Such kind words from another HD family

Attention Hirschsprungs Disease families.  You are not alone.  We were fortunate enough to meet with another family who has a boy with HD.  Our respective wives had become close friends thanks to the internet and Facebook.

We met in the place of all places, Disneyland in Orlando.  Here is a link to Keaton’s Blog: Eat, Breathe, Poop

We are blessed to have met this wonderful family. We (HD families) are not alone.

2 Responses

  1. Anna July 12, 2013 at 9:17 pm | | Reply

    Hello. Jag am from Sweden och have a daughter with total HD. She lives with help of CVK och 100% of nutrition goes through it. So I wonder if there are children wich stomi and CVK on this site. Thanks for your answer.

    1. Brenda Weiss September 29, 2013 at 9:55 pm | | Reply

      This blog is only about my son who has LSHD so I cannot help you w/ the nutrition issues you are facing. There is a wonderful supportive HD group on yahoo and also facebook has at least 5 HD groups. I’m SURE there are people there who can help you with this. good luck

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