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You may take a look at http://www.cff.org/LivingWithCF/AssistancePrograms/. The CF Foundation has a list of resources-depending on which enzyme she is on, the manufacturer may offer assistance.
You may take a look at http://www.cff.org/LivingWithCF/AssistancePrograms/. The CF Foundation has a list of resources-depending on which enzyme she is on, the manufacturer may offer assistance.
You may take a look at http://www.cff.org/LivingWithCF/AssistancePrograms/. The CF Foundation has a list of resources-depending on which enzyme she is on, the manufacturer may offer assistance.
You may take a look at http://www.cff.org/LivingWithCF/AssistancePrograms/. The CF Foundation has a list of resources-depending on which enzyme she is on, the manufacturer may offer assistance.
You may take a look at http://www.cff.org/LivingWithCF/AssistancePrograms/. The CF Foundation has a list of resources-depending on which enzyme she is on, the manufacturer may offer assistance.
I am guessing insurance doesnt cover it? Sounds like a ridiculous ?? I know, but want to be sure.
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<br />Check out this thread for assistance programs
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<br /><a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.com/forums/messageview.cfm?catid=902&threadid=17395&highlight_key=y&keyword1=assistance%20programs">http://www.cysticfibrosis.com/...=assistance%20programs</a>
Call your doc and ask for the contact info for the pharma rep that services the clinic.
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<br />they'll give you the latest @ greatest info on programs to help <img src="i/expressions/face-icon-small-smile.gif" border="0">
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