Jenny McCarthy

admin's picture

I just found out today that celebrity Jenny McCarthy has a child with autism. She writes for a site called Indigo Moms. I haven't had a chance to really check it out myself. So I'm not exactly sure how good the information is, but it's another resource.

I have been promoting

jaymers's picture

I have been promoting ThreeLac on this site,and been giving it to my son for two years. HOWEVER I just read a couple of articles out there that there is a strain of bacteria in threeLac that can be dangerous! It is the enterococcus faecalis, which is only found in this probiotic. The Australian Health Department baned it in their country. This type of bacteria can be found in some sick hospitals. Studies are showing that this bacteria can make a person resistent to antibiotics as well. I will post the full article, and please if you know any information on this, please feel free to share it with me thank you. I started my son on Yukcult drink

http://www.yeastinfectionadvisor.com/threelacreview.html

I am into biomedical world,

jaymers's picture

I am into biomedical world, I have heard many good things about this. GFCF didnt work tried forever. I have been using oral chelation and clay bath since it is a cheaper way to use it. However I have been on the MB12 (methyl-B12) for around off and on almost two years now. Initially I had to pay 750 dollars for the evaluation of the DAN! Dr. then 60 bucks a month for the injections. And one follow up for 200. Now hes refusing to renew the B12 injections for me unless I make a evaluation appointment every year! thats 750 a year! Im concerned that I smell a scam. However I have seen little improvement in my son, but still have noticed! I feel awful that I cant afford 750, since I hear people drop thousands at a time. I live in a middle class home, but have four other mouths to feed. Do you think he is scamming me? or is this protocol for Mb12 injections

I am going through similar

KaeLainne's picture

I am going through similar myself. At first, I was so in LOVE with DAN! and our DAN! doctor... then I seriously started to realize that the questions I asked, she often had to look up the answer... I can do that, why am I paying $125 a visit to look shit up? She stopped returning my emails when my questions got more in depth.. While I still feel she is an amazing woman, I just feel that the answers we seek are NOT only available at a DAN! doctor's office. I have learned SO much more through talking to others parents like me and then researching what they have done.
We were blessed that the gf/cf diet DID work for my daughter. She has had one dose of Mb-12 at the DAN! but that's it.. I did pay $125 for 5 other supplements though... horrific tasting powdered capsules that I can't get her to ingest... pretty much a waste of money, you'd THINK, being a DAN! and working with children with sensory issues... to have maybe the liquid form to recommend and sell (there are many in liquid)...
I'm rambling.. I feel guilty leaving our DAN!, yet also feel like I have wasted money..

Rakesh Patel, R.Ph. MBA We

Pharmacist-WELLHealth Rx's picture

Rakesh Patel, R.Ph. MBA

We work with several DAN Dr.s at our Pharmacy. We dont recommend one over another, but will be happy to give you a list. Call me at the pharamcy or send me an e-mail. The address is: www.wellhealthrx.com

Not all DAN! Doctors are

Ozma's picture

Not all DAN! Doctors are created equal- but actually I would be impressed with a doctor with the humility to look things up in your presence- they all look stuff up, most docs just hide it from you to appear omniscient. The best advice I can give is to shell out for the best- we took our daughter to Doctor Bradstreet, in Florida ( we live in Ohio). He is expensive, but he knows his stuff. We are not wealthy, we live in a tiny shoebox house in a rural area. But it was worth every dime. Our daughter is doing so well, no one knows she is autistic! Many relatives have decided this autism thing was just something I was being hysterical about. She is taking three languages at school this year, French, latin, and Chinese, to use her savant skills to their best advantage. Keep your heads up peeps, there is light at the end of the tunnel. My daughter is 16 and the future is as bright as our faith.
gfcf recipes @ http://wogglebug.com

How old is your son? Can he

cunning29's picture

How old is your son? Can he swallow pills? Methyl cobalamin is available without a prescription or doctor being involved. Last I knew, it was available from swansonvitamins.com and was very reasonably priced, although I forget offhand how much it was. Yes, I'd say you may very well be being scammed.

Rakesh Patel, R.Ph. MBA You

Pharmacist-WELLHealth Rx's picture

Rakesh Patel, R.Ph. MBA
You are correct, Methylcobalamin (Methy B-12) can be found in a tablet. However, bioavailably is very, very, very low (my guess is less than 1%). Please remember just because a vitamin manufacture places an ingredient into a tablet, does not mean it will work. The only way to “get” some vitamins is by injection. Methy B-12 is one of these.
On a side note, if you can find a vitamin with L-methlyfolate this will be absorbed better. But still not 100% in my opinion. A RX only vitamin called Cerefolin contains this ingredient. Call our Pharamcy if you have any more questions about Methy B-12. The contact number can be found on our web site: www.wellhealthrx.com

Dose the clay baths and oral

Marlin's picture

Dose the clay baths and oral chelation work? Also, instead of B vitamin injections can one use a reputable high quality B tablet or nose gel?

For my son I have seen minor

jaymers's picture

For my son I have seen minor improvement over the months. the b12 has to be injected in the subcutaneous tissue for it to be effective. Trust me it took months for me to be brave to use a shot, but the shot is small as a diabetic needle, and you can purchase the numbing cream to put on the area where you are going to inject the b12, my son doesnt even feel it.

this site tells you how to use b12
http://www.youtube.com/watch?v=wdIWkym4dAA&feature=related

www.tacanow.org and click on the menthyl b12 area under biomedical treatments, and there is a plethora information there regarding b12.

Thank you for sharing the

Marlin's picture

Thank you for sharing the helpful information, there are so many miracle claimed treatments out there one has to be careful in what they choose to give their child.

Marlin Goff

I agree it can be tricky.

jaymers's picture

I agree it can be tricky. And its hard to say but I think sometimes some of them are scams. Its like finding a needle in a haystack on which one to choose

I have to add on a side note

jaymers's picture

I have to add on a side note of my previous blog, that even though I disagree with some of the approaches that Jenny Mcarthy implies in her books ie "autism is curable" "you should fork over thousands for biomedical treatments" I do think she should be praised in her efforts to bring attention about this particular disorder. By using her semi-celebrity status, I think she brought more awareness to others in our community about autism.

I agree with you about

ChunWong's picture

I agree with you about praising her efforts. The rest of us can try our hardest to raise autism awareness but it's nothing compared to what a celebrity can do by going on chat shows, writing books and being able to publicize them effectively, doing interviews and getting out there and being heard by a worldwide audience. I'm not saying that we shouldn't try, I'm just saying that I applaud Jenny for her efforts.

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

I think she is really

Ozma's picture

I think she is really brave. She could have hushed it all up, she had written books on parenting for pete's sake, and it could have all blown up in her face. Lots of people criticize her, but not me. I never judge moms of autistic kids, really. Everyone is doing the best they can, every day. Thank goodness for people like Jenny, who are willing to lay it all on the line for others.
gfcf recipes @ http://wogglebug.com

I guess my only concern is

Jon the Storyteller's picture

I guess my only concern is that she professes to be the advocate and voice for all parents of children living with autism. On CBS' "The Early Show" a couple weeks ago, she said she's "advocating for all parents" and to me, that's a bit self-righteous. Not all share her beliefs and not all believe her son is cured. I have no problem with putting autism in the forefront, but to express "cures" is dangerous, even when you disclaim that they "may not work for everyone". For many unfortunately, her celeb-status alone makes her credible. I'm not trying to downplay the importance of awareness, but the information being professed should be carefully tempered when dealing with a frustrated and sometimes desperate audience.

Jon Gilbert
Co-Chair
Exceptional Parents of Exceptional Children

http://thesamechild.blogspot.com

I agree Ozma and I don't

ChunWong's picture

I agree Ozma and I don't understand how people can be so nasty about her. I know that many don't agree with her opinions about autism and vaccinations etc. but people get so personal and attacking about her and there's just no need for it. As you say, she could have hushed it all up, kept her privacy (and no-one would have blamed her) but she used her experience to teach others and raise awareness.

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

I tried to contact three

abbylovestwins's picture

I tried to contact three different rescue angels from Jenny's Generation Rescue Site...I emailed three different women and not one of them emailed me or called me back. It has now been over a month, so I am not to thrilled with a resource she offers on her site that does not pan out. Maybe I should try one more time to contact one, but usually in my book, three strikes and you are out. I will have to see if I think it's worth it to try try again.

I am a Rescue Angel on the

KaeLainne's picture

I am a Rescue Angel on the site. My DAN! recommended I sign up, as there were NONE in my area. I have been told that some Angels ignore their requests and that REALLY bothers me. One, it's negative reflection on the site. Two- if these people signed up, they need to step up and answer the emails. I answer mine the DAY I get them. But then again, I literally live and breathe Autism and Biomedical.
It's unfortunate that the treatments don't work for all of our children. It's like anything else- One size does not fit all. There is no right answer, when each of our children are so very different. I just encourage parents to read up on current treatments and talk with other parents and see if they can find something that seems to fit for their family. We have been VERY fortunate and the gluten free diet was a life saver for us. Removing casein had little effect on her developmentally, but physically, the change was dramatic. The dark circle vanished and her swollen belly eased and her stool FINALLY firmed up. This was a chronic issue for her.
The greatest thing for us was Antioxidants. On day two of that supplement, she potty trained herself. The days I cant sneak that one in now are not good days...
I am very sorry you had, not one, BUT TWO bad experiences with Rescue Angels Abbylovestwins. I would be MORE than happy to talk with you. As a rescue angel or just mom to mom. This goes for anyone on here. I'll never push anything on anyone, just help you find info you may be looking for!
As for Jenny- while I may not agree with everything she says, it IS because if her that I didn't listen when our doctor said "Your daughter has Autism. Mourn the loss of your hopes and dreams, there is NOTHING YOU CAN DO FOR HER". (word for word). Jenny was on Oprah days later and I found Biomed. My daughter entirely non-verbal and began speaking within days of removing gluten. For this, I will be eternally grateful to Jenny McCarthy. I have since learned that not only does she not have all the answers. NO ONE DOES and it's up to us to find them for ourselves.

http://biokae.com/home/

That's really bad, perhaps

ChunWong's picture

That's really bad, perhaps your email went into their spam folder or something. I would give them the benefit of the doubt and try again or contact Generation Rescue and explain the situation.

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

Being at a place in my life

Ozma's picture

Being at a place in my life where the worst days of autism are behind me, and having had lot and lots of success with the diet and DAN! treatments, I am always willing to help a desperate mom who needs help. I am not a doctor, but have been in the trenches for 15 years. Drop me a note if you need some help, and if I have answers, I would be happy to share. Keep your chin up! And for all the peeps who say that DAN treatments are too expensive, well, so are soccer, piano lessons and designer sneakers. We just choose to spend our meager funds on what will most benefit our child. Not every one can afford it, but there is a lot you can do. And as For the gluten free caesein free diet being expensive, I find it to be much less expensive than the hospital, the psychologist, and the special tutoring she needed before. I would much rather spend my meager money at the grocery store buying healthy food, than spending it on asthma equipment and therapy that goes no where. Give the diet a good solid try- it really does work for a lot of people!
gfcf recipes @ http://wogglebug.com

First, I commend you for

jaymers's picture

First,
I commend you for being positive and encouraging. But your justification for the treatments from the DAN Dr is a far cry from a small soccer fee. And yes in the long run the GFCF diet could help on dr fees, but for me my son became really really ill, and this is not me just giving up cause I tried it several times in his five years of life. By the way, I tracked my cost of GFCF food (i went to all the stores bought books, ordered online food, my son is REAL picky about food ) and my cost with just GFCF food for one son was 135 for two weeks of food! This is not including the food for my other three children. We are talking thousands here not hundreds for DAN dr examination fees and testing, and not including the treatments. It just urks me that these Drs are charging so much money for this! Im sorry but I dont have thousands of dollors in my pocket people!

Heres an example of a DAN drs exploit. I paid 750 to see him for the first time to get B12. I couldnt afford to do the whole testing (whole comprehensive testing is about 3 grand), so I decided to do the B12 for now. He said no problem just pay 700 and 50 something a month to a lab and thats all you have to pay. So i was like ok that fine. Then he calls me up and demands me to fork over thousands for testing (this is not including the treatment costs by the way) and if i dont he will stop me from getting the B12 for my son! I begged him to wait so thats where it is now. Later on down the line I might get a basic test.. (urine, stool) to see how many metals are in my sons system. Thats a few hundred. I can do that, that is workable..

Im just trying to throw out there to not beat yourself up if you dont have thousands on hand. Do it a little at a time, as much as you mom and dads can.
Another Bio-medical treatment I am hearing about from this guy on YouTube called PhilCommander2. (by the way he is real good subscribe to him!) is the Glutothine IV. I called my DAN! Dr. and they said its only 65 dollars a treatment! It helps improve the cellular level (like repairing)

It can be very expensive,

Ozma's picture

It can be very expensive, yes, but we are taking the long view. We actually took out a second mortgage on our house to cover her treatment. We went with Dr. Bradstreet, who is the best there is. I think the docs get pushy sometimes, because they know how much these things are going to help out. I am not sure how old your child is, and where you are on this path, but for some perspective, my daughter who is 16 recently won prizes in the state science fair, and got asked out to prom, and went independently! To put it into perspective, she used to spend most of her time under a table screaming. The DAN! and the diet are worth the time effort and money. At least they were for us. We have used the B12 and the glutithione, they both worked very well, we saw lots of improvements.
gfcf recipes @ http://wogglebug.com

Ozma, it's fantastic that

ChunWong's picture

Ozma, it's fantastic that you have seen such improvements with your daughter - what a great story and so encouraging for others!

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

Thank you for sharing your

jaymers's picture

Thank you for sharing your personal story. It gives me encouragement for my 5 year old son, who is improving slightly but I worry about his future. Thanks

We are on the diet, and it

abbylovestwins's picture

We are on the diet, and it is making a huge difference in Michael's life. Eliminating the milk has made the most difference. I was just frustrated with these ladies not responding to my cries for help. I just went on and researched on my own and asked questions.

OK, so I am worried about one thing...when you have a kid who is on this diet, who doesn't eat much variety like my Michael, I worry about him not getting enough of the good stuff. He eats no veggies and no fruit. He eats mostly dry things, except gluten free bacon. The kicker is that he is a pain to get any kind of medicine or vitamins in without a traumatic pin him down and force feed it to him kinda thing...which we despise doing. So, do you have any suggestions as to ways of getting him the vitamins/supplements he is lacking? He won't chew any vitamins or willingly swallow any liquid supplements. I worry about his bones, with so little calcium in his diet. He is only two and a half. He has lost some weight from taking milk away, but it's not worrying me too much yet. He is like so many, a creature of habit and just won't try new things. We went out and bought a variety of gluten and caesein free snacks from pretzels, cookies, donuts to cereal and he just pushes it all away. Thank God for sunkist fruit snack and bacon! So if you have any ideas, techniques or suggestions, I so welcome them and thank you very much!

Oh right now I am using V8

jaymers's picture

Oh right now I am using V8 Fusion (the drink that has veggies and fruit) my son loves to drink it so that gives me the peace of mind for the time being. And when my other son who eats his veggies and fruits, I place it near my little picky one too. He is starting to bite it here, but not even close to eating it yet. Little by little I think if you at least introduce it and show it to him or her, they will more likely try it one day

Our daughter was also the

Ozma's picture

Our daughter was also the type where we had to hold her down and make her swallow. Those were not fun days. We get so used to such a high level of drama, don't we? Some suggestions, for getting foods into picky eaters:
One of the things I have found in my own family, and in others that I talk to, is that lot of our kids self select very unhealthy food for themselves, because they are trying to get their gluten fix. My daughter ate only bread for the longest time, until her nickname was loaf! I find lots of parents are too exhausted to argue with this, and resort to giving their kids nothing but snacks, you are not alone in this. But we need to get healthier food into them, it is not just about gfcf, that is only a start. It is about getting the best quality nutrition in them as possible, because they need proper fuel. It really is true that you are what you eat. I learned not to buy the 7 dollar pretzels, and the 12 dollar cereal- I make lots of food from scratch, so it takes more of my time, but it is much less expensive and better for my children. I keep it simple, that is my mantra. There are lots of ways of sneaking fruits and veges into your kid!! The best way is the almighty muffin. There is not anything you can't hide in a muffin. I have put all kinds of small amount of cooked veges into a really yummy looking muffin, and it is hilarious to watch them shovel them down. As for calcium, you can get orange juice that is calcium fortified. We also liked the Super Nu-Thera powder, and we put it in sweeetened drinks, because it was better than nothing. ( It is a powdered vitamin, formulated specifically for autism, and you can get it from Kirkmanlabs.com) As my daughter got older, we were able to sprinkle her meds on her food, and then she graduated to taking pills. It does get easier, for many people. One of the other things that many parents have reported is that their child gets less picky the longer they do the diet, and the stricter they are with it- this was my experience. Taking her off milk showed the most dramatic results, but taking her off gluten had many more subtle and long term effects. Once all the gluten and casein were cleared out of her system she became much less picky, and now she eats all kinds of things. I couldn't find it for you, but on Tacanow.com, she has a protocol that you do with you child to introduce new foods that sounds like a great idea- I never had to do it, my daughter got less picky by strictly adhering to the diet, but it sounds like a great plan. I know it sounds like I am flogging my website, not really, it is just where I store all my info- I have lots of ideas up on there for what to put in your child's gfcf lunchbox, and what to make when you are in a hurry, etc, that won't cost you an arm and a leg, so give it a look. (woggle-bug.com) I also hear lots of people say, oh they will eat when they are hungry enough. And I know that sometimes our kids have the stubborn streak a mile wide, where they really would rather starve. Do the best you can, and God bless you.

gfcf recipes @ http://wogglebug.com

I was exactly in the same

jaymers's picture

I was exactly in the same position as you are few years ago. For me in my case, it got so bad that I had to take him off the diet. Too much weight loss, getting too sick. For me it didnt work, that doesnt mean it wont work for you, because I had others in my son's class who did work out on it. I tried Rice Milk to supplement his calcium intake. You can get them at Trader Joes or Clarks, but beware of Rice Dream it does have gluten in it. I think Full Circle has a rice milk that is a good choice, but make sure its not the fat free kind since your child needs the nutrients in it. For vitamins I used the Gummie chewies, they taste like gummy bears, and I read the label and I dont see any gluten or casein, but you probably have to call the company.

Also I bought a book that was really helpful to me when I had to go shopping at the grocery store and didnt have time to read every label. This book is alphabetized,and has every kind of food group that you would ever need for your child. In each category, it has every brand that uses GFCF ingredients. Its the Bible for GFCF shoppers. www.gfcfdiet.com or email: products@gfcfdiet.com

I appreciate your

abbylovestwins's picture

I appreciate your suggestions. I am going to look into the gummy vitamins for sure. We tried the rice milk option and it was a no go. It is an expensive diet. One bag of pretzels costing 8 dollars. But, since Michael and his twin Kaylee are so picky and eat so little, it is working out ok for us thus far. We buy snack food more than anything for them, like cereals and pretzels, and since they don't eat too much it is ok for now. If I had to cook all GFCF meals for them I could not afford to feed them. We have not gone to any DAN doctors as of yet because of course they don't take our medicaid insurance and we have five kids so seeing doctors not covered by insurance is just not an option right now. Kaylee is not autistic but she is delayed in many ways so we figured we might as well put her on the diet to see if it helps.

Thanks for the link too. Very cool.

I think this word "cured"

jaymers's picture

I think this word "cured" out there is being used incorrectly for autism. Our autistic children are not diseases that need to be "cured" from. However through this world of bio-medical threats, these, at least in my case, helps improve their life. Autism as I was told at a convention, is not degenerate, this needs to be known to parents who have children with autism. Do not worry mom and dads, autism is not degenerate. Therefore there is nothing to go but up! The brain will develop in its own pace. And there things you can do to help this process even more: Gluten Free Casein Free diet. (this can get expensive, and it is difficult to do, but people have done it, I however couldnt do it, tried it 4 times in my child's 5 years of life) There is Methyl-B12 which is suppose to be the most effective (90 percent success) and the cheapest (50 dollars a month, this doesnt include the examination fee of the DAN! Dr which for me was 700 dollars). go to www.tacanow.org for more info on b12
There is Chelation, which for us non-rich folks, with all the testing that the DAN dr charges, and the treatments, it cost thousands! Dont beat yourself up if you feel that "hey I just dont have like 4 grand laying around!" On a side note, that's what bothered me about Jenny's book, she implied that you were not a good parent if you did not fork over thousands, charge up your credit cards, and loose you house for Bio-medical treatments! this to me was hogwash, she has no clue obviously what its like being just middle class family, that has other dependents other than her only child.
OK back to Chelation. www.evenbetternow.com sells oral chelat drops and a detox clay baths for children and adults. These are reasonable prices too! And you dont have to loose your home over it!
Another treatment I have been using for my son is ThreeLac (recommended in Jenny's book) It is a probiotic, and helps control the "leaky gut issues" this is the cheapest seller of ThreeLac. www.threemax.biz you can order it by email or by phone: mwinicki@yahoo.com or 716-373-0983. This is also reasonable 50 something bucks every two months.
So there are ways to get around the who total DAN! Dr expenses. I am a middle class mom, and I can afford all of these treatments. So far all of these: Chelate, detox clay bath, B12, and probiotic. seems to be helping my 5 year old, I have seen an improvement in him! and so has his teachers (ABA teachers, OT, and speech)

Yeah, perhaps "recovered" is

ChunWong's picture

Yeah, perhaps "recovered" is a better word to use although I think that if your child's symptoms have disappeared then you can happily use the word "cured". It's great that you are seeing suc an improvement with biomedical treatments - what improvements have you noticed?

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

ya I agree with you

jaymers's picture

ya I agree with you "recovered" might be the better term

Improvements in the last month: My 5 year old son is just now starting to understand the concept of language. He has always repeated words, but now that I am telling him to do something he is going and doing it! Its more simplified one step commands, but this is brand new.

Whether or not your child is

Ozma's picture

Whether or not your child is "cured" is debatable, but I look at it like this- I think before my girly girl was on the diet, she was continuing to receive brain damage from everything she was sensitive to. Now that she is on the diet, and we have chelated her, etc. (DAN! Treatments galore) She is no longer getting daily brain damage, so in a sense she is "cured". There will always be a certain amount of brain damage left, which will always be with us- autism will always be with us. We have had some really great success reversing some of the damage with HBOT treatments, and seen her grow and prosper in ways we thought weren't possible before. And before the treatments none of it was possible- it didn't matter if she had therapy, none of it stuck. Now she can really learn. Anyway, she is 15 now. Hang in there, Moms and Dads, it gets better as they get older for a lot of these kids.

gfcf recipes @ http://wogglebug.com

This might be a too personal

jaymers's picture

This might be a too personal question for you. I understand if you are not willing to answer, but if you can, could you tell me how much you paid for the HBOT treatments? is that the hypoberic chamber? I heard good results from it, but when i found a person who does it in my area she wants to charge me 4 grand!

Hi Ozma, That's so great

ChunWong's picture

Hi Ozma,

That's so great that you have noticed such improvements in your daughter from biomedical treatments and I'm so pleased that you've seen her flourish in such a way. I think it is important that parents retain hope.

Chun
***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

Well if want information

clairelouise82's picture

Well if want information that gives flase hope then visit jennys site or site jenny is featured on. Jenny claims her son is cured from autism! U decide!

Her son had a seizure

Amy's picture

Her son had a seizure disorder and gluten issues. She fixed that, not autism. Her whole shtick is ridiculous and stupid!

I saw her on a special on

MDDdoll's picture

I saw her on a special on television and she said "my son was having seizures where his heart would stop. so i took him to a neurologist and the neurologist told me my son had autism. and i just knew it was true". EHEM but if MY neuro told me that my son was having seizures that made his heart STOP and he told me "oh he has autism" I would be SERIOUSLY pissed. My 2 cents.

I don't think that's true.

ChunWong's picture

I don't think that's true. Her son Evan was diagnosed with Autism and has now moved off the autism spectrum.

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

It is possible. My son has

shootingstars's picture

It is possible. My son has started off about medium functioning and is rising on the spectrum. Someday he may be barely on the tip, or he could regress back. I recently found contact with some family I lost as a child and found out one of my other cousins has Autism and my uncle told people he was told she would grow out of it...

Of course I think it is not growing OUT of it rather it is growing INTO it. It is coming to understand oneself and a bit about the world around them. It is coming to accept your limits and learning emotions rather than having them control you. My son is still controlled by his emotions, but we are teaching him he has to move on from them.

I am not saying I think she has CURED her son. I especially how she was quoted taking all the credit. How she prayed to God to cure her son and she would show the world how she did it... Managing Autism is a team effort... Doctors, therapists, family ect.

I agree with you

ChunWong's picture

I agree with you shootingstars, treating and managing autism is definitely a team effort - everyone working together for the child's benefit.

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

Agreed.

shootingstars's picture

Agreed.

I have not yet read the

kcpurple's picture

I have not yet read the book, so i do not have an opinion on it one way or the other. I do however, have a question. What is a DAN doctor? I have heard of many treatments for people on the spectrum, but I have never heard of a DAN doctor. I have a son with PDD and wonder if this could be helpful to me. Thanks.

*****

ChunWong's picture

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****

DAN! stands for Defeat Autism Now!, an initiative by the Autism Research Institute to inform and educate parents about biomedical treatments for autism and biomedical based research. A DAN! doctor is a physician or therapist is someone who believes that traditional psychotropic drugs are not the best approach to treating autism and that biomedical interventions, that treat the root cause or trigger of the autism, are best. Biomedical treatment can include supplements, chelation, dietary changes/improvement, hyperbaric oxygen therapy (HBOT) and gut treatments.

You can read more about DAN! on the Autism Research Institute site http://www.autism.com/dan/index.htm

I googled DAN doctor, here's

Cindy's picture

I have not read the new

AutismClassroom.com's picture

I have not read the new book. Is it worth checking out?

AutismClassroom.com
Question. Discuss. Learn.

Asperger’s syndrome is a

Luca's picture

Asperger’s syndrome is a form of mild autism that often goes undetected. New years 2008: my little brother Chris dropped dead - a moving testimony to a brother with asperger's syndrome, by zen peace. This is an enlightening new book that details a doctor's decline into depression, and highlights the signs of Asperger's Syndrome in childhood, adolescence and adulthood. A good primer.

While I have read the book I

monkey1's picture

While I have read the book I find it informational and hope it helps millions.  Although, I think her son had a unique situation I feel it gives false hope to all of us who have tried all of the remedies and our children have not gotten better.  I saw her on Larry King and while I admire her for her perserverence I feel that her solutions are not the only ones and as you all know every child with autism is different just as every typical child is.  Just my 2 cents!

*****

ChunWong's picture

***** http://www.newautismcure.com/blog - Biomedical answers to Autism *****
I have seen an interview with Jenny McCarthy where she says that what helped Evan won't work for every child, just like chemo won't work for everyone with cancer, but that you don't find out until you try these things. Yes, every child is different and there does not seem to be a "cure all".
I too admire Jenny for her perseverance and for getting the word out about autism.

I am an Early Childhood

Melissa's picture

I am an Early Childhood Special Education teacher. I teach an ECLIPSE program, which is a model program for children with and without disabilities. The school that I work in is a title 1 school... based on the amount of low-income families in the community whose children attend our school. I just finished reading Jenny McCarthy's book, "Louder Than Words," and I loved it! It left me with several ideas of options to give to the parents in my class who have children with autism. I know that they will not be able to afford many of these things, but it at least gives them information that they might not be able to find elsewhere; to help them better understand what their child may be going through and ways that we can help. We can take these ideas and options and come up with more "real life" ways to use them. I really enjoyed reading this book and am looking forward to her next one!
~Melissa