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!
We are always happy to receive updated medical information for the children we represent. Daniels new information is from July 2023, and we will be getting new photos and video soon. Daniel was born February of 2018 and his diagnoses is Spastic cerebral palsy with localized (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial convulsive seizures. Asthma with a predominant allergic component.
Due to the congenital disease of the child, the development of motor skills does not meet the basic requirements and indicators of age. Daniel can keep his head upright while held by the wheelchair. He has no support in his legs. He turns and spins in bed. He kicks, stretches his arms, and turns from his back onto his stomach. He moves his fingers but has a weak grip. He reaches for hanging objects. He tries to hold a toy in his hand but can only do so for a short time.
A rehabilitator is working on schedule with Daniel on a project from a foundation. Daniel has a personal “Grandma” who takes care of him. Grandma is a special educator who works to develop skills to assist in daily service and acquire useful habits. He is now learning to use a cup. He likes to listen to children’s songs and stories. He laughs loudly when teased. He cannot sit on his own.
Video from June, 2022
Cute little Daniel has been assigned to us for advocacy. He was born February of 2018 and almost didn’t survive. He was very close to death. He was revived and is diagnosed with cerebral palsy, severe degree quadriparesis; symptomatic epilepsy and bronchial asthma. Despite all this his caregivers say his state of health is satisfactory, given his main diagnosis. Keep watching this site as new photos, videos and information is coming soon.
A report from 2019 says Daniel receives physical therapy three times a week and has improved a lot. Previously he could not hold his head up at all but now he can hold it up for a short time. He has started opening his fingers more easily and moving his arms. His right arm moves more easily than his left arm. He is unable to grab and hold toys but the caregiver says from time to time he grabs a toy and holds it for a few seconds then drops it. While he does not have speech, he is able to laugh loudly when happy. Daniel follows with his eyes moving objects and people but he is unable to focus or make eye contact. He reacts with a smile and opens his mouth wide and laughs when someone is talking to him He reacts and turns his eyes and head towards the speaking person. Daniel enjoys being teased. He does not like being put in the stroller with belts to hold him in.
Initially Daniel could only drink milk or finely pureed food through a bottle. Now he eats food mashed with a fork and tiny pieces of bread and most general food. He is fed by an adult with a spoon. He eats well and has a good appetite. He drinks water from a bottle or with a spoon. He has also learned to drink some tea with a spoon. He is unable to drink from a cup.
Daniel is said to be very sociable and smiles a lot. The agency representative who met him in 2019 said the following: “He reacted happily when I was talking to him. It is obvious that he knows his baba and reacts to him talking to him. He would follow me with his eyes and would turn his head towards me when I was moving around. I did not see him reacting to his name but he reacts immediately to people talking to him or giving him toys. He is unable to hold toys or to transfer them from one hand to another. The child is unable to sit; he only lies in bed and moves his head and arms. The baba alleges that he understands what is being said to him but I did not see such reactions. He only reacted to sounds and moving people and toys.” We would love to find a family who is familiar with Daniel’s special needs.
Video from approx.12-2021
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.
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.