Guest guest Posted August 6, 2004 Report Share Posted August 6, 2004 , I just looked at my responce to your question and I'm afraid it looks like I just snapped back a reply. How insensitive of me. I remember how frazzled I was when I began this diet and if someone had spoken to me like that I would have been crushed. Yes, it does seem like a daunting task but really our kids respond so well (for the most part) that after time it is easy to see that the benefit outweighs the frustration. I daily curse the foods I can no longer feed my son. I cringe every time he says he's hungry and I can offer him peas, again. I hate that the sweetest thing he's eaten since Easter is a pear. It frustrates me to no end to see all variety in the GF/CF things that I can no longer give him, that 6 months ago I thought was limited. I hope you don't take my words as unkind as I'm afraid they appear. I know you are very busy and really need encouragement and support now. Please forgive my insensitivity Hang in there. It will get better. Helen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2004 Report Share Posted August 6, 2004 Here is the story of one of the first children who did SCD.This might help you figure out how long this diet would need to be followed. http://lyris.dundee.net/read/messages?id=259549#259549 Mimi -------------------------------------------------------------------- Hi there, Here is the story. I didn't have a science to it--as I was the first mom of a child on the spectrum to try the diet. I basically did a trial and error. First, I tried meats and veggies. We added nut flour after a month and he would start laying around lining up trucks again....we knew it was too soon. So, I went back to meats and veggies for three months. We added fruits on the fourth month. After month five, we cut out all supplements and finally tried goat yoghurt. We were so brainwashed from the last diet. He did great on the yoghurt. Huge growth and development improvements. He stayed on the det for 1 1/2 years. We've tried to go off of the diet 2 times since. He does not do well off of it for too long. His villi are healed and he never goes back to the old days (autistic behavior, diar.), but he gets hyperactive if he is off it. My belief is that it's because of the metals. He has 7 toxic metals. We are using C and zinc only right now. I don't want to do anything that violates the diet. He is currently on Ester C, zinc with B, and the quinn be strong and A LOT of probiotics. We use Lucy's now. He didn't do well on it at first but he does now. I say this: Don't do as I say. Each child is different. Colin had such severe Dia. at first I had to cook his veggies for months...fruits at first two. He really didn't do well on raw foods for a while. He also had troubles (breathing) with eggs and any trace of cow milk at first--and an aversion to beef. He now can have beef and eggs too. It takes time to heal. Get to know your child one food at a time. I believe the yoghurt and probiotics are key. Also, chelating the body is very taxing on your system. I wouldn't have ever tried it on Colin in the early days. He wasn't strong enough. He is so healthy now. Colin's development is good. He has friends, he's caught up to grade level, and he has a vivid imagination (pretend friends). He is also extremely emotional. He is 6 and the light of my life! He just learned to read; read me his first book yesterday. Hang in there. Colin is still not 100% healed but he is almost there. Please be extremely patient every step of the journey. Luv, Jen > I want to know if this diet, which we are on day 2 of, is a lifetime > necessity, or can kids on the Austism spectrom return to a regular > diet at some point? > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2004 Report Share Posted August 6, 2004 >> I want to know if this diet, which we are on day 2 of, is a lifetime necessity, or can kids on the Austism spectrom return to a regular diet at some point? << , When I went on SCD about two and a half years ago, I read the part in Elaine's book about how her daughter stayed strict SCD for two years, and then gradually returned to eating " normally " . Elaine typically recommends strict SCD for one year after the last symptom has disappears (for gut disorders). For ASD, we only have about two years worth of data, so it's hard to say. <grin> We have seen some miracles, though! I loved whole wheat bread, and whole wheat pasta and brown rice, and thought that giving that up was going to be hard, hard, hard. I figured I would go on the diet, get my gut in order, and then get back to real food. Well, this autumn, I'll be hitting my third anniversary on SCD. Know what? I have NO desire to go back to the way I once ate. I won't deny that it's a nuisance to have to make sure I have half & half yogurt cheese on hand to make ranch salad dressing, or to need to remember that I have to use the mayonnaise-based remoulade dressing / sauce up within two weeks and that I have to remember to use a clean utensil dipping it out. But I like the taste of my homemade food better. And I don't have to accept some faceless manager somewhere deciding what spices I will like on my food this week. Harry (my husband) and I are eating better than we ever have. Because we're no longer buying expensive processed stuff, we're able to afford free-range meats, seafood, vegetables and eggs from our local Farmer's Market. I like this -- the idea that not only am I getting better quality food, but that my food dollars are going directly to the people who actually did the work of raising my food, not some middleman. My sister, who went SCD despite not thinking she had any gut problems, has so much energy it's insane. (She has a husky, and takes the husky running for ten miles every day, rain or shine. She's now working a farmer's market near her home in Ohio.) My niece, who was told that because of her gut and thyroid problems, she would probably never be able to get pregnant, let alone carry to term without major medical interventions, went on SCD, and four months later, she was pregnant. Young Master Liam just passed his 3 month " birthday " . My mother, who is not SCD, but who is on a low-salt diet for her congestive heart failure has benefitted because I have learned so MUCH about food preparation! I now make her a salt-free honey-mustard salad dressing, and do gourmet meals on Mondays for my parents. I also make a salt-free chicken salad spread which she uses for sandwiches when she goes some place where she can't be sure the food is safe. My husband, who is about 97% SCD (he uses wheat bread for his lunch sandwiches five days a week) has discovered that SCD has significantly reduced his chronic fatigue. I'm betting if he'd go 100%, he'd see a complete amelioration, but he hasn't QUITE reached the point where he's willing to give up ALL bread. Not only is my gut healing (I was sick for 25 years: urgency, soft, mushy, stinky stools, constant embarassment, etc. etc. etc.), but my ADD symptoms have all but vanished. The point I want to reach is where I can eat out and not have to be QUITE so concerned about whether they are using a commercial spice mix for the Cajun seasoning, or if a little flour happened to cross contaminate my meat on a grill. We've seen lots of reports from kids who are reaching this point -- exposure to a food that in previous times might have meant miserable days or even weeks for both child and parent not longer has an effect, or has a minimal effect. For myself, I plan to stay SCD for the rest of my life. When I was on Day Two, I couldn't imagine feeling this way. Now I can't imagine why I was ever addicted to grains and processed foods in the first place. -- Marilyn (New Orleans, Louisiana, USA) Undiagnosed IBS, SCD 2.5+ Years Darn Good SCD Cook No Human Children Shadow & Sunny Longhair Dachshund Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2004 Report Share Posted August 6, 2004 > >> I want to know if this diet, which we are on day 2 of, is a lifetime > necessity, or can kids on the Austism spectrom return to a regular diet at > some point? << > > , > > When I went on SCD about two and a half years ago, I read the part in > Elaine's book about how her daughter stayed strict SCD for two years, and > then gradually returned to eating " normally " . Elaine typically recommends > strict SCD for one year after the last symptom has disappears (for gut > disorders). For ASD, we only have about two years worth of data, so it's > hard to say. <grin> We have seen some miracles, though! > > I loved whole wheat bread, and whole wheat pasta and brown rice, and > thought that giving that up was going to be hard, hard, hard. > > I figured I would go on the diet, get my gut in order, and then get back to > real food. > > Well, this autumn, I'll be hitting my third anniversary on SCD. > > Know what? I have NO desire to go back to the way I once ate. hday " . > Except for the fact that I have no husband named Harry our stories could have been written by the same person. SCD has made a good cook of me too, one with spontaneous imagination and a sense of adventure. Others who taste my SCD food find it better than conventional too. Carol F. **** There is no substitute for the right food! Quote Link to comment Share on other sites More sharing options...
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