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<blockquote data-source="post: 2765"><p>I know what you're saying, but there have been some parents who have gotten their doctors to look at this. Some are printing information or getting the videos of the conference to show their doctors that this is credible. There recently was a section added specifically for doctors who have questions. </p><p> </p><p>I don't know exactly what the guidelines are for the NIDS study, but that may be an option if one of the drawing stations is accessable. The only one I know about so far is in New Jersey. There is alot or red tape to go through to get this going.</p><p></p><p>They are in the process of developing a national public relations campaign and have already had preliminary meetings with several pharmaceutical companies. They are working very hard to remove any obstacle to early application of clinical therapies for our children.</p><p></p><p>There are immune modulators that the drug companies have already developed, that they are trying to get available for our children. That is what I am waiting for. </p><p></p><p>I know that medicare has paid for some of the kids, I have Blue Cross and they pay. But its because my son has a medical diagnosis.</p><p>Cheryl</p></blockquote><p></p>
[QUOTE=", post: 2765"] I know what you're saying, but there have been some parents who have gotten their doctors to look at this. Some are printing information or getting the videos of the conference to show their doctors that this is credible. There recently was a section added specifically for doctors who have questions. I don't know exactly what the guidelines are for the NIDS study, but that may be an option if one of the drawing stations is accessable. The only one I know about so far is in New Jersey. There is alot or red tape to go through to get this going. They are in the process of developing a national public relations campaign and have already had preliminary meetings with several pharmaceutical companies. They are working very hard to remove any obstacle to early application of clinical therapies for our children. There are immune modulators that the drug companies have already developed, that they are trying to get available for our children. That is what I am waiting for. I know that medicare has paid for some of the kids, I have Blue Cross and they pay. But its because my son has a medical diagnosis. Cheryl [/QUOTE]
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