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I don't think the original antibody screening is done in a plool. I believe that the antibody test is done on each unit of blood. Perhaps someone who knows for sure will post and explain how this happens.
Cost-effectiveness has its benefits and risks. We used to have school inoculation programs and to save money, the same needle was used for everyone.
When I was dx with hepc a letter went to the State and then my local Board of Health was notified and then my local B of H called me to question me and discuss treatment of the disease.
Since Red Cross initially said you had it, I would call them again and ask them how soon the letter goes out to the State. I am GUESSING, but I have a feeling it goes right out -pronto - those 16 names in that pool, and that 'might be the reason' that though she said you are negative, you still CANNOT donate......In other words, that would involve more paper work of them contacting the State and saying you (and the other 14 people) are neg. And we know how corners get cut everywhere you go today, so more paper work??- thats pulling teeth.
Its probably easier for them to just exclude those 16 people from donating though only one was infected. Nothing makes sense the way things are done today, so you have to try to think of the most stupid way to do something and thats usually where you will find the answer.
But IF this is how they do things and your case is not unusual, its no wonder we go thru blood shortages.
But anyhow, I would, yes, definitely get tested by my own doc again and if neg - no antibodies, I would ask him to send a letter (and call) to Red Cross and have them send you and the STATE a letter stating that you DO NOT have hep c. I would also tell RED CROSS that the State needs to take you off that list, (if you are on it) and that you ALSO want a letter back from the STATE saying you do not have hepc. I would then go to your local Board of Health and explain what happened and ask if they received any letter from the State and if they did, I would make sure I didn't leave without the letter in my hand - a copy.
The RC probably might tell you they won't do this or whatever, but I would not let them get away with having my name on a State list of having hepc (if that has happened) if I didn't have hcv. What if it came back positive also for HIV, syphliss etc, and then they said, oh that wasn't you, it was one of the other 15 people,,,,,,would you be listed as having those diseases too? I would want to know.
It was expressed by some, including myself, that it felt crumby to be put on that State list, but, we DO have/or had hepc......I know how I would feel if I didn't have it and was put on the list just because they are looking to cut corners(?) in their screening process. Or at least it appears that they are looking to cut corners. If I were you I would be curious to see what your doctor thinks about this new screening process from his medical perspective - safety issues etc.
And with ALL that said,,,,,You may NOT be on the STATE list, I am just saying what I would do and what I would check into.
Good luck,
MO
The only way I found out that my STATE was notified was I asked the lady from my local board of health how she was notified and she said the State notifies the Local. The State has never notified me - just the Board of Health. So evidently some people get letters from the State and some get calls from the Local - but when it comes down to it - we are on the list one way or another.
When you said "Finally" the girl told you how it was done - the screening process,,,,that tells me that if you didn't really push hard enough for answers, you may not have been told.....so keep on pushing;o)
take care,
MO
Bobby