Guest guest Posted November 9, 2001 Report Share Posted November 9, 2001 Does anyone know if LActaid would work like the pepcid AC? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2001 Report Share Posted November 9, 2001 We only use olive oil for cooking eggs. We use Fleischmann's unsalted marg instead of butter. We try to only bring gfcf food into the house... makes it much easier. Dona Vickrey Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2001 Report Share Posted November 9, 2001 > I am writing for several reasons. To introduce myself, to unload, to rejoice > and to ask a question. Obviously until we get really good at this, there are > going to be slips such as the one this morning. When such things happen, how > do you deal with the reaction. Do you just sit and watch, try to control it, > wait it out, or use some of the therapy techniques, like brushing or > swinging? Or does it really make any difference? I use enzymes for my child, from this url http://www.houstonni.com/ You can also use enzymes from this url http://www.kirkmanlabs.com/ > We are homeschooling, I homeschool also, here is my family's story, if you are interested. My son no longer qualifies as autistic. http://home.pacbell.net/cscomp/myson.htm Here is my homeschool section http://home.pacbell.net/cscomp/parentin.htm#homeschool Here is my therapy section http://home.pacbell.net/cscomp/parentin.htm#therapies If you go to my main parent information page, I have a lot of other topics that might interest you also. http://home.pacbell.net/cscomp/dmain.htm Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2001 Report Share Posted November 9, 2001 Sherrie, You could try enzmes with his meals in case he eats something he shouldnt. go to www.kirkmanlabs.com and read about Enzyme Complete with DPP-IV. everyone makes mistakes. it happens and luckily its just a short setback and then we get our kids back. Best of luck to you from another adoptive mom of a beautiful almost 5 yr old boy. karen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2001 Report Share Posted November 9, 2001 Sherrie - Welcome to the list. You are doing a great thing for your boy - it is hard work, but it will pay off. It sounds like your husband is very much on board with you regarding the diet - that is great. I am lucky to have an extremely supportive husband who is totally in this battle against Autism with me. It makes a big difference. I know how it feels to feed your kid " poisons " - early on I bought the wrong kind of ricemilk that had wheat in it - it said " wheat protein " right on the ingredient list, and I missed it. I felt like banging my head against the wall! But, thanks to a supportive husband, we just used it as a lesson to be more diligent. Sounds like you guys have the same strength. Use this as an inspiration to know that all your hard work is worth it. You should feel really good about that. Some folks don't always see an immediate reaction and it makes it really hard to continue to be so diligent with the diet. Also, don't beat yourself up about time lost. I sometimes go down that road too and it is a waste of energy. I once heard somebody say, " If you fall down when you are walking down the street, do you just stay there on the ground? NO! You get up and start walking again. " So - keep walking. We are all in this together, we will all make mistakes, we will share our setbacks and triumphs - just know that we are all still moving forward. One thing we did to make the diet easier for us was to make the entire house GFCF. My husband and I eat what we want outside of the house, but at home, everything is " safe " for my son. It just makes it a user friendly environment and reduces stress. I remember going to a family wedding early in this journey and there was an entire banquet table set up for the buffet - it was filled with rolls and breads.... It scared the s**t out of me. I viewed it as a table full of poisons that would take my son away from me. It was very stressful, but we survived that wedding without any accidents. So - having our home be a place that is safe takes away a lot of stress for us. Also, my hubby and I discovered that he is severely lactose intollerant and I have allergic reactions to milk. So it is good that we don't have it at home. Anyway - a long winded welcome to you and yours. Moira mom to Vico (4.5 ASD) and Culzean (18 months) > Can this be a whole new world that is opening up to me? Am I about to be > introduced to my son for the first time since his adoption 5 years ago? > Please let it be so. I'm new here. My name is Sherrie. My little boy, > was 5 in June. He was diagnosed (rather skeptically) at the age of 3 > with PDD. Because the diagnosis was half-hearted I tended to rock along a > bit longer than my nature usually allows me. I did not pursue answers. > Instead I waited to see if thy were right. He is now 5 and I cry when I > think that I " wasted " so much time. When I read about the hallucinogenic > effect of dairy and gluten on these little guys, my heart breaks to think of > the " treats " I offered my son that were turning his world into a whirling > tornado of confusion. Every cookie, granola bar, and milkshake have haunted > me. One week ago yesterday my husband and I read Karyn Seroussi's book and > one week ago today we removed dairy and subsequently gluten from his diet. > > The first five days: from bad to worse. Sleep walking every night (urinating > on walls and doors, thinking he was in the bathroom) ; Scooting his forehead > on the floor (something he has never done) ; Extreme stimming. > > BUT, interspersed throughout the last two of those days were other things we > have never seen; getting up in the morning quietly (he usually stomps from > the time he gets out of bed) listening to a story being read even while > other children are playing in the same room; showing remorse for spilling a > drink; noticing and commenting on the clothes I was wearing; less wandering > and darting; more cooperative. > > Yesterday was a wonderful day. (No sleepwalking the night before) He played > in the Mcs playground without once creating a need for us to apologize > to the other parents there. (A big thing!) When it came time to go home he > came when he was called, the first time! Wow. > > Today, the scene: Breakfast. Mom and Dad looking hopefully at one another > that we are getting our precious little boy back. Big brother and little > brother munching away. Suddenly throws his arms into the air and > screams, jumps out of his chair and crashes to the floor with squeals. My > husband and I look on with horror (remember that one week ago this was > common behavior) We look quickly at his plate, minds racing to determine the > culprit. It didn't take long, I asked, " Did you cook his egg in butter? " > Ohhh, how I wish I had been the one to make this slip. My poor husband > looked as if he had unknowingly slipped his son poison. It brought him to > tears. He scooped up the little guy who was thrashing about and carried him > to the sofa and held him tightly, asking him for forgiveness. It has been 2 > hours now and we see him coming `back down " He is playing fairly quietly > with only an occasional outburst. > > I am writing for several reasons. To introduce myself, to unload, to rejoice > and to ask a question. Obviously until we get really good at this, there are > going to be slips such as the one this morning. When such things happen, how > do you deal with the reaction. Do you just sit and watch, try to control it, > wait it out, or use some of the therapy techniques, like brushing or > swinging? Or does it really make any difference? We are homeschooling, and I > can see the potential of losing a whole day of school if a little butter > slips into his diet during breakfast. Is there some way to counteract the > effects so that they are minimal and not as distracting to the whole family' > s schedule? > > I know I'll have loads more questions and I am very glad to find this list, > but for now I just need to know, like the old song in Camelot, " What do you > do while they're doing it? " > > Sherrie > " The name of the Lord is a strong tower, the > righteous runs into it and is safe. " Proverbs 18:10 > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2001 Report Share Posted November 9, 2001 I dont think so -lactaid is made to help digest lactose in the milk-it would not help with the protien which is casein you would need an enzymes made to digest the casein protien not the lactose.F Re: Is this my kid? > Does anyone know if LActaid would work like the pepcid AC? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2001 Report Share Posted November 9, 2001 Hi Sherrie, It's Kirstin. (I've been meaning to write you back....hopefully I'll get a chance to this weekend!!!) I am soooooooooooooo thrilled about the changes you are seeing in !!!!!!! We have not begun the diet yet with Caleb - I'm still trying to figure out just what direction I need to go in. We have so many upheavals in our life as it is right now that experimenting with diet (since it's hard to know which approach will work best for what child - I want a hard and fast rule LOL!!!!!) is not what I'm wanting to do right now! But I want to learn as much as I can in case the time comes for us to go this route. I tell you what, although Caleb isn't as old as is, I can understand how you feel badly for the way things have been. But like others have said, you can't work with information that you don't have! I am so thankful for the internet when it comes to Caleb. If it hadn't been for my internet friends, we never would have suspected that anything was even wrong with Caleb. Since hs is not severe at ALL, we just though he was a little quirky. Or airheaded. Or clutzy. ;-) But I mentioned a particular behavior to some friends and they said, hmmmmmm you might want to get that checked, especially since his language is so poor. I kind of blew them off, but I did go ahead and get him a speech evaluation. The speech pathologist noticed some behaviors and is the one who really got us going down this road. But that's as far as we've gotten because of moves and such, and I found out today that it will be about 6-8 more weeks before we can get a full evaluation because of the backlog at the clinic! I'm so thankful for the internet so I can learn more about PDD in the mean time AND possibly all those " weird alternative " treatments that actually seem to hold more promise than the typical ones in the medical world. I would be completely clueless if it weren't for the internet and groups like this!!!!! Love, Kirstin <>< Wife to Bobby (7 years) Momma to Grant (4.5), Caleb (3), Libby (1.25), and " Lil' Bit " (due 4/26/02) I sell books kids love!!! I'm an Usborne Books at Home Independent Consultant! http://usbornekirstin.tripod.com/ Quote Link to comment Share on other sites More sharing options...
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