My Nonprofit Reviews

When my son was born with HLHS in 1997, Anna was the first person I talked to who had a similar experiences. She gave me a parent’s perspective on raising a child with HLHS. It was desperately needed. Over the years, Anna helped me numerous times as my son had a stroke and then went through a very difficult heart transplant. I was happy to be able to give back and participate in several podcasts. HUG has helped so many over the years and provides a great service to the CHD community.

My son was born 15 years ago with hypoplastic left heart syndrome and I went searching for help and found the Congential Heart Information Network. I have gotten both practical and emotional support and been able to connect with others with similar situations. This group of parents facilitated by tchin have truly become my friends who understand. They have seen our family thru 3 open heart surgeries and a difficult heart transplant just last year. It made a huge difference to our family to know there were others around the country and the world providing thoughts and prayers for my son as well as "been there, done that" support. Things would have been far tougher without tchin. I recommend them often to other parents in similar situation. As a matter of fact, I did so again today.

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