Wednesday, November 26, 2008
Thankful
I don't have the answer to that question, but I have my own theory: knowing and loving Bridget keeps me from getting in the way of myself.
As Bridget's mom, I've stopped looking to others to help me gauge my own worth. I am no longer concerned with what others might be thinking about me. I am not self-conscious.
If I take my daughter's lead, I live Life jubilantly. I trust. I try. I love. I don't rush. I don't judge. I don't miss a thing.
Bridget is so full of Life and beauty--and Life with Bridget, in turn, is full of dimension and meaning.
Bridget embodies goodness and honesty. She is light and truth, and she reminds me daily--this is it--this is what Life is all about.
This love,
this joy~~
that arrived with Bridget.
The significance,
and brilliance
in our days.
The moments of discovery,
and reflection.
Moments of peace~~
and laughter~~
and light.
I am so thankful for this little girl, and for this beautiful journey...
Thankful
I don't have the answer to that question, but I have my own theory: knowing and loving Bridget keeps me from getting in the way of myself.
As Bridget's mom, I've stopped looking to others to help me gauge my own worth. I am no longer concerned with what others might be thinking about me. I am not self-conscious.
If I take my daughter's lead, I live Life jubilantly. I trust. I try. I love. I don't rush. I don't judge. I don't miss a thing.
Bridget is so full of Life and beauty--and Life with Bridget, in turn, is full of dimension and meaning.
Bridget embodies goodness and honesty. She is light and truth, and she reminds me daily--this is it--this is what Life is all about.
This love,
this joy~~
that arrived with Bridget.
The significance,
and brilliance
in our days.
The moments of discovery,
and reflection.
Moments of peace~~
and laughter~~
and light.
I am so thankful for this little girl, and for this beautiful journey...
Sunday, November 23, 2008
Ending one day and starting another...
My own advocacy efforts will be growing in scope over the upcoming year. I will share more as plans are finalized...
This past three weeks have been a bit of a blur. We've all been sick at one point or another with a variety of beginning-of-the-winter bugs (postponing our playdate with the Elliott's), and Chris has been out of town on business more than usual. The boys' basketball season started and school conferences have come and gone. Late at night, when the house has been quiet, I've started and finished my holiday shopping on-line. And now, more boxes are arriving than I can find space for.
Anyway, when Chris was gone recently, Sara slept in his spot. All the kids stay in the room with me when he's away, and the girls take turns sleeping next to me. The boys have an air bed on the floor, and there is another single bed on the floor for Emmy or Sara, whichever one is not with me.
There is a pack-n-play right next to my bed for Bridget, but she likes to snuggle as she falls asleep. I pulled her into bed with me and Sara the other night. She was sandwiched between us, all of our cheeks in a row. The three of us took up only the space in the middle of the bed. We fell asleep like that, together, with Sara's arms around Bridget, and my arms around Sara. Sometime in the middle of the night, I lifted Bridget from Sara's arms and laid her in the pack-n-play next to me.
In the morning, Bridget was the first to wake. I heard her tiny voice before daylight: "Mom Mom". I pulled her back into bed just as Sara's alarm sounded. Sara's eyes were still closed, but she sighed when she felt Bridget next to her. "What a great way to fall asleep and wake up...with this little girl beside me," she whispered.
Ending one day and starting another...
My own advocacy efforts will be growing in scope over the upcoming year. I will share more as plans are finalized...
This past three weeks have been a bit of a blur. We've all been sick at one point or another with a variety of beginning-of-the-winter bugs (postponing our playdate with the Elliott's), and Chris has been out of town on business more than usual. The boys' basketball season started and school conferences have come and gone. Late at night, when the house has been quiet, I've started and finished my holiday shopping on-line. And now, more boxes are arriving than I can find space for.
Anyway, when Chris was gone recently, Sara slept in his spot. All the kids stay in the room with me when he's away, and the girls take turns sleeping next to me. The boys have an air bed on the floor, and there is another single bed on the floor for Emmy or Sara, whichever one is not with me.
There is a pack-n-play right next to my bed for Bridget, but she likes to snuggle as she falls asleep. I pulled her into bed with me and Sara the other night. She was sandwiched between us, all of our cheeks in a row. The three of us took up only the space in the middle of the bed. We fell asleep like that, together, with Sara's arms around Bridget, and my arms around Sara. Sometime in the middle of the night, I lifted Bridget from Sara's arms and laid her in the pack-n-play next to me.
In the morning, Bridget was the first to wake. I heard her tiny voice before daylight: "Mom Mom". I pulled her back into bed just as Sara's alarm sounded. Sara's eyes were still closed, but she sighed when she felt Bridget next to her. "What a great way to fall asleep and wake up...with this little girl beside me," she whispered.
Friday, October 31, 2008
Thoughts from Dad...
Sure, I’m proud of her in so many ways as any father would be. I'm proud to see her smile and laugh, interact with her older siblings, communicate with sign language (most fathers don't get that experience), crawl, stand, take first steps, even raise her index finger high in the air when we say "Go Bucks!"...and the list goes on. I'm proud of the way she expresses herself, of her joyful spirit, and of the depth of her determination.
That feeling of pride extends much farther, though, into areas I would not really have expected.
I am proud of my other children for having such a pure acceptance for who Bridget really is as a person, not only as a child with Down syndrome. I’m proud of their willingness to try to contemplate the lives of others with disabilities and to view and appreciate them as individuals.
I am proud of their young friends for being willing to take the lead from our children in finding an understanding, acceptance and pure enjoyment of Bridget.
I am proud of my friends and extended family for celebrating Bridget, versus judging her as a child with a syndrome that makes her different, and for supporting our entire family in our advocacy efforts.
I’m proud of my wife for her willingness to provide information, along with a sense of peace and understanding, to other parents who will have children with Down syndrome and are uncertain as to what that really means and what the future may hold.
Just two years ago we were in that uncertain position, and I’m proud to say that our life is much more complete and full with Bridget in it!
**This post from Chris marks the end of Ds Awareness Month. Although it also marks the end of our participation in 31 for 21, we will continue to advocate, on all days, for Bridget and for all people with Down syndrome.
Thoughts from Dad...
Sure, I’m proud of her in so many ways as any father would be. I'm proud to see her smile and laugh, interact with her older siblings, communicate with sign language (most fathers don't get that experience), crawl, stand, take first steps, even raise her index finger high in the air when we say "Go Bucks!"...and the list goes on. I'm proud of the way she expresses herself, of her joyful spirit, and of the depth of her determination.
That feeling of pride extends much farther, though, into areas I would not really have expected.
I am proud of my other children for having such a pure acceptance for who Bridget really is as a person, not only as a child with Down syndrome. I’m proud of their willingness to try to contemplate the lives of others with disabilities and to view and appreciate them as individuals.
I am proud of their young friends for being willing to take the lead from our children in finding an understanding, acceptance and pure enjoyment of Bridget.
I am proud of my friends and extended family for celebrating Bridget, versus judging her as a child with a syndrome that makes her different, and for supporting our entire family in our advocacy efforts.
I’m proud of my wife for her willingness to provide information, along with a sense of peace and understanding, to other parents who will have children with Down syndrome and are uncertain as to what that really means and what the future may hold.
Just two years ago we were in that uncertain position, and I’m proud to say that our life is much more complete and full with Bridget in it!
**This post from Chris marks the end of Ds Awareness Month. Although it also marks the end of our participation in 31 for 21, we will continue to advocate, on all days, for Bridget and for all people with Down syndrome.
Happy Halloween!

Here are a few pics of Miss Bridget dressed up last night for Trick or Treat.
She was a really, really cute cat--who really, really did not want to wear her mask :). She knew exactly where it was supposed to go, and would hold it up to her face or head, but did not want it strapped on. I can't say I blame her...it was squishing her little eyes!




Happy Halloween!

Here are a few pics of Miss Bridget dressed up last night for Trick or Treat.
She was a really, really cute cat--who really, really did not want to wear her mask :). She knew exactly where it was supposed to go, and would hold it up to her face or head, but did not want it strapped on. I can't say I blame her...it was squishing her little eyes!




Thursday, October 30, 2008
Holy Cow!
Make that a big Holy Cow...Just One, Though. I'll explain...
I follow the blogs of several of Bridget's peers. I love keeping up with these other kids and families. My kids all know each of the children by name, and often ask about them.
One local family (who lives on the other side of town, and who we have yet to meet) has a precious little girl, Leah, who is close to Bridget's age. I will often take Bridget to the computer and show her pictures of Leah and the other kids whose blogs I browse.
One day, Leah's mom Mary posted Leah Walks, a video of her proudly taking some steps (at the end, you can hear Mary shouting with excitement, "Holy Cow!!").
When Bridget woke up from her nap that day, I took her to the computer and said, "Leah is walking. Want to see?" She was totally engrossed, and smiled throughout the 30-second clip. And at the end, she clapped and raised her hands above her head. It was adorable. I showed her the video about 10 times that day and we clapped together at the end of each one.
Bridget had been free standing and standing against things, but had not ventured out...until that night. I set her against our back door and said, "Can you walk like Leah?" No joke, she came toward me squealing with her shoulders up by her ears. She took 5 or 6 steps to me, giggling the whole time. She was like, Yep, I can take steps by myself, too. She was inspired to walk by Leah walking. I was blown away.
The funny thing is...no one else was home to see Bridget walking but me. Since that night she has taken a few steps here and there without help, but she usually wants to hold at least a finger for moral support. She is fully capable of walking on her own, but she is holding out on us. When asked, "Bridget, please stand up and take a few steps," she initially furrowed her brow, shouted "NO!" and pinched her little index finger and thumb together with vigor. She now replies sweetly and with a smile, "no". She honestly just says "no" while signing "no" at the same time. So, my Holy Cow post has been modified :).I do love how animated Bridget gets when she sees other babies and kids. I would love to find her a few friends who have the extra chromosome in common.
Bridget is surrounded by kids at home and in our neighborhood, but there are no little girls who live nearby and also have Ds. There are a few boys close to her age in our community, and I am going to reach out to their families and see if we can get together.
We have loved reading about her peers like Leah, Ella Grace, Vince, and Reid through their blogs. Thank you to all of these parents who write about their children and their experiences. They keep us company and inspire us without even knowing it.
Holy Cow!
Make that a big Holy Cow...Just One, Though. I'll explain...
I follow the blogs of several of Bridget's peers. I love keeping up with these other kids and families. My kids all know each of the children by name, and often ask about them.
One local family (who lives on the other side of town, and who we have yet to meet) has a precious little girl, Leah, who is close to Bridget's age. I will often take Bridget to the computer and show her pictures of Leah and the other kids whose blogs I browse.
One day, Leah's mom Mary posted Leah Walks, a video of her proudly taking some steps (at the end, you can hear Mary shouting with excitement, "Holy Cow!!").
When Bridget woke up from her nap that day, I took her to the computer and said, "Leah is walking. Want to see?" She was totally engrossed, and smiled throughout the 30-second clip. And at the end, she clapped and raised her hands above her head. It was adorable. I showed her the video about 10 times that day and we clapped together at the end of each one.
Bridget had been free standing and standing against things, but had not ventured out...until that night. I set her against our back door and said, "Can you walk like Leah?" No joke, she came toward me squealing with her shoulders up by her ears. She took 5 or 6 steps to me, giggling the whole time. She was like, Yep, I can take steps by myself, too. She was inspired to walk by Leah walking. I was blown away.
The funny thing is...no one else was home to see Bridget walking but me. Since that night she has taken a few steps here and there without help, but she usually wants to hold at least a finger for moral support. She is fully capable of walking on her own, but she is holding out on us. When asked, "Bridget, please stand up and take a few steps," she initially furrowed her brow, shouted "NO!" and pinched her little index finger and thumb together with vigor. She now replies sweetly and with a smile, "no". She honestly just says "no" while signing "no" at the same time. So, my Holy Cow post has been modified :).I do love how animated Bridget gets when she sees other babies and kids. I would love to find her a few friends who have the extra chromosome in common.
Bridget is surrounded by kids at home and in our neighborhood, but there are no little girls who live nearby and also have Ds. There are a few boys close to her age in our community, and I am going to reach out to their families and see if we can get together.
We have loved reading about her peers like Leah, Ella Grace, Vince, and Reid through their blogs. Thank you to all of these parents who write about their children and their experiences. They keep us company and inspire us without even knowing it.
Wednesday, October 29, 2008
Ds and Nutritional Supplementation
I was looking for basic information about Down syndrome and what we might experience with Bridget. I found the incredibly comprehensive and helpful Riverbend Down Syndrome Support Group website, and printed out sections of interest to read at the hospital.
I was mostly concerned with things that applied to Bridget's first three months of life. I spent quite a bit of time researching the nutritional needs of premature babies and feeding issues in babies with Down syndrome. I really wanted to nurse Bridget and was determined to do everything I could to give us the best chance at successful breastfeeding.
Knowing that each child is unique, and that there were many things I could do little more than worry about at that point, I tried to not look too far into the future.
I came across information on Targeted Nutritional Intervention (TNI) and NuTriVene-D. I was skeptical at first, but came to the conclusion that nutritional supplementation was something I should at least consider. I did not feel the need to "fix" Bridget, or to change her...but I certainly didn't want to miss an opportunity to improve her health or to help her fulfill her own potential. Chris and I knew right away that we wanted to be open and creative in parenting and caring for Bridget, and in giving her a great start in life.
I printed out detailed information about TNI and gave it to our pediatrician to look over. She felt that Bridget may benefit and that it was not likely to do harm. She would have supported us if we'd decided to try it.
After careful consideration, we decided not to use TNI. There were three main reasons: (1) We wanted to get to know Bridget without medications or supplements. I felt strongly that waiting several months to start TNI would not be harmful. (2) Once she was able to leave the hospital, it was clear to us that Bridget was thriving. Her muscle tone was good, and she was alert and active. (3) After reading testimonials, talking to people who had used TNI, and fact-checking as much as possible, we still were not convinced of the benefit. (Additionally, Bridget had some minor GE reflux issues, and the literature explained that increased reflux was a potential side effect of the treatment.)
We are very content with our choice not to use nutritional and dietary supplementation with Bridget. She's been incredibly healthy so far. I'm always interested, though, in hearing about all the ways children with Down syndrome may be helped to meet their full potential.
Our pediatrician recently asked if I had seen the Changing Minds Foundation website. I had not. (One of her other patients with Ds wanted her professional opinion on the Changing Minds protocol.)
I am curious to hear what others have found and experienced. Please post here, or email me if you are using, or have used TNI or the Changing Minds Foundation protocol.
Ds and Nutritional Supplementation
I was looking for basic information about Down syndrome and what we might experience with Bridget. I found the incredibly comprehensive and helpful Riverbend Down Syndrome Support Group website, and printed out sections of interest to read at the hospital.
I was mostly concerned with things that applied to Bridget's first three months of life. I spent quite a bit of time researching the nutritional needs of premature babies and feeding issues in babies with Down syndrome. I really wanted to nurse Bridget and was determined to do everything I could to give us the best chance at successful breastfeeding.
Knowing that each child is unique, and that there were many things I could do little more than worry about at that point, I tried to not look too far into the future.
I came across information on Targeted Nutritional Intervention (TNI) and NuTriVene-D. I was skeptical at first, but came to the conclusion that nutritional supplementation was something I should at least consider. I did not feel the need to "fix" Bridget, or to change her...but I certainly didn't want to miss an opportunity to improve her health or to help her fulfill her own potential. Chris and I knew right away that we wanted to be open and creative in parenting and caring for Bridget, and in giving her a great start in life.
I printed out detailed information about TNI and gave it to our pediatrician to look over. She felt that Bridget may benefit and that it was not likely to do harm. She would have supported us if we'd decided to try it.
After careful consideration, we decided not to use TNI. There were three main reasons: (1) We wanted to get to know Bridget without medications or supplements. I felt strongly that waiting several months to start TNI would not be harmful. (2) Once she was able to leave the hospital, it was clear to us that Bridget was thriving. Her muscle tone was good, and she was alert and active. (3) After reading testimonials, talking to people who had used TNI, and fact-checking as much as possible, we still were not convinced of the benefit. (Additionally, Bridget had some minor GE reflux issues, and the literature explained that increased reflux was a potential side effect of the treatment.)
We are very content with our choice not to use nutritional and dietary supplementation with Bridget. She's been incredibly healthy so far. I'm always interested, though, in hearing about all the ways children with Down syndrome may be helped to meet their full potential.
Our pediatrician recently asked if I had seen the Changing Minds Foundation website. I had not. (One of her other patients with Ds wanted her professional opinion on the Changing Minds protocol.)
I am curious to hear what others have found and experienced. Please post here, or email me if you are using, or have used TNI or the Changing Minds Foundation protocol.
Tuesday, October 28, 2008
Gifts...
I'm not saying that it is always easy, because sometimes being a parent is just plain exhausting. But I am thankful every day for this sense of comfort in my own skin, & for Bridget--for her sweet little self & for all of the gifts she's brought into our lives...
Gifts...
I'm not saying that it is always easy, because sometimes being a parent is just plain exhausting. But I am thankful every day for this sense of comfort in my own skin, & for Bridget--for her sweet little self & for all of the gifts she's brought into our lives...
Monday, October 27, 2008
Evaluations & Assessments
The way the system works, service providers need to evaluate Bridget and record their observations in order to justify the specialized help. I have given much thought to the process of evaluation and assessment--of defining the need for assistance and, by default, pointing out all the ways a person is "broken" and needs "fixed".
I realized recently that this process will be a fixture in our lives for some time to come. I have considered (heavily) my role in supporting Bridget, and how much to push--how far to go to see results.
Our own feelings regarding interventions and therapies began to come into focus early. After being in the hospital for Bridget's first month of life, we were enjoying our days with her at home. We spent the first several months just caring for Bridget and getting to know her. That time allowed us to develop not only routines, but also strong bonds with Bridget. It provided stability for our whole family. We first met with Help Me Grow when she was two months old, but chose not to start services for several more months. I truly feel that we made the right decision.
We have a great Early Intervention (EI) team. We work together to track Bridget's progress and to determine how best to encourage and support her learning. We see Bridget’s EI team (team leader, OT, PT) once a month, and have her therapists out on an as-need basis. For us, home-based and family-centered services are best whenever possible. There are many families that include outside therapy as much as once a day, but what works best for one individual or family may not work for another.
I write monthly updates on Bridget's progress in all areas, and on what we have been doing at home each month. I also provide information on any medical appointments or tests, or any changes in status that her team should know about. They, in turn, provide me with feedback after each visit as well as support materials to accomplish goals we have set together.
I am open with all of our intervention specialists and am very active in helping Bridget move to the next stages of development, but I've asked not to be given every detail of her assessments. General areas of strength and areas needing focus are plenty of information.
Bridget was just over five months old when we had her first evaluation with her EI team. She was a "superstar", hitting all the marks for a baby in her age range (adjusted for prematurity--she was six weeks early). In the "social/emotional" category, she actually ranked above other babies her "real" age--including "typical" babies. She was alert, and aware, and strong. She was rolling over both ways, vocalizing a lot, bringing objects to her mouth, bringing her hands together, trying to imitate singing, clearly communicating her needs and wants, and lifting her head and shoulders off the floor when on her tummy. She was nursing well and getting ready to begin solid foods.
I already knew she was thriving, but the evaluation was exciting and affirmed all my own thoughts. The team clearly enjoyed Bridget, and they seemed really happy--although a little bit surprised, I think--to see how well she was doing. There was lots of smiling, and clapping, and "Yeah, Bridget!" I was gently cautioned that the evaluations are "harder" (as they include more specific tasks) as children grow. Generally, for kids with Down syndrome, the "lag" gets more obvious as time goes by.
At her nine month evaluation, Bridget did all sorts of great things. She sat independently; experimented with many different sounds (short bursts & long strings of sounds, loud & quiet sounds, squealing); she stood with help; passed toys freely from one hand to the other; and was generally animated and willing to show all of her skills. She showed only minor delays in that evaluation. She could not, however, hold a cracker and eat it herself, so she did not get a check in that box--it had to be left empty and she "lost points" for not possessing that skill.
This was a critical moment in my understanding of my role in Bridget's growth and development, and in determining how far to take interventions and therapies. How important was it that she was a "superstar"--proving everyone wrong that said she would never (fill in the blank), or would not (fill in the blank) within the "typical" time frame, or would not (fill in the blank) as well as her peers? I could have let the fact that she was unable to feed herself a cracker eat me alive. In the past, I just might have. I might have decided: Okay...we are going to do this...we are going to make sure she can eat a cracker for the next evaluation. She'll show them. We'll show them.
The truth is, I had never really given her crackers to eat herself. I tried once. She could easily hold the cracker and bring it to her mouth, but shoved the whole thing inside. She had no teeth, and little saliva, and was not really "chewing", so it just was not the right time. I lunged forward to swipe the cracker out of her mouth, and she ended up sobbing. It was not the best start to independent eating :).
The evaluation reminded me that many 9-month-old babies are feeding themselves crackers, and Bridget was not. With tons of work (and me letting go of my fear of choking), Bridget might have been able to perform this skill earlier. But when I really thought about it, I realized that it just didn't matter. Was I going to cling to every point on these evaluations? Was I going to make sure we focused on every little thing that was pointed out? Was I going to drive us all crazy with daily therapy sessions and working tirelessly on all the things Bridget could not yet do?
I knew Bridget was learning. I knew Bridget was working toward milestones. I knew she was happy, healthy and secure. Our whole family was involved in her development by playing with her, talking to her, and generally making her an important part of everything we do.
I knew right then that I had to put my (or anyone else's) motives aside and look instead for Bridget to reveal her own. We look to her for readiness "cues".
We've all learned the signs for things in our everyday life that are important to Bridget, and we've learned techniques to help her reach milestones in all areas of her development. With her, our work is play, and our play is really "work". Together, we are making lots of progress, its just that we are making it fun and following her lead...
**The ages of birth to three are truly the foundation for a person's learning. Early Intervention programs are important and necessary. For us, and with Bridget's own personality, less has been more. We make it a priority to be active learners along with Bridget, and to surround her with books as well as educational toys and experiences--and a lot of love.
**Jennifer Graf Groneberg's Perfectly Imperfect also takes a look, although much more eloquently :), at this same issue.
Evaluations & Assessments
The way the system works, service providers need to evaluate Bridget and record their observations in order to justify the specialized help. I have given much thought to the process of evaluation and assessment--of defining the need for assistance and, by default, pointing out all the ways a person is "broken" and needs "fixed".
I realized recently that this process will be a fixture in our lives for some time to come. I have considered (heavily) my role in supporting Bridget, and how much to push--how far to go to see results.
Our own feelings regarding interventions and therapies began to come into focus early. After being in the hospital for Bridget's first month of life, we were enjoying our days with her at home. We spent the first several months just caring for Bridget and getting to know her. That time allowed us to develop not only routines, but also strong bonds with Bridget. It provided stability for our whole family. We first met with Help Me Grow when she was two months old, but chose not to start services for several more months. I truly feel that we made the right decision.
We have a great Early Intervention (EI) team. We work together to track Bridget's progress and to determine how best to encourage and support her learning. We see Bridget’s EI team (team leader, OT, PT) once a month, and have her therapists out on an as-need basis. For us, home-based and family-centered services are best whenever possible. There are many families that include outside therapy as much as once a day, but what works best for one individual or family may not work for another.
I write monthly updates on Bridget's progress in all areas, and on what we have been doing at home each month. I also provide information on any medical appointments or tests, or any changes in status that her team should know about. They, in turn, provide me with feedback after each visit as well as support materials to accomplish goals we have set together.
I am open with all of our intervention specialists and am very active in helping Bridget move to the next stages of development, but I've asked not to be given every detail of her assessments. General areas of strength and areas needing focus are plenty of information.
Bridget was just over five months old when we had her first evaluation with her EI team. She was a "superstar", hitting all the marks for a baby in her age range (adjusted for prematurity--she was six weeks early). In the "social/emotional" category, she actually ranked above other babies her "real" age--including "typical" babies. She was alert, and aware, and strong. She was rolling over both ways, vocalizing a lot, bringing objects to her mouth, bringing her hands together, trying to imitate singing, clearly communicating her needs and wants, and lifting her head and shoulders off the floor when on her tummy. She was nursing well and getting ready to begin solid foods.
I already knew she was thriving, but the evaluation was exciting and affirmed all my own thoughts. The team clearly enjoyed Bridget, and they seemed really happy--although a little bit surprised, I think--to see how well she was doing. There was lots of smiling, and clapping, and "Yeah, Bridget!" I was gently cautioned that the evaluations are "harder" (as they include more specific tasks) as children grow. Generally, for kids with Down syndrome, the "lag" gets more obvious as time goes by.
At her nine month evaluation, Bridget did all sorts of great things. She sat independently; experimented with many different sounds (short bursts & long strings of sounds, loud & quiet sounds, squealing); she stood with help; passed toys freely from one hand to the other; and was generally animated and willing to show all of her skills. She showed only minor delays in that evaluation. She could not, however, hold a cracker and eat it herself, so she did not get a check in that box--it had to be left empty and she "lost points" for not possessing that skill.
This was a critical moment in my understanding of my role in Bridget's growth and development, and in determining how far to take interventions and therapies. How important was it that she was a "superstar"--proving everyone wrong that said she would never (fill in the blank), or would not (fill in the blank) within the "typical" time frame, or would not (fill in the blank) as well as her peers? I could have let the fact that she was unable to feed herself a cracker eat me alive. In the past, I just might have. I might have decided: Okay...we are going to do this...we are going to make sure she can eat a cracker for the next evaluation. She'll show them. We'll show them.
The truth is, I had never really given her crackers to eat herself. I tried once. She could easily hold the cracker and bring it to her mouth, but shoved the whole thing inside. She had no teeth, and little saliva, and was not really "chewing", so it just was not the right time. I lunged forward to swipe the cracker out of her mouth, and she ended up sobbing. It was not the best start to independent eating :).
The evaluation reminded me that many 9-month-old babies are feeding themselves crackers, and Bridget was not. With tons of work (and me letting go of my fear of choking), Bridget might have been able to perform this skill earlier. But when I really thought about it, I realized that it just didn't matter. Was I going to cling to every point on these evaluations? Was I going to make sure we focused on every little thing that was pointed out? Was I going to drive us all crazy with daily therapy sessions and working tirelessly on all the things Bridget could not yet do?
I knew Bridget was learning. I knew Bridget was working toward milestones. I knew she was happy, healthy and secure. Our whole family was involved in her development by playing with her, talking to her, and generally making her an important part of everything we do.
I knew right then that I had to put my (or anyone else's) motives aside and look instead for Bridget to reveal her own. We look to her for readiness "cues".
We've all learned the signs for things in our everyday life that are important to Bridget, and we've learned techniques to help her reach milestones in all areas of her development. With her, our work is play, and our play is really "work". Together, we are making lots of progress, its just that we are making it fun and following her lead...
**The ages of birth to three are truly the foundation for a person's learning. Early Intervention programs are important and necessary. For us, and with Bridget's own personality, less has been more. We make it a priority to be active learners along with Bridget, and to surround her with books as well as educational toys and experiences--and a lot of love.
**Jennifer Graf Groneberg's Perfectly Imperfect also takes a look, although much more eloquently :), at this same issue.
Sunday, October 26, 2008
Doing the Dreaming for Herself
We were concerned foremost with her health. We decided we would learn whatever we could to advocate for her in every way we could. We agreed that we would focus on getting her well enough to come home. We discussed large issues like education, driving, and marriage. Would Bridget be able to attend a regular school? Would she ever drive? Was marriage out of the question for her?
We also wondered about everyday life. Would she be sick often? How would raising her be different from raising the other kids? How would their lives be impacted? Would we be able to take family vacations? What about leaving the kids with a babysitter? Would we always be worried about Bridget?
The questions were endless at first, and the process is one we needed to go through to realize: things are not much different than what we anticipated when we found out we would be adding a new member to our family. The truth is, we never know what a child will be like, what he or she will require, achieve or struggle with. We never know if a child will be healthy, independent, happy, and so on. Who's to say if any of our children will drive, go to college, get married, or live independently. We really don't know at this point. We're not consumed by the need to know how it will all play out. And, honestly, the future for our children is not for us to plan out.
Once we'd talked through all these issues, Chris and I realized that many of these things are outside of our control, and what's most important to us is that our children are happy & able to contribute to the world in some way. Each one of us has a unique personality. We all have our issues and our strengths. We will all go through times when we require more attention or more support than usual. We all have something valuable to contribute.
With Bridget, we are learning to be hopeful without expectations. We have plans and goals to help Bridget in her growth and development, and while those plans are necessary and important--we cannot be tied to them. Bridget is on her own path, and will develop in her own ways on her own time. We can provide her experiences and exposure to things which may influence her development, but her own personality and abilities will dictate what she accomplishes and when.
We don’t want others to judge her against an arbitrary standard of development or of what’s acceptable. We’ve learned that we can’t do that either. There is a fine line between wanting the best for our children, and asking that they meet our ideal. Typical, healthy or not…we cannot dream for our children.
Doing the Dreaming for Herself
We were concerned foremost with her health. We decided we would learn whatever we could to advocate for her in every way we could. We agreed that we would focus on getting her well enough to come home. We discussed large issues like education, driving, and marriage. Would Bridget be able to attend a regular school? Would she ever drive? Was marriage out of the question for her?
We also wondered about everyday life. Would she be sick often? How would raising her be different from raising the other kids? How would their lives be impacted? Would we be able to take family vacations? What about leaving the kids with a babysitter? Would we always be worried about Bridget?
The questions were endless at first, and the process is one we needed to go through to realize: things are not much different than what we anticipated when we found out we would be adding a new member to our family. The truth is, we never know what a child will be like, what he or she will require, achieve or struggle with. We never know if a child will be healthy, independent, happy, and so on. Who's to say if any of our children will drive, go to college, get married, or live independently. We really don't know at this point. We're not consumed by the need to know how it will all play out. And, honestly, the future for our children is not for us to plan out.
Once we'd talked through all these issues, Chris and I realized that many of these things are outside of our control, and what's most important to us is that our children are happy & able to contribute to the world in some way. Each one of us has a unique personality. We all have our issues and our strengths. We will all go through times when we require more attention or more support than usual. We all have something valuable to contribute.
With Bridget, we are learning to be hopeful without expectations. We have plans and goals to help Bridget in her growth and development, and while those plans are necessary and important--we cannot be tied to them. Bridget is on her own path, and will develop in her own ways on her own time. We can provide her experiences and exposure to things which may influence her development, but her own personality and abilities will dictate what she accomplishes and when.
We don’t want others to judge her against an arbitrary standard of development or of what’s acceptable. We’ve learned that we can’t do that either. There is a fine line between wanting the best for our children, and asking that they meet our ideal. Typical, healthy or not…we cannot dream for our children.
Saturday, October 25, 2008
Audiences Across the Country Get the Message a Second Time
A little surprise awaited us, also. As the show began, a video played on a large screen above the stage. SYTYCD co-creator Nigel Lythgoe introduced the top five most memorable auditions for the 2008 season. I started to tear up as soon as the clip started for memorable audition #4, which I immediately recognized as the Brett Banford audition. Most of us in the Ds community have seen it, but for anyone who hasn't, please click on the link here and watch the video of Banford's segment on the Disability News site (along with a partial transcript of the judges' comments).
In May, 25-year-old Banford appeared on national t.v. during prime time with the show's recap of the Salt Lake City auditions. He grooved on stage, and was clearly enjoying his time in the spotlight. With great composure and with a goal to "represent" for people with disabilities, Banford said after his performance, “I’m just here to prove to people that people with disabilities can actually have a normal life and live it. And that’s what I’m here to represent.” Amidst the whooping and hollering of the audience, he continued, “It’s not about winning or losing. It’s about having fun.”
I was completely thrilled--and more than a little overwhelmed--that his audition (and message) was getting another round of play to audiences around the country. Last Wednesday night, at the Jerome Schottenstein Center on the Ohio State campus, around 10,000 people watched Banford's clip. He got lots of applause while it played--and when it was over, the woman next to me leaned to her friend and said, "That was awesome." It truly was.
Big, big kudos to SYTYCD for highlighting Banford and his message once again. And big, big kudos to Brett. You make us all proud!
p.s. The live show was AWESOME. For fans, it was well worth the cost of tickets and being out late on a school night :).
Audiences Across the Country Get the Message a Second Time
A little surprise awaited us, also. As the show began, a video played on a large screen above the stage. SYTYCD co-creator Nigel Lythgoe introduced the top five most memorable auditions for the 2008 season. I started to tear up as soon as the clip started for memorable audition #4, which I immediately recognized as the Brett Banford audition. Most of us in the Ds community have seen it, but for anyone who hasn't, please click on the link here and watch the video of Banford's segment on the Disability News site (along with a partial transcript of the judges' comments).
In May, 25-year-old Banford appeared on national t.v. during prime time with the show's recap of the Salt Lake City auditions. He grooved on stage, and was clearly enjoying his time in the spotlight. With great composure and with a goal to "represent" for people with disabilities, Banford said after his performance, “I’m just here to prove to people that people with disabilities can actually have a normal life and live it. And that’s what I’m here to represent.” Amidst the whooping and hollering of the audience, he continued, “It’s not about winning or losing. It’s about having fun.”
I was completely thrilled--and more than a little overwhelmed--that his audition (and message) was getting another round of play to audiences around the country. Last Wednesday night, at the Jerome Schottenstein Center on the Ohio State campus, around 10,000 people watched Banford's clip. He got lots of applause while it played--and when it was over, the woman next to me leaned to her friend and said, "That was awesome." It truly was.
Big, big kudos to SYTYCD for highlighting Banford and his message once again. And big, big kudos to Brett. You make us all proud!
p.s. The live show was AWESOME. For fans, it was well worth the cost of tickets and being out late on a school night :).