Showing posts with label autism preschool. Show all posts
Showing posts with label autism preschool. Show all posts

Sunday, May 23, 2010

The GF/CF Lunchbox

I had a really wonderful opportunity last month to teach a little class about food sensitivities. I shared our family's stories, (see food sensitivities part 1 and food sensitivities part 2,) and demonstrated some really delicious chicken recipes that we have run across and found helpful with our son. One of the moms that was there asked me what I put in my son's lunches that he takes to school. I had a couple of ideas ready, and I thought I would post them here, along with afew other things I have sent him with. Some of these things will seem odd, like the pasta with peas stirred in, but since this is the main way that I can get green things down him, I take advantage of that, for sure. Every child will tolerate different things of course, but I hope that this list helps some parents out with ideas.

* I should probably mention that my son's lunches are more than just GF/CF. They are also corn, soy, sugar, additive, preservative, and coloring free.


Special things I make for his lunch


pizza
brown rice or Lundberg's brown rice couscous cooked in veggie broth, salted, with peas added
rice flour tortilla with filled with flavored re-fried beans
falafel
chicken nuggets (recipe adapted from eatingglutenfree.com)

Leftovers from dinner
making extra dinner is a great way to have an easy ready made lunch

chicken soup made with rice
chili
tortilla soup
stir fry
brown rice pasta (he won't eat spaghetti sauce, so he gets earth balance spread on his noodles with salt added, often with green peas or mix veggies stirred in.)

Other
things I add to above listed main courses

apple slices
carrots
raisins
peas
green beans
olives
cucumbers
green pepper strips
all natural potato chips
GF/CF muffins
GF/CF crackers (homemade 'fake' graham crackers or store bought rice ones)

I'm sure I am forgetting some things... I will add as I remember. I always send my son with his little klean kanteen full of filtered water as well as a healthy "suits his system" meal.

Sunday, December 6, 2009

Speech Progress!

Autism causes caused developmental delay that often severely tampers with speech development. Our son not only has autism, (inherited from the family,) he also has additional issues with speech. (Also inherited from the family.) He has had many "Eli" words for many of his favorite things for a long time. For example, "Go-Go" was Gordon the train from Thomas and Friends for quite a while. I just had to write a little post to say that we have had some things going for us in the speech department lately.

Eli's doctor has put him on a pretty high dosage of vitamin E, which of course he monitors. He said that it helped with speech development. Also, at Eli's new autism preschool he receives significantly more speech therapy than he used to. (Next week the speech therapist is even meeting with me to teach me things we can to at home with him. Exciting!) The result of these changes has been just pure awesomeness. Yesterday after some coaching Eli learned how to say "Thomas" correctly. He has always loved Thomas the Tank Engine, but for the longest time he has called him "Boo-Ess," then he was "Mum-Ess." Now at age 4 and 1/2 he can finally call him Thomas! We could not be prouder. Now if I can just get him to stop saying "Bups" for "Grapes."

Thursday, November 12, 2009

Parent Training

My son's autism preschoool has parent training nights and I think it is so wonderful because parent education makes all the difference. Tonight after coming home from one, however, I have to admit I am alittle frustrated. Some parents were discussing "the diet" and basically putting down biochemical intervention. It was obvious that they had not tried to educate themselves on it. I told them I have been doing biochemical intervention for a year, I told them about the monumental difference (his social smile, understanding discipline, etc.) I said there is a book they can read, (Changing the Course of Autism, by Dr. Bryan Jepson,) and that I am willing to talk to anyone about it. After that I tried to keep my mouth closed. It was hard because I feel like even if they choose not to do it, they should not discredit it. To me that is wrong. One parent approached me afterward, and she understood exactly how I felt! "Some people are so ignorant about food," she said. I can't explain how relieved I am that there is another parent like me in the group and I look forward to talking to her again on the subject.

One of the handouts we got tonight was a little story. I read it once in Jenny McCarthy's Mother Warriors book, and I have to tell you it never looses significance for me. I think the author got it head on.

WELCOME TO HOLLAND

by
Emily Perl Kingsley.

c1987 by Emily Perl Kingsley. All rights reserved

I am often asked to describe the experience of raising a child with a disability - to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this......

When you're going to have a baby, it's like planning a fabulous vacation trip - to Italy. You buy a bunch of guide books and make your wonderful plans. The Coliseum. The Michelangelo David. The gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland."

"Holland?!?" you say. "What do you mean Holland?? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy."

But there's been a change in the flight plan. They've landed in Holland and there you must stay.

The important thing is that they haven't taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.

So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around.... and you begin to notice that Holland has windmills....and Holland has tulips. Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy... and they're all bragging about what a wonderful time they had there. And for the rest of your life, you will say "Yes, that's where I was supposed to go. That's what I had planned."

And the pain of that will never, ever, ever, ever go away... because the loss of that dream is a very very significant loss.

But... if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things ... about Holland.

Sunday, October 25, 2009

The Pictures Don't Lie

These are snapshots I took of Eli's preschool pictures. In the first one he is barely 3, and in the second he is 4 and 1/2.

Photobucket

This one with the glass glare was taken early in 2008. Although not really smiling, he is looking in the general direction and seems to show curiosity on the photographer.

Photobucket

I was so shocked and pleasantly surprised to pull this packet out of Eli's backpack last week! What a difference! Here he is obviously engaged... what progress.

Biochemical therapy has made him so much more available for learning. His schooling, and life experiences, and activities with mom and dad have been more beneficial for his learning than ever. His academic progress has been phenomenal. (He can read many words.) But it is his social progress that makes me the most proud of all, and these pictures are a clear documentation of that.

Thursday, October 8, 2009

Dr. South and Recycled Clothing

It has been alittle while since I have updated. Even though Eli has been in school, I have somehow been very busy. One thing that has been occupying my time is creating products for the upcoming Beehive Bazaar in Provo this next month. I was so thrilled to be accepted because it is a very trendy artsy type of show.

thebeehivebazaar.com


The products I am submitting are eco friendly. I am producing clothing made from pre existing fabric. Most of it is from donated pre loved clothing and linens. I was required as part of the application process to tell them why I do what I do. The answer is simple: Less toxins in our environment means less cases of autism, and as an autism sibling and mom that is important to me.

reconstruction

Photobucket

Acouple of weeks ago I went to a meeting all of the Giant Steps parents were invited to on BYU campus. The meeting was led by Dr. South and his students in the psychology department. At this meeting I learned that the Giant Steps program is in constant danger of losing funding, and has been threatened especially so this school year. The research that Dr. South and his students do is in part right in the preschool program. I am so excited about this because if they can come up with the actual documentation to show how essential the program is to the kids, it is far less likely to get funding cut because the results are then proven in numbers.

Some of the senior students of Dr. South's presented research on how autistic children reacted to trials differently then typical children. Their findings were interesting, but I kept thinking to myself, autism effects the whole body, not just the brain! Being a parent who is a biochemical therapy convert is maddening at times. I feel that more answers could be found if only all symptoms were taken into account.

Sunday, August 23, 2009

The Move

I haven't posted for awhile because of all the chaos of our recent move. It is all over though, and we are happy with our new place! The reason for our move was the autism preschool located in Orem, Utah, called Giant Steps. It is public, but it is funded by the Wasatch Mental Health Department. Translation: it is free and the program is cutting edge. The downside is that our son had to be on the waiting list for this program for 2 years. We had to be living in Utah County for him to attend, but that was OK because anything out of the county was just too far to commute for a one car family. So here we are! This program is totally worth the move and we are pumped! It is an ABA based program, (although they will use whatever method works for the individual,) and it is four days a week, with full school days!
Photobucket
Photobucket
Our last move was back at the end of December of last year when we moved north in order to complete hubby's education. That move was hard on Eli, as you would expect for a young one with autism. We had lots of uncooperative behavior, vocal outbursts, sleep disturbances, etc. He stopped being manageable with taking supplements for a while there, too, but we kept trying. Once we started getting the supplements down him again, things started getting better, and then he started school at the public school there, and things got even better. We have kept with the biochemical intervention for this whole year this last month and let me tell you how great he is doing! Eli now calls me "mom" and his dad "dad." His vocabulary is growing everyday. If he is looking for a favorite toy train he will say "Gordon go?" He tells me about things in his little shows he likes to watch. He is starting to have more and more of a social smile. This recent move has been such a switch from the one back in December! No regression at all.
Photobucket
Eli had some very kind little friends in our town we lived in up north who taught him so much about interaction, playing and friends. We miss all of you sweet little people! These are some pictures to show his friends how happy Eli is at the new place. There is a swing in the backyard that is cut from an old tire.