Guest guest Posted November 28, 2007 Report Share Posted November 28, 2007 Hi Beth, My son is 6 years old, and about 20 kg. We started last year per reccomendation of a biochemist (from Mannatech) at 1/4 tsp 3 times per day, with meals and before bed, after 21 days, he told me to increase the dose to 1/2 tsp 4X/day, with every meal and before bed. Maybe you can start at half of this dose and work yourself up as his body adjusts. I buy the Classic Ambrotose powder and mix it with his milk, cereal, yougurt, mac n cheese, juice, just about anything. He also mentioned that if you buy Granulated Soy Lecithin ( Labs has a good one) and give it at the same time (also same amount) of the Ambrotose, it improves its potency. Talk to the person that sold you the Ambrotose and discuss the cell memory effect, this means that your child can get the symptoms of a cold when you start, but this is just the cells recalling any illnesses that he/she had in the past. The most important thing with Ambrotose and any other supplement is consistency and continuance. They are not medicine and it usually takes a while to see benefits. Let me know if you have any other questions. Deborah > > Hi > I have purchased tub of ambrotose powder as i'm interested in trying it > with Torin. Can someone tell me how much i should be giving Torin > please? He's about 11kg and is 17 months old. Any suggestions > concerning dose and method would be great. thanks so much > > Beth mum to torin, bilateral PMG (excluding frontal and opcipital lobes) > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2008 Report Share Posted February 26, 2008 Hi! I am a bit late to respond to this, but if you still have it, I'd be interested. Thanks. Sue Mom to Meghan(12) and (6)BFPP, mod spastic quad CP > > Hi all, > > I have an unopened 5.3oz container of Ambatrose complex powder with an expiration date of 1/09. I am asking $50.00 plus shipping. As always, first to ask gets. > > Jim > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2008 Report Share Posted February 27, 2008 Hi Sue, I have still have it. I can check on shipping costs today, but, through the USPS it shouldn't be too much. I'll write when I get the cost. Jim Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2008 Report Share Posted February 28, 2008 Hi, I drop in rarely to check on things, as my daughter seems to be doing fine and her diagnosis is actually pachygyria rather than polymicrogyria. Anyway, I wanted to offer my 2 cents on your son's breathing issue. My daughter had a boy in her class, and I am not sure of his diagnosis, but he was on oxygen full time until he had an operation that allowed his lungs to expand appropriately. Apparently the rib cage was not growing appropriately, thus not letting the lungs to grow or to expand. Just a thought, may be worth looking at. And since he has a trach now, it seems that the growth in his throat isn't the main obstacle. Maybe have them x-ray his chest, etc. Beth Beth Troutman Special Education Partners, LLC P.O. Box 10786, Burke, VA 22009; a All information provided by Special Education Partners,LLC is for informational purposes only. Reference to treatment, therapy, program, or legal options, or to providers of these services, is not an endorsement by Special Education Partners,LLC. Special Education Partners,LLC assumes no responsibility for use of this information. This message is for the designated recipient and contains private information--use of the email by any other recipient is prohibited. Quote Link to comment Share on other sites More sharing options...
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