Guest guest Posted June 17, 2002 Report Share Posted June 17, 2002 wow!! That is great! Tell me more tell me more!! Jenn > Hi Jenn, > My friend and I have met a man that has a great zapper > .He works closly with Dr.. The interesting thing > is that he has a harness that works for animails too. > > I have worked on my self with the zapper and with my > cats, family and friends. It is very effective. > > If you or anyone else would like to know more shoot me > an email. The zapper itself is very affordable and is > true on the frequency (not unstable). > > Take care, > Georgi > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2002 Report Share Posted June 18, 2002 hi i would love to know more about the zapper you mentioned. thanks rita >From: Georgi Murray <georgimurray@...> >Reply-Dr >Dr >Subject: Jenn >Date: Mon, 17 Jun 2002 18:19:42 -0700 (PDT) > >Hi Jenn, >My friend and I have met a man that has a great zapper >.He works closly with Dr.. The interesting thing >is that he has a harness that works for animails too. > >I have worked on my self with the zapper and with my >cats, family and friends. It is very effective. > >If you or anyone else would like to know more shoot me >an email. The zapper itself is very affordable and is >true on the frequency (not unstable). > >Take care, >Georgi > >__________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2002 Report Share Posted June 18, 2002 The original message is: Cord Blood and Parkinson Plus Questions I would like for someone to answer my questions. I have access to cord blood from the Umbilical Cord from a family member when the baby is born. I am a 62 year old male who was diagnosed with Parkinson Plus a couple years ago. Have you done Parkinson Plus research or with cord blood? What is your recommendation and treatment? How do I find if, I am compatible with the cord blood? If I have a donor, what is the procedure for capturing and storing the same? What is the success of this procedure? Who will give me the injection? Please EMAIL your responses. Thanks Joe Nichols Jenn>Date: Mon, 17 Jun 2002 18:19:42 -0700 (PDT)>>Hi Jenn,>My friend and I have met a man that has a great zapper>.He works closly with Dr.. The interesting thing>is that he has a harness that works for animails too.>>I have worked on my self with the zapper and with my>cats, family and friends. It is very effective.>>If you or anyone else would like to know more shoot me>an email. The zapper itself is very affordable and is>true on the frequency (not unstable).>>Take care,>Georgi>>__________________________________________________> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 7, 2002 Report Share Posted October 7, 2002 In a message dated 10/5/2002 9:41:03 AM Eastern Daylight Time, jgadeberg@... writes: ... i am attempting to try the whole repositioning thing but he favors that side of his head.. so he screams when he cannot turn his head that way.. when feeding Hi, Welcome to the group! This sounds very much like torticollis, a tight neck muscle, which is making your son physically unable to turn in that direction. Ask your ped to check him for torticollis, its important so that you can start with physical therapy to stretch out that tight muscle. I will also attach a link that helps give you an idea of what types of exercises help, and a great carrying hold to help seperate that neck and shoulder. If your child is tilting his head also, this is another sign of tort. Some kids tilt, some do not. Some have great range in both directions, and only have a tilt- so tort in itself can get very complex. It sounds as if the tort started inutero, much like my son, only now I can say that in hindsight we see the signs, at birth we didn't see it as clearly. Your Doctor may want a neurologist to look at your son, and also schedule an MRI to rule out anything other than just a muscular problem, some tort is caused by fusion of the spine abnormally, very rare, most tort is muscular. Also, check out www.torticolliskids , compare pics and see if it looks familiar. I would urge you to begin now with the process, tort is not an overnight fix of stretching out that muscle, it can take a few months honestly, but it is very treatable and for that very slim chance that pt is not working it out, surgery is used as a last resort. You can do things to help now also, position interesting toys to the side he does not want to turn to, prop the head midline in the carseat, limit time on the back of the head, and reposition, reposition, reposition as much as you can. Good luck to you and if I can help in anyway, please email me. There are many tort moms on board as well, and can offer you great advice as well. Hang in there! It may seem overwhelming, but just know that if it is tort, my son was severe and we have reached resolve. 'Mom (dx with tort at 2mnths, pt from 3-9/10 months, DOC grad 5-8mnths old) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 20, 2004 Report Share Posted November 20, 2004 I think the purpose of the hot probe inserted into the disc is to actually shrink the disc by heating the contents to an elevated temperature. I briefly discussed the treatment with my PM doctor but since my thoracic disc is calcified it wouldn't do much good. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 20, 2004 Report Share Posted November 20, 2004 I think the purpose of the hot probe inserted into the disc is to actually shrink the disc by heating the contents to an elevated temperature. I briefly discussed the treatment with my PM doctor but since my thoracic disc is calcified it wouldn't do much good. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2007 Report Share Posted January 13, 2007 Jenn, My daughter has had an eeg already. No seizures showed up at the time. She hasn't had the blank stare thing in a while, so maybe part of the dietary things I am doing is helping her. I have been doing what I can with her diet based on the book Nourshing Traditions by Sally Fallon. We are currenly looking for a new autism doctor, the one we were using went out of practice. Hoping that we can take her to PA at the haverford wellness center and do the protocol of Dr. Kane. We'll see after hubby gets back from his Iraq tour.(in august 07) How old is your daughter? What all have you done with her? Have long have you been doing the enzymes? Ginger Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2007 Report Share Posted January 13, 2007 The military requires you to have vaccines especially when you deploy. So needless, to say, yes he has been pumped full. However, he got out of getting the flu one and said that he had already gotten it. ) I know that my daughter received a lot of junk from me.(viruses, heavy metals) I have six lovely silver fillings in my mouth which I want to get taken out in the near future. My daughter is 6 and is still pretty much non-verbal.(in other words, nothing really consistent) I am really not interested in the Dan! protocol because although it is in the right direction, I don't think they focus on fats enough. I mean 1tsp isn't enough. Our children are severely deficient in omega 3's and 6's. Ginger Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2007 Report Share Posted January 13, 2007 Just because no seizures showed up at the time, it may not mean that it's not a problem. Dietary does help seizures. My dd has been on SCD for 20 months. I think the die-off really triggered them. It is the body's way of resetting itself. My dd is 6. We have done a whole lot with her. I will email you that in a different email because it's lengthy. We haven't been doing only the candidase enzyme against the yeast. We have had this much improvement without them so far. We are though going to add them in next week. I can't wait. I hope she doesn't get anymore high fevers like last night. We are doing biotherapeutic drainage with her right now through a ND to open all her blockages up to allow her to drain. The inflammation produces alot of mucous in the body. Without this drainage, toxins build up in the tissues when released through chelating. This is proibably step #1. DAN! docs and others cannot possibly be helpful if they want to supress conditions. How old is you little girl? You say your husband is in Iraq? God Bless you. How long has he been in the service? Did he have certain vaccines? The parent's toxic load, especially mom's has a huge impact on our unborn babies health. I think the vaccines were just the last straw. Every person has a toxic threshold. Our kid's met their match. I know a young man who became ADHD, and inusulin dependent due to a very bad virus he got when he was a teenager. He was NT before that all his life. That was his final straw of toxins. His body was too gunked up to deal with it. We ALL need the drainage. Jenn L ginger587@... wrote: Jenn, My daughter has had an eeg already. No seizures showed up at the time. She hasn't had the blank stare thing in a while, so maybe part of the dietary things I am doing is helping her. I have been doing what I can with her diet based on the book Nourshing Traditions by Sally Fallon. We are currenly looking for a new autism doctor, the one we were using went out of practice. Hoping that we can take her to PA at the haverford wellness center and do the protocol of Dr. Kane. We'll see after hubby gets back from his Iraq tour.(in august 07) How old is your daughter? What all have you done with her? Have long have you been doing the enzymes? Ginger Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2007 Report Share Posted January 13, 2007 My dd up until yesterday, was VERY picky about saying anything. Her speech is not well understood but, she did try to use 2 words at a time sometimes. She is now doing really well saying new words today probably at a quicker speed now that she is calmer. I am sorry to hear about the toxin overload. We are too. When was your dd born? I agree about them not getting enough fats. Their bodies need it for repair. I give K 3 tsp. fish oil & 3 CLO caps almost everyday switching on/off to krill oil & using coconut oil, free-range chicken & beef fats, & organic cooking oils too. Good for your husband saying he already got his flu shot! Smarty! I simply just tell everyone that I got a milk & egg allergy and they don't bother me. Sometimes the allergies to foods CAN be just sensitivities that cause some sinus infx. etc. so, no one pushes any further. I am a nurse aide among other things. This is where I feel I am toxic. I'll let you know how we do with the enzymes next week. Jenn L ginger587@... wrote: The military requires you to have vaccines especially when you deploy. So needless, to say, yes he has been pumped full. However, he got out of getting the flu one and said that he had already gotten it. ) I know that my daughter received a lot of junk from me.(viruses, heavy metals) I have six lovely silver fillings in my mouth which I want to get taken out in the near future. My daughter is 6 and is still pretty much non-verbal.(in other words, nothing really consistent) I am really not interested in the Dan! protocol because although it is in the right direction, I don't think they focus on fats enough. I mean 1tsp isn't enough. Our children are severely deficient in omega 3's and 6's. Ginger Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 14, 2007 Report Share Posted January 14, 2007 Ginger, Just to let you know, there is no specific protocol with DAN for fatty acids. The good DAN docs treat each child individually and prescribe what is needed. I have three children involved with a DAN pediatrician and two others as well. All take way more than a tsp. of EFA's a day. I have seen wonderful things with all my children using higher doses of EFA's. I agree, fats are important. Blessings to you and your family. You have a lot on your plate! Anne > > The military requires you to have vaccines especially when you deploy. So > needless, to say, yes he has been pumped full. However, he got out of getting the > flu one and said that he had already gotten it. ) I know that my daughter > received a lot of junk from me.(viruses, heavy metals) I have six lovely > silver fillings in my mouth which I want to get taken out in the near future. My > daughter is 6 and is still pretty much non-verbal.(in other words, nothing > really consistent) I am really not interested in the Dan! protocol because although > it is in the right direction, I don't think they focus on fats enough. I mean > 1tsp isn't enough. Our children are severely deficient in omega 3's and 6's. > > Ginger > > > > Quote Link to comment Share on other sites More sharing options...
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