All three kids are attending school this year!!! Katie is loving Kindergarten and is really beginning to find her niche. Andrew is in a regular 3rd grade class. We had the expected beginning of year issues with Andrew, but he now seems to be settling in nicely. The biggest change is that Benjamin went back to school this year after 2 years of homeschooling. He is in the autism/behavioral class at our local school and is also mainstreamed into the regular 3rd grade class for a good portion of the day. He is doing fantastic! We've had a few hiccups (of course), but his good days have far outnumbered his bad ones. The teachers see his potential and are working diligently with him to help him to achieve it.
I get asked almost daily: "WHAT will you do with all of your time now that they are in school." My answer to them is almost always, "Sleep!" While I have taken my fair share of naps over the last few weeks, that is definitely now how I spend the majority of my time. For one, I am back to going to the gym at least 4 days a week; I was also finally able to get my bedroom and bathroom deep cleaned (after I don't know HOW long... longer than I care to admit); I am blogging again; I am enjoying going to the grocery store without having to drag my three kids with me; I am sometimes going to breakfast with my husband... because we CAN. Basically, I am enjoying my few hours of kid-free time every morning and am starting to feel more in control of my life.
While homeschooling, I felt like everything was getting out of control. I was overwhelmed with having to work very closely with Ben to get him to do his schoolwork while still homeschooling Kate so that she was prepared for Kindergarten. Then, I always had a deadline to finish our schooling for the day so that I could pick up Andrew from school, work with him in the afternoon and still fit in all of our after school activities, including therapy. My housework and workout routine were the hardest hit with the chaotic nature of our schedule. I often felt frustrated that I couldn't achieve all that I wanted to in a day.
One biggest benefit of them all being in school this year is that I am back to the more patient, fun-loving mommy that I want to be. I have a lot more patience with Andrew when he comes home exhausted and overstimulated from a full day of hard work at school. I am far more patient with Katie when she asks to read 4 or 5 books when I know I should be cleaning. I am far more patient with Ben when he runs away when I tell him to get up to the table for homework. I am playing with my kids more. We have spent a lot of time outside and I am loving that they are all begging me to jump on the trampoline with them or ride bikes with them. The few hours to myself during the week allows me to focus on me. That is something that I haven't been able to do for the last 9.5 years and I think everyone is benefiting from it.
A collection of stories, kid bloopers and parenting/homeschooling ideas from a family with two special needs kids and a "typical" preschooler.
Sunday, September 29, 2013
Saturday, September 28, 2013
Feeding Issues? Understatement!
Ben: "Mom? Can I have some chocolate chips and fruit snacks and Doritos please?
Kate: "Mom!? Can I have some peaches and some red and green peppers and some carrots for snack? Make sure you give me lots of red ones! And broccoli for dinner!" (This is not a dramatization...this was a real conversation I had with my children an hour ago).I stare at both of my children dumbfounded and wonder where I went wrong with my son and how I could have possibly done better with my daughter. Then, I wonder why it is that I am bribing my son to eat 9 grapes (since he is 9 years old) with the aforementioned junk. At least THAT answer is fairly easy.
Benjamin has feeding issues. He isn't picky in the traditional, "my kid doesn't like veggies" sense. It goes far beyond that. Some feel it is from the lack of strength in his jaw from the CP. Some feel it is one of his autistic traits, some feel it is just behavioral. One thing that I am sure of is that it is one of the worst parenting issues I have ever had to face.
When he was a baby, he left the hospital a month after Andrew because he had a difficult time with taking a bottle. He got the hang of it eventually, but feeding was still an hour long ordeal. I made all of their baby food once they transferred to solids and noticed that Ben did not like increasing textures. He tolerated some eventually and around age 1 was moving to table foods.
Then, he got a cold. He was coughing so badly that anytime he ate anything not completely puréed, he would vomit. Being fearful of my underweight, high risk preemie losing weight, I fed him baby food and yogurt to get him through his illness. After that, he refused to eat anything with texture to it.
We began very expensive feeding therapy, which only made it worse. It made him anxious at meal times and suspicious of hiding foods in the textures he would eat. At age 3, he was eating 6-8 jars of 3rd stage baby food in a sitting and supplemented his diet with yogurt and Pediasure. There was talk of feeding tubes if he did not continue to gain weight, but I was not about to give up on him learning to eat.
On Easter when he was 3.5, I walked in his room to see him scarfing down M&Ms from his Easter basket. I immediately went downstairs and threw away all baby food in my pantry. If he could eat candy, he could eat other things.
And so began the excruciatingly slow process of getting Benjamin to eat. I scoured the Internet for ideas and suggestions. I was very fearful of feeding therapy from our past encounters, but I did ask some therapists for some advice.
We started with "take a bite, get a bite." If he took a bite of a new food, he would get an M&M. It was very slow going. He would often "pocket" the food in his mouth and refuse to swallow. He would cry and I would cry. Mealtime was dreaded.
He soon learned that he liked Cheetos, graham crackers and chocolate chips. Soon after came the first real meal he ever ate...ravioli with meat sauce. That opened up a whole new world for us. We had called the ravioli "spaghetti" at first, so anything with red sauce was soon called spaghetti. He liked spaghettios, spaghetti, ravioli, and lasagna and freely ate those without any issues and eventually without bribery. We still supplemented with Pediasure daily.
He is now 9 years old and I would love to say that he eats a well balanced, completely healthy and diverse diet. While he has now expanded tremendously from his 3 year old diet of baby food and yogurt, mealtimes are often frustrating. His favorites are still red sauce based foods, but have expanded to include "chili a la spaghetti," "enchiladas a la spaghetti," and cheese pizza. He loves plain canned pumpkin (weird, I know) and loves when I add it to pancakes. Sandwiches are new within the last year or so and we are now able to get him to eat bites of most of our family meals without too much fighting. He loves chicken nuggets. He will voluntarily eat bananas and raisins and will eat broccoli, grapes and green beans fairly easily. His old rewards of chocolate chips, M&Ms, chips and fruit snacks are still items he wants on a regular basis. The most exciting event this year was the transition to milk instead of Pediasure. We have been working on that for about 2 years.
It has been a long, frustrating experience. Whereas Kate just picked up her food and ate it as a toddler, we had to fight for every bite with Ben. People just plain don't understand why we were so excited the first time Ben ate a donut or a hotdog or a bite of ice-cream... Or why I cried hysterically on the day that Kate ate her first Cheerio, which happened to be the same day Ben ate his first Cheerio.
If you are dealing with feeding issues with your special needs child, know that you are not alone and that there are those of us who understand the daily struggle. It isn't easy and is extremely emotional. Other parents don't get it because they can't. Having Kate has made me realize that there is a lot that parents of typical kids take for granted and that's just the way it is. Like so many things, you have to live it to understand it.
Labels:
Cerebral Palsy,
Feeding issues,
Parenting,
Special Needs
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