On July 6th, our little princess turned 3! She was soooo excited about her birthday that I'm surprised she slept the night before. After she woke up in the morning, she got to open her gifts from us. She got the Bullseye character from Toy Story that she has been asking for since Christmas and boy was she happy!! She also got the game Candy Land and a new alarm clock that looks like a monkey. She did a great job opening the gifts all by herself. After presents, we went out to lunch at Billy McHale's and they put Hailey's name on their train that goes around the restaurant. Every time that train went by, she would point up to her name with excitement! She also got a huge ice cream sundae as a birthday treat.
After lunch, it was time to enjoy the sunny day by doing some splashing at the splash park. It took Hailey a little bit to feel comfortable playing in the water (there were tons of other kids there), but after she warmed up, she enjoyed herself although she still stayed close to us. then it was home for naps, and Jeff had to head to work. After dinner, I took Hailey down to the toy store to pick out a birthday toy. This toy store sent Hailey $2.00 in birthday bucks to spend so I told her she could pick out anything she wanted. What did she pick? She went straight for the .99 cent table and picked out 2 princess figures. Since they were so cheap, I told her she could get 2 more of them, so she picked out Belle, Ariel, Snow White and Cinderella. I even tried to get her to pick out something more expensive, but she wanted those princesses so badly. They were a great pick too, because she hasn't put them down yet.
We are doing a family and friend birthday party this weekend at Whatcom Falls Park, it should be a good time!
Saturday, July 9, 2011
Tuesday, July 5, 2011
1st visit with Children's
What a long day! Jeff, my mom and I all worked graveyard on the 4th of July, and got just a couple hours of sleep before heading down to Seattle to meet with some doctors from Children's Hospital. We started off with an ultrasound that lasted over an hour. The room we were in was SO warm and the lights were dim, we were all struggling to stay awake. It didn't help that the ultrasound tech wasn't very talkative, so we had no idea what we were seeing on the screen most of the time. The tech took all of Madeline's measurements to make sure she is growing and gaining weight. Which she is, so that is great news.
Next, we met with Edith Cheng, who is the Director of the Prenatal Genetics Program. She went over some basic information regarding Gastroschisis and what to expect with upcoming appointments, and what would happen in the event that I went in to labor early. Shortly in to our meeting, a pediatric surgeon joined us and went through a power point of what we can expect with pregnancy, labor, delivery, and surgery. He also explained different levels of Gastroschisis (simple and complex), and the different surgery options that will be considered. Basically, we won't know until Madeline gets here if she will need surgery right away or not. It all depends on how much of the bowel is outside the body and what condition it is in. The surgeon said that Madeline will most likely have to stay at Children's for 2 months, possibly up to 4 months, depending on how she responds to surgery and how quickly she learns to eat and gain weight.
Our next ultrasound will be at our OB's office in Bellingham in about 4 weeks, and they will take more measurements of Madeline, and then send them to UW and Children's. We will meet with doctors at the UW in late August for another ultrasound.
Overall, we learned a lot, but there are still so many unanswered questions that can't be answered until Madeline arrives. So we will continue to wait!
Hailey is finally feeling better, and we can't believe that she is turning 3 tomorrow! Where has the time gone? She is such an amazing little girl and she continues to surprise us each day with her knowledge and humor. Life is good!
Next, we met with Edith Cheng, who is the Director of the Prenatal Genetics Program. She went over some basic information regarding Gastroschisis and what to expect with upcoming appointments, and what would happen in the event that I went in to labor early. Shortly in to our meeting, a pediatric surgeon joined us and went through a power point of what we can expect with pregnancy, labor, delivery, and surgery. He also explained different levels of Gastroschisis (simple and complex), and the different surgery options that will be considered. Basically, we won't know until Madeline gets here if she will need surgery right away or not. It all depends on how much of the bowel is outside the body and what condition it is in. The surgeon said that Madeline will most likely have to stay at Children's for 2 months, possibly up to 4 months, depending on how she responds to surgery and how quickly she learns to eat and gain weight.
Our next ultrasound will be at our OB's office in Bellingham in about 4 weeks, and they will take more measurements of Madeline, and then send them to UW and Children's. We will meet with doctors at the UW in late August for another ultrasound.
Overall, we learned a lot, but there are still so many unanswered questions that can't be answered until Madeline arrives. So we will continue to wait!
Hailey is finally feeling better, and we can't believe that she is turning 3 tomorrow! Where has the time gone? She is such an amazing little girl and she continues to surprise us each day with her knowledge and humor. Life is good!
Our first trip to the ER
It started last Tuesday when I picked up Hailey from Preschool. She looked really sad and cried when she saw me, which was unusual. The staff said she had been complaining of her head hurting. When we got home we took her temp and it was 101 F. No wonder her head hurt! So we gave her Ibprophen and figured she would be fine by the next day. The fever continued to linger, but we were able to keep it down with Ibprophen. By Friday, her fever had gotten up to 103 F, so I made an appt. to have her looked at. At the doctor's office they checked her over and collected a urine sample (which was really fun), and said that she probably had a viral infection.
On Saturday, Hailey woke up screaming at 6am, which is not normal. She was SO hot but strangely not sweating at all. Jeff checked her temperature and it was 104 F, and Hailey seemed totally out of it. I called my mom at work for her opinion. She suggested going to the ER, which is what I thought, but I didn't want to overreact. So we quickly loaded up and flew to the ER. There were some shady characters in the ER, but it was quieter then expected. They got Hailey checked out quickly, and gave her Ibprophen. Then we took a seat and waited to be called back. After about 30 minutes, they called us back to the exam area. We had to wait another good 30 minutes before we saw the doctor, but in the meantime, Hailey made friends with her nurse named Lucy. Hailey asked her lots of questions about her cats, who her cousins are, and even got to play with her stethoscope. Finally the doctor came in, and Hailey told him she was hungry and wanted cereal. He asked her what her favorite cereal was and she said "Raisin Bran!" It was really cute, and I was so glad she didn't say "marshmallow cereal" which she gets occasionally! The doctor took one look in her throat, and said "Wow." Then he had her open so we could see her throat, and it was so swollen and red, and covered in white sores. Which can signify strep throat. The doctor said he wasn't going to test her for strep, because the results are often inconclusive, and that regardless of the results, he was going to put her on antibiotics. Poor Hailey! We couldn't believe after seeing her throat that she never once complained about it. So after 4 hours at the ER, we went home and Hailey ate some otter pops, then it was nap time for all of us. Poor Jeff had only slept for 2.5 hours, as he worked the night before.
It was hard to spend the sunny 4th of July weekend holed up inside, but Hailey's fever was still coming and going, so we laid around and watched Snow White and Toy Story 3. She is finally starting to feel better, but is still taking Ibprophen every 6 hours to control her fever.
Hopefully she is feeling 100% by Wednesday, her 3rd birthday!
On Saturday, Hailey woke up screaming at 6am, which is not normal. She was SO hot but strangely not sweating at all. Jeff checked her temperature and it was 104 F, and Hailey seemed totally out of it. I called my mom at work for her opinion. She suggested going to the ER, which is what I thought, but I didn't want to overreact. So we quickly loaded up and flew to the ER. There were some shady characters in the ER, but it was quieter then expected. They got Hailey checked out quickly, and gave her Ibprophen. Then we took a seat and waited to be called back. After about 30 minutes, they called us back to the exam area. We had to wait another good 30 minutes before we saw the doctor, but in the meantime, Hailey made friends with her nurse named Lucy. Hailey asked her lots of questions about her cats, who her cousins are, and even got to play with her stethoscope. Finally the doctor came in, and Hailey told him she was hungry and wanted cereal. He asked her what her favorite cereal was and she said "Raisin Bran!" It was really cute, and I was so glad she didn't say "marshmallow cereal" which she gets occasionally! The doctor took one look in her throat, and said "Wow." Then he had her open so we could see her throat, and it was so swollen and red, and covered in white sores. Which can signify strep throat. The doctor said he wasn't going to test her for strep, because the results are often inconclusive, and that regardless of the results, he was going to put her on antibiotics. Poor Hailey! We couldn't believe after seeing her throat that she never once complained about it. So after 4 hours at the ER, we went home and Hailey ate some otter pops, then it was nap time for all of us. Poor Jeff had only slept for 2.5 hours, as he worked the night before.
It was hard to spend the sunny 4th of July weekend holed up inside, but Hailey's fever was still coming and going, so we laid around and watched Snow White and Toy Story 3. She is finally starting to feel better, but is still taking Ibprophen every 6 hours to control her fever.
Hopefully she is feeling 100% by Wednesday, her 3rd birthday!
Tuesday, June 28, 2011
Her name is....
We chose the name Madeline for our little princess. We originally thought her middle name would be the same as mine (Renee), but I wasn't dead set on it. Then one day Hailey randomly said that Madeline's middle name should be Belle (from Beauty and the Beast). I laughed about it and thought it was cute, but after some deeper thought and help from my friend Michelle, We realized how beautiful the name is, and it makes it so much more special that Hailey helped pick out her name. We can't wait to meet our little Maddy Belle!
Zoo trip
On Monday we went to the Zoo. We were hoping it was going to be hot, but we settled for it being warm with a few sprinkles here and there. On the way home, we stopped at Babies R Us and shopped around for things. Hailey picked out a little pink doggy for her sister...although she has been sleeping it with it since we bought it so I'm not sure it will end up being the baby's afterall. Then we headed over to Buca Di Beppo for dinner. It was such a fun family day.
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| She LOVES this fox! |
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| Hailey liked petting the goats. |
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| Our beautiful almost 3 year old! |
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| We got to feed an elephant named Chai. Hailey thought it was really cool! |
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| 22 weeks and feeling huge! |
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| Hailey always loves feeding these birds, thankfully they were hungry today! |
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| Could she be any cuter?! |
Wednesday, June 15, 2011
UW visit #1
So on June 6, we headed to UW for our first appt. We were nervous and didn't really know what to expect, but we were hopeful that we would get our questions answered. We started out with an appt. with a Genetic Counselor, which is normal when a baby has a birth defect. She told us what we already knew, that Gastroschisis is not a genetic disorder, and it is a rare occurrence which isn't known to have a cause. She also went over our family tree and medical history.
Next up was the in depth ultrasound. Our doctor had told us that UW has the best ultrasound technology, which made us feel more confident that we were getting the best care possible. Our ultrasound lasted about an hour, and our ultrasound tech was absolutely great. She didn't skirt around the reason we were getting an ultrasound, she was very upfront about what she was doing and looking for, which I really appreciated. She told us that we were only the 3rd people to have this particular ultrasound done, which focused on taking lots of measurements of the baby's tummy and bowels. She also was able to see and hear the blood flow throughout the baby's body including through the bowels, which is important because if there isn't proper blood flow, the bowels to die.
After the ultrasound, we met with the Perintologist, who went over what Gastroschisis is and what to expect for delivery and after birth...So I have to deliver at UW, and I will need to be induced at 35-37 weeks due to an increased risk of stillbirth in baby's with Gastroschisis. It isn't necessary for me to have a C-section. The doctor explained that there is no increased risk to the baby or I with a vaginal delivery. I was happy to hear this because I didn't want to deal with the recovery time that a C-section would require. After delivery, the baby will be put in to a silo, which is a sterile sack that will cover the lower portion of her body and will keep the bowels clean and sterile. The baby will then be transported to Children's Hospital, which is a couple miles down the road, to be evaluated. They won't know until she gets here if she will require surgery right away or not. But we can expect her to be in the NICU at Children's for 6-12 weeks. Baby's with Gastro are normally on the small side, and then add in inducing 4 weeks early...we are expecting her to be pretty small.
We aren't sure yet of what the housing situation will be after I get discharged from UW. I know there is housing available, but I don't know if or how we qualify for it. That is something we will learn when we meet with Children's. It's going to be a long road, but in the end we hope to be taking home a perfectly healthy baby girl.
Our next appt. will be a Children's Hospital on July 5. We will have another ultrasound, meet with a pediatric surgeon and meet with the program director of the Prenatal Diagnosis and Treatment Program at Children's.
Next up was the in depth ultrasound. Our doctor had told us that UW has the best ultrasound technology, which made us feel more confident that we were getting the best care possible. Our ultrasound lasted about an hour, and our ultrasound tech was absolutely great. She didn't skirt around the reason we were getting an ultrasound, she was very upfront about what she was doing and looking for, which I really appreciated. She told us that we were only the 3rd people to have this particular ultrasound done, which focused on taking lots of measurements of the baby's tummy and bowels. She also was able to see and hear the blood flow throughout the baby's body including through the bowels, which is important because if there isn't proper blood flow, the bowels to die.
After the ultrasound, we met with the Perintologist, who went over what Gastroschisis is and what to expect for delivery and after birth...So I have to deliver at UW, and I will need to be induced at 35-37 weeks due to an increased risk of stillbirth in baby's with Gastroschisis. It isn't necessary for me to have a C-section. The doctor explained that there is no increased risk to the baby or I with a vaginal delivery. I was happy to hear this because I didn't want to deal with the recovery time that a C-section would require. After delivery, the baby will be put in to a silo, which is a sterile sack that will cover the lower portion of her body and will keep the bowels clean and sterile. The baby will then be transported to Children's Hospital, which is a couple miles down the road, to be evaluated. They won't know until she gets here if she will require surgery right away or not. But we can expect her to be in the NICU at Children's for 6-12 weeks. Baby's with Gastro are normally on the small side, and then add in inducing 4 weeks early...we are expecting her to be pretty small.
We aren't sure yet of what the housing situation will be after I get discharged from UW. I know there is housing available, but I don't know if or how we qualify for it. That is something we will learn when we meet with Children's. It's going to be a long road, but in the end we hope to be taking home a perfectly healthy baby girl.
Our next appt. will be a Children's Hospital on July 5. We will have another ultrasound, meet with a pediatric surgeon and meet with the program director of the Prenatal Diagnosis and Treatment Program at Children's.
Monday, June 13, 2011
Ultrasound: 5/31/11...It's a girl!
Finally it was the day for our ultrasound. Hailey had preschool that day so it worked out nicely. We were both really nervous, but also trying to stay positive about the whole situation. I tried to imagine how things our lives would change if we did have a child with a debilitating disability, then I felt guilty for feeling this way. I just went through so many strange and uncomfortable thoughts that I think only happen in situations like this.
Our ultrasound tech told us that she was going to do a thorough check of the baby from head to toe and capture images for the doctor to look over. She told us that the doctor would go over them with us. I know that the ultrasound tech's aren't allowed to tell you if something is wrong, but I was hoping she would tell us that everything looked great during our hour long session. She didn't. I tried analyzing everything she was doing and her facial expressions, but she didn't really give out any cues. I found myself throughout the ultrasound wiping away tears because I think I just knew something wasn't right. She seemed to be focusing a lot around the heart and capturing a bunch of picture of that area, but she wasn't saying a whole lot. That was a huge red flag for me.
However on a positive note before I continue, it was during this ultrasound that we found out that we were having another girl! I was so excited because I really wanted two little girls who could grow up with an amazing friendship.
After the ultrasound, we waited in the exam from for about 30 minutes while the doctor looked over the ultrasound images. Another red flag. When he finally came in, he told us to follow him in to another room. Red flag. He took us in to a room with a computer screen filled with our ultrasound pictures and movies. He started by explaining a little about what AFP levels are and what they are an indication of. I wasn't really listening and was already starting to cry. He said that our daughter didn't have Spina Bifida. Thank God. But she does have a birth defect called Gastroschisis. More tears. He went on to explain that Gastroschisis is when the bowels are on the outside of the body. Sobs. He told us that it isn't known what causes this defect, so it was nothing we did wrong, and it occurs in women under the age of 30. I'm 29. He told us that the baby would need to be delivered at UW, and she would have to stay there for awhile after birth, and that she may require surgery. Hearing all this was just too much. Even though he also explained that this defect is not normally life threatening, I couldn't get my head around any of it. He asked if we had questions, and I couldn't think straight, neither could Jeff. What is there to say? We felt like we had been hit by a truck. He drew us a picture so we could understand a little better, but I wasn't grasping it. I was hearing birth defect, surgery, UW, organs outside of body...
Our doctor brought in a nurse to explain what would happen next. She would refer us to UW and they would call in the next few days to set up an appointment. Okay, now what? More waiting. On the way home from the appt. I called my parents who were vacationing in Italy. It was probably midnight their time, and thankfully my dad answered the phone. I'm not even sure if he knew what I was saying because I was crying so much, he woke up my mom and put her on the phone. Somehow she was able to make out what I was saying and reassured me that everything would be okay. When we got home, I crawled in to our bed and just cried. I felt so helpless knowing that something was wrong with our baby and there was absolutely nothing we could do about it, but wait. It was an awful moment.
I had to return to work the next day, and I knew that I wasn't ready but I didn't want to use a sick day because I felt like I needed to save them all up for when the baby comes. I should have called in sick because I must have cried a handful times, in private. It was awful.
When I got home, I did some research on Gastroschisis and I started to feel a tiny bit better. It really helped talking to Jeff, our families and close friends. It's always nice to hear reassuring words from the people you love.
UW called us 2 days later and set up an appt. for June 7. They told us we would meet with a Genetic counselor, have an in-depth ultrasound and then meet with a Perinatologist, which we learned is a doctor that cares for the mother and baby in a high risk pregnancy.
More waiting, but things were getting easier with each day. It was easier to talk about what we were going through without crying and I was able to see the big picture in that finding out our daughter has Gastroschisis was better then finding out she has Spina Bifida.
Our ultrasound tech told us that she was going to do a thorough check of the baby from head to toe and capture images for the doctor to look over. She told us that the doctor would go over them with us. I know that the ultrasound tech's aren't allowed to tell you if something is wrong, but I was hoping she would tell us that everything looked great during our hour long session. She didn't. I tried analyzing everything she was doing and her facial expressions, but she didn't really give out any cues. I found myself throughout the ultrasound wiping away tears because I think I just knew something wasn't right. She seemed to be focusing a lot around the heart and capturing a bunch of picture of that area, but she wasn't saying a whole lot. That was a huge red flag for me.
However on a positive note before I continue, it was during this ultrasound that we found out that we were having another girl! I was so excited because I really wanted two little girls who could grow up with an amazing friendship.
After the ultrasound, we waited in the exam from for about 30 minutes while the doctor looked over the ultrasound images. Another red flag. When he finally came in, he told us to follow him in to another room. Red flag. He took us in to a room with a computer screen filled with our ultrasound pictures and movies. He started by explaining a little about what AFP levels are and what they are an indication of. I wasn't really listening and was already starting to cry. He said that our daughter didn't have Spina Bifida. Thank God. But she does have a birth defect called Gastroschisis. More tears. He went on to explain that Gastroschisis is when the bowels are on the outside of the body. Sobs. He told us that it isn't known what causes this defect, so it was nothing we did wrong, and it occurs in women under the age of 30. I'm 29. He told us that the baby would need to be delivered at UW, and she would have to stay there for awhile after birth, and that she may require surgery. Hearing all this was just too much. Even though he also explained that this defect is not normally life threatening, I couldn't get my head around any of it. He asked if we had questions, and I couldn't think straight, neither could Jeff. What is there to say? We felt like we had been hit by a truck. He drew us a picture so we could understand a little better, but I wasn't grasping it. I was hearing birth defect, surgery, UW, organs outside of body...
Our doctor brought in a nurse to explain what would happen next. She would refer us to UW and they would call in the next few days to set up an appointment. Okay, now what? More waiting. On the way home from the appt. I called my parents who were vacationing in Italy. It was probably midnight their time, and thankfully my dad answered the phone. I'm not even sure if he knew what I was saying because I was crying so much, he woke up my mom and put her on the phone. Somehow she was able to make out what I was saying and reassured me that everything would be okay. When we got home, I crawled in to our bed and just cried. I felt so helpless knowing that something was wrong with our baby and there was absolutely nothing we could do about it, but wait. It was an awful moment.
I had to return to work the next day, and I knew that I wasn't ready but I didn't want to use a sick day because I felt like I needed to save them all up for when the baby comes. I should have called in sick because I must have cried a handful times, in private. It was awful.
When I got home, I did some research on Gastroschisis and I started to feel a tiny bit better. It really helped talking to Jeff, our families and close friends. It's always nice to hear reassuring words from the people you love.
UW called us 2 days later and set up an appt. for June 7. They told us we would meet with a Genetic counselor, have an in-depth ultrasound and then meet with a Perinatologist, which we learned is a doctor that cares for the mother and baby in a high risk pregnancy.
More waiting, but things were getting easier with each day. It was easier to talk about what we were going through without crying and I was able to see the big picture in that finding out our daughter has Gastroschisis was better then finding out she has Spina Bifida.
Where to start...
I keep going back and forth in my head about whether I wanted to blog about this or not, but I decided that I did because it's part of our pregnancy journey that I want to be able to look back on just as we do with our blog posts about waiting for Hailey to arrive. So here goes...
I had a routine 16 week appt. back in May, which happened to be a day before we went on a 2 week vacation. The doctor couldn't see me because he was delivering a baby, so I left to get a routine blood test. The next day, while enjoying a sunny day on the beach at Deception Pass, I got a phone call from my doctor regarding the results of my blood test. I was immediately concerned because the doctor himself was calling and not the nurse who normally calls. He said that my AFP levels were unusually high, which was concerning because it could indicate there is a neural tube disorder, such as Spina Bifida. My heart sank. He said the only way to find out more was to do an ultrasound. So I tried to schedule an ultrasound as soon as I could, but with our upcoming trip to Winthrop we couldn't make something work before we left, so we had to wait our entire vacation (15 freaking days) until we could get in. I even tried to get one for that day knowing that we would have to pack up everything, but there wasn't an opening.
After hanging up with the doctor, I told Jeff what was going on, and immediately called my mom to figure out exactly what this all meant. Of course I'm crying and assuming the worst because it's just what I do. She didn't know too much about AFP levels but she said she would Google it and see what she could find. At the same time, Jeff called his sister, who works in the medical field, to see what she knew. Thankfully, Hailey was running around playing the entire time, not knowing that anything was going on. So my mom calls back and says that from what she found on the internet, 90% of women whose AFP levels are found to be high, end up having healthy babies. This made me breath a little easier, but Jeff and I were still shaken up, and we couldn't help but worry...I told myself that I wouldn't Google it while we were camping which I did, until I realized that there is WAY too much negative information out there, so I stopped.
We continued on with our camping trip, which was so much fun. We had perfect weather, and enjoyed having the campground all to ourselves. After we got home from camping, my best friend Jen and her son Cal came all the way from Oregon to visit for the weekend! It had been a year since we had seen them, so it was just so great to sit down and have girl talk with my bestie, especially about this baby stuff. After Jen and Cal left, we packed up again and headed over to Winthrop via Highway 2 to meet our friends KC, Jenny and their son Tristen. We had a great week long stay at the cabins at the Sun Mountain Lodge. The kids had a blast playing and the adults had fun catching up. All the while though, I couldn't stop thinking about the ultrasound and I was just anxious to get home so we could find out some more information.
I had a routine 16 week appt. back in May, which happened to be a day before we went on a 2 week vacation. The doctor couldn't see me because he was delivering a baby, so I left to get a routine blood test. The next day, while enjoying a sunny day on the beach at Deception Pass, I got a phone call from my doctor regarding the results of my blood test. I was immediately concerned because the doctor himself was calling and not the nurse who normally calls. He said that my AFP levels were unusually high, which was concerning because it could indicate there is a neural tube disorder, such as Spina Bifida. My heart sank. He said the only way to find out more was to do an ultrasound. So I tried to schedule an ultrasound as soon as I could, but with our upcoming trip to Winthrop we couldn't make something work before we left, so we had to wait our entire vacation (15 freaking days) until we could get in. I even tried to get one for that day knowing that we would have to pack up everything, but there wasn't an opening.
After hanging up with the doctor, I told Jeff what was going on, and immediately called my mom to figure out exactly what this all meant. Of course I'm crying and assuming the worst because it's just what I do. She didn't know too much about AFP levels but she said she would Google it and see what she could find. At the same time, Jeff called his sister, who works in the medical field, to see what she knew. Thankfully, Hailey was running around playing the entire time, not knowing that anything was going on. So my mom calls back and says that from what she found on the internet, 90% of women whose AFP levels are found to be high, end up having healthy babies. This made me breath a little easier, but Jeff and I were still shaken up, and we couldn't help but worry...I told myself that I wouldn't Google it while we were camping which I did, until I realized that there is WAY too much negative information out there, so I stopped.
We continued on with our camping trip, which was so much fun. We had perfect weather, and enjoyed having the campground all to ourselves. After we got home from camping, my best friend Jen and her son Cal came all the way from Oregon to visit for the weekend! It had been a year since we had seen them, so it was just so great to sit down and have girl talk with my bestie, especially about this baby stuff. After Jen and Cal left, we packed up again and headed over to Winthrop via Highway 2 to meet our friends KC, Jenny and their son Tristen. We had a great week long stay at the cabins at the Sun Mountain Lodge. The kids had a blast playing and the adults had fun catching up. All the while though, I couldn't stop thinking about the ultrasound and I was just anxious to get home so we could find out some more information.
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