Guest guest Posted March 23, 2009 Report Share Posted March 23, 2009 Maggie,Thank you for taking the time to tell about the experiences behind your comment. I'm sorry to have jumped to the conclusion I did without knowing that you have been subjected to some really unfair criticism on this topic. Call me naive, but I would never assume that people would have the nerve to say things that unkind to you about your choices for your child. I guess I had a kneejerk reaction to the feeling that those same kinds of words were being put into my mouth. For me, being for one thing doesn't mean I'm automatically against someone doing something else. I like hearing about how people are succeeding, no matter their approach. No one knows our children like we do and I believe every autism parent works extraordinarily hard (and makes hard choices!) everyday. I truly didn't mean to offend you. --Tammy Re: The importance of diet We did give the GF/CF a solid try before going to enzymes. Maybe you'd understand why I put that sentence in after seeing some of the comments I've received about not doing the diet. I've been referred to as lazy, not willing to "go the distance" and of putting my own needs in front of my son's. I've also been told my son probably wouldn't recover if I didn't put him on the diet. I feel like I have to make it known that just because I found an alternative to GF/CF doesn't mean I don't put in extraordinary effort into my son's recovery. If you don't want to participate in these boards don't try to use my statement as a scapegoat. I will not take any responsibility for YOUR decisions. As it is, I have a son who is recovering from moderate/severe autism. I have received help from these boards as well as given it in return...this is not my first day. If we are going to discuss the importance of diet then I feel it is not only my right, but my obligation to let people know that there are some of us who do not have our children on special diets. > > > > "In my beginning years, I finally saw I had two sets of kids, the > > ones who were getting better and better and the ones who did not. After a few > > years it became clear to me that almost invariably the attitude and diligence to > > the dietary restriction was what made the difference whether a child got well or > > not. It got to the point where I could predict who would get well by the way > > the parent responded to the necessity to get the offending foods out of their > > kids' diets, especially after I finally got it > > that it was sugar just as much as casein and gluten and soy." > > > > -Dr. McCandless > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2009 Report Share Posted March 23, 2009 Maggie,Thank you for taking the time to tell about the experiences behind your comment. I'm sorry to have jumped to the conclusion I did without knowing that you have been subjected to some really unfair criticism on this topic. Call me naive, but I would never assume that people would have the nerve to say things that unkind to you about your choices for your child. I guess I had a kneejerk reaction to the feeling that those same kinds of words were being put into my mouth. For me, being for one thing doesn't mean I'm automatically against someone doing something else. I like hearing about how people are succeeding, no matter their approach. No one knows our children like we do and I believe every autism parent works extraordinarily hard (and makes hard choices!) everyday. I truly didn't mean to offend you. --Tammy Re: The importance of diet We did give the GF/CF a solid try before going to enzymes. Maybe you'd understand why I put that sentence in after seeing some of the comments I've received about not doing the diet. I've been referred to as lazy, not willing to "go the distance" and of putting my own needs in front of my son's. I've also been told my son probably wouldn't recover if I didn't put him on the diet. I feel like I have to make it known that just because I found an alternative to GF/CF doesn't mean I don't put in extraordinary effort into my son's recovery. If you don't want to participate in these boards don't try to use my statement as a scapegoat. I will not take any responsibility for YOUR decisions. As it is, I have a son who is recovering from moderate/severe autism. I have received help from these boards as well as given it in return...this is not my first day. If we are going to discuss the importance of diet then I feel it is not only my right, but my obligation to let people know that there are some of us who do not have our children on special diets. > > > > "In my beginning years, I finally saw I had two sets of kids, the > > ones who were getting better and better and the ones who did not. After a few > > years it became clear to me that almost invariably the attitude and diligence to > > the dietary restriction was what made the difference whether a child got well or > > not. It got to the point where I could predict who would get well by the way > > the parent responded to the necessity to get the offending foods out of their > > kids' diets, especially after I finally got it > > that it was sugar just as much as casein and gluten and soy." > > > > -Dr. McCandless > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2009 Report Share Posted March 23, 2009 sorry to butt-in..But maggie are you not doing the gf/cf diet ,cos I feel like a little guikty not doing the diet too,I dont mind doing the enzymes or biomeds but doing thid gf/cf diet is draining me down,as my boy just wont eat now !!!! Kind Regards.. Parveen Waris Subject: Re: Re: The importance of diet: maggieTo: mb12 valtrex Date: Monday, 23 March, 2009, 1:36 PM Maggie,Thank you for taking the time to tell about the experiences behind your comment. I'm sorry to have jumped to the conclusion I did without knowing that you have been subjected to some really unfair criticism on this topic. Call me naive, but I would never assume that people would have the nerve to say things that unkind to you about your choices for your child. I guess I had a kneejerk reaction to the feeling that those same kinds of words were being put into my mouth. For me, being for one thing doesn't mean I'm automatically against someone doing something else. I like hearing about how people are succeeding, no matter their approach. No one knows our children like we do and I believe every autism parent works extraordinarily hard (and makes hard choices!) everyday. I truly didn't mean to offend you. --Tammy Re: The importance of diet We did give the GF/CF a solid try before going to enzymes.Maybe you'd understand why I put that sentence in after seeing some of the comments I've received about not doing the diet.I've been referred to as lazy, not willing to "go the distance" and of putting my own needs in front of my son's. I've also been told my son probably wouldn't recover if I didn't put him on the diet. I feel like I have to make it known that just because I found an alternative to GF/CF doesn't mean I don't put in extraordinary effort into my son's recovery.If you don't want to participate in these boards don't try to use my statement as a scapegoat. I will not take any responsibility for YOUR decisions. As it is, I have a son who is recovering from moderate/severe autism. I have received help from these boards as well as given it in return...this is not my first day. If we are going to discuss the importance of diet then I feel it is not only my right, but my obligation to let people know that there are some of us who do not have our children on special diets. > > > > "In my beginning years, I finally saw I had two sets of kids, the > > ones who were getting better and better and the ones who did not. After a few > > years it became clear to me that almost invariably the attitude and diligence to > > the dietary restriction was what made the difference whether a child got well or > > not. It got to the point where I could predict who would get well by the way > > the parent responded to the necessity to get the offending foods out of their > > kids' diets, especially after I finally got it > > that it was sugar just as much as casein and gluten and soy." > > > > -Dr. McCandless > >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2009 Report Share Posted March 23, 2009 No, we do not do gf/cf, just Houston Enzymes. Here is a link to their page, and you can call Dr. Houston and talk to him as well... http://www.houston-enzymes.com/ > > > > > > " In my beginning years, I finally saw I had two sets of kids, the > > > ones who were getting better and better and the ones who did not. After a few > > > years it became clear to me that almost invariably the attitude and diligence to > > > the dietary restriction was what made the difference whether a child got well or > > > not. It got to the point where I could predict who would get well by the way > > > the parent responded to the necessity to get the offending foods out of their > > > kids' diets, especially after I finally got it > > > that it was sugar just as much as casein and gluten and soy. " > > > > > > -Dr. McCandless > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2009 Report Share Posted March 23, 2009 Please explain how they work, is this a long-term solution? How many do your children take with meals? Are they recovered from this treatment? I have always understood that there must be an enzyme particle for every particle of food needing digestion...in other words, the enzymes are recommended for those who are already on a restricted diet who may have small particles of food they are sensitive to in their food from cross-contamination. The enzymes help digest particles left over in the intestines that can cause yeast overgrowth and leaky gut. > > > > > > > > " In my beginning years, I finally saw I had two sets of kids, the > > > > ones who were getting better and better and the ones who did not. After a few > > > > years it became clear to me that almost invariably the attitude and diligence to > > > > the dietary restriction was what made the difference whether a child got well or > > > > not. It got to the point where I could predict who would get well by the way > > > > the parent responded to the necessity to get the offending foods out of their > > > > kids' diets, especially after I finally got it > > > > that it was sugar just as much as casein and gluten and soy. " > > > > > > > > -Dr. McCandless > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2009 Report Share Posted March 23, 2009 You're exactly right. Our intestinal cells normally have enzymes that break down food within our intestinal tract. Many kids with ASD have blunted/damaged cells and lack enzymes, or excess mucous as a protective measure which prevents food from coming into contact with the enzymes, or poor enzyme production. Foods that sit undigested within the intestinal tract, feed bacteria leading to pathogenic overgrowth. The bacteria release toxins as part of their natural life cycle, which causes further damage, leading to poorer digestion which feeds more bacteria and it becomes a vicious cycle. Enzymes taken with meals, help to digest food as eaten, placing less strain on the body and decreasing amounts of undigested food particles in the GI tract. There are different types of enzymes for different types of food. Many kids on restricted diets still require enzymes until their GI tract has a chance to heal. > > > > > > > > > > " In my beginning years, I finally saw I had two sets of kids, the > > > > > ones who were getting better and better and the ones who did not. After a few > > > > > years it became clear to me that almost invariably the attitude and diligence to > > > > > the dietary restriction was what made the difference whether a child got well or > > > > > not. It got to the point where I could predict who would get well by the way > > > > > the parent responded to the necessity to get the offending foods out of their > > > > > kids' diets, especially after I finally got it > > > > > that it was sugar just as much as casein and gluten and soy. " > > > > > > > > > > -Dr. McCandless > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2009 Report Share Posted March 23, 2009 That is a wonderful explanation of how enzymes work. I would just like to add that enzymes are considered extremely safe and along with aiding in the digestion of food they are also helpful with absorption of supplements. In the long term they are also helpful with any antiviral protocol as they eat away at the outer layer of viral surface cells, exposing them and allowing anti-viral supps to attack the exposed cell. > > > > Please explain how they work, is this a long-term solution? How many do your children take with meals? Are they recovered from this treatment? > > > > I have always understood that there must be an enzyme particle for every particle of food needing digestion...in other words, the enzymes are recommended for those who are already on a restricted diet who may have small particles of food they are sensitive to in their food from cross-contamination. The enzymes help digest particles left over in the intestines that can cause yeast overgrowth and leaky gut. > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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