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fatin.rochon. It’s Down Syndrome Awareness Month!!! This one right here stole our he

It’s Down Syndrome Awareness Month!!! This one right here stole our hearts the day she was born. It wasn’t until she was almost four weeks old that we were told Catherine has DS. And now in a few months she will be TWO! We are thankful every day to God that He entrusted her to me, Josh and David! To the one who will pose for this amazing picture then keep me on my toes the REST OF DAY... I love you!! #downsyndrome #awareness #t21 #beautiful #upsideofdownsyndrome #shesnotadownsbaby #shescatherine #notdefined

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We had a great time meeting families at the Down Syndrome Association of South Texas Buddy Walk today! The @dsastx were FANTASTIC hosts and we had a blast being a part of the day. If you’re a parent of a child with Down syndrome in the South Texas area, we encourage you get to connected with this amazing organization. Also, if you’re a parent of a child with Down syndrome one year old, or older, and live in the United States, we invite you to become a Hope Advocate by visiting the link in our bio.

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Spek ku patah Dah tiba masa, migraine makin menggila, Spek lama dah innalillah . Imran patahkan Imran rawatkan Imran roll roll rollkan minyak EO Claritie kat badan, kepala dan leher ibu kesayangan. . Alhamdulillah pagi ni Ibu boleh senyum nampak gigi Hasil sentuhan kasih sayang anak lelaki Drop of love tagline diberi ❤️ . #narinar #narinarmelaka #dropoflove #aromatherapyrocks #downsyndrome #downrightperfect

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geauxmomma. The Down Syndrome Association of Central Texas (DSACT) was the first o

The Down Syndrome Association of Central Texas (DSACT) was the first organization to help my family even in the months before Bryan was born. He was 18 months old for our first Buddy Walk in 2002, and he’s now an 18-year-old Senior in high school! Bryan’s Buddy Walk team is at 35 percent of its goal. All donations are greatly appreciated and tax deductible too! Thank you for your consideration and you’ll find the link in my bio! 💙💛 #buddywalk #dsact #bryansbowiebuddies #bowiebuddies #downsyndrome #downsyndromeawarenessmonth #t21 #t21club #dsactbuddywalk

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my_extra_ordinary_life. thumbs up!! .... stubborn kid🤦🏽‍♀️ Inflatable fun!! THANK You @kelly

thumbs up!! .... stubborn kid🤦🏽‍♀️ Inflatable fun!! THANK You @kellyannhale Aunt Kelly and girls for hanging out with him!!! #downsyndrome #Downsyndromeawareness #adventureontheslide

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fresno_state_nsslha. Thank you to all of our NSSLHA chapter's hardworking volunteers! Altho

Thank you to all of our NSSLHA chapter's hardworking volunteers! Although we did not get photos of every volunteer, you are all greatly appreciated! Thank you to the Down Syndrome Association of Central California, for allowing us to be a part of this amazing event. #downsyndrome #stepupfordownsyndrome #nsslha #fresnostate #fresnostatebulldogs #makeadifference #slp2b #aud2b

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wird_wirld. Sweetest face. 🥰😍
#downsyndrome #morealikethandifferent

Sweetest face. 🥰😍 #downsyndrome #morealikethandifferent

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balfour_to_balfive. Timmy embraces the chaos and then ups it a notch. 🥳#treasuringtimothy

Timmy embraces the chaos and then ups it a notch. #treasuringtimothy #theluckyfew #downsyndrome #nothingdownaboutit

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downsyndromemagazine. Down syndrome is togetherness ☺️ Ellie is Eli’s biggest fan. She follo

Down syndrome is togetherness ☺️ Ellie is Eli’s biggest fan. She follows him everywhere he goes and mimics his every move. She carries a huge love for family togetherness. Every morning she insists on a big family hug 🤗 #downsyndromeis

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stevefrissell. We are almost ready for our Mabel

#downsyndrome #downsyndromeawarenes

We are almost ready for our Mabel #downsyndrome #downsyndromeawarenessmonth #theluckyfew

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Celebrating with @clubtwentyone Down syndrome awareness and Annabelle’s 3rd birthday plus her 1 year heart anniversary. We are so blessed and happy she’s doing amazingly well and thriving. Going to preschool 25hrs a week and modeling, her dreams are already coming true! We love building a community of friends and feel privileged to be apart of such a great resource for children with Down syndrome! They have helped bring inspiration to our lives. If you are able please consider donating to Club21 on Annabelle’s behalf we set a goal of $500 . https://www.ds-stride.org/club21walk/profiles/team/HopeforAnnabelleMoon . . . . . #lifeisbetterwithyou #extra #bettertogether #differentlyabled #upsyndrome #nothingdownaboutit #morealikethandifferent #everyonebelongs #downsyndrome #downrightperfect #theluckyfew #inclusion #chd #heartwarrior #chromosomallyenhanced #dsdn #joy #love #community #extrachromosome #changingthefaceofbeauty #downsyndromelife #trisomy21 #t21

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thegolbergers. I love standing her up now that she has her SMOs. She’s so tall and sh

I love standing her up now that she has her SMOs. She’s so tall and she looks so grown up. Twice this trip we ran into kiddos with Down Syndrome. It was so fun talking to their parents. Both girls were older than Isla so we got a little sneak peek at what the future could look like for her.

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皆勤賞🏅 表彰〜〜おめでとう㊗️ #downsyndrome #congrats #chupachups #けんたマン #皆勤賞 #ダウン症

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doris_down_up. My baby girl laughing #downsyndrome

My baby girl laughing #downsyndrome

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iam.iro. Brown Bear,
Brown Bear,
What do you see?が、イロちゃんに大好評だったのでPanda Bearバージョ

Brown Bear, Brown Bear, What do you see?が、イロちゃんに大好評だったのでPanda Bearバージョンも購入🐼 * 色がいっぱいなのと、リズムがあるのが面白いのかな〜✨ * Amazon で買うと、Brown Bearと同じ大きめのハードカバーと、ひと回り小さめのボードブックがあって、今回はめくりやすそうなボードブックの方を買ってみた。 * でもハードカバーの方が画面が大きいから子供は喜ぶのかな? そうなると、頑張って画面大きい方めくれよ👶🏻ってなるのかな? * とりあえず試してみよう🙋🏻‍♂️

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enablesnp. At ENABLE Special Needs Planning, LLC, we believe that everyone has th

At ENABLE Special Needs Planning, LLC, we believe that everyone has the ability to be impactful in the lives of others. This ability is what gives each of us a sense of purpose in life.⁠ .⁠ Traditional Special Needs Planning only helps families prepare for what will happen to their child when the parents are no longer around to provide for him or her. While creating a transition plan is absolutely essential, at ENABLE we help families plan comprehensively.⁠ .⁠ The primary purpose of comprehensive Special Needs Planning is to enable individuals with special needs to live purposeful, impactful lives every day, based upon their own unique abilities, dreams, and goals.⁠ .⁠ .⁠ .⁠ #ENABLEsnp #specialneedsplanning #specialneeds #autism #cerebralpalsy #downsyndrome #epilepsy #spinabifida #BeImpactful #autismawareness #adhd #inclusion #autismmom #disability #asd #love #specialneedssiblings #specialneedsparent #specialneedsawareness #specialneedsparenting #specialneedsministry #specialneedsadoption #specialneedsmom #specialneedsparents #specialneedskids #specialneedschildren #specialneedsteacher #specialneedsfamily #specialneedsfamilies #specialneedsdads

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morgy_smits. This little man gets cooler by the day! 😎

This little man gets cooler by the day! 😎

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👋Milo meeting Milo!👋 A study conducted by the U.S. National Institute of Health analyzed surveys from 284 people with Down syndrome. Of those surveyed, nearly 99% of people with Down syndrome indicated that they were happy with their lives, 97% liked who they are, and 96% liked how they look. Nearly 99% people with Down syndrome expressed love for their families, and 97% liked their brothers and sisters. Years ago, before I even met my husband, I thought really hard about what I wanted in life. I peeled back the layers until I uncovered this one paramount truth: all I really wanted in life was that my children (unborn at the time) were happy. Naturally, reading these statistics in the hospital hours after Milo was diagnosed gave me great comfort. #milobbenton #downsyndromeawarenessmonth

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paigesidra. Tristan & Siena...Love these two rascals! Our sweet godson Luke was na

Tristan & Siena...Love these two rascals! Our sweet godson Luke was napping so that cute boy missed all the selfies! 😂🙈 We love play dates with this family. My husband went to college with Luke and Siena’s daddy & now the wifeys are besties and our kids love each other too! Do you have any longtime friends like that?!

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paigesidra. Day 1️⃣6️⃣ of Down Syndrome awareness month! 
I’ve missed some posts b

Day 1️⃣6️⃣ of Down Syndrome awareness month! I’ve missed some posts because life got busy & I’ve been mulling over sharing this for a few days, but I remembered my commitment to transparency and wanting real, positive change, so here we go! There’s been, what feels like, a rise in prenatal diagnosis, or maybe the fact that it’s DS month just highlights it. I’m not sure really. This also means, many mamas are debating whether or not to choose life. I’ve been honored to have had intimate conversations with several of them. I will ALWAYS, always, always, advocate for life here. I will also always let them know the feelings of devastation, hopelessness, and grief are all valid when walking through a diagnosis or possible diagnosis, but the hope we find in the gift of life, has the power to change it all. It’s that simple, and that complicated all at the same time. Choosing life for Tristan has changed our world. We didn’t even realize that was a choice to be made at first. It shattered me when I realized it, when we were going through the ringer with multiple, grim, possible diagnoses. I would choose him, in any world, in any version of reality. I would find him, and choose him. He’s so unbelievably worthy of any extra effort it might require to raise him, and loving him comes so easy. Some of these mamas chose life, some didn’t. My heart hurts for those babes, they would have certainly been something special earth side. Please come alongside me and pray for them all, and their precious mamas. We educate and we advocate so one day, no one has to feel like that’s a choice they need to make. I advocate so choosing life will be a little easier, so they’ll know the joy and the incredible gift that awaits them.

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