|
|
First Month Updates--November 2005 Go to Most Recent Updates (2008 & 2007) (If you e-mail us at roberts99@insightbb.com and ask nicely, we will place you on our e-mail update list) Go to June-December 2006 Updates Go to March/April/May 2006 Updates Go to January/February 2006 Updates Go to December 2005 Updates Go to First Month Updates (November 2005) Go to Pregnancy Updates (July-October 2005) 2007 Year in Review Video, Roberts Hooligan 2nd Year Slideshow, Chair Wars, 2005 Year in Review Slideshow, Birth Announcement, Pregnancy Announcement, Emily Anne Roberts Memorial Slideshow, First Birthday "Thank You" Video, First Birthday "All Things New" Video, and Christmas 2006 Laughter/Motion Video Savannah Morning News Article on the Roberts Family & Emily's Passing Thanksgiving Day Arizona Republic Article on the Roberts Family
November 29, 2005
Dear Family & Friends, We wanted to give you an update of what’s going on with us… Benjamin, Casey and Danielle have all had little ups and downs, but have done fairly well in the last few days, with no earth-shattering news or major problems. Infections appear to be completely gone, and breathing/eating seems to be progressing fairly well. Danielle’s head has grown a little bit faster than what we’d like, and a head ultrasound and some consultation will show if she’s getting close to hydrocephalus or not—if so, some temporary measures can drain some fluid, with the hopes that a permanent shunt still won’t be needed. Yesterday, Danielle was allowed to move from a jet ventilator down to a conventional ventilator, which is a step in the right direction toward getting her off of ventilators altogether. Please pray that her lungs and body will react favorably to this change. We would like to see her on CPAP, which the brothers are on, in the next few weeks. Weights are 2-10 for Danielle, 2-9 for Benjamin and 2-6 for Casey (it is interesting to see how they jockey for the title of “family heavyweight”). Yesterday we had a funeral service here for Emily. We debated on whether to do a more open service at the church, or to do a smaller service in the hospital chapel. We opted for the smaller service in the hospital chapel, and were glad that we did, for one reason in particular. It allowed about fifteen NICU doctors and nurses, who knew Emily personally and loved her and cared for her, to attend the service simply by coming down the elevator. We cannot even express how much these people mean to us, and meant to Emily, and how much it meant that they came. We also asked the four pastors from First Christian Church who had met Emily personally to read Scripture and lead singing. And my Dad and I were both able to talk a little bit about Emily’s life and the confidence that we have in knowing that she’s truly home now. Of course, it was a somewhat emotional and bittersweet service, but was helpful in verbalizing feelings and beliefs that a loved one’s passing is supposed to help us clarify. Our good friend Jennifer Nagy left on Saturday morning. Jennifer arrived the previous Saturday, at the height of Emily’s sickness and our coming to grips with it, and was here through Emily’s death and Thanksgiving and the beginning of our grieving time. We cannot even begin to describe how much it meant that she would sacrifice her Thanksgiving and some vacation time to be with us—she definitely was thrown into the fire, and came out intact, as she selflessly watched Ashley during a time when it was hard for us to do much toddler-stuff. Ashley definitely enjoyed her time with Jennifer, who taught her all kinds of fun songs, as well as being with all three of her grandparents for the last few days. My parents left yesterday afternoon after three days with us, and Lisa’s mother (Nana to Ashley) is here for four more days before returning to Atlanta. It has been good to have family here during this time. Lisa and I are doing well—holding up through waves of emotions, and grateful for our time with Emily and the four babies that we are blessed to still be here for. Again, the constant encouragement and prayers of friends and family, and even those that we haven’t met, have been such a steadying factor for us. Thank you. We love and miss so many of you, and wish we could have more return dialogue with you, but know that you understand. We will keep you posted, every few days if things hopefully level out for us some. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily (November 4-23, 2005)
November 25, 2005
Dear Family and Friends, Happy Thanksgiving! We were reminded yesterday so much of how grateful we are to God for providing for us, and always holding us safely in His hand. We called to mind the original Thanksgiving meal in 1621, celebrated in gratitude to God after nearly half of the Mayflower’s passengers (many of them their children) had not survived the previous winter. In the same way, the loss of our little girl cannot stop us from giving thanks to God for so many blessings, including our time with her. About an hour after Emily passed away, when tears had dried and her belongings were being gathered, I was washing my hands at one of the sinks in the NICU. One of the nurses, whom I had not met and who just knew that we were parents of quadruplets, was standing next to me, and said hello, not knowing about what had transpired. She looked over at the four isolettes, noticed that one of them was different, and cheerily said, “Oh wow! It looks like one of your kids came off of the ventilator. Who was that?” (I immediately felt so bad for her, because I wasn’t sure what to say, and knew she would feel awful.) I politely said, “Well, one of our babies just passed away.” As she began to apologize (and did feel awful for what she had said), I said to her, “But you’re exactly right. The good news about Emily is that she did come off of the ventilator. She’s somewhere now where she doesn’t need any more ventilators or tubes or IVs.” And that really is the good news. We miss her greatly, and we mourn the loss of the time and the plans that we had reserved for her here with us, but we are not worried about her anymore. We are so grateful that so many of you share that faith (true, specific faith in knowing exactly where she is and who she’s with), and have expressed it to us. Those of you who have shared your own stories of loss—and hope—with us have comforted us far more than you will ever know. Those of you who have no way to relate to this (as we didn’t just a few days ago), but who have just told us that we are in your prayers—that too is a great source of comfort, and we thank you so much. We will meet with a funeral home later this morning to discuss some of the details of Emily’s burial. A very small and very private funeral service will be held for her in the hospital chapel, and then we will have her body transported and privately buried somewhere in the Savannah area before we are able to return. After we return to Savannah, we will have a memorial service for Emily, in which everyone will be invited to participate. Thank you for your willingness to wait for the large public service that we would like to have now, but can’t. In lieu of flowers, you may make contributions to an account that has been set up to help with the children. It was mentioned in the very nice article that came out in yesterday’s Arizona Republic (http://www.azcentral.com/arizonarepublic/arizonaliving/articles/1124quads1124.html)—it is a general account that was originally intended for general help with the quads, but we will use half of any undesignated contributions in Emily’s memory, as well as any contributions that we know were specifically intended for her memorial. The Bank of America account name is “Philip Roberts for Roberts Quads” and the account number is 0046 5433 8810. Thank you in advance for any contributions—we are excited about trying to do something very meaningful in Emily’s memory. The other three children had a very good day and night yesterday, which was a great relief to us, in that we have not really had any non-tense days (on someone’s behalf) in the last four weeks. Danielle still has a long way to go, and you may focus a lot of prayer on her in regard to her breathing and brain bleeds and issues related to them. The boys really seem to be thriving—all three of the kids weigh right around 2 lbs. 4 oz., so they are slowly gaining weight. (By the way, while I’m thinking of it, they will never technically be “triplets,” but the correct terminology would be “three surviving quadruplets” in case you are understandably confused as to how to refer to them.) As you can see, Ashley is keeping us on our toes, and Jennifer Nagy, my cousin Melissa Casey, and Lisa’s mom Patti (all of whom shared Thanksgiving with us) have been great in harnessing Ashley’s energy during a very busy time. Our journey has not worked out in exactly the way that we had hoped or prayed for or planned for, but it is our journey, and God has been faithful, and having company along the road is one of the things that has made it bearable. Thank you for sharing it with us. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily, 11/4/05-11/23/05 November 23, 2005 (part 2 of 2)
Emily Anne Roberts November 4, 2005-November 23, 2005 Outside the hospital, in a beautiful garden in the fresh air and sunshine, Emily Anne Roberts went from her Mommy and Daddy’s arms into the arms of Jesus. With no more IVs or tubes, and wearing a beautiful pink and white dress, she looked at Mommy and Daddy for a moment before she left this life peacefully, as she heard words of love and adoration, songs, Scripture and prayers. We thank the Lord for every moment that we were able to share with her, and for the prayers of all those who came to love her so quickly, and through our tears we yearn for the day when we are reunited with her again. matthew 6:19-21
we held in our arms a treasure for a moment yesterday— her beauty, beyond measure or words we knew to say
try as we would her life to keep, this jewel we cannot own; we smile at her, and softly weep and know she’s not alone
and though it hurts with all we feel (this leaving—so abrupt), we place her where no thief can steal nor moth or rust corrupt
Jesus, heal our precious child as we so wanted to— and till the day we’re reconciled we lay Emily up with you
November 23, 2005 (part 1 of 2) Dear Friends & Family, May God bless you for all your kind notes of comfort to us. None of them has gone unread or has not touched us deeply, even short notes in which you don’t really know what to write. The fact that you’re reaching out to us at all is overwhelming, and holds us in that place of peace that we need to be in. We wish we could reply more personally, but we know you understand. Please know that we know that it probably feels to some of you like you should do something else for us, say something else to us—something to make it easier. Your prayers and encouragement, even when you don’t know what exactly to say (and who would?), are quite enough. Some very dear friends of ours who lost their son a few years ago directed us to a book called When There Are New Words, by Charlie Walton. It helped us know how better to reach out to those who are dealing with grief, and if it helps you too, we highly recommend it—you can probably find it on Amazon.com. Some of you have offered to help financially, and we appreciate that. We don’t know exactly what our needs will be at this point, but know that they will be provided for. We will be setting up a fund in Emily’s name that you could contribute to—we are presently trying to come up with a way to use any such resources in a way that will uphold and honor her memory, and will at the same time be used for a high purpose (a higher purpose than diapers). Please let us know if you have any suggestions. Emily has been slowly slipping away from us, as you well know. The earthly miracle we prayed for seems not to be part of the plan, while the far greater heavenly miracle is clearly about to take place. Of course we are sad, and of course we grieve (but not like the rest of men, who have no hope), but our comfort is that Emily will soon be fulfilling our highest dream for her. As parents, all that we ultimately want for our children is for them someday to be in heaven with Jesus. For Emily, that someday is very soon, probably today. No explanation that we can come up with can adequately explain (to us, while we are still here) why she has to leave us now, but we do take comfort in knowing that her short life has by no means been meaningless: too many people already have been drawn toward the Lord through this little girl’s life. If Emily’s life has done anything for us, it has caused us to reconsider and reaffirm what it is that we put our complete hope in, and why. We believe that Jesus was not just some good teacher or a good religious option or a comforting thought—we believe that He was and is God, who left the glories of heaven to redeem a world corrupted by sin and pain and death and the kind of infections that take the lives of innocent little girls. We do not hate God, since on our behalf He became subject to all of these horrors even as He conquered them—instead, we hate the tsunamis and the corruption and the sadness that are the consequences of living in a fallen world. We rejoice to see them soon rendered powerless in the life of Emily, who won’t suffer long, and we rejoice further that a day is coming soon when all of them will be finally extinguished. More than anything, Emily’s leaving makes us long even more to see Jesus face to face, and to experience that reunion which our hearts are crying out for as we weep for our little girl. Lisa and I spent several hours with all four of the babies yesterday. Of course, we spent most of our time with Emily, and it was good for us. I finished reading The Lion, the Witch and the Wardrobe to her, and was overcome with emotion at several points—to read about the sacrifice of the Lion on behalf of his children, and the little girls’ love for him, and the way that he breathed life back into those whose bodies had been stilled by the witch’s curse. Last night I read to Emily some passages from the Bible as sort of a crash course for what she is about to experience—about the good news of Jesus’ arrival in Bethlehem, about the way that Jesus loves children, about the way that Jesus wept for His friends Mary and Martha even as He worked the resurrection of their brother, about His death and burial and resurrection, about “the most excellent way,” and about the ultimate conquering of sin and death and the new place prepared for all of us. We have no doubt that Emily is prepared to meet Jesus. And we hope that her life will be a reminder that you and I need to be as well. The other babies seem to be doing well—stable, still tiny, still subject to the same dangers that every tiny premature baby faces. Please continue to pray for them. We love you, we are grateful to you for holding us so close, and we thank you for sharing our tears and our ultimate joy. We will keep you updated as well as we can. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily November 22, 2005
Dear Friends & Family, First of all, thank you for reaching out to us in our hour of sadness. We cannot express to you how much your kind notes have meant—we have learned that it is unwise to read e-mails without Kleenexes in hand. When we get a note from one of you whom we already know has dealt with this kind of grief, we begin to cry before we even start. Thank you for sharing the heartache part of our journey as well as the more inspiring parts. Emily is steadily declining, despite all of our prayers. Even though she is very sick and does not look at all like herself, she is still so beautiful to us, and we love every moment with her. It occurred to us yesterday that we have a very short window of opportunity in which we could gather our family of seven together. Ashley is allowed one visit to the NICU per sibling during the course of their stay, and we had planned to bring her for her first visit when the babies were a little bigger and more stable and could come out and play with her a little more easily. We also wanted to wait till Ashley was a little more “mature.” During her ten or so visits to see Lisa in the hospital within the past month, her attention span was just long enough to say “Hi, mommy” and then want to leave the hospital room and start roaming the halls. And so we weren’t sure what we would experience when we got her into the NICU. We asked the doctors if it was okay for her to visit—from a giving and receiving of infection standpoint—and they said that it would be fine, as long as she didn’t make contact with any of the babies. We prepped her that she was going to meet the 1-2-3-4…babies, Benjamin, Casey, Danielle & Emily, and that we were going to sing songs and blow kisses to them. Our good friend Jennifer Nagy, who has sacrificed her normal non-roller-coaster Thanksgiving week to be with us, came with us and met the babies and took pictures of us. I would never want to put pressure on anyone to take good pictures of us, but it was really important to me that we got some great photos of this meeting. And Jennifer came through for us bigtime! We don’t know what possessed Ashley. Frankly, during the last two or three days she’s been sort of an uncharacteristically wild child who wants to do what she wants to do and go where she wants to go (enabling parents’ excuse: she is cutting a bottom molar, we just discovered). But last night, in the NICU, she was the perfect child. She was sweet, not overly shy, and stayed in Daddy’s arms and blew kisses and looked at the babies with delight and said their names and said “love you” and helped us sing. We sang “Jesus Loves Me” (with verses “Yes Jesus loves Ashley”, “Yes Jesus loves Benjamin and Casey” and “Yes Jesus loves Danielle & Emily” and we also sang a special alphabet song that we wrote using their five alphabetical names). We hope and pray that someday Ashley will smile when she gets to see pictures of her meeting with Emily (whose name she has always been partial to anyway), and will be proud that she behaved so wonderfully. Mom and Dad behaved pretty well too. We have shed many, many tears in the last few days, but somehow kept our composure during this particular visit and drank in the joy of just being together as a family. Lisa got to hold Benjamin for a few minutes while we were there, and we just enjoyed it all (maybe we were just in shock that Ashley seemed so comfortable in the NICU!). It was a wonderful ten-minute visit. You will also see in several of the pictures Emily’s main nurse, Jane Hodges (she’s also cared for Benjamin lately too). Jane is actually from the part of Ohio where I ministered for seven years, and is a childhood acquaintance/friend with Ernie and Vicki Graf, friends of ours at Northside Christian Church there. Jane drew Emily “randomly” on the day that they were born, but we have always felt that she was the perfect nurse for her (Jane’s mother’s name is Emily; 87 years old, and the mother of eleven children!). Jane is another great example of servanthood in the NICU, and we know that her own heart is breaking almost as much as ours is. Last night I was able to go back for a couple of hours to be with the babies and read to them. I went around to each of them and read a book called “Guess How Much I Love You,” which I found in the church bookstore about a year ago. I used to read it to Ashley at least once a day—it’s the best book for small children that I’ve ever read, and is just a short account of a baby rabbit and a daddy rabbit who have a back-and-forth dialogue about how much they love each other (I won’t give away the surprise ending, but the daddy rabbit sort of wins the “argument”). Then I stayed with Emily and read her a couple chapters of The Lion, the Witch and the Wardrobe, remembering fondly how my own dad used to read it to my brother and sister and me (yes, it really was a rather good book before it became a major motion picture). We are struggling with the all-too-human desire to know the answers to “why?” concerning Emily and her leaving, and we are doing the only thing that we can do, which is to lay those “why?” questions at the feet of Jesus, trusting that He never wanted Emily to be sick at all and that He loves her more than either of us ever could. We find ourselves with Mary and Martha, who felt that sense of heartache that comes with losing someone you love, and desperately wanted to know why Jesus had allowed things to happen as He did, and then never got an answer from Him to the “Why?” question. But we also find ourselves with Mary and Martha, who watched Jesus weep on their behalf, and who—before very long at all—were reunited with their loved one through the resurrection. This is our hope and our joy…and our peace. Even through our tears. Thank you for sharing them… In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 21, 2005
Dear Friends & Family, Thank you again so much for all of your prayers and your expressions of kindness, especially over the last couple of days. We are asking the Lord to work a miracle in Emily’s little body. She is very, very sick, and her kidneys have still not been keeping up. It appears that the infection is still very present (in her blood as well as her central nervous system). If it is not the Lord’s will to provide the miracle we’re praying for, then she will be going home to be with Him sometime in the next few days. We rest assured that her presence with us in the first place is a miracle, and we know that Jesus loves her. If the miracle of her healing here on earth doesn’t happen, then we have peace and assurance that the miracle of her ultimate healing is about to happen. Lisa and I have cried a whole lot together in the last couple of days—it is so difficult to say goodbye to someone that you love, especially when she is so tiny and when we have just begun to get to know her. Yesterday, we asked to be able to hold Emily for a few minutes, and the nurses allowed us to do that. I can only say that it was hard, and it was emotional, and yet it was one of the most wonderful moments of our lives. To hold her in our arms, kiss her, say how much we love her, and smile at her through our tears…we thank God for those moments, while she’s still with us, that so many grieving parents never get. We also were able to hold the other three yesterday. Danielle is doing just well enough that they were willing to allow us to do that, and I got to hold Casey for my first time yesterday. Both of us being able to hold all four of them means a whole lot to us after all that we’ve been through. Please pray for protection from infection for everyone, and that Casey’s PDA will not require the surgery. We will try to keep everyone posted on how things are about once a day. For the next little while, we will probably not get a good chance to return e-mails (but we will read them and cry through them and will know that we’re not alone) and it really drains both us and our batteries to do much talking on the phone right now. That is hard for us, and I know that it is hard for you because many of you would like to call and talk with us, and it would certainly be good to talk to you. We appreciate your understanding, and hope that we convey to you how much your thoughts and prayers and messages mean to us. On a similar note, some of you who are close to us may have the urge to fly out here to comfort us. While we would normally appreciate that very much, that would really not be helpful at this time. If Emily should leave us, we will probably have a private family-only service for her here, and then would like to do a larger memorial service once we return home to Savannah. We will cross that bridge if we come to it, but just don’t want anyone to spend money for a plane ticket at this time, and we need so badly to focus on the other children during this still-volatile time. In my e-mail the other day, I listed the people who had visited the babies. I realized today that I had neglected to mention Mark and Jena Hall, who were one of the first ones to meet them (and who saw Lisa through the hardest part of her ordeal). My apologies for the omission on that one—I’ll correct it on the website. We love all of you and thank you so much for laughing and crying and praying with us. God has been so good to us… In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 20, 2005
Dear Friends & Family, Here’s the latest… All four of the babies are flirting with some degree of some kind of infection or another, and so we really need your prayer for all of them. Emily right now is really—to be honest—teetering on the edge of life and death, as she has been now for most of the last week or so. The infection that she has is not only in her blood and central nervous system, but could also be getting into her brain and lungs right now as well. The kind of virus that she has is a wicked type, which over the last decade or two has mutated to a place where it’s resistant to most of the antibiotics that knock out most infections. As a result, Emily’s little body is getting hit with a high dose of heavy-duty antibiotics. Part of this double-edged sword is that the healthy parts of her body can have adverse reactions to those antibiotics. If you want to pray hard and fast for anything right now, please pray for Emily’s kidneys to kick in and produce some serious urine output. In general, we believe that Emily really needs a miracle in order to stay with us here and to live any kind of semi-normal life. Her best-case scenario includes a weeks-and-weeks long tooth-and-nail fight, which she has already begun. Thank you for your prayers. Casey is really doing well. Even though his tests showed meningitis, which always produces some potential long-term brain issues, he is fortunate that his actions seem to indicate that he is for all material purposes “better.” He is fortunate to have a much easier type of virus than Emily does—though he was sick the other day, the virus itself is easier to kill in both the blood and central nervous system. He is almost back to where he was with his breathing before the sickness started, and he looks and acts quite healthy (he’s had his eyes open a lot the last few days). Unfortunately, his PDA (heart valve) did come open, which is not unusual with an infection (but kind of discouraging to us, since early on he had shown zero signs of it being an issue at all—we had no idea that it even could come open at this point), but hopefully a drug called endomethazin (sp.?) will cause it to go shut on its own now without surgery. Please pray that Casey’s recovery from infection will be complete, and that he will not require the PDA surgery. Danielle has really really improved. Her progress has been slow, but you may remember that we almost lost her just two days after she was born, and that she required the PDA surgery, and that the surgeon came and told us that the state of her lungs was very, very bad. Danielle has slowly gone down on how much she needs the ventilators, and various levels are looking a lot better, and we are nearing a point where we can attempt some new things, such as: going from a ventilator to a CPAP machine; feeding her Mommy’s milk through her tube; and possibly even letting Mommy and Daddy hold her!!!!! She has shown possible signs of having an infection on some tests, but has shown no real symptoms. Please pray that Danielle does not have any kind of full-blown infection, and that her progress continues. Benjamin is kind of in the same boat. Tests indicate signs of him having at least a slight infection, but nothing on the surface would indicate that his body is sick in any way, shape or form. Yesterday, Benjamin came off of his CPAP and started breathing through a nasal cannula (a steady supplement of oxygen through two very non-invasive little prongs in his nostrils). He tolerated this very well, and we hope that he will not have to go back on to the CPAP again (but if he does, we still love him). I had the privilege of holding Benjamin last night, which was so much easier and enjoyable without some of the bigger breathing tubes all around him. We enjoyed a great father-son rocking time for a good 30 minutes. Benjamin’s feedings are purely breastmilk now, with no fluid supplements, which is great. Please pray that Benjamin keeps doing great, and that there is not even a hint of any kind of infection from here forward. The two of us and Ashley are doing fairly well. (We may start renting Ashley out to some of you who need some stress relief—though she creates some toddler-induced stress of her own, she is such a bright-eyed, innocent, ornery, hilarious, beautiful little girl, and represents the absolute best picture of what we’re praying for with the other four.) One great friend from Savannah Christian Church—Mary Brown—was replaced by another—Jennifer Nagy—who is actually going to spend Thanksgiving with us, for which we are so grateful. We are rejoicing with the babies, and daily holding up under the strain of seeing one of our little ones in particular who is walking through the valley of the shadow. Thank you for your concern, encouragement, faith and joy that you’ve expressed to us recently. Most importantly, we thank you for your prayers. They mean the world to us. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 18, 2005 Dear Friends & Family, It seems that the last few days have held a lot of bummer news for our children. Daily, and moment-by-moment, we are all too aware of the dangers and potential consequences of some of this news. Without minimalizing any of it, or living in DenialLand, we still believe this: At the end of the day, the Lord has been so gracious and so merciful to us and to these four little babies. We wanted to offer you a sampling of some of the ways that we’ve seen this mercy and grace in the last two weeks, so that while you’re relentlessly praying for us, you can remember to rejoice at the same time… Four Beautiful Babies We don’t know why God chose to answer our prayer for children so suddenly and so dramatically. For whatever reason, we have the opportunity to be Mommy and Daddy to a super-cute toddler and to the most beautiful little foursome we’ve ever laid eyes upon. With daunting issues and challenges and hurdles in their way, they have all turned two weeks old! Whatever comes, we have been blessed to lay our eyes and on our hands upon them, and we will never be quite the same again. For fourteen days and running, all four of them have heard over and over and over again that Jesus loves them, that people are praying for them, and that their Mommy and Daddy love them and are very, very proud of them (we know of many who have waited a lifetime to hear those kinds of words, just once, from their parents). We are absolutely in love with (from left to right) Benjamin, Casey, Danielle & Emily… Angels with Stethoscopes Our friend and former professor Dr. Bert Allen wrote to us in an e-mail shortly before their birth: “You can be certain that an angel band are walking with you and even perhaps playing a few tunes! Can you hear them? I think that some of them are wearing scrubs and have stethoscopes around their necks.” He was exactly right: All of the doctors and other specialists have been incredible with both Lisa and the babies. But, specifically, our hats are off to the nurses, in Labor & Delivery, and then in the adult ICU, and now in the NICU with these little ones, who have demonstrated a special kind of love and compassion toward both us and our children, in such a way that we would never have believed it possible if we hadn’t experienced it. The around-the-clock attention and care given to all four of them, and to us, is amazing. Pictured below are two of the excellent night nurses, Gretchen and Megan, as well as some of the celebratory signage that they have creatively produced for our children (in cases where kids in the NICU are abandoned or are removed from their homes, these works of art go with the child to their foster or adoptive home, as a record of the first real love that they received when they were brought into this world)… If you expand each of the footprint/handprint files below up to 4” x 6” size, it will be just a little bigger than the actual size (Benjamin’s file is two 4x6es scanned together, so actual size would be just under 8x6). Casey’s has yet to be done…
From the Mouths of Babes We are encouraged by the prayers and compassion and encouragement of everyone, but for some reason (and I think you’ll understand this) it means even more to us when we hear that other children are praying for these little ones. Some of you may have noticed a picture of some children in the background of the kids’ isolettes. The pictured children are Burke, Boone, Turney and Aubrey Russell—they live in the greater Nashville area with their parents Steve and Barrett, and they happen to be quadruplets. When these four-year-olds heard about our kids, they asked if they could be assigned one of our kids as their own personal “prayer baby” (the two-boys/two-girls combo worked out nicely). Barrett just sent us an updated version of the picture (see below), and included samples of the prayers that each of them have been praying, which are as follows: Burke: "Please help Casey to grow up big and to like broccoli like me. And help him to breathe good." Turner: "God, please help Emily grow up to be a Mommy and to love baby dolls like I do. Then her baby doll and my baby doll can be friends." Aubrey: "God, please help Danielle not be sick. I want her to have a big girl bed and grow up strong." Boone: "I pray that Benjamin will like camouflage and donuts just like me. And I love Benjamin." We are connected online to numerous other families of high-order multiples who have sent us pictures and have told us their children are praying for ours, and we continually get the assurance that many other children are doing the same. Our friend Mary Brown, here with us right now, and her husband Kevin have a small group at our church, Savannah Christian Church. When Mary arrived in Phoenix just the other night, she showed us the cards that the kids in their small group had made for our babies. I wish that I could include a sample of all of them—they all moved us very deeply—but I scanned in just a couple of them that you can see below. Our eighteen-month-old, Ashley, knows the babies’ names and occasionally decides to say them without any prompting. (Often, we say “Benjamin” and she proceeds with the names of the other three). At every mealtime we have her repeat their names during the prayer. There is not a more beautiful sound in the world. Isolette-side Visitors In addition to Mommy and Daddy’s frequent visits, these babies have been blessed to get to meet personally a whole host of friends and family who love them. First and foremost among them are their three active grandparents (my parents and Lisa’s mom), who flew from very far away to come meet them. We are very comforted that—should anything happen to any of them—they all got to know all of their grandparents. In addition, they have also been visited by—not necessarily in this order—my first cousin Melissa Casey; Stacy Baker and Donita (sorry, Donita, can’t remember your last name [it is Evans]) who are children’s ministers at First Christian Church of Phoenix; Kenyon Ackeberg and Debbi Dilk, also FCC ministers; Mark and Jena Hall, dear friends of ours from Savannah (earlier I had omitted their names); our close friend Dave Allgire, a minister at Savannah Christian Church; Janie Magruder, our new friend from The Arizona Republic, and Tom the photographer; DeeDee (sorry, don’t know the last name there either), who’s another quad mom who lives in Phoenix; Amanda Pommerenck, our great friend and neighbor; Mary Brown, who goes to church with us in Savannah; my first cousin Ron Dove; and Lisa’s incredible ICU nurse Denielle Headley. [Most recently, our incredible Savannah friend Jennifer Nagy also got to meet them.] If I’ve omitted anyone, please let me know, and accept my apology in advance. The important thing is that you realize that Benjamin, Casey, Danielle & Emily sleep in isolettes, but have not been isolated from people who love them. Prayers of the Saints We are reminded daily by e-mail of the hundreds of people who are lifting up these babies in prayer. We will not even try to list them all, because we will leave someone out and get someone mad at us (which would defeat the purpose of an uplifting e-mail). We know that our church family in Savannah is praying for us, and that many people from First Christian Church here in Phoenix are doing the same. Churches like Victory Christian Center in Macon, Georgia (my sister’s church), Bethel Christian Church in Conyers, Georgia (Lisa’s home church, where we were married), Grandview Christian Church in Johnson City, Tennessee (my parents’ church, also the church that ordained me), and several others have specifically focused concentrated prayer on the babies. A common scenario that we keep finding is that people we’re e-mailing will forward on our updates to their own friends and acquaintances in other places, who end up praying for the babies too. We don’t know if someone in every state has prayed for these babies, but we wouldn’t be surprised if that were the case, and we know that people in other countries (such as Canada, Zimbabwe, Mexico, and even Michigan [just kidding, but…Go Buckeyes!!!]) have lifted them up to the Lord as well. We don’t believe that it’s already been definitely decided what will happen to our babies. We believe that prayer works, that God wants to hear us and tells us to petition him about such things, and we believe that He does answer prayer, even if not always the way that we want. Because we believe this, we know that your prayers really do matter to us and to God as well…and they mean the world to these innocent little ones. The Good Physician More important than anything we’ve mentioned is the fact that we are certain that these babies are never alone. We don’t believe that Jesus is some kind of legend or mantra or angel or phantom (whose likeness shows up on clouds or toast). We believe that Jesus really is God, that He lowered Himself to come to earth to be like us and so that we could know Him, that He didn’t immunize himself or His followers from physical suffering, and that He literally died in our place, and then overcame death by rising from the dead. As a result of those convictions, we believe that He’s not only right here with us, but that He’s always present in the NICU. We know that He loves children, we know that He weeps when our little ones are hurting, and we know that there’s nothing that they could experience right now—even death—that would separate them from His love and from their place in His kingdom. That’s the ultimate good news whenever not-so-good news comes at us in this whole experience. That’s our peace.
Many of you have commented that we seem to be at peace, and holding up well, and not caving in when things are going downhill. When you say that, maybe you’re just making an observation, but maybe you’re asking us how that’s possible with all that’s happened to us in the last three weeks. And if that’s what you’re asking, we’d love to tell you more. Please just ask. Thank you for sharing in all of our news, and we hope that this e-mail will give you some reasons to really really rejoice, right along with us, in the midst of what’s happening in our lives…and in yours. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 17, 2005 (part 2 of 2) Dear Friends & Family, Sorry to be writing you again so soon, but we have some more news, which is not necessarily good… Casey does indeed have meningitis also. His infection was a different one than Emily’s, and fortunately an easier infection to fight off, but it is still a big concern when the infection has reached the fluid of the central nervous system. With both Emily and Casey, a 21-day (minimum) round of antibiotics will be given to try to knock out the infection in the central nervous system (which is more under-the-surface than just a basic blood infection). Please pray that both of their bodies will respond well to this, that the antibiotics will not adversely affect their kidneys or other organs, that their infections will be knocked out in both the blood and the c.n.s. fluid, that none of their siblings or other babies in the unit will get the same infections, and that the long-term effects of their meningitis will be minimal. The last few days have seen us inundated with several pieces of not-so-good news concerning at least one of our children. This has been somewhat discouraging, mostly because it keeps coming to us right at that point where we think, “Okay, maybe things are starting to calm down a little.” One of the things that makes it especially difficult is that there’s no way to predict what some of these issues are going to mean in the long-term, and there’s no way to really get our arms around all of the potential scenarios even in the short-term (multiply it times four, and you can believe that we really just throw our hands up and ask God to do what’s best for the babies). The negative things that have happened are really hard to put our finger on exactly, and we think and hope and pray that at least some of them won’t have a major permanent effect. We believe that the positive things that are happening, on the other hand, are very easy to identify and do definitely have a major permanent effect on us. In light of that belief, the next e-mail that we send out is going to focus strictly on some of those really positive things, and is going to hopefully shed some light on why we’re not falling apart whenever we get some not-so-great news like we’ve gotten. I look forward to writing it, and putting it together, and we’ll look forward even more to sharing it with you. Thank you for sharing our lives with us. Please keep all four of the babies, and Ashley too, in your prayers. We believe that—if we’ll just pray—the Spirit will compensate for those unique situations where we’re not sure exactly how to pray or what exactly we need to ask for. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 17, 2005 (part 1 of 2)
Dear Friends & Family, Good morning! We just wanted to give you the latest on the gang… Casey’s day improved yesterday. He still hasn’t completely turned the corner, but he doesn’t seem to be in any danger, and will hopefully just get better and better, and soon be back to where he was. In a day or two, they will do a test of his spinal fluid (actually, fluid that goes throughout the central nervous system, even to the brain), to see if the infection crossed from his blood into that. This would be called meningitis, and is a very serious thing, and we don’t want him to have to deal with that… Which brings us to Emily. Her test for meningitis yesterday came back positive. We are saddened by that, and concerned, and aren’t exactly sure what all of that means, except that she will be on antibiotics for a long time, in order to make sure that this is completely out of her system (both blood and central nervous system). She is definitely doing well thus far in terms of her body’s recovery from the infection (septic shock), but she still has a long way to go. Like Danielle’s brain bleed diagnosis, we will have to just wait and see how this meningitis will affect her long-term (fortunately, my only previous knowledge of meningitis happened when I was about ten years old. A baby in our church in Indiana, Sara Wiley, was the little sister of one of my buddies. She had meningitis, and we prayed for her recovery and her long-term outcome. Last year, we watched Sara, all grown up, in the Miss America Pageant, as Miss Indiana—the cause she was supporting was meningitis research! http://www.tftj.com/Miss/MAO/a_04States/IN/a_IN.htm Even if Emily never becomes Miss Indiana, we will gratefully look at Sara as an example of the power of prayer and a reason not to give up hope, and we’ll see if we can get in touch with her and tap into some of the resources that she can point us to.) Because of the two infections, all four of our babies have their own special section now—they are all four right together. When we go see them, we need to wear a gown and gloves, and if we touch one of them, we need to discard the gown and gloves and go put on new ones before seeing another baby. This may be less intimate and a slight inconvenience, but we are very thankful that the doctors and nurses are taking great care not to pass any infection on from one baby to another, or to any other baby in the NICU nursery. (Dr. Ianni last night even worked with the housekeeping folks to make sure that they were being cautious when they changed the trash cans, etc.!) We are glad that they are so close to each other, but are sad that sickness was the thing that brought them so close together. We joke about having our own wing, our little country club, an exclusive section…right now, RobertsWorld is the name Benjamin is excelling the most right now, and is the only one who’s able to take Lisa’s milk. Last night I got to hold him for an hour, and he even took his feeding while I held him. Please pray that he will be infection-free. Danielle is still kind of holding steady. Her weight was 2 lbs. 0 oz., which is good (probably a little bit skewed from receiving blood and fluids, and probably she didn’t go to the bathroom right before she got weighed, but she is still moving in the right direction with her weight. We’re not sure of the other weights.) Ashley is having fun with her buddy Mary Brown. She is learning a lot of words (Ashley, not Mary), and has handled all of the changes very well. We were never quite sure how much she understood about the babies, except that when we say “1-2-3-4” she will say “babies.” She was also able to go to Mommy’s belly (sometimes lifting her shirt up) when we talked about the babies, and we’re not sure if she thinks that they’re still there. Ashley is not really able to go into the NICU and see the babies (maybe in a month or so, maybe not ever with some of these infection issues), and so Ashley’s world has really not significantly changed. She’s going to enjoy a pretty good grace period of feeling like the only child, even if she’s not anymore. Lisa’s neck is not perfect, but feeling a lot better after last night’s massage from our friend Emily Ackeberg (whose sweet daughter Raegen came and played with Ashley right after karate-time). Thanks for praying for her too. Sorry about the lengthiness of this. And sorry to leave you hanging about Casey. We will get these updated as much as we can. Thanks again for all of your encouragement and prayers. If you’re not sure where to start in praying for us, we understand (we’re kind of at that point too). Just pray for a few semi-stable days, and for continued peace. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 16, 2005 Dear Friends & Family, Sorry to include you on the roller coaster part of our ride, but we just found out that during the night Casey began to show some signs of a pretty serious infection of some kind. We are heading over to the hospital right now to see him, but wanted to ask that you pray specifically for him and for his durability and recovery during the next 24 hours or so. The other three had a very good night. Thanks for your prayers. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 15, 2005 Dear Friends & Family, Thank you again for your prayers and encouragement. Here’s the story, as best as we can decipher it… Emily has apparently turned the corner with her infection. We are so grateful. The neonatologist who has worked nights this week told me that when she went home on Monday morning, she wasn’t sure if Emily would still be alive when she returned to work on Monday night. During the night last night, things started turning around, and today she has had a really, really good day. She is not completely out of the woods, but things are really looking positive. Unfortunately, this was a serious enough infection that Emily will be extremely shielded from infection during the rest of her NICU stay. Also, there is a possibility that there could be some long-term damage from the infection and some of the low oxygen that she got while she fought it (no way of telling that now). The good news is that she is alive, and that somewhere along the line her PDA seems to have taken care of itself again (patent ductus arteriosus—heart valve problem, alluded to in earlier e-mails, see latest updates page on www.expandingrobertses.com ). We really believe that this is the result of specific prayer, and that it will save her already-taxed little body from going through a surgery. Please pray that that will stay closed. And just keep praying for her little body to keep fighting. Danielle seems to be holding her own, making some slow progress but not breaking any records, and not in a hurry to move down on the kind of ventilator that she’s on. She looks so much better than she did just a week ago, and her future seems to look a whole lot brighter than it has up until now. Please pray for her to start steadily improving. Benjamin and Casey have been doing extremely well. Typically in the NICU units it’s the girls that seem to excel; in our case, so far, it’s been the boys, and we’re praying that the girlpower will kick in and that Danielle & Emily will catch up with their brothers. Our biggest prayer for the boys is that nothing would deter them from how well they’re doing. Please pray that infection and any other type of hindrance would not be able to touch them. Lisa has been dealing with a big pain in the neck (I’m referring to a literal pain in her literal neck). We saw the doctor today, who determined that it was a muscle spasm, which will probably go away fairly soon, but that it might need some help to make it disappear. She has a massage scheduled from a friend of ours at the church, Emily Ackeberg (a true Renaissance woman: in addition to being a massage therapist, she’s also Ashley’s hairstylist, a recent Nepal mission trip veteran, and an FCC praise team singer extraordinaire, among other things). Pray that Lisa’s sharp neck pain will go away quickly, so that she can focus on some other things. Okay, while you’re praying for everyone else in the family, pray for me too: that I’ll have good stamina and a good balance of rest and diligence. So far, that’s been going pretty well, and—as I mentioned with Benjamin and Casey—I just don’t want anything to derail that. Today was a big transition day in terms of our out-of-town helpers—I actually visited the airport three times today! My mom, who came on the spur of the moment before the babies were born and ended up staying for two whole weeks, left this morning, and then our good friend Amanda Pommerenck left early in the afternoon. This evening, our wonderful friend Mary Brown (from Savannah Christian Church) flew in, and she is looking forward to hanging out with her buddy Ashley for the next three days. We have been so blessed to have such supportive friends and family who have been able to come visit us. Yesterday we met for a couple of hours with Janie Magruder, a feature reporter for the Family section of the Arizona Republic (Phoenix’s newspaper). An article about our family will be featured on Thanksgiving Day. Meeting with Janie was great for us, first because she was such a pleasant person to talk to, and also because our conversation helped us articulate where we’ve been and what we’re facing and where God fits into all of it. We are really excited about this, and hope that it will be a blessing and an encouragement to those who read it. I cannot say that our recent journey has been fun. It has been bumpy, uncertain, and very harrowing at times…and in the midst of it all somehow incredibly joyous. But we have never traveled an inch of it alone. And for that we are extremely grateful. Thanks for helping us keep our heads above water. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily P.S. We’ve been camera-lazy over the last couple of days. Please forgive us. We won’t let it happen again. P.P.S. Some of you didn’t receive some of our updates last week. I think I may have to make some adjustments to the mailing lists that I have. If you don’t get something from us over a period of several days, check the website in the Latest Updates section to see if you’ve missed anything.
November 13, 2005
Dear Friends & Family, How are you? Pretty good here. The ups and downs of NICU life are definitely evident to us… Danielle has been doing a whole lot better—thank you for your prayers. By no means should you take that to mean that she’s home free, but she has had a series of better days and has even been ok’ed to start getting feedings, which will be Mommy’s milk, something that will help her immune system. Both of the boys (Benjamin and Casey) are doing extremely well. Lisa and I have had a chance to hold them, as you can see in the pictures attached. Everyone seems to be very pleased with their progress. Emily has had a rough day and really needs your prayers. She hasn’t been breathing as well, and seemed like she wasn’t feeling so good. They moved her back onto the ventilator that she had been on, and then discovered that the PDA (patent ductus arteriosus—heart valve not closing on its own) was still slightly a problem, even though they thought last week that it was closed. This will probably require surgery, like Danielle’s. Today they began to think that she might have some kind of infection, and found out that that was the case. They started her on an antibiotic, which should cover a whole host of infections, but noticed some evidence of yeast on her skin. If her infection is a yeast-based infection, it will be harder to knock out than a regular infection, and will require an antibiotic that will be harder on her body and will make it hard to do the PDA surgery. Please pray for Emily (but don’t slack off on praying for Danielle!), and pray specifically that she will have just a normal, non-yeast-related infection that will begin to get better with regular antibiotics in the next day or so, so that she can have her PDA surgery quickly and start moving in the right direction once again. Please understand that an infection is a very common thing for any premature baby, and that this is more of a setback, at least at this point, than it is a detriment to her health. It is still no fun to hear that one of our little ones has moved backward a little. We are of course concerned, and need your prayers that we won’t allow worry to creep in, since we know that God is in control. A ladies’ group (the Girlfriends group) from Broadway Christian Church down in Mesa/Gilbert had asked a while back if they could help us out in any way, or do something special for us. I told them that it would be nice if they could decorate our house for Christmas in mid-November. Even though the babies came so early, these ladies still stuck with their plan to decorate…and they did an incredible job. We had a great time today with Jason and Marlene Graham and their formerly preemie 13-month-old daughter Madison, along with Angie Cole and Fran and Jo. They were so nice, and the house really looks great with their decorative flair. (Jason helped get the tree up, and helped watch his daughter—he is not an official member of the Girlfriends group.) Lisa is still doing better. Getting milk to the babies (with the help of a pump) is both very tiring and very satisfying. She is going with me to the NICU in the afternoons, and I am trying to get there once in the morning and once in the evening as well. This allows us to keep up with the babies’ status and to meet each of their nurses during both day and night shifts. Again, we thank you so much for your prayers and encouragement and concern. We are so grateful for how the Lord has worked during the last ten days, and know that He is very very good to us. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 12, 2005
Dear Family & Friends, Good morning! We were discharged from the hospital yesterday (okay, really just Lisa was, but her roommate came with her) and finally were back at the house having the best night’s sleep we’ve had in weeks. It was really great to be home, although it’s no fun not to be able to hop on an elevator to see the babies. The babies all had a really good day yesterday. Danielle seems to be staying calm, which is what we want her to do right now. All of the babies had head ultrasounds yesterday—they came back clear, with the exception of Danielle’s, but her test seemed to indicate that the bleeds had not progressed since Monday’s test, which is exactly what we were praying for! This makes us hope that there will be no hydrocephalus, or a shunt, etc. Time will tell. Lisa got to hold the babies yesterday. Danielle is not ready to be held, but it was legal for the other three. Lisa held both of the boys (Benjamin and Casey), but was very tired when it was time to hold Emily. Since they like the babies to be held for at least an hour if they come out of their isolettes, we decided that one or both of us would hold Emily today. She seems very forgiving. With the help of a pump, Lisa is also able to express milk, which is added to the preemie formula that the babies are receiving through a tube that goes to their stomach (with the exception of Danielle, who needs to recover and progress some before she can receive a regular feed). This milk from mommy, even though it’s just a few drops, is very very helpful to these tiny babies and their immune systems during this time. We have had some great visitors, with more on the way. Dave Allgire flew in on Thursday night, and has been visiting with us and taking some camcorder footage of the babies and the NICU—this has been great, since Dave is a very close friend, and a fellow pastor, and a NICU dad himself from a couple of years ago. Huge encouragement to us. Last night my dad flew in, and will have to leave Sunday—it was wonderful for him to get to meet his four new grandbabies. This morning our great friend Amanda Pommerenck (former next-door neighbor and Lisa co-worker; she and husband Derek built our house in Savannah) is flying in, and we look forward to several great days with her. And this morning, Lisa’s first cousin once removed (or something like that) Marie Miller, and her son Tiffin (second cousin?) will be meeting us for the first time, which we are very excited about. Probably the biggest news of yesterday came before Lisa checked out. The cardiologist who has been seeing her gave her the okay to leave, and talked about how amazingly well she had bounced back from the peripartum cardiomyopathy (sp.?) that she had developed (this is a condition that anyone can develop; it is not particularly associated with pregnancy/preeclempsia). He encouraged her to see a cardiologist for the next year. He then talked to her about the seriousness of what she just recovered from. He said that the mortality rate for this condition is 20-60%, and that Lisa’s echocardiogram showed that her case was very severe. I asked him if he meant, by mortality rate, that Lisa would have needed medication, and that this would cause her death when she was 80 years old or something, and he said that—no—he meant mortality in the short term, as in this past week when it was diagnosed. He said that she should mark November 6th on her calendar, because it was when her heart suddenly started doing twice the work that it had been doing the day before. When we asked if she was in danger of having a heart attack and dying right then and there (on November 5thbefore things turned around), he said that it would have been considered heart failure rather than a heart attack, and that they were a very short step away from putting her on a heart transplant list. We were very aware that Lisa’s condition was very serious (I will tell you sometime later the traumatic circumstances of her fast trip up to the ICU twelve hours after delivering the babies), but we were not aware that her chances of dying had become statistically greater than her chances of making it. We are grateful that she has bounced back, and we are extremely grateful for your prayers. We know that we asked for prayer for her on November 5th and the morning of the 6th, and that those prayers were answered. We have prepared ourselves all along for the difficult possibility of having to say goodbye to one of our babies—I don’t know that I was at all prepared to say goodbye to Lisa. Thank you for lifting us up. It is making all the difference. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily P.S. For those of you just added to the list, please understand that we are getting further and further behind on replying to personal e-mails (drives me crazy!). But please also understand that they are a huge encouragement to us. Thank you!
November 10, 2005
Dear Family & Friends, Thank you again for your prayers…and encouragement. Even though we are a couple of days behind in reading e-mails, and even though we can’t reply to many of them individually now, it means so much to us. Several of you sent us accounts of your own children, or others, some of them now grown, who started out with grade 4 brain bleeds and didn’t necessarily end up completely impaired for life. That was very helpful to us, in re-realizing that God—and not x-rays or ultrasounds or medical knowledge—really is in control of what happens to each of our children. Today has been an up-and-down day. Lisa’s improvement is more and more evident, and the cardiologist who saw her a couple of days ago is very pleased. She was moved down to a regular room yesterday, and will probably be discharged tomorrow. She wouldn’t let me take a picture of her, but she is absolutely beautiful, and looks like Lisa again (as opposed to the coughing, puffed-up, oxygen-masked, IV-everywhered version of Lisa that was here just a few days ago). The doctors really seem to think that there will be no residual heart damage from all of this, which would be a huge answer to prayer. The really great part of this is that Lisa got to meet the babies!!! We went down once yesterday, and twice today. She did very well in dealing with this, and—as if there were another option or something—immediately fell in love with them. Tomorrow will be the first day that we may get to hold at least some of them, as they will be a week old! Danielle had her PDA surgery today to close the valve that I mentioned in yesterday’s e-mail. It had gotten bigger, and the doctors believed that closing it would be a great advantage to her, in light of some of the breathing/bleeding/blood pressure challenges that she has already faced. The surgery went very well, and the problem was taken care of, but the surgeon felt obligated to tell us that Danielle’s lungs are very, very unhealthy…filled with fluid, and with evidence of some bleeding, even recently. He stressed to us that she has a huge uphill battle still ahead of her, and that she really can’t afford to have a bad day. Her recovery from what’s already taken place will be a slow process that would take several weeks or even months. Right now, her stats look pretty good, but those can change quickly. Please pray for Danielle. If you can’t remember all of our kids’ names (and gosh, if you had quadruplets, we probably couldn’t remember all of their names, so don’t feel bad), please at least remember Danielle’s name and lift her up in prayer. We know that she belongs to God, and we have surrendered her to Him and are at peace with whatever His will is for her, but we really really really want Danielle to be with us for the long haul, and we will love and accept her in whatever form she comes. The other kids seem to be doing very well in terms of breathing and tube feedings and everything else. We will try to get some good pictures of them in our arms tomorrow. We can’t wait. We love you and thank God for you. In Christ, Phil, Lisa, Ashley, Benjamin, Casey, Danielle & Emily
November 9, 2005 Dear Friends & Family, Another day, another update. Before I forget, I updated the website yesterday, with several pictures, and had been working on a kind of birth announcement slideshow thing, which is now on the homepage. The website, by the way, is www.expandingrobertses.com . Feel free to check it out. Lisa is doing much much better and will almost certainly go from ICU down to a regular OB room later today. We are very excited about this, as she has come off all of her IVs, her swan catheter has been removed, and she is basically on a few oral medications. She looks 100% better than just a couple of days ago, and feels much better, although there is a definite combination of fatigue, meds, hormones, and “what happened” questions that have been a little tough. I am hopeful that she can see the babies (and Ashley) sometime today, but please pray for that to go smoothly, mostly from an emotional standpoint, as it’s kind of an overwhelming thing for her right now. I am SO excited about her getting introduced to them. The babies are doing really well too. Danielle has definitely stabilized, but still seems to be behind the others. All four of the babies, most likely, to some degree had what is called PDA (if I remember right, it’s patent ductus arteriosus), which is very common in early preemies. I’m going to explain it from memory, and some of you medical folks can laugh at my explanation if it’s a little off: a duct on both sides of the heart (lung side and body side) closes naturally when a baby is born just a few days after birth. In preemies, it often doesn’t close on its own and can potentially present problems in regulating blood flow, blood pressure, oxygen, etc. Danielle’s PDA seems to be most severe, and very likely caused her bleeding episode(s) the other day. Unless it closed on its own in the last couple of days, she will probably require a short routine surgery either today or tomorrow in which (again, the layman’s explanation) a doctor would cut a small incision and take some tweezers (not the medical term) and pinch the two sides of the valve shut. The results are then immediately seen. We look forward to seeing this happen with Danielle. Fortunately, with the other three, Emily’s closed after she was given medication, Benjamin’s may not be enough to even mess with, and Casey’s stats are so good that they said there’s no reason to even check to see whether he has it or not. Other than that, the babies all seem to be holding their own, and all four have had a really good couple of days. The nurses and doctors in the NICU are great. It’s clear that it takes a very special type of person to work in the NICU—and I have to think that it would be |