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Cancer has spread/Metastasized - JMS

Oh No Associated with Pancreatic Cancer. Posted on October 29, 2013 View this journey (1 Experience)

I have written a journal about my experiences, at least for the first 18 months following diagnosis. Anyone wanting to read it could just let me know. I've tried to highlight the patient side of the story since my family could not find much information from this perspective following my diagnosis.

5 Comments
  • geekling's Avatar
    geekling

    I am very sorry to hear such news.

    What will you do now?

    Please do not give up.

    Since you have family, I'm sure your "things and effects" are already in order so you have time to look over to new horizons if the conventional treatments have failed you.

    If/when you have time and energy and willingness, please investigate "chaga mushroom" extract, "nigella sativa" oil from the mid east, graviola, and artimisinin.

    If I knew more about you I could suggest other things but please look into these to start. These are all wild foods which are on the planet to be gathered and used when needed.

    Except for the expense of gathering/buying the items and learning how to use them for your personal protocol, these foods can do you no harm. Chaga is specific for [pancreatic] cancer, nigella sativa (black seed) shrinks tumors, graviola (soursop) is eaten and then withdrawn in stages as is artimisinin (an herbal derivative).

    I do hope that you might also consider a sharp right turn in food intake. No meat, no dairy, no high heat .. lots of juicing and sprouts. Try looking up the Hippocrates Health Institute (WPB, FL), the Living Light Institute (Atlanta, Ga), and Optimum Wellness (San Diego, Ca & Austin, TX)

    It is always best to live in the now.

    Enjoy the holidays.

    almost 8 years ago
  • tibby150's Avatar
    tibby150

    I would love to read you journal

    almost 8 years ago
  • geekling's Avatar
    geekling

    I would read what you've written too but, preferably, not posthumously. Get well.

    almost 8 years ago
  • Rick1970's Avatar
    Rick1970

    Hello JMS, God bless you for your willingness to share your experiences. I'll be extremely grateful for any information that may help my wife of 43 years. She'll begin her 4th treatment of FOLFIRINOX on Dec 26th. I'm trying to develop an understanding of what side-effects to expect as her treatments continue. The neuropathy and sensitivity to cold already seems to be increasing. Rick

    almost 8 years ago
  • Rick1970's Avatar
    Rick1970

    Hello JMS, How's it going? Have you any thoughts about potential regimen's after FOLFIRNOX? Thanks for any suggestions you may have to share. Rick

    over 7 years ago

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