I start by using this Suave kids detangler spray and making sure every strand is nice and wet. It’s almost impossible to brush curly hair dry, not to mention really painful. I start from the ends (you may have always started at the root, but this way actually reduces breakage!) and work my way up with our Tangle Teezer brush. This brush has been our go to even with Honey – no more tears are shed once we started using it! I will also section off pieces (using starting with the underneath area as it’s usually the least knotted) and work on them in these individual chunks so it’s a little less for both of us to get through.

Once everything is smooth and tangle free, I will use my fave curl cream (I use this on my own curls!) and work it into all strands of her hair. After that, I give it a little scrunch but most of the curls are already forming natually at this time. I don’t diffuse it unless she’s going to bed or it needs to be dried for some reason, so it just air dries on it’s own. Using the cream helps the frizz stay away and also helps the shape stay in tact which will create less tangles later on too.

This is our routine when she hasn’t taken a shower and just wakes up in the morning with frizzy/wild hair. On days she showers and we wash her hair, I’ll use a leave in condition that I spray in right after the shower and I know her hair is clean.

That’s it! It’s really not complicated, but it can be a little time consuming. Right now she sits pretty well for me and lets me get through it with just holding or chewing on a toy, but I’m sure as she gets older she might get more antsy.

To make it easy, all of these products I’ve chatted about plus our fave spray bottles are all linked in one photo on my LTK, here!

My whole goal is for her to do this herself and do it confidently one day. I have faith we’ll get there and it won’t be something she dreads doing with support and knowledge. Have a question for me about curly hair or our routine? Leave a comment and I’ll get back to you! ➿

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Filed in: Mom Hacks, Motherhood, Style, Uncategorized • by angmdisney •

Prime Day 2022

July 13, 2022

This post contains affiliate links.

Prime Day 2022 is here but will be gone in a blink! You might be here because you saw my IG reel on 4 Prime Day sale items I use in my home daily — you can find a link to those here.

Now to the good stuff you don’t want to miss!!! Here’s a round up of “the best of” home, organizing, baby, and more!

TECH/SMART HOME

all products linked here

BEAUTY

all products liked here

CLEANING/HOUSEHOLD

all products linked here

ORGANIZING

all products linked here

FOR THE KITCHEN

all products linked here

BABY

all products linked here

I’m going to try and round up a list of things we purchased as a family too!! I’ll update this post and also post to my IG stories, so stay tuned!!

Filed in: Gift Guides, Style • by angmdisney •

Try It Tuesday: Neutral Summer Nails

July 13, 2022

Maybe you’re like me and you like a little nail flare, but aren’t into the loud colors. I’m rounding up a few ideas that are still more on the neutral side but have some fun to them.

Above are two that I recently got done – both times I stuck with white on all of them except my middle and ring finger. I opted to get a design on those two each time – once with some neutral tan flowers and another time with a mauve color and gold stars!

Here are some others I’m really liking right now (I do not own the rights to these images):

Hope this gives you a little bit of inspo to try something new next time you go!

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Filed in: Style, Try It Tuesdays, Uncategorized • by angmdisney •

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Welcome In!

Welcome In!

Hey and welcome to my little corner of the internet! I’m Ang Disney (yep, DISNEY!): a believer, wife, mom of 4, and an entrepreneur. Some of my favorite things in life are brunch, HGTV, white chocolate, long walks through Target, and 90's music - if that's you too… let's be friends!! :)

In this space I hope to inspire you. I genuinely enjoy sharing my fave mom hacks that I use in my every day, home decor, DIY, easy recipes, and attainable fashion for yourself + kids on a budget. Grab a cup of your fave drink and stay a while!

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Easter Bunny Cookies

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@disneysinthedesert

disneysinthedesert

What an incredible opportunity to go (live!!!!) on What an incredible opportunity to go (live!!!!) on @arizonasfamily yesterday! 🎥✨

We were able to share some of Colly’s story along with our fundraiser with @picazzositalian that’s supporting Colly’s pediatric therapy clinic, @bloomkidz_az 💚 In April, $1 of every dessert sold at all 6 stores is being donated here. We are so grateful to be able to give back to such an incredible organization that’s been monumental in Colly’s progress and unwavering in support to our family the last 2.5 years. 

Thank you to @cerretanews for taking the time to chat with us and to @elainavpr for always advocating for our family so generously and in such a special way!! 🤍 

#rettsyndrome #rettsyndromeawareness
If you’re still looking for an easy treat to bri If you’re still looking for an easy treat to bring to dinner tomorrow, try this!! The cutest 💛🐰💖🐇🩵

Wishing you the happiest Easter, knowing He did it for me and you ✝️🕊️
Colly works so hard 🙏🏻 At age 4 and by this Colly works so hard 🙏🏻
At age 4 and by this stage of this savage disease, eating by mouth (chewing and swallowing) plus gaining (and even maintaining) weight is extremely difficult. Additionally, most girls cannot use their hands for anything with purpose at this time as well 💔

Please join us in praying that Colly will continue to have hand strength + the ability to use them, that she can tolerate eating by mouth, that she stays seizure AND med free, and that she continues to grow and gain weight. Thank you friends!!! 🫶🏻 Forever grateful for this community who encourages and cares about us.
Obsessed with our new zebra blinds from @lustrowin Obsessed with our new zebra blinds from @lustrowinhome! This was a dream collab for me and it really elevated the windows in our family room, kitchen, and living room ✨ I love how these blinds easily allow for light to pour in during the day while still providing privacy at night. 

They have so many beautiful, modern, and stylish options of window treatments for any home! Use code “DISNEY” to save sitewide at Lustrowin - link in bio!

#ad 
#lustrowin
#homefinds
#homedecor
#windowtreatments
#modern organic
Just received this video from Colly’s PT 2 days Just received this video from Colly’s PT 2 days ago and have already watched it on repeat about 100x 🥹 The squeal of joy is something we don’t take for granted when much of her short life has been consumed with crying, anxiety, pain, and frustration. She genuinely seems so happy and joyful 🥹😭

Also can we also just take a second to acknowledge how much motor planning and brain power it takes to repetitively jump up and down like this?! THAT’S OUR GIRL!!!!! 💪🏻🧠✨

We believe in the power of prayer and humbly ask everyone reading this to please keep praying for her. I will always desperately want more for her, and I am believing in His perfect timing that it will happen. 

#rettsyndrome #rettsyndromeawareness
This is long, but worth a watch!! Colly has been a This is long, but worth a watch!! Colly has been absolutely CRUSHING Rett Syndrome this past month. Literally saying, “Rett who?!?!” 🤯🤗👊🏻 November we witnessed so many miracles happening for Colly. It wasn’t without some bumps, but we have SO much to be thankful for. 

By age 3.5 (she’s so close to 4 now!), most girls with this disease no longer have purposeful use of their hands. Every day she’s able to still use them in any capacity is a miracle, but the fact that she’s doing even more beyond that…is almost unbelievable. 🥹 She is not doing what medical text says she should at this stage of the disease. 

We wouldn’t be where we are today without her massive team at @bloomkidz_az where she receives 5 different therapies M-F full time, and the last couple of months adding in weekly appointments with @dr.connerbor. The impact all of these treatments are having on her is huge, and at this point, essential to her development and continued progress. 

It’s so exciting to be able to post happy + encouraging updates about Colly after so much darkness, sadness, and confusion. Please pray we are able to keep her on this stable track of good health, pray for her team to have the wisdom they need to continue to help her, and pray for even more strength for her body and brain! 💪🏻🧠✨ We can’t thank you enough for cheering our family on as our sweet little girl continues the fight of her life.
The most healing Halloween + diagnosis day yet 🕊️

It’s not a secret that I still carry a heavy grief over Colly’s life. Ultimately, the prognosis of Rett is very dark but seeing her progress since she was diagnosed is nothing short of inspiring. We have so much hope for her future and although there is still much uncertainty, she has an amazing team of therapists, doctors, and supporters. She has treatment plans and goals. She has a family who loves her and will never stop pushing for more for her. 

I was telling a friend recently that this day will always be a reminder of the ending of the dreams/life I saw for her, but how can I wallow in sadness when there is so much joy? Colly IS that joy ✨🪽

God has revealed a lot to me these last two years and has pulled me out of a really scary pit. He’s wiped my tears, softened my heart, and given me strength to be a better mom, caregiver, and person for Colly + my other children. Instead of dread, my excitement for life is returning and I can’t wait to see where we’ll be next Halloween 🤍
Really they are so much fun 🦇💀🎃👻 I lov Really they are so much fun 🦇💀🎃👻 I love making my iced coffee at home in them!

Some have sold out but there are a few styles left! Linked on my blog as well as my LTK shop (in bio!) www.disneysinthedesert.com
Finally sharing the small update I did earlier thi Finally sharing the small update I did earlier this year in Colly Girl’s room! I used a wall stencil from Amazon + the colors are Snowbound and Warming Peach by @sherwinwilliams for the paint 🤩 

I’m personally obsessed with how it came out!! More details on my blog tonight (link in bio)! ☀️🧡🧸☁️
We are beside ourselves and elated 😭😭 If you We are beside ourselves and elated 😭😭 If you are new here, Colly had a handful of words before her second “Rett Regression” in 2023 where she lost them all and went completely silent. A few of those words returned this year with the regression ending (praise the Lord) but “Dad” was never one of them. 

She had said “ddddaaaa” in January of this year but not much came after that. Fast forward to the end of this month, and now when we ask her to say it on command - she seemingly is doing just that 🤯🤯🤯🤯🤯🤯🤯 Absolutely blown away. I swear she’s even saying, “eeeee” at the end a few times as if to say “daddy”! 

We were told Colly would never verbally communicate amongst so many other heartbreaking (and a slew of other WAY MORE terrifying) things that accompany this disease. Honestly, verbally talking fell off of our wishlist a long time ago because we’ve seen her face many other struggles that make every day life so much more challenging for her. My hope has been renewed lately and I’m adding it back onto my dreams for her. 💫☁️ I know she will likely never verbally speak in sentences, but to have a few words would be incredible and I’m sure would do wonders for her anxiety and frustration levels as well. 

Continued in comments 🥹

#rettsyndrome #rettsyndromeawareness
Switched out the drum coffee table we’ve had for Switched out the drum coffee table we’ve had for a few years for this space saving, fluted one! It’s more sturdy (the drum slid around a lot) and also goes with the room better IMO 😍

It’s currently 20% off and I shared more deets about it on my blog + LTK shop tonight (in bio) ✨

#homedecor #cozyvibes #homestyle #arizonahomes
Summer break ended almost 3 weeks ago for us, but Summer break ended almost 3 weeks ago for us, but the temps will be summer-y for a long time to come 🥵🔥 If it’s really hot where you live and your kids love 🍉, try this treat!

Only 3 ingredients and so simple, but I did list the “how to” on my blog (link in bio!) 🍉🍧💚
So much can change in one year 🥹❤️‍🔥 So much can change in one year 🥹❤️‍🔥

In June 2023, we were 7 months into a devastating diagnosis - which would be Rett Syndrome, a rare neurological disease that is a whole body disorder and affects every single thing the body does for us voluntarily. We were told Colly may never walk, she would face severe motor challenges, have so many limitations of her life, and worst of all, a shortened life span. She was also in the midst of her Rett Regression, which is where children rapidly lose any acquired skills they DO have (basic things - like using their hands and swallowing food). It also causes so many issues with mood, breathing, sleep, and much, much more. The only way to put it is non stop suffering, and absolutely gut wrenching. 

One year later and I think we can say Colly is out of her regression and new skills are emerging. In June of 2023, she was just learning to tolerate more time standing up and attempting assisted steps with a walker and bearing weight on her feet. Her mood has improved so much by gaining this independence of walking where she wants and she seems so much more stable. 

“Believing gets hard, when options are few” has never felt so real in my life. I am pretty sure I was circling the drain and at the bottom of the bottom in June 2023. Life was so hard, DEPRESSING, scary, and uncertain. I refuse to give up on God though, because He doesn’t give up on me. While we know Rett is a savage beast, we are believing Colly will continue to defy the odds and she WILL keep surprising us 🥹💫 If you asked me last year if she’d be walking next June, I’d probably try to sound hopeful but I would tell you it was maybe *hopefully* going to still happen in a year or two. AND LOOK AT HER GO!!

If you are in your circling moment, just hang on. Miracles happen every day, EVEN IF it’s not in the way you or I pray about. I know the author of Colly’s story is STILL writing a beautiful one, so I’m going to trust and hold onto that. 

Ephesians 3:20

#rettsyndrome #curerettsyndrome #rettsyndromeawareness
@beddys Summer Launch is kicking off TODAY! 🥳🎉

Ella & Ryan (shown on my bed, here!) are two new colors joining the line up of best-selling Beddy’s at their lowest price point. Not only are they the most wallet-friendly styles, but you can save even more with my *limited time* INCREASED discount code + free shipping!!! Use code ANGDISNEY for 25% off 6/4-6/11! 🤍 

If your bedding could use a little upgrade, this is the best time to shop! We have been using Beddy’s for almost 8 years and couldn’t love and recommend them more!!!!
Last min teacher baskets/gifts! I put these togeth Last min teacher baskets/gifts! I put these together for the kids’ teachers a couple of weeks ago for Teacher Appreciation Week, but they’d be great as an end of the year treat too! I made one for the girl + guy teachers, because they do have both this year!!! Linked everything on my blog tonight with more deets (in bio)! 🍎💕👩🏻‍🏫📝
Definitely a memory made though 🙃😆⚾️ . Definitely a memory made though 🙃😆⚾️

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#momlife #momof4 #momofboys #momofgirls #motherhood #momlifebelike #momproblems
With today being #rarediseaseday, it felt very rig With today being #rarediseaseday, it felt very right to share this now. In the beginning of January, we had the opportunity to discuss one of the first pediatric gene therapy trials for Rett Syndrome happening NOW in the USA!! It is a very exciting time and we are cautiously optimistic about our daughter, Colly, having the chance to receive this life saving treatment. 

We were also so thankful to chat about our fundraiser with @picazzositalian which donates $1 of every chocolate chip cookie dessert sold to @rsrtig (which is the only foundation solely dedicated to the cure) and how raise awareness about how this devastating disease has impacted our sweet girl and  so many others who are suffering from it. 

We need this cure!! Without it, Colly will continue to struggle for life’s basic necessities - BREATHING, eating, sleeping, walking, talking and using her hands. Rett is a severe neurological disease that affects every aspect of her life, everything our brain tells our bodies to do for us is disrupted for a girl with Rett Syndrome. 

Full video is in the link in my bio if you’d like to watch more! BIG thank you to @elainavpr for facilitating this for us, and to @arizonasfamily for allowing us to share 🤍

#rettsyndrome #rett #rettsyndromeawareness #curerett
Happiness comes from a fresh set these days ❤️ Happiness comes from a fresh set these days ❤️‍🩹 Bookmark it for next year! 🏹💘💌
Loved these light fixtures we’ve had in the loft Loved these light fixtures we’ve had in the loft, especially because they aren’t hard wired. However… I hated the cord - so kind of defeated the purpose. I cut the cords and added these battery powered lights and problem solved! 💡 Also added some different battery operated ones to our olive tree to give it a little shine! ✨ 

Linked both of these on blog and LTK tonight (in profile)!
My kids’ birthdays have ALWAYS been emotional fo My kids’ birthdays have ALWAYS been emotional for me. I cry every year on the day that they turn a year older. That reality hits so much harder with Colly, and the fragility of her life. The “bittersweet” of a new year: what it symbolizes and how time moves on for others, but it really doesn’t for Colly. I’m really trying to still be grateful, even through all of the hard. I just wish things were easier for her. I have to keep trusting that God’s plan is so much bigger and better than mine. 

I love you, my angel, Sweetpea Girl 💗 Happy 3rd Birthday.

#rettsyndrome #curerett #rettsyndromeawareness
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