Over the years, since losing my son, Hunter, to severe PE in 2005, I have visited the site/forum to share thoughts and see if there's others who share similiar stories. We all share something in some form or another. I'm happy to share that I'm stronger knowing I'm not alone. Today, I took an extra step and filled out the volunteer form. I live/work in the Charlotte NC area and I'm still amazed that this area doesn't have more of a preeclampsia awareness presence.
Again, just a simple thank you to the Preeclampsia Foundation for giving me comfort & support.
Carla M. Gaydos
Hunter Presley Gaydos 08/03/2005 (23 weeks old)
Would you like to share your appreciation for the Preeclampsia Foundation? Please post your comments here...
1 post • Page 1 of 1
Users browsing this forum: No registered users and 0 guests