ANSWERS: 3
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If not...Where the hell should I go from here...?
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I have never heard of PKD before but did some quick research. The suggestions I found are rather limited.. Check out the site below, they seem to be the largest source on the web for information. I hope you can find some help.. Best wishes http://www.pkdcure.org/site/PageServer
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@csimme01 and the Ninja Cooper: Ah, yes, PKDcure. They are the company I wrote to that gave me the worst news I could ever get. I love their site though. It's helped me out so much. But the woman who replied to me told me there is absolutely nothing I can do...I was just hoping someone whose had experience with this might help me. And PKD is Polycystic Kidney Disease. It's hereditary disease that affecfts the kidneys at first. Cysts form in the kidneys, over time they break, causing a lot of pain for the carrier. ADPKD is a rare form, where it's not in the family gene--it forms spontaneously. It's unfair in my opinion...But it's not curable, so I can complain about it being unfair all I want. It won't do any good... But thank you for trying to help me.
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