
I think a lot of people assume we searched out a child with special needs. There are a lot of amazing families who do just that. Their hearts are aching to help those kids that others toss aside. That wasn’t our story though. I never imagined being a mother to a child with Down Syndrome.






I was looking at the websites of the adoption centers and In 2012 I found Marina, a girl with DS and made a decision to take her into our family. She was only 3.6 years old, was only 84 cm (33 inch) and almost couldn’t walk. Marina has easily adapted to her new home and family and started to go to the developmental preschool. Although due to the health problems she couldn’t attend preschool every day I have realized how much she loves other children and being a part of the group so I started to think about another baby.
One of my friends told me about a girl with DS that has been directly influenced by the new law of “Dima Yakovlev”. This law has prohibited foreigners to adopt children in Russia and one American family who came to meet Yana, didn’t manage to adopt because of this law. In December 2013 I took Yana into our home. She is very sweet and funny girl, although she had huge problems with tvision, because of this, she almost couldn’t walk. We had to do an operation and purchase special glasses. Yana started to feel much better, started to develop faster, walk and even run. Marina and Yana became very good friends and Marina started to teach Yana how to play and help her around. After awhile they became real sisters.
One of the orphanages for the children without disabilities was located next to our home and once when passing there I saw a boy with DS seating alone in the snow, other children were playing and not giving him any attention. I was very surprised, as usually children with DS stay in other institutions. On a few occasions during this winter, when going out, we had been going around this orphanage and saw this boy always seated alone. In the spring we caught his attention and he smiled at us. For the next few next days we were coming closer and calling him to come to the fence and talk to us, so after awhile he started to recognize us. We began to think about adoption, but the decision to adopt was not coming easy until we heard this boy’s story. He was living with his family until he was 4 years old, but in November 2014 his family had another “healthy” child and decided to give Vladik away, that is how he came to the orphanage. In September 2014 Vladik came to our home. He turned out to be very independent and serious boy who could do many things by himself and was trying very hard. I think for a long time he was very scared we would give him back so we changed so we would never walk close to this orphanage where he was located before.
need for so many anymore. Out local adoption centre was also closing and we were asked if we would want to take the last child – a girl with DS. We though that a house with 4 children has a place for the fifth one and she was the same age as Sima. This is how Milana became a part of our family in December 2016, which is less than a year now.



But then, as the months went by I began to learn that
Yes it is in practical matters – double diaper changes etc. But they do therapy appointments and specialist appointments at the same time. They entertain and play with one another. As far as my older 2 children (age 12 and 9) – they have grown so much from having Jude and Max as siblings. They are more aware of differences in others and strive to make everyone feel included. They share with friends and others about Down Syndrome and disability.
Whittney married her high school sweetheart and together they have 4 children. After the birth of their 3rd son and his Down Syndrome diagnosis, the entire family became passionate about raising awareness to reduce the stigma of disability. This past year the Moody’s adopted their son Max from China who is also rocking an extra 21st chromosome. The Moody’s live in Georgia and have started a 5k race on World Down Syndrome Day to raise support for families adopting children with Down Syndrome. You can follow Max & Jude on Facebook at 



he has Down syndrome?” My answer has always been the same. Why not? Down syndrome is not scary. Down syndrome is beautiful. My message to the world is that there is hope in all things. People, including people with Down syndrome, all want to be loved, accepted and included. Having an open mind and embracing heart led me to motherhood and has resulted in so many blessings. The extra chromosome in Wyatt’s body has made it possible for me to experience extra love, extra happiness, extra patience and a plethora of knowledge I would never have had without him. Wyatt came to us through domestic infant option. A lot of people say he was lucky to have been adopted. The truth is he is not the lucky one, we are.
Bio: Nichole and her family live in rural north Texas. She left her career in behavior analysis to open a licensed in home child care business when Wyatt was born. Today she is a stay at home mother of 3 who enjoys gardening, yoga, crocheting and refinishing furniture. Nichole is a strong advocate for open adoption and Down syndrome. Follow along on Instagram