Guest guest Posted February 28, 2008 Report Share Posted February 28, 2008 Here's one more archive message of our experience (after the list of links to help your research). Please do follows 's advice and research very thoroughly the MB12 treatments ahead of time, the probable and potential side effects (including temporary behavioral implications), how you shouldn't make ANY other dietary changes or supplement changes during the first 5 weeks to allow a clean evaluation of whether the patient responds or not and how, additional mineral/vitamin/other supplements that you may need to add as the MB12 starts working. Stay in contact with your doctor to discuss in a short timeframe all changes observed and be ready to alter the program including stopping it, if deemed necessary. (This applies to ANY type of medical or other treatment for any of us and does not mean the treatment is unsafe.) Resources about various MB12 therapies www.drneubrander.com www.stankurtz.com http://www.childrenscornerschool.com/mb12nasalspray.htm http://www.talkaboutcuringautism.org/medical/methyl-b12-treatments.htm Discussion groups on MB12 (but it is talked about about on most autism boards) mb12 valtrex/ Scientific studies about MB12/Methylation Cycle http://www.drneubrander.com/Files/Oxidative Stress.pdf (Dr Jill ) http://www.drneubrander.com/Files/Deth Testimony.pdf (Dr Deth) http://www.autismweb.com/forum/viewtopic.php?t=8529 & postdays=0 & postorder=asc & Here are a few of the compounding pharmacies (does require prescription)..price shop and check out MB12Valtrex where they are in the know about pricing comparisons. I don't think sublingual drops require a prescription though but check all ingredients if you don't get it compounded clean. http://www.coastalcompounding.com/ http://www.collegepharmacy.com/ http://www.fallonpharmacy.com/ http://www.hopewellrx.com/wellness/links.shtml http://www.leesilsby.com/contact.html On 05July2007 momresearch wrote Hi Wendi Here's some info based on our experience... The MB12 shots are given with a syringe and tiny tiny needle (the ones used to give insulin) - and it's given in fatty tissue just below the surface. It's nerve-wracking on the first one you give - we give our son his while he's sleeping about 5am (my husband is up that early - not me) so we take advantage. I tried giving it after he was just asleep but often I'd fall asleep waiting for him to get asleep good enough. I even tried the Emla cream for a while but that would wake him up twice (once to put on the Emla and once to give the shot). It really is a painless shot - if one does have pain it is probably because the pH of the formula is too high (that has happened to some peoples batches that the pharmacy replaced for free). As for there not being side effects........that's not so true. The MB12 alters the body's metabolic system in some way too...not only can there be hyperactiveness for up to several months, there can also be insomnia, increased mouthing of objects (like putting things in your mouth like an infant, eating dirt or licking things you wouldn't expect). My son had a neurologic reaction that was rare but it happened for several weeks...but improved after adding in folinic acid (that we had to them remove because it made him spacey...not present). We did get some pluses mixed in with the period of adjustment for his body to get used to the new changes -- he would go to his own bed when I'd say it was time for bed and WANTED TO, his eye contact clicked in, he could distinguish between hot and cold, he acknowledged and communicated pain when he hurt himself - before he was indifferent. He could say and understand more things, too, so there was an improvement in his auditory processing system. His digestion also changed for the better but that was due to a combination of treatments and which cannot be attributed to any single treatment by itself. The MB12 wasn't a magic talking shot, but has helped his global well-being. (oh - and he hasn't eaten meat in 3 years so he doesn't get much B12 in his diet otherwise due to his severe food selectivity) As you begin this process, observe objectively, keep an open dialogue with your DAN! for ANY odd changes or questions/doubts you may have....it may take several weeks to notice some changes - good or bad or none. Check out Dr. Neubrander's questionnaire (it's on his website)...he also has a forum where he and his brother Rick respond to questions. And remember not to make any other dietary or supplement changes during the first 6 weeks - unless some of the negative symptoms might warrant the addition of zinc or folinic/folic acid earlier (with your DAN! ok). At the end of 6 weeks, discuss with your DAN! and decide together if your child " responded " or not - not all kids do. P.S. Don't worry about a build up because the MB12 is water soluable. If you accidently were to inject into muscle (i.e. too deep which is hard to do with the tiny needle) the urine would be red where the MB12 is expelled from the body. Quote Link to comment Share on other sites More sharing options...
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