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Hi there, my name is Orleans. I was diagnosed with the dry form of FIP at 12 months in July of 2019. My human mom researched what treatments had shown some promise and decided on the GS protocol. I was a fairly large, young adult which meant that the shots were really large. Man did I hate how those things stung in spite of the efforts of my humans to numb the shot sites. I finished my treatment protocol with the oral version of the medication and it was much easier to handle. I am now more than four months post treatment, the hair is growing back where they did my last ultra-sound and I am back to racing around with my siblings. I hope that all who are receiving treatment meet with success!