Hi Chrissey,
We are such strong people, with all the challengers that are thrown at us and we beat them down. The continuous hurdles we need to jump and as you said we need to take each day as it comes and to take the bad days with the good and go with the flow. I was lying on the CT table being mapped out for yet again more radiation and I thought to myself, "what are normal people doing" then out came the tears. (not that I'm not normal), but I would love to be well and working and spending lots of time with my children and grandchildren without getting this terrible fatigue. I've stopped counting how many times I've been diagnosed with new mets, but most times I am silently distraught for the first couple of days of being told then have a day of tears. It's just how I except the news. I have met so many beautiful people since being originally diagnosed, it will be 12 years September. My second granddaughter was born September 26th and I was diagnosed the following day. I call her my little guardian angel. I wish you all the very best, cheers from Annette