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Re: CF awareness Melbourne/MAIA

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By Guest guest
in Health, Medicine and Natural Healing 02

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Guest guest

Posted
Posted

Sounds just like the Cystic Fibrosis Foundation in the USA; I would

be complaining, too---maybe to there central offices tomorrow--usual

ly these things are primarily publicized to donors and sponsors.

Who spend money that could go to research---oh, do not get me going,

or I will really bore everyone------GRRRRRRRRRRRRRRRRRRR!!!!

Cheers and love,

n Rojas

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