How beautiful to see this simply adorable little girl be given a chance to achieve goals that in the past through ignorance they were often hidden away and never given the chance to develop their full potential. ❤❤❤❤ Good on you Daddy and Mummy and siblings for giving time and nmost of all love to a special little gift from Above😇😇
I must say your daughter is adorable/beautiful! my cousin had downs and passed in his late 60's. our family always laughed with him, not at him. we loved him so very much and yes he was very special.
Please keep telling us about her progress we are following you we are concerned and we are happy and may God bless her you and your whole lovely family🙏🏽😘😇
I love this. My daughter is 2 years old with down syndrome and there literally identical it seems like. And also seems like we were very blessed with healthy daughters. Thank you for sharing this. Great video! God bless you and your family
little Naomi is very adorable and yeah I agree she is really smart!!! love that she knows how to open her toy and how to get down to step safely! God bless you sweet girl!!!
Hi there! I just subscribed to your channel! I have a little girl named Zoe who is 2, with Down Syndrome, and she absolutely mimics your sweet daughter! They are so much alike. I know the video I watched was from a year ago, but I'm excited to follow your journey! You're obviously doing a fantastic job and your daughter is just so brite and happy!
I love watching your channel! I have a two year old grand daughter, Reece, with DS and when I watch your videos, it makes me realize that she’s right on track. My husband and I watch her while her momma works, so we do quite a bit of her developmental therapy. We get a list every month from her physical and speech therapist that we work on during the time we have her. I found your channel when I decided to start introducing her to the potty. Not so much to start the actual potty training, but to get her used to it and hopefully make a connection with what it’s all about. I went to you tube to search for potty training for children with DS and fell in love with your channel. Thank you for helping us to understand the progress and milestones that we can expect or at least get an idea of how you do things and the results you have.
Hi new supporter here friend #546! she is a lovely baby! love to hear all the improvements with her! she is a happy girl! and wow she is helping you fold the clothes that's amazing!!! big thumbs up from us liked #33!
My daughter with SETD5 had a similar progression but later. She was doing the things you showed around age 3.5. She was still non-verbal at that time though. I love that you can use sign language. That didn’t work for Sophie because of severe fine motor delays.
I love that we have so much in common. It so challenging at times and we all need to know we’re not alone. Thank you so much for all of your shares. ❤️ God bless Sophie too.
So nice to see Erick. Leylani, you are an incredible woman. Shoresh David is blessed to have you and your family involved with the mishpocha. Shalom Shalom.
Since you did a 3 year and 2 year, could you do a video about what Naomi was doing at 1 year. My son is 1 year and I feel like he won't be doing this stuff by 2 years old. He is not crawling yet, but I'm hoping soon. Your daughter is so beautiful, smart and strong.
I have to look through my videos, therapy reports and my memory. It's been so long, it feels. She never really crawled, she was a butt scooter. The Physical Therapist hated it! So the butt scoot went straight to the walk. It does take a while and everything takes a while. Do you have an Occupational or Physical Therapist. They are wonderful resources and set my mind to ease a ton of times.
@@LivingWithEve Yes, he does have a Physical Therapist that we see once a week, but since the virus, it's been online which is not as helpful. He can stand with leaning on his table for a few minutes so I am thinking of trying the treadmill with him for walking.
Ooh that sounds really interesting. I know we hate the teletherapy thing. It’s not the same thing and the internet keeps going out on us. Plus, it’s hard work! Good luck!
I love to hear about her progression!! Her smile and how proud of herself she was for flipping her lion over, turning it on, then resuming playing is amazing! She is a happy girl and I’m happy to see her moving around more! You’re doing amazing Leilani keep up the great work!
I just found your channel, and can’t wait to get to know y’all. My name is Regan and I have a cerebral palsy, my channel is all about my weekly adventures with positivity sprinkled in. I’m also a teachers aide for my local day program for adults with mental challenges. I hope to hear from you.
Cool! Nice to meet you! After a year of playing around I decide to really focus on on my daughter’s journey. Sound like we’re in the niche! I will for sure check you out!!!
Hi ! I have a 3 years old boy with Down syndrome , he can’t talk still, can’t comunícate much, I good to see Eve her progress, that mean I have to work more with my baby, question how often she got therapy, probably that’s my problem too, he don’t have much therapy.
She still doesn’t completely communicate much. Maybe 50 clear words and a few phrases. But she’s trying and she understands everything. With speech we were able to get a communication device (tablet). We do speech two times a week, and possible 3 very soon.
How many months is she? My daughter Sandy is 20 months, going into her 2nd birthday soon. She has recently started walking. Saying little words. Very exciting.
Lol, Eve is actually her middle name. There is a story behind it. I wanted her name to be Eve, Dad want Eva. We settled on Naomi Eve. Eve means life. So when naming my channel I though of that, because it’s not just about Naomi, it’s about life. Also the idea of Adam and Eve, in the garden, the Fall. We’re dealing with imperfect people, plus we’re imperfect. And we’re all just relying on God, learning from each other and trying our best, as parents to be successful and raise our children in this imperfect world.
Asslam o alikum I,m from Pakistan my daughter has also down syndrome,she is 1year,and 8 months she is no walking yet no speeking I,m worries about her ,your videos are very helpful for me about her but I want to know that who medicine can use for speeking and walking herplz infrom me.....u understanding what I say ......
Hi Irfan, We actually don't have her on any medication. Be patient, it will come when she is ready. Keep working with her, doing exercises, modeling for her, and if you can get her pictures to help her communicate, that would be helpful. Hope this helps.
Calaykuma slaaam brother also my daughter has down syndrom and she can,t walk still she is one year and 7 months how about you doughter is she walk yet
Some walk early and some not until about 3yrs. My friend’s daughter did not walk until after 3yrs and she was a good Irish dancer. She was also very independent and I used to see her out walking by herself.
@@Hamdi-di5muIt is not advisable to compare as all children are different. My daughter (now 40 yrs) sat up at 7 months, walked at 1.5yrs, fully trained 2.5 yrs. She had no health problems. Taught her to read at 3.5yrs, By 5 she could read about 5 children’s books, the first two readers of Primary School. Best reader in mainstream class for 2 years and then class caught up and passed her out. She could do simple addition and subtraction for a while but lost it later. She enjoyed books like Catherine Cookson and Lives of Saints in her 20s, and was very independent. Got job in Investment Insurance Co. doing tracks and trackers. Travelled to and from work on bus into City. Comprehension good and speech articulate. Unfortunately was only child and siblings would have been good. After death of father and change to independent living at 40yrs anxiety set in. Still struggling with that. Also an important part is maintaining friendships of people with DS. All children with DS develop at different stages but meet the same goals. The love and loyalty these children give is immeasurable. To get their needs met is the problem after school.
How beautiful to see this simply adorable little girl be given a chance to achieve goals that in the past through ignorance they were often hidden away and never given the chance to develop their full potential. ❤❤❤❤ Good on you Daddy and Mummy and siblings for giving time and nmost of all love to a special little gift from Above😇😇
I must say your daughter is adorable/beautiful! my cousin had downs and passed in his late 60's. our family always laughed with him, not at him. we loved him so very much and yes he was very special.
I just want to ask of how did you know if the babyor new born baby have a down syndrome
@cassyandcandy4499 well there is a test they run, it’s bloodwork and there will be markers.
Your daughter is so cute and loving. I like how she spontaneously will give you a hug. It's great that you work with her to maximize her potential.
Please keep telling us about her progress we are following you we are concerned and we are happy and may God bless her you and your whole lovely family🙏🏽😘😇
Check out the never videos. She has actually come a long way,
I love this. My daughter is 2 years old with down syndrome and there literally identical it seems like. And also seems like we were very blessed with healthy daughters. Thank you for sharing this. Great video! God bless you and your family
She's such a busy little thing! Super cute and yes, super smart! Personality+ ! Look out, world! 🥰
My daughter, who also has Down Syndrome, will be two in August. I appreciate you sharing Naomi's milestones when she was two!
little Naomi is very adorable and yeah I agree she is really smart!!! love that she knows how to open her toy and how to get down to step safely! God bless you sweet girl!!!
I have a daughter with down syndrome, she is 13 months old. It is confronting for me to watch this video but it sure does makes me feel hopefull.
Feel hopefully. They will be who God made them to be and they will surprise you!
Kindly tell me is she now walking or not my niece is 1.5 years old but she is not walking.
Hai dear...i never miss to see your videos...
I love how honest you are and it helps me know that the way I feel is normal too because I relate to you often. Thank you
Ahh thank you. ❤️
Hi there! I just subscribed to your channel! I have a little girl named Zoe who is 2, with Down Syndrome, and she absolutely mimics your sweet daughter! They are so much alike. I know the video I watched was from a year ago, but I'm excited to follow your journey! You're obviously doing a fantastic job and your daughter is just so brite and happy!
Cool! Thanks!
All babies with DS are a gift from God. They are real angels to bring you pure joy & true love. You are lucky & blessed to have a child with DS.
She’s so cute and fresh just getting around all over the place like a big girl she’s adorable and a blessing to you all👼🏼😘🙏🏽
She can give me a hug any day
I love watching your channel! I have a two year old grand daughter, Reece, with DS and when I watch your videos, it makes me realize that she’s right on track. My husband and I watch her while her momma works, so we do quite a bit of her developmental therapy. We get a list every month from her physical and speech therapist that we work on during the time we have her. I found your channel when I decided to start introducing her to the potty. Not so much to start the actual potty training, but to get her used to it and hopefully make a connection with what it’s all about. I went to you tube to search for potty training for children with DS and fell in love with your channel. Thank you for helping us to understand the progress and milestones that we can expect or at least get an idea of how you do things and the results you have.
Ahh thank you! ❤️it’s not me alone, I have my wonderful therapist to help me too. Without them I have no idea what I would do.
You are a really good mama and you are doing a super good job with your children.
She is so precious!
Hi new supporter here friend #546! she is a lovely baby! love to hear all the improvements with her! she is a happy girl! and wow she is helping you fold the clothes that's amazing!!! big thumbs up from us liked #33!
Yes we love our little girl. She is teaching us so much about life! I hope you will continue to enjoy our journey and learning with us.
Fantastic update 😊💕💕
My daughter with SETD5 had a similar progression but later. She was doing the things you showed around age 3.5. She was still non-verbal at that time though. I love that you can use sign language. That didn’t work for Sophie because of severe fine motor delays.
I love that we have so much in common. It so challenging at times and we all need to know we’re not alone. Thank you so much for all of your shares. ❤️ God bless Sophie too.
You are an amazing mom, and your daughter is so beautiful. Thank you for sharing.
Thank you so much!
This was amazing! Her progress is incredible! Cutest girl ever 💖
Here is a new friend to your channel. Good job Keep going
So nice to see Erick.
Leylani, you are an incredible woman.
Shoresh David is blessed to have you and your family involved with the mishpocha.
Shalom Shalom.
Ahh! Thank you! We already miss you guys!
watching you again sweet Eve! 🎃🍁🍂😍💖❤😘
Love watching Naomi and seeing all the changes and progress.
Esta Hermosa su hija que dios Los bendiga.....felicidades....🙏👍❤
She is so cute and sweet!!! 🥰 I loved this video, thank you for sharing.
Thanks!
Since you did a 3 year and 2 year, could you do a video about what Naomi was doing at 1 year. My son is 1 year and I feel like he won't be doing this stuff by 2 years old. He is not crawling yet, but I'm hoping soon. Your daughter is so beautiful, smart and strong.
I have to look through my videos, therapy reports and my memory. It's been so long, it feels. She never really crawled, she was a butt scooter. The Physical Therapist hated it! So the butt scoot went straight to the walk. It does take a while and everything takes a while. Do you have an Occupational or Physical Therapist. They are wonderful resources and set my mind to ease a ton of times.
@@LivingWithEve Yes, he does have a Physical Therapist that we see once a week, but since the virus, it's been online which is not as helpful. He can stand with leaning on his table for a few minutes so I am thinking of trying the treadmill with him for walking.
Ooh that sounds really interesting. I know we hate the teletherapy thing. It’s not the same thing and the internet keeps going out on us. Plus, it’s hard work! Good luck!
Love seeing her progress.
She is just too cute! I love hearing updates about how well she is doing! Just subscribed for future videos and updates :)
Naomi is growing so quickly! And hitting those milestones like a champ!
Now I am hinge watching to catch up! Yes She s smart! I teach child development and special needs classes ...Go Naomi!
Thanks❤️
Great video! She is doing so well ! Keep up the great work!! 💕
I love these updates
Love the video and seeing Naomi's progress! New friend to your channel! 💗
Children with special needs are a blessing from God!
I love to hear about her progression!! Her smile and how proud of herself she was for flipping her lion over, turning it on, then resuming playing is amazing! She is a happy girl and I’m happy to see her moving around more! You’re doing amazing Leilani keep up the great work!
Thank you so much!❤️
AWWWWWWWWWW your Daughter is soo cute and pretty shes very beutifual
Thank you !
@@LivingWithEve your welcome
She is beautiful
Omg she is adorable and very smart
I catching up on your videos. So cute
Yeah! I see that. Thank you so much! I am glad she brings you joy. You are always welcome here.
I just found your channel, and can’t wait to get to know y’all. My name is Regan and I have a cerebral palsy, my channel is all about my weekly adventures with positivity sprinkled in. I’m also a teachers aide for my local day program for adults with mental challenges. I hope to hear from you.
Cool! Nice to meet you! After a year of playing around I decide to really focus on on my daughter’s journey. Sound like we’re in the niche! I will for sure check you out!!!
@@LivingWithEve Thank you so much! I truly hope you enjoy
Hi ! I have a 3 years old boy with Down syndrome , he can’t talk still, can’t comunícate much, I good to see Eve her progress, that mean I have to work more with my baby, question how often she got therapy, probably that’s my problem too, he don’t have much therapy.
She still doesn’t completely communicate much. Maybe 50 clear words and a few phrases. But she’s trying and she understands everything. With speech we were able to get a communication device (tablet). We do speech two times a week, and possible 3 very soon.
Kindly share how many days physical and speech therapy in a week
1 PT, 1 swim Physical therapy , 3 OT and 2 speech a week. All an hour long.
And for 7 months how many times therapy in a week
Plz tell me as now adays i m trying my best so that she sits independently. She is 7 months but can’t sit
How many months is she? My daughter Sandy is 20 months, going into her 2nd birthday soon. She has recently started walking. Saying little words. Very exciting.
In this video, Naomi was 30 months. Does Sandy have DS or another disability?
Still learning....a
Will you do a growth and development of a 4 year and 5 year old
I probably should. Lol
She’s the cutest! Who is Eve?
Lol, Eve is actually her middle name. There is a story behind it.
I wanted her name to be Eve, Dad want Eva. We settled on Naomi Eve. Eve means life. So when naming my channel I though of that, because it’s not just about Naomi, it’s about life. Also the idea of Adam and Eve, in the garden, the Fall. We’re dealing with imperfect people, plus we’re imperfect. And we’re all just relying on God, learning from each other and trying our best, as parents to be successful and raise our children in this imperfect world.
@@LivingWithEve I was trying to work that. Out 🐤🐣🐥💛
Hi MOM YOUR LITTLE GIRL IS VERY BUSY AND GREAT THING LOVE TO ALL 🌿🐤🌴🌿🐣🌿🌴🐥🌿
Thank you.❤
Asslam o alikum I,m from Pakistan my daughter has also down syndrome,she is 1year,and 8 months she is no walking yet no speeking I,m worries about her ,your videos are very helpful for me about her but I want to know that who medicine can use for speeking and walking herplz infrom me.....u understanding what I say ......
Hi Irfan,
We actually don't have her on any medication. Be patient, it will come when she is ready. Keep working with her, doing exercises, modeling for her, and if you can get her pictures to help her communicate, that would be helpful. Hope this helps.
Calaykuma slaaam brother also my daughter has down syndrom and she can,t walk still she is one year and 7 months how about you doughter is she walk yet
Some walk early and some not until about 3yrs. My friend’s daughter did not walk until after 3yrs and she was a good Irish dancer. She was also very independent and I used to see her out walking by herself.
Hello
Your daughter is two year
Is she walking
@@Hamdi-di5muIt is not advisable to compare as all children are different. My daughter (now 40 yrs) sat up at 7 months, walked at 1.5yrs, fully trained 2.5 yrs. She had no health problems. Taught her to read at 3.5yrs, By 5 she could read about 5 children’s books, the first two readers of Primary School. Best reader in mainstream class for 2 years and then class caught up and passed her out. She could do simple addition and subtraction for a while but lost it later. She enjoyed books like Catherine Cookson and Lives of Saints in her 20s, and was very independent. Got job in Investment Insurance Co. doing tracks and trackers. Travelled to and from work on bus into City. Comprehension good and speech articulate. Unfortunately was only child and siblings would have been good. After death of father and change to independent living at 40yrs anxiety set in. Still struggling with that. Also an important part is maintaining friendships of people with DS. All children with DS develop at different stages but meet the same goals. The love and loyalty these children give is immeasurable. To get their needs met is the problem after school.