I started this podcast thinking I’ll let other Moms know that they aren’t alone and share some stories of fellow Wegener’s warriors, because rare diseases make it difficult to find people to connect with. It took a few months, but I quickly found out that being a Mom life podcaster and sharing about my kids wasn’t a good fit for me.

I don’t know where this will lead… and if you were here for the mom life stuff, and this whole Vasculitis, Rare Diseases, Chronic Illness life isn’t your thing. I get it. I’m sorry if I’m letting you down at all, and I deeply thank you for your support this past year. This is something I have to do.