Why does time seem to fly by so fast? Can't it just slow down a bit? I feel like I'm taking so many pictures to capture just every moment, every memory. I'm looking back on all these photos with mixed emotions. Just so happy, and thankful that we are all together, and healthy and able to enjoy these moments, and at the same time remembering what we've been through, and the children who are still fighting, and the children who have lost the fight. It is always on my mind. London's last MRI was this past October 2015. Her MRI looked great!, Her urine markers VMA and HVA were normal! Thank you God! She is doing great! She will be turning 5 next month! Wow! Kindergarten in the fall! I just cant believe it. I am so blessed. There was some conversation as to whether or not we could move London's MRI's out to every year, instead of every 6 months. I received a phone call yesterday from her doctor, explaining that she would like London to have 1 more MRI this spring, before moving out to every year. She explained how London's case is so irregular, not "normal" to what they've seen. So we have scheduled another sedated MRI for this May, and a follow up appointment right after at the Jimmy Fund Clinic with her doctor, and nurse practitioner. I love pictures and will add some below. I know I haven't updated this post since last spring 2015, and I apologize. Over the summer we got to meet up with Team Forward again from the PMC (Pan-Mass Challenge) who ride many, many, many miles to raise funds for cancer research and treatment. A huge Thank you to you all! Heroes! That's what all of you are! It was nice seeing you all again! We also went to the annual Jimmy Fund Festival over the summer, you'll see pictures below of that also. We had a great time! London's oldest brother AJ has been away now for almost a year, serving in the Army, stationed in South Korea. London's brother Cullen is currently serving in the Marines, and stationed in Okinawa Japan. We are so proud of both of you, and we miss you more than anything. London's oldest sister, Jordynn, will be graduating from high school this year! Her other sister, Madison is starting to drive! Nolan (our 11 year old) just made Star rank in boy scouts. We are so proud of you all! Like I said time flies. Enjoy each and every day. Each and every moment. Today is a blessing from God. A gift. That's why its called the "present". God Bless.
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London had her MRI on April 6th. It was a Monday, the day after Easter. Following her MRI, we had a follow up appointment at the Jimmy Fund. We were told her scans looked great! Her blood work was normal. She has been just doing great! We went home and resumed living life. Have you ever gotten a feeling that something is off? About midweek, I'm not sure why,( I call it mothers intuition) I started to think about her urine test. Now I don't know why I thought of this because all along even when we knew there was active neurobalstoma, London's urine markers, HVA and VMA,(what they test her urine for) have always been normal. Our home phone rang about 3pm on Friday April 10th. It was London's nurse practitioner telling me that we needed to talk about London's urine test. She told me her HVA was elevated to 49. Normal value for London would be 0-22 ratio. London's VMA was normal. I knew what this test result could mean. HVA and VMA are diagnostic indicators for neuroblastoma. Neuroblastoma cells secrete these proteins, aka catecholamines and end up being excreted by the kidneys into the urine. I felt my whole body begin to shake, I was having difficulty taking a breath. London's RNP told me we would start by repeating the test in a few weeks. She told me that certain amounts of foods in high doses could potentially raise a catecholamine in the urine. She also told me that normally neuroblastoma will come back where it was prior and London's scans looked great. She gave me a list of foods to avoid for a few days prior to London's next urine test. After hanging up, I also did my own research. The scary thing, the pessimist in me, kept thinking back to the statistic that if neuroblastoma is going to come back, it mainly comes back within 2 years. London will be 2 years at the end of this May. I also knew that chemo would no longer be an option. That these cells build up a cell wall of resistance to any chemo in the future. I was starting to panic. I looked at London, who had no idea any of this was going on, just happily playing with her brother and sisters without a care in the world, and it hit me. This is not in my hands. I am not in control. I write in a journal every time London has some sort of medical test/exam, to keep track of dates, results, future plans. I also write some spiritual notes in a different section. Words that give me peace. On one page I had written in big letters, Trust In GOD. That was what I needed to know, what I needed to do. And the phrase Jesus speaks, " Remember, I am always with you". That always gave me peace. On the same page, the last thing I had written was from Proverbs 3: 5-6 " Trust in the Lord with all your heart and lean not on your own understanding, in all your ways acknowledge him, and he shall direct your paths". This is not an easy thing to do, to just give it over to GOD. To let go. I started asking for GODs peace. I was able to let go of my fear. I started having faith that no matter what, London would be just fine. I honestly believed this. I felt a peace come over me. I continued to thank GOD daily for her healing. I prayed for her urine to be normal. We were lucky to have planned a family vacation to Disney the following week. This allowed us to keep our mind off of the future testing date. We were very busy in Florida and had a lot of fun. We also celebrated London's 4th birthday there! When we returned, London was to have her re-test of her urine. This was Thursday, April 30th back up at the Jimmy Fund. It would be another few days until the results were back. We were told most likely Monday the 4th. Over the weekend I came upon a short story someone had written about how powerful prayer can be, and to be very specific for what you are asking GOD for. I also remembered reading in the bible and hearing that when more than one are gathered in Jesus' name, he is there. All of my family and myself had been praying non-stop. But I thought to myself, I'm going to do this right now. It's Sunday night, her results might be back tomorrow, I'm going to get up, get all my kids and do this. So Sunday night, I got everyone up, all at the same time, with the same prayer (being very specific that London's urine test come back normal) prayed together out loud. We believed. We had faith. The next morning my phone rang around 9am. It was London's nurse practitioner, calling me as soon as she got the results, that London's urine came back NORMAL!!!!!! I just dropped to my knees. Praising GOD, Thanking GOD. I cried and cried. I was still crying as I called my husband at work to tell him the incredible news. I sent my daughter a text message in school to let her know. She texted me back, " it worked mom!" Was this just some fluke thing? Was there more to this than coincidence? I don't know. What I do know with all my heart is prayer works. GOD doesn't give us all the understanding of this world. This was another reminder, another lesson on faith, and the power of prayer. London will go back again in 6 months for another MRI and labs. Then from there we are planning to move to yearly MRI's! Thank you GOD!
London had her MRI on Thursday, October 16th. She did wonderful! I want to jump right ahead and tell you her MRI "looks great!" Praise to you GOD! They did a scan of her neck and spine. Her previous MRI had shown some "fatty tissue" or "scar tissue" on the spine at the site of T11. Now that is totally gone also. They think that was how the bone was healing. The day of her MRI she was prepared. She new where she was going and why. She was ok with it. She was debating on the car ride up if she wanted the "pinch" to make her fall asleep and wake up with goofy legs- as she says, or "the mask". She is extremely smart. I really can't get too much past her. She had decided on the mask. So I was surprised when she was asked what she wanted, she told them the pinch. She was very brave. London's favorite thing to play right now is Nurse Nancy. When London was in the hospital a while back, my mother gave London a book that was around when she was young. The title was from a Golden Book, Nurse Nancy. So we have read this, and re-read this quite a few times. London picked up on the idea of the book, and takes care of all her dolls putting bandages on, using her stethoscope, checking blood pressures. She loves it! Since London's middle name is Nancy(after her great grandmother), we started calling her nurse Nancy at home. I had told one of the nurses this over the phone. So the day of the MRI we come walking in and they say, " Well, this must be Nurse Nancy". She was so happy! A huge smile spread over her face, she just lit up. She took the doctors blood pressure. She helped with her "pinch". She was awesome! She had her urine tested for the neuroblastoma protein markers, and her blood work done. Her white blood cells and her anc (absolute neutrophil count) were on the low side. They said it was just under normal but on the low side and they were not concerned, and would continue to monitor her. The plan again is to have another MRI and be seen in 6 months, which should bring us around the month of April(when London will be turning 4!!! I can't believe it!). We all enjoyed our summer, and are now enjoying the cool fall days. We were lucky to get to meet up with Team Forward (formerly Team Scorpion) from the PMC. A gigantic, huge Thank You to all of you. Raising money and riding all of those (many, many, many...)miles (sometimes in the rain) to find a cure. You are our heroes. Another Thank You to Pink Heals. Thank You for coming to our home to surprise London. It was just so heartfelt and we greatly appreciated it. London loves to take walks still up the road to "feed her friends" the horses, and see "her friends" the cows. She is a huge animal lover. We visit the zoo where her best animal friend lives... Kate the elephant. A funny story recently. My oldest son played the trumpet in middle school. It has now been passed down to my youngest son(now in middle school). One morning Nolan said to me, " Mom, I taught London how to play the trumpet". I told him wow, great job, and went on with whatever I was doing. The next thing I hear is music -trumpet music, being blasted down the hallway. London is actually playing the trumpet! Not just making sounds, but holding a note, and playing actual notes Nolan taught her! She told me it sounds like Kate. She wants to bring the trumpet to the zoo to play for Kate. (We will most likely be kicked out!). So far when we go to the zoo, Nolan is in school with the trumpet (luckily). I could go on and on about her. We are just all so amazed. So grateful to GOD for her healing and for giving us all of our children. What a miracle these children really are. I am not so good with electronics. Her new biggest thing is she wants to be on TV. Inside she tells me one of her cartoons she watches. Jake and the Never Land Pirates to be specific. I tell her we will see. For now I have a recording of her singing one of her many made up songs about her love for her family. I will try to attach it on here somehow. If I can't I apologize in advance. Thank you for your prayers and checking in on London and our family. Please continue with your prayers for London. Pray for a cure. There are so many babies fighting this neuroblastoma, fighting for their life here on this earth first. If you are reading this because you found this site because your child or someone you know has been diagnosed with neuroblastoma know that prayer does work. When London was first diagnosed I would spend nights on my computer searching and reading through other children's sites. There were stories of such incredible strength, and faith and hope. It was very humbling. Your whole life changes. The way you look at life changes. I know I say this often and it is easy with the everyday things in life to become side- tracked, but Every Day Is a Gift. Its true. GOD does not promise any of us a tomorrow. Make the most of your day Today. Live. Have Faith. Believe. Be Thankful for everything GOD has given you. I will end this note with a passage from the bible that I find comfort in. Be humble in the presence of GOD's mighty power, and he will honor you when the time comes. GOD cares for you, so turn all your worries over to him. 1 Peter 5:6-7 and remember Jesus heals. * I think I figured out the video .... check out the last picture box on this page London had her MRI on April 26th, just a few days after she turned 3. Can you believe she is already 3?!!! The time goes too fast. She had an MRI of her neck and spine. She did pretty well this time with her anxiety. She was so brave! She let the nurse take her vitals, and she changed into her pj's herself. She didn't need anything to calm her down either, which was great. She got her IV("the pinch" as London calls it) after she was asleep(sedated). In the post-op she recovered quite quickly and by the time we arrived back at home she was running around her normal self again. For the past few months in between the last MRI and this one, London's been pretty healthy. She continues to amaze me. She's so smart and just loves being with her family and her friends. She makes us all laugh the things she does and says. Just the other day she was asking her daddy if he was going to come to her wedding. When he replied "of course London, who are you going to marry", she blurts out Harry Styles from 1 Direction, then continues to discuss what she is going to wear and the white dress that Harry will also be wearing. She is at that age now where she wants to dress herself and refuses to be persuaded. So the bright orange shorts, 3 shirts, rain boots, and headbands is how we go out(even when it is still cold....where are you spring?).Her f/u appt to go over the results and a check-up were 2 days later on Monday April 28th. We were told the MRI looks great! They don't see anything on her neck(cervical), and on the T11 site(spine-thoracic) it showed fatty tissue, which we were told is consistent to post chemo, and was normal! I feel like the luckiest person in the world. I have faith and know that Jesus healed her. I feel so blessed, so grateful. I look at her every morning and just thank GOD over and over for healing her. For giving us her and all of our children. What a true miracle. We got some other good news too. London will be 1 year cancer free as of May 30th. They are going to count this MRI as her year, and move her to a schedule of every 6 month MRI's instead of every 3 months. So London won't have to go back until October! We thank GOD for our blessings, and continue to pray for a cure. Please send your prayers and praise up above for London and all the other children battling this. Prayer works. Jesus heals. I want to put in a note here to Team Scorpion, who ride many, many(many) miles on bikes and raise money for pediatric cancer research. I was reading in one of my magazines the other day a quote, and as I read it, I thought of all of you guys. The quote said," Be someone who makes someone else look forward to tomorrow". You guys not only do this, but you raise money for a cure so that there is a tomorrow. Thank You in advance. We look forward to seeing you all again this summer. Yesterday London went for her MRI. Our arrival time was 6:15am in the morning. So we were up and getting ready very early. I am happy for this time because we get in first. There are so many kids in our family, that someone is always at some point or other at a doctors appt. So I let London know in advance that tomorrow would be her "turn". She didn't really seem to mind then. Driving in to the city(the following morning), it was still dark out but she knew exactly where she was going, and started screaming. She has a horrific fear of the hospital. So needless to say, by the time we got her into the building and into the MRI dept, she was extremely distraught. Mad at me even. She would not let anyone come near her. They gave her a sedative called Ketamine, which totally calmed her down. but almost to a point of sedation. Giving her this was my decision and I feel bad having to give her this to calm down, but at the same time, which is worse? To see her so distraught(to the point of dry heaving) or medicating her? The MRI was shorter than I expected because normally they do spine, neck and abdomen. This time it was just spine and neck. From there she went into PACU(recovery). Two of my other children were with me, Jordynn(London's oldest sister) and Nolan. I think this is the first time that Nolan has come into the PACU with me. London was hooked up to a breathing tube/mask, had leads on(monitor heart), IV tubes in her hand. While this is all normal and expected, I was in such a rush to go and see her, that it didn't occur to me at the time how Nolan would see his sister. I could tell by his face he was a little scared, but he is such a sweet, caring big brother, he went right to her and was rubbing her hand, calling her his silly names he has for her, and when she woke up she was so happy to have him and JoJo(London's name for Jordynn) there. I need to add a note in here, that my other daughter, Madison really wanted to go with us, she never missed one, but I said no because she has a bad cold and I didn't want her out or around immunocompromised children. She understood though. We had an appt in another building @ the Jimmy Fund after that, with London' s oncologist. My kids love it up there, there are wonderful people who work there and volunteer their time. Many activities going on to keep the kids busy and having fun. London just wanted to be out and walking around and playing with all the kids but her balance and strength were not back yet from sedation. She then started vomiting, which continued until about 4pm. Right after that is when she was back to herself, eating, playing and on the run! London's oncologist told us that London's MRI looked great! That it shows the scar tissue healing. We are just so lucky and so thankful. The plan will be again to do another MRI in 3 more months. Meanwhile, we will go back into our comfort zone. Back to "normal" life. Keep praying, and always remembering Each Day Is A Gift. Here is to a Happy and Healthy New Year! We had the honor of meeting Miss Rhode Island in person last night at our house! Jessica Marfeo was crowned Miss Rhode Island 2013, this past June, and recently(this September) represented our state in the 2014 Miss America pageant and was a finalist for 2 Miss America scholarships. Jessica is an inspiration to many. She and London share a common bond. Jessica is a survivor of neuroblastoma. She was diagnosed she told us at the age of 5 years old after a bout with pneumonia. She came to meet London and our family. London got to try on her "princess" crown! Jessica is just a beautiful person inside and out. I can not begin to list all of the things she is involved in. She is so young and is accomplishing so much. She is a junior at URI studying biology and elementary education and pre-med. She told us she is working to earn a masters for physician assistant to specialize in OB-GYN. She volunteers countless hours visiting schools to talk about healthy relationships and anti-bullying. She also spends her time working in a local hospital playroom with the children who are hospitalized and being treated for cancers, on top of being Miss Rhode Island! Congratulations again Jessica! You are amazing! Her story and meeting her, knowing she is a survivor of this horrible cancer has just given our family so much hope, as I'm sure it does to many others who know her. London was still talking about her today, and how she was wearing her crown. I overheard her tonight telling my husband, " Daddy, a princess came to visit me" Jessica if you are reading this, Thank you again for taking the time to come and visit us and share your story. It meant so much. GOD Bless. We received a phone call on Monday, September 16th, letting us know there was an opening in the schedule for an MRI for London for the next day, Tuesday 9/17 @ 10am. We had to cancel the previous one since London was sick, and were put on the schedule for October, and were placed on an opening list pending cancelations. So, we took it. Which to me was a blessing because I had that October date kind of always in the back of my mind, waiting, thinking about it. Now there was no time to think, just go. Get it done with. I thank the good Lord each day for sweet Jesus saving our baby girl. It's the anxiety about going to the hospital. Remembering what London's already been through, and all those other beautiful babies still going through it, or just beginning. London's MRI went well, she was under for about 3 hrs. I had emailed London's doctor that morning to let her know London was called in for an MRI, that there had been an opening in the schedule, and that I would make an appt to see her the following week. She emailed me back the next day, " MRI looks Great! See you next week". Thank you Dear GOD! London's appt was on Thurs 9/26. She is almost 3 ft tall now, and her weight is up to 12.7kg(which is almost 28lbs - I think). They checked her labs, and took urine again to check for those proteins neuroblastomas can excrete in the urine. Developmentally she is doing great! So smart! Very proud mom! We were told MRI looks great, the same as it looked post chemo(scar tissue). London will go again for another MRI and f/u appt either end of Dec or beginning January. London's hair is growing in more thickly now. I am still hoping for curls to return, although her hair is growing in lighter than it had been. Very cute! You will see in the picture. London continues on her medicine 3x's a week because her immune system is still not back to "normal". She will do this through November. Then we are behind on some 2 yr old vaccines, we will see her pediatrician to get them and get caught up. London will also need to get her flu shot, as well as everyone in the house(the shot, not the one that is squirted in your nose), and anyone else who has direct contact with London frequently. She is at a higher risk of contracting. She did have the influenza virus back in May of this year(we were in hospital). We are hoping it will pass by us this year. So we are enjoying the days, the beautiful weather! Remembering how fragile life is and how fast time goes by, taking every day with meaning, appreciating the moments. There was a calendar recently put out by another pediatric cancer hospital and on the cover is a picture of a beautiful little girl, her name is Azalee. Anyone who is reading this please keep her also in your prayers. She is currently battling neuroblastoma for the 2nd time. Pray for her and her family. Send praise up to GOD for London. We are just so lucky. So blessed. Thank you sweet Jesus for healing London Nancy. Has it been 3 months already? Time seems to be flying by. I wish it would slow down a bit. I look back to old pictures on this site and London is changing. She looks more like a little girl and not a baby. How sad, yet how wonderful! London is doing great! We are all enjoying our summer. The kids start back to school next week. Some of them are thrilled about this, and some are not! London was scheduled for her MRI last week, which had to be postponed due to a bad cough she had that actually went through the family and lasted a little more than 3 weeks. London has to be sedated for her MRI(so she remains still for the pictures) and her MRI's last for about 3 hours. It was not worth the risk. So her new date for her MRI is early October. Then the following week, she will be seen again by her doctor. I had been waiting to update after her MRI, but since it was postponed, I wanted to give everyone an update on her and some things we did this summer. Health wise, London's cough has resolved, she is eating well, gaining weight, growing taller, running around like any other 2 year old. Which we are just so lucky and so grateful for. Her hair is starting to come back in, although it is much lighter- as you'll see in some of her recent pictures(I am still keeping my fingers crossed for her curls). I continue to thank GOD everyday for London's healing. Cancer can change you, it can make you feel alienated, but it also makes you appreciate things that were previously taken for granted. Life has new meaning to it. Everyday is a blessing. This summer we were lucky enough to meet an amazing group of guys who form a team called Team Scorpion for the Pan Mass Challenge. This team consists of 8 guys who raise thousands of dollars to support pediatric cancer research through Dana Farber and the Jimmy Fund. These men rode bicycles for London. London was their pedal partner. We met up with them midway at a break spot. There were activities, music and food. We took pictures with them(see below). All the children who were matched with a pedal partner had their picture taken a while back, and was then made into posters which were on the side of the road all lined up before the break spot. So riding in, you see all these beautiful little sweet faces, who these wonderful people are riding for. My husband got out of the car to take a picture of London's poster on the side of the road, it was actually taken at the Jimmy Fund before she started her treatment. Thank you again Team Scorpion(Jim, Tom, Scott, Jason, Don, John, Mark, and Paul) for helping to save children's lives! We look foward to seeing you all again next summer. It was so great to meet you all! This summer we also went to the Jimmy Fund Festival. That was such a great event. We all enjoyed ourselves. We met other families with children who were either starting treatment, or who have finished. It makes you feel like you are not alone in this. These families are going through something similar, even if it is a different type of cancer, the fear, the hope it is still the same. There were games, and rides and petting zoo's and food and activities for everyone in the family. Her favorite of all was the petting zoo, London is an animal lover or as London says it, " I'm a luva mom". London continues on her Bactrim medication 3x's weekly to prevent a pneumonia from low immune system (post chemo). She will likely be on this through November of this year. She is behind on her 2 year old vaccines. She won't be able to have them until around December. This is all due to post chemo and her immune system. We also want to say a big ThankYou again to Dave and Dan and to your families, to Cal Ripken(West Warwick), our family, friends(old and new), neighbors, to all the people who donated and gave your support for London. Thank you for thinking of London and our family. It was just so heartfelt what you all did. We will never forget it. Londons MRI (test) went well on Tuesday. We were there for most of the day and evening. The scan itself takes about 3 hours to scan her full spine and abdomen, and she had to be sedated for this to remain still. So after the scan, we go to a recovery. She did great. Wednesday, we hung around the house and every time the phone rang, jumped. I could literally feel my heart leap into my throat. I had a good feeling about the test. Still, its the waiting that gets to you. We didn't end up hearing anything on Wednesday, and my good feeling started to become a small knot in my stomach. I knew I was going into the clinic on Thursday to see Londons doctor, labs and possibly the 5th cycle of chemo. Thursday morning we left early for a 9am appt. Londons doctor and nurse practitioner met with us and went over the results. Londons MRI images came back great!, the only thing they can see is a small area on her thoracic part of the spine(this is where the biopsy was done and showed active neuroblastoma), that looks like scar tissue! We were told that a lot of research had been done and Londons case was discussed with many physicians(because her case is so different)and stopping the chemo now would be the plan. We were told she would be treated like a baby. (Depending when you present with neuroblastoma, affects how drastically your treatment will be). Also London's pathology of her original tumor- everything you would want to have(chromosomes dividing, 1 mycn amplication, etc)London had, it was considered favorable-and yet we were told it should have not done what it did(metastasized)-this being said, we were reminded that looking back from the previous hospital scans, this was there most likely all along. I trust London's doctor, she is very good. We also trust GOD and prayed that not only for London's complete healing (with a vengeance), but also prayed to guide the doctors to make the right decision. So, I can't begin to tell , you how I felt in that room. I felt overjoyed, shock-that this was over, incredible happiness, so much so I could not stop myself from crying. The tears just kept coming down the whole ride home. We are very grateful to all of you for praying for London, words cannot express how thankful we are for all of you. Last night we celebrated by going to one of Londons favorite places, the beach. Everyone had a great time. London still has some things up the road. She will be going back to the clinic in 3 weeks, London is having recently frequent episodes of complaints of pain in her lower back and both her knees, they think this is from that shot London received while in the hospital to increase her white count, but should be going away. She will also on this day have an echo(heart test-because one of the chemos can affect the heart), and a repeat hearing test. Following this, she will be scheduled, most likely July, for surgery to have her port removed. After all this, London will continue to have every 3 months of MRI's for a year, then decreasing. There is still some discussion on how best to approach London's testing, since everything came back negative except the MRI, there maybe a new machine which scans the whole body. London is still running around being her feisty, happy 2 year old self. If you ask her how she is doing, she'll tell you, " Jesus healed me!". Praise GOD! Our prayers were heard and answered! London came home from the hospital yesterday afternoon(Sunday). She is doing great! While in the hospital, she received a shot called CGSF (neupogen) once daily on Fri, Sat, and then yesterday afternoon before coming home. This shot boosts or stimulates new white blood cell growth in the bone marrow. Saturday her anc(white/neutrophil count) was up from 0 to 300. Sunday it was up to 350. They like to get you over 1000, because some of these cells since they are being stimulated to make them, die off, so sometimes the count will go down after you stop the shot. London's red blood cells were going down, they talked about transfusing, but we held off since she was not acting tired and her heart rate was good. Today London went for labs and we are very happy because her red blood cells went up-so she won't need a blood transfusion, and her ANC is up to 1228!!!!!! Yeah!!! so even if it drops off by 1/2 she will still be above the 500(neutropenic) mark! She is on her way back to recovery! That being said, we received a phone call this morning telling us London's nose swab came back + for influenza B (the flu). This must have started last Monday and it has been a week now and it is almost gone. London did get the flu shot last fall, and I am glad she did or this could have been very bad. She is home now acting like we were never gone and that she was never sick. It amazes me how resilient these kids are!. I am lucky to have help from my husband and family. I wonder how single parents and people with no family manage this. We will go for labs again later this week, and then next week is the big MRI. Thankyou everyone for your prayers and concern. Please continue with them- your prayers are working!! |
AuthorKerri and Aram Hinz, parents of London Nancy Hinz.
March 2016
Categories |
London's Bridge to Recovery
Thankyou to everyone who is taking the time to read about our special baby girl. Please pray for her healing and a long healthy life on this Earth first. Thankyou so much, and GOD Bless.