The easiest way to avoid or reduce your exposure to chemical coloring is simply to avoid a lot of processed food.  Check your gluten-free labels always.

FD&C on a label means the FDA allows the dyes to be used in food, drugs and cosmetics.  Sometimes you’ll see FDA Red 40 or FD&C Red 40, so these are just 2 ways the labeling is used.

The FDA allows nine synthetic color additives to this date despite consumer advocacy groups showing mass evidence of the 2 dyes; Red 40 and Yellow 6 linked to hyperactivity, hence attention disorders.

Also, the term artificial colors means “dyes from plants and minerals”, not a synthetic source.  Two of these are caramel (used in cola) and annatto extract from a tropical seed and used in some cheeses to make the color desired.

Click here to read Part 1 on how chemical food dyes are linked to hyperactivity.

Tina Turbin
www.TinaTurbin.com

Chemical dyes are in all types of foods and despite evidence of some of them wreaking havoc; the FDA has allowed them to remain on the “safe list”.

Manufacturers like to use them due to their capabilities to enhance foods, gums etc.  The results are vivid, consistent and very appealing.

The FDA monitors the production of nine synthetic color additives they consider safe.  Consumer advocacy groups have linked two of these dyes, Red 40 and Yellow 6, to hyperactivity in many children.

It is said that sometime in late 2010 the European Union will require any product containing these dyes to be labeled as such “May have an adverse effect on activity or attention in children”.  Some companies in Britain have already phased them out.

Tina Turbin
www.TinaTurbin.com

Dear Friends,

I’m sending this out to say THANK YOU to all of you for your continued support – it’s a tremendous help and been quite an avenue to meet such nice people. I love reading all of your communications too.

A special thanks to many of you for calling and sending in the many questions for the past near two years of radio shows, your suggestions, your invaluable feedback, your questions and for listening in on the various shows. I have been on a 4-month break from the radio shows and interviews I was accepting, enabling me to focus on some exciting projects as a children’s author, a fully grain-free (and of course gluten-free) cook, my work in the celiac arena and of course my studying which is very important to me.

I am being very selective ( or picky as you may say) and will do just a few shows this year, keeping you informed. Some very exciting and very wonderful projects are moving forward. Things have really expanded beautifully.

Wishing you all an amazing 2011 and wishing you all success and accomplishment in your goals.

Tina Turbin
www.TinaTurbin.com
r.n.

Children’s literacy is one of the most important issues facing us today. Fortunately, many groups, organizations, and individuals are dedicated to reversing the staggering statistics. However, as hard as people are working to get kids reading, there are some kids—such as the visually- impaired ones—who get left out.  Thanks to Stevie Wonder, though, visually-impaired literacy is getting some of the attention it deserves.

Stevie Wonder recently appeared before the World Intellectual Property Organization (WIPO) of the United Nations urging for global copyright laws to be changed to the benefit of the 300 million print-reading-disabled global citizens, to whom millions of books are inaccessible to them as audiobooks due to the current copyright system.

According to the Huffington Post, the way the system is currently set up requires that many audiobook versions of the same work be produced, which carries a higher cost, the burden of which falls on the visually-impaired public. What’s more, some poor countries can’t even afford to make their own versions of works, so that they’re not available at all to their blind citizens.

Here is part of Wonder’s address, courtesy of The New Yorker:

“While I know that it is critical not to act to the detriment of the authors who labor to create the great works that enlighten and nourish our minds, hearts and souls, we must develop a protocol that allows the easy import and export of copyright materials so that people with print disabilities can join the mainstream of the literate world.”

“According to the AFP,” reports The New Yorker, “aides to Wonder said that just ‘five percent of printed materials and books are available in a readable form for the blind or visually impaired in industrialized nations, and just one percent in developing countries.’”   You may wonder, as I certainly did, how come such a small amount of books get translated into formats accessible to the visually-impaired, such as Braille and audiobooks. Ian Crouch of The New Yorker interviewed Paul Schroeder, the Vice President of Programs and Policy at the American Foundation for the Blind to find out more about this issue.

According to Shroeder, while several developed countries have different copyright laws allowing books to be reproduced in Braille, audio, and electronic or large print, the materials must fulfill two limitations, first that the books only go to those who are unable to read print books due to a disability, and secondly that the books are made by “specialized format producers who work with people with print-reading disabilities.”

In the U.S. the copyright provisions, also known as the Chafee provisions after former Senator Lincoln Chafee, allow these specialized producers to reproduce books in formats that are accessible to people with print-reading disabilities. A problem arises, however, with the fact that the provisions don’t allow for export outside the U.S., a law that other counties have in common with us.

According to Shroeder, “We definitely want to see a treaty or other mechanism that allows books to be shared across borders for use by people with print disabilities.” Stevie Wonder’s advocacy work is in alignment with this goal.

It’s an inspiration to see other artists working on behalf of children who aren’t typically represented in the children’s literacy issue.  After visiting with the bright children of Blossom Montessori School for the Deaf on my East Coast book tour, I released Danny the Dragon Meets Jimmy, the first book of my children’s book series, on DVD with a sign interpretation, and the profits are going to the causes of literacy and education. Now the DVD has been released by iStorytime, of Dreamworks and Shrek Forever After, as an app for the iPhone, iTouch, and iPad. I hope to see other artists and individuals follow in Stevie Wonder’s example by championing causes that are special to them, and I look forward to seeing progress in developing a global system whereby the millions of visually-impaired are able to enjoy the books we ourselves are lucky to have access to.

Tina Turbin

www.TinaTurbin.com

Resources:

New Yorker: Stevie Wonder and Books for the Blind http://www.newyorker.com/online/blogs/books/2010/09/stevie-wonder-and-books-for-the-blind.html#ixzz10K3xYhi1

Huffington Post: Stevie Wonder To UN: Ease Copyrights For The Blind http://www.huffingtonpost.com/2010/09/20/stevie-wonder-to-un-ease-_n_732281.html

As an author, researcher, and gluten-free advocate, I work to raise awareness for celiac disease and gluten intolerance because with increased awareness comes more research, more diagnoses, and even better treatments. I’d like to give you an example of how the work of just one researcher, Dr. Fasano of the Center for Celiac Research at the University of Maryland, can make a difference:

In Scientific American, Dr. Fasano poses in his article, “Surprises from Celiac Disease,” the question of why some celiacs develop the disease later than others, even though all celiacs share a genetic predisposition to it.

According to Dr. Fasano, the different onset time among celiacs is associated with the microbiome—that is, the community of bacteria or microbes which live in the digestive tract. Dr. Fasano explains that the microbiome varies among different people and even in the same individual over time. Furthermore, Dr. Fasano says these microbes can have an effect on the genes which are active in their host. Therefore, someone genetically predisposed to celiac disease may have been able to handle gluten for a long time, but upon a shifting of the microbiome, and a subsequent activation of the gluten intolerance gene, the symptoms of celiac disease will appear.

Not only do Dr. Fasano’s studies shed light into a question that has been perplexing researchers for some time, but it also opens the door to a treatment for, or even prevention of, celiac disease—good bacteria for the digestive tract, otherwise known as “probiotics.”

I look forward to hearing more from Dr. Fasano about this fascinating topic!

Tina Turbin
www.GlutenFreeHelp.info

If you’ve been keeping up with me for a while, you’ve probably heard me mention and quote the benefits of a GF multivitamin on the gluten-free diet. After all, it’s common sense health advice. Now there’s scientific evidence that shows that taking a daily multivitamin also increases longevity!

The study in the Journal of Clinical Nutrition shows that with a daily vitamin supplement, telomeres were lengthened by 5.1%. Not just any vitamins were taken, but specifically the powerful antioxidants, Vitamins B12, C, and E.  Telomeres are considered to be the anti-aging “key.” Part of the DNA, they’re found in every cell in the body. As cells divide, however, telomeres become shorter, which means that cells are getting “older,” and lengthening telomeres will lead to a longer, healthier life.

You can take B12, C, and E regularly in supplement form, but it’s important to also get these in your diet as well. Food sources of Vitamin B12 include grass-fed beef, salmon, tuna, and milk; vitamin C can be found in produce such as kiwi, strawberry, orange, grapefruit, and red and green bell peppers; and vitamin E can be found in spinach, broccoli, almonds, peanuts, olive oil and kiwi.

Here are the minimum daily values recommended in supplements for keeping telomeres long: 100 mcg of Vitamin B12, 3,000 mg of non-synthetic Vitamin C, and 200 to 400 IU of vitamin E in mixed tocopherols form, the last of which needs to be taken with food because it is a fat-soluble supplement, requiring fat in order to be absorbed.

Now you have no excuse not to take your GF multivitamin every day—not only is it “insurance” to make sure you’re getting all the nutrients you need, but it’s also an effective anti-aging method at minimum cost and maximum convenience!

Tina Turbin
www.GlutenFreeHelp.info

I used to be a nurse and midwife before David and I got married in 1969 – we then went on to have 5 daughters between 1972 and 82! I first became aware of having difficulties in digesting wheat within 24 hours of giving birth to Naomi my oldest daughter in 1972, and with each successive child birth the problem got worse, eventually leading to my doctor sending me to hospital for allergy tests, which proved nothing!! It wasn’t until my 4^th daughter was born in 1978 that I finally got round to doing an exclusion diet and guess what my symptoms disappeared! Since then I have been wheat free and since 1998 I have been totally gluten free. Unfortunately since going down with *ME/CFS (Alternate names/abbreviations for chronic fatigue syndrome) 2002 I have had to deal with a lot of food allergies and exclusion is always the best way to deal with it, but I have discovered that quite a lot of these allergies/intolerances are transient which is quite interesting so my diet goes up and down as to what I can and can’t eat – but gluten is always a complete no no.

When Naomi my oldest daughter was diagnosed with being on the Autistic Spectrum at the age of 28 in 2000 she was completely addicted to all wheat products! At her new autism specific residential home they even in 2000 knew that gluten could effect the severity of the autism and so Naomi was put on a gluten reduction diet which she keeps to even now 10 years on. Her health has vastly improved with her carers being brilliantly observant to her dietary needs and how it effects her autism.

2. Tell me a bit about being a professional interviewer – what does it entail?

Am I a professional interviewer? That is a moot point because many times I have been told that as an amateur and a voluntary worker that my interviews are quite often better than the professionals and in the fact that I get a lot more information from my interviewees by being more conversational. But I have to act as professional as I can even though I am the amateur!

3. I’m intrigued by the fact that you created programs for hospital radios, please explain what this entails.

Here in Britain we have had hospital radio run by volunteers for many decades. I became involved with my local hospital radio in 1985 and because I was much older than the other people there I decided to carve myself out a niche of doing interviews with celebrities and book authors! In 1986 I was doing so many, that myself and another hospital radio volunteer started up a charity called H.O.P.E. – Hospital Oriented Programme Enterprises and made programmes for hospitals around Britain. I also roped in students from a local university and both my husband David and I taught them how to do old style cut and splice tape editing and good quality interviews. It was a great deal of fun and even my kids got in on the act!!

4. What does BFK stand for?  Can you share some details about this, please?

BFK stands for Book Fiends Kingdom – people who love to read books, but because people kept getting it confused with Friends instead of Fiends I shortened the title to BFK – and it grew until now we have www.bfkbooks.com, www.bfkautism.com, www.bfkmusic.com and www.bfkdvd.com the BFK family of websites to cater for most tastes.

5. Please provide details you’d like to share about YOUR mission for these sites.

My original website www.bfkbooks.com came into being in 2007 to Raise Awareness and Funds for the Care of Adults with Autism because Naomi read voraciously before she became Special Needs, the website was set up in honour of her reading and her many interests. I would like all the websites to grow and raise funds to help adults with autism. At the moment we are helping the Disabilities Trust’s Adult Autism Specific Services but the more money we can raise the more people we can help.

6. What particular circumstance inspired you to create your sites?

Naomi being diagnosed in 2000 at the age of 28 with being on the Autistic Spectrum. Once she was settled in a good Autism Specific Residential Home run by the Disabilities Trust in 2000 it gave our family a chance to heal emotionally and physically. In 2006 I felt I was healed enough to begin to give back to the people who had cared so much for Naomi so she become my inspiration for setting up all the websites.

7. If you could share 1 key piece of advice with parents that are raising an autistic child, what would it be?

Raising an autistic child is one of the hardest things to do because you have to forget self and become like a Rottweiler to fight for the right kind of care for your child. My advice for all the parents in this position is to take time out for themselves, even if it’s to just stand in the garden and listen to the birds singing. Parents are so tired with all the battling they do that they quite often become ill so taking time out is a necessity. Here’s an article written by Anna Van De Post on Coping http://www.bfkautism.com/articles-on-autism/coping-by-anna-van-de-post Anna is a mum here in England who’s autistic son is now 17 and who has gone through a lot of trials and tribulations in trying to cope – I asked her to share her experiences in this article.

8. Any particular touching memory or experience that you would like to share about your daughter and her progress which may help others?

When Naomi went to Hollyrood the adult autism specific residential home she was very ill and in crisis – as one would expect she completely lost her ability to talk, laugh and write which she loved to do. Over the decade she has been there and now in a community home, her talking has come back and so has her humour – which is quite wicked at times! She can now write the odd poem or two but I think most importantly she can now express what she is feeling much more coherently. These changes have not come overnight but piecemeal throughout the decade. We find we can now take her out to restaurants, to the Blue Bell Railway (steam engines) and she came to her middle sister’s  wedding 2 years ago and will be going to her 4^th sister’s wedding in July this year. When we look back over the last 10 years so much has happened and now she is a completely different person to who she was when she went through the front door of Hollyrood in 2000.

9. As a child, did your daughter stick to a specific vitamin regimen or anything else in particular as regards nutrition or diet?  If so, is this still the case?

As a child we thought Naomi was eccentric but normal – so she ate normally in keeping with the rest of the family. Now she is on a good diet with no supplements other than horse chestnut for her varicose veins.

10. How might one have a glimpse into the life of an autistic person such as your daughter, to read a bit more into their true story(ies)?  Any blogs or resources that you care to share?

I’ve recently started a rolling news on Naomi http://www.bfkautism.com/content/news-on-naomi and an overview of her life http://www.bfkautism.com/content/naomi with more info to go on. I’ve also started with another mum Heather on her son Josh http://www.bfkautism.com/content/heather-and-josh and http://www.bfkautism.com/content/news-on-heather-and-josh . In a few weeks another mum Anna will be talking about a group of mums and will have a rolling news on them as well.

I also highly recommend the www.autismfile.com which does a lot of campaigning for the rights of children with autism and their need for good medical treatment and care.

In America there are so many fantastic websites which I Googled and have been left feeling quite inspired by them.

Last but not least http://www.autism-awareness.org.uk/ which is run by the Disabilities Trust – their standards of care are second to none.

For resources – this is where Google comes into its own. Each country is very different but in the future for my autism website maybe a generic resources article that will take on board the needs of the autistic people of that country. Dr Andrew Wakefield has a website www.callous-disregard.com and in the links page are many associations and societies that can help people in many ways – from wills to how to get the best health treatment for your child.

11. You have taken on the honorable task of shedding light on a portion of our society that largely goes un-noticed: adults with autism.  Please explain the variety of ways that you help this population.

I am slowly building up on articles on the autism website talking about the different aspects of adults with autism. I also do a lot of talking on the ground and always carry leaflets explaining what autism is. You never know who you may meet standing on a train station platform or bus queue! At least 50% of the people working with me are on the autistic spectrum but at the high end of it. Trying to educate people about adults with autism are the forgotten people and tweeting of course!! I also try to mentor some adults with autism as well.

12. With all of the various “hats” that you wear, I can see that you’re a very busy woman!  What is a typical day with “Vicky” like?

Gosh – now you’re making me think, because everyday is different depending on what I’m doing! In the morning it’s reading my emails, making phone calls to sort out interviews for the websites. After lunch I do a lot of my review posting across 3 of the websites and sorting out articles for the autism one and making new contacts for the articles on autism. Walking the dog and when things get too overwhelming on the website front I take to my sewing machine and make quilts or do lace knitting!

I also have to make time for reading books on all subjects for the interviews,  have days when I go out to meet people either interviewing them for the websites or talking about the autism side. Believe it or not the London Book Fair is a great place to talk about Adults with Autism!

All of the above is done with a background of medical appointments for David’s chronic lung disease – he has Granular Sarcoidosis of the Lungs and I have Diabetes and am on Insulin as well as having ME/CFS! As well as that we have regular review meetings with Naomi’s carers and see Naomi on a regular basis along with her sisters.

13. What role does a gluten-free diet play in the lives of people that are living with autism?

From my own personal experience of going gluten free and that of Naomi (my autistic daughter) is that for me I am not grumpy! Add a bit of gluten and even my friends and family will pick up on it. For Naomi – her autism is much, much better and instead of needing 3-1 care she now only needs 1-1 care. Being gluten free does make the autism less severe – it never goes away but becomes more manageable.

14. You shared with me the immense cravings your daughter has for some specific foods which are not beneficial to her. What can you share about this with other parents of autistic adults or children?

Having an immense food craving can mean that the person is addicted to what they are eating, but weaning the person off of the offending food is not easy and has to be done in small stages. I remember how grumpy and angry Naomi was in the beginning but the effort was worth it to see how she has progressed. I know that between us – the parents – and Naomi’s carers a lot of thought was put into how to do everything. Take it slow and find a substitute like gluten free bread and biscuits – look for food that has maize, corn or rice in the ingredients – if soya is tolerated or spelt flour also gram flour and buckwheat flour which is great for all sorts of cooking. Even now we keep a look out for things like corn pasta and spaghetti and for you Tina, your gluten free website is just brilliant.

15. Please share some of the GF resources that you would typically suggest to both children and adults with autism.

Our supermarkets here in Britain are now building up on their Free From produce and our good health food shops are very good as well. In America I know that your health food shops are very good and even in 2002 when I was last in America there was a lot I could eat without feeling hard done by.

There are now lots of books published on gluten free cooking which can be bought from www.amazon.com and www.amazon.co.uk.

16. Do you personally have any statistical information that sheds light on the differences and successes between an autistic person eating a non-GF diet as compared to a GF diet?

I personally don’t have any stats on this, only personal anecdotal info, but I know that in America some of the doctors dealing with autism are very aware that autism and gluten really don’t mix and there is some research going on there.

17. If anyone cared to make a donation to the BFK Autism website, how might they do so?

For any donations, go to www.justgiving.com/BFKautism. This is the link to the Just Giving charity which was set up many years ago to collect money for charities from marathons or events and pass it on to the relevant charity – in my case the Disabilities Trust Adult Autism Services. All donations bypass me and go straight to the Disabilities Trust

18. What are the funds and donations used for?

All the funds and donations are used to help with the facilities for adults with autism, e.g music centre with instruments, sensory room,  multi media raised gardening beds, art – paints, paper, clay etc, pottery room – all the adults love going here and much, much more. There is so much but these are just a few things that the money goes towards helping the adult with autism progress – I certainly know that all of this creative care was instrumental in bringing Naomi out of her severe autistic crisis.

19. Your love of reading shines through on your BFK Books website.  What book(s) are you reading currently as well as interested in?

Ooh – where do I start! These are just a very select few right across the board:

The Red Velvet Turnshoe by Cassandra Clark – an historical crime novel set in the late 1400s – she’s a brilliant writer.

The Holy Man and The Holy Man’s Journal by Susan Trott – Two beautiful novels that are very spiritual and dare I say it healing to read.

Fear The Worst by Linwood Barclay audio book – crime story read by Jeff Harding – had to send a friend into the garden whilst I finished the disc I was listening to! It is just brilliant and addictive listening!

The Mummy Snatcher of Memphis – by Natasha Narayan – a very well researched children’s book set in Victoria times – a good rollicking adventure – loved it.

Horrid Henry audio books are the best stress busters ever – these are officially children’s books but parents will get a great deal of fun from them as well!

Praise of Folly by Desiderius Erasmus – translated by Roger Clarke – this book was first published in 1511 – a classic published by Oneworld Classics. Desiderius pokes fun at the establishment and I have to say – nothing has changed at all!

I Heard the Owl Call my Name by Margaret Craven – an extraordinary book of how a dying priest is sent to the wilds of British Columbia to work with the indigenous people. Loved it.

Callous Disregard by Dr Andrew Wakefield – can only be bought in America on www.amazon.com tells the true story of what happened with the MMR vaccine and the GMC. Quite an eye opener of a book with loads of info.

Stradivari – this is about the violin and how it is made – it is a very sumptuous book with lots of pictures!

20. How many author interviews do you personally conduct in a year (average)?

Approximately 30 plus – can’t believe that but we do a lot!

21. You’re providing a tremendous service by shining the spotlight on these authors, do you have any success stories to share from any of the individuals you’ve interviewed?

Ian Rankin who wrote the Rebus books – I interviewed back in the early 90s on his very first book and he has become a huge success! I was able to do a catch-up interview with him a couple of years ago.

Terry Pratchett – way back in 1992 when I interviewed him – he’s huge now with his discworld series and now TV specials.

Philip Reeves and his Mortal Engine series – teenage books that are so creative and set in the Victorian era.

22. I see that you have also created the BFK Music and DVD site. They look terrific!  What types of music and DVD genres can one expect to find?

With the music website we’ll be reviewing all sorts of music – from Glee to Queen – and all in between. I love Southern Gospel music and folk so they are my areas; Gareth loves classic rock and the classics, whilst Riff who’s just joined us will be doing Be Bop and jazz.

DVD genres: all sorts both modern and classic with a look at the world cinema genre as well.

23. In terms of the DVD site, do you only review contemporary or “new releases”?  Or do you include the classics also?

We review both latest releases, but I think well be specializing in some much older films – everything from the big musicals and the old classic 40s and 50s films, to Avatar and all in between. We’ve also been taking a look at all the old TV classics too.

24. Please share the name of the last DVD you reviewed and a bit about it?  What was your favorite part in this DVD??

Last DVD reviewed but not posted yet is a world cinema film called Riding Alone for Thousands of Miles – a Chinese film about a man who on hearing that his son is dying, rushes to his son’s bedside but his son doesn’t want to see him. His son’s wife gives him a film to watch so he can get to know his son – a promise on the video sends the father on a journey into the heartland of China to film a very special folk dancer. Along the way he meets so many different people and films them.

This is a beautifully shot film that is slow in its build-up but so satisfying. When you come to the end you really feel you have been on a journey with the father. I more than highly recommend this film.

Avatar – a brilliant film that translates to the small screen exceptionally well.

25. Do you work with a team of book/music/DVD reviewers?  If so, how many?

I do work with a team of reviewers – there are about 8 of us right across the board but I guess most of us do book reviews as well!

26. Where do you reside?

I live in England (Britain); always have  – so everyone lives local to me here.

27. Do you sell advertising space at any of your sites?  If not, please explain why.

My webmaster and I made a decision at the beginning not to sell advertising space because it just clutters everything up and doesn’t look good. This is not set in stone and may change in the future.

28. If you provide a newsletter or a way to subscribe to receive updates on new reviews and interviews, how might one subscribe to this?

This is something we are looking at – we do have a Feeds free subscription bit which came into being in March 2010 but I have to say I haven’t really used it yet – this is part of our build-up on the websites and does take some getting used to as it’s based on us inputting into the news several times a week which at the moment I haven’t done. So thank you for reminding me to be a bit more proactive on this one.

29. Now let’s talk about the direction that you’re heading with your cause, what is your vision or long-range plan?

Wow – the big 4 way split in March was one of our long range plans that happened sooner than expected. With the book, DVD and music websites it is a case of providing good quality reviews, interviews and articles such as Spotlight and of course building up on the news side. We will be encouraging more autistic adults to join us with their personal reviews that we can post on the websites and in some cases write their own experiences of how they cope with being on the autistic spectrum..

The autism website because it is so different it is still evolving but I foresee it as an all encompassing site with source info, articles and interviews all in the autism genre. I do have a scientist who is about to come on board. I’d like to see more personal anecdotal stories from parents around the world – so we can build up a picture of how each country is helping or not the parents with autistic children and adults.

I would like to raise a lot of money so that the Disabilities Trust can have a drop in centre for young adults to get diagnosed and have specialized counseling and also for some outreach workers who can go to families caring for autistic children and need help and support. Once we have the prototype then it can be rolled out across the country, but this takes time to be refined and honed locally to Hollyrood in England.

I would also like to be properly sponsored for the websites – paying my webmaster would be good etc!

Education is so important but education for parents so that they know their rights in getting the right kind of help for their children and how to do it.

30. Do you have plans to create more programs in the future?

Yes – these will evolve as more people join us and new ideas are brought forth.

31. Any other specific plans for expansion we can look forward to?

That happened in March and will evolve, refine and hone as we go along, and as website life goes on new ideas come in and I would expect us to expand but how – I think I just need to get over this expansion first!

32. And my last question – Please share one piece of advice you’d like others to read and really understand, taking this advice straight from Vicky’s heart!

The Dalai Lama in one of his quotes said “Never Give up” and I guess that is my mantra from my heart – because if you keep at it, it will happen – also, be like water – flow around the rock, don’t bash yourself on it thus giving yourself serious injury!

Thank you for your time and all you have shared with us, Vikki.

Tina Turbin

www.GlutenFreeHelp.info

* ME: Myalgic means muscle pain or tenderness. Encephalomyelitis means inflammation of the brain and spinal cord. Encephalopathy means altered brain function and structure caused by diffuse brain disease. Alternate names for chronic fatigue syndrome (CFS).

As a children’s author, researcher, and humanitarian, I have been growing increasingly alarmed at the growing rate of autism diagnosis. Whereas in the 1980s, a study shows that 4 in every 10,000 children exhibited signs of autism, a study conducted recently by Cambridge University’s Autism Research Center showed that approximately 1 in 60 children have autism. Several years ago, I myself was diagnosed with celiac disease, caused by a reaction to gluten, a protein found in wheat, barley, and rye, after many years without proper diagnosis for my painful symptoms. I am now happily gluten-free and pain-free. Lucky to have been correctly diagnosed and had my symptoms handled with the natural treatment of a gluten-free diet, I am passionate about helping children to avoid the same pain of misdiagnosis and to find natural remedies for their health problems. According to a recent article on NaturalNews.com, one such natural remedy for autism is calcium Bentonite clay. I had to share this information!

The use of Bentonite clay has been rising in popularity in autism treatment centers. Calcium Bentonite clay, also known as “Living Clay” and one of the most sought-after for its healing properties, has a particularly strong negative ionic charge which magnetically attracts positively-charged substances such as bacteria and metals, for example, and absorbs them, eliminating toxins from the body. It is used both internally and externally and is a rather simple procedure.  In autism treatment centers, Bentonite clay baths are used to safely remove metals and toxins from the body to increase the chances of success when used in conjunction with other therapies.

As autism diagnosis increases, so does the controversy over its causes. Most researchers seem to be searching for a genetic factor, but others are showing evidence of environmental causes. “There`s really the role for something in the environment that could be triggering someone who is genetically susceptible,” says Dr. Gary Goldstein, a child neurologist and director of the Kennedy Krieger Institute, located in Maryland.

The research supporting the impact of environmental toxins has spurred the search for detoxification therapies that can remove them from our systems.  Already large numbers of doctors are recommending chelation and detoxification programs in conjunction with behavioral therapy for autistic children, noting that with these toxins removed, other therapies are more effective. Chelators are substances that fix themselves to heavy metals. Chelation therapies are typically effective, but they’re expensive and carry a higher risk of side effects such as headache, diarrhea, fatigue, fever, and cramps, particularly for children. Calcium Bentonite clay is considered more effective and safer for children.

While many autism clinics are citing successful results with clay therapy, its use isn’t being promoted to doctors due to the fact that clay can’t be patented by the pharmaceutical companies.  Similarly, celiac disease affects 1 out of 100 Americans, and since its treatment is simply a gluten-free diet—requiring no pharmaceutical products, doctors are failing to recognize the symptoms of the disease and diagnosis it correctly, leaving only three percent of celiacs properly diagnosed. However, just as in the cause to increase celiac and gluten-free awareness, by taking it upon ourselves to promote natural therapies for children’s autism, we will surely bring about increased awareness on the effectiveness of calcium Bentonite clay treatment, just as I’ve witnessed awareness of celiac disease and gluten-free grow a great deal over the years.

Tina Turbin
www.GlutenFreeHelp.info

Tina Turbin

Tina Turbin