Hi everyone. My name is Pat and I'm 45 with a 17yr old son and mostly dh.LOL I live here in western MT. I was re-dxd with MCTD 2 years ago. First dxd with RA 9 years ago. I have several cross-overs like lupus, and also pulmanary hypertension. Am on O2 24/7. The RA is most obvious in my hands and feet. Painful to walk! The first 2-3 years were the worst. I was angry, in denial and in pain. Life has changed a lot for the whole family since then. RA certainly does change things, doesn't it?!
Nice to be here. Good to have folks to share with and learn from. Look forward to the chat room re-opening. See you there!