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Grand Opening Celebration of our new website!
█► All-day open chat room — Experts from Toronto's Hospital for Sick Kids and HEA leaders will be available to answer your questions
█► Membership sign up
█►Check out our Message Board
█►Find others like you: Sign up for the New HEA Connections searchable directory
█►More information can be found here.
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Help support HEA by using this link to search and shop!
Go here for instructions and for links to Amazon, Orbitz, Hotwire, and
eBay Giving Works.
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Welcome to Our Internet Community
The Hypospadias and Epispadias Association (HEA) is a 501(c)(3) non-profit organization founded for the education & support of people born with hypospadias or epispadias and their families and loved ones.
Although HEA is based in the USA, we invite participation from all people in all countries who have an interest in these congenital anomalies.
We offer resources and support so that people with HS/ES and their families can make informed decisions about surgery, self-esteem, self-acceptance, relationships, and sexuality.
Our message board, chat rooms, shared stories, and conferences ensure that no one needs to feel alone.
Because feelings of guilt and shame are self-destructive and are not based in fact, we provide opportunities to develop pride in ourselves and compassion for others by volunteering to serve our community through becoming members of the board or committees, reaching out to new members, advocating for better care and better choices, and educating the public.
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Listen to our Public Service Announcement.