Our day started out with a Halloween parade at Savannah's school. We got everyone in costume and out the door by 8:45. Quite the accomplishment. Thank goodness daddy was home. Once Savannah's class paraded through the sanctuary and stopped upfront for pictures, I had come to the realization that I have "that kid." Yes, that kid is Miss Grace the child who really doesn't like people. However, when it comes to standing up in front of more than 100 people and pretending to be a 5 year-old (as she did when she just squeezed her way into the line of Savannah's class and stood there like she belonged while all the parents took pictures) Lila Grace is in her element. She smiled and knew that she was getting away with something.
Soon after we headed back home and tried to get a few pictures of the twins before their therapist came. Wouldn't you know that Lila Grace would pose for 100 parents that she doesn't know but wouldn't sit for even a second while smiling when I am behind the camera. So much for the "picture."
After therapy, the girls ate lunch and went down for an early nap while Savannah and I helped one of her friends celebrate her birthday at a local farm. We were exausted when we got home and passed out for a quick power nap. It wasn't long after that we were, getting costumes on, face painting and quickly trying to inhale our dinners. Miss Grace pulled at the stool while I was working on Savannah and said, "Up please." I thought she wanted to watch but then she was doing her Lila jargon and pointing at her cheek. She wasn't going anywhere until she got her face painted too. How is that time races away on a day like Halloween. I tried to plan everything but still felt rushed at dinner time. Thank goodness, Elmo seemed to take the edge off the girls while I was running around and organizing their costumes. Lila and Savannah were very cute all snuggled up watching their show.
The girls had a wonderful time trick-or-treating. I think they were out longer than most of the other kids in our cul-de-sac. It took a little while for them to get the hang of it, as seen in the video, but by the third and fourth time, they were pros. Lila Grace would lead the way up to the door and say, "Trick-or-Treat" while taking as much candy as the adult would allow. Adeline was right there with her and said, "Trick-or-Treat" most time too. Savannah enjoyed going to all of the different houses and soon realized that she was going to bring home a very large amount of candy. The girls took breaks every now and then in their stroller but were on their feet and walking up to houses the majority of the time. There was no fussing, crying or complaining. It was truly a fun-filled family outing. I couldn't be more proud of how they interacted with their neighbors, their display of great manners (please, thank you and bye bye were often heard) and how well the twins caught on to the sequence of trick-or-treating. I love it when my children surprise me.
Off and running
She sees an airplane
Miss Justine had special goldfish for us!!!
Why tear off the wrapper when you bite right trough it?
Savannah and her friends
Can you get your hands on any more things at one time?
Lila was fast asleep in bed. Possibly, Adeline should join her?
Will the sugar high ever end?
Friday, October 31, 2008
Thursday, October 30, 2008
Messy Play
During Adeline's last speech therapy session, she was engaged in messy play. She had finger paints on just about every surface of her and the room. I was please that she was engaged and not distressed. This is a very small step closer to being able to accept the "not so everyday experiences" into her life.
Of course, big sister had blast joining in on the painting. Luckily, little sister was pacified with Elmo in my bedroom or the whole thing would have gotten out of control.
Big sister looks so old in this picture. It was picture day and I had put her hair in hot rollers before she went to school. It didn't stay too well but the body in her hair made her look more grown up than ever.
Of course, big sister had blast joining in on the painting. Luckily, little sister was pacified with Elmo in my bedroom or the whole thing would have gotten out of control.
Big sister looks so old in this picture. It was picture day and I had put her hair in hot rollers before she went to school. It didn't stay too well but the body in her hair made her look more grown up than ever.
Wednesday, October 29, 2008
Third Annual Pumpkin Carving with the Anstines
We just completed our third year of carving pumpkins with the Anstines. The first year our girls were still in the NICU right beside their little girl Charlotte. This year they were all running, jumping and playing around while we tried to discern what shapes they wanted on their pumpkins. Lila Grace tried really hard to like the taste of the pumpkin while Adeline tried to not let the wet stringy pieces force her off my lap. We had a great time and celebrated how lucky we are to have three healthy and thriving girls.
Our first year. . . still in a state of exhaustion and disbelief as our girls have not even made it home yet
Year two. . . happy that all the girls are making tremendous strides in their development
Sunday, October 26, 2008
Guess Where We Went Today
For those of you who are at a loss, we went to Sesame Place. I remember taking Savannah her first time and the excitement that was elicited by merely driving into the parking lot which is adorned with character signs. The same was true for Lila and Adeline. Lila Grace expresses it more energetically, but Adeline was pretty excited as well. If you couldn't gather it from the video clip, Ernie is Lila's favorite! Elmo is a close second and is number one with the other two girls.
Sesame Place was decorated for Halloween. The girls got to go around to different stations and collect various treats. The favorite was the orange Legos that make a pumpkin. We were invited to attend this even by the Variety Charity It is an organization that supports children with disabilities and developmental delays. It was certainly worth the drive. The girls didn't fuss once and we were there for four hours. They were beside themselves as they tried hard to absorb all characters and Sesame stuff. Oddly enough, they sat still for an Elmo Live show, something their oldest sister wouldn't do until she was four.
We saw all of the important characters. The babies did a double take at first but soon it was hard to hold Lila Grace back. She couldn't wait to run up to Ernie and give him loves. She snuggled him and talked to him. It was hard to get her turn around for a picture. She couldn't believe that "her Ernie" was snuggling her. She didn't want to leave him. The same was true for Zoe and, of course, Elmo. Adeline was excited to see the characters from distance. Their fur was a bit much for her. She was happy for me to hold her take her up close and personal but didn't want to touch them herself. Her love for Elmo almost got her over the hump as she walked right up to him. She then suddenly turned to me and said, "up please."
I will post pictures later. We really had a nice day!
Wednesday, October 22, 2008
Through the Eyes of Children
After a rough couple of days I have started to think that this world of prematurity has taken its toll. I feel as though I look at least five years older than when I had the girls, my patience is lessened and I am no certainly no longer the fun and young teacher I was when I got pregnant with the twins (well a few months before). Times have changed and I feel like more of a referee (as my husband put tonight) and a no fun mom. Definitely NOT a young, happy go lucky mom. I don't have the energy to do what I once did and things seem more like a burden than an adventure (yikes, am I really admitting this). It took my neighbor to make a hair appointment for me in order for me to get a hair style (it had been a year) and I am just starting back on the working out which has been neglected for years. Makeup? Isn't that something my girls are supposed to play with when they sneak in my bathroom because it certainly hasn't made it in my hands recently. Clothing, well, in the very few pictures I post of myself on my blog, one can see that it isn't a priority. My point is that I have turned into the frumpy mom. I promised myself I wouldn't but I AM.
Just when I think I have given into the world of frump and frown (isn't that what the not so fun moms did when I was growing up - frown all of the time?) little Abby throws me a rope. On my way to pick up Savannah and her neighborhood friends from art class tonight, Abby and Libby have a discussion about me. "Miss Sara, we don't think you look old enough to be a mom. Libby, doesn't she look so young?" Thankfully Libby agreed. Frown no more. I look too young to have kids!!! Yeah, right us more like it but I will take what I can get from an eight year old!
Just when I think I have given into the world of frump and frown (isn't that what the not so fun moms did when I was growing up - frown all of the time?) little Abby throws me a rope. On my way to pick up Savannah and her neighborhood friends from art class tonight, Abby and Libby have a discussion about me. "Miss Sara, we don't think you look old enough to be a mom. Libby, doesn't she look so young?" Thankfully Libby agreed. Frown no more. I look too young to have kids!!! Yeah, right us more like it but I will take what I can get from an eight year old!
Tuesday, October 21, 2008
Another One of Those Days for Adeline
Today was a terrible day for Miss Belle. During her physical therapy, an orthotist came by to measure her orthotics and stretch her calf and ankles. He was looking for symmetrical range of motion. Of course, Adeline screamed because she hates being manipulated. It is really hard to get a good feel for her range because she fights it so much. The conclusion was that she is tighter on one side. According to her PT, it is slight but the orthotist seemed to think it was significant.
He is a really nice guy but he really needs to watch his delivery. After stretching her he asks, "What is the diagnosis?" I just want to scream - THERE IS NO DIAGNOSIS!!! Do people not get there she can be delayed without a syndrome or a condition? It told him she was a preemie and he said, "That's it?" I am sitting there wondering, does she really look that bad? Does she stand out like a sore thumb? We don't get "the look" from people in public (at least not any more because there isn't a cannula taped to her face). How does someone who doesn't know her presume that there is no chance of normal?
The orthotist made the recommendation that we start stretching her at night in order to loosen her up. Thus, she will wear braces that go up to her knees and hold her ankles static (most preferable beyond 90 degrees). Joy oh joy. She is really going to like this! What is even better is that he had to cast each of her legs to fit her for the braces. Well, as you can imagine, having a cast put on her legs while they are bent in an uncomfortable position (let's not even go into the sensory component) made her irate. She was crying so hard that he she wasn't keeping her sats. It was beyond anything I have experienced in some time. I was the lucky one holding her in my lap. It was truly miserable and brought me right back to the NICU and past hospitalizations. There have been so many times where I have held her down for terrifying and painful procedures. It was much easier when she was little (never easy but not nearly as hard as today) because I didn't see the shear terror in her eyes piercing my own.
It is times like this that I want to scoop her up and run away. Enough is enough. It seems like positive yardage always presents us with a new problem. For example, she is walking very well now and able to use both legs with symmetry. It took a long time for her to accomplish this. Shouldn't this mean the intervention backs down? Not in Adeline's case. Because with walking behind us we are now focused on tone and her latest trick, toe walking. We always seem to ramp it up. Here we go gain. New orthotics during the day and stretching braces at night. When will it end for my sweet girl?
This miserable hour during our morning set the tone for the rest of the day. She has been quite miserable for the past couple of days (most likley the result of a flu shot) so this morning was like a double does of hysterics. We went to Hippotherapy tonight and had to cut it short because she was a blubbering mess. It is the first time I have every seen her come running to me in tears. Usually, she finds her bunny and waits for me to come to her. She was so upset when she turned the corner and saw me waiting for her. I hope this doesn't screw up Hippotheraphy. Once something rubs her the wrong way, it takes a long time to get her going on it again.
He is a really nice guy but he really needs to watch his delivery. After stretching her he asks, "What is the diagnosis?" I just want to scream - THERE IS NO DIAGNOSIS!!! Do people not get there she can be delayed without a syndrome or a condition? It told him she was a preemie and he said, "That's it?" I am sitting there wondering, does she really look that bad? Does she stand out like a sore thumb? We don't get "the look" from people in public (at least not any more because there isn't a cannula taped to her face). How does someone who doesn't know her presume that there is no chance of normal?
The orthotist made the recommendation that we start stretching her at night in order to loosen her up. Thus, she will wear braces that go up to her knees and hold her ankles static (most preferable beyond 90 degrees). Joy oh joy. She is really going to like this! What is even better is that he had to cast each of her legs to fit her for the braces. Well, as you can imagine, having a cast put on her legs while they are bent in an uncomfortable position (let's not even go into the sensory component) made her irate. She was crying so hard that he she wasn't keeping her sats. It was beyond anything I have experienced in some time. I was the lucky one holding her in my lap. It was truly miserable and brought me right back to the NICU and past hospitalizations. There have been so many times where I have held her down for terrifying and painful procedures. It was much easier when she was little (never easy but not nearly as hard as today) because I didn't see the shear terror in her eyes piercing my own.
It is times like this that I want to scoop her up and run away. Enough is enough. It seems like positive yardage always presents us with a new problem. For example, she is walking very well now and able to use both legs with symmetry. It took a long time for her to accomplish this. Shouldn't this mean the intervention backs down? Not in Adeline's case. Because with walking behind us we are now focused on tone and her latest trick, toe walking. We always seem to ramp it up. Here we go gain. New orthotics during the day and stretching braces at night. When will it end for my sweet girl?
This miserable hour during our morning set the tone for the rest of the day. She has been quite miserable for the past couple of days (most likley the result of a flu shot) so this morning was like a double does of hysterics. We went to Hippotherapy tonight and had to cut it short because she was a blubbering mess. It is the first time I have every seen her come running to me in tears. Usually, she finds her bunny and waits for me to come to her. She was so upset when she turned the corner and saw me waiting for her. I hope this doesn't screw up Hippotheraphy. Once something rubs her the wrong way, it takes a long time to get her going on it again.
Sunday, October 19, 2008
Tyler Arboretum
This post is very overdue and would have been skipped had I not recently come across these crazy pictures of my very CRAZY Lila Grace.
We had to opportunity to see a tree house display at our local arboretum about a month ago. The weather was wonderful, daddy was home and the Anstines were able to join us. The girls had fun running around in large open spaces, Alex and I enjoyed nurturing our need for outdoor time and Savannah had fun examining the tree houses paying careful attention to the details. Our favorite was the last tree house which had bells attached to ropes that the kids could pull.
Here are some pictures from the trip. Check out Lila Grace when she comes down the slide of a tree house.
We had to opportunity to see a tree house display at our local arboretum about a month ago. The weather was wonderful, daddy was home and the Anstines were able to join us. The girls had fun running around in large open spaces, Alex and I enjoyed nurturing our need for outdoor time and Savannah had fun examining the tree houses paying careful attention to the details. Our favorite was the last tree house which had bells attached to ropes that the kids could pull.
Here are some pictures from the trip. Check out Lila Grace when she comes down the slide of a tree house.
Saturday, October 18, 2008
Friday, October 17, 2008
Hippotherapy
Adeline started Hippotherapy last week. This involves riding a horse (full size) while a lead walks the horse around the rink and physical therapist positions Adeline. It sounds rather simple and at first I asked myself, "Is this just a trend?" but once seeing it - I BELIEVE. I was in awe of how right it seemed for Adeline. These horses are so docile that they allow the kids to snuggle in. Of course that is the last thing Adeline wanted to do to a horse's head considering the head is bigger than her body and very hairy. She must might be the smallest kid they have had up on a horse (they start at age two). It almost seems like these horses are rooting for the kids they carry.
The biggest struggle for Adeline was the helmet. Not a surprise considering a lot sensory issues stem from her head. She growled and eventually screamed when Miss Alana was trying to get the helmet on. I told her to go ahead and shove it on because Adeline is never going to just allow it. She did and there were screams but the screams disappeared the minute the horse started moving. All the sudden the disorganized and very stressed little girl was quiet, focused and working more muscles than she knew she had. There is something about watching your tiny 20 pound child on top of a horse that makes you realize how physically demanding it is for her to counter the horse's movements in order to maintain balance.
Once she was settled I left the rink and went into the observation room. As I watched from a distance, tears filled my eyes. Here is my sweet Adeline sitting on a horse, which she would never want to be around if she had a say, cooperating, and suckering those around into loving her. The women who were working with her couldn't get enough of her sweet disposition and social smile. Somehow, the horse was symbolic of Adeline's world. So big, scary and constantly moving. And there was my girl going with the flow, working hard to stay afloat and not bothered that she has to work twice as hard as the next kid to find her way in this world. I love her for that! If there is a perfect disposition, she has it - hands down.
Tuesday, October 14, 2008
Drowning in my Kids
I had a conversation with a woman I recently met. She has a son that has issues but does not have a diagnosis. She has put her life on hold and is desperately working with therapists and doctors in order to fully understand his needs. Of course, this bonded us immediately as I feel that I am doing the same thing with Adeline.
She mentioned in an email that I had said, "I am drowning in my kids." I don't remember saying it but when reading her email, the phrase struck me at my core. I am trying everyday to give my children all that they need. Unfortunately, they need more than most children. I end up orchestrating a juggling act between therapy, appointments, therapy centered play, and just enjoying and loving my girls. Drowning is right! As I continue to strive for a balance, I am beginning to realize that balance isn't the answer. It just seems to be the first thing out of everyone's mouth that recognizes the difficulty of our situation. There is always need for more therapy, medical opinions and evaluations. My girls could use a great deal more from me in the therapy centered play and of course, the one that beats me up most at night is the too few moments of just loving my girls. If I really want to balance this, then all areas are going to be cut back. Clearly, there is need for more of each so really what we all need is more daylight hours, patience and money. Daylight hours so that we can squeeze in more play and therapy in one day. As it is, I can barely fit all of their therapists into a week. I find myself ready to sit down and hold and love my girls at 7:45 at night when they are already late for bed. More patience is like stating the obvious. I can only do something for so long without getting annoyed that my child isn't cooperating, or that another child is trying to pull me away from what I am trying to accomplish with her sibling. Finally, more money. Yes, money. There is a need because alternative therapies aren't covered and the top doctors that see special cases like Adeline are often not considered in-network. We just scheduled Adeline to be seen at the Kennedy Krieger Institute where you pay upfront ($1500 that is) and pray that your insurance kicks in retroactively. So no, there is no balance. There is always a need for more and balance isn't the answer. All, balance does for me is find away to fit a little bit of everything into a day. I still go to bed feeling that everything we do is just inadequate. I just can't come up with a "fix."
Ultimately, I am drowning in my kids.
She mentioned in an email that I had said, "I am drowning in my kids." I don't remember saying it but when reading her email, the phrase struck me at my core. I am trying everyday to give my children all that they need. Unfortunately, they need more than most children. I end up orchestrating a juggling act between therapy, appointments, therapy centered play, and just enjoying and loving my girls. Drowning is right! As I continue to strive for a balance, I am beginning to realize that balance isn't the answer. It just seems to be the first thing out of everyone's mouth that recognizes the difficulty of our situation. There is always need for more therapy, medical opinions and evaluations. My girls could use a great deal more from me in the therapy centered play and of course, the one that beats me up most at night is the too few moments of just loving my girls. If I really want to balance this, then all areas are going to be cut back. Clearly, there is need for more of each so really what we all need is more daylight hours, patience and money. Daylight hours so that we can squeeze in more play and therapy in one day. As it is, I can barely fit all of their therapists into a week. I find myself ready to sit down and hold and love my girls at 7:45 at night when they are already late for bed. More patience is like stating the obvious. I can only do something for so long without getting annoyed that my child isn't cooperating, or that another child is trying to pull me away from what I am trying to accomplish with her sibling. Finally, more money. Yes, money. There is a need because alternative therapies aren't covered and the top doctors that see special cases like Adeline are often not considered in-network. We just scheduled Adeline to be seen at the Kennedy Krieger Institute where you pay upfront ($1500 that is) and pray that your insurance kicks in retroactively. So no, there is no balance. There is always a need for more and balance isn't the answer. All, balance does for me is find away to fit a little bit of everything into a day. I still go to bed feeling that everything we do is just inadequate. I just can't come up with a "fix."
Ultimately, I am drowning in my kids.
Saturday, October 11, 2008
Apple Picking
Due to our amazing fall weather, we were able to get out early friday and pick apples at Highland Orchards. Picking apples with three young children is interesting. Lila Grace found one apple on the ground and had to hold it the entire trip. This made it very hard for her to pull an apple off the tree as she needed both hands. It took her a very long time to give up her apple in order to pick another and put it in the bag. Savannah enjoyed herself but was a bit frustrated at first when all the apples were out of reach. Eventually, we found a patch that both she and Lila Grace could reach. Miss Adeline was a completely different story. For her, standing and walking in the orchard grass amongst apples that were rotten was about all she could handle. I would pull a branch out to her that was pretty clear of leaves but she would have nothing to do with picking the apple. Too much to quick.
As for the apples themselves, they were delicious. Savannah and Lila couldn't get over the fact that they could pull tiny apples off of the trees and just bite right in. They loved it. Adeline was skeptical. I finally got an apple up to her mouth which gave her a chance to taste them. You could tell that her brain wanted so badly to take a bite but her body was overloaded by the wet, rough feel of the apple. She would lean in and then once a half inch away from taking a bite, quickly pull away. These are the moments that remind me she has a lot going on inside her. Managing it is taxing and often she just gives up as she did on the apple.
As for the apples themselves, they were delicious. Savannah and Lila couldn't get over the fact that they could pull tiny apples off of the trees and just bite right in. They loved it. Adeline was skeptical. I finally got an apple up to her mouth which gave her a chance to taste them. You could tell that her brain wanted so badly to take a bite but her body was overloaded by the wet, rough feel of the apple. She would lean in and then once a half inch away from taking a bite, quickly pull away. These are the moments that remind me she has a lot going on inside her. Managing it is taxing and often she just gives up as she did on the apple.
Subscribe to:
Posts (Atom)