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Angelina (@aestheticartist_angelina), Instagram profile photo
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Angelina

Digital creator
@aestheticartist_angelina
Wife, Mom of 4 šŸ©µšŸ’›, Cosmetologist, CF-L2 Sharing motherhood, beauty & Hank’s Down Syndrome journey Faith•Fitness•5 Min Makeup•Curly Hair Matthew 5:16 ✨
  • Travel
  • Following 1.4K
  • Followers 84.5K
  • Engagement 476.08%
  • Avg comments 13.2K

About Angelina

Angelina (@aestheticartist_angelina) is a Digital creator creator on Instagram, also filed under Travel. The account has 84,500 followers and 211 published posts. Recent posts average 469,266 likes and 13,180 comments, an engagement rate of 476.08%.

With 84.5K followers, Angelina is a micro creator by the common 10,000 to 100,000 definition. Set against 1,384 accounts followed, the audience works out to about 61 followers per account Angelina follows. Angelina uses an Instagram professional account. Flinque files Angelina under Digital creator, with Travel as a secondary category.

The Instagram bio for Angelina runs to 23 words across 4 lines. Emoji sit alongside the words. The latest activity Flinque has on record for Angelina dates from April 2026.

Story Highlights

Unlocking shows the title and cover image of every story highlight this creator keeps pinned to the profile.

211 Posts

Of the 10 most recent posts shown for Angelina, 9 are videos and 1 is a carousel. That mix leans toward videos. 211 published posts give Angelina a moderate archive on Instagram. Against the audience, that is roughly 400 followers for each post published. Angelina also keeps 9 story highlights on the profile. All 10 carry captions, averaging 188 words each. The captions are written mainly in English. Words that recur across them include been, hank, downsyndrome, things and know. The captions tag #downsyndrome, #theluckyfew, #specialneedsmom, #downsyndromemom and #specialneedsparenting.

Hank, your first birthday has come and passed🄺
I love you more than I ever could have imagined possible. I am endlessly grateful that God chose me to be your mom. You have already made such an impact...you've made our family better, our hearts softer, and our faith deeper.

I promise to keep standing up for you, advocating for you, and helping the world see your incredible worth. I also promise to take care of myself so I can be the healthiest, strongest mom I can be for you, for every milestone, every challenge, every victory, and every adventure God has planned for your life.

Love,
Your mama

We spent the day together as family at the. I had a feeling he would love all of the visual stimulation, and it was perfect. He opened a few presents at home, and celebrated with a vanilla Greek yogurt birthday treat...I had bigger plans for his dessert, but you know, life šŸ˜….

This passed year has also been one of the hardest years of my life. Hank’s diagnosis changed me. I’m not the same person I was before, and I’m still figuring things out. It exposed strengths I had, along with weaknesses I didn’t know existed. Through all of it, I believe God has been intentional. He has been faithful in ways I couldn’t have imagined, even on the days that felt so difficult.

Thank you to everyone who wished him a happy birthday. We are so very thankful.

#downsyndrome #firstbirthday #downsyndromemom #theluckyfew #specialneedsmom
Before Hank, I probably wouldn’t have noticed the wheelchair accessible pathways, the communication boards, the sensory-friendly play features, or all the thoughtful details that make an accessible playground welcoming for children of all abilities. Even the fence, for possible eloping.
I didn’t even capture everything this playground had to offer, but I left so impressed.

Sometimes you don’t know what you don’t know until your perspective changes.

I almost feel guilty for not being aware of these things before. But honestly, many of us don’t realize how important accessibility is until someone we love needs it. I’m grateful for the people who have been advocating for inclusive play long before families like ours ever needed it.

Because of them, Hank and so many other children get to experience what every child deserves: playing, exploring, and belonging alongside everyone else.

My hope is that we continue to see more inclusive playgrounds in communities everywhere, so that children of ALL abilities can play together 🄹

#inclusion #accessibilitymatters #downsyndrome #inclusiveplay #specialneedsparenting
In an e-bike and iPad era, we want our kids to know that movement matters. That showing up even when you don’t feel like it matters. That doing hard things builds confidence, that strength is beautiful and resilience is learned. CrossFit and physcial fitness has really impacted our family.

The kids are watching how we do things, how we handle things, what we consume...

We want them to understand that caring for their bodies isn’t about chasing perfection, it’s about building strength for life. It’s about longevity, health, and creating habits that will serve them for decades, both inside and outside the gym.

We want them to see the community of people who cheer eachother on, check up on one another and support eachother along the way.

Hank's been a 'crossfitter' since before he was born and has been at the gym for nearly every workout since. As coaches, we’re grateful for the understanding of movement, development, and mind/muscle connection.
We can’t wait to see what his version of CrossFit looks like with Down Syndrome.

This isn’t about saying CrossFit is the only way to be healthy, there are many. However, the lessons we learn in the gym...consistency, discipline, resilience, and doing hard things carry into every part of life.

We strive for a life where we steward the bodies God has given us, have the strength and endurance to serve others well, embrace challenges instead of avoiding them, and teach our children to do the same.

For our family, that’s been the CrossFit effect

#crossfit #familyfitness #faithfamilyfitness #specialneedsparenting #fitfamily
Gave Hank his first haircut the other day!!
Watch for the cute after pictures!
My plan was to do it in the salon after meeting/class on Monday, but he seemed a bit off so we decided to do it at home (if you’ve been watching my stories, you know he ended up coming down with a pretty bad sickness).
It worked out well! Dad got to hold him, and his silly sisters did everything they could to keep him entertained. He was having a party and didn't have too many sensory issues! šŸ™ŒšŸ¼
He did really well and looks so grown up, what do you think?!

(I know Rich needs a haircut too 😩I literally did everyone's hair here this weekend except his.. we are a little exhausted but I'm doin' my best hunnay)

#firsthaircut #hairstylistmom #specialneedsmom #downsyndromelove #hairstylistlife
We’ve been asked a lot about Hank’s vibration plate therapy that we do at home, so I decided to share a little glimpse into one of our sessions with a little help from our boxer, ChipšŸ¶šŸ¤

Vibration plate therapy can provide vestibular and sensory input, encourage muscle activation, improve body awareness, and create opportunities to work on skills like reaching, balance, and coordination.

Chip decided he wanted in on the attention, and it was perfect! With Hank reaching for him, he was naturally working outside his base of support, exploring different textures, and getting extra sensory input by petting him.

One thing I’ve learned is that some of the best therapy happens through real-life moments. Sometimes the things that motivate don't feel like work, they just feel like fun and play.

I personally think that petting a dog is therapy in itself šŸ˜

The vibration plate we use is

#dogtherapy #downsyndrome #doglover #specialneedsparenting #occupationaltherapy
Watching a very public conversation about a prenatal Down syndrome diagnosis unfold online brought me right back to 14 weeks pregnant, sitting in an ultrasound room after being told our baby’s heart wasn’t complete and that he likely had Down syndrome. I remember the fear, the uncertainty, and the questions about the future.

What I needed most during that season wasn’t more fear. I needed hope.

I needed to see families who were actually living this life. Families who were honest about the hard, but also willing to share the joy. Families who showed me that a diagnosis is not the whole story.

That’s why I share Hank. Not because our experience is everyone’s experience, and not because there aren’t challenges. But because I know there may be another scared parent searching for answers the same way I once was.

If that’s you, please don’t let fear be the only voice you hear. Seek out families who are living this life. Listen to different experiences. Find hope alongside the hard.

Most of all, know that your child’s worth is not determined by a diagnosis. Their value is not found in their chromosomes, abilities, or independence. They are worthy because they are human, and they are worthy because they are loved.

The families who shared their stories gave me hope when I needed it most. My prayer is that by sharing ours, we can do the same for someone else.

ā€œLet your light shine before others, that they may see your good deeds and glorify your Father in heaven.ā€ Matthew 5:16

#downsyndrome #downsyndromemom #trisomy21 #downsyndromelove #t21
I have struggled finding grace in my words after watching the viral video of a family sharing their decision to terminate their pregnancy at 21 weeks after receiving a Down syndrome diagnosis.

My heart feels broken. It’s heavy.
Not because I don’t understand fear. Not because I don’t understand uncertainty. Every parent experiences those emotions. My heart breaks because so many families are still being given a diagnosis filled with worst-case scenarios, outdated information, and fear instead of hope, support, and the stories of real people living beautiful lives. I have received countless messages and emails from women who are pregnant and struggling with a decision, I have stake in this game, because I was in their situation too.

I’m here to tell you that Down syndrome may mean a different life than expected, but different does not mean less valuable. Different does not mean less worthy of love, belonging, joy, purpose, or dignity. That video absolutely does not portray that.

I’ve found myself praying a lot these past 24 hours because my first reaction has been anger. Anger for the families who never get to hear the good stories. Anger that termination is often presented as an option before families are connected with the Down syndrome community. Anger that so many people will watch that video and walk away with a misunderstanding of what life with Down syndrome actually looks like.

My heart aches for those who choose not to have their children like Hank..I look at his smile, his determination, the joy he has brought to our family, and the ways he has changed us for the better. I can’t imagine life without him.

Every life has value. Every life has challenges. Every life deserves the chance to be lived.

My prayer is that when families receive a diagnosis, they are given truth, support, resources, and hope alongside the hard conversations. Because a diagnosis should never be the end of the story.

#downsyndrome #downsyndromeawareness #morealikethandifferent #theluckyfew #trisomy21
We had the best time BUT.. this is more important than it seems!

Down syndrome can come with sensory sensitivities, so we’re starting early with things like this. Letting him feel the water, the cape, the comb… all in an environment that is familiar and with mom 🄰

We had so much fun making this and Hank LOVED his hair being combed, he was nodding off šŸ˜….

#firstsalonvisit #downsyndrome #morethanhair #behindthechair #specialneedsmom
We don’t even know what to say… this has been unreal! šŸ¤

I shared the video because I loved it so much and thought to share it on my feed vs stories… watching what it has done has been an amazing surprise!

Your messages, your kindness, the love you’ve shown our boy… it’s meant everything. We are so grateful!

We’re so excited to be here and I can’t wait to share more of our life and journey with you

#downsyndrome #specialneedsmom #theluckyfew #blessed #momlife
Hank’s First words!! What looks small to the world feels monumental to us… how proud we are!

Behind this moment are daily therapies, challenges, tears, prayers… and a whole lot of faith. Down Syndrome/Trisomy 21 comes with neuro differences and hypotonia, making things much more challenging. None of this I knew before Hank but having him has taught me so much more awareness and created softness in my heart.
This season has been hard and a bit isolating at times BUT it’s so much more bright than the internet or doctors lead us to believe.
Learning to surrender, trust God’s plan, let go of some things and to find myself again are things I’m actively working on.

God doesn’t waste a single step and he’s building something new, I’m learning to rest in that and I’m SO grateful to have Hank as our proof He is working and blessing us in unique ways

#downsyndrome #theluckyfew #inclusionmatters #downsyndromelove #downsyndromemom

Angelina's engagement

Angelina's engagement rate on Instagram is 476.08%, over 6%, more than 6 likes and comments per 100 followers. A typical post draws likes and comments in numbers close to the size of the audience itself. An average post collects 469,266 likes and 13,180 comments, close to 36 likes for each comment.

Engagement rate

476.08%

Avg likes
469.3K
Avg comments
13.2K
Interactions : followers
1 : 1

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Frequently asked questions

These answers about Angelina are generated from the Instagram profile data Flinque holds for the account.

Who is Angelina?

Angelina (@aestheticartist_angelina) is a Digital creator creator on Instagram, also filed under Travel. Angelina uses an Instagram professional account. The Instagram bio for Angelina runs to 23 words across 4 lines.

How many followers does Angelina have?

Angelina has 84,500 followers on Instagram (84.5K). Set against 1,384 accounts followed, the audience works out to about 61 followers per account Angelina follows. 211 published posts give Angelina a moderate archive on Instagram.

What is Angelina's engagement rate?

Angelina's engagement rate on Instagram is 476.08%, over 6%, more than 6 likes and comments per 100 followers. A typical post draws likes and comments in numbers close to the size of the audience itself. An average post collects 469,266 likes and 13,180 comments, close to 36 likes for each comment.

What does Angelina post about on Instagram?

Flinque files Angelina under Digital creator, with Travel as a secondary category. Of the 10 most recent posts shown for Angelina, 9 are videos and 1 is a carousel. The 10 recent Instagram captions Flinque holds for Angelina repeatedly use the words been, hank, downsyndrome, things and know. Angelina's captions carry hashtags such as #downsyndrome, #theluckyfew and #specialneedsmom. Angelina writes those captions mainly in English. Angelina keeps 9 story highlights, which open with a free Flinque account.

How do I contact Angelina for a collaboration?

Angelina's contact details are not published on Flinque's public profile. The Instagram bio links to 2 external sites, and a free Flinque account opens those links. Brands with a free Flinque account can shortlist Angelina and use Flinque's outreach tools wherever a contact route is on file.

Angelina's own Instagram profile is the one outbound link Flinque publishes for the account, and the 2 bio links open after signing up.

Public profile data sourced from Instagram. Flinque is not affiliated with Angelina.

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