tag:blogger.com,1999:blog-272166488914759029.post5028896185290005431..comments2023-10-29T02:41:30.197-07:00Comments on Maxton David Standifer: 4 monthsMaxton's Mommyhttp://www.blogger.com/profile/02582713864323407882noreply@blogger.comBlogger9125tag:blogger.com,1999:blog-272166488914759029.post-33296855811788918392008-11-17T11:23:00.000-08:002008-11-17T11:23:00.000-08:00Hi Ashley... I just read your message on BOH and c...Hi Ashley... I just read your message on BOH and came to read your blog. I am Tricia, and my daughter, Cadenne, is nearly a year old. <BR/><BR/>One thing I'd recommend is reading blogs that represent lots of different paths. I learned SO much from the families that went before us. I felt like I was really "pre-informed" when doctors would come tell us things. I knew terminology, treatments, etc. and I feel that knowing it ahead of time helped me to process things as they came in that post-partem emotional time.<BR/><BR/>As for Cadenne, she was an ECMO baby, in hospital for 12 weeks, and came home with a g-tube. (just to give you an idea of what kind of "path" she had! :) ) Today she is doing fabulously... g-tube is gone and we have very few issues that relate to CDH.<BR/><BR/>Our blog address is: http://kariabi.blogspot.com if you want to read more! I will add yours to my list! :)Triciahttps://www.blogger.com/profile/02622366355652306645noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-46579715151329952462008-11-15T14:25:00.000-08:002008-11-15T14:25:00.000-08:00Enjoy the joy. Take it as it comes. Trust me the...Enjoy the joy. Take it as it comes. Trust me the last three months of pregnancy dragggggg... ;-)<BR/><BR/>Keeping you in my thoughts & prayers and sending Max some LUNG FUNCTION chants!<BR/>ElizabethElizabethhttps://www.blogger.com/profile/16490413342578432553noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-17925558047673969132008-11-13T06:01:00.000-08:002008-11-13T06:01:00.000-08:00trust what these follks say. they have won their b...trust what these follks say. they have won their battles and know what lies ahead for you and your family. stay strong and keep you faith! prayers for all of you guys!casauhttps://www.blogger.com/profile/03651590603207360298noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-4333656240362927262008-11-11T20:13:00.000-08:002008-11-11T20:13:00.000-08:00Have faith in God and don't give up hope. Stay pos...Have faith in God and don't give up hope. Stay positve and God will give you the strength.Liz and Shanehttps://www.blogger.com/profile/10259533868125774997noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-71271873273380048712008-11-11T15:05:00.000-08:002008-11-11T15:05:00.000-08:00Many continued prayers for you and your family, an...Many continued prayers for you and your family, and especially baby Maxton. CDH babies do amazing things and have such a will and fight within them and Maxton will amaze you too!! Stay strong and before you know it, your little boy will be here. Hugs!!<BR/><BR/>Tracy Meats - mom to Ian, born with a LCDH on 4/3/04 and WY and CO State Rep. for CHERUBSTracy Meatshttps://www.blogger.com/profile/12549931664862571288noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-10509252954905210772008-11-11T14:09:00.000-08:002008-11-11T14:09:00.000-08:00Baby Maxton is constantly in our prayers and thoug...Baby Maxton is constantly in our prayers and thoughts. Please let us know if there is anything we can do for your family.Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-83470249437723318542008-11-11T08:02:00.000-08:002008-11-11T08:02:00.000-08:00Many continuos prayers for you and baby Maxton :)F...Many continuos prayers for you and baby Maxton :)<BR/>Fer<BR/>CHERUBS Mexican Rep.Ferhttps://www.blogger.com/profile/02399525219852871525noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-48595102026884574642008-11-11T06:30:00.000-08:002008-11-11T06:30:00.000-08:00Welcome to the CDH Family. I hate that you have t...Welcome to the CDH Family. I hate that you have to be a part of this family, but it's a wonderful and supportive one. I saw your post on BOH and wanted to wish you the best with your journey. We're right in the middle of ours with Carter and certainly filled with huge ups and huge downs, but you WILL get through it. Try to stay positive for Max and we can't wait to meet him. Please don't hesitate to contact me if you have any questions or concerns. kzmyers@yahoo.com<BR/><BR/>Carter's mom, Kellie*super dude and super dog*https://www.blogger.com/profile/00506572597464180765noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-14644669374354053772008-11-10T23:46:00.000-08:002008-11-10T23:46:00.000-08:00from one CDH family to another, i want to extend m...from one CDH family to another, i want to extend my warmest wishes to you and my blessings! this is a hard road and an uphill battle at times, but your strong, and remember to keep faith, God has a plan. our son Zach was born last oct and just turned one, he had left sided CDH and was born at 33 weeks due to polyhydrominos, due to him not swallowing any longer. he was placed on a vent for 2 months, and had many other issues arise from everything, but he is here with us, and he makes each day brighter. he has given us so much, pride, respect, inspiration,determination, insight. please feel free to contact me if you want, i found your info from BOH website. my email is roses4me777@yahoo.com and our carepage (blog) is at www.carepages.com, you will need to sign up, its easy and free, and our page name is Zacharydavis no spaces. we will keep you and Maxton in our prayers!!! stay strong<BR/>Zach's momma<BR/>DottyDottyhttps://www.blogger.com/profile/12624318675496736214noreply@blogger.com