Guest guest Posted June 15, 2008 Report Share Posted June 15, 2008 Yes, it is all McCarthy's and the moms who have not stopped getting the word out fault that my son is on the road to recovery. It is also their fault that my 5,2, and 1 yr old will not end up with Autism. God Bless you all m McCarthy Just thought you all might find this interesting. ...Our new director has a small baby and when he took him for hiswell-visit he got into a little feisty argument with the pediatricianbecause he doesn't want to vaccinate "too many too soon."The pediatrician' s comment?"This is all McCarthy's fault." Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2008 Report Share Posted June 15, 2008 It's McCarthy's fault that I felt like a human being again this spring. Darn her. So many of us were enjoying feeling isolated, voiceless and disenfranchised. Now I have people telling me they saw Larry King, believing me about what happened to my children and some don't even look at us like we're freaks anymore. Tsk. > > Just thought you all might find this interesting.... > > Our new director has a small baby and when he took him for his > well-visit he got into a little feisty argument with the pediatrician > because he doesn't want to vaccinate " too many too soon. " > > The pediatrician's comment? > > " This is all McCarthy's fault. " > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2008 Report Share Posted June 18, 2008 YOu are a much better person then me, because we would have before that doctor looked at my child and not just my asd kid, any of my kids. Primer who lives in Oceanside but is in Carlsbad Unified School District Tired of the energy crunch? Fuel your body with something healthy and delicious. The energy of the future is Verve. All your daily Vitamins, Essential Minerals, Mangosteen and Aloe in an energy drink. ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich McCarthy I was in the ped's office today.There was an "anti-jenny" article, copied on colored paper and laminated, hung above the sink in the exam room. It was written my an MD w/an adult sister w/ASD.We did not discuss it,CGF Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2008 Report Share Posted June 18, 2008 Imagine the guilt building up in the pediatric community. That niggling little voice that is probably still locked in the subconscious mind, " Did I do this to these kids? Could I have helped my sister? Was I sold a bill of goods in exchange for free lunches and a bunch of pens? Am I culpable? Will I get sued and lose my career? Is my wife cheating with the boy who shags balls at the practice range? " KS > > I was in the ped's office today. > > There was an " anti-jenny " article, copied on colored paper and > laminated, hung above the sink in the exam room. It was written my an > MD w/an adult sister w/ASD. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2008 Report Share Posted June 18, 2008 I don't believe the peds are thinking such things yet. My SIL is a pediatrician and she still seems truly convinced vaccines are totally safe and effective. She has tried to convince my husband and me to vaccinate our boys. And she even has a son on the spectrum! > > > > I was in the ped's office today. > > > > There was an " anti-jenny " article, copied on colored paper and > > laminated, hung above the sink in the exam room. It was written my > an > > MD w/an adult sister w/ASD. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2008 Report Share Posted June 18, 2008 Think about how some parents are filled with anger and guilt for giving their 1 kid about 30 shots..... Now think of a doctor who has given about 1000 kids 30,000 shots...... No wonder they can’t accept it. Plus- they are scared to lose everything they own in a law suit. - I don't believe the peds are thinking such things yet. My SIL is a pediatrician and she still seems truly convinced vaccines are totally safe and effective. She has tried to convince my husband and me to vaccinate our boys. And she even has a son on the spectrum! > > > > I was in the ped's office today. > > > > There was an " anti-jenny " article, copied on colored paper and > > laminated, hung above the sink in the exam room. It was written my > an > > MD w/an adult sister w/ASD. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2008 Report Share Posted June 18, 2008 Kirby talked about this in Null's vaccine nation (the dvd passed out at the rally). I can't remember his exact words but something along the lines of it being " human nature " for someone who got in a profession to help people, not wanting to hear any evidence that they inadvertently could have harmed thousands. He worded it much better than that, and it made perfect sense. > >>> > > > >>> > > I was in the ped's office today. > >>> > > > >>> > > There was an " anti-jenny " article, copied on colored paper and > >>> > > laminated, hung above the sink in the exam room. It was written my > >> > an > >>> > > MD w/an adult sister w/ASD. > >> > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 McCarthy's Mother Warriors Book Tour Check your local listings for stations and time: Oprah Sept 24 (Oprah.com that night) GMA Sept 29 CNN American Morning Sept 30 CanadaAM - Sept 30 Access Access <s Sept 29, 30 Possibly Oct 1 Ellen Degeneres October 3 KTTV/Good Day LA October 2 > > seen lots of ads for the show tomorrow. Jim Carrey is also on with her. Remember that Oprah's show also airs at night on cable if you miss it during the daytime. > > Maurine > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 I like her don;t get me wrong PLEASE.. .Glad she brought our struggles to the fore front but I have a few little issues with her experience. She has alot of fund to use for Evan's health. She really is not limited in income. If I had alot of money---even 50K I could use t for my son's betterment also but I don't and us as regular people's insurnace is really hard to get adequate care for our kids (I have 6 ot a YEAR for 's Aspies--I may as well have none) I don't believe Evan is in a full day of school yet. Us with kids on the spectrum know how much a school cna help for good and bad for our kids. . structure--good. . long day--bad. Again she has the funds to adjust his schooling to his needs.. . how wold he do in " regular public school. " I know I am going to take a beating for this but also where ate the Stars who's kids have been hurt by vacines?? Would be nice to see them out fighting too. . or do we commoners have the only affected kids?? People see these kids who are in a remission and then ask us why our kids are stillhaving issues. . It all comes down to the most powerful thing. .he who has the unlimited money--get the best services. Grace -- In EOHarm , Primer wrote: > > YOu are a much better person then me, because we would have before that doctor looked at my child and not just my asd kid, any of my kids. > > > > > > > McCarthy > > > I was in the ped's office today. > > There was an " anti-jenny " article, copied on colored paper and > laminated, hung above the sink in the exam room. It was written my an > MD w/an adult sister w/ASD. > > We did not discuss it, > CGF > > > Primer who lives in Oceanside but is in Carlsbad Unified School District > Tired of the energy crunch? Fuel your body with something healthy and delicious. The energy of the future is Verve. All your daily Vitamins, Essential Minerals, Mangosteen and Aloe in an energy drink. > ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 I don't think you should hold it against her that she has a lot of money. She is out there fighting for all of us. There are people with a lot of money that may or may not recover their kids and they aren't out there helping the rest of us and making this all public. Let's be glad she has a public face and popularity from the past so she can make people sit up and listen to her. Maurine>> YOu are a much better person then me, because we would have before that doctor looked at my child and not just my asd kid, any of my kids.> > > > > > > McCarthy> > > I was in the ped's office today.> > There was an "anti-jenny" article, copied on colored paper and > laminated, hung above the sink in the exam room. It was written my an > MD w/an adult sister w/ASD.> > We did not discuss it,> CGF> > > Primer who lives in Oceanside but is in Carlsbad Unified School District> Tired of the energy crunch? Fuel your body with something healthy and delicious. The energy of the future is Verve. All your daily Vitamins, Essential Minerals, Mangosteen and Aloe in an energy drink. > ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 I don’t think at the time had “unlimited” money. She was in the middle of a divorce that was costing her a lot. Plus, she works hard for what she has. Have you ever seen a movie shoot- where the actors work 18 hour days- many times in the middle of the night? It’s not easy work. Also, I think there is a misconception that those with money heal their kids and all the poor kids stay sick (to simplify it). That is just not true. I know many families who put THOUSANDS of dollars into their kid’s treatments and got very little improvements. And, on the other hard, take my situation. I have very little money- no savings- no home- rent a crappy apartment, etc. We are very lucky that our insurance covers most of the testing and chelation for my son. Of course his Dad has been away in the military for 9 years- so we all make different sacrifices. Also, we live on Long Island- where back when my son was dx, the school district would give you 30-40 hours a week of ABA, Speech, OT, etc. in your home (no cost to you). My son went to a preschool 6 hours a day starting at age 2.5 yrs. Now he is in a school district with a special “autism” classroom and all these other services. Again, no cost to me. I could live in a house in VA and have crappy services. Or I could live in a crappy apartment in NY with great services. I know it’s hard because some people have never left their own state and don’t know what is out there- but if you don’t have any services- think about moving. It could save you a lot of money in the long run. I also do a lot of research- online and at conferences. I learned ABA myself- so I don’t always need to pay someone to help me solve a problem. My son has been Gluten/Casein/Soy/Nut free for the last 6 years. I get a lot of stuff through Amazon.com by the case and it’s a lot less expensive then buying at the health food store. Overall, I’ve probably spent $5000 in 9 years on my kid’s autism (extra food, supplements, doctors). Plus, I’ve spent hours and hours “volunteering” for the cause (but that’s a whole other story). But anyway, my son is doing great- he’s out of the “autism” classroom and into a 15-2. He’s starting violin lessons at school on Thursday- he’ll be in the band. I really have no complaints. Ok- he’s not “recovered” and still has issues. But, he’s getting there. Life is good. He’s happy. Those of you who have met him know what I’m talking about. I’ve met Evan at the rally in DC. It was hard to tell if he was 100% recovered. But, the kid looked pretty good to me. Yes- only time will tell. But, in my experience- I’ve meet a few recovered kids and people just don’t believe it. Which is sad. Because some of these kids are- no doubt. Another thing- One must understand that society has been brainwashed that vaccines are good. Those who are anti-vaccine are thought to be crazy. I’ve experienced this in the media as well as the Health department. Talking to politicians is fun too- having to tread lightly. I give a HELL of a lot of credit for getting out there and saying what she says. She doesn’t do it because she has all this money fall on her lap. She has risked everything she has- which makes it even more amazing. She has more to lose. But, she still does it. And she is a mother- just like the rest of us. She cried with her son in her arms- just like the rest of us. But, I really find it offensive that people belittle her actions and say “well- she’s rich”. Yes, some things are easier when you have money. But, she has a whole other set of problems that most of us don’t have. I wouldn’t want to trade places with her. Her son died and came back. I would never want to see my own son go through that- or see him have a seizure. - I like her don;t get me wrong PLEASE.. .Glad she brought our struggles to the fore front but I have a few little issues with her experience. She has alot of fund to use for Evan's health. She really is not limited in income. If I had alot of money---even 50K I could use t for my son's betterment also but I don't and us as regular people's insurnace is really hard to get adequate care for our kids (I have 6 ot a YEAR for 's Aspies--I may as well have none) I don't believe Evan is in a full day of school yet. Us with kids on the spectrum know how much a school cna help for good and bad for our kids. . structure--good. . long day--bad. Again she has the funds to adjust his schooling to his needs.. . how wold he do in " regular public school. " I know I am going to take a beating for this but also where ate the Stars who's kids have been hurt by vacines?? Would be nice to see them out fighting too. . or do we commoners have the only affected kids?? People see these kids who are in a remission and then ask us why our kids are stillhaving issues. . It all comes down to the most powerful thing. .he who has the unlimited money--get the best services. Grace -- In EOHarm <mailto:EOHarm%40yahoogroups.com> , Primer wrote: > > YOu are a much better person then me, because we would have before that doctor looked at my child and not just my asd kid, any of my kids. > > > > > > > McCarthy > > > I was in the ped's office today. > > There was an " anti-jenny " article, copied on colored paper and > laminated, hung above the sink in the exam room. It was written my an > MD w/an adult sister w/ASD. > > We did not discuss it, > CGF > > > Primer who lives in Oceanside but is in Carlsbad Unified School District > Tired of the energy crunch? Fuel your body with something healthy and delicious. The energy of the future is Verve. All your daily Vitamins, Essential Minerals, Mangosteen and Aloe in an energy drink. > ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 I have to stick up for here. I know the last place you want to be is on a movie set or doing a shoot acting HAPPY when your child needs you home to help them.But she has to earn a living. We cant put her down or say its wrong she has more money then us. personally..i work in the same field.I'm on sets as well but I'm not an actor I'm an agent so the hours the talent has to work is harsh to say the least sometimes double shifts and dieting on top of that and exercising to stay fit because that's how she gets paid.I know all I wanna do eat when I get stressed. I only had a full day option for my daughter..and that sucked let me tell you because they are sucking up all my daughter day and only accomplishing 2 hours a therapy the whole week!! So I'm doing her ABA at home now..we do 3 to 4 hours a day now.I'm taking an ABA training course so I officially know how to take data and do chaining.They teach it at a local autism education place here in my state.When there is a will there is a way! For Christmas..relatives ask..what does my daughter want for Christmas..I give them the list of supplements and websites to order..I say that any of those things on the list would really help instead of toys that we have 4 million of anyway. didn't ask for a child with Autism ..none of us did and it doesn't matter how much or how little money we have..Its difficult no matter what we have to be supportive of one another not be mad because someone may have better resources or has a better job. We all struggle for sure so lets just open our hearts to mothers who are fighting for us to make headway here. Deo Productions: Talent and Model ManagementContact www.sAngels.com APRIL IS AUTISM AWARENESS MONTH.>> YOu are a much better person then me, because we would have before that doctor looked at my child and not just my asd kid, any of my kids.> > > > > > > McCarthy> > > I was in the ped's office today.> > There was an "anti-jenny" article, copied on colored paper and > laminated, hung above the sink in the exam room. It was written my an > MD w/an adult sister w/ASD.> > We did not discuss it,> CGF> > > Primer who lives in Oceanside but is in Carlsbad Unified School District> Tired of the energy crunch? Fuel your body with something healthy and delicious. The energy of the future is Verve. All your daily Vitamins, Essential Minerals, Mangosteen and Aloe in an energy drink. > ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 Grace, even children that have families with endless resources have Autism. We are all coming in at a time where nobody knows the cure. What works for one child doesn't work for another. has used her stardom to give us a voice. We don't have a ton of money, but I use the law and the resources available to help my child. Do some advocating, go to the free classes that are provided. Join a support group, get involved, it doesn't cost allot of money to fight for your child and bring awareness. One step at a time. Let's get to it and get help for our children. Thanks to all the proactive parents we are being heard and it doesn't cost allot of money. Candyce McCarthy> > > I was in the ped's office today.> > There was an "anti-jenny" article, copied on colored paper and > laminated, hung above the sink in the exam room. It was written my an > MD w/an adult sister w/ASD.> > We did not discuss it,> CGF> > > Primer who lives in Oceanside but is in Carlsbad Unified School District> Tired of the energy crunch? Fuel your body with something healthy and delicious. The energy of the future is Verve. All your daily Vitamins, Essential Minerals, Mangosteen and Aloe in an energy drink. > ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 Did you read her book? If not, you don't know the whole story. Although their story is one you've heard many, many times, it's a good, easy read if you want to pick it up. Free at the library, CGF > > ...I have a few little issues with her > experience... > Grace > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 Yes I red her book--got it for mothers day. I know he had seizures and alot of issues. . I know she divorced over it . . .But Society looks at her and says if her son is " cured " why isn't yours?? My son with AS is A typical AS and he is dealing with a pretty severe imunization injury which has hurt his communication abilities he DID have with the AS. She no where lists the amount she spent on all these drs interventions ect. Yes I am glad she is out there getting press and stuff but she also has alot more monies than I can even get in a lifetime. Bio Medical is a great route but my son is alergic to Lithium and many suplements are made in production areas where lithium pills or similar compounds may of been produced. I have contacted many DAN dr's about it and it is a very rare alergy and some have said I've never delt with it. The two where I live won't even touch him. . (not that I have the 3000 they want when you walk in the door) > > > > ...I have a few little issues with her > > experience... > > Grace > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 There are some shcolarships out there. places you can contact are NAA, TACA and some DANs themselves have scholarships or will charge you a lot less if your financial status warrants it. maurine Subject: Re: McCarthyTo: EOHarm Date: Tuesday, September 23, 2008, 2:45 PM Yes I red her book--got it for mothers day. I know he had seizures and alot of issues. . I know she divorced over it . . .But Society looks at her and says if her son is "cured" why isn't yours?? My son with AS is A typical AS and he is dealing with a pretty severe imunization injury which has hurt his communication abilities he DID have with the AS. She no where lists the amount she spent on all these drs interventions ect. Yes I am glad she is out there getting press and stuff but she also has alot more monies than I can even get in a lifetime. Bio Medical is a great route but my son is alergic to Lithium and many suplements are made in production areas where lithium pills or similar compounds may of been produced. I have contacted many DAN dr's about it and it is a very rare alergy and some have said I've never delt with it. The two where I live won't even touch him. . (not that I have the 3000 they want when you walk in the door)> >> > ...I have a few little issues with her > > experience.. .> > Grace> >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 Hi Grace, I'm so sorry that you are feeling overwhelmed by the lack of resources you have to pay for Autism treatments. I understand completely. My husband is self-employed and he works non-stop so that I can stay home and be with our boys (both are on the spectrum). We also have 2 daughters (that's 4 kids total). There are days when I cry and cry and I think "if we just had more money we could be all done with Autism..." But then I remember that God has a different path for each of us to walk, and if I spend my time wishing for what I think might be an easier path, I'm missing the blessings that God has for me along my own path. Get creative-I asked for cash for birthday presents so that I could pay for tests/treatments. I teamed up with another mom who also has 4 kids/2 on the Spectrum to do several fundraisers such as a spaghetti dinner, a large yard sale, selling Tastefully Simple items...I've written letters explaining the costs of Autism and asked people if they're thinking of us just set $10 aside for the next time they see us, as every little bit helps. Get a good cookbook and learn how to make GFCF foods that taste good so that you aren't always buying pre-made items that are more expensive...include lots of foods that are naturally GFCF-potatoes, rice, lots of fruits and vegs, meats...and only spend $$$ on the things you can't make (like crackers or pretzels for instance...and if you're talented, you can even make those.) I hope I've been supportive and helpful. My heart truly does go out to you... Meg Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2008 Report Share Posted September 23, 2008 If you haven't been spending years on supplements because of this lithium allergy, I'd say find yourself a homeopath who can do the recovery WITHOUT the supplement issue.RoxSubject: Re: McCarthyTo: EOHarm Date: Tuesday, September 23, 2008, 6:45 PM Yes I red her book--got it for mothers day. I know he had seizures and alot of issues. . I know she divorced over it . . .But Society looks at her and says if her son is "cured" why isn't yours?? My son with AS is A typical AS and he is dealing with a pretty severe imunization injury which has hurt his communication abilities he DID have with the AS. She no where lists the amount she spent on all these drs interventions ect. Yes I am glad she is out there getting press and stuff but she also has alot more monies than I can even get in a lifetime. Bio Medical is a great route but my son is alergic to Lithium and many suplements are made in production areas where lithium pills or similar compounds may of been produced. I have contacted many DAN dr's about it and it is a very rare alergy and some have said I've never delt with it. The two where I live won't even touch him. . (not that I have the 3000 they want when you walk in the door) > > > > ...I have a few little issues with her > > experience.. . > > Grace > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2008 Report Share Posted September 24, 2008 has said that her son isn't cured but recovered. I wonder if he was taken off the diet and other interventions she is doing how he would be. Also, the other recovered children, are they on an maintanence of interventions? C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2008 Report Share Posted September 24, 2008 she has stated in the past that she will always say recovered and not cured. M Subject: Re: McCarthyTo: EOHarm Date: Wednesday, September 24, 2008, 9:59 AM has said that her son isn't cured but recovered. I wonder if he was taken off the diet and other interventions she is doing how he would be. Also, the other recovered children, are they on an maintanence of interventions? C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2008 Report Share Posted September 24, 2008 > > has said that her son isn't cured but recovered. I wonder if he was taken off the diet and other interventions she is doing how he would be. Also, the other recovered children, are they on an maintanence of interventions? > > C. > My son is one of the lucky ones, he recovered (started diet/supps in 2002). He is no longer gf/cf but still takes some supplements (less than half as before). I still try to limit his sugar. We pretty much only drinks water and unsweetened brewed iced tea at our house. We have stayed away from milk so he doesn't do cereals. He has the occasional ice cream and cheese. I've noticed if there is too much dairy his eczema will flare up. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2008 Report Share Posted September 24, 2008 I saw speak at a conference last Fall and she openly states that she believse Evan would regress if she stopped the diet and other interventions. She truly believes that his diet is what was driving the autism. Ever since I heard her speak I have a newfound admiration for her. Her fight was different than mine, our children have different issues, but I read her first book about autism and realized she WAS in the same boat as alot of us when our children were first diagnosed - being put on waiting lists for everything, not getting straight answers, etc. And then I met her and she is just an incredible speaker. > > has said that her son isn't cured but recovered. I wonder if he was taken off the diet and other interventions she is doing how he would be. Also, the other recovered children, are they on an maintanence of interventions? > > C. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2008 Report Share Posted September 24, 2008 We are in a similar situation, and if my son eats even a cross contaminated food we have a regression. I can't imagine how bad his regression would be if he were to go even one meal off the diet. So although he appears quite 'typical' he is one diet slip away from being very much disabled. We have only had a few small diet mixups and the impact it has is beyond description--shocking. He takes about 2 weeks to get back to himself. If we didn't homeschool I dont think he could get through it during the schoolyear. I am guessing this is what you would find among most'recovered' kids. As far as other interventions, the supplements we do really help, but it takes a week or so off of them before you can tell any change, and it is slight. He struggles with very obvious 'depressed' mood when he goes without his cod liver oil for more than week, but is still able to get along with school and other activities ok. When he does without supernuthera for a while we can see a real change in his ability to stay on task with schoolwork (being mom and teacher makes me painfully aware of every little change). So I think he could live without the other interventions, but the diet is his lifeline to being 'recovered'. Hope this helped answer your question. It is a tricky issue, are they or are they not autistic anymore? When one goldish cracker causes you to manifest so many symptoms, I don't think that is a question that can be answered definitively. > > has said that her son isn't cured but recovered. I wonder if he was taken off the diet and other interventions she is doing how he would be. Also, the other recovered children, are they on an maintanence of interventions? > > C. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2008 Report Share Posted September 25, 2008 I agree. When I first saw her website indigo child, long before she told the world her kid had autism, I thought, is this the new age way to cover up Autism. 4 years ago when we started this journey people looked at us like we had 2 heads that Austin was on diet and enzymes, because of people think its common to see recovery. My kid is far from recovered, but because of I get lots of feed back from parents I only see during football season (husband is a high school football coach) about what a difference a year has made in Austin. may have more money then us, but she still mortgaged her house, she still did the poop smears, she still cares for her child largely on her own. Instead of keeping her kid hidden like many celebs, she is out walking the walk and talking the talk. It would have been easier for her to take our techniques and walk away with a recovered kid, she took the hard road and came out fighting. Watching the web cast today, she really is just a regular woman who loves her kid and wants to help all our kids. Primer who lives in Oceanside but is in Carlsbad Unified School District ~All truth passes through three stages. First, it is ridiculed. Second, it is violently opposed. Third, it is accepted as being self-evident. -- Arthur Schopenhauer ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich McCarthy> > > I was in the ped's office today.> > There was an "anti-jenny" article, copied on colored paper and > laminated, hung above the sink in the exam room. It was written my an > MD w/an adult sister w/ASD.> > We did not discuss it,> CGF> > > Primer who lives in Oceanside but is in Carlsbad Unified School District> Tired of the energy crunch? Fuel your body with something healthy and delicious. The energy of the future is Verve. All your daily Vitamins, Essential Minerals, Mangosteen and Aloe in an energy drink. > ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 25, 2008 Report Share Posted September 25, 2008 I am sure this has been covered but on the webcast tonight she said she still monitors Evan;s diet and that she packs a lunch when he goes to party. Personally I think recovered does not have to mean off diet, if your allergic to peanuts you could recover from the allergic reaction but you can't eat some more. Primer who lives in Oceanside but is in Carlsbad Unified School District ~All truth passes through three stages. First, it is ridiculed. Second, it is violently opposed. Third, it is accepted as being self-evident. -- Arthur Schopenhauer ~Well-behaved women seldom make history~ Laurel Thatcher Ulrich Re: McCarthy has said that her son isn't cured but recovered. I wonder if he was taken off the diet and other interventions she is doing how he would be. Also, the other recovered children, are they on an maintanence of interventions? C. Quote Link to comment Share on other sites More sharing options...
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