Guest guest Posted July 11, 2003 Report Share Posted July 11, 2003 If you had changed the she's to he's you would have described my son at that age. He is now 19 and in his second year of college. Jas has always been a very sweet and caring child. He IS basically happy yet never smiles. He always looks serious and laughs inaapropriatey and usually overly loud, yet is overly sensitive to sounds from other sources. He literally walks into walls as he has major balance issues. He walks strangely. He is largely a loner with those not of the family. Yet.. I have found that if someone makes the effort to get to know him and finds a commonality he can talk with them for hours. My younger 2 children have always had alot of friends and alot of phone calls. My oldest barely talks on the phone if I call home- all yes no answers and all right (rather loud) if he gets frustrated by my repeating something. Now he has a friend who calls him (he still hasn't gotten to the he can call part yet) and they talk (about card strategies) for hours. sometimes its just a matter of finding the key that fits. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 11, 2003 Report Share Posted July 11, 2003 I just wanted to welcome you. I have two boys on the spectrum. Ages almost 10 and just turned 3. I just wanted to comment on the European accent. A good friend of mine who just came back from overseas swears my son sounds British. This friend is well traveled and has studied languages. Currently she is working towards a degree in speech pathology. She was just so sure somewhere along the line our family had British ties or that my ds had been exposed to it from a speech teacher or whatnot. However he's pure mutt. Very Americam. Noone British anywhere nearby. Interesting that you mentioned this too. a > Hello, I've just signed up to this site and am hoping to get some feedback from other parents of Asperger's children, in particular, parents of girls, since I've read so many times that this syndrome is not as common in girls. has unusual speech (her teachers and the speech therapist at school comment that she speaks almost with a European accent > Thanks, I appreciate any feedback anyone can give! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 12, 2003 Report Share Posted July 12, 2003 <<<<<I just wanted to comment on the European accent. A good friend of mine who just came back from overseas swears my son sounds British.>>>> my ds speaks English with a Russian accent. dito. F Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2003 Report Share Posted July 20, 2003 My older son spoke with a " cajun " accent from 3-5. Pam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2003 Report Share Posted July 20, 2003 Theresa...just curious how much Zoloft your daughter takes per day? Pam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2005 Report Share Posted January 3, 2005 Hi My name is Lori, I have a little boy who is 6 years that is disabled due to a chromosome disorder called isodicentric 15. Because of this disorder not only he non verbal & mobile but he has seizures and constant consitpation. I'm starting to look into all the great links but if anyone has any similar issue;s can you tell me what worked for you? Thanks everyone Lori Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2005 Report Share Posted January 3, 2005 > My name is Lori, I have a little boy who is 6 years that is disabled due to a chromosome disorder called isodicentric 15. Because of this disorder not only he non verbal & mobile but he has seizures and constant consitpation. Seizures can be related to food intolerance issues, and enzymes can help with that, altho not always. Something good to consider tho. Constipation ideas http://www.danasview.net/constip.htm Consider having him tested for metal toxicity, which is a common cause of seizures and constipation http://www.danasview.net/chelate.htm Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2005 Report Share Posted January 3, 2005 Hi Dana we did alot of testing with a DAN doctor and found out that due to all the antibioxtics he took he has yeast in his stool.. The seizures are apart of his disorder, he started having them when he was 9 months old. Lori -------------- Original message -------------- > My name is Lori, I have a little boy who is 6 years that is disabled due to a chromosome disorder called isodicentric 15. Because of this disorder not only he non verbal & mobile but he has seizures and constant consitpation. Seizures can be related to food intolerance issues, and enzymes can help with that, altho not always. Something good to consider tho. Constipation ideas http://www.danasview.net/constip.htm Consider having him tested for metal toxicity, which is a common cause of seizures and constipation http://www.danasview.net/chelate.htm Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 4, 2005 Report Share Posted January 4, 2005 > Hi Dana > > we did alot of testing with a DAN doctor and found out that due to all the antibioxtics he took he has yeast in his stool.. Yeast can be constipating. > The seizures are apart of his disorder, he started having them when he was 9 months old. Definitely consider having him tested for metals, also possibly viruses. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 18, 2005 Report Share Posted May 18, 2005 The FAQ's are a good place to start. Then read more here: http://home.earthlink.net/~moriam/ http://www.danasview.net/parent3.htm A lot of great information here to learn more. Jackie---- > Hello everyone. i am new to the site and still trying to navigate my > way around it. A friend referred me to you. I have a five year old son > who has dx of severe apraxia, ADHD, and a rule out diagnosis of PDD- > NOS. There is so much info out there its hard to know where to turn. > My son gets ST and PT. We have tried Proefa, but that is the only supp > we use and no meds. I have recently taken interest in looking at my > son's vitamin and mineral levels as well as looking into the > possiblity of lead or mercury toxicity. I understand someone posted a > message to see if anyone would be interested in an enzyme trial. I am > very interested. My son has sever language delays, mostly expressive, > and his impulse control and attention is not the best either. I would > love more info on getting involved with this. > Thank you, > Chrissy (mother to Ian age 5) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 18, 2005 Report Share Posted May 18, 2005 I would take your son to a DAN! practitioner as soon as possible. ARI stands for Autism Rsearch Institute Their project is DAN! Defeat Autism Now! Pamela " Courage is doing what you're afraid to do. There can be no courage unless you're scared. " Eddie Rickenbacker, top US fighter ace, WWI _____ From: [mailto: ] On Behalf Of cferrell79 Sent: Wednesday, May 18, 2005 2:16 PM Subject: [ ] new to site Hello everyone. i am new to the site and still trying to navigate my way around it. A friend referred me to you. I have a five year old son who has dx of severe apraxia, ADHD, and a rule out diagnosis of PDD- NOS. There is so much info out there its hard to know where to turn. My son gets ST and PT. We have tried Proefa, but that is the only supp we use and no meds. I have recently taken interest in looking at my son's vitamin and mineral levels as well as looking into the possiblity of lead or mercury toxicity. I understand someone posted a message to see if anyone would be interested in an enzyme trial. I am very interested. My son has sever language delays, mostly expressive, and his impulse control and attention is not the best either. I would love more info on getting involved with this. Thank you, Chrissy (mother to Ian age 5) ======================================================= Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 19, 2005 Report Share Posted May 19, 2005 >>I understand someone posted a > message to see if anyone would be interested in an enzyme trial. I am > very interested. This was on the enzyme forum / >>My son has sever language delays, mostly expressive, > and his impulse control and attention is not the best either. I would > love more info on getting involved with this. Here is my general info page on chelation, with links to other areas for more info http://www.danasview.net/chelate.htm Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 19, 2005 Report Share Posted May 19, 2005 > I would take your son to a DAN! practitioner as soon as possible. I wish it was that simple. Unfortunately a lot of them just mess your kid up worse. It is no different than mercury injecting pediatricians - most doctors think it is OK to just blindly follow a recipe without taking any responsibility to see if it is a good one. To say the least, the DAN! protocol is not yet perfect. There is no substitute for educating yourself and being able to make your own informed decisions. > ARI stands for Autism Rsearch Institute > > Their project is DAN! Defeat Autism Now! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 Hi! Sorry that your son was recently dx with autism. But, we are all here to help,if possible! I have not heard of the connection between enzymes (in drinks/foods) and reflux? I can tell you we have NOT experienced that at all. Anyone else heard of that one? Lori --- bignelson5 <gdnelson5@...> wrote: > Hello to all....My precious son is almost 3 years > old and has been > diagnosed with autism. I am completely overwhelmed > with all of > the 'therapies and treatments.' I am desperate to > know how to help him. > I keep coming across the issue of enzymes. My sons' > tests showed high > allergy to dairy and casein products...but our > doctor also feels he > should avoid gluten. The diet is so hard...and I am > not sure if it is > helping him at all. What form of enzyme is > recommended? When we saw our > doctor last she mentioned enzyes would be > great...but wanted to wait > until he could swallow the capsules...she felt the > powder in food would > cause reflux. I would like to try enzymes but don't > know where to > start. I feel parents are the true > professionals....any advice??? > Deanne > > > > > > __________________________________ for Mobile Take with you! Check email on your mobile phone. http://mobile./learn/mail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 I give all three of mine powder and have not had reflux issues. In fact my daughter used to spit up all the time, and I mean all the time!, until I put enzymes in her bottle. No more problems. Many of use Houston's enzymes, me included. I don't know if it would be best to try the diet first or just go to enzymes? We just found out about the enzymes a few months ago. Before that we did a gfcf as well as soy and nut free diet for about 3 years. Not fun but you do get used to it. There are a lot of good resources if you are going to do the diet. Special Diets for Special Kids was my first book purchase and I really loved it. The recipies were actually kid friendly. As far as seeing results...it may take a few weeks to couple months and then again, these kids are great for not really showing any reaction to diet or supplements until you take them away. Then you remember what it was like before...! Has happened to me more than once. With the diet also, if he is really sensitive every bit of gluten or whatever must be out of his diet. Any little bit can cause you not to see progress. Hang in there though...this stuff really helps...promise! Lori Yurtin <loriyurtin@...> wrote: Hi! Sorry that your son was recently dx with autism. But, we are all here to help,if possible! I have not heard of the connection between enzymes (in drinks/foods) and reflux? I can tell you we have NOT experienced that at all. Anyone else heard of that one? Lori --- bignelson5 <gdnelson5@...> wrote: > Hello to all....My precious son is almost 3 years > old and has been > diagnosed with autism. I am completely overwhelmed > with all of > the 'therapies and treatments.' I am desperate to > know how to help him. > I keep coming across the issue of enzymes. My sons' > tests showed high > allergy to dairy and casein products...but our > doctor also feels he > should avoid gluten. The diet is so hard...and I am > not sure if it is > helping him at all. What form of enzyme is > recommended? When we saw our > doctor last she mentioned enzyes would be > great...but wanted to wait > until he could swallow the capsules...she felt the > powder in food would > cause reflux. I would like to try enzymes but don't > know where to > start. I feel parents are the true > professionals....any advice??? > Deanne > > > > > > __________________________________ for Mobile Take with you! Check email on your mobile phone. http://mobile./learn/mail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 Hi , I too have an almost three year old. He turns three this Sunday. No functional language and lost of issues. I came to this site about three months ago and haven't found a better group or resource any where. I feel lucky that I found this group. Like you, I have been broken hearted and hurt and sometimes frightened about my child's future. There is a lot we can do. For me listening to my son's pediatricians have often been a set back, so, I double check their recommendations with this group. My son started enzymes in his drink at the start of my joining this group (about 3 months ago) with Houston Naturacuetical Inc Zyme Pryme and a month later I added AFT Peptizide by the same company. Then I started the Gluten Free Casein Free diet. We are on our third week and I love the diet and Enzyme combination. Finally on Monday after I saw blood in my child stool, I took him to a pediatrician who totally dismissed that, so, I started No-PHenol enzyme and I am amazed. Suddenly, a child that has had 3-6 BM per day (every day of all his life) has one only yeasterday. His behavior and cognitive development has improved greatly and he is a happier person. I mix the powders in his drink and have seen no signs of reflux. Also, Huoston also makes two of these enzymes in chewable forms. At the beginning the GFCF diet seemed so impossible to me, but after the enzymes, my sons appetite improved and not being in tummy ache all the time, he became more open to new stuff. His eye contact improved greatly and he runs and gives me hugs many times a day. Our children are special human beings and we must help them thrive and respect their uniqueness. After all no major accomplishment in the history of humanity has come from people who were perfectly Neuro Typical (if such thing exist). Welcome, You couldn't join a better group to help your child. And the following URL is were I get my son's enzymes. You can call them and they are very helpful on the phone as well. There are other reputable companies as well but I have only used Houston's and I love them. http://houstonni.com/Merchant2/merchant.mvc? Also, are you in an area to get him to a DAN (Deafeat Autism Now) doctor? I am sending you my two favorite autism websites. I read them extensively to learn about my options of helping mt child. http://www.generationrescue.org http://www.autismwebsite.com/ari/index.htm Best to you and your precious child and remember when you get him recovered, you have quite story to tell. Haleh > > --- bignelson5 <gdnelson5@...> wrote: > > > Hello to all....My precious son is almost 3 years > > old and has been > > diagnosed with autism. I am completely overwhelmed > > with all of > > the 'therapies and treatments.' I am desperate to > > know how to help him. > > I keep coming across the issue of enzymes. My sons' > > tests showed high > > allergy to dairy and casein products...but our > > doctor also feels he > > should avoid gluten. The diet is so hard...and I am > > not sure if it is > > helping him at all. What form of enzyme is > > recommended? When we saw our > > doctor last she mentioned enzyes would be > > great...but wanted to wait > > until he could swallow the capsules...she felt the > > powder in food would > > cause reflux. I would like to try enzymes but don't > > know where to > > start. I feel parents are the true > > professionals....any advice??? > > Deanne > > > > > > > > > > > > > > > > > __________________________________ > for Mobile > Take with you! Check email on your mobile phone. > http://mobile./learn/mail > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 Deanne - go here, shed a tear, grab some hope and join the club _www.findingthewords.org_ (http://www.findingthewords.org) Click on view trailer - its about 5 mins, thats more than enough for the message! Mandi in Dorset UK Wife to (Self Dx AS), mum to Tom 10 NT, Joe 9 NT and Sam 8, 47XYY, Autism, Heavy Metal Toxicity, possible Seizure Disorder and Severe cute-ness Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 Haleh... God bless you for such a beautiful message. Talking to other parents brings such comfort. I am in a pit of fear and sadness.....autism has become my life. I have lost all sense of balance and peace. How inspiring to learn of how many parents are fighting this thing.....and have hope. You use the word 'recover'....what a amazing concept...does one dare to dream such a thing!!! That would mean a new life....and new dreams for our son. Thanks for the enzyme site....what about kirkman products? We use vitamins through them...and have noted that they make enzymes too. I have no idea which he needs...how often...and what to look for. We have started seeing a DAN doctor...she has ordered many blood tests. She is the one who mentioned holding off on enzymes now as he will not swallow pills. Your son sounds like such a joy. WOW...hugs. What a great thing. Take Care and God Bless Deanne Re: New to site Hi , I too have an almost three year old. He turns three this Sunday. No functional language and lost of issues. I came to this site about three months ago and haven't found a better group or resource any where. I feel lucky that I found this group. Like you, I have been broken hearted and hurt and sometimes frightened about my child's future. There is a lot we can do. For me listening to my son's pediatricians have often been a set back, so, I double check their recommendations with this group. My son started enzymes in his drink at the start of my joining this group (about 3 months ago) with Houston Naturacuetical Inc Zyme Pryme and a month later I added AFT Peptizide by the same company. Then I started the Gluten Free Casein Free diet. We are on our third week and I love the diet and Enzyme combination. Finally on Monday after I saw blood in my child stool, I took him to a pediatrician who totally dismissed that, so, I started No-PHenol enzyme and I am amazed. Suddenly, a child that has had 3-6 BM per day (every day of all his life) has one only yeasterday. His behavior and cognitive development has improved greatly and he is a happier person. I mix the powders in his drink and have seen no signs of reflux. Also, Huoston also makes two of these enzymes in chewable forms. At the beginning the GFCF diet seemed so impossible to me, but after the enzymes, my sons appetite improved and not being in tummy ache all the time, he became more open to new stuff. His eye contact improved greatly and he runs and gives me hugs many times a day. Our children are special human beings and we must help them thrive and respect their uniqueness. After all no major accomplishment in the history of humanity has come from people who were perfectly Neuro Typical (if such thing exist). Welcome, You couldn't join a better group to help your child. And the following URL is were I get my son's enzymes. You can call them and they are very helpful on the phone as well. There are other reputable companies as well but I have only used Houston's and I love them. http://houstonni.com/Merchant2/merchant.mvc? Also, are you in an area to get him to a DAN (Deafeat Autism Now) doctor? I am sending you my two favorite autism websites. I read them extensively to learn about my options of helping mt child. http://www.generationrescue.org http://www.autismwebsite.com/ari/index.htm Best to you and your precious child and remember when you get him recovered, you have quite story to tell. Haleh > > --- bignelson5 <gdnelson5@...> wrote: > > > Hello to all....My precious son is almost 3 years > > old and has been > > diagnosed with autism. I am completely overwhelmed > > with all of > > the 'therapies and treatments.' I am desperate to > > know how to help him. > > I keep coming across the issue of enzymes. My sons' > > tests showed high > > allergy to dairy and casein products...but our > > doctor also feels he > > should avoid gluten. The diet is so hard...and I am > > not sure if it is > > helping him at all. What form of enzyme is > > recommended? When we saw our > > doctor last she mentioned enzyes would be > > great...but wanted to wait > > until he could swallow the capsules...she felt the > > powder in food would > > cause reflux. I would like to try enzymes but don't > > know where to > > start. I feel parents are the true > > professionals....any advice??? > > Deanne > > > > > > > > > > > > > > > > > __________________________________ > for Mobile > Take with you! Check email on your mobile phone. > http://mobile./learn/mail > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 Lori...thanks for that info. If a child is on enzymes...do they still need to be on a restricted diet? Pardon my ignorance. We have been doing the GFCF diet...only to learn that he now has intolerances to rice and soy too. It seems that the more we limit him...the more intolerances he develops. I try to rotate...but the choices he will take are so limited. What a dream it would be if enzymes enabled him to eat more things. Deanne Re: New to site I give all three of mine powder and have not had reflux issues. In fact my daughter used to spit up all the time, and I mean all the time!, until I put enzymes in her bottle. No more problems. Many of use Houston's enzymes, me included. I don't know if it would be best to try the diet first or just go to enzymes? We just found out about the enzymes a few months ago. Before that we did a gfcf as well as soy and nut free diet for about 3 years. Not fun but you do get used to it. There are a lot of good resources if you are going to do the diet. Special Diets for Special Kids was my first book purchase and I really loved it. The recipies were actually kid friendly. As far as seeing results...it may take a few weeks to couple months and then again, these kids are great for not really showing any reaction to diet or supplements until you take them away. Then you remember what it was like before...! Has happened to me more than once. With the diet also, if he is really sensitive every bit of gluten or whatever must be out of his diet. Any little bit can cause you not to see progress. Hang in there though...this stuff really helps...promise! Lori Yurtin <loriyurtin@...> wrote: Hi! Sorry that your son was recently dx with autism. But, we are all here to help,if possible! I have not heard of the connection between enzymes (in drinks/foods) and reflux? I can tell you we have NOT experienced that at all. Anyone else heard of that one? Lori --- bignelson5 <gdnelson5@...> wrote: > Hello to all....My precious son is almost 3 years > old and has been > diagnosed with autism. I am completely overwhelmed > with all of > the 'therapies and treatments.' I am desperate to > know how to help him. > I keep coming across the issue of enzymes. My sons' > tests showed high > allergy to dairy and casein products...but our > doctor also feels he > should avoid gluten. The diet is so hard...and I am > not sure if it is > helping him at all. What form of enzyme is > recommended? When we saw our > doctor last she mentioned enzyes would be > great...but wanted to wait > until he could swallow the capsules...she felt the > powder in food would > cause reflux. I would like to try enzymes but don't > know where to > start. I feel parents are the true > professionals....any advice??? > Deanne > > > > > > __________________________________ for Mobile Take with you! Check email on your mobile phone. http://mobile./learn/mail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 I don't understand what is happening to our children. It seems that autism is creeping up everywhere. My husband and I are overwhelmed with grief over our son. What happened?? What will the future be like for him? I am trying to search for answers and help. This site is wonderful. You parents are wonderful. This is the first time I hear people talking about recovery....and believing it. What a hope!!!!! I want to know how.... Deanne Re: New to site Hi! Sorry that your son was recently dx with autism. But, we are all here to help,if possible! I have not heard of the connection between enzymes (in drinks/foods) and reflux? I can tell you we have NOT experienced that at all. Anyone else heard of that one? Lori --- bignelson5 <gdnelson5@...> wrote: > Hello to all....My precious son is almost 3 years > old and has been > diagnosed with autism. I am completely overwhelmed > with all of > the 'therapies and treatments.' I am desperate to > know how to help him. > I keep coming across the issue of enzymes. My sons' > tests showed high > allergy to dairy and casein products...but our > doctor also feels he > should avoid gluten. The diet is so hard...and I am > not sure if it is > helping him at all. What form of enzyme is > recommended? When we saw our > doctor last she mentioned enzyes would be > great...but wanted to wait > until he could swallow the capsules...she felt the > powder in food would > cause reflux. I would like to try enzymes but don't > know where to > start. I feel parents are the true > professionals....any advice??? > Deanne > > > > > > __________________________________ for Mobile Take with you! Check email on your mobile phone. http://mobile./learn/mail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 Have you been to the Generation Rescue website... www.generationrescue.com There are stories of recovered children on there, helps when you are feeling overwhelmed...something to shoot for! Good luck. gdnelson5@... wrote: I don't understand what is happening to our children. It seems that autism is creeping up everywhere. My husband and I are overwhelmed with grief over our son. What happened?? What will the future be like for him? I am trying to search for answers and help. This site is wonderful. You parents are wonderful. This is the first time I hear people talking about recovery....and believing it. What a hope!!!!! I want to know how.... Deanne Re: New to site Hi! Sorry that your son was recently dx with autism. But, we are all here to help,if possible! I have not heard of the connection between enzymes (in drinks/foods) and reflux? I can tell you we have NOT experienced that at all. Anyone else heard of that one? Lori --- bignelson5 <gdnelson5@...> wrote: > Hello to all....My precious son is almost 3 years > old and has been > diagnosed with autism. I am completely overwhelmed > with all of > the 'therapies and treatments.' I am desperate to > know how to help him. > I keep coming across the issue of enzymes. My sons' > tests showed high > allergy to dairy and casein products...but our > doctor also feels he > should avoid gluten. The diet is so hard...and I am > not sure if it is > helping him at all. What form of enzyme is > recommended? When we saw our > doctor last she mentioned enzyes would be > great...but wanted to wait > until he could swallow the capsules...she felt the > powder in food would > cause reflux. I would like to try enzymes but don't > know where to > start. I feel parents are the true > professionals....any advice??? > Deanne > > > > > > __________________________________ for Mobile Take with you! Check email on your mobile phone. http://mobile./learn/mail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2005 Report Share Posted August 19, 2005 I could not pull it up on my ancient computer!! Thanks for the thought... Deanne Re: New to site Deanne - go here, shed a tear, grab some hope and join the club _www.findingthewords.org_ (http://www.findingthewords.org) Click on view trailer - its about 5 mins, thats more than enough for the message! Mandi in Dorset UK Wife to (Self Dx AS), mum to Tom 10 NT, Joe 9 NT and Sam 8, 47XYY, Autism, Heavy Metal Toxicity, possible Seizure Disorder and Severe cute-ness Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2005 Report Share Posted August 20, 2005 Do you have the book by DeFelice, Enzymes for Digestive Health and Nutritional Wellness? It covers so much about what can happen to our stomachs which then affects our brains. Best book I have on health, and I have a lot of them. It covers autism and everything else you can think of. Her two boys recovered. Susie > I don't understand what is happening to our children. It seems that autism is creeping up everywhere. My husband and I are overwhelmed with grief over our son. What happened?? What will the future be like for him? I am trying to search for answers and help. This site is wonderful. You parents are wonderful. This is the first time I hear people talking about recovery....and believing it. What a hope!!!!! I want to know how.... > Deanne > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2005 Report Share Posted August 20, 2005 I have ordered it from Amazon. Thanks... Re: New to site Do you have the book by DeFelice, Enzymes for Digestive Health and Nutritional Wellness? It covers so much about what can happen to our stomachs which then affects our brains. Best book I have on health, and I have a lot of them. It covers autism and everything else you can think of. Her two boys recovered. Susie > I don't understand what is happening to our children. It seems that autism is creeping up everywhere. My husband and I are overwhelmed with grief over our son. What happened?? What will the future be like for him? I am trying to search for answers and help. This site is wonderful. You parents are wonderful. This is the first time I hear people talking about recovery....and believing it. What a hope!!!!! I want to know how.... > Deanne > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2005 Report Share Posted August 20, 2005 > I keep coming across the issue of enzymes. My sons' tests showed high > allergy to dairy and casein products...but our doctor also feels he > should avoid gluten. The diet is so hard...and I am not sure if it is > helping him at all. What form of enzyme is recommended? If you want to consider adding back gluten and/or casein [or soy], then consider Peptizyde or AFP Peptizyde from HNI http://www.houstonni.com/ When we saw our > doctor last she mentioned enzyes would be great...but wanted to wait > until he could swallow the capsules...she felt the powder in food would > cause reflux. Enzymes eliminate reflux for many kids, even if mixed into food. Dana Quote Link to comment Share on other sites More sharing options...
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