Showing posts with label My daughter. Show all posts
Showing posts with label My daughter. Show all posts
Wednesday, October 17, 2018
Underestimating her abilities
It's been a long time, but we've had a lot of big changes.
Her little brother, baby A, is potty training and both kids are big fans of Peppa pig. So, baby A ended up with Peppa pig undies next to his Spider-Man ones. Big A decided that she wanted to wear Peppa pig. And that is when it hit me.
Why was I potty training her little brother and not trying with her? She was showing interest, she has been sitting every morning for at least a year and knows how to use the equipment. Second, she's in a very supportive preschool and is getting ready to move up to the pre-K room where the school no longer supports potty training. They are willing to move her up, but we are doing a disservice to her by not trying her out on it while she has the supports in place.
So, we brought it up with the preschool. I think they were surprised we were asking them to do this after all my discussion on how it might be later for her. It still might, but we should allow her to try. I'm not entirely sure if all my work to convince them we should wait had been too effective because I didn't get the impression the school was entirely happy with my change of heart.
We started her at home over the weekend and there were a lot of messes.
A lot.
But, she seems to get it. At least with a timer, but she's doing it on a schedule. A few times I caught her walking to the rest room, but not going in there on her own.
She's getting it!
For school, it dawned on me that a social story would help, so I tossed on together. The preschool told me that really helped. She would ready it and get to the picture of the little girl with blond hair like hers and try.
I'm proud of her no matter where this goes. She's getting it and I hope we have given her enough time with the right supports to keep getting this.
Labels:
Advocating,
Down Syndrome,
My daughter,
social story
Tuesday, September 5, 2017
Preschool blues
We have made the decision that Anna should be with kids her own age who are neurotypical. You would think this would be easy to find, call a few local preschools and just sign her up, but it isn't.
The moment I mention that she has Down syndrome, I suddenly have to prove that she belongs there. If it's in person, there's hand ringing, or the standard, "I don't know if this will work out..." These preschools who list "inclusive" on their web pages are scared to death of having to actually follow through with what inclusive means. Or, perhaps they don't realize how exclusive they truly are.
We went through the search for child care a few years back and it took searching high and low to find a day care that not only would take her, but wanted her there. You can tell. You can tell when the provider is scared and you can tell when they think Anna is the problem. However, we found one that not only wanted her, they embraced her.
This was not an easy thing to find. The search began when she was 17 months old. She had just had her G-tube taken out a few months earlier and was still learning to eat orally. Her primary source of calories was liquid. She had limited core strength and needed side support in chairs. She wasn't really climbing, but was walking, just walking. We thought we had found one in a great church day care, but I brought her in for her first day and they walked us into the infant room. The next oldest child wasn't even rolling over. I left her there, because I felt I had no choice, but I bawled in the parking lot.
They told me they couldn't handle her in the room with the kids her age. What's to handle? She was on a bottle which she held herself, but they didn't want to even try.
On the third day, I said enough, and picked her up. She had gotten sick at the day care and when I called a few weeks later they let me pull her out and told me to forget any fees for the month. I think they were glad to see her go and the problem family was gone. They were able to go back to thinking they were inclusive and pretending that they welcomed someone who works a little harder to learn skills.
We found a home day care, but that also wasn't working. They were not staffing the rooms. Every time I stopped by during the day, it was one worker and no other staff. She kept telling me this was not normal, but it was consistent. Anna came home with massive bites on her. We were on the search for something that was safer for her.
We finally found a center near my office. At this point, I had interviewed and visited 20-30 day cares. I walked in, assuming more of the same, and asked the director if she would allow Anna in the room with kids her own age. She looked surprised and said back to me, "Why wouldn't we? Yes, of course." I think I cried in the office.
Anna did really well at this preschool and day care. The staff found a high chair that allowed Anna to sit at the same level as the kids at the table for meals and brought it into the room. Within four weeks, Anna had figured out how to sit in the big kid chairs and the high chair disappeared. A few weeks in, I was picking Anna up and one of the room teachers told me to hide for a second and watch. She was explaining how they were trying to figure out which kid was helping Anna get up onto the play structure when they finally saw that she had figured out how to get up on it all by herself. I watched my little girl, who just recently learned to walk, climb up on a play structure and go down the slide. It was magical.
The gains in her skills just being around the other kids her age cannot be quantified. There was no PT service, no OT service, no magic therapist that led her to make such big gains in skills as what she learned from the other kids. She started to eat traditional foods, watching the other kids eat lunch, she wanted to try it. This was huge! We finally were able to back off on formulas and start to push real food. This was not the feeding therapist, it was kids showing her what to do that helped her.
Anna started developmental preschool right after her 3rd birthday. There are no peer models in her room. She had started potty training at the day care and this seemed to come to a stop in developmental preschool. Words stopped, big skills stopped emerging.
We put her back on the wait list at the preschool/day care that had been so good for her and I returned to work. A spot opened up this September and we made the decision that a truly inclusive setting is best for Anna. We decided that Anna's best setting is with her peers and decided to pursue what it would involve doing her therapies without attending the preschool program.
Of course, when I called the school district, they are not willing to bus her for her therapies because the preschool is just outside the district. So, all her therapies end or I have to leave my job that I really enjoy. I have long ago written off Anna's SLP at the school as useless when she told me in an offhand comment that Anna would never speak. However, her fine motor skills are still behind. I worry this will be what blocks the kindergarten teacher from welcoming her. And how will we manage her orthotics?
I've called preschools within the district and we are back to proving Anna should be allowed to be there. I have to provide a copy of her IEP to one preschool so they can analyze if they think she would be a good fit. Would they ask for that level of scrutiny from any other child who has an IEP? They also told me she must be potty trained. I brought up that this would be an ADA issue and that didn't go over well. The thought of going through the search, the depressing, search, again, is hard to stomach.
Someone's ability to welcome my child says a lot more about that person as a human being, more than anything they say to me as a person. To welcome someone without question says a lot because it says that they belong in this world. She belongs in this world and I wish I didn't have to fight so hard to prove this. However, someone who welcomes my child is far and few between and the world needs more of that.
The moment I mention that she has Down syndrome, I suddenly have to prove that she belongs there. If it's in person, there's hand ringing, or the standard, "I don't know if this will work out..." These preschools who list "inclusive" on their web pages are scared to death of having to actually follow through with what inclusive means. Or, perhaps they don't realize how exclusive they truly are.
We went through the search for child care a few years back and it took searching high and low to find a day care that not only would take her, but wanted her there. You can tell. You can tell when the provider is scared and you can tell when they think Anna is the problem. However, we found one that not only wanted her, they embraced her.
This was not an easy thing to find. The search began when she was 17 months old. She had just had her G-tube taken out a few months earlier and was still learning to eat orally. Her primary source of calories was liquid. She had limited core strength and needed side support in chairs. She wasn't really climbing, but was walking, just walking. We thought we had found one in a great church day care, but I brought her in for her first day and they walked us into the infant room. The next oldest child wasn't even rolling over. I left her there, because I felt I had no choice, but I bawled in the parking lot.
They told me they couldn't handle her in the room with the kids her age. What's to handle? She was on a bottle which she held herself, but they didn't want to even try.
On the third day, I said enough, and picked her up. She had gotten sick at the day care and when I called a few weeks later they let me pull her out and told me to forget any fees for the month. I think they were glad to see her go and the problem family was gone. They were able to go back to thinking they were inclusive and pretending that they welcomed someone who works a little harder to learn skills.
We found a home day care, but that also wasn't working. They were not staffing the rooms. Every time I stopped by during the day, it was one worker and no other staff. She kept telling me this was not normal, but it was consistent. Anna came home with massive bites on her. We were on the search for something that was safer for her.
We finally found a center near my office. At this point, I had interviewed and visited 20-30 day cares. I walked in, assuming more of the same, and asked the director if she would allow Anna in the room with kids her own age. She looked surprised and said back to me, "Why wouldn't we? Yes, of course." I think I cried in the office.
Anna did really well at this preschool and day care. The staff found a high chair that allowed Anna to sit at the same level as the kids at the table for meals and brought it into the room. Within four weeks, Anna had figured out how to sit in the big kid chairs and the high chair disappeared. A few weeks in, I was picking Anna up and one of the room teachers told me to hide for a second and watch. She was explaining how they were trying to figure out which kid was helping Anna get up onto the play structure when they finally saw that she had figured out how to get up on it all by herself. I watched my little girl, who just recently learned to walk, climb up on a play structure and go down the slide. It was magical.
The gains in her skills just being around the other kids her age cannot be quantified. There was no PT service, no OT service, no magic therapist that led her to make such big gains in skills as what she learned from the other kids. She started to eat traditional foods, watching the other kids eat lunch, she wanted to try it. This was huge! We finally were able to back off on formulas and start to push real food. This was not the feeding therapist, it was kids showing her what to do that helped her.
Anna started developmental preschool right after her 3rd birthday. There are no peer models in her room. She had started potty training at the day care and this seemed to come to a stop in developmental preschool. Words stopped, big skills stopped emerging.
We put her back on the wait list at the preschool/day care that had been so good for her and I returned to work. A spot opened up this September and we made the decision that a truly inclusive setting is best for Anna. We decided that Anna's best setting is with her peers and decided to pursue what it would involve doing her therapies without attending the preschool program.
Of course, when I called the school district, they are not willing to bus her for her therapies because the preschool is just outside the district. So, all her therapies end or I have to leave my job that I really enjoy. I have long ago written off Anna's SLP at the school as useless when she told me in an offhand comment that Anna would never speak. However, her fine motor skills are still behind. I worry this will be what blocks the kindergarten teacher from welcoming her. And how will we manage her orthotics?
I've called preschools within the district and we are back to proving Anna should be allowed to be there. I have to provide a copy of her IEP to one preschool so they can analyze if they think she would be a good fit. Would they ask for that level of scrutiny from any other child who has an IEP? They also told me she must be potty trained. I brought up that this would be an ADA issue and that didn't go over well. The thought of going through the search, the depressing, search, again, is hard to stomach.
Someone's ability to welcome my child says a lot more about that person as a human being, more than anything they say to me as a person. To welcome someone without question says a lot because it says that they belong in this world. She belongs in this world and I wish I didn't have to fight so hard to prove this. However, someone who welcomes my child is far and few between and the world needs more of that.
Labels:
childcare,
Down Syndrome,
My daughter,
special education
Wednesday, May 17, 2017
Don't use the R-word
The R-word. Seriously, you have to have a better term, unless you're really just that incapable of coming up with anything witty. Because The R-word is not witty. It's not funny and it's not something you should use.
It's insulting to anyone who has developmental delays. It should be insulting to everyone. It is an outdated term and the R-word is no longer used in medical texts.
I "hear" it more often than I used to. I don't think it is used more often than it used to be, but I'm more aware of, or at least more sensitive to the true meaning.
I notice it when people use it perhaps because it stings.
It is hopefully unintended, but using that word as a joke is a derogatory way to talk about my daughter. You see, my daughter is blessed with an extra chromosome.
However, the R-word has changed meaning over time. Our language is a living thing and that medical term has become a joke and an insult.
It is no longer a medical term. The medical community recognized what the word had become and removed it from their descriptions of developmental delays.
The negative assumptions of her capabilities are what make it "funny." The things she works so hard to accomplish are summed up as a joke. Even today I am advocating to allow her to be involved in activities with typical peers because the world assumes she is not capable of being part of that world. That's the joke you are inferring when you use that word. The ha-ha, the funny. This is the history of segregating persons with developmental delay from the rest of society.
Don't pull my daughter out of the world because you cannot accept differences.
Most of all, don't use the R-word. Come up with something better.
Most of all, don't use the R-word. Come up with something better.
Tuesday, November 15, 2016
Hey, School District!
Last night our district held a school board meeting. A segment of the meeting allows audience members to address the school board. This is what I told our school board.
Good evening
I am here to talk to you about inclusive education at the preschool level.
My husband and I have four children. My oldest son is in middle school, my oldest daughter is in elementary school, and my 3 year old is in Preschool at a different Elementary. My youngest is not yet in school.
Anna, my 3 year old, is blessed with an extra chromosome. She has Down syndrome and she is a fire cracker. She is in the developmental preschool program atelementary. Her teacher really shows so much love for the kids and we know she is in good hands while she is at school. Anna lights up when she sees her bus and is excited to go to school.
When I dropped her off at school a few weeks ago, I watched as all the big kids flooded off the buses and onto the playground. Then the kids on the little buses were escorted to their classroom. I know there is an age difference between my daughter and the kids on the playground, but what a missed opportunity to have kids together at something that is just such a normal, everyday thing as playing on the play ground before school.
This event caused me to look at Anna’s schooling differently.
It is one of the reasons I am here tonight.
When Anna was too young for school and both of my older kids were in the same elementary school, one of the kids came home from school and asked me, “Where are all the kids with Down syndrome, mommy? Will Anna be allowed at my school?”
I didn’t have an answer.
I volunteered and went to events at the kid’s school. I looked around and there was not one child like my three year old in the school. We started to seek out local groups that we could take the kids to that involved kids their own age who have Down syndrome. I needed my kids to know that Anna was ok. Finding these groups was really good for my kids. They went to one event and watched movies with some kids. They have a lot of the same interests, likes and dislikes. They are all just kids.
This is our normal, but it shouldn’t be the abnormal. I shouldn’t have had to seek out situations for my kids to be around kids who happened to be blessed with an extra chromosome.
I want my kids to be in a world that welcomes them and I want them to be in a world that allows them to participate with the rest of the world. I want this world for all four of my kids.
I want both my daughters to go to school with the kids down the street. I want my kids to be in the same school if possible. I plan for a world that encourages all four of my kids to go to college and the opportunity to fully participate in the community.
I want my kids to learn to take care of themselves, to reach for the stars and to stand up for others.
Tonight I am giving you a copy of the recent joint Policy statement on inclusion of children with disabilities in early childhood programs. by the US Department of Education and the US Department of Health and Human Services released in September of 2015.
The policy statement outlines that districts should “Strongly communicate inclusion as a shared responsibility and a top priority, and demonstrate a commitment to inclusion through policy changes and appropriate resource allocation at all levels.”
Meaningful inclusive education needs to happen.
I am going to read you a segment from the IDEA’s Least Restrictive Environment Provisions. I know I am likely preaching to the chior, but I want you to think about these words:
(IDEA’s LRE provisions are found at §§300.114 through 300.117.) Each public agency must ensure that—
(i) To the maximum extent appropriate, children with disabilities, including children in public or private institutions or other care facilities, are educated with children who are nondisabled; and
(ii) Special classes, separate schooling, or other removal of children with disabilities from the regular educational environment occurs only if the nature or severity of the disability is such that education in regular classes with the use of supplementary aids and services cannot be achieved satisfactorily. [§300.114(a]
As a district, we can make a difference and we need to look at what we can do together to bring this population into the classrooms with other kids.
A recent Dutch study published in June of this year in the Journal of Policy and Practice in Intellectual Disabilities outlines that people with Down syndrome with lower IQs in inclusive settings did better than their counterparts with higher IQs in segregated settings. The data shows that being part of the classroom with typical kids, kids did better.
One of the barriers to inclusion is the fear of a negative impact on typical kids. What’s really cool is the data shows this is not the case. Many studies show that an inclusive education classroom actually benefits all students.
A 2001 study states:
“In the area of academic progress, Waldron, Cole, and Majd (2001) report that more students without disabilities made comparable or greater gains in math and reading when taught in inclusive settings versus traditional classrooms where no students with disabilities are included.”
A 1998 study states “Further evidence for the positive effects of inclusion on students without disabilities is reported by McGregor and Vogelsberg (1998). They found:
- inclusion does not compromise general education students’ outcomes
- typical peers benefit from involvement and relationships with students who have disabilities in inclusive settings, and
- the presence of students with disabilities in general education classrooms leads to new learning opportunities for typical students.
Inclusive education is a huge benefit to all students, not just the students receiving special educational services.
Saturday, November 5, 2016
The short bus
My little girl started developmental preschool. She takes the little bus. The bus stops at the top of our driveway and she happily climbs on to go to school.
I have my misgivings about school. I like her teachers, I like the care and respect everyone has for us, but I wish she had peer models.
I dropped her off at school once this year and left very upset.
First, I watched as all the big buses came. The kids came pouring out the doors of the buses onto the playground. We were trying to get Anna to her class and were turned away at the door because they weren't ready for her. I asked if she should go to the play ground and I was told, "no!"
We were told to wait by the bus drop off, so we walked back to the front of the school and watched the kids run past us to the play ground. After all the big buses emptied and left, the short buses pulled up. It was like a dance, one group left and the next group came on stage. However, none of the kids got off. They sat on the bus and waited for the helpers. Then the kids were escorted off to their separate classes.
It took everything I had not to start crying for my little girl right there.
My little girl, who I had been asking to be around typical kids missed another opportunity. I didn't see one child get off the short bus and head to the play ground with the other kids. Not even the older kids who were the same age as the elementary school kids on the play ground.
I think about my big kids who asked me where the kids with Down Syndrome are in their school. How can they not think something is wrong with Anna if she's not allowed in the classes with other kids.
I think about Anna and how much she learns being around typical kids. She learned to climb at the day care. She started potty training because the other kids were doing it at the day care.
To be included and loved, that's what we want for our kids, not separated from the rest of the world like there is something wrong with them.
This is Anna. She is perfect just the way she is.
I have my misgivings about school. I like her teachers, I like the care and respect everyone has for us, but I wish she had peer models.
I dropped her off at school once this year and left very upset.
First, I watched as all the big buses came. The kids came pouring out the doors of the buses onto the playground. We were trying to get Anna to her class and were turned away at the door because they weren't ready for her. I asked if she should go to the play ground and I was told, "no!"
We were told to wait by the bus drop off, so we walked back to the front of the school and watched the kids run past us to the play ground. After all the big buses emptied and left, the short buses pulled up. It was like a dance, one group left and the next group came on stage. However, none of the kids got off. They sat on the bus and waited for the helpers. Then the kids were escorted off to their separate classes.
It took everything I had not to start crying for my little girl right there.
My little girl, who I had been asking to be around typical kids missed another opportunity. I didn't see one child get off the short bus and head to the play ground with the other kids. Not even the older kids who were the same age as the elementary school kids on the play ground.
I think about my big kids who asked me where the kids with Down Syndrome are in their school. How can they not think something is wrong with Anna if she's not allowed in the classes with other kids.
I think about Anna and how much she learns being around typical kids. She learned to climb at the day care. She started potty training because the other kids were doing it at the day care.
To be included and loved, that's what we want for our kids, not separated from the rest of the world like there is something wrong with them.
This is Anna. She is perfect just the way she is.
Monday, September 5, 2016
We have had a lot of changes in our household.
We've moved back to the wet side of the mountains. Big N is in middle school. Little N is in her final year of elementary school. Big A is a big A. Yes, since I haven't been posting a lot of blog updates there has been a little A.
So, to say things are moving forward is the understatement.
I've taken a hiatus from work to care for Big A and little A. I've done some consulting now that she is healthier. That's been a nice change of pace.
We've moved back to the wet side of the mountains. Big N is in middle school. Little N is in her final year of elementary school. Big A is a big A. Yes, since I haven't been posting a lot of blog updates there has been a little A.
So, to say things are moving forward is the understatement.
I've taken a hiatus from work to care for Big A and little A. I've done some consulting now that she is healthier. That's been a nice change of pace.
Friday, January 4, 2013
Home sick from school and feeling better activity
Tuesday, December 4, 2012
Polka Dots!
Little N was helping me go through some hand-me-down maternity clothes the other day and came across a great little polka-dot sleeveless shirt. The shirt had gigantic black polka dots sprinkled across it. She immediately squealed in delight. Little N ran to her closet and produced her Easter dress from last spring. Wouldn't you know it, her Easter dress also has gigantic black polka dots sprinkled across it.
Little N informed me that I was to wear this polka dot shirt to church and she would wear her polka dot sundress. However, it was December and not exactly sundress weather. We dug around to find sweaters for both of us to wear during this non-sundress weather.
I had a lovely day being a polka dot twin with my little girl.
Wednesday, June 13, 2012
Worms in dirt on cupcakes
Little N is coming to the end of her year at kindergarten. When I picked her up today, she was taking her time leaving the classroom. This is a regular occurring event for Little N. She starts to chat with her friends, slowly puts on her coat, wanders the room in circles. She takes her time at school, she takes her time at home, I've tried rushing the girl, and sometimes it's just not worth the fight. We tend to pick our battles and give her plenty of time when we can.
Today, when she was done wandering the classroom, she chatted with her teacher on the way out the door. Since everyone else had already left, she had the teacher's full attention (perhaps she had a plan for her wandering). Little N suggested to her teacher that she would like to bring snacks for tomorrow. The teacher looks at me, raises an eyebrow as a question mark and I said, "why not." I, of course, underestimated Little N's grand plans.
As we were driving away from the school, Little N started to describe grandiose, flower covered cupcakes. It turns out that watching the food network can backfire on you. I had to break it to Little N that Mommy cannot make a frosting flower and I wasn't sure where we could find edible flowers as a substitute.
I suggested gummy worms on chocolate cupcakes, to which Little N suggested that we needed to make "dirt" for the worm to crawl out of. My super creative Little N thought of the chocolate graham crackers we have in the cupboard and the worms in the dirt cupcake was born.
This evening we made cupcakes. Little N did all the measuring and ran the mixer. Once we frosted the cupcakes, she put a worm on each cupcake and then dipped the top into the ground up graham crackers. She wanted the worms to look "dirty" and she was very successful. Big N helped, too. He was the official worm tester.
Photo Sharing - Video Sharing - Photo Printing
Saturday, April 28, 2012
Please pass the pees
Pees be wif you.
And also with you. Love you, Little N.
Wednesday, November 23, 2011
Girls like dinosaurs, too!
Princess dinosaur Hat
Auntie Sarah gave Big N a dinosaur hat when he was three. He still loves this hat and it miraculously still fits now that he is almost 8. Little N tries to steal it on occasion, which never ends well for her. However, I can see her point. What is not to love about wearing spikes on your head?
Big N wearing his hat
When I spoke to Little N about making her a dinosaur hat, she was very specific on the color combination. It had to be pink. It had to be purple. It had to be all that and made for a princess. It also could not have purple spikes.
Little N helped me make the pattern. We traced Big N's hat and added a 1/2 inch seam allowance. She then cut out the pattern pieces for me. I opted to sew it when she was in bed to surprise her this morning.
Little N was thrilled! I skipped the velcro chin closure because it covers her ears just fine. I think it looks a little more feminine as it is.
Tuesday, November 15, 2011
Very Persuasive
Little N is in half day kindergarten. I pick her up just before lunch to drive her to day care on the days Pete is unable to. On some special occasions, we have taken her out to lunch. It is fun and I enjoy it because I know we won't have this opportunity next year.
One day when I picked her up, she asked, "Mommy, can we go out to lunch with Daddy?"
I wasn't able to that day and told her no. She asked again, "Please Mommy, can we go out to lunch we Daddy?"
I repeated my earlier answer and told her no. She then got very upset with me. "Mommy! That isn't how it works! You say no, I talk you into it and then you say yes!"
It appears I am a push-over.

One day when I picked her up, she asked, "Mommy, can we go out to lunch with Daddy?"
I wasn't able to that day and told her no. She asked again, "Please Mommy, can we go out to lunch we Daddy?"
I repeated my earlier answer and told her no. She then got very upset with me. "Mommy! That isn't how it works! You say no, I talk you into it and then you say yes!"
It appears I am a push-over.
Tuesday, September 27, 2011
Little N starts Kindergarten
Little N is now in Kindergarten. She was very excited to start on her first day. Her big brother walked her to her classroom, even though she already knew how to get there.
She got right down to business when her teacher suggested that she go play, she did just that! She also was very good at picking up her toys (never her favorite task at home).
She was fine when I left, barely looking at me as she said good-bye. Little N was very happy to finally follow her big brother's footsteps to kindergarten.
When I picked her up, she had a great day. Her only complaint was that she had to leave.




She got right down to business when her teacher suggested that she go play, she did just that! She also was very good at picking up her toys (never her favorite task at home).
She was fine when I left, barely looking at me as she said good-bye. Little N was very happy to finally follow her big brother's footsteps to kindergarten.
When I picked her up, she had a great day. Her only complaint was that she had to leave.
Sunday, August 21, 2011
The sites in Yellowstone
One of the first places we visited in the park was the mud volcanos on the west side of the park.

Both kids loved hiking through the mud volcano site. Little N listened well and stayed on the path, which made our lives a lot easier. Big N was pretty thrilled using my old digital camera to take his own photos.


Little N was not a fan of the sulfur smell that was prevalent at the geothermic sites in the park.


I harassed one of the other park visitors in order to get a rare photo of the entire family.


Later that day we stumbled across the Lower Falls at Yellowstone. This area appears to be responsible for the name of the park. It was spectacular to see.




Both kids loved hiking through the mud volcano site. Little N listened well and stayed on the path, which made our lives a lot easier. Big N was pretty thrilled using my old digital camera to take his own photos.
Little N was not a fan of the sulfur smell that was prevalent at the geothermic sites in the park.
I harassed one of the other park visitors in order to get a rare photo of the entire family.
Later that day we stumbled across the Lower Falls at Yellowstone. This area appears to be responsible for the name of the park. It was spectacular to see.
Thursday, August 4, 2011
Kindergarteners get the short end of the stick
My little girl is starting kindergarten, however, once again the school district is giving the kindergartners the short end of the stick. The kids will not even start school until September 14th. I wonder what this actually does to help the students, other than watch their siblings go to school and spend more time in day care.
I wonder if this means that like my son's first year of school, my daughter will not meet the state mandated minimum number of days in school.
Let's also point out that the school district ignores the fact that many families have both parents working. I'll assume that was something they concerned themselves with when they decided not to offer bus service in the middle of the day for the kindergartners.
Thanks a lot Ellensburg school district. Way to go on dropping the ball when it comes to your youngest students, once again.
I wonder if this means that like my son's first year of school, my daughter will not meet the state mandated minimum number of days in school.
Let's also point out that the school district ignores the fact that many families have both parents working. I'll assume that was something they concerned themselves with when they decided not to offer bus service in the middle of the day for the kindergartners.
Thanks a lot Ellensburg school district. Way to go on dropping the ball when it comes to your youngest students, once again.
Sunday, July 17, 2011
Seeing Thomas
Today Thomas the Tank engine came to visit Seattle, well, Northbend. The kids were thrilled! The major hit of the day, other than the ride, was the garden railroad display at the railroad museum. Big N would have stood there all day if we had let him.
The second big event was having Thomas run over some pennies. The kids thought that was pretty cool.
We are convinced that this may be the last year that the visit to see Thomas is a magical event. Big N enjoyed the visit, but it wasn't quite like the time we saw it when he was three.
Friday, July 1, 2011
Off to the Park
We have taken a two week vacation! I cannot remember ever taking this much time off in my adult life, other than maternity leave.
We started off heading towards Yellowstone National Park. After a few days, we headed to Rocklake North Dakota. After the trip to North Dakota, we headed to South Dakota to visit My Rushmore. It has been a whirlwind trip. Overall this has been a very positive family vacation.
It did start out a little hard for Little N. We drove two days to go to Yellowstone Park. As we're driving through the park to reach our campground passing herds of Bison and beautiful rivers, we hear from the back, "Where is the slide and the swings at this park?"
Little N was heartbroken to find out that a National Park is a different designation of the word park. She started crying, but we were able to make her smile after that.

Swedish Fish made it better
We started off heading towards Yellowstone National Park. After a few days, we headed to Rocklake North Dakota. After the trip to North Dakota, we headed to South Dakota to visit My Rushmore. It has been a whirlwind trip. Overall this has been a very positive family vacation.
It did start out a little hard for Little N. We drove two days to go to Yellowstone Park. As we're driving through the park to reach our campground passing herds of Bison and beautiful rivers, we hear from the back, "Where is the slide and the swings at this park?"
Little N was heartbroken to find out that a National Park is a different designation of the word park. She started crying, but we were able to make her smile after that.
Swedish Fish made it better
Tuesday, May 31, 2011
Tooth Fairy
The tooth fairy came to visit Little N while she slept last night. The tooth fairy left five dollar coins in Little N's borrowed tooth pillow. However, Little N's wild sleeping habits sent the pillow flying and one of the dollars disappeared.
Little N was disappointed, Big N was convinced her tooth must not have been clean enough since there was only $4 in the pillow. Big N had received $5 for his first lost tooth just over a month ago. This really didn't help the morning go well.
Luckily, we did find missing dollar this evening. It had become tangled up inside her pillow case. As far as Little N is concerned, all is now right with the world.
The tooth fairy and I need to chat about possibly switching to paper money in the future.

Little N was disappointed, Big N was convinced her tooth must not have been clean enough since there was only $4 in the pillow. Big N had received $5 for his first lost tooth just over a month ago. This really didn't help the morning go well.
Luckily, we did find missing dollar this evening. It had become tangled up inside her pillow case. As far as Little N is concerned, all is now right with the world.
The tooth fairy and I need to chat about possibly switching to paper money in the future.
Toothless Tuesday
Little N lost her first tooth yesterday evening! I was horribly unprepared, expecting her first tooth to come out much later using her older brother as a reference. Once again, I have proven to myself that by having two children all I am really sure of is how completely different they both can be.
Luckily for me, Big N jumped in and offered his monster tooth pillow for the tooth fairy visit. Little N was un-phased at not having her own pillow. In fact, I think she was very excited to use Big N's special pillow. He was very excited to let her share it, which brought out a little bit of my momma pride in him. It was a sweet moment in the household.
My little girl is growing up so fast and enjoying her toothless Tuesday.

Luckily for me, Big N jumped in and offered his monster tooth pillow for the tooth fairy visit. Little N was un-phased at not having her own pillow. In fact, I think she was very excited to use Big N's special pillow. He was very excited to let her share it, which brought out a little bit of my momma pride in him. It was a sweet moment in the household.
My little girl is growing up so fast and enjoying her toothless Tuesday.
Monday, May 30, 2011
Little N is ready for the summer!
My latest project has been a swim suit cover-up for Little N. It had to twirl and it needed a hood for wet hair. I also thought a pocket would be nice. The cover-up is loosely based off of one I came across on crafterhours blog. I used a sweatshirt to build my pattern and added a big front pocket.
Little N could not have been more thrilled with the outcome. She wants to wear it as a dress.
I started with two towels with complementary colors in them.
I then traced a dress that fit's Little N well and added a very generous seam allowance. My thoughts are that the beach cover-up should be loose and slightly large. I made the dress a little boxier. I also shortened it and planned on a 7-inch ruffle on the bottom of the dress. I used a sweatshirt to figure out how large the hood should be and how to modify the back piece to attach the hood.
I used my overlock machine for all of the seams. I only ended up using the sewing machine to attach the pockets, bias binding and hem the bottom.
I have one happy little girl who is ready to swim!
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