Parents get a feeling of hope and strength by connecting with other parents who also have children with CHD through our meetings and social events. Members also have access to a private facebook chat page just for parents of children born with CHD.
Carefully trained volunteers make hospital visits, phone calls and emails to parents who sign up for our parent matching program. We understand what you are going through and are here to help.
MLH Chapters provide educational resources online, as printed material, through educational workshops, at local and national events and webinars. We also share current CHD related research and news.
Several times a year, members are invited to fun stress relieving social events such as a day at the park, holiday party or something else fun the members choose.
We work to educate people in the community and across the nation about CHD related topics such as pulse-ox testing on newborns, CPR, the need for organ donors, and research.
We connect parents with resources that are available to families who have a child born with CHD. Click here to view a list of resources and links that are available to CHD children and their families in our area.
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Contact us at: firstname.lastname@example.org