tag:blogger.com,1999:blog-826454922362512247.post1056282552284151504..comments2009-06-30T14:11:22.566-07:00Comments on The Jack Ryan Gillham Foundation: Jack's StoryThe JRG Foundationhttp://www.blogger.com/profile/08955445812653294159noreply@blogger.comBlogger3125tag:blogger.com,1999:blog-826454922362512247.post-22110040456336393322009-01-23T10:17:00.000-08:002009-01-23T10:17:00.000-08:00Hi Again Bethany,I tried to email you to get your ...Hi Again Bethany,<BR/>I tried to email you to get your e-newsletter and to see if I could use the JRG Foundation button on my blog but the email bounced back...<BR/>Do you have my email? If not just leave a comment on my blog and I'll email you back.<BR/>darcy<BR/>http://ittybittyblog.wordpress.comDarcyhttps://www.blogger.com/profile/16280603933019108782noreply@blogger.comtag:blogger.com,1999:blog-826454922362512247.post-80698755566538715102009-01-22T09:58:00.000-08:002009-01-22T09:58:00.000-08:00Hey Bethany,This is great! My husband, Owen and I ...Hey Bethany,<BR/>This is great! My husband, Owen and I have sent our blood off for the Mass General research study (we did it last March I think). I would be happy to do any others if you know of others. You guys are doing such a great job!<BR/>darcy<BR/>http://ittybittyblog.wordpress.comDarcyhttps://www.blogger.com/profile/16280603933019108782noreply@blogger.comtag:blogger.com,1999:blog-826454922362512247.post-45803347543070914012009-01-21T18:31:00.000-08:002009-01-21T18:31:00.000-08:00Hello I too am a cdh mommy. My daughter is once ag...Hello I too am a cdh mommy. My daughter is once again struggling with the effects of this "cdh monster" as I call it! WE nearly lost her just three short months ago and she is 2. <BR/><BR/>I just think it is so heroic of your family to help so many others. God has really used your son in an outstanding way! I'm truly sorry you can't physically hold your son but he is in so many people's hearts! <BR/><BR/>Please let me know if I can help your foundation. Feel free to drop by and read about our little Ava.<BR/><BR/>~Terri L. Helmick<BR/>http://avaslifewithcdh.blogspot.com<BR/>http://cdhawarenessvideos.blogspot.com<BR/>Carepage: avahelmickHope for congenital diaphragmatic herniahttps://www.blogger.com/profile/02815771123190989855noreply@blogger.com