Autism Therapy: intravenous (IV)

definition of intravenous (IV): Route for giving medications or other liquids (i.e. salt solutions or liquid foods) by injection directly into blood vessels. Single injections or bags of fluids may be given I.V.

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Journal of Nutritional and Environmental Medicine, by Boris, M., Goldblatt A., and Edelson SM, published in 2006, summarized Nov 22, 2006

Monthly treatment with intravenous gamma globulin (IVIG) may improve hyperactivity, inappropriate speech, irritability, lethargy, and stereotypy in children with autism.

This open retrospective study included 27 children with autism, who had failed to show improvement with dietary elimination of dairy and gluten, vitamin and mineral supplementation, and behavioral educational therapies. Previous studies have suggested that children with autism may have immunological disorders. The group of children in this study had many signs of an overly strong immune response including a high level of antibodies to myelin basic protein, thyroid, and DNA. IVIG is an approved immunological therapy that is considered to be safe for individuals with autoimmune diseases. The authors found that IVIG therapy for six months resulted in improvement in all measured aberrant behaviors.


Arch Dis Child., by Wang, HS, Kuo MF, Chou ML, Hung PC, Lin KL, Hsieh MY, and Chang MY, published in 2005, summarized Oct 21, 2006

This article reports that certain types of epilepsy can be controlled with vitamin B6 supplementation, and may be even better controlled with PLP supplementation.

It is known that vitamin B6 can help reduce the seizures of children with epilepsy. The authors of this article wanted to determine whether supplementation with PLP, the active form of vitamin B6, would work even better than supplementation with vitamin B6. This study focused on 94 children with severe idiopathic epilepsy (8 months to 15 years old). These children received PLP intravenously. In eleven patients, seizures stopped after PLP treatment, and in these patients, vitamin B6 supplements (50 mg/kg body weight per day, or about 909 mg for a 40-pound child) were used instead of intravenous PLP. After the switch to vitamin B6, six of the eleven patients were still free of seizures. No significant side effects were observed. The authors note that it is not yet known why some children with epilepsy respond to vitamin B6 or PLP treatment.


Jennifer Blaton of Shreveport, LA, like a lot of parents, will stop at nothing to help her daughter with autism. At the foundation of her daughter's treatment is a gluten- and casein-free diet; this appears to have made the biggest different in Darbee's integration. In addition, Blaton gives her daughter vitamin supplements including B12 and magnesium sulfate cream. Her daughter receives regular testing for the presence of heavy metals in her body as well as monthly intravenous chelation treatments. While Darbee is non-verbal, she makes straight As in school.

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One parent's story of success

Oct 26, 2006 by Anonymous

My daughter Katie was diagnosed with PDD-NOS when she was 26 months. A follow-up visit to a Developmental Pediatrician suggested a move to the diagnoses of Autism as she fit the DSM-IV criteria. The suggestion was that it would also be easier for me to get appropriate services for my daughter, in which case she was very correct.

Our story is long as most of us who experience this diagnosis and I won't get into the advocacy and struggles we encountered along the way. When Katie was diagnosed my research confirmed that an ABA type approach would most likely produce the best results. I understood that the most benefit would be made if we began early. And I understood that we needed a program that involved my daughter in 30+ hours of intervention.

We relocated rather then continue to debate approaches with our EI team. We enrolled our daughter in the Margaret Murphy Center for Children in Lewiston, Maine. They used an approach that follows the teaching's of ABA, an approach referred to as Verbal Behavioral Therapy, www.drcarbone.com.

Katie began at 32 months for 15 hours a week. She napped after that and I involved her in social activities in the afternoon. There were lots of drills and repetition, but within 2 months, the child who had no need for any expression of language, the child who made no requests, began using sign language. In 4 months she had 20 signs that she was using appropriately.

When she turned 3 Katie qualified for 30 hours of ABA. Three was a tough age. As Katie became more a part of the world and wanted more from it, she also tantrumed more and appeared even more "autistic" to me. We observed an increase in stereopathy, she started flapping, and her tantrums sometimes involved self-injurious behavior. I expressed my concerns during this time. The team adjusted Katie's program and gave her more flexibility which resulted in improved behavior.

Designing a program around a child's particular needs rather the keeping a program "by the book" is very possible and can still produce fabulous results. There are many misconceptions about ABA. Don't believe it, find out for yourself. I called different centers and spoke to parents. I observed and pick the location that I felt comfortable with. I had two other children so therapy in the home would not work for us.

I had difficulty figuring out how to support Katie at home, she wouldn't do for me what she would do at school. But then I'm the mom and decided to keep it that way. I found support from another agency that provided in-home support to children with significant disabilities. We trained her at Katie's school. She played with Katie in the afternoon while I engaged my other children and prepared dinner.

I enrolled Katie in Gymnastics, swim lessons and attended a church with a Sunday School program so she could be with typical peers her own age.

All of these steps were critical in determining Katie's readiness for preschool part-time while continuing her program.

Katie's language soared shortly after enrolling in a preschool program. There were concerns about the acceptance of Katie's behaviors by her peers. Her peers were fabulous, and a community began to be developed of people who understood Katie and accepted her for who she was.

Katie used to be happy playing alone, but now she would prefer to be among her friends more then anything else. Katie is a typical 5 year old child in her kindergarten class. She has many friends and goes on playdates. Another mother picks her up afterschool one day a week for a playdate and then takes her daughter and mine to gymnastics where I meet them after my son's piano lessons. My girlfriend doesn't believe that Katie has autism and thinks it must have been a mistaken diagnosis. I chose not to tell her about what Katie looked like at three.

We no longer use formal ABA techniques. Katie is still working on fine tuning her social and communication skills. But if you were to meet her and strike up a conversation, you would not notice her to be any different then any other child of her age. Katie's outlook is bright as a result of using ABA techniques to help address her autism.


Stepping up to the plate

Oct 24, 2006 by Anonymous

Autism can happen to anyone, it doesn't matter your socio-economic background, your level of education or your genetics. It is an epidemic. I can't mention Katie's autism without hearing that someone knows someone else with Autism/Asperger's/PDD.

 

I have a Masters in Counseling, so I've studied the DSM-IV, but that was before ASD (Autism Spectrum Disorders) became popular. I say that tongue in cheek because I do not believe that ASD is just a "popular" diagnosis. I have been an adult long enough to have seen that there are many more children with the traits of autism running around.

 

So what's in a label?? Well, when it comes to qualifying for services or getting appropriate intervention, depending on your state and your school, the type of Autism your child is diagnosed with can be critical.

 

Katie was "upgraded" as I chose to call it, to "Autism" shortly after a team diagnosed her with PDD-NOS. She fit the criteria and the Developmental Pediatrician knew that it would be easier to get Katie what she needed with the proper diagnosis. It hurt a bit, like a slam of reality, but she was right...it made all the difference in the world........

 

 



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