Guest guest Posted September 5, 2009 Report Share Posted September 5, 2009 Hi I have been reading all the posts and never posted infact this is my first post. I heard Yaskos's protocol and I just want to hear from parents who have used her protocol. please share the good or bad experience you have experienced.It realy will help my disission Before I do any move. Please share what ever idea you have. Thank you. Magt Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 6, 2009 Report Share Posted September 6, 2009 I have been doing Yasko for about 3 years - with a 5 month side trek to do biofilm - i think the genetic testing is very helpful - guiding which supplements to use - and the metal program has been great for my son - as well as the ammonia program to get his ammonia levels under control - downside - very expensive - very- when we are in full metals program it could be about $75.00 a day. - i think Yasko is a great foundational program - to get the methylation process cleaned up - as well as the gut program - very important - - i worked with a practitioner in New Jersey b/c i was so overwhelmed and confused in the beginning - but there is a very good chat board with very experienced parents to help. lisa c > > Hi I have been reading all the posts and never posted infact this is my > first post. I heard Yaskos's protocol and I just want to hear from parents > who have used her protocol. please share the good or bad experience you have > experienced.It realy will help my disission Before I do any move. Please share what > ever idea you have. > Thank you. > Magt > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 6, 2009 Report Share Posted September 6, 2009 Mag, Well, we are using Dr. Amy's protocol. . .sort of. I find her system of working through the email and not talking directly to us to be a little difficult and she doesn't really offer a lot of direction. I ordered the genetic testing for my son and it called for certain supplements. Many he had already been taking (purchased through vitacost). Others, I had tried but were not impressed with any results from them. But she has supplements that she specificially likes for sale on her site but they would cost between $1-2,000 per month if I used them all so I just stick to buying them from vitacost. One thing she has that others do not, is the RNA drops. They are specific for they type of mutation problems the child has and so that has helped to know which ones to buy and they do seem to help. Also, she has digestive enzymes that are cheaper than anyone else's ($20 for 100). She says, "Learn the science." Well, I can't figure out the science and I've tried. It is too complicated for me--I have an art background, not science. Another thing is that we are supposed to have tests done monthly to monitor the results. This is another $3-400 and I cannot afford that, either. Maybe others have better luck but I have not been wowed. Maybe I just don't have the resources to follow her program. sally To: mb12 valtrex Sent: Saturday, September 5, 2009 8:35:25 AMSubject: Amy yasko's protocol Hi I have been reading all the posts and never posted infact this is myfirst post. I heard Yaskos's protocol and I just want to hear from parentswho have used her protocol. please share the good or bad experience you haveexperienced. It realy will help my disission Before I do any move. Please share what ever idea you have.Thank you.Magt Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.