Guest guest Posted September 23, 2009 Report Share Posted September 23, 2009 Hi, my son was 6mm off. He has been in the helmet for 8 weeks now and will get his first scan tomorrow. He probably has another 2 - 4 weeks to go. I felt very uneasy about banding my son, but am glad that i did it. The hard part is only the first week. After that u dont even remember that they are wearing it. U get so used to it. Feel better, I hope this helps u. I dont have any decorating ideas, my son is wearing a tornado style starband so no decoration is needed. Good Luck Miriam Mom to ely 7 months old, 8 weeks in starband > > My 4 month old daughter needs a helmet for plagiocephaly. I need some decorating ideas for the helmet....it's the only thing making feel better about the whole thing right now. Any suggestions. Also, curious to know how long other people's kids had to wear the helmet for. She 8mm off. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2009 Report Share Posted September 24, 2009 WELCOME! Look thru pics to see how others have decorated and shee what you like. Our band came in pink so we just did cute flower sticker. Vellum stickers work best. The paper ones don't stay on as well. Also, there are tips in the deco file. HTH! Jen Mom to Luli - 3 yrs old Torticollis, Plagio, Syringomyelia Newbie My 4 month old daughter needs a helmet for plagiocephaly. I need some decorating ideas for the helmet....it's the only thing making feel better about the whole thing right now. Any suggestions. Also, curious to know how long other people's kids had to wear the helmet for. She 8mm off. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2009 Report Share Posted September 24, 2009 Hi! I would also like to add that scrap booking stickers work very well. I apply a layer of clear nail polish over the stickers as well to add a little extra protection. I have found great selections for the stickers @ s and Target. Have fun! BrouseUnderwriting AssistantU.S. Specialty Insurance CompanyA subsidiary of HCC Insurance Holdings, Inc.mailto:rbrouse@...Tel: (972) 381-4803 From: Plagiocephaly [mailto:Plagiocephaly ] On Behalf Of JenandLuli@... Sent: Thursday, September 24, 2009 1:03 AM Plagiocephaly Subject: Re: Newbie WELCOME! Look thru pics to see how others have decorated and shee what you like. Our band came in pink so we just did cute flower sticker. Vellum stickers work best. The paper ones don't stay on as well. Also, there are tips in the deco file. HTH! Jen Mom to Luli - 3 yrs old Torticollis, Plagio, Syringomyelia -----Original Message----- From: mantevy <mantevy > Plagiocephaly Sent: Wed, Sep 23, 2009 11:23 am Subject: Newbie My 4 month old daughter needs a helmet for plagiocephaly. I need some decorating ideas for the helmet....it's the only thing making feel better about the whole thing right now. Any suggestions. Also, curious to know how long other people's kids had to wear the helmet for. She 8mm off. This e-mail contains confidential information, and may contain privileged information, which is the property of the sender, and is intended solely for the attention and use of the addressee. If you are not the named addressee, you must not disclose, copy or retransmit this transmission or take any other action in reliance upon this transmission, and you should notify us as soon as possible. ______________________________________________________________________ This email has been scanned by the MessageLabs Email Security System. For more information please visit http://www.messagelabs.com/email ______________________________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2009 Report Share Posted September 24, 2009 > > My 4 month old daughter needs a helmet for plagiocephaly. I need some decorating ideas for the helmet....it's the only thing making feel better about the whole thing right now. Any suggestions. Also, curious to know how long other people's kids had to wear the helmet for. She 8mm off. > My son is 6 months and just started wearing the STAR band last week. Yesterday was his first day at 23 hours. I took his to get it airbrushed. We are in Houston and did it at Airbrish Brothers at I-10 and Silber. They did an excellent job. I will post pictures today. I have heard you can put stickers and stuff but I was not impressed on how they looked and they can come off. I paid $35. and it will last the entire time that he has to wear it. You can get pictures off the internet of what you want and take it to them to work from. Hope this helps some. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2009 Report Share Posted October 1, 2009 Dr. Cutler knows. He will tell you to chelate yourself and your children. You need to get the mercury out. See my other reply. And yes, babies get our mercury. Mine got some from my amalgam fillings, and the rest from his vaccines and environment. I got rid of my anxiety and depression by getting mercury out. So I've no doubt this can help you. Everything your telling me about your kids....mercury. Get the hair tests for them, and possibly yourself. Read about Andy Cutler low dose chelation, antifungals for yeast, vitamin supplements for chelation. Getting on Flax seed or cod liver oil might help you also, it will help them. There is treatment for this. Andy Cutler chelation. > > I was hopitalized in 1990 for Mercury Poisoning and in ICU for a week. My blood oxygen level was in the 30's when I was admitted. NOW.......I cannot find anyone that knows anything about my future health. > > I have 2 children aged 9 & 11 and they have ADD/ASD/OCD. I do not medicate, but am learning that Mercury could be the cause. > > Did I transfer mercury to my children? I assume that the Mercury is till in my body. I have anxiety. I have never been diagnosed with anything but anxiety/depression. I have mood swings and Effexor seems to be the only thing that helps me. > > I am more concerned about my children and would like to know what your opinions are. I just read about the hair test and was wondering if I should even bother for myself, since I know I was poisoned by Mercury. > > I joined the GFCF group and am researching to go that route with the diet. Also, I believe that we are dealing with Yeast Overgrowth as well. My son has severe allergies and was tested very young. He responded to all the molds. He was observed during a short time in private school by the public school ASD psychiatrist. We were told he had traits of autism. But never went beyond that. > > I thought my daughter was fine. But, she does have a problem with attention and now we are learning about the OCD behaviour. Had colic when she was a baby and always screamed and cried alot. I just thought this was tummy issues. Did not even let her grandparents hold her until she was over 2 years old. > > Thank you all very much, > Sharon > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2009 Report Share Posted October 1, 2009 > > I was hopitalized in 1990 for Mercury Poisoning and in ICU for a week. My blood oxygen level was in the 30's when I was admitted. NOW.......I cannot find anyone that knows anything about my future health. > The mercury needs to be chelated out in the proper way. It is good that you found this group because the chelation method developed by Cutler, PhD is best. He has posted in this group since it started. > I have 2 children aged 9 & 11 and they have ADD/ASD/OCD. I do not medicate, but am learning that Mercury could be the cause. > > Did I transfer mercury to my children? That is possible. They were also exposed to mercury in the standard childhood vaccines and possibly dental amalgam. > I assume that the Mercury is till in my body. Yes. Once toxicity reaches a certain level it interferes with the bodies ability to remove it. Clearance from the brain is very slow. So, chelation is needed to remove it. ALA is the only chelator that will remove it from the brain and internal organs. It must be used in small doses, every 3 h, day and night for some days on and some days off. See the FAQ of this group and H Cutler's 2 books www.noamalgam.com All amalgam fillings must be safely removed before chelation. Chelation is actually very simple once you know how to do it. You likely will be able to chelate yourself and your children easily without a physician. You can ask your physician for help if needed. > I have anxiety. I have never been diagnosed with anything but anxiety/depression. I have mood swings and Effexor seems to be the only thing that helps me. > The basic supplements to support chelation plus some extras will help with symptoms during chelation. See Andy Cutler's " depression " post: frequent-dose-chelation/message/15287 frequent-dose-chelation/message/28048 > I am more concerned about my children and would like to know what your opinions are. I just read about the hair test and was wondering if I should even bother for myself, since I know I was poisoned by Mercury. > It is important to take care of yourself first. You need to start with chelation in order to get better and stay well in the long term. You will need your health in order to chelate your children. It is best for all of you. It would be good to have hair tests for all 3 of you. There are other things that show up on the tests that may help you when making treatment decisions. > I joined the GFCF group and am researching to go that route with the diet. Different people respond to different diets. See Andy Cutler's file " Diet-How to pick the right one for your kid " in the files section. > Also, I believe that we are dealing with Yeast Overgrowth as well. See the file " Neutrophils.html " by Andy Cutler in the files section, and many posts from Andy in archives. > My son has severe allergies and was tested very young. He responded to all the molds. He was observed during a short time in private school by the public school ASD psychiatrist. We were told he had traits of autism. But never went beyond that. > > I thought my daughter was fine. But, she does have a problem with attention and now we are learning about the OCD behaviour. Had colic when she was a baby and always screamed and cried alot. I just thought this was tummy issues. Did not even let her grandparents hold her until she was over 2 years old. > They will both improve with proper chelation. Be careful not to use methods other that Andy's. There are many chelation protocols out there, promoted by companies out for profit and well meaning medical professionals who don't understand chelation, that will make everyone worse because the metals are moved around without eliminating them. There is another group focused primary on adult chelation with Andy Cutler's protocol. It is the frequent-dose-chelation group. We have collected many of Andy's posts (links section of that group) that are most helpful to read. Also see Moria's pages (linked to from the loveletters link on the autism mercury home page and in the links section of the chelation groups). J > Thank you all very much, > Sharon > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2009 Report Share Posted October 4, 2009 try blingyourband.com thats where i ordered the decals form y daughters helmet. They do custom so pretty much anything you want. > > > > My 4 month old daughter needs a helmet for plagiocephaly. I need some decorating ideas for the helmet....it's the only thing making feel better about the whole thing right now. Any suggestions. Also, curious to know how long other people's kids had to wear the helmet for. She 8mm off. > > > My son is 6 months and just started wearing the STAR band last week. Yesterday was his first day at 23 hours. I took his to get it airbrushed. We are in Houston and did it at Airbrish Brothers at I-10 and Silber. They did an excellent job. I will post pictures today. I have heard you can put stickers and stuff but I was not impressed on how they looked and they can come off. I paid $35. and it will last the entire time that he has to wear it. You can get pictures off the internet of what you want and take it to them to work from. > Hope this helps some. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2010 Report Share Posted January 20, 2010 Jen - You are by far not alone -- and I'll tell you what - as far as the schooling goes -- aspies can do well in the younger grades .. my son is in third grade -- he is in public school and he is managing though we are now looking at special ed privates because I know that as the work gets harder and more complicated -- it will be increasingly difficult for him to keep up.. not to mention the social game is very difficult as the kids get older, too -- I think social skills classes are the most important things for these kids ... they really need to be told over and over again how to read people, how to react, how to play ... They also need strong behavior supports and a therapist can help you with that both at home and at school. My son is great with order, structure and relies heavily on these -- use this trait of aspies to your advantage.. Once we put something into place -- my son will be the first one to remind me to give him his pill after breakfast -- or that he needs to brush his teeth before bedtime. The routine becomes a comfort.Also -- consider looking into integrated schools where special ed and mainstream kids share a classroom -- My son was in one for K & 1 and it was wonderful for him. From: H <jenuhferr@...>Subject: ( ) Newbie Date: Wednesday, January 20, 2010, 9:55 AM Hi, I am a SAHM to my daughter Em who just turned 5 two days ago (ack). My husband, Em and I live in Upstate NY in the capital region. Em was diagnosed on the spectrum at exactly 2 yrs old (PDDNOS, sensory processing disorder, speech delay, fine motor delay) although I knew something wasn't right before then and she has had services at home and then in special preschools since then. Her current diagnosis is Asperger's and she gets speech at her preschool (reg teacher and sped teacher) along with seeing the social worker. Academically she is doing very well... the ABCs were her soothing splinter skill at 3 years old. She will probably be approved to continue the preschool through the summer and then the "plan" right now is to get her into regular kindergarten in the fall... However, I've always done a lot of research.... on my own medical issues and of course hers since she was diagnosed... heck I researched her birth! I put a lot of weight into people's experiences along with my research. What I'm hearing about Aspie's in school is not good. I'm basically trying not to be terrified at the idea of her going into public school and trying not to be terrified at homeschooling. .. I have no idea what to do. I have materials to read about different types of homeschooling but it's just so MUCH! And you know what? I'm NOT smarter than a 5th grader!! I have a bachelor's degree in biology/psychology but I couldn't tell u my butt from my elbow at this point! How am I going to teach my incredibly intelligent daughter anything??? I can't get her to sit and write her letters... I have no idea how they manage to do that in school. I'm not a trained sped teacher... Plus, if she goes to public school then I could work and help us out of our financial hole but that is less important than what is best for Em. I have so much reading and research to do and I'm not well myself. Some days are a real struggle. Em's main issues are her emotional regulation and ability to socially interact appropriately. One tiny example.. she can't do something so she just throws herself on the floor in another room and I hear her complaining that she needs help. If I ignore her hoping she will 'get it' and come to me and ask for help, it never happens. I have to tell her to come and talk to me. She's already been called a "retard" at the pool and pushed around my "mean kids" as she calls them at public play places. She has a target on her head because she loves everyone and it so insanely friendly and outgoing!! She doesn't get it when the kids want her to GO AWAY. She is very affected by these episodes and we end up discussing them and how to act appropriately and talk about feelings about them, etc... She tells random adults we meet that she loves them! We've just finally gotten her to not talk to people unless Mommy or Daddy are talking to them (stranger idea just doesn't work). Now we're trying to explain other ways she can say she likes someone she meets (nice meeting you) and that 'i love you' is only for family. Saying close friends would just be too confusing... . ack! Well, that's a lot! I'll stop now! LOL! Jen -----Inline Attachment Follows-----No virus found in this outgoing message.Checked by AVG - www.avg.com Version: 8.5.432 / Virus Database: 271.1.1/2634 - Release Date: 01/20/10 09:12:00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2010 Report Share Posted January 20, 2010 HI there, My grandson is almost five and has the same diagnosis….I can relate to everything you are saying. He is also starting mainstream kindergarten in the fall It has taken almost a year and a half for figure out that most of his problems are sensory. Try these two books to see if her face is on so many of the pages just like DGS’s was The sensory sensitive child / & Gouze Sensory Processing Disorder - Answer Book / Tara Delany We have changed the way we are doing some things per the books and have his starting OT with a therapist specializing in Sensory processing next week. So far he is responding in a very positive way Good luck Teri From: [mailto: ] On Behalf Of Sent: Wednesday, January 20, 2010 7:38 AM Cc: jenuhferr@... Subject: Re: ( ) Newbie Jen - You are by far not alone -- and I'll tell you what - as far as the schooling goes -- aspies can do well in the younger grades .. my son is in third grade -- he is in public school and he is managing though we are now looking at special ed privates because I know that as the work gets harder and more complicated -- it will be increasingly difficult for him to keep up.. not to mention the social game is very difficult as the kids get older, too -- I think social skills classes are the most important things for these kids .... they really need to be told over and over again how to read people, how to react, how to play ... They also need strong behavior supports and a therapist can help you with that both at home and at school. My son is great with order, structure and relies heavily on these -- use this trait of aspies to your advantage.. Once we put something into place -- my son will be the first one to remind me to give him his pill after breakfast -- or that he needs to brush his teeth before bedtime. The routine becomes a comfort. Also -- consider looking into integrated schools where special ed and mainstream kids share a classroom -- My son was in one for K & 1 and it was wonderful for him. From: H <jenuhferrnycap (DOT) rr.com> Subject: ( ) Newbie Date: Wednesday, January 20, 2010, 9:55 AM Hi, I am a SAHM to my daughter Em who just turned 5 two days ago (ack). My husband, Em and I live in Upstate NY in the capital region. Em was diagnosed on the spectrum at exactly 2 yrs old (PDDNOS, sensory processing disorder, speech delay, fine motor delay) although I knew something wasn't right before then and she has had services at home and then in special preschools since then. Her current diagnosis is Asperger's and she gets speech at her preschool (reg teacher and sped teacher) along with seeing the social worker. Academically she is doing very well... the ABCs were her soothing splinter skill at 3 years old. She will probably be approved to continue the preschool through the summer and then the " plan " right now is to get her into regular kindergarten in the fall... However, I've always done a lot of research.... on my own medical issues and of course hers since she was diagnosed... heck I researched her birth! I put a lot of weight into people's experiences along with my research. What I'm hearing about Aspie's in school is not good. I'm basically trying not to be terrified at the idea of her going into public school and trying not to be terrified at homeschooling. .. I have no idea what to do. I have materials to read about different types of homeschooling but it's just so MUCH! And you know what? I'm NOT smarter than a 5th grader!! I have a bachelor's degree in biology/psychology but I couldn't tell u my butt from my elbow at this point! How am I going to teach my incredibly intelligent daughter anything??? I can't get her to sit and write her letters... I have no idea how they manage to do that in school. I'm not a trained sped teacher... Plus, if she goes to public school then I could work and help us out of our financial hole but that is less important than what is best for Em. I have so much reading and research to do and I'm not well myself. Some days are a real struggle. Em's main issues are her emotional regulation and ability to socially interact appropriately. One tiny example.. she can't do something so she just throws herself on the floor in another room and I hear her complaining that she needs help. If I ignore her hoping she will 'get it' and come to me and ask for help, it never happens. I have to tell her to come and talk to me. She's already been called a " retard " at the pool and pushed around my " mean kids " as she calls them at public play places. She has a target on her head because she loves everyone and it so insanely friendly and outgoing!! She doesn't get it when the kids want her to GO AWAY. She is very affected by these episodes and we end up discussing them and how to act appropriately and talk about feelings about them, etc... She tells random adults we meet that she loves them! We've just finally gotten her to not talk to people unless Mommy or Daddy are talking to them (stranger idea just doesn't work). Now we're trying to explain other ways she can say she likes someone she meets (nice meeting you) and that 'i love you' is only for family. Saying close friends would just be too confusing... . ack! Well, that's a lot! I'll stop now! LOL! Jen -----Inline Attachment Follows----- No virus found in this outgoing message. Checked by AVG - www.avg.com Version: 8.5.432 / Virus Database: 271.1.1/2634 - Release Date: 01/20/10 09:12:00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 Hi .. This is just from my own personal experience, not recommending that anyone do what I did .... but I saw a surgeon first, he biopsed and scheduled me for a lumpectomy. I never saw an oncologist until 18 mos later. So glad I did. I think I knew, even tho the dx was a shock, that I would refuse chemo & radiation. But I saw nothing wrong with surgery to debulk. My surgeon did breast surgeries all the time & was a very experienced surgeon. He was patient with me & seemed to sense that I was gonna be a 'maverick'. He never fussed at me... just encouraged me to be knowledgable. He did recommend that I buy the book Dr. Love's Breast Book. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 Just my personal opinion. Neither Cheri > > I just found out that I have breast cancer.I had a biopsy.(no details yet about which stage) Who do I talk to first? Oncologist or surgeon? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 Hi , I was diagnosed with Breast Cancer (invasive ductal carcinoma) in both breasts in Jan/2008. I refused allopathic treatment. I was diagnosed with Stage 4 breast cancer in Jan/2010. , no matter what kind of breast cancer you have, if it's only in your breast, you'll be offered complete mastectomy or lumpectomy followed by radiation. They'll also do a sentinal node biopsy to see if it's moved to the axilla lymph nodes. If I had it to do all over again, I'd have had a lumpectomy in both breasts, lied to the surgeon and said I'd take the radiation, then I'd refuse that and go to a professional natural practitioner to help me with detox and killing off any residual cancer cells in a more gentle manner. If you have Ductal Carcinoma In Situ DCIS, your need for treatment is not anywhere near as urgent as this is just " precancer " . If I would have only had DCIS, and I had it to do all over again, I'd have found a professional natural practitioner to help me reverse the situation. , stage 4 is a lot harder to overcome than stage 1 or 2. Stage 1 or 2 is still curable. Please consider this when you are making your decision. If you need more advise, please message me privately. Also, please let us know of your diagnosis once received ok? Louise > > I just found out that I have breast cancer.I had a biopsy.(no details yet about which stage) Who do I talk to first? Oncologist or surgeon? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 Read the book Cancer-Free by Bill . Visit Cancertutor.com. Bill Corley From: J Sent: Tuesday, February 23, 2010 I just found out that I have breast cancer.I had a biopsy.(no details yet about which stage) Who do I talk to first? Oncologist or surgeon? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2010 Report Share Posted February 23, 2010 , I would concure on that one with Cheri, but it is not exactly a constructive one. You may do yourself a great favor and I would strongly advice at this time to talk to Tony Isaacs on " Oleandersoup " on . With kind regards, SLavek. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 24, 2010 Report Share Posted February 24, 2010 I know I was a bit blunt. Sorry personal garbage getting in the way. Surgery is an option so if I was to see anyone that would be the person. The problem is that they will want to check your lymph nodes. If they find cancer you will have to option to say leave them as you will be under anesthesia. No way will I give them a chance to take the lymph nodes. Cheri > > , > > I would concure on that one with Cheri, but it is not exactly a > constructive one. > > You may do yourself a great favor and I would strongly advice at this > time to talk to Tony Isaacs on " Oleandersoup " on . > > With kind regards, SLavek. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2010 Report Share Posted March 26, 2010 john wrote: > > Hello all, > > Newbie dad here, I have a 2 year old son that has autism. I can't thank > you all enough for sharing your experiences and insights. I just ordered > Andy's book > I would suggest getting BOTH. > and am working to get up to speed with issues regarding > heavy metal poisoning and chelation, but let me ask a goofy question, do > I need to be worried about toxic metals from my wife's amalgam fillings > passing to either of my sons through the mouth (kissing)? > Goofy answer: Not unless she is kissing them in an inappropriate way (saliva to saliva contact). In all seriousness, even then the exchange of mercury would be minimal. Mercury leaks from the amalgams in minute amounts. It is exposure over time that builds up body stores. You do need to worry about whether the mercury-toxic status of your wife will affect the care that will be needed in the process of addressing your son's toxicity. In plain English, she should really have the amalgams removed and chelate herself as well. > I hate having > to ask such a question, but I can't afford to let awkwardness or > ignorance hurt my family anymore. Thanks and God bless. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2010 Report Share Posted March 26, 2010 Thanks for the reply . By " both books " do you mean " /Amalgam Illness: Diagnosis and Treatment/ " and " Hair Test Interpretation " ? Thanks again. Ross wrote: > john wrote: > >> Hello all, >> >> Newbie dad here, I have a 2 year old son that has autism. I can't thank >> you all enough for sharing your experiences and insights. I just ordered >> Andy's book >> >> > I would suggest getting BOTH. > > >> and am working to get up to speed with issues regarding >> heavy metal poisoning and chelation, but let me ask a goofy question, do >> I need to be worried about toxic metals from my wife's amalgam fillings >> passing to either of my sons through the mouth (kissing)? >> >> > Goofy answer: Not unless she is kissing them in an inappropriate way > (saliva to saliva contact). > > In all seriousness, even then the exchange of mercury would be minimal. > Mercury leaks from the amalgams in minute amounts. It is exposure over > time that builds up body stores. > > You do need to worry about whether the mercury-toxic status of your wife > will affect the care that will be needed in the process of addressing > your son's toxicity. > > In plain English, she should really have the amalgams removed and > chelate herself as well. > > > > >> I hate having >> to ask such a question, but I can't afford to let awkwardness or >> ignorance hurt my family anymore. Thanks and God bless. >> >> >> > > > > ------------------------------------ > > ======================================================= > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2010 Report Share Posted March 26, 2010 Hi! Welcome! My mercury free dentist said " Yes " . The mercury vapor can be released out of your mouth. I am really careful breathing in my kids faces (talking close to them). I still kiss them (of course my 10-year-old will not let me) but my 5-year-old I will kiss her on the cheek with my mouth closed or on her head after prayers at bedtime. Some things can't be helped you don't want to keep your distance or anything. I just try to limit my kids exposure. I am in the process of getting my amalgams removed but it is going to take awhile due to the cost and insurance. Here is a video on it: > > Hello all, > > Newbie dad here, I have a 2 year old son that has autism. I can't thank > you all enough for sharing your experiences and insights. I just ordered > Andy's book and am working to get up to speed with issues regarding > heavy metal poisoning and chelation, but let me ask a goofy question, do > I need to be worried about toxic metals from my wife's amalgam fillings > passing to either of my sons through the mouth (kissing)? I hate having > to ask such a question, but I can't afford to let awkwardness or > ignorance hurt my family anymore. Thanks and God bless. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 26, 2010 Report Share Posted March 26, 2010 > > Hello all, > > Newbie dad here, I have a 2 year old son that has autism. I can't thank > you all enough for sharing your experiences and insights. I just ordered > Andy's book and am working to get up to speed with issues regarding > heavy metal poisoning and chelation, but let me ask a goofy question, do > I need to be worried about toxic metals from my wife's amalgam fillings > passing to either of my sons through the mouth (kissing)? No. >I hate having > to ask such a question, but I can't afford to let awkwardness or > ignorance hurt my family anymore. Thanks and God bless. > Andy http://www.noamalgam.com/index.html Amalgam Illness: Diagnosis and Treatment http://www.noamalgam.com/hairtestbook.html Hair Test Interpretation: Finding Hidden Toxicities http://www.noamalgam.com/nourishinghope.html Nourishing Hope for Autism: Nutrition Intervention for Healing Our Children http://www.noamalgam.com/biologicaltreatments.html Biological Treatments for Autism and PDD Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2010 Report Share Posted April 27, 2010 Welcome to the group. There are certainly ups and downs. I chose (after great deals of wondering "WHY") to accept all of this as a gift, but it took me years to get to this point. We all understand what you are going through, and please post all of your questions, concerns, and your joys on here as we may all benefit from you. From: Mayne <jazjamloch@...>" " < >Sent: Mon, April 26, 2010 10:43:58 PMSubject: ( ) Newbie Hi, I am new to this group. My teenage son has Aspergers and I was looking for a way to share the ups and downs with someone who understands. KelSent from my iPhone Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2010 Report Share Posted April 27, 2010 Hi, there. I am also new...and right there inthat boat with you!! Share away! > > Hi, > I am new to this group. My teenage son has Aspergers and I was looking for a way to share the ups and downs with someone who understands. > Kel > > Sent from my iPhone > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2010 Report Share Posted April 27, 2010 Hi all. Thanks for the welcome. During the night all of the messages came through, when reading them I realised you all write mom not mum! I did not realise this was not an Australian group, do you think that matters? Kel Sent from my iPhone Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2010 Report Share Posted April 27, 2010 no maam, it does not matter, we are all here to help! Asperger's is all over! From: Mayne <jazjamloch@...>" " < >Sent: Tue, April 27, 2010 5:32:27 PMSubject: ( ) Re: Newbie Hi all. Thanks for the welcome. During the night all of the messages came through, when reading them I realised you all write mom not mum! I did not realise this was not an Australian group, do you think that matters? KelSent from my iPhone Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2010 Report Share Posted April 27, 2010 NO PROBLEM!!!!!! Ahhhhh, Laughter................Robin > From: Mayne <jazjamloch@...> > Subject: ( ) Re: Newbie > " " < > > Date: Tuesday, April 27, 2010, 4:32 PM > > > > > > > > > > > > > > > >  > > > > > > > > > > Hi all. Thanks for the welcome. During the night > all of the messages came through, when reading them I > realised you all write mom not mum! I did not realise this > was not an Australian group, do you think that matters? > > Kel > > > > Sent from my iPhone > > > > > > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 27, 2010 Report Share Posted April 27, 2010 We like Australians! You can stay and participate all you like and welcome! Roxanna Whenever I feel blue, I start breathing again. ( ) Re: Newbie Hi all. Thanks for the welcome. During the night all of the messages came through, when reading them I realised you all write mom not mum! I did not realise this was not an Australian group, do you think that matters? Kel Sent from my iPhone Quote Link to comment Share on other sites More sharing options...
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