Guest guest Posted November 29, 2004 Report Share Posted November 29, 2004 all the hyper behaviour I thought was enzymes when we started turned out to be yeast die off. We had three months of it! I hope yours doesn;t last that long, its bad enough with a 60 pounder LOL. Give it time, add the inositol and keep up the good work IMHO Mandi in UK is still hyper-Can be due to the enzymes which I just recd my second batch of regular so I would like to finish them first before I switch to the AFP and SCD (if this continues) or it could be yeast due to the Antibiotic he is on which I started to use Candex/Culturelle with,(giving 1 Candex 1hr before meal in am and 1 Candex 2hr after meal in pm) so I think it is too soon to say if it is yeast or Enzymes. Also can the negatives reoccurr after increasing the dose to 2 instead of 1 PEP with meals. I am trying to figure this all out. His teacher said he was anxious and compulsive in school today. He is just loud and hyper and jumping at home(imagine this 220lb guy jumping like a 5 year old)!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2004 Report Share Posted November 29, 2004 i didn;t realise what is was at first - we came stright off the diet with the very first enzymes, this was 3.5 years ago when they first came out and we didn't have the guidlines we have now. I first thought it was the enzymes, then I realised that in my joy in giving him 'real food' he was getting more su gar again. The enzymes were helping with the yeast - creating a long term mini die off but extra guns were needed and we did GSE. After things were back under control the improvements shone through and the hyper was gone. Stuff takes a while longer with the older ones. The hyper may just be the outcome of dealing with new feelings. Your Candex/Cullturelle protocl sounds fine. Syick ewith it and the enzymes MAndi in UK Did you treat this die-off. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2004 Report Share Posted November 29, 2004 Did you treat this die-off. I am getting everyone confused and I cant remember if you told me about the Candex and Culturelle-SOrry EIleen >From: Mum231ASD@... >Reply- > >Subject: Re: Adult son >Date: Mon, 29 Nov 2004 18:20:02 EST > >all the hyper behaviour I thought was enzymes when we started turned out to >be yeast die off. We had three months of it! I hope yours doesn;t last that >long, its bad enough with a 60 pounder LOL. Give it time, add the inositol >and >keep up the good work IMHO >Mandi in UK > > is still hyper-Can be due to the enzymes which I just recd my >second batch of regular so I would like to finish them first before >I switch to the AFP and SCD (if this continues) or it could be yeast >due to the Antibiotic he is on which I started to use >Candex/Culturelle with,(giving 1 Candex 1hr before meal in am and 1 >Candex 2hr after meal in pm) so I think it is too soon to say if it >is yeast or Enzymes. Also can the negatives reoccurr after >increasing the dose to 2 instead of 1 PEP with meals. I am trying >to figure this all out. His teacher said he was anxious and >compulsive in school today. He is just loud and hyper and jumping >at home(imagine this 220lb guy jumping like a 5 year old)!!! > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2004 Report Share Posted November 29, 2004 Thanks Mandi: Im in this for the long haul. I want to run out and start all the testing just to know where he's at, but we are going to Pfeiffer in February and they will do the testing. I did GSE one day with the NO FENOl to avoid phenol problems but really cant seem to tolerate the NF, so I opted for the Candex. I'll stick with this awhile I think. Thanks again Eileen PS My daughter went to London for Classes a few summers ago with College. She was there for 3 weeks-She fell in love with England.. She stayed in Oxford. I have familiy in Ireland and my husband has familiy in France. We thought she would travel to either place of her ancestory but she just had too much fun in London. >From: Mum231ASD@... >Reply- > >Subject: Re: Adult son >Date: Mon, 29 Nov 2004 19:39:28 EST > >i didn;t realise what is was at first - we came stright off the diet with >the very first enzymes, this was 3.5 years ago when they first came out and >we >didn't have the guidlines we have now. I first thought it was the enzymes, >then I realised that in my joy in giving him 'real food' he was getting >more su >gar again. The enzymes were helping with the yeast - creating a long term >mini >die off but extra guns were needed and we did GSE. After things were back >under control the improvements shone through and the hyper was gone. Stuff >takes a while longer with the older ones. The hyper may just be the >outcome of >dealing with new feelings. Your Candex/Cullturelle protocl sounds fine. >Syick >ewith it and the enzymes >MAndi in UK > >Did you treat this die-off. > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2004 Report Share Posted December 2, 2004 > Dana: I am using tablets for Ca/Mg. Citracal for CA, dont remember the > name of Mg. I am using 2:1 ratio. 1000 mg CA (broken up am and dinner > time-just got to this dose level) and 350 Mag so far (also broken up am and > just before bedtime). Well, 500 mg Mag would be 2:1 ratio, so if it turns out that he is tolerating the Mag, try giving him a little more. > I am going to order the AFP and SCD also to see if that makes a difference. > Are there any negative behaviors to watch for with this switch. Not usually. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2004 Report Share Posted December 2, 2004 > > Hi it's me again: I have something to throw out there. Has anyone > had problems with sore throats since starting enzymes. I have to > tell you my son has been so sick for the last 2 weeks( on again off > again). Started with double ear infections and sore throat, then > went to Stomach virus(did determine that this was a virus and not > antibiotics), now he's complaining of a sore throat the past few days > again (no fever) throat is slightly red. Yeast, or die off, can do this in my family. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2004 Report Share Posted December 2, 2004 Thanks Dana: I really am suspecting this is what is going on. I thought maybe I was looking a little too hard for explanations!!! By the way I stopped the CA/MG for now until I get the Candex/Culturelle in order. He has slept much better and much less hyper past 2 days. Thanks Again Eileen > > > > Hi it's me again: I have something to throw out there. Has anyone > > had problems with sore throats since starting enzymes. > > > > again). >Yeast, or die off, can do this in my family. > >Dana > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2004 Report Share Posted December 4, 2004 >>By the way I > stopped the CA/MG for now until I get the Candex/Culturelle in order. He > has slept much better and much less hyper past 2 days. Sounds good. If/when you start the cal/mag again, start one at a time, mag first. It took me five different calcium types/products before I found one my son tolerated, so you might be having a similar problem. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2004 Report Share Posted December 17, 2004 Hi -Eileen I am so sorry about your story. You are not lonely. My son be Dx as an autistic when he was alomst 2 years old. I have been cried for alomst 2 years. I believe that you are suffer more than I am. I just want you know you are not lonely. I wish you will feel better tomorrow and find the way to help your son. -- In , " eileen brischoux " <ebrischoux@h...> wrote: > Hi Sorry to be a bother. My son just had a total melt down and I need to > write. I am by nature a very strong person but I just am at my whits end. > The meltdown was precipitated by him throwing his dish in the sink, which he > was corrected for. Well he just lost it. Rage behavior which i havent seen > in a very long time. I tell you I am ready to call it quits. He is pretty > strong and it took everything in me to restrain him. Boy he can pinch and > knows all the right spots. He now has added shoving along with the grabbing > of the wrists. > > His teacher called today and told me school has been tough this week. She > apologized for not writing as gets upset when she writes in his book. > So she just told me that he has been anxious this week. I told her I > stopped the magnesium and I was not aware there was problems so now I have > to look at what else is going on. She also has not given him any more fruit > so its not from that. Could be the inositol which I am also stopping. I > have him crying in his room and Im crying in the other room. (I am not a > cryer) > > Anyway, I think I will just do enzymes for now. Not add anything else. His > menu at home hasnt changed either. Well thanks for the shoulder. Eileen > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Dear Mandi, ,, Laurie and Yenju and everyone esle that is so supportive: Thank You for all your kind words and encouragement. After a good nights sleep I am ready to start again. I didnt realize that I was not alone with the rages. He too has had problems with any SSRI drugs in the past just cant handle them. Wasnt aware of this with inositol. THanks for the info. I didnt think of the Charcoal. I really should have some in the house. He was very calm last night and gave a hug (his way of apologizing). Part of the problem is when he gets like this there is just no way of stopping it. Walking away doesnt work, he follows and continues the rage. He was drenched in sweat and shaking. I am still waiting for the Hair Element test kit to get to me and I cant wait for Feb to have other tests done to see what is going on internally with him if nothing else. I think my other fears are the changes he will be going thru when he graduates and I am just not happy about his choices, actually I am scared to death about this transition. This board has been a saving grace for me and I cant thank you all enough. I will keep pecking away at this (as you all knew I would, hehe) pure exhaustion talking last night. Thank Eileen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 My son is the same, however my son hits me and himself about the head area and sometimes bites. His latest development is the he will lean against the wall and bang his head, I have many holes in the wall from this... he has been much worse lately. However, my son doesn't tolerate the enzymes at this time. He has many GI problems and they get worse when I try the enzymes. My son's psychiatrist (who also believes that food is a factor in behaviors) thinks maybe he needs raw milk. So when I get some extra money I will try this. I have not found a type of magnesium or calcium that my son will tolerate. I do use l-glutamine, that seems to help calm him. My son is 21 years old, and mainly non-verbal. VickiB > Hi Sorry to be a bother. My son just had a total melt down and I need to > write. I am by nature a very strong person but I just am at my whits end. > The meltdown was precipitated by him throwing his dish in the sink, which he > was corrected for. Well he just lost it. Rage behavior which i havent seen > in a very long time. I tell you I am ready to call it quits. He is pretty > strong and it took everything in me to restrain him. Boy he can pinch and > knows all the right spots. He now has added shoving along with the grabbing > of the wrists. > > His teacher called today and told me school has been tough this week. She > apologized for not writing as gets upset when she writes in his book. > So she just told me that he has been anxious this week. I told her I > stopped the magnesium and I was not aware there was problems so now I have > to look at what else is going on. She also has not given him any more fruit > so its not from that. Could be the inositol which I am also stopping. I > have him crying in his room and Im crying in the other room. (I am not a > cryer) > > Anyway, I think I will just do enzymes for now. Not add anything else. His > menu at home hasnt changed either. Well thanks for the shoulder. Eileen > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Hello Eileen, will you please chart when this happens compared to when your son eats(how long after) and chart what he has eaten...when this happens-- I think you will find a corlation between the 2( is this a reaction to Aspartame the sugar substitute) OR your sons thyroid is not telling your son body when and how to use energy right.-peoples who thyriods are under active really can not control themselves at times- is this how you would decribe your son? We use to not be able to tell my son " no " for fear of an outburst he is very even tempered now. I love to send web pages to explain why I have these ideas and my son use to rage and does not any longer.. so there is a reason.. This is a procces.. you must go on I know you want to stop the supplements and medications -- I have never had my son on any medication and would love everyone to find natural ways to help our kids like I have.. this is a process-that means supplements ; at one point I remember reading that adrenaline( a stress hormon) and phenolic foods are made of the same kind of 5 ring alcohol compounds( I want to send you to the web page but can not) Will you find that a phenol food is making your son have a adrenaline rush like mine was ? if you have not been to web page you need to do some reading http://www.enzymestuff.com/nofenolfile.htm-- I have to go now I will pray the answer will come to you- It is strange... your own gut will tell you if it is the right course of action - follow your gut. My 2 cents Ann Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 > The meltdown was precipitated by him throwing his dish in the sink, which he > was corrected for. Well he just lost it. Rage behavior which i havent seen > in a very long time. Have you tried raging back at him? Now this probably won't be a good idea if he is 6'4 " and 250 pounds, and you are 4'10 " and 90 pounds. But my son is 8-1/2, and about when he was age 6, he raged at me one day, and I turned around and just screamed and ranted right back at him. [My other 3 kids all disappeared into the dark recesses of the house!] My son was so absolutely shocked at this that he literally just froze and stared at me for maybe as long as a minute. Then he started to cry and I gave him a big hug. Since that time, he has NEVER raged at me again. I am fortunate tho, in that his typical reaction to intolerances is that he gets giggly and spacy, and starts waving his hands in front of his eyes. He does not have meltdowns, and in fact this one that I referenced above, was probably one of the 3-4 times in his life that he has done that. > Anyway, I think I will just do enzymes for now. Not add anything else. His > menu at home hasnt changed either. This sounds like a good idea. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Eileen So glad to hear from you this morning! I've been thinking of you and hoping things had calmed down again. Our doctor felt that our sons rages were actually a form of seizure activity. Something you might want to check into. Someone else mentioned Aspartame and this will definitely trigger rages in my son and we avoid that stuff like the plague. It is in so many kids supps and medicines!! I know what you mean by not being able to walk away from it. If only!! If he has had problems with SSRI's I'd definitely wonder about the inositol. So glad to hear about the hug! They really don't mean to get this way and it really isn't their fault. It is so heartbreaking to see them go through this. Things are so much better for my son now but I still worry that those behaviours will come back. It takes a long time for mom's to recover emotionally from this Keep us posted! Laurie > Dear Mandi, ,, Laurie and Yenju and everyone esle that is so > supportive: > > Thank You for all your kind words and encouragement. After a good nights > sleep I am ready to start again. I didnt realize that I was not alone with > the rages. He too has had problems with any SSRI drugs in the past just > cant handle them. Wasnt aware of this with inositol. THanks for the info. > I didnt think of the Charcoal. I really should have some in the house. He > was very calm last night and gave a hug (his way of apologizing). Part of > the problem is when he gets like this there is just no way of stopping it. > Walking away doesnt work, he follows and continues the rage. He was > drenched in sweat and shaking. I am still waiting for the Hair Element test > kit to get to me and I cant wait for Feb to have other tests done to see > what is going on internally with him if nothing else. I think my other > fears are the changes he will be going thru when he graduates and I am just > not happy about his choices, actually I am scared to death about this > transition. > > This board has been a saving grace for me and I cant thank you all enough. > I will keep pecking away at this (as you all knew I would, hehe) pure > exhaustion talking last night. Thank Eileen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Dear Eileen, I really feel for you. We had been dealing with such behaviors from my daughter as she hit puberty. From trial and error and talking to other parents on this list, we started a calming amino acid called glycine first, It took about 2 weeks to see any benefit. While it greatly reduced many of her aggressive rages and melt downs, she started having problems again as we got into the December month. I switched over to TMG, which naturally raises your serotnin levels and within 2 days we had our sweet girl back. By the way, is 15 1/2 now, doing very well at school and hasn't had an aggressive incident at school in over (minor grab) 3 months. Just type in calming neurotransmitters or TMG and autism into your search engine and you'll find lots of valuable info to help you. It was a God send here. Re: Adult son > > Hi Sorry to be a bother. My son just had a total melt down and I need to > write. I am by nature a very strong person but I just am at my whits end. > The meltdown was precipitated by him throwing his dish in the sink, which he > was corrected for. Well he just lost it. Rage behavior which i havent seen > in a very long time. I tell you I am ready to call it quits. He is pretty > strong and it took everything in me to restrain him. Boy he can pinch and > knows all the right spots. He now has added shoving along with the grabbing > of the wrists. > > His teacher called today and told me school has been tough this week. She > apologized for not writing as gets upset when she writes in his book. > So she just told me that he has been anxious this week. I told her I > stopped the magnesium and I was not aware there was problems so now I have > to look at what else is going on. She also has not given him any more fruit > so its not from that. Could be the inositol which I am also stopping. I > have him crying in his room and Im crying in the other room. (I am not a > cryer) > > Anyway, I think I will just do enzymes for now. Not add anything else. His > menu at home hasnt changed either. Well thanks for the shoulder. Eileen > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 18, 2004 Report Share Posted December 18, 2004 Thank you : I will look up this info. 's negative behaviors also started during puberty. Very bad time for us. He was finally put on risperdal and gained 60 lbs in a few months. He is still on this with the addition of trileptal. My main goal in all this was to get him off these meds. He has been on risperdal for 8 or so years now. I didnt realize there were so many other parents with older children on this board. I knew a few but I have had many responses and I thank you all. EIleen >From: " Dougherty " <JBelle456@...> >Reply- >< > >Subject: Re: Adult son >Date: Sat, 18 Dec 2004 11:41:24 -0500 > >Dear Eileen, > I really feel for you. We had been dealing with such behaviors from my >daughter as she hit puberty. From trial and error and talking to other >parents on this list, we started a calming amino acid called glycine first, >It took about 2 weeks to see any benefit. While it greatly reduced many of >her aggressive rages and melt downs, she started having problems again as >we >got into the December month. I switched over to TMG, which naturally raises >your serotnin levels and within 2 days we had our sweet girl back. By the >way, is 15 1/2 now, doing very well at school and hasn't had an >aggressive incident at school in over (minor grab) 3 months. Just type in >calming neurotransmitters or TMG and autism into your search engine and >you'll find lots of valuable info to help you. It was a God send here. > > Re: Adult son > > > > > > Hi Sorry to be a bother. My son just had a total melt down and I need >to > > write. I am by nature a very strong person but I just am at my whits >end. > > The meltdown was precipitated by him throwing his dish in the sink, >which >he > > was corrected for. Well he just lost it. Rage behavior which i havent >seen > > in a very long time. I tell you I am ready to call it quits. He is >pretty > > strong and it took everything in me to restrain him. Boy he can pinch >and > > knows all the right spots. He now has added shoving along with the >grabbing > > of the wrists. > > > > His teacher called today and told me school has been tough this week. >She > > apologized for not writing as gets upset when she writes in his >book. > > So she just told me that he has been anxious this week. I told her I > > stopped the magnesium and I was not aware there was problems so now I >have > > to look at what else is going on. She also has not given him any more >fruit > > so its not from that. Could be the inositol which I am also stopping. >I > > have him crying in his room and Im crying in the other room. (I am not >a > > cryer) > > > > Anyway, I think I will just do enzymes for now. Not add anything else. >His > > menu at home hasnt changed either. Well thanks for the shoulder. >Eileen > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2005 Report Share Posted June 11, 2005 I have not posted in awhile as has been having some real problems and I have been trying hard to figure out what was going on. I was going to wait until Dr. visit to inform the group but feel it is important enough to mention now. was just dx with Lyme, present and past exposure. I have an appt with a lyme literate doctor late this month and will know more than I hope. I read an article relating Autism and lyme and had testing done on a hunch. I have never seen a tick on him but we do live in a lyme epedimic area and have had many tics in the house from pets. I am hoping that this underlying,albeit horrible desease is the reason why my son has had such a hard time with every intervention we try. My hope is that once he gets the proper treatment from a knowledgable lyme doctor than he will start to feel much better and not be in so much pain. If anyone suspects lyme, please have your child tested. I plan on having my entire family tested. My husband shows signs of lyme and after doing some reading so do I. I'll keep you all informed as you have always been so much help to me. Eileen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2005 Report Share Posted June 11, 2005 Is there a particular test to ask for to test for Lyme? I know someone doing SCD that had trouble 'getting anything to work'. Her son and other members in the family were found to have Lyme. Thank you for posting this. . Quote Link to comment Share on other sites More sharing options...
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