Guest guest Posted February 26, 2004 Report Share Posted February 26, 2004 I think that in all of the studies, they only rely on what was reported to the government agencies. There are doctor-patient confidentiality privileges that would prevent your doctor from reporting things to anyone. I remember reading that in CA, when they quote the number of kids with " autism " , it is the number of kids who have filed with our Regional Center program (which handles benefits for such kids), but to be in this program, you have to have a straight-on autism diagnosis. Kids with PDD-NOS or Asperger's generally aren't eligible and so they dont get counted in CA's numbers. So, yes, I think this means that everyone's numbers are below the number that are truly on the Spectrum. Best, Lora _________________________________________________________________ Get fast, reliable access with MSN 9 Dial-up. Click here for Special Offer! http://click.atdmt.com/AVE/go/onm00200361ave/direct/01/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2004 Report Share Posted February 26, 2004 I tried to send a reply before, but it didn't work - I hope this one does. If the reaction isn't in your son's medical record, it wasn't reported to VAERS. This is a big problem with the whole system. PARENTS should be able to report it, not depend on the doctor, because what happened to you happens all too frequently, skewing the whole program. I had a client whose son had a 105 degree fever and a rash after the varicella vax - her doc told her this was a normal reaction. I urged her to phone him and insist he report it. He told her he wouldn't. I believe that the varicella vax is particularly underreported from the reactions I have seen. I wonder if it would be worth contacting a vaccine attorney anyway since your INTENTION was to report a reaction at the time. This is just not right. It's one thing for those of us who refused to believe that it could have been the vaccines. I will have to live with my ignorance. You, on the other hand, did the best that one would expect and reported it. Shame, shame, shame on the system. Uh. BLESSINGS ON YOUR DAY. You're a good mom. , mom to and [ ] accuracy of vaccine adverse event reporting data base I never reported my son's autism to VAERs -- or whatever the acronym is. I assume that this is the case for many of us. I bring this up because I read that the Geirs correlated children who had mercury containing vaccinations with children who developed autism by looking at the vaccine adverse event reporting database. Would my son's data be in that database, even if I never reported it to them? I wonder if the rate of autism is even higher than the Geirs found by looking at the vaccine data base because I am sure we are not the only family who has not reported. I suspected a vaccine reaction, but my phone calls to the nurse are not even recorded in my son's medical record and my suspicions were poo-poo'd by the nurse. Just curious, ======================================================= Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2004 Report Share Posted February 26, 2004 I reported Allie's reaction to VAERS myself. A parent is perfectly able to report it, it does NOT *have* to be filed by a medical person. In fact, I recently spoke with a woman whose son had a mild fever whose doc poo pooed it as " minor common reaction " and I told her to file a report because *any* reaction is supposed to be reported. The vaccine fact sheets should really be updated to contain information that any reaction can be reported by parents and should be reported. Of course, that would mean a huge percentage of vaccine recipients would need their parents to file. Debi > If the reaction isn't in your son's medical record, it wasn't reported to VAERS. This is a big problem with the whole system. PARENTS should be able to report it, not depend on the doctor, because what happened to you happens all too frequently, skewing the whole program. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2004 Report Share Posted February 26, 2004 I remember reading that in CA, when they quote the number of kids with " autism " , it is the number of kids who have filed with our Regional Center program (which handles benefits for such kids), but to be in this program, you have to have a straight-on autism diagnosis. Kids with PDD-NOS or Asperger's generally aren't eligible and so they dont get counted in CA's numbers. Wow! That sure puts an end to the " better reporting " myth that so many experts point to as a cause of the increase of cases. 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.