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Jennifer and I send our greetings to everyone. Our Taylor would have been 8 years old on June 22nd, had we not lost her to complications associated with Jennifer's pregnancy. Much has changed since then, but much has stayed the same. Eight years since her death, and you can now find numerous references to HELLP Syndrome on the Internet. There have been foundations established and societies formed, surveys have been done, articles and books have been written, money has been raised, questions have been asked, websites and newsletters created. People who don't know each other, but know each others fears and pain, comfort and console one another. Much has changed, but much has stayed the same. Despite all that we do and all that we have accomplished, mothers and babies still die and we don't know why. It is at times like these that we must reflect on the past and look to the future.
I want to formally thank everyone who has volunteered in any way to further the goals of the HELLP Syndrome Society over the past eight years, including those who have created memorial gifts and made donations to our cause. I also want to formally remember all of our loved ones that we have lost to this terrible condition. It is in the memory of these precious loved ones and all who have suffered from HELLP Syndrome that we dedicate our work
Steve Bohach Co-founder, HELLP Syndrome Society, Inc.
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