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Cliff Douglas's avatar

Thanks, Howard, for continuing to shine light on these issues and challenges. Based on your well-documented story and the personal experiences shared here and elsewhere by our AS comrades, I do wonder about the potential for pursuing legislative and/or regulatory changes in our state legislatures - Illinois and well beyond. The insurance industry lobby might be expected to use its great influence to interfere, but as Allan G. says in his comment, "I am at a loss as to why they refuse to take money from someone whose doctor is willing to say that the potential client is as much or as little a risk as virtually anyone else, given the Gleason 6, low risk diagnosis. They refuse to take your money because of their lack of understanding/lack of reasonable intelligence in connection with medical diagnoses and opinions." That makes sense to me at face value, so it may be worth identifying sympathetic political leaders -- what do you want to bet this very issue has touched some of them personally? -- to start strategizing needed change.

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Jeff Coleman's avatar

As most people might say, "Don't get me started about insurance companies!". I have not yet personally had to deal with any insurance company after being diagnosed with PCa. That may still come.

Unfortunately, it always seems to take pressure from a specific interest group to lobby lawmakers into passing legislation and essentially force the insurance companies to make changes.

However, my opinion would be that until Gleason 6 gets "de-classified" as cancer, that battle might be lost from the start.

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