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One of the significant limitations in global estimates related to spastic children is that they often only account for those currently residing in homes. This narrow focus overlooks the unique challenges and needs of spastic children. We must broaden our perspective to truly understand and address the specific circumstances faced by this exceptional group.
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Mothers are often the primary caregivers and know what their families need most to succeed. Our programs are designed in true partnership with the mothers, encouraging them to participate in defining benefits and services for their children.