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Maia

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As a parent of a cfer who was treated all along for cf, but not officially

diagnosed until age 26, all I can say is that we parents (with and with

out cf ourselves) get awfully tired of this one. I would be happy not to

have cystic fibrosis, but after all these years, the evidence just mounts.

As with any chronic illness, when one finally has a differential diagnosis,

an " explanation, " perhaps after many years, doubting it does not con

sole either parent or child--unless the child has miraculously suddenly

attained perfect health and is totally sign and symptom free!!!!

This is about as irked as I have ever gotten on line and I do not like my

own tone here, but constant doubt can lead to tragic psychological con

sequences for both child and parent.

n Rojas, wcf, mom of 3 adults, 2cf carriers and 1 wcf--and in all

cases there is no doubt and the expression of it would only give false

hope and create confusion----I may be cheerier next time around!

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