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@christina3444

Dear janemc, Well, you could be right. After I was diagnosed with PV I told two “friends” and was shocked by the lack of reaction. Neither asked me what the prognoses was or even how I felt. And, in subsequent conversations that did not change.
Maybe you’re right about “comprehension” but they’re pretty smart and know how to use Google.
I knew these two to be caring people who I thought I could depend on for some support while I myself came to know more about the condition. I was wrong.
I guess it’s just not as “sexy” as other diagnoses! And, I am glad for that.
I’m not a joiner and it took me a long time before I started participating in this forum and I’ve felt better since I did. Both for being able, I hope to provide some help to others, and for being able to “speak” with others who appreciate what Im going through.

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Replies to "Dear janemc, Well, you could be right. After I was diagnosed with PV I told two..."

As if a mysterious and scary diagnosis weren't bad enough . . . I'm really sorry your "friends" weren't kinder. Sadly, yours was not an isolated incident.

My sister, whom I've supported through two kinds of acute cancer, informed me that she'd researched ET, and it wasn't anything to worry about. All I had to do was eat more cinnamon! (Huh?)

This forum really saves my sanity.