changingthefaceofbeauty

97,317 Photos and Videos

1 hour ago

Nikki continues to share her story (2/7) makatonwithlucinda At my 20 week scan, my world fell apart. The sonographer detected a heart defect and referred me for more detailed scans. There are literally no words on this earth like ‘I think I can see something wrong with your baby’s heart’. They are the hardest words I have ever had to hear. We hadn’t wanted to know the sex of our baby, but once they said they could see a heart defect, I felt like I needed to know ‘who’ we were rooting for. Every part of me wanted it to be my heart, not hers – I still do. The sonographer wrote our baby’s sex on a piece of paper and stapled it shut so we could decide later, back at home whether to look or not. Back at home, we asked Zack to open it for us, and we learnt that we were expecting a baby girl 💗. I will cherish that ripped (thanks, zack, I know you were only 4 but carefully would have been fine.) piece of paper forever. PositiveAboutDS ChallengingPerceptions SmashingStereotypes CelebratingDownSyndrome CelebratingDS UpSyndrome NothingDownAboutIt TheLuckyFew MoreAlikeThanDifferent DontBeSorry DSAwareness DownSyndrome NewMummmy changingthefaceofbeauty pregnancy congenitalheartdefect

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2 hours ago

Today Marnie is 14 months. Her personality is something else. Her understanding is second to none. Her purity and innocence shines through every single day. She eats everything I give her, including olives 😂. She chats away all day and is a fantastic mimic. She is my heart and I am her voice❤ changingperceptions nothingdownaboutmarnie beautifulbabygirl 14monthsold downsyndrome trisomy21love changingthefaceofbeauty upsyndrome lifeisbetterwithyou downsyndromerocks theluckyfew

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3 hours ago

Norah has raised ₹2,55,316 INR in 10 days with kettoindia to help mann_org vivek_m23 and I are just her voice till she finds her own. Her positivity and love has radiated to 2,63,000 viewers who have seen our story and even if half of them have changed their outlook towards Down Syndrome and have seen the blessing then Norah has truly shattered one thick glass ceiling. Our hope is to change the false image that has been portrayed for decades about Down Syndrome by age old textbooks and doctors and show what holds true Our hope is to SAVE Down Syndrome and not try to eradicate a human race that’s different from us.Our hope is build the ability in people to see beauty and power in diversity and inclusion Our hope is to create awareness on Down Syndrome, mental health and work towards building an inclusive environment for everyone who is born different We have a month left to raise our goal amount of ₹5,00,000 INR for mann_org via kettoindia. Help us in whichever way you can🙏🏾 theluckyfew fundraisers norahmittal meetthedetermined downsyndrome warriorprincess proudmama daughtergoals happinessisachoice mentalhealthsupport confidentlybeautiful advocatelikeamother nothingdownaboutit savedownsyndrome lifeofadventure diversityandinclusion candidchildhood motherhoodintheraw fundraising proudofyou changingthefaceofbeauty iamworthy loveislove thisisus almostfamous littleandbrave strongereveryday downrightperfect positivelifestyle breakingthemould

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3 hours ago

The possibilities are endless 👏🏼👏🏼👏🏼 pushing our treatments for the best possible results and healthy, happy, glowing skin 💫 ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ skinrevision cutera lasergenisis scarrevision acne cameraready redcarpetready changingthegame beauty happyskin glowingskin skintherapist healthyskkn thinkingtherapist facial skintreatment agemanagement pigmentation steppingitup skinnerd skineducation changingthefaceofbeauty skinfluencer mood skinclinic auckland

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4 hours ago

Look who’s a big girl now🥰🥰 You guys know that, for almost 3-4 months she’s using swing in side position and today we achieve front seating in swing. It’s really tough for her to balance and weight shift while swinging, but look at this strong girl. She did it so beautifully💖 Veda’s spine is much more stronger than her abdominal muscles that’s why she use to fall back when it comes to balancing on any platform. I am so proud of you munchkin. lovemakesafamily extrachromieveda theluckyfew letthembelittle raisinggirls homiewithanextrachromie blessedwiththebest nothingdownaboutit trisomy21 adoptionislove morealikethandifferent proudmama downsyndrome downsyndromeawareness adoptionrocks advocatelikeamother motherhoodunplugged changingthefaceofbeauty igmotherhood downrightperfect upsyndrome lifeisbetterwithyou childhoodunplugged magicofchildhood wouldntchangeathing candidchildhood daughtergoals documentingmotherhood clickinmoms indianmomblogger

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5 hours ago

Well hello there sweet baby girl. I’m loving these cloudy days. We took a break from mommas endless editing today to take these photos mid day. For anyone who lives here in the desert, you all know that isn’t an easy thing to do. We normally have never ending sun. This softness in the lighting is a welcome change for this lady. Now if we could manage it without the wind that would be amazing! • • • • • • • • • • ourblessedlife2019_365 let_there_be_delight morealikethandifferent the_sugarjar shared_joy candidchildhood jj_it_kids my_magical_moments pocket_sweetness thesincereststoryteller follow_this_light changingthefaceofbeauty heaventhroughmylens ourjourneywithds pixel_kids boldemotionalcolorful wildandbravelittles hazelgrace runwildmychild theluckyfew vintagetrucks celbrate_childhood enchantedchildhood livingwithalittleextra uniteinmotherhood ourcandidlife tutudumonde babiesintutus tutuskirt tutubaby

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6 hours ago

We have some new friends here! Welcome to our journeymy name is Hollyce and I'm stepmama to Tyler (14) and Emily (12) and mommy to our son Hudson (2) who rocks an extra chromosome (Down syndrome - Trisomy 21). I'm married to my super hot husband David and we live in the north burbs of Chicago. Here, I want to share our joy as a speciallyblended family and our laughter and adventures along the way. ⠀⠀ ⠀⠀ It's time to play 4 truths and a lie! Ready??⠀⠀ ⠀⠀ 1. I have shaved my eyebrows off as a kid. ⠀⠀ 2. I won a watermelon eating contest. ⠀⠀ 3. I visited Liverpool by myself. ⠀⠀ 4. My oldest son picked out Hudson's name. ⠀⠀ 5. I bought a dog with my high school graduation money.⠀⠀ ⠀⠀ Which one is the lie? Comment below! Let's go holdingmoonbeams

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6 hours ago

If you’ve ever questioned the value of social media, know this Today, just a few hours ago, the Louisiana Senate voted 34-0 to make it illegal to discriminate against someone with a disability in the organ transplant process LARGELY because of connections made on social media. EviesLaw is officially headed to the Governor’s Office to be signed into law and as crazy as it sounds, in so many ways, we have FB and IG to thank An IG post by an awesome DS mom ( sweet.on.sutton) inspired by a post by another awesome DS mom ( downrightwild) made us here in Louisiana question, How on God’s green Earth are with disabilities being denied organ transplants simply because they have a disability??? But then we saw more posts and we knew we had to do something That’s when we found the National DS Society’s page ( ndssorg) and the incredible resources they provide in conjunction with the Autistic Self Advocacy Network. With their help, we were able to draft an anti-discrimination bill for LA. And we knew exactly who to reach out to We’d been Facebook stalking this incredible, super mom and advocate Katie Corkern ( kscorkern) for YEARS and even though we had never met, we KNEW she was just the rockstar to take us to the next level! And sure enough, right away she hooked us up with the sweetest, most passionate legislator, Rep. Malinda White ( malinda_brumfield_white) . With their help - bolstered by the advocacy of the coolest group of DS parents on social media upsidedownsla - and all of YOUR support following our journey and blasting legislators with emails at every step we did it. 🙌🏼 Evie’s Law is a real thing. It’s happening Guys, we may literally save lives and we have all of you and all the amazing connections made from these silly apps to thank. So thank you. Thank you. THANK YOU _ _ EvieLove DownSyndrome TheLuckyFew NothingDownAboutIt T21 CTFOB Trisomy21 DownSyndromeAwareness SaveDownSyndrome ChangingTheFaceOfBeauty DownSyndromeRocks DSDN MoreAlikeThanDifferent UpSyndrome DownSyndromeLove LIFEisbetterwithyou savedownsyndrome spencer_is_spicy downwithhayden julierharrison

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7 hours ago

Is it possible to have too many pictures of your own baby? Asking for a friend 🤷‍♀️🤣 In the past couple weeks I've had a couple moms with a new Down syndrome diagnosis either prenatally or at birth reach out to me. That is why I share so many photos of this incredible girl. I want new moms on this journey to see love, joy, and beauty. I want them to look into these gorgeous eyes and know that it is going to be ok. In fact, it's going to be amazing If you are a new mama to this amazing Down syndrome or special needs tribe, please reach out. You are not alone 💓 incredibleivy theluckyfew lifeisbetterwithyou downsyndrome downsyndromelove nothingdownaboutit upsyndrome downrightperfect downsyndromerocks trisomy21 morealikethandifferent lovedoesntcountchromosomes designergenes shoutthierworth somuchworth worthy chromosomallyenhanced shiftthenarrative extrachromosomeextracute changingthefaceofbeauty upgradedto47 babiesofinstagram instababy hollandtourguide tulipswindmillsandrembrandts savedownsyndrome motherhoodunplugged joyfulmama fearfullyandwonderfullymade prenataldiagnosis

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7 hours ago

We had so much fun going to the Kick Off Party for the Ducky Derby Chicago! What an AMAZING group of people! We are so excited to get to know more of the specialolympicsillinois community! 💙💛💙💛💙💛

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7 hours ago

Terminando un fin de semana XL exquisito🙌🏻 mañana de vuelta a la rutina y a las clases🤓 pero con ánimo que esta semana es cortita💕 Buenas noches y que tengan un excelente miércoles❤️

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7 hours ago

T H U G L I F E

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8 hours ago

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8 hours ago

“If I’m being honest, Nurse’s have just about the most important role when it comes to quality care. ••••••••••••••••••••••••••••••••••••••••••• Being sick for 6 years I have had both good and bad Nurse’s, I think because the nurse isn’t a doctor many people overlook the importance of having a nurse who has compassion, who will help advocate for you when they see something is wrong and someone who you can trust with your life You might be shocked to find out that on multiple occasions a nurse has played a huge part in saving my life, I have so many names of people I remember that have cared for me in the very start of my health battle Yesterday we finally got to flush and draw labs from my port, while my current home nurse is out of town I was delighted to see the amazing women who had been my home nurse 6 years ago when I was around 14 years old and I was super new to the idea of Feeding-Tubes This is all to say to those who are a nurse or know one please remember how important you really are, many times when I’ve been upset about my situation you are the one who helped keep a smile on my face, allowed me to laugh even when it hurts to laugh Thank you so much, for being in my life and teaching me how to make the most of my life even with all my hardships. 💕 *if you are friends with/are a nurse please comment or tag down below, I want you to know how important you are*

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8 hours ago

That smile is what happens when you take your kiddo to AbilitiesExpo! Betting this picture was taken right after she conquered the adaptive climbing wall. 💪 Heads up, Chicago! We're coming to you next. See you June 21-23 at the Renaissance Schaumburg Convention Center. It's all free so get registered. Link in the bio. Repost amazingabigailgrace • • • • • Just some more pictures from out first ever Abilities Expo We will absolutely be back next year! 🙌🏻💛✨ abilities_expo • • • • abilitiesexpo changingthefaceofbeauty numotion permobil inspiredbydrive disABILITY theloyalbrand accessibility inclusion

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9 hours ago

Day 21 Williams syndrome awareness month ☝️STRENGTH 🧬 Sunny got both ears pierced today and she didn’t even flinch. 🤭 Fate whispers to the warrior "You cannot withstand the storm" and the warrior whispers back "I am the storm" 🧬 Strength=Sunny Jewel. My daughter We long for carefree days, yet sometimes, God takes our hand and leads us straight into the darkest of times. Not to harm us, ever. But to bring greater strength, character, trust, beauty, and perseverance to the deepest part of our souls. sunnyjeweldobbs williamssyndrome theluckyfew unique beautiful williamssyndromeawareness ws love strength photooftheday amazing picoftheday cute us fun changingthefaceofbeauty onlyupfromhere ourstory

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9 hours ago

Morning chats in bed

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9 hours ago

Go check out itssamuelsstory post on inclusion, it’s 👌 Start with kindness 🖤

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11 hours ago

Today’s blog post is about my major struggle with PTSD, and anxiety after Cam’s surgery. It’s just a surface scratcher, but opening up about these things is important for me to be able to grow and heal. I want anyone struggling to know I FEEL you. I hear you. I’m with you. Link in bio if you’re interested 🖤 ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀ ⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀⠀ chromiecommunity theluckyfew morealikethandifferent chdwarrior savedownsyndrome savedownsyndromeambassador littlestwarrior homiewithanextrachromie downsyndrome dsdn trisomy21 tripplethreat jbcpresets advocatelikeamother advocate awareness nothingdownaboutit thisisdownsyndrome CTFOB downrightperfect 21reasonswhy shouttheirworth changingthefaceofbeauty designergenes livingwithalittleextra lifewithds hobbyblogger momblogger blogspot

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12 hours ago

Had the pleasure of doing this challenge for allure magazine along side ryburk agussuga_mua went with my go to on this! 🗣GLITTER💙(Nipsey Blue)💙✨ anywho swipe left and enjoy!

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13 hours ago

We went and visited our friend Miss Mary at my old job today. The first person Scarlett ever jumped out of my arms to go see. Oh how we miss seeing her every day. The gal I talked everything baby with when we were supposed to be working 🤫 Excitingly telling her to give me her hand every time I felt Scarlett kick. Such sweet days we had, but it’s even more sweet taking Scar to visit. She just loves watching her grow. Thank you for loving on my girl. We love Miss Mary! 💛

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14 hours ago

Just making a little music today. Were trying to do things that don’t involve a ton of moving because it is burning up in our house. Our ac went out Saturday for who knows what reason and it looks like its going to be another week before we can even get someone to come out and look at it. Looks like we are going to have a ton of outdoor water play and lake time threenager upsyndrome myahnicoleflores theluckyfew downsyndrome downsyndromelove downrightperfect changingthefaceofbeauty candidchildhood nap momarazzi momswithcamera perfection

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14 hours ago

A picnic at Wheeler Farm with my Jaynerbug! We ate our lunch, fed the ducks, took a ride on the cow train and saw all the animals, including a brand new baby sheep!🐑 Jayne did not want to leave the sheep but could not understand how the baby was eating 😂 It was so funny The best part though was just talking with her. When it’s just the two of us, she has so much to say and I love it! We were walking along and she told me that her favorite colors are pink, purple and yellow and then asked me what my favorite colors are.👏 😳 This may seem like a simple thing but inside I was doing a little happy dance and told her how nice that was of her to ask. We have been working on her communication skills—looking people in the eye, asking questions about them, etc and she is getting it! I am SO so proud of her!👏 . One of the best parts of having a with Down Syndrome is that you learn to appreciate the little things and realize that every milestone—big and small—is worth celebrating! This is a BIG thing in my book and a victory worth celebrating! 🥳 jaynerbug picnic wheelerfarm downsyndrome nothingdownaboutit upsyndrome theluckyfew itsthelittlethingsthatcount t21 shemakesmehappy changingthefaceofbeauty

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14 hours ago

“Today you are you, that is truer than true. There is no one alive who is Youer than You” - Dr Seuss ⁣ ⁣ Look at this passionate participation award winner! I can’t believe the school year is over. It couldn’t have ended in a better way. I was so nervous sending my buddy off way back in August. We did it though! We went w our guts even when things didn’t seem right. ⁣ ⁣ Cameron has progressed and shown so much growth. He has made friends, some that will be forever. He has become more confident and independent. We are so grateful for his teachers and his therapists. They are part of our big Team Butler and I hope they realize how important they are. I am so proud of Cameron! And you know what? I’m proud of myself and the rest of the 6 pack. We really do all of this together! 👊🏼

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15 hours ago

Everybody wants happiness. Nobody wants pain, but you can’t have a rainbow without a little rain. When I found out Lucie would be born with Down syndrome I thought the storms had come and they were here to stay. How wrong I was. Is every day sunshine ☀️ and rainbows 🌈? Absolutely Not. But are most days sunshine and rainbows? Heck yes! This little ray of sunshine is worth every drop of rain. ☔️ Rainbow boutique bow from cinderellabowtique Use code Lucie15 for a discount! Link in bio

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15 hours ago

Another couple of great sessions at smallstepscharity, where we get to work with the best physios and conductive educators 🙌🏻We’ve been learning about different countries can you guess the two we’ve just learnt about from the pics? 😝 happy love conductiveeducation physio charity blessed dontbesorry downsyndrome trisomy21 dsdn wouldntchangeathing nothingdownaboutit downsyndromeawareness changingthefaceofbeauty lifeisbetterwithyou extrachromosomeextracute positiveaboutdownsyndrome downrightperfect theluckyfew babyboy sebastian teamzebedee downsyndromebaby babiesofinstagram ourboy ourworld learning fun dressingup toomuch

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16 hours ago

🌱❤️ L i l s i s & b i g s i s ❤️🌿 Å ha en storesøster med et ekstra kromosom betyr at du (nesten) alltid har en venn som er klar for lek og moro 🥰👭❤️❤️ downsyndromerocks

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16 hours ago

These girls are always up and ready to go to school. They love school! They have such an amazing team who support them and are always looking at ways for them to succeed. It’s such a blessing to know my girls are loved and safe when they are in school. Makes this mommy so happy

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17 hours ago

Nino Genua (20 yrs old) is: - A student at Bath College 2nd Year on LILS Course - Assistant Community Coach with Bristol Bears - Parliamentary Award Winner 2016 for his work with the Bristol Bears - Captain of Bristol Sharks SO Competitive Swim Squad - Goalkeeper for Keunsham Mencap Football Club - Model signed to Zebedee Management - Health, Fitness and Sports Fanatic - 100% Loved - 100% Amazing nino_genua iamable theluckyfew downrightperfect thisisme * * We would love to celebrate your or your little one’s ability! Send us a message or email summer ablefinder.com.au to share your story ❤️✨

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1 day ago

Ramps, wheelchair accessible play equipment, suitable supports and equipment for blind and deaf people, sensory play areas, accessible toilets - they should all be standard in new playgrounds. thefutureisaccessible

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4 days ago

Thank you all so much for praying for Amellia and her bloodwork yesterday. The good news is that her white blood cell count is higher than it has been in a year. The bad news is it’s still too low, so our doctor will consult with other doctors around the world who treat patients with DS with similar numbers and then decide where we go from here. We love you all! Thank you for your support for our family. ❤️ Also, can we talk about this picture of Amellia taken by the lovely lilyglass? 😍🥰 amelliabelle theluckyfew downsyndrome kidsmodel changingthefaceofbeauty