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!
Precious Jayda was born June of 2012. Her special need is listed as epidermolysis bullosa. Jayda’s condition has been treated and the symptoms have improved. Jayda is able to sing and dance following the teachers. She is also able to say some simple sentences. She is able to recognize and say aunt, uncle, sister and other people. She is able to know some common objects. She is able to feed herself. She can play alone and can do some simple housework and can do some simple crafts. She is a relatively shy girl. An update from April of 2019 shows questions and answers as follows:
- New measurements to include – height, weight, head circumference height 106cm, weight 15kg, head size 54cm.
- Is she attending school? Not yet.
- How does she compare to her peers in terms of her mental capabilities? Almost normal.
- How does she compare to her peers in physical capabilities. Her physical capabilities are a little slow.
- What are some things she struggles with? The current difficulty is that his hands and feet have herpes. Sometimes bleeding, and movement is inconvenient.
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.
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