Description
The England Grant of $2500 may be available for qualifying families.
Individualized grant funding for qualifying families may be available through our President’s Grant. Contact us for more details!
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We just received an update on darling Scotty. Please see the questions and answers below as well as his new videos.
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Can he walk?
He can walk by himself holding onto the railing and can stand alone.
2. Can he understand directions?
A little
3. What is his personality?
A little quick temper
4. Please tell us if he still has Nystagmus. If yes do they do anything to help that eye?
He has a little nystagmus. It is better than before.
5. Please take a close-up picture of his eye. Also some video of him playing walking babbling etc.
Height is 86cm and weight is 10kg. He can’t say any words for now. Compared with the same age of Down’s syndrome children, his development is normal.
Videos:
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Scotty looks like he is ready to fly into your arms! Scotty was born in December of 2016 and has Downs Syndrome and Nystagmus of both eyes. His update is from October of 2017 and says the following: Scotty is now ten months old. He is very cute and likes stretching out his tongue, has less slobber, likes the caretaker touching him and talking to him face to face. When the caretaker did the passive exercise and moved his limbs, he can stare at the caretaker, and sometimes he makes sounds of “enenen” to respond. He can change from supine to prone position, prone to supine position with turning over at 360 degrees. He can lean forwards and sit alone for a while with his hands propping. When he is prone on the mat, he can prop with both hands to raise his head, can move his head and neck freely, can prop with one elbow with the other hand picking the toy before him. When he is happy, he can use the belly on the mat, open both arms and raise both feet, “flying” position. When he was supine on the mat, he can use one hand to pull the toy hanging under the toy shelf before his chest to wave it, or use one hand to stir or move the toy on the toy shelf to make it turn or move, also can hold his feet with both hands. He can put off socks when he is naughty. When holding him erectly, you do not need to hold his neck. He can track the moving toy left and right with his head and eyes. When he is sitting against the caretaker or in the children’s chair, he feels comfortable. He can grasp the toy when it is passed before him, he can hold one toy in each hand. When the toy drops, he can take a look. He likes interaction with the caretaker. When the caretaker plays hide and seek and puts the towel on his face, he can remove the towel. The caretaker often lets him lie prone on the bucky ball, so the ball can practice his waist muscle as it turns forwards and backwards. He knows his name. When calling his name face to face, he can gaze at you. When the familiar caretaker calls his name, he can turn back to search for the sound source. He likes his caretaker. When the caretaker stretches out her hand and says “ mom hugs you”, he can reach his hands to the caretaker. The caretaker cuddles him up and says “ touch mom’s face”, he can stretch out hands to touch mom’s face. He rejects the stranger. When the stranger calls his name, he can stare at the stranger. But the stranger hugs him, he cries. When sent to his caretaker’s arms, he stops crying. In the sunny day, the caretaker often takes him to the garden to enjoy the sunshine and breathe the fresh air.
Could you be darling Scotty’s forever family?
For more information, please contact: Kathy@wiaa.org. You will be asked to complete a parent eligibility form before any file information can be released.
Please be aware that children on our waiting list may be under review by multiple families. Additionally, a child’s availability status may change on short notice. Please contact Kathy@wiaa.org for the most up-to-date status of a child.
Disclaimer:
WIA is not responsible for the medical information summarized here. Medical information sent by other countries may be inaccurate or incomplete. Prospective Adoptive Parents reserve the right to have medical information evaluated by a medical professional in the United States.
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