With reference to twins, it can occur in one and not in the other.
Most researchers believe that DIPG is caused by something that happens during the development of the children who have DIPG. There are specific mutations that are prevalent in DIPG--much more prevalent than in children without DIPG. This type of information has really only become widely available over the past 6 years due to tumor tissue donations by families of children who have died of DIPG.
A disease is defined as rare in the USA when it affects fewer than 200,000 Americans at any given time.
Dipg is caused by vaccination I don't care what anyone says not once was I asked about jaydes bringing up ie breastfed (which she was) where she lived what she ate etc etc and you would think with dipg (which they state don't know what causes it) they would be trying to find a common denominator but no they are not even interested read small print on vaccination side affects and one is brain tumor the doctors know they just won't admit it
In her words, how can you cure something if you don't know what it is or where it came from... Since I began this quest back in 2009 I've found several common denominator's between our children.. The survey is being updated on the back side so please if you feel a question should be asked and it's not there add it to the comments...http://www.surveygizmo.com/s3/1480532/Aimee-s-Army-Survey
We already know that children with NF1 have an unusual amount of birthmarks, which is a sign of the disorder. What if there is a yet known disorder that causes a child to be at risk for developing DIPG, and their physical features are a sign of that?
Right now you can fill out the Parent Profile, and I will email you once the surveys are ready to be completed.http://www.surveygizmo.com/s3/1937460/DIPG-Parent-Profile
DIPG works on the Pons part of the brain and so does many vaccinations and Polio sabin.
Most researchers believe that DIPG is caused by something that happens during the development of the children who have DIPG. There are specific mutations that are prevalent in DIPG--much more prevalent than in children without DIPG. This type of information has really only become widely available over the past 6 years due to tumor tissue donations by families of children who have died of DIPG.
A disease is defined as rare in the USA when it affects fewer than 200,000 Americans at any given time.
Dipg is caused by vaccination I don't care what anyone says not once was I asked about jaydes bringing up ie breastfed (which she was) where she lived what she ate etc etc and you would think with dipg (which they state don't know what causes it) they would be trying to find a common denominator but no they are not even interested read small print on vaccination side affects and one is brain tumor the doctors know they just won't admit it
In her words, how can you cure something if you don't know what it is or where it came from... Since I began this quest back in 2009 I've found several common denominator's between our children.. The survey is being updated on the back side so please if you feel a question should be asked and it's not there add it to the comments...http://www.surveygizmo.com/s3/1480532/Aimee-s-Army-Survey
We already know that children with NF1 have an unusual amount of birthmarks, which is a sign of the disorder. What if there is a yet known disorder that causes a child to be at risk for developing DIPG, and their physical features are a sign of that?
Right now you can fill out the Parent Profile, and I will email you once the surveys are ready to be completed.http://www.surveygizmo.com/s3/1937460/DIPG-Parent-Profile
DIPG works on the Pons part of the brain and so does many vaccinations and Polio sabin.
I am so glad you have spoken out! I have suspected vaccines also. Out of 7 of our children only 1 is vaccine free. My biggest regret is that our other 6 aren't!
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