Category: tests

Sharing my cancer story. It might be helpful, it might be interesting, it might be informative.

  • The right care team

    I’ve settled on one particular support group as being the best fit for me: LACNETS, which is a 90-minute Zoom meeting once a week. I like it for several reasons. It focuses on my my specific kind of cancer (neuroendocrine), it’s a good blend of emotional support and practical advice, it’s very professionally run, and…

  • One year after surgery: a retrospective

    I’m still coming to terms with my new identity as a life-long cancer patient, as well as the transition from Librarian to not-Librarian. Most importantly, however, I have absolutely been loving being home after school with my daughter and eating dinner together. With my previous schedule, on an early day I’d get home at 6:45pm,…

  • The decision to stop working

    Ever since my metastatic diagnosis almost exactly a year ago, the idea to stop working has been in the back of my mind, but I just wasn’t ready to make the leap. In the two months between my diagnosis and the Big Surgery I was in crisis management mode, focusing on tying things up, both…

  • I’m looking at you, lymph nodes

    It’s been a mostly relaxing four months since I’ve been back at work. We’ve been ramping up for a big event that took place this week, and I’m excited I got to be a part of it. In the meantime, I’ve been going in for my monthly Sandostatin shots. I’m continuing to have flushings, so…

  • My support network

    As the year winds down, I am preparing to return to work on January 3. I am so incredibly lucky to have had over 3 months to recover from my surgery. Here is a starter list of everything I am grateful for: What’s next for me: I’m going to continue to have monthly injections of…