Guest guest Posted April 6, 2005 Report Share Posted April 6, 2005 Welcome to the list. Many on this list chelate without a doctor. S <tt> <BR> hello.. im from the Philippines and I want to get my son started on Chelation. Can you refer a doctor who can get us started on the process because I really want to or If there's no doctor who is willing to do that will It be wise to wait til I migrate to the US which is in 2 or 3 years. <BR> <BR> __________________________________________________<BR> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 6, 2005 Report Share Posted April 6, 2005 Any tips on how to get started with the process.. Leirs (Manila) & Philbert (US)- 07.15.00 Joshwa 01.16.01 (Manila) __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 6, 2005 Report Share Posted April 6, 2005 Read the FAQs of this list. If the individual to be chelated has any mercury amalgam dental fillings those need to be removed according to proper protocol by a mercury-free dentist before beginning chelation. S <tt> <BR> Any tips on how to get started with the process..<BR> <BR> <BR> Leirs (Manila) & Philbert (US)- 07.15.00 <BR> Joshwa 01.16.01 (Manila)<BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> __________________________________________________<BR> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2005 Report Share Posted April 8, 2005 > > Have there been cases where the child was chelated for 2 years and has still not improved.. My son needed much more than just chelation to show major improvement. He also needed anti-virals and several supplements. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 12, 2005 Report Share Posted April 12, 2005 _http://home.earthlink.net/~moriam/HOW_TO_hair_test.html_ (http://home.earthlink.net/~moriam/HOW_TO_hair_test.html) could not get into the link please resend< would likehair tesitng done on kids thanks Sorry punctuations not working need to reboot Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 13, 2005 Report Share Posted April 13, 2005 Take out the underline at the end. http://home.earthlink.net/~moriam/HOW_TO_hair_test.html Re: [ ] hi _http://home.earthlink.net/~moriam/HOW_TO_hair_test.html_ (http://home.earthlink.net/~moriam/HOW_TO_hair_test.html) could not get into the link please resend< would likehair tesitng done on kids thanks Sorry punctuations not working need to reboot Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 13, 2005 Report Share Posted April 13, 2005 Hi, -Clare - Love it! Isn't it wonderful when the words come out - you just are so happy, excited, proud of our kids! Josh doest the " fart " thing, too, only when he does it, we look at him and says " Clyde-o farted! " (the dog) or " Mommy farted " then finally laughingly fesses up to being the one to pass the gas. What a jokester! Sherry mcdalzell@... wrote: Hi to All, With all the hard work our son does to speak sometimes the words just flow. Last night I said I love you as I tucked him in. He said " love you too mommy " now I know I may not hear those words for a long time but I hold them close in my heart:) Just thought I would share. Now for the humor side of life for us. We were all seated down at the dinner table and we heard a gassy sounding noise. Lee says as clear as a bell Who farted?! My husband and I looked at each other and said did he say what we think he just said? As our older son said not me! I tell you never a dull moment here. This too I hold close to my heart. LOL Wishing everyone a great week. -Clare Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2005 Report Share Posted April 22, 2005 , You need a DAN Dr.!!! [ ] hi My name is sue and I have a 2 1/2 year old daughter named Cameren she only has about 12 words so far and looking for other mothers who have been through this process, we are already enrolled in our early on program here in Michigan...looking for support and tips thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2005 Report Share Posted April 22, 2005 Hi Sue and welcome! I'm not sure who talltex99 is -but doesn't look like they read your post that well (since you say in the first sentence your name is Sue) If your child is a two and a half year old late talker with 12 words -just want to let you know that the first step is not a DAN doctor, or any doctor other than your child's pediatrician! The first step if not done yet is a thorough speech and hearing evaluation. What are the 12 words your child can say -and does he or she ever attempt to string any words together? Your child is also entitled by Federal Law (if you live in the US) to Early Intervention through your state -up till the age of three, and through your town's school from three up. Is your child in Early Intervention, and has your child been diagnosed with any disorder of speech or do they suspect it may be a simple delay? If it ends up that your child has just a simple delay in speech, the sessions of speech therapy will be fun and stimulating for your child and may even encourage the speech to come in sooner -if it ends up the reason for the delay is an impairment of speech vs. a simple delay -the Early Intervention you can provide now is priceless! Private exams recommended after a speech and hearing could be an OT (occupational therapy) exam, and 'then' if something like apraxia is suspected -a visit with a neuroMD (pediatric neurologist or developmental pediatrician) There are many great parents and medical, speech and education professionals in this group -and even though many of them lurk -hope some of them email you to welcome you and provide you with new member support and advice! Have you read The Late Talker? Oh -and PS -if you decide to see a DAN doctor -please know not all are medical doctors and some are not doctors at all. If I ever took Tanner to a DAN doc, I would make sure they were a medical doctor. In our large in person support group half felt it was a waste of money. (Now that I think of it -perhaps because only half saw DAN MDs and the other saw DAN " Dr.s " ?) ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2005 Report Share Posted April 23, 2005 --what is a DAN dr??????? > > > > My name is sue and I have a 2 1/2 year old daughter named Cameren she > only has about 12 words so far and looking for other mothers who have > been through this process, we are already enrolled in our early on > program here in Michigan...looking for support and tips > > thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2005 Report Share Posted April 23, 2005 HI, My Thank you for your response I guess he came up with from our email its my husbands name...We have had Cameren in an ISD program here in michigan she goes to class an hour a week and then the teacher comes to the house for a hour a week...I took Cami to the ped. nero this week at the U of M...she did some blood and wrote a script for speech theapy .Cami also has low muscle tone but she has great fine motor and gross motor skills the Isd did some test on rated her at about a 15 mth level in Jan her speech was in 5th precentile...The words she has now are like uh oh and dora hank you ...but very few I am having her tested Monday for hearing....I am unsure what a DAN dr is ...Cami is my 4th child and all my other talked early so needless to say this has been a changle for us...Thank you for your reply any help would great Sue Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2005 Report Share Posted April 23, 2005 Below is a link that describes the DAN protocol. It will take an hour to complete. Not all children on this list have needed a DAN protocol, but those that have seeked the biochemical procedures, like myself, have seen my child come out of the " fog " . http://www.talkautism.org/video/df/index.asp?id=3# Maureen McDonnell is a registered nurse, nutritionist who helped my son immensely. all the best, Joanne ---------------------------------------------------- This mailbox protected from junk email by MailFrontier Desktop from MailFrontier, Inc. http://info.mailfrontier.com [ ] Re: hi > > > --what is a DAN dr??????? >> >> >> >> My name is sue and I have a 2 1/2 year old daughter named Cameren she >> only has about 12 words so far and looking for other mothers who have >> been through this process, we are already enrolled in our early on >> program here in Michigan...looking for support and tips >> >> thanks > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2005 Report Share Posted April 29, 2005 Welcome, Pinar ! F " When the power of love overcomes the love of power the world will know peace. " -- Jimi Hendrix ( ) Hi Hi,I am the mother of 5 years old sweet boy, Mehmet Selman, who has Autism. I think I'll learn so many thinks from you. Thanks. Pinar. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2005 Report Share Posted May 3, 2005 Pinar Bahceci <pinar_bahceci@...> wrote: Hi,I am the mother of 5 years old sweet boy, Mehmet Selman, who has Autism. I think I'll learn so many thinks from you. Thanks. Pinar. Pinar, WELCOME to our list! Feel free to jump in anytime you like! Roxanna Look alive. Here comes a buzzard. -- Pogo __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 I wish I could help you. Best of luck. Terryfowlereagles2004 <fowlereagles2004@...> wrote: I have a ? does anyone else have friends that get scared of getting HCV? If so what do you do?__________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 People are generally not well-informed about Hep C, and therefore are scared of it. For the most part, the better informed they become, the less apprehensive they will be. It's just whether or not they 'want' to take the time to find out, is all..... > I have a ? does anyone else have friends that get scared of getting > HCV? If so what do you do? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 6, 2005 Report Share Posted May 6, 2005 Those who didn't understand after I gave them all the info, are no longer around. Sharon --- fowlereagles2004 <fowlereagles2004@...> wrote: > I have a ? does anyone else have friends that get > scared of getting > HCV? If so what do you do? > > > Stay connected, organized, and protected. Take the tour: http://tour.mail./mailtour.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 7, 2005 Report Share Posted May 7, 2005 Kick 'em to the curb. My wife hasn't caught my hep-c in over 32 years. Almost all cases are blood to blood contact. A good friend passed away a few months ago. She got it from a blood transfusion many, many years ago. She was 77. HCV is not easily transmitted. That is not to say it is totally safe, but as we all know, casual contact (kissing, etc.) will *not* pass it and it would appear that normal sex does not either. If someone is that hung up over HCV, it would spare your nerves to simply forget that person until that individual comes around to his/her senses. Best regards from Rochester, NY Jim [ ] hi I have a ? does anyone else have friends that get scared of getting HCV? If so what do you do? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2005 Report Share Posted May 8, 2005 > I have a ? does anyone else have friends that get scared of getting > HCV? If so what do you do? At first I was afraid of giving hep c to people But knowing more about how it is transmitted to other people Just dont share razors toothbrushes combs or brushes And of course covering up cuts right away with bandages. there is very little chance of transmitted it through sex. I learned that no worry about it from someone drinking after you either. Annita Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2005 Report Share Posted May 15, 2005 Hi I am so pleased for you to have got so far with your Son. You give me great hope, thank you for posting. Re the restricted diet - know how you're feeling, dealing with that now! I was thinking J my son might well turn out this way. He will only eat chips/organic chicken and organic locks sausages and fruit at the moment. Odd bit of yoghurt when he can cope with the texture. Spoke to other ASD Mums - apparently I am lucky! There is a brilliant writer/psychologist in US who deals with food issues, I've just read her book (borrowed) with loads of hints but I can't remember her name! I'll know on Tues when I see my friend and will post. It would be easy to say " Your Son's in recovery, don't worry " but food definitely has a major impact on life both socially and physically; I understand how you feel, keep the faith, look at how far you have come. Good luck, Eileen littlegirlcurls <littlegirlcurls@...> wrote: Hi all, I am new to this group and am using pca-rx and af-x plus an antioxidant/anti inflammatory drink that have greatly helped my son who is almost four at the end of this month and diagnosed with autism. I also for dietary benefit am adding a huge variety of enzyme's like berry green, perfect food, fruits of life, goatein, o- zyme, a digestive enzyme from baseline nutritionals as well as buying organic fruits and really raw honey. My biggest concern at this point as he has gone from many autistic behaviors to almost completely typical is that he is barely trying new foods and its a major struggle. he is eating either french toast all organic and whole wheat bread for breakfast or peanut butter sandwhich with goatein sprinkeled in it, vitamin c and a digestive enzyme plus berry green, then for lunch is always a peanut butter sandwhich with a little goatein, perfect food and fruits of life and for dinner is sometimes boneless skinless chicken (not organic) a table spoon of bbq sauce and a couple tiny bites of yellow potato. His snacks are organice apples, pears or bananas, his diet is to say at the very least frustrating. Everything else other than if we go out to eat once every two weeks is a flat out refusal, fit and then sleep. He drinks 100% straight carrot juice once a day and water the rest and he take a viactiv supplement as well (caramel kind not chocolate). AS we took him off of milk and yogurt a year ago with great success to irritability mood swings. He has come such a long way and am so proud of him but what the heck do i do about his diet? Thanks, littlgirlcurls --------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2005 Report Share Posted May 15, 2005 Hi I am so pleased for you to have got so far with your Son. You give me great hope, thank you for posting. Re the restricted diet - know how you're feeling, dealing with that now! I was thinking J my son might well turn out this way. He will only eat chips/organic chicken and organic locks sausages and fruit at the moment. Odd bit of yoghurt when he can cope with the texture. Spoke to other ASD Mums - apparently I am lucky! There is a brilliant writer/psychologist in US who deals with food issues, I've just read her book (borrowed) with loads of hints but I can't remember her name! I'll know on Tues when I see my friend and will post. It would be easy to say " Your Son's in recovery, don't worry " but food definitely has a major impact on life both socially and physically; I understand how you feel, keep the faith, look at how far you have come. Good luck, Eileen littlegirlcurls <littlegirlcurls@...> wrote: Hi all, I am new to this group and am using pca-rx and af-x plus an antioxidant/anti inflammatory drink that have greatly helped my son who is almost four at the end of this month and diagnosed with autism. I also for dietary benefit am adding a huge variety of enzyme's like berry green, perfect food, fruits of life, goatein, o- zyme, a digestive enzyme from baseline nutritionals as well as buying organic fruits and really raw honey. My biggest concern at this point as he has gone from many autistic behaviors to almost completely typical is that he is barely trying new foods and its a major struggle. he is eating either french toast all organic and whole wheat bread for breakfast or peanut butter sandwhich with goatein sprinkeled in it, vitamin c and a digestive enzyme plus berry green, then for lunch is always a peanut butter sandwhich with a little goatein, perfect food and fruits of life and for dinner is sometimes boneless skinless chicken (not organic) a table spoon of bbq sauce and a couple tiny bites of yellow potato. His snacks are organice apples, pears or bananas, his diet is to say at the very least frustrating. Everything else other than if we go out to eat once every two weeks is a flat out refusal, fit and then sleep. He drinks 100% straight carrot juice once a day and water the rest and he take a viactiv supplement as well (caramel kind not chocolate). AS we took him off of milk and yogurt a year ago with great success to irritability mood swings. He has come such a long way and am so proud of him but what the heck do i do about his diet? Thanks, littlgirlcurls --------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2005 Report Share Posted May 15, 2005 Eileen, Thanks so much your post was very encouraging to read. And yes I feel too he is in recovery. His teachers can not believe that this is the same boy but of course getting the " its a blessing but not the diet changes " (do you think anyone would be offended here if I calld them idiots?! <-- just personal opinion) I feel rather blessed of course, and am praying for the wisdom of the right things to try and so far have been pretty lucky. Haven't wasted a whole lot of things to try or time. My main concern is " and realize that I know they don't understand enough about autistic children " that family and friends raising their eyebrows that he would rather eat 3 organic peanut butter sandwhiches a day with the supplements and even getting the french toast and chicken in there is a major struggle. I follow the body for life program for losing weight and toning body and have dropped 30 pounds so far. I have been trying to have my kids follow it as close as possible as It's the healthiest I have found except that trying to get protien into a child you don't want on dairy or soy is proving a big big problem. Like I said he will eat egg in the french toast to which I had a table spoon of goatein so it tastes like vanilla cake (i soooo know this is cheating lol) and a few nights a week I have done the boneless skinless chicken (how in the heck do I afford organic by the way on a family of 5 who has chicken like 3-4 nights a week in different ways?) and so in his peanut butter sandwhiches I am slipping in the whole foods like perfect good and berry green and fruitoflife while also a few raw organic fruits he will allow and the carrot juice ....so he is following decently close but am more frustrated that my youngest daughter who is typical will eat anything and my oldest daughter if finicky but will eat like any other 5 year old but what do I do to expand him eating something like tunafish once a week or more preferably a small peice of chinook salmon, or i guess gfcf yogurt? is this at any organic food store? are there any things I should watch out for other than the red40 dye? I figure I can bring in yogurt in with a half peice of fruit to get the lean protien plus high fiber card for the balanced meal. I personally dream of the day when he will eat organic veggies lol. Thanks again, for such an encouraging post, I just feel so much better and good about myself. Heavyness tends to run in my family and my hubbies too but I think I am finding its all about how healthy you eat, whether you are eating balanced meals so your body dosen't go into a blood sugar rollercoaster, getting rid of build up in the intestines and heavymetal poisoning that is hidden in fat that can slow down metabolism, etc. etc. the more I learn the more I apply the better I feel. I want that for my children as they grow up. If I teach them responsible eating for body energy and health now then they won't have the issues I am experiencing now. Its just so hard with a child with these types of food restrictions mentioned in the first post to feed him properly. I appreciate your time, littlegirlcurls > Hi all, I am new to this group and am using pca-rx and af-x plus an > antioxidant/anti inflammatory drink that have greatly helped my son > who is almost four at the end of this month and diagnosed with > autism. I also for dietary benefit am adding a huge variety of > enzyme's like berry green, perfect food, fruits of life, goatein, o- > zyme, a digestive enzyme from baseline nutritionals as well as buying > organic fruits and really raw honey. > > My biggest concern at this point as he has gone from many autistic > behaviors to almost completely typical is that he is barely trying > new foods and its a major struggle. he is eating either french toast > all organic and whole wheat bread for breakfast or peanut butter > sandwhich with goatein sprinkeled in it, vitamin c and a digestive > enzyme plus berry green, then for lunch is always a peanut butter > sandwhich with a little goatein, perfect food and fruits of life and > for dinner is sometimes boneless skinless chicken (not organic) a > table spoon of bbq sauce and a couple tiny bites of yellow potato. > His snacks are organice apples, pears or bananas, his diet is to say > at the very least frustrating. Everything else other than if we go > out to eat once every two weeks is a flat out refusal, fit and then > sleep. He drinks 100% straight carrot juice once a day and water the > rest and he take a viactiv supplement as well (caramel kind not > chocolate). AS we took him off of milk and yogurt a year ago with > great success to irritability mood swings. > > He has come such a long way and am so proud of him but what the heck > do i do about his diet? > > Thanks, littlgirlcurls > > > > > > > --------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2005 Report Share Posted May 16, 2005 I know, don't you just LOVE the mental disconnect between change in diet and change in bahaviour/outcome? Re: Hi His teachers can not believe that this is the same boy but of course getting the " its a blessing but not the diet changes " (do you think anyone would be offended here if I calld them idiots?! <-- just personal opinion) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2005 Report Share Posted May 16, 2005 Thanks Eileen!!! Eileen McLennan <eileen_mclennan@...> wrote:Yes right! Thanks that has helped me too, its beautifullly put and has put into words exactly how I feel Eileen x --------------------------------- Discover Have fun online with music videos, cool games, IM & more. Check it out! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2005 Report Share Posted May 16, 2005 Thanks!!! ebrischoux <ebrischoux@...> wrote:Beautifully said. > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.