Guest guest Posted October 10, 1999 Report Share Posted October 10, 1999 thanks for all the vaccine info, patti. that explains a lot! @}{~{<<~~~~~~~~~~~~~~~~~~~~ debbie s. - dlsherman@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2000 Report Share Posted February 11, 2000 Hello all, Here is the reference for the OCD Storybook that was mentioned recently: Blink, Blink, Clop, Clop: Why do we do things we can't stop? by E. Katia Moritz, Ph.D. and Jablonsky. Available from Childswork Childsplay 1-800-962-1141. It may also be on the OCF website www.ocfoundation.org. It is a bit long for really young children, but for 5-7 year olds it's a good length for parents to read in a sitting or so, and there are illustrations that potentially a child could color to get more involved with the story. Best, Tamar Chansky, Ph.D. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 12, 2000 Report Share Posted February 12, 2000 I typed the whole thing out, did you all get it? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2000 Report Share Posted June 25, 2000 Hi Kati Jay, My nams is Ann and I am so new to the list that you are the first leter I've seen yet. A very brief on me My battle to put an end to candida is really an amazing story and I hope to one day share it with all of you. understanding candida and how it goes on in each individual and assisting them in there struggle has been my lifes commitment for the last 8 years. In learning all that I could, and continuing to further my education, I became a colonic therapist and work in the phx. area. One of my main focus is candida. My time, unfortunatly, is very limited so I must get out what I would like to say in regards to advertising. although I have not seen the adds that your are refering to, I feel that if it is someone who has tried the product and it has worked for them and they are willing to share their story in detail and answere any questions others may have then I am interested. But if you are talking about commercial advertising then I agree with you 100%! I do not know if the list is moderated and I would like to see what comes of this. I feel so lucky to have access to something like this. we could all learn so much from each other and suport and encourage one another and I would hate for us to be disbanded because of advertisers, BUT if that is what happens so be it! I joined to hear peoples story's and methods of living under thier own personal conditions NOT to see adds for products. Ann >From: " Jay " <kj-mj@...> >Reply-candidiasisegroups ><candidiasisegroups> >Subject: Re: Digest Number 393 >Date: Sun, 25 Jun 2000 11:11:40 -0700 > >I don't think this list should be used for advertising. Is this list >moderated? I'm not going to stay if this issue is not addressed. > > > > > Digest Number 393 > > >------------------------------------------------------------------------ >Turn your EGROUP into a GROUP BUYING GROUP! Join beMANY! today. >1/4124/12/_/469673/_/961922273/ >------------------------------------------------------------------------ > >Send blank message to candidiasis-unsubscribeonelist if you want to >UNSUBSCRIBE ! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2000 Report Share Posted June 25, 2000 Dear Ann If you have your personal candida experinces on computer I for one would be very interested to read it. Email it to me direct not to the list. I was diagnosed June 6th when I had never heard of candida, but having learnt all about it since then, I realise I have suffered (and I mean *suffered*) from it for 20 years. (I am a 42 yr old woman). I intend to type up my own story one day. Right now I am so busy enjoying life to the full, after years of being half-dead, that I don't have time! Lee Hastings England UK Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2000 Report Share Posted June 25, 2000 I don't think this list should be used for advertising. Is this list moderated? I'm not going to stay if this issue is not addressed. Digest Number 393 ------------------------------------------------------------------------ Turn your EGROUP into a GROUP BUYING GROUP! Join beMANY! today. 1/4124/12/_/469673/_/961922273/ ------------------------------------------------------------------------ Send blank message to candidiasis-unsubscribeonelist if you want to UNSUBSCRIBE ! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 14, 2000 Report Share Posted September 14, 2000 In a message dated 9/13/00 11:33:00 PM Central Daylight Time, egroups writes: << Karyn: has ADHD big time, and we have tried that combo recently....at first, the Clonidine made him very sleepy, then he became " used " to it and we went up to a full 1 mg, 3 x's a day, in addition to about 7.5mg of Adderral a day.......worked for about 2-3 mos. then wasn't effective at all. But every kid is different..... >> , Thanks for the info. My foster son has been on clonidine for almost a year now and it still makes him drowsy. At least I think it is the clonidine. He gets drowsy mid-morning and then recovers. I'm thinking that we may need a dose of clonidine after school to get through to bed time. Oh well, we'll try the adderal first and see if it works. Karyn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 19, 2001 Report Share Posted May 19, 2001 This concerns me. My daughter is 15 months old. I have been using a flouridated nursery water (bottled water) product for her. She does not drink tap water. Because I am using this, the pediatrician did say he would not prescribe any flouride drops or anything like that. I used this water also to mix her powdered formula when she was an infant. I do know that this nursery water has far less flouride that other flouridated bottled water products on the market. Since she is not getting the flouride from the tap water, then is this the same as drinking tap water and not excess flouride? Hmmmmmmm..... Jeanne [ ] Digest Number 393 >_ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2002 Report Share Posted October 4, 2002 Hi there , sorry it has been so tough for your son .I think people who arent doctors need to be careful when talking about normal.My daughter was in hospital for 5 days after her last mastoidectomy ,so that she could have IV antibiotics , because infection had ruined previous grafts. That was April and now she is fine.When you talk about bandaging ,maybe you mean packing ,and 6 to 8 weeks is normal.Maybe your child had a complication.Ears are peculiar objects ,and your doctor will know your sons ear well. But maybe you need to ask more questions. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 7, 2003 Report Share Posted March 7, 2003 Marina, I'm sorry to read about your trouble. My daughter (7) has similar behaviors(hand biting, throwing herself to the floor) but not to such an extent. We have been able to curb them and relieve some of her frustration through a sensory approach. Deep pressure, joint compressions and having a trampoline available. If you haven't tried this already if may be an idea. If you'd like more info, feel free to contact me privately. It seems my daughter needs a lot of sensory input in order to compose herself. Good luck, Ann > > Message: 1 > Date: Thu, 6 Mar 2003 22:04:59 -0800 > From: " Marina Siddoway " <tsidd@...> > Subject: SIBs > > Hello! > I just joined this list because we have a 12 yr. old daughter with > autism who has terrible self-injurious behaviors. She hits herself in > her face; has blackened her eye and cheek recently, and also head-bangs > against walls, the floor, windows. It is very terrifying at times when > she gets very bad. She bites her hands, but not hard enough to draw > blood. She also leaps into the air and then propels herself to the > floor very hard, so her knees, elbows and tops of her feet are all > bruised, too. > > We are at our wits end lately. I have read and read about meds for > this, and all seem to have terrible side effects and it appears it's a > total crap-shoot to find " the right one " , so have been trying > nutritionally to find some answers, but just when I think I have her > supplements figured out, the behaviors escalate again. I am also > reluctant to use medication because of poor liver function, but at this > point, we may have no other choice. > > I would appreciate any experiences, thoughts, ideas on this, Rx or > supplements anyone has used with success. > > Thanks. > > Marina, mom to Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 7, 2003 Report Share Posted March 7, 2003 Marina, I'm sorry to read about your trouble. My daughter (7) has similar behaviors(hand biting, throwing herself to the floor) but not to such an extent. We have been able to curb them and relieve some of her frustration through a sensory approach. Deep pressure, joint compressions and having a trampoline available. If you haven't tried this already if may be an idea. If you'd like more info, feel free to contact me privately. It seems my daughter needs a lot of sensory input in order to compose herself. Good luck, Ann > > Message: 1 > Date: Thu, 6 Mar 2003 22:04:59 -0800 > From: " Marina Siddoway " <tsidd@...> > Subject: SIBs > > Hello! > I just joined this list because we have a 12 yr. old daughter with > autism who has terrible self-injurious behaviors. She hits herself in > her face; has blackened her eye and cheek recently, and also head-bangs > against walls, the floor, windows. It is very terrifying at times when > she gets very bad. She bites her hands, but not hard enough to draw > blood. She also leaps into the air and then propels herself to the > floor very hard, so her knees, elbows and tops of her feet are all > bruised, too. > > We are at our wits end lately. I have read and read about meds for > this, and all seem to have terrible side effects and it appears it's a > total crap-shoot to find " the right one " , so have been trying > nutritionally to find some answers, but just when I think I have her > supplements figured out, the behaviors escalate again. I am also > reluctant to use medication because of poor liver function, but at this > point, we may have no other choice. > > I would appreciate any experiences, thoughts, ideas on this, Rx or > supplements anyone has used with success. > > Thanks. > > Marina, mom to Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 18, 2005 Report Share Posted May 18, 2005 Hi, Does anybody have experience with making high-speed interenet connections friendly to people with EHS. We got a DSL connection not to long ago, and I've had no end of trouble with it. Even though I sleep 40 ft from the phone line it still causes trouble sleeping. I've wrapped the phone line in aluminum foil which partially helps. Was thinking of trying cable modem, though I've heard ground currents can be a problem with cable, as well as the high frequency stuff. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2005 Report Share Posted June 27, 2005 I am an avid tea drinker. I discovered KT and began making my own when GT Dave ran out at my Co-op. Thus far I have experimented with all different types of tea. White Peony, Qunicsenchia, Phoenix Dragon (Hand-rolled Jasmine), Wenshan Baozhong Formosa Oolong, Black Dragon China Oolong and Copenhagen Earl Grey. I have mixed some using two teaspoons of Oolong and White Peony, the others I haven't mixed half black & half green. White Peony by itself was fantastic, as is the Jasmine. I'm looking forward to trying the Earl Grey (my favorite tea). I would like to try making this with a Dammann Framboise which is a rich black tea flavored with a high quality raspberry oil. If my Earl Grey turns out I will try the Dammann. I also make a sourdough starter for bread from teh Oolong & Peony mix. The bread is also fantastic. Catharren Quote Link to comment Share on other sites More sharing options...
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