• DaveWaz's Avatar

    DaveWaz wrote on brockm1's wall

    Welcome. Thank you for taking the time to register and share your journey. I know we have several people on the network with cancer or the unknown primary experience so when you are ready please do not hesitate to reach out to them. They are here for the same reasons you are.

    If you need anything (e.g., emotional support, help finding support/care resources, insights, you can post in our Questions section. You can do this by clicking on the "Ask Network" link on your logged in home page or the "Questions" link at the top of this page. When you post needs/questions using our question feature, we route your question to everyone in the network who might be able to help. Also, know you can use the "Update" feature on the site to keep anyone who might be following you on WhatNext up to date.

    I look forward to reading about your progress.
    - David, Founder, WhatNext

  • brockm1's Avatar

    brockm1 asked a questionCancer of Unknown Primary

    My husband was diagnosed with Cancer of Unknown Primary in February.
    He is stage4. What can we expect as the desease progresses?

    • RuthAnne's Avatar
      RuthAnne

      Hi Brockm1,

      Because metastatic cancer can take so many different (and somewhat unpredictable) routes, it is hard to say what to expect. You can probably get a better answer from the oncologist(s) who is familiar with the extent of the metastases, which organs are affected, and how your husband is responding to any treatment he is receiving.

      Best of luck to you both.

      11 months ago
    • Betty1948's Avatar
      Betty1948

      I am a 64-yr.-old female who was diagnosed with SQUAMOUS CELL CARSIMONA in March 2012. I was never a "sun-worshipper" or smoker. I was told that the mass in the lower-left side of my neck
      was "a secondary site". I was sent to hospital for general anthestic to do multiple biopsies on tissues of my tongue, neck and sinuses. Nothing was found, meaning my Immune System had destroyed the "primary". I was told this is common -- to not be able to locate the primary or initial site of this type cancer.

      I had (for the past 5 years) faithfully taken 12 food and vitamin suppliments. My Oncologist told me to stop the regiment because "it was the fuel that was feeding the cancer" so I did stop 2 weeks before beginning my CHEMO. I am now in my 9th week and into recovery.

      However, it also means that my Immune System was healthy enough to destroy the INITIAL CANCER SITE. So I see this as good and bad. I was told that once my CHEMO / RADIATION is completed (late Sept. 2012) I can resume my vitamin/food suppliments.

      My Oncologist predicted that 1/2 way thru my CHEMO the 6 cm. Lymph Node mass would disappear. It doubled in size between the time I found it and starting Chemo. (a month) meaning it was very agressive. His prediction was accurate...I can no longer find it.

      You are welcome to follow my progress here or on FACEBOOK
      (Elizabeth A. Scott/Florida).

      11 months ago
    • Teri's Avatar
      Teri

      What is his treatment plan?

      9 months ago
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