Long time readers and friends will know that I have had a past experience with FIP and I absolutely hate the disease with a passion. I hate that in 2008 we not only don't have a 100% accurate test for it, we don't have a cure, we don't have a vaccine, we don't even know why it happens (although it is thought to be something genetic that helps with the mutation)
There is research being done out there.
I ran across this website today. Just thought I'd spread the word.
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