Guest guest Posted August 20, 2000 Report Share Posted August 20, 2000 In a message dated 8/20/00 4:34:34 PM Pacific Daylight Time, gldcst@... writes: << So what if we were ALL to write the Sunshine Foundation and tell themour child's dream is to have a conference for all kids withDS/Autism? hmmmm. Sherry >> Sherry! Wonderful idea~~!!!!!! I second the motion! Jeannie Mom to Mark and ! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2000 Report Share Posted August 20, 2000 I like this idea Sherry????? Better yet, our kids want our MOM'S to go to camp and wish for a break for US. Don't you think would want that for you? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2000 Report Share Posted August 20, 2000 So what if we were ALL to write the Sunshine Foundation and tell themour child's dream is to have a conference for all kids withDS/Autism? hmmmm. Sherry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2000 Report Share Posted August 20, 2000 I third it! S On Sun, 20 Aug 2000 19:35:42 EDT JVal987@... writes: > In a message dated 8/20/00 4:34:34 PM Pacific Daylight Time, > gldcst@... > writes: > > << So what if we were ALL to write the Sunshine Foundation and tell > themour > child's dream is to have a conference for all kids withDS/Autism? > hmmmm. > Sherry > >> > Sherry! > Wonderful idea~~!!!!!! I second the motion! > Jeannie > Mom to Mark and ! > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 21, 2000 Report Share Posted August 21, 2000 In a message dated 08/20/2000 6:34:33 PM Central Daylight Time, gldcst@... writes: << So what if we were ALL to write the Sunshine Foundation and tell themour child's dream is to have a conference for all kids withDS/Autism? hmmmm. Sherry >> Love this idea! We would be there for sure! Followed by a week for the parents only at a resort on some breathtaking Carribean beach - with massages and terrific food! Whadya think? Maureen (Daydreaming in Naperville) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 21, 2000 Report Share Posted August 21, 2000 In a message dated 8/21/00 9:37:56 AM Eastern Daylight Time, MRASMUS@... writes: << Love this idea! We would be there for sure! Followed by a week for the parents only at a resort on some breathtaking Carribean beach - with massages and terrific food! Whadya think? Maureen (Daydreaming in Naperville) >> Maureen, What's this? You want us all dead? LOL That sounds like heaven to me....Won't ever happen in my LIFEtime! LOL Gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 22, 2006 Report Share Posted July 22, 2006 Thanks so much for posting - this is great - just what I needed to hear!!!! Jacqui > > hi mandi asked me to cross post this regards my boy from AM, hes > currently on dmsa/ala following andy protocol: > > hi > > weve been chelating low doses of ala and dmsa for kai probably > averaging once a fortnight, since xmas, ive seen some improvements > overall but not many. > > BUT > > i went to parents meeting on friday, and they didnt half make me > smile. Kai is doing very well, at Key stage 2, he has straight c's > in english, straight a's in maths and science, as and bs in history > and geography and she said that he will be going for sats in year 6, > bearing in mind kai is in a special school for children with > autism, they are absolutely delighted, also they then mentioned we > dont know quite whats going on with kai, but over the last 4 months > we have seen real surges of improvment!!! and that if he kept up > like this we were looking at an intergrated resource and possibly > gcse's at high school. I quietly smiled to myself - as they dont > know that i began chelating since just after xmas. > > also his physiotherapist saw him 2 weeks ago, she hasnt seen him > since before xmas and she was stunned at the improvements hed made, > she said she couldnt understand why and how hed managed to improve > so much. > > just thought id share, > > emma > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 22, 2006 Report Share Posted July 22, 2006 In a message dated 23/07/2006 07:41:53 GMT Daylight Time, editorial.hillbury@... writes: Emma, how old is your lad? We just started DMSA with Dr Heard and I wasbeginning to think we'd left it a bit late. Our son has recently turned 7 >>>Its never too late, 20 somethings are seeing gains with a proper chelation protocol. Mandi x Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 In a message dated 22/07/2006 12:56:12 GMT Standard Time, eeejay174@... writes: I quietly smiled to myself - as they dontknow that i began chelating since just after xmas.also his physiotherapist saw him 2 weeks ago, she hasnt seen himsince before xmas and she was stunned at the improvements hed made,she said she couldnt understand why and how hed managed to improveso much.just thought id share,emma Go Emma and Kai! Great to hear. Also, thanks for posting about your son's negative reaction to Bio-Care Multivit. My son's EXTREME hyperactivity and aggressiveness immediately went away when I discontinued the vitamins. Unfortunately it left him completely wiped out and feverish again <sigh> oh well, that's one to strike off the list anyway! Darla Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 Emma, how old is your lad? We just started DMSA with Dr Heard and I was beginning to think we'd left it a bit late. Our son has recently turned 7 Gillian On 22/7/06 19:31, " npower2003 " <jacqui@...> wrote: > Thanks so much for posting - this is great - just what I needed to > hear!!!! > > Jacqui > > >> >> hi mandi asked me to cross post this regards my boy from AM, hes >> currently on dmsa/ala following andy protocol: >> >> hi >> >> weve been chelating low doses of ala and dmsa for kai probably >> averaging once a fortnight, since xmas, ive seen some improvements >> overall but not many. >> >> BUT >> >> i went to parents meeting on friday, and they didnt half make me >> smile. Kai is doing very well, at Key stage 2, he has straight c's >> in english, straight a's in maths and science, as and bs in history >> and geography and she said that he will be going for sats in year > 6, >> bearing in mind kai is in a special school for children with >> autism, they are absolutely delighted, also they then mentioned we >> dont know quite whats going on with kai, but over the last 4 months >> we have seen real surges of improvment!!! and that if he kept up >> like this we were looking at an intergrated resource and possibly >> gcse's at high school. I quietly smiled to myself - as they dont >> know that i began chelating since just after xmas. >> >> also his physiotherapist saw him 2 weeks ago, she hasnt seen him >> since before xmas and she was stunned at the improvements hed made, >> she said she couldnt understand why and how hed managed to improve >> so much. >> >> just thought id share, >> >> emma >> > > > > > > > > > DISCLAIMER > No information contained in this post is to be construed as medical advice. If > you need medical advice, please seek it from a suitably qualified > practitioner. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 hi kai is 8, i did kind of think the same thing, but i thought even so its still worth a go, and in my opinion looking at how he is, there really doesnt outwardly appear to be huge improvements, but something somewhere is clearly improving, we do have horrendous trouble with yeast, which could well be disguising any other improvements, im just keeping my resolve in that i hope that the yeast will eventually clear up on its own with the chelation, but im over the moon, so much more than i could have hoped for. emma > >> > >> hi mandi asked me to cross post this regards my boy from AM, hes > >> currently on dmsa/ala following andy protocol: > >> > >> hi > >> > >> weve been chelating low doses of ala and dmsa for kai probably > >> averaging once a fortnight, since xmas, ive seen some improvements > >> overall but not many. > >> > >> BUT > >> > >> i went to parents meeting on friday, and they didnt half make me > >> smile. Kai is doing very well, at Key stage 2, he has straight c's > >> in english, straight a's in maths and science, as and bs in history > >> and geography and she said that he will be going for sats in year > > 6, > >> bearing in mind kai is in a special school for children with > >> autism, they are absolutely delighted, also they then mentioned we > >> dont know quite whats going on with kai, but over the last 4 months > >> we have seen real surges of improvment!!! and that if he kept up > >> like this we were looking at an intergrated resource and possibly > >> gcse's at high school. I quietly smiled to myself - as they dont > >> know that i began chelating since just after xmas. > >> > >> also his physiotherapist saw him 2 weeks ago, she hasnt seen him > >> since before xmas and she was stunned at the improvements hed made, > >> she said she couldnt understand why and how hed managed to improve > >> so much. > >> > >> just thought id share, > >> > >> emma > >> > > > > > > > > > > > > > > > > > > DISCLAIMER > > No information contained in this post is to be construed as medical advice. If > > you need medical advice, please seek it from a suitably qualified > > practitioner. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 hi kai is 8, i did kind of think the same thing, but i thought even so its still worth a go, and in my opinion looking at how he is, there really doesnt outwardly appear to be huge improvements, but something somewhere is clearly improving, we do have horrendous trouble with yeast, which could well be disguising any other improvements, im just keeping my resolve in that i hope that the yeast will eventually clear up on its own with the chelation, but im over the moon, so much more than i could have hoped for. emma > >> > >> hi mandi asked me to cross post this regards my boy from AM, hes > >> currently on dmsa/ala following andy protocol: > >> > >> hi > >> > >> weve been chelating low doses of ala and dmsa for kai probably > >> averaging once a fortnight, since xmas, ive seen some improvements > >> overall but not many. > >> > >> BUT > >> > >> i went to parents meeting on friday, and they didnt half make me > >> smile. Kai is doing very well, at Key stage 2, he has straight c's > >> in english, straight a's in maths and science, as and bs in history > >> and geography and she said that he will be going for sats in year > > 6, > >> bearing in mind kai is in a special school for children with > >> autism, they are absolutely delighted, also they then mentioned we > >> dont know quite whats going on with kai, but over the last 4 months > >> we have seen real surges of improvment!!! and that if he kept up > >> like this we were looking at an intergrated resource and possibly > >> gcse's at high school. I quietly smiled to myself - as they dont > >> know that i began chelating since just after xmas. > >> > >> also his physiotherapist saw him 2 weeks ago, she hasnt seen him > >> since before xmas and she was stunned at the improvements hed made, > >> she said she couldnt understand why and how hed managed to improve > >> so much. > >> > >> just thought id share, > >> > >> emma > >> > > > > > > > > > > > > > > > > > > DISCLAIMER > > No information contained in this post is to be construed as medical advice. If > > you need medical advice, please seek it from a suitably qualified > > practitioner. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 What a great bit of news there!! We are starting TTFD shortly and i so hope for a similar outcome followed by chelation. I don't intend to tell anyone either. > > > In a message dated 22/07/2006 12:56:12 GMT Standard Time, > eeejay174@... writes: > > I quietly smiled to myself - as they dont > know that i began chelating since just after xmas. > > also his physiotherapist saw him 2 weeks ago, she hasnt seen him > since before xmas and she was stunned at the improvements hed made, > she said she couldnt understand why and how hed managed to improve > so much. > > just thought id share, > > emma > > > > > Go Emma and Kai! Great to hear. > Also, thanks for posting about your son's negative reaction to Bio- Care > Multivit. My son's EXTREME hyperactivity and aggressiveness immediately went > away when I discontinued the vitamins. Unfortunately it left him completely > wiped out and feverish again <sigh> oh well, that's one to strike off the list > anyway! > Darla > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 What a great bit of news there!! We are starting TTFD shortly and i so hope for a similar outcome followed by chelation. I don't intend to tell anyone either. > > > In a message dated 22/07/2006 12:56:12 GMT Standard Time, > eeejay174@... writes: > > I quietly smiled to myself - as they dont > know that i began chelating since just after xmas. > > also his physiotherapist saw him 2 weeks ago, she hasnt seen him > since before xmas and she was stunned at the improvements hed made, > she said she couldnt understand why and how hed managed to improve > so much. > > just thought id share, > > emma > > > > > Go Emma and Kai! Great to hear. > Also, thanks for posting about your son's negative reaction to Bio- Care > Multivit. My son's EXTREME hyperactivity and aggressiveness immediately went > away when I discontinued the vitamins. Unfortunately it left him completely > wiped out and feverish again <sigh> oh well, that's one to strike off the list > anyway! > Darla > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 Emma I am so pleased for you with the improvements in your child.Hope Kai continues on this road to recovery. welldone you for all that hard work. Kind Regards caroline, Aberdeenshire Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2006 Report Share Posted July 23, 2006 Emma I am so pleased for you with the improvements in your child.Hope Kai continues on this road to recovery. welldone you for all that hard work. Kind Regards caroline, Aberdeenshire Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2009 Report Share Posted March 10, 2009 Just to let you know I am just about 10 weeks pregnant (after 3 miscarriages in past 18 months). I have just had my 3rd scan & all is well!! Thank you particularly to Sheila for all her kind advice. I had another blood test today so hope that my levels are still as good as before. I feel pretty sure that the reason things are different this time is the Armour. At the moment I have a good supply & don't think any doctor would be foolish enough to try & change my treatment while pregnant. I did mention this at my appointment last week & he seemed to think that I'd be able to continue to get Armour prescribed throughout this pregnancy. P.S I'd love to hear from anyone who has gone through pregnancy on Armour as the prospect has terrified my endo.......... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 10, 2009 Report Share Posted March 10, 2009 Congratulations . Regarding your question about being pregnant on Armour, I can assure you that you have nothing to worry about. My friend, who had been trying for years, told that her thyroid was normal, went to see Dr. S who prescribed Armour for her. Within months she was pregnant. All went well during the pregnancy, she gave birth to a normal weight baby boy, who is now 6 years old. She was on Armour all during the pregnancy and after. Lilian Quote Link to comment Share on other sites More sharing options...
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