I'm gobsmacked as my mother would say. I didn't. I didn't certainly didn't expect that. I'm so grateful for the people that have told me that they enjoyed the show the critics who have been so kind, but I'll tell you the most powerful thing is when there was a woman who came up to me and who said, you know, the words that I've come to fear, because I don't want to hurt anyone's feelings. And she said, You don't remember me, do you? Would you help me? And she said, we took Irish dancing lessons together when we return. And I said, Oh, yeah, but actually, I did remember that when she made the connection. Anyway, she had recently moved back to the Detroit area to care for her 93 year old mom who is not doing well. She told me in an email after the show how powerful it was and how so many of the supermom was an Irish immigrant as well. But how many of the stories really resonated with her but how it helped her as her mom's caregiver and it relieved so much of the guilt that she felt? Because here's one of the biggest things I've learned about being a family caregiver, of of a person with dementia. No matter how good you are, no matter how hard you work, how you think of everything, all the resources, all the medical professionals, if you're a person who's used to getting the job done making things happen, you know, you're a fixer. This can't be fixed. And so many people feel guilty because their loved one is still declining, or that what worked today isn't working today. So they think Oh, I'm doing this wrong, what can I do? How can I help? And it's so frustrating. It's exhausting. It's overwhelming. And people don't talk about it. And so I'm hoping that through Mrs. Kelly's journey home, that when we see a person with dementia, we realize the dementia is not who they are or who they were, or it is not the totality of, of them as an individual. And the people who care for them need support, and need help, because it's so hard. And people when they tell me they feel seen, they feel heard, that they learn things, and that they have a laugh, and they have a different attitude, about hospice, about end of life and about being a caregiver, that that's, that's the biggest reward that I get. But I certainly appreciate the reviews and the awards and things like that.