Guest guest Posted July 29, 2002 Report Share Posted July 29, 2002 At 08:13 AM 7/29/02 +0000, you wrote: >does that depend on the type of bottle? I've had EO mixes in a plastic >bottle for >at least two years without any problem. of course it depends on the type of plastic...they will do fine, in dilution, in PET plastic.... but in general, no...they won't do well. >Doesn't vodka contain too much water to allow an emulsion? depends on the proof...low proof may not work, everclear will work, or high proof vodka > I also thought EO's >didn't need polysorbate. polysorb will allow them to dissolve in the water... without SOMETHING to dissolve them, the eo's will form a layer and float on the top. Your source for superb Essential Oils, Aromatherapy Accessories, Information, Books and more! Visit us at: <http://www.naturesgift.com> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 20, 2003 Report Share Posted January 20, 2003 Dale, hope Katy feels better soon. I have a brother with diabetes he is now 32 and he struggled with teenage rebellion with his illness, he wouldn`t listen to his dr`s or family. I think they just want to be considered " normal " . She`ll come through it ok. Carol _________________________________________________________________ Add photos to your e-mail with MSN 8. Get 2 months FREE*. http://join.msn.com/?page=features/featuredemail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 6, 2003 Report Share Posted February 6, 2003 > Are there any pretzels on the market that don't have corn syrup in > them (or a bunch of other nasties)? Thanks. Snyder's has lots of pretzels without corn syrup and artificial stuff...of course, they have wheat. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2003 Report Share Posted May 30, 2003 Count me in! My challenge ends July 4th, but I never offically entered so I will this one, might as well get some free products I use anyway, lol. in Texas > ________________________________________________________________________ > > Message: 5 > Date: Fri, 30 May 2003 14:20:17 -0000 > From: " " <cmsteph@...> > Subject: june 1 challenge > > who else is doing the june 1 challenge? dh and I are going to do it > (for the $150 gift certificate!) > steph > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 2, 2003 Report Share Posted September 2, 2003 dennis, kristie, mario, hi i'm mick ( nick name) i received 4 shots also starting in 99, a week after first shot the flu symptoms started and lasted for ever it seemed. the headaches were bad, and still are. after receiving the 3 rd or forth can't recall now, i started have severe abdominal problems to add to the list. soon i was admitted to the local hospital put on antibiotics released, admitted again underwent surgery to remove part of my colon, while in this time discovered i was hyperallergenic and came close to dying, for real. went to icu to keep me stable. admitted for a third time to get infections under control. joint pains, muscle pain fatigue, depression you know what all i'm talking about. started having chest pains tho nothing was ever found. have been on a myrad of meds, am doing somewhat better then i was, better living thru chemistry. after 16 months i finally got to see a VA nurse that took down a med history and asked some questions from a question aire. that was my VA exam ! then i get the letter denying me...... the systems is rediculous, the politicians offer lip service reguardless of party , dod refuses to admit that they made us sick, and we are left to fend for ourselves...... thats some debt of gratitude for service to your country. sorry if i'm a lil hostile toward " The System " but it has gotten so old to keep hoping for something thats probably never going to come. later all Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2004 Report Share Posted November 3, 2004 In a message dated 11/2/2004 11:36:34 PM Eastern Standard Time, writes: Whew...after all that I just have one question for now: why magnesium in boiling water? I mix Gregor's capsules with water and give them via oral syringe, but just use cold water or juice, but I'm always keen to find better ways of doing things! thanks, Edinburgh ----- Original .. .. >>>>> To increase it's absorption, that's why. We've been doing this for three years. An alternative to dissolving Magnesium in boiling water that we now use is taking Milk of Magnesia. MoM has 400 mg of Magnesium per teaspoon. There are also several brands of LIQUID Magnesium of other types on the market. You have to experience the difference for yourself. mjh http://foxhillfarm.us/FireBasil/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2004 Report Share Posted November 3, 2004 In a message dated 11/2/2004 11:36:34 PM Eastern Standard Time, writes: Date: Tue, 2 Nov 2004 08:40:43 -0500 From: " Mike Mchugh " <mcpitza@...> Subject: Re: New piece to our puzzle Barb, That center sounds great... are you aware there is a similar one here in the US. In Philadelphia called the Institute for Human Achievement. Here is there website: http://www.iahp.org/ Click on the side panel box " Programs for Brain Injured Children " - they consider any seizure disorder a brain injury. Good luck . .. .. >>> The problem with the Institute for my son is that he is now 39 years old and the Institute will not treat him. mjh http://foxhillfarm.us/FireBasil/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2004 Report Share Posted November 3, 2004 In a message dated 11/2/2004 11:36:34 PM Eastern Standard Time, writes: From: " Don Vance " <dvance@...> Subject: Re: Experience with VNS Walt, I also have a son with epilepsy named . He has not had an early morning hiccup type seizure now for 4 weeks! Just reporting in as instructed. I have him taking only a 1/2 ounce of BodyBalance as he is about 40 lbs. Recommended dosage is 1 ounce per 100 lbs! Free quarts to try are being given away at www.healthgotit.com I plan to ask his doctor to back off on the two meds he is taking slowly, one being clonazepam, and the other is lamictal. I will continue to report on his condition, while using this awesome liquid nutrition thats absorbed to the cellular level at 98% in just minutes. Remember this is a giveaway, nobody is selling here as no one has to pay for the product. That helps all of the " yea butters " you know, " yea but " , to go ahead and prove how worthless it is to themselves, without a hit in their pocketbook! Don ----- Original Message ----- .. .. >>>> Liquid minerals from WalMart, Sam's Club, etc for $10.00 a quart (month's supply) is another option here. I have a quart right here in my son's hospital room. We have been in this hospital now for six weeks. He is now off bag feeding as of yesterday and today I will slowly restart his supplement program, beginning with the liquid minerals. mjh http://foxhillfarm.us/FireBasil/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2004 Report Share Posted November 3, 2004 I have attended the brain injured child course. Its a hefty fee (apx.$900) for a week long course, but the information you get makes it very worthwhile.The program is very time consuming, but it works.I have met parents of children who made REMARKABLE improvements, and recoverys. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2004 Report Share Posted November 3, 2004 WOW!!!!Yeah, i was referring to the course in Philidelphia. It was like $895 or something like that. I just attended in June of this year. Happy the price dropped for me Did you do the programs? What kind of results did you get? Did you do the masking program for seizures? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 3, 2004 Report Share Posted November 3, 2004 > I have attended the brain > injured child course. Its a hefty > fee (apx.$900) for a week long > course,... SARAH: Are you referring to the Doman course at IAHP in Philadelphia, PA; or this one, M.A.P.S., in Canada? I would have assumed you were talking about the IAHP course, but when you said $900, it threw me off because the cost for us was $1600 in 2001. Tim but the information you get makes it very worthwhile.The > program is very time consuming, but it works.I have met parents of children > who made REMARKABLE improvements, and recoverys. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 Hi! The brain injured child course is a 5 day course from around 8am to around 6 or 7 p.m. It was founded by an excellent neurosurgeon and physical therapist i believe around the 50's or 60's. They studied the brain and how it develops. They traveled around the world studying the different ways children develop, due to their enviroment and ways of living. Any neurological problems, they believe is a brain injury. They came to the conclusion the brain heals itself, with enough stimulation, and opened the institutes to heal brain injury. The staff consists of different kinds of doctors, and therapists. During the week long course you learn so much about the brain and development of children. Their are many interesting lectures. They give demonstartions on how special needs kids think, see, hear, etc., the world. They help you figure out what cognitive level your child is on, and show you the stimulation programs that are best for your child. They have children already on the program demonstrate the achievements THEY have made, you can talk to their parents as well. I met a man from France in the bed and breakfast I was staying at, whos daughter ate a poisonous mushroom, and lost all her abilities. The doctors said she'd be a vegetable forever. They came to the institutes, and have been bringing her to the institutes for 2 years. When I met her, she had already regained her ability to talk and was crawling, beginning to learn to walk. The institutes philosiphies are if you start at the bottom of their " developmental profile " , and work your way up step by step, your brain can heal itself. They do " patterning " to help the brain learn what its sposto be doing. It is VERY interesting, and amazing when you meet the kids this program is helping. I will admit this program is very time consuming once you bring it home to do with your child. You definetly need 2 people quite a few times a day to help with the patterning. There is sensory stimulation programs. Auditory processing. Mobility. Tactile stimulation. On the program, my daughter has learned how to " read " some sight words. she has learned how to kick, and throw a ball. Her fine motor skills improved, she can open jars now and unlock doors. She was very sensitive to touch, and that has improved. She is also listening better to what i say, before it was like she wouldnt hear me. I have only been doing the program for about 2 1/2 months. I dont do it nearly as much as the institutes recommend. Unfortunetly it is only me and my daughter, and i dont have the help needed. I stayed at a bed and breakfast for $55 a night right across the street. It was nice, cuz the only people that were there is parents who were also attending the program, so we had eachother to talk to, and lean on. I know i wrote alot, but i do believe this program is well worth it, and would recommend anyone with a cognatively impaired child go. They also believe kids with seizures shouldnt be on aed's. They have weaned kids off and found the majority do better with out. They believe a seizure is a sign of the brain healing itself, and say the drugs prohibit it from doing so. Their website is http://www.ihap.org Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 > Happy the price dropped for me Me too. > Did you do the programs? No. We opted not to do it. Tim Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 , Can you please tell me how you went about it and how it works? Also, has it worked for you and where do you live? I live in Florida, did you have to find a place to stay while there? Thanks! Grace I have attended the brain injured child course. Its a hefty fee (apx.$900) for a week long course, but the information you get makes it very worthwhile.The program is very time consuming, but it works.I have met parents of children who made REMARKABLE improvements, and recoverys. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 , Can you please tell me how you went about it and how it works? Also, has it worked for you and where do you live? I live in Florida, did you have to find a place to stay while there? Thanks! Grace I have attended the brain injured child course. Its a hefty fee (apx.$900) for a week long course, but the information you get makes it very worthwhile.The program is very time consuming, but it works.I have met parents of children who made REMARKABLE improvements, and recoverys. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 , Can you please tell me how you went about it and how it works? Also, has it worked for you and where do you live? I live in Florida, did you have to find a place to stay while there? Thanks! Grace I have attended the brain injured child course. Its a hefty fee (apx.$900) for a week long course, but the information you get makes it very worthwhile.The program is very time consuming, but it works.I have met parents of children who made REMARKABLE improvements, and recoverys. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 Yes, the book is very interesting also. You really have to read into it to understand, though. They have a bookstore on line with different books and packages that go into more depth about the specific programs you will be doing with your child.I believe they even have lectures on tape. sarah Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2004 Report Share Posted November 4, 2004 , Thank so much for your post and for the info about the program and I must say that when you got to the part about seizures and that they don't believe that children should be on AEDs, that's what I'm believing as well. I was contacted by the program registrar and explained that I cannot leave right now for the program and she told me to buy the book How to help your brain damaged child and I've already bought it through Amazon.com and will read it and work on some of the things until I can go there, if that ever becomes possible. She said that I can do the homestudy program which the book will tell me about. Have you read the book and does it help alot? Grace sarahbri813@... wrote: Hi! The brain injured child course is a 5 day course from around 8am to around 6 or 7 p.m. It was founded by an excellent neurosurgeon and physical therapist i believe around the 50's or 60's. They studied the brain and how it develops. They traveled around the world studying the different ways children develop, due to their enviroment and ways of living. Any neurological problems, they believe is a brain injury. They came to the conclusion the brain heals itself, with enough stimulation, and opened the institutes to heal brain injury. The staff consists of different kinds of doctors, and therapists. During the week long course you learn so much about the brain and development of children. Their are many interesting lectures. They give demonstartions on how special needs kids think, see, hear, etc., the world. They help you figure out what cognitive level your child is on, and show you the stimulation programs that are best for your child. They have children already on the program demonstrate the achievements THEY have made, you can talk to their parents as well. I met a man from France in the bed and breakfast I was staying at, whos daughter ate a poisonous mushroom, and lost all her abilities. The doctors said she'd be a vegetable forever. They came to the institutes, and have been bringing her to the institutes for 2 years. When I met her, she had already regained her ability to talk and was crawling, beginning to learn to walk. The institutes philosiphies are if you start at the bottom of their " developmental profile " , and work your way up step by step, your brain can heal itself. They do " patterning " to help the brain learn what its sposto be doing. It is VERY interesting, and amazing when you meet the kids this program is helping. I will admit this program is very time consuming once you bring it home to do with your child. You definetly need 2 people quite a few times a day to help with the patterning. There is sensory stimulation programs. Auditory processing. Mobility. Tactile stimulation. On the program, my daughter has learned how to " read " some sight words. she has learned how to kick, and throw a ball. Her fine motor skills improved, she can open jars now and unlock doors. She was very sensitive to touch, and that has improved. She is also listening better to what i say, before it was like she wouldnt hear me. I have only been doing the program for about 2 1/2 months. I dont do it nearly as much as the institutes recommend. Unfortunetly it is only me and my daughter, and i dont have the help needed. I stayed at a bed and breakfast for $55 a night right across the street. It was nice, cuz the only people that were there is parents who were also attending the program, so we had eachother to talk to, and lean on. I know i wrote alot, but i do believe this program is well worth it, and would recommend anyone with a cognatively impaired child go. They also believe kids with seizures shouldnt be on aed's. They have weaned kids off and found the majority do better with out. They believe a seizure is a sign of the brain healing itself, and say the drugs prohibit it from doing so. Their website is http://www.ihap.org Quote Link to comment Share on other sites More sharing options...
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