On May 27, 1999 we had a baby girl who we named Janine Bobbi O'Brien. She only lived 37 short minutes. She was born with a rare birth defect called Potters Syndrome. I belong to a On-Line support group for people who have had this tragic defect effect their lives and in this group is a wonderful lady (one among many),Michele who did a Memorial web site for my Daughter before I knew how to make them myself. I feel I have bothered her enough over the last year and a half by adding Awards that Janine's site has won, or adding graphics I have found and liked, even adding special things on holidays. So, now that I now know how to build a site myself I will add all of these things here! I would LOVE for you to go visit our Daughter's Memorial page and read about her story. |