Demystifying Alternative Therapies for Children with Autism

Reposted with permission from Healthism.

For parents of children on the Autism Spectrum figuring out treatment can be tough. The spectrum is vast and children have different symptoms and triggers that require different treatments. There are a number of ways to treat your child’s needs through different therapies – from the way you eat to different activities you do. That is why we’ve contacted the BEST of the best when it comes to Autism specialists to find out more about each treatment.  Here is what they had to say:

  1. GLUTEN FREE & ALL NATURAL DIETS

    WHAT IS IT?
    Improving your child’s health by changing what they eat.

    HOW DOES IT WORK?
    Children with Autism tend to have food sensitivities more than food allergies, the biggest offenders can be gluten and casein (casein is a protein in dairy products and gluten is found in wheat, barley, rye, and some oats). Some autistic children have vast improvements on a Gluten Free Casein Free diet (GFCF) while other do not.

    Also, a diet of minimally processed, or foods in as close to their natural state as possible, can help some children with Autism. One common symptom of Autism is gastrointestinal (GI) upset because children with Autism often lack, or have very low levels, of detoxification and digestive enzymes. This leads to poor digestion and absorption of food and nutrients resulting in a multitude both behavioral and physical symptoms. Minimally processed or all natural foods contain less potential GI and behavioral triggers which can mean all the difference to a child with Autism.

    HOW DOES IT HELP? The first major improvement is an almost immediate reduction in GI distress. The effects vary, but some parents have actually proclaimed to have “gotten their child back” due to the vast improvement in behavior and reduction in autism symptoms.

    Also, almost everyone notes a positive change from shifting to a natural diet. A recent study found that autistic children who experienced chronic GI distress had the greatest improvements in behavior and social interaction when compared with autistic children without significant GI distress.

    Colleen Hurley, RD is a Wholistic practitioner, Registered Dietitian, Certified Kid’s Nutrition Specialist, and a Master Gardener offering wellness education through services and her website at www.colleenhurleyrd.com.

    Debi Taylor, Autism Specialist; www.SpiritOfAutism.org

  2. CRANIO-SACRAL THERAPY WHAT IS IT? Improving Health by Allowing The Breath of Life to Do It’s Job

    HOW IS IT ADMINISTERED? Biodynamic Craniosacral therapy orients and magnifies the forces that direct cells to do their job. It has one foot rooted in anatomy, and another in what practitioners call the breath of life that breathes in all of our cells every second. Healing occurs by these forces communicating more strongly, and clearly in a person’s energy field and body and tissue field. It works at the root level of health which is the quantum physics of the body.

    The breath of life is the similar to electricity in that it’s used everyday as it breathes and directs each cell. Practitioners do not quite understand how it happens, but with Autism these forces can be blocked by various conditions at birth, in-utero, from genetics, and from environmental toxins. Biodynamic Craniosacral therapy allows the body to show the practitioner what level it wants to work on. It orients towards the forces that are present from conception on, to magnify them to heal areas where the body is less connected to these baseline forces specialists call the breath of life.

    When cells and the entire body connect more to these forces of health, the body heals on emotional, mental, physical, and energetic levels. Craniosacral therapy will improve one’s health by strengthening the body’s innate intelligence and a sense of well being occurs.

    HOW DOES IT HELP? Some practitioners have had good results with this, as Craniosacral therapy supports whatever is needed at anytime. The affects are direct and indirect. Treatment can magnify other therapies as well as support maximizing the child’s brain development. When children and their parents receive Craniosacral therapy (as both should be treated since they are all in a unit) it supports their nervous system, immune system, and more, as healing happens where it is needed.

    It is believed that only the body knows exactly what it needs, the practitioner just holds the proper container for healing to happen. While the practitioner is tracking what is happening with their client, they make sure to “get out of the way” to allow the breath of life to do the job.

    Dr. Kate Klemer has been practicing Cranial work since 1986. She has studied various forms of the work. Over the past 10 years she has been training to be a teacher of biodynamic craniosacral therapy. www.drkateklemer.com.

  3. EQUINE-ASSISTED THERAPY WHAT IS IT? Help through horseback riding.

    HOW DOES IT WORK? After an initial application and intake process is done, a child may start a specific treatment plan specific to their needs. This will include elements of occupational, speech and language, physical, and cognitive behavioral therapies. While a child may spend up to 45 minutes riding they also work on daily living skills. They are taught the daily care of a horse like grooming and feeding which is paralleled to their own self daily care. LifeStriders Therapeutic Riding Center also makes sure to include sensory integration, so the children are playing games and doing activities while riding.

    HOW DOES IT HELP? Many people with disabilities don’t have a normal gait, a common symptom of many children with Autism. When a person is not moving how they were meant to move the brain doesn’t get certain kinds of stimulation. With Equine-Assisted Therapy a horse carries four beats per step, so a child’s brain is getting stimulation they wouldn’t get with their normal two beats per step.

    There have also been studies that show that oxytocin, or the bonding hormone, is released during riding. A result of this is an increase in sustained contact. And while the brain is stimulated week after week they’ve seen increased verbalization in most of their non-verbal patients. Many non-verbal students even say their first words during riding, which is music to a parent’s ears.

    Veronica Sosa Agnoli, MS, LPC is the Executive Director of LifeStriders Therapeutic Riding Center, establishing LifeStriders as a leader in the field of Equine Facilitated Learning/Mental Health and therapeutic riding.

For more articles discussing tips for teachers, preparing them for college, great resource roundups, and more, visit http://blog.healthism.com/.

Have you used either of these therapies with your children? What have you seen that works or doesn’t work? Is there an alternative therapy you use that we haven’t covered?

Practical Gluten & Casein Free Substitutes

I perpetually have the best intentions in trying to eliminate gluten and casein from my child’s diet (to read about why you should consider a GFCF diet for your autistic child, see my previous post). However, I’m a single mom with a grocery budget, so going the extra mile for organic and special brands aren’t always practical! Add to the mix an older child that is one of the pickiest eaters in the universe and sodium and sugar restrictions on my own diet… it is not unusual for me to buy and prepare three separate menus in this house.

I thought I would put together a small list of some common items found at your local grocery store that are gluten and casein free. Some may not be the healthiest, but it is nice to know that there are options to sometimes buy these common brands, saving a trip to the ATM a health food store.

Snacks

Juices/Drinks

Candy

Cereal

What are some of your experiences? Feel free to head over to the Spirit Of Autism Facebook Fan Page and post some of your successes, strategies, and struggles with the GFCF diet in your home! I’d love to hear from you.

DENIED! Why am I Doing the Happy Dance?

Six months ago I applied for SSI Disability to help me provide for my Autistic son. Meeting the income guidelines for this assistance, I jumped through all the required hoops of their dog and pony show. I supplied them with a 92-page history and timeline of all Justin’s diagnoses, school records, IEP copies, behavioral and developmental assessments, medication history (yes, I at one time investigated that route out of sheer desperation – a story for another day), and every behavior slip, suspension and punishment notice he’d ever received.

I saw their doctor. I followed up, week after week, inquiring about their decision. All the while, in my journey, I was learning about my son and Autism. I was not happy with the doctor visits, the medication attempt, the rigid recommendations, the books, the cookie-cutter approaches.

In this journey I came across a book by Dr. Robert Melillo called Disconnected Kids. Along with the centers he founded, this book offered a scientifically proven theory about a hemispheric imbalance in children with Autism, ADHD, Dyslexia, Tourette’s, and other disorders. I voraciously digested this information and began applying what I learned immediately. I tested and modified some of the sensory exercises and techniques. I expanded my research on the nutritional guidelines. I drew some new conclusions.

I began supplementing with EFT, teaching my son to tap and performing surrogate tapping when he could not. I also began graciously opening my heart and accepting the gifts of his beautiful mind. The docile nature of our beautiful Alaskan Malamute, Juno, has also had an extremely calming effect on him.

These things combined have changed our world. Oh, our journey is nowhere complete, as he still cannot tie his shoes or ride a bike; we still have days where a trip to the grocery store is a nightmare. It still takes an Act of Congress to get him ready in the morning on time for school. We are working on it, as I refine the techniques that have shown me hope and success. He is now able to smell and recognize scents; we can go to the movies and sit through an entire film; I don’t receive calls to pick him up from school early for being out of control… and he was denied for SSI.

According to my letter, “… the evidence does not show that these conditions are severe enough to be disabling. We have decided that Justin’s condition is not disabling under our rules.”

I’ve been denied, and I’m ecstatic! What mother would not want this kind of news?