Wednesday, March 11, 2009

Taking it on the Road: Tip 2




Tip #2 Call or Google ahead to locate Health Food Store availability.

This tip might be in the wrong order and may be best as number one - that is because we won't go anywhere or plan a trip before we have this tip taken care of. Finding a good source for all your needs is vital to a successful vacation. We google and call the store directly with our list of needed items. If this is done with adequate enough time the store can order items that they don't normally carry. This is a great win-win for you and the store. You don't have to pack a whole lot of food from home and when you arrive at the store all your goods are packed and ready for pick up. The store wins with your business and your customer satisfaction.
This is a great source for locating a wide range of health food stores from the giants of Whole Foods to the tiny corner shop: http://www.greenpeople.org/healthfood.htm

If you are one of the lucky ones who can do resturants without negative side effects you can check out this website http://www.glutenfreerestaurants.org/ to find a GF (not necessarliy DF) resturant for your family dinning pleasure.

I also recommend locating the local farmers markets. This has been a great money and time saver for our fresh produce, as well as a fun outing for the whole family.

Taking it on the Road: Tip 1


We are gluten-free, dairy-free, corn-free, soy-free, egg-free, rice-free, and stress-free as we vacation in Nevada today. So what am I doing writing a post when I am suppose to be on vacation? I am having such a nice time with my husband and two great kids as they frolic in the dessert sun in the crystal blue pool water at the Cancun resort. Their smiles warm my heart more than the hot Nevada sun as they splash off the water slides for the 100th time. I think to myself how blessed we are to be on vacation despite the challenges of dietary implementation.
I think this is amazing that we are on vacation with a special needs child with severe food allergies, multiple nutricuticle needs and no predictable routine and we are having FUN!. We have come a long way over the past 8 years of biomedical and behavioral treatments and days like this are proof that consistant work pays off. This is our second family vacation (not including visits to family) where we take the show on the road. And I thought to myself...I wish others with kids with dietary and biomedical needs could experience the joy and thrill of making lasting family memories despite it all. For this reason I am writing - To share tips that may encourage families to take the show on the road. It will prove to be rewarding and freeing for the whole family.


TIP 1: PLAN AS A FAMILY
Take the time to plan your vacation location and destination with your entire family. Post pictures of the location and talk daily about fun things you are hoping to do together (don't set anything in stone...you don't want to build false hopes and grounds for serious meltdowns). Talk about the plane trip. What kind of plane will you be traveling on, what to expect in the airport security, and who gets the window seat. Play airport, show pictures of the ports you will be passing through (direct flights are best). We always enjoy watching videos of possible attractions, airplane rides and vacation related things on YouTube (you will be amazed on the helpful things you can find. We spent a great deal of time watching subways and monorails for vacation preparation once).
If you are traveling by car, mark a map and highlight cities you will stop in along with the attractions. Look at pictures of each city on the internet as well as the hotels you will be staying at. We always make sure we stay at ones with pools (and in the cooler months indoor pools are a must).
Whatevery type of transportation you decided to take this vacation, preparation can help increase enthusiasm and reduce stress for most. It brings a sense of partnership and ownership to the entire family in regards to vacation planning.

Mark your calendar and start counting the days together. The anticipation can be half of the fun!

Tuesday, February 24, 2009

Hope and Help for Picky Eaters



Julie Matthews: Autism Nutritionist Expert

Hope and Help for Picky Eaters






I know what you are thinking, "My child is picky and very inflexible with eating new foods. I'm never going to be able to get him to eat anything other than wheat and dairy, and never mind anything 'healthy.'" I also understand that you are really wondering if an autism diet will help your child and their symptoms.I appreciate these concerns. I have had some very picky eaters in my nutrition practice-many children ate only bread and dairy, others subsisted on just pancakes and fries. When the body creates opiates from foods, one can become addicted to them and thus crave nothing but those foods, or when yeast overgrowth is present, a preference for only carbs and sugars can result. Children eventually narrow their food choices to include only those that make them "feel better" (in the short term). It's worth trying diet (whether it's GFCF, SCD, or another) because once the child gets passed the cravings (a few days to a few weeks), they often expand food choices dramatically and it becomes much easier to do. Most of my clients with autism eat limited amounts of vegetables-if any. However, it's also very common that once they apply diet (and the cravings diminish and appetite increases), children begin eating more vegetables (or meat)-often for the first time. In fact, this is the experience with a majority of my clients. Now, there are some children that are very self-limiting, and it takes time to change their diet. But keep at it.

NOTE: Don't remove all foods with the expectation that "if they're hungry, they'll eventually
eat." While this may be true for many children, some have real feeding challenges and may stop eating altogether, which could be very problematic. Add new foods before removing others. Be sure to seek professional guidance from a feeding specialist or qualified clinician if your child won't add any new foods.Addressing picky eating is essential for expanding the diet and implementing an autism diet, but sometimes the diet won't expand until certain foods are removed. Don't let picky eating stop you from implementing an autism diet. Find a few foods your child will eat before implementing a new diet, then after the problematic or addictive foods are removed, expand little by little.

Here are solid reasons why children can be so one-sided in their food choices:

"Addictions" to opiates (gluten/casein) can cause consumption of primarily wheat and dairy containing foods. According to this theory, gluten (wheat) and casein (dairy) when not broken down properly by digestion, create compounds that fit into opioid receptors in the brain and feed opiate (morphine-like) cravings/addictions. The child then becomes restricted to only the foods that fuel this addictive cycle, creating very limited and picky eating.

"Addictions" to chemicals (MSG, artificial additives) can cause restriction to one brand or a strong preference for processed foods. These chemicals can also be addicting like opiates. MSG is known to create "excitement" in the brain by stimulating the glutamate (excitatory) receptor, making food seem to taste much better. Artificial ingredients such as artificial colors and flavors can also affect similar cravings.

Nutrient deficiencies (such as zinc) can make all foods taste bad or bland. When zinc is deficient, a common finding in children with autism, sense of smell is reduced and food tastes boring or unappetizing. Texture can then become an even bigger factor, imagine eating mashed potatoes if you can't taste the potato flavor - a bland mouthful of mush.

Yeast, viral, and microbial overgrowth may cause focus on eating mainly high carb and sugar foods. Yeast and other microbes feast on carbohydrates and sugar. They can actually get their "host" to crave the food that feeds them by giving off chemicals that get kids to crave refined carbs and sugar. This can create self limitation to only these foods.

Sensory sensitivities can result in restriction of foods of certain textures. For children with sensory issues such as tactile and sound sensitivities, food texture can be a big hurdle. Crunchy foods can be too loud, and mushy foods can be intolerable. In these cases, it's advised to seek an occupational therapist or other professional that help you work through these sensory integration challenges. Once you've identified possible causes of your child's finicky eating habits, begin to look for creative ways to address them. Sometimes as occupational therapy or sensory integration begins to address food textures, a child begins to expand more. Until then, get creative and make foods crunchy or smooth based on their preferences. Begin to add new food options such as gluten-free pasta before removing the existing food. Be aware that brand preference, may be because of MSG or other additives that can be addicting and make that food "exciting." Add enough salt to make your versions of their favorites more flavorful--don't go overboard but don't feel you need to limit salt. Be creative with food. Begin to add vegetables where you can and slowly introduce foods slightly different than they have had before. See if you can make food a little different each day--not so much that they reject it, but just enough that they don't expect sameness--and to get in new nutrients. Add purees to pancakes, apple sauce, meatballs, or sauces. Make vegetables crunchy by making carrot chips, sweet potato fries, or vegetable latkes. Hide meat in pancakes. Try mixing or diluting a brand of food/beverage they like with a healthier version in very small amounts until the item is swapped for the new food-this works well for milks, peanut/nut butters, apple sauce and other foods that blend well.

The following are ideas to help picky eaters become introduced to new foods:
Always provide food child likes in addition to one "new" food.
Involve your children in food preparation of "new" food.
Introduce it to them on a separate plate. Don't require them to do anything other than get familiar with it. Consider incorporating the food into therapy or play time.
First have them touch it and lick it without eating it.
Inform them. Let child know whether it is sweet, salty or sour. Eat some yourself and tell them how delicious it is-enlist others at the table to do the same.
Let them chew it and spit it out.
Start with only a small taste ~ 1/2 teaspoon. Let child determine amount.
Try and Try Again! At least 15 times!
Get creative. Try new food in preferred texture - crunchy, smooth.
Avoid being emotionally "attached" - children sense anxiety. Keep mealtime calm. Visualize child eating/enjoying new food.
Avoid forcing or pushing - maintain trust.
Choose rewards or other encouragement.
Make sure whole family participates - serve everyone at the table.
Make it fun!Also, if one parent is or was a picky eater themselves, try having the spouse feed the child. I know it can be frustrating cooking food and having them refuse it, but make sure you don't project that energy of frustration. Children are very sensitive and pick up on these cues. If they don't eat it, don't give in and prepare something completely new. Instead, make sure the meal already includes something they will eat for the meal along with the new food. Or when they are hungry at snack time, try a new food. This is a good time to do so because while they may skip a snack, they will not be going without a main meal, and you won't teach them that if they hold out you will fix them something new. They will also be a little hungrier at dinner and may be more motivated to try something new.Applying healthy diet is an important step to health and healing. Try implementing diet and adding nutritious foods step by step. You can do it-and your child can too! I have seen countless children expand their diet. Once food addictions, texture, and exposure to a new food are addressed, you'll be surprised what your child may eat. Visualize that they can do it. Get creative. Try things in a texture they like. Taste it yourself and make sure it tastes good. I bet you'll be pleasantly surprised when they eat that first vegetable!

The information expressed here comes from Julie's experience as a Certified Nutrition Consultant with clients that are picky eaters and their parents' experiences. Julie is not a feeding specialist. This information in intended to help parents find creative ways to feed their children healthy food. It is not intended to act as or replace professional feeding therapy or medical needs. Parents of children with serious feeding issues should seek professional and medical guidance.

Tuesday, February 17, 2009

Cuckoo for Coconuts!



I have officially gone nuts over coconut and had to share the benefits of this wonderful food with you all. The benefits of coconut oil are not only for our kids on the spectrum but for every BODY. It is really amazing the healing properties of such an unattractive fruit.
I stumbled onto the nutritional benefits of coconut in relationship to autism about a year ago and continue to hear about the wonderful improvements others are experiencing.

Hear are just a few of the many benefits on and off the spectrum. It is a wonder that more people do not indulge in this wonderfilled fruit.

Brain - The Brain tissue is very rich in complex forms fats needed for proper neural transmission. Every brain needs to have the proper fats and ratios to produce brain health and improve conductivity. Coconut oil has been shown to increase brain function.

Immunity - Coconut oil is good for the immune system. It strengthens the immune system as it contains antimicrobial lipids, lauric acid, capric acid and caprylic acid which have anti fungal, antibacterial and antiviral properties. The human body converts lauric acid into monolaurin which is claimed to help in dealing with viruses and bacteria causing diseases such as herpes, influenza, cytomegalovirus, and even HIV. It helps in fighting harmful bacteria such as listeria monocytogenes and heliobacter pylori, and harmful protozoa such as giardia lamblia.

Skin - Coconut oil is beneficial in treating various skin problems including psoriasis, dermatitis, skin infections and eczema (which many of our kids suffer from due to diet).

Digestion - Coconut helps improve the digestive process and can also prevent various stomach and digestive problems. Due to the anti microbial properties coconut oil helps in dealing with various bacteria (YEAST), fungi and parasites. Coconut oil also helps in absorption of other nutrients such as vitamins, minerals and amino acids (especially calcium).


Infections - Coconut oil is very effective against a variety of infections due to its antifungal, antiviral, and antibacterial properties. According to the Coconut Research Center, coconut oil kills viruses that cause influenza, measles, hepatitis, herpes, SARS, etc. It also kills bacteria that cause ulcers, throat infections, urinary tract infections, pneumonia, and gonorrhea, etc. Coconut oil is also effective on fungi and yeast that cause candidiasis, ringworm, athlete's foot, thrush, diaper rash, and more.

For Us Moms (and Dads)
Promotes weight loss
Supports healthy metabolic function
Provides an immediate source of energy
Helps keep skin soft and smooth
Helps protect against skin cancer and other blemishes
Helps prevent premature aging and wrinkling of the skin
Reduces risk of atherosclerosis and related illnesses
Helps prevent osteoporosis
Helps control diabetes

How to use VCO (virgin Coconut Oil)?

CHILDREN: A reasonable amount to add to the diet of a child would be about ¼ teaspoon of coconut oil for every 10 pounds that the child weighs, 2 or 3 times a day. Also, some children may like the taste of coconut milk, in which case about 1 ½ to 2 teaspoons can be added to the diet 2 or 3 times a day. If you use coconut milk be sure to refrigerate it and toss after two days if using coconut milk for a child.

ADULTS: Researchers state that the optimal amount for an adult is between 3 and 4 tablespoons per day three times a day at meal times. It us recommend that you begin with a smaller amount and build up to the recommended dosage if necessary.

  • Cooking oil: Since it is a stable cooking oil, one can simply replace unhealthy oils in the diet
  • Spread: VCO at room temperature can be used as a butter or margarine substitute for spreads or for baking.
  • Recipe replacement: Any recipe calling for butter, margarine, or any other oil can be substituted with VCO.
  • Spoonful: Many people simply eat it by the spoonful.
  • Directly into food.
  • External applications: VCO can also be massaged into the skin and in the hair.

FOOD IDEAS

Use coconut oil instead of butter on toast, English muffins, bagels, grits, corn on the cob, potatoes or sweet potatoes.
Mix coconut oil into hot cereal.
Add coconut oil or coconut milk to your favorite smoothie recipe.
Mix coconut oil into rice, vegetables, noodles, pasta.
Mix coconut oil half and half with salad dressings. If the salad dressing is cold from the refrigerator, pour some into a small bowl, or other microwavable container, and warm it for about 10-12 seconds in a microwave oven and then add the coconut oil. If added to cold liquids or foods, coconut oil tends to harden.
Mix coconut oil into your favorite soup, chili or spaghetti sauce. Use a measured amount of coconut oil to stir fry or sauté any of your favorite dishes.

Caution Die Off Possible(regression)- The lauric acid in coconut oil is antibacterial, anti-protozoal and antiviral and there could be a "die off" effect as offending organisms are removed from the body. This could cause diarrhoea (not in itself a bad thing under the circumstances) but it could be inconvenient. It is probably best not to start with the daily recommended dosage of 3 to 4 tbsps. but build up to it over the course of a few days if necessary. Spread out whatever amount you decide to take over the course of the day (three times with meals is best) and reduce your intake if there are side effects. It is unlikely, but some people could possibly have an allergic reaction - although coconuts do not fall under the classification of being a nut.

RECIPE:

Nut Butter

Ingredients:
2 cups (480 ml) Crispy nuts, such as peanuts, almonds, or cashews
3/4 cup (180 ml) Omega Nutrition Coconut Oil
2 Tbsp (30 ml) Raw honey
1 tsp (5 ml) Sea salt

Directions: Place nuts and sea salt in a food processor, and grind to a fine powder. Add honey and Coconut Oil, and process until "butter" becomes smooth. The resulting "butter" will be somewhat liquid, but will harden when chilled. Store in an airtight container in the refrigerator. Serve at room temperature.

Monday, February 16, 2009

The 411 wrist band


411 Wristband are designed to give parents peace of mind when dropping off children at birthday parties or field trips, or even when taking them to amusement parks. Other adults or caregivers have a means to contact the child’s parent or to learn vital information by looking at their 411. The disposable wristbands include the child’s first name, the parent’s first name and cell phone number and any allergies or special needs the child may have. These can be customized to fit any parent’s needs.

Thursday, February 12, 2009

IEP Boot Camp


I thought this was a good interview and overview of some of the things you may need to know for an IEP. It was written by Michelle Diament for Disabiliyt Scoop.

They chat about the rights of students with disabilities with special education attorney Marcy Tiffany of the law firm Wyner & Tiffany in Torrance, Calif.


Since the enactment of the Individuals with Disabilities Education Act (IDEA) in 1975, students with disabilities have the right to a free appropriate public education (FAPE). Accordingly, each student deemed eligible for special education has his or her own individualized education plan known as the IEP. But things can get sticky when parents and school staff sit down at so-called IEP meetings to decide what’s needed to educate a student.
Marcy offers must-read advice for anyone headed to an IEP meeting. She tackles everything from preparing for and participating in an IEP meeting to what rights students with disabilities have under the law.


Check out what Marcy has to say and then submit your own questions to her by clicking here.

Disability Scoop: Tell us about the work that you do.


Marcy Tiffany: I represent students with disabilities in an educational context. I deal with school districts and assist parents in developing appropriate IEP’s. If that doesn’t work, I represent parents in mediation and due process hearings and also in federal court proceedings.
Disability Scoop: If you’re a parent of a student with a disability, what should you expect from the IEP process?


Marcy Tiffany: School districts are obligated to provide a free appropriate public education (FAPE). This includes an annual IEP that includes goals and objectives that are measurable and that address the student’s areas of need.

Given the financial constraints most school districts suffer under and the chronic lack of full funding of the IDEA, there’s an inherent tension between what the student really needs and what resources are available to the school district. Understanding that this is at the root of many of the difficulties in the IEP process is important. It’s not that the school district doesn’t want to serve the children, it’s that they don’t have money.


Disability Scoop: What rights do students have that families are often unaware of?


Marcy Tiffany: There are two recent changes in the IDEA that came with the 2004 reauthorization. One is the emphasis on and the requirement that school districts use research-based teaching methodology wherever possible. The other change many people are not aware of is the requirement that there be functional goals as well as academic goals. For example, in a college bound student you might want to look at functional skills like being able to take notes. For some children, functional skills include social development.


Disability Scoop: Is it necessary for schools to follow research-based methodology in their teaching practices when it comes to students with disabilities?


Marcy Tiffany: Schools are supposed to use research-based teaching methods whenever possible. It’s important for parents to do as much research as they can to see what kinds of programs are out there and what research supports them so that they can walk into an IEP meeting armed with this information and be effective advocates for their children’s rights.


Disability Scoop: Tell us the top three things you should keep in mind when preparing for an IEP meeting.


Marcy Tiffany: Try to avoid becoming adversarial. You want to focus on what the child’s needs are, not simply complain about what’s not happening. Once an IEP meeting becomes adversarial, it’s usually not going to be very productive. Many parents bring food, which helps to relax the environment.
Another mistake is lack of preparation. You must know what it is that you want to focus on and don’t rely on the school district to set the agenda.
The third mistake is to consent at the IEP meeting (i.e. sign the parent signature section). We always advise our clients, no matter how well the IEP meeting went, to take the IEP home and think about it. Make sure you’re comfortable with everything that’s been said. You have a right to supplement the IEP. It’s important to read the narrative and make sure what was discussed at the IEP meeting was included. Along the same lines, we always recommend taping an IEP meeting. School districts are used to it. It’s very important to have a complete record of what was said and if you just have notes, sometimes they’re complete and sometimes they’re not.


Disability Scoop: Tell us about writing a supplement to an IEP.


Marcy Tiffany: Write out what it is that you felt wasn’t adequately covered or you disagreed with. Then, you can say “here’s an addendum to the IEP and I’d like it to be included.”


Disability Scoop: When you request to think about the IEP and bring it back, are you simply withholding your signature from the IEP until you feel comfortable and have thought about things?


Marcy Tiffany: Yes, I’m not saying don’t consent. Keep in mind that you can partially consent. For example, let’s say that you think your child needs two hours of speech and language but the school district only offers one hour. Well, consent to the one hour and indicate that you don’t think this is sufficient but that you’re consenting because some services are better than no services.


Disability Scoop: How do you indicate which elements you agree with in the IEP versus those that you don’t?


Marcy Tiffany: You can indicate this in a separate statement with your consent. The IEP usually has a place for a parent’s signature. You can sign the IEP with an asterisk that says, “please see detailed consent.” Or, you can say “we’re consenting with the exception of blank and blank.” Typically, however, we write a separate consent that says here are the things we consent to, here are the things we don’t consent to and we reserve our rights to object to the entire IEP as not providing of FAPE (Free Appropriate Public Education).


Disability Scoop: What can you do to make sure your priorities are the focus of the IEP meeting?


Marcy Tiffany: Again, try to avoid becoming too adversarial. Prepare before you walk into the IEP meeting so that you know what you’re saying and can say it concisely and clearly. Start with the old IEP. Look at what those goals and objectives were and see if your child has achieved them in your opinion. All too often the description of the present levels of performance are very vague. Johnny has “improved” in his reading ability. Johnny’s spelling is “better” than it was last year. These kinds of statements mean absolutely nothing. The present levels of performance need to be articulated in terms of the previous goal. Visit with the child’s teachers ahead of the IEP meeting. Go over the goals and, equally importantly, go over the content standards, which most states have available online (check your state’s Department of Education Web site). For example, here’s what Johnny should be doing in sixth grade math, is he doing it or isn’t he? It’s important for parents to really understand their child’s current levels of performance and to do so in terms of the content standards.
It’s also important for parents to understand the nature of their child’s disability. If you don’t understand your child’s disability, you’re never going to have an effective IEP.
We also strongly recommend private assessment. If a parent disagrees with the school district’s assessment or can simply afford to go out and get a private assessment, they should do so. With a private assessment they can get a more detailed explanation about what the nature of the disability is and also obtain recommendations they can take with them to the IEP meeting.


Disability Scoop: Is there a way you can force the school district to pay for a private assessment?
Marcy Tiffany: Yes. If the school district conducts an assessment and you disagree with it, you can request an independent educational evaluation (IEE). What the law requires is that the school district either pay for the IEE, or the school must file for due process to establish that its own educational evaluation was appropriate. Something the school districts are now doing, is the minute a parent requests an IEE, the school district files for due process, which in turn intimidates the parents who then withdraw the request.
Another tactic school districts use is they’ll say, “okay we’ll pay for it but only if you have it done by this particular individual.” This, of course, doesn’t end up being an independent educational evaluation because it’s done by providers selected by the school district. The school district is supposed to provide guidelines for IEE’s. They can also provide a list of providers in the vicinity who are qualified, so there’s a fine line in helping the parents obtain an IEE and having the school district control it.
Again, the key would be disagreeing with the evaluation. Sometimes you don’t know whether to agree or disagree until you get the independent evaluation. What you might want to do is take the school district’s assessment to an independent assessor who you think is qualified and ask for an opinion. Do you think this is a good assessment? Did they do all the testing they should do? You have to be prepared before you ask for that independent educational evaluation.


Disability Scoop: You talked before about content levels. Were you talking about general standards for each grade level for any child?


Marcy Tiffany: Yes. They vary from state to state, not dramatically, but they differ some and parents ought to know, what is my child supposed to be learning in fifth grade? Should they be able to write a single paragraph or should they be able to write a multi-paragraph essay? If you don’t know what it is that they should be doing then you don’t know what the areas of focus need to be.


Disability Scoop: When you’re going to an IEP meeting, what should you make sure to have with you?


Marcy Tiffany: I would certainly have the previous IEP. I would have the most recent assessments that have been done on the student. I would have work samples.


Disability Scoop: Are there any other things you would recommend bringing with you?


Marcy Tiffany: Food!


Disability Scoop: What are the hallmarks of a good goal versus a bad goal?


Marcy Tiffany: I rarely see good goals and I see lots and lots of bad goals. One of the most frequent errors is having a goal that appears to be measurable on the surface but really isn’t. Frequently you’ll see, “the student will do x, y and z with 80 percent accuracy in three out of five trials.” It looks great on paper, but you need to ask, “what does this mean as a practical matter?” When we come back to this IEP meeting a year from now, what are you going to show me to prove that this goal has been achieved? What evidence? What documentation? What would the student have to do in order to achieve this goal?
Another common mistake with goals is having too many skill sets in a single goal. For example, a child will initiate a conversation and respond and maintain a conversation. Well, initiating a conversation is different from responding to someone else’s initiation, which is different from maintaining the conversation. So which is it? If a child initiates a conversation, is that goal going to be achieved even if the child is not responding and not maintaining? So trying to make sure that the goal has enough specificity so that what’s being measured is clear.


Disability Scoop: What are the commonalities among goals you’ve seen that are good and productive?


Marcy Tiffany: They have a very specific focus relating to the content standard. You want to make sure that you understand what grade level the goal is at. Also you want a goal that is measurable in a meaningful way. For example, if the proof of the goal is work samples, then insist that those work samples be provided to ensure that the goal has actually been achieved. A typical way of looking at progress is data collection. Make sure the data is being collected. Who’s going to collect the data? What is it going to look like? What does the data collection sheet look like? When you have that kind of specificity, you’re going to have a good goal.


Disability Scoop: If you’re feeling discouraged about the outcome of your IEP or the way the process is going, where can you turn for help?


Marcy Tiffany: There of course are advocates who are non-attorney lay people who can go to IEP meetings and assist in the IEP process. And then of course there are attorneys and there are lots of different places to find out who the attorneys are in your community (check the Disability Scoop resources page).


Disability Scoop: If you’re unhappy with the IEP that your team has created, what type of recourse do you have?


Marcy Tiffany: There are various procedures in different schools. If you’re not happy with an IEP, it’s important to act quickly. I’ve seen students go for multiple years without a signed IEP and that’s not supposed to happen. If the IEP isn’t signed, the school district is supposed to initiate due process. If you’re not happy with the IEP, then you need to get legal counsel. We have cases that we get resolved without the need to file for due process. Sometimes, obviously we need to file. Once you get into a hearing, all too often the real focus is on a battle of the experts and the school district already has their experts so you need to get yours. Until you have that information, all you know is that you’re unhappy. So, seeing an attorney as early as possible is very important so you can get the pieces in place so that you can file a due process case that will be a winning case.


Disability Scoop: What about mediation?


Marcy Tiffany: Mediation is an integral part of due process. Mediators are provided for free by the agency that conducts the hearings and a good mediator can be very helpful in resolving a dispute. Most cases are resolved by settlement, usually as the result of mediation.
Disability Scoop: When is it appropriate or necessary to involve an attorney?
Marcy Tiffany: If you don’t feel your child is making progress, it’s useful to consult an attorney. Sometimes we can resolve a case without having to go to due process if we can get to it early enough. Waiting until it’s been a year and nothing is happening and you’re totally frustrated is a mistake.


Disability Scoop: If you do want to go forward with an attorney, how can you find one and what qualifications should you look for?


Marcy Tiffany: There are some web sites. Wrightslaw has a listing of attorneys in various states and advocates and that’s certainly one place to look. The Department of Education is supposed to keep a list, at least in California, of special education practitioners, which they will provide to parents upon request. (Check with your state’s Department of Education or check the Disability Scoop resources page.) I think probably word of mouth is the way most parents learn about who’s good.


Disability Scoop: Where can you find free or low cost legal advice pertaining to special education law?


Marcy Tiffany: This varies from state to state. My firm’s Web site lists some agencies that provide free legal advice in California. Also, some law schools have special education clinics that can provide assistance. (Also, check the Disability Scoop resources page.)
Disability Scoop: What’s the best advice you would give to families about approaching the IEP process?


Marcy Tiffany: Ask a lot of questions. Keep asking until you understand and feel comfortable. Ask about the previous IEP and what’s been achieved. Ask questions of the teachers about what the child is doing and isn’t. Ask how goals are going to be measured. Ask questions of the assessor. What is the specific nature of my child’s disability? How does it impact my child’s functioning in the educational environment? Ask other parents what they’ve been through. Ask until you get answers that you really understand.

Wednesday, February 11, 2009

Bad Wrap


Most of you know that wrapping your child's (and your) food in plastic wrap, bags and bowls exposes them to a PVC plasticisers and BPA that disrupt the endrocrine system (a complex network of glands including ovaries, testes, thyroid, adrenals and intestines) and chromosomal DNA (the basic structure of life). In additioin to the above mentioned disruption plastics and plastic wraps contain carcinogenics (dethylhexyl)adepate (DEHA).

With a large subset of children with autism having a compromised immune system and gastrointestinal issues this topic should be an area of concern for our loved ones on the spectrum (and each one of us). So what to we do? How do we store our left overs? What about school lunches?
Alternate Solutions
Tomato film: the latest researchers have developed an edible film using a tomato puree base. The edible film will protect food from contamination by many types of bacteria, including E. coli. The researchers belive that their tomato based film may even be beneficial to health due to the inherent health benefits of eating tomatoes.
Diamant Film
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The incentive behind the experiment is that there is increasing need for natural food coating films that contain antimicrobial properties. This is due to the growing consumer concern about synthetic preservatives. The researchers thought that their tomato based film may even be beneficial to health due to the inherent health benefits of eating tomatoes.