Some History...

We welcomed Phoenix into our family on November 24, 2007. I was 37 weeks pregnant at the time, but our little boy came into this world weighing 3 lb. 14 oz. Come to find out later it was due to a blood clotting disorder I didn't know that I had at the time. Phoenix scored low on his Apgars, was groaning, and did not cry (he never has cried to this day). He was sent to Children's Hospital in Milwaukee where he spent his first three weeks of life surrounded by loving nurses, visitors, and family. Doctors there found that Phoenix had been experiencing minor seizures, which went away after a few months time.

As Phoenix grew, we noticed that he didn't meet the normal developmental milestones that he should have. There were times where we would say, "can he see?", "can he feel pain?", "can he hear?", "can he talk?", etc. Phoenix was involved in the Birth to Three program from the age of 3 months to 3 years. At the age of 3 he started Early Childhood Education.

Due to his developmental and social delays, we had him evaluated at age three to see if there was anything that the neuropsychologist could tell us. After extensive testing, and 4 long visits later, they informed us that Phoenix had Pervasive Developmental Disorder-Not Otherwise Specified, which is to say Phoenix diagnosis falls on the low end of the Autism Spectrum.

As parents, we wanted to do everything that we could for our little man. We implemented a gluten-free and caisen-free diet, which has helped tremendously. At age four Phoenix is acedemically developed every bit of his four year age; however in other areas of developement Phoenix is still at a 2.5 year old level or below. Trying to be an informed parent, we searched the internet looking for a way to help Phoenix. This is when we stumbled upon a site for Brain Balance Centers which uses a natural, non-drug approach to normalizing brain and body functions. We are fortunate to have a center in Mequon, about 40 minutes away from our home. After talking to parents who have sent their children to Brain Balance with positive success, we started taking Phoenix as of 11/28/2011. This blog is Phoenix's Journey towards an improved way of life.

How It All Started...

A few months ago, I was researching Autism and options to help Phoenix with his PDD-NOS and came across a website for Brain Balance: Achievement Centers. As I looked at the site, I noticed that there were seminars in the area that gave an overview of the program. On a Wednesday night, my mother and I went to meet Dr. Jeremy Fritz and hear a lecture on what Brain Balance is all about and what the program entails. My mother and I were very impressed. It made complete sense... Through research they understand that the underlying cause of many of the disorders is a functional imbalance of brain activity between the right and left sides of the brain. After much discussion and reading the book Disconnected Kids by Dr. Melillo (the founder of Brain Balance) we scheduled an appointment to have Phoenix evaluated to see if he was a good candidate for the program. A week later, we met with Dr. Fritz who went threw the evaluation results. Being very cautious I recieved a list of parents that have taken their children to Brain Balance and asked them about their children, their experience, and what thoughts they may have. It was AMAZING! They had success with their children. There was one parent I talked to that her son was nonverbal and within the first 4 weeks he started to talk. There was a parent as well that her son had sensory issues and was not calm at all and within weeks he was calmer. The mothers I talked to, including one I met in the waiting room today, said that the time and expense were worth the success their children have had with Brain Balance. A few days later, I called and signed Phoenix up for this new program. I can't wait to see the little or big successes that Phoenix will have. http://www.brainbalancecenters.com/

Wednesday, May 9, 2012

Week 19

Phoenix has been chewing on his shirts for quite some time.  He will sit and just chew away while his collar and chest area get soaked and full of small holes. Once it gets to that point, we take off his shirt and sometimes even throw them away.  I am a little bummed because someday I would have liked to have a rummage and sell them, but can't.  

So, this weekend I decided to do some research and came across this article: 

http://recoveringnoah.blogspot.com/2007/09/answer-to-noahs-shirt-chewing.html


(a bonus article about potty training autistic children)

After reading about the shirt chewing and the experience this mom had, I thought I would experiment and take palm oil out of Phoenix's diet. On Friday we switched from peanut butter sandwiches to turkey, his butter was thrown out, and his healthy fruit snacks were no longer added to our grocery cart.  They all contained palm oil.  With those items eliminated, we saw a change by Saturday.  Phoenix was able to sit and not chew his shirt constantly.  He does have instances where he will still bite it, but only when he is upset or angry. For this past week, Phoenix has not had a wet shirt!  I think this is progress! 

As for the instruction that Dr. Fritz gave us regarding his diet, we are no longer giving Phoenix french fries and have eliminated sugar thus far and I have increased his natural juice.  So far so good.   

 


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