tag:blogger.com,1999:blog-272166488914759029.post3880637698977017082..comments2023-10-29T02:41:30.197-07:00Comments on Maxton David Standifer: Extra prayers today please!Maxton's Mommyhttp://www.blogger.com/profile/02582713864323407882noreply@blogger.comBlogger12125tag:blogger.com,1999:blog-272166488914759029.post-48417349074104638982009-03-10T06:35:00.000-07:002009-03-10T06:35:00.000-07:00Keep your head up and keep your eye on the prize. ...Keep your head up and keep your eye on the prize. We pray for you every night (I think Reggan just likes saying baby maxton) in hopes that every little prayer will help your little miracle. Ryann is your personal angel (we have had the talk) and is there to help him fight this!<BR/><BR/>With LOVE, the Smith'sJaime Smithhttps://www.blogger.com/profile/11677841352664886653noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-43173421805524898882009-03-09T19:49:00.000-07:002009-03-09T19:49:00.000-07:00Of course we'll say extra prayers for Maxton. We c...Of course we'll say extra prayers for Maxton. We check your blog daily and hope for good news :)<BR/><BR/>Don't feel guilty about one thing. You have done nothing but be an awesome, loving mother- exactly what Max needs!Ashworth Familyhttps://www.blogger.com/profile/12954955105533808295noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-24157230392794122032009-03-09T19:30:00.000-07:002009-03-09T19:30:00.000-07:00Keeping you all in my thoughts and prayers. I hop...Keeping you all in my thoughts and prayers. I hope that there is a change and it gives more options. Don't feel guilty about ECMO - I so recall not wanting her on it and then once she was - knowing it helps but also knowing the risks too. Scary stuff.<BR/><BR/>Sending Maxton prayers and Lung Function Chants too,<BR/>ElizabethElizabethhttps://www.blogger.com/profile/16490413342578432553noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-42555282008114631182009-03-09T18:41:00.000-07:002009-03-09T18:41:00.000-07:00We are praying really hard for Maxton. He sounds ...We are praying really hard for Maxton. He sounds so much like Wyatt. Wyatt too had a brain bleed- an IVH grade 4 and was on ECMO for CDH. He has had a roller coaster of a ride, but is doing fine. Keep your faith and think positively. <BR/><BR/>Gina<BR/>Wyatt's Mom<BR/>http://wyattjameskoger.blogspot.com/Ginahttps://www.blogger.com/profile/13786147882900140854noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-61535695807911351322009-03-09T16:14:00.000-07:002009-03-09T16:14:00.000-07:00Ash, this is your old roomate! I'm so glad to hear...Ash, this is your old roomate! I'm so glad to hear that Maxton is fighting so hard. I'm adding your family to my church prayer list. You are of course in my prayers, and will continue to be.Beatrice Blounthttps://www.blogger.com/profile/18412115311766270612noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-28515365663806638172009-03-09T15:19:00.000-07:002009-03-09T15:19:00.000-07:00We pray for little Maxton often! We want nothing b...We pray for little Maxton often! We want nothing but the best for you all of you.<BR/>We're so sorry that you're on this CDH roller coaster...we're all learning how much it stinks!<BR/>Just keep the faith and know that Maxton is giving it his all! :-)<BR/>Sending our love and prayers,<BR/>Sheryl & TomJaime's Worldhttps://www.blogger.com/profile/02164450421168557829noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-76142420645638025042009-03-09T13:46:00.000-07:002009-03-09T13:46:00.000-07:00Praying for your little boy that he can be strong ...Praying for your little boy that he can be strong and you see a change today. I hope the brain bleed is gone and his support can be weaned too. Maxton is fighting hard and we all are praying and cheering him on. Fight Maxton fight, show those doctors how strong you are!<BR/><BR/>Sending you 3 lots of love, positive thoughts and energy for today, 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-11358824742440497412009-03-09T13:19:00.000-07:002009-03-09T13:19:00.000-07:00I know you don't know me, I'm a friend of ...I know you don't know me, I'm a friend of Racheal Phillips. She has been askign me to keep baby Maxtonin my prayers and I want you to know that I have been & with your permission, I'd like to link your blog to mine so I can ask my friends to keep you in their prayers as well. I also know someone who has a prayer blog... <BR/><BR/>I'm continuing to pray for your little fighter and for you daily!!Joyhttps://www.blogger.com/profile/04012901168005426842noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-65789064816216590942009-03-09T13:16:00.000-07:002009-03-09T13:16:00.000-07:00I will be praying for you. I'm sorry Max is having...I will be praying for you. I'm sorry Max is having to fight so hard, but he can do it, I have faith. I follow many CDH blogs. My friend's blog is called "Letters to Catherine." They are a wonderful family, the Davis'. Will Continue to pray for strength, and progress. Love you.Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-41178995387866916562009-03-09T12:46:00.000-07:002009-03-09T12:46:00.000-07:00First of all, don't feel guilty for anything! You...First of all, don't feel guilty for anything! You know you always have Maxton's best interests in mind when it comes to anything you do. I pray for him at least once an hour and plead for God to see him through this. This is part of the rollercoaster, I hope this bump in the ride passes quickly.The Daher Familyhttps://www.blogger.com/profile/04630215897890650917noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-40011902970198574062009-03-09T12:43:00.000-07:002009-03-09T12:43:00.000-07:00Ashley-It kills me that Maxton is having to fight ...Ashley-<BR/><BR/>It kills me that Maxton is having to fight so hard. I will pray for the brain bleed to be gone and <BR/>ECMO will again be an option. It sounds like you and David are staying strong--Max can feel that. I am just a mess thinking about this CDH rollercoaster, and knowing that I am next in line for the ride. It is so crazy that things change from one minute to the next, but we are all pulling for him.<BR/><BR/>God is with you and Max, and he is listening to all our prayers. Keep us posted :)Craig and Kristi Kuehlhttps://www.blogger.com/profile/01823742035504045016noreply@blogger.comtag:blogger.com,1999:blog-272166488914759029.post-41900627272240157912009-03-09T11:58:00.000-07:002009-03-09T11:58:00.000-07:00MANY prayers being sent, if you dont mind i will a...MANY prayers being sent, if you dont mind i will also post some of your info on my carepage for zach, the more prayers the better right? Zach also had a bleed in his brain, subdermal hematoma, it wasnt caught until 9 months old though, and it was old then, however it had caused a big seziure and thats how they found it. i know how scary all of this is. i pray for peace, comfort, healing and more for you all. your a strong momma and Maxton is a strong baby. hang in there!! keep your faith!<BR/>God Bless<BR/>zach's mom cp=zacharydavisDottyhttps://www.blogger.com/profile/12624318675496736214noreply@blogger.com