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Hi everyone , just been diagnosed, (multiple myeloma. ) It all happened so fast , I arrived at hospital with severe anemia. After 6 blood transfusions I felt myself again , I’m living in France and don’t speak French. I was carried along with little explanation and no time to deal with the diagnosis. After a 2 week hospital stay with lots of antibiotics on a line , and one chemo I got very ill, pain in back and ribs , sense of smell and taste became acute and I stopped eating and drinking water. I had no understanding that this was side effects . I got shown no results or photos of scans , I was on my own , restricted to the bed and toilet, being sick on an empty stomach , coming out both ends at same time , thought I was dying, so I signed myself out. The pain left after 7 days and I was able to walk unaided again. Cost so far is over 55,000. I want to hear from people who didn’t take the treatment . On the up side I’m getting married next month before I get disabled . I have lesions in my spine and ribs , ( information I got from a doctor I found after hospital. I’m 60yrs.  No one asked if I’d prefer to go back to Scotland for free treatment , your all braver than me 

  • Hi jo100,

    I understand and agree on the fragility.

    I don't generally worry about my health and prognosis (I do what I can to look after myself and the rest is beyond my control). However, only yesterday I was talking about a historic heroic person to my son, and got a bit tearful. A little embarrassing for me as a man, but this damned disease takes a toll both physically and mentally.

  • Hi Jo100, I started to read the link too but stopped because I feel exactly  the same way you do.  We have to talk tough or we may not get thru this journey  but underneath it all some of us are extremely fragile.

  • I was going to read it but decided not to as I am very weepy all the time. 

  • Hi Kizi  I have days like that too especially when I look at my 3 sons and my 13 beautiful grandchildren but then I have days when I'm very upbeat and positive.   I'm sure it's all part of this journey we are on.  Try to stay positive,  we are all here to help.  Take care. 

  • My first ?? why was a sedative (thamidome) being given to pregnant women? Makes you wonder. Dallas buyers club comes to mind . I’m taking assiac tea n vts , iron . Will test my blood n urine every 2 months ,30 euro .  Try n not stress my bones . For now alls good , I feel for you all , lots of friend support in a foreign land .best of luck , I need hunter for info of whe dc n they started the testing of thalidomide etc

  • Hi River.

    You confirmed in a previous post that your treatment includes Bortezomib. It is weird stuff: Things that are normally good for you interfere with Bortezomib.

    For example,  a couple of years ago (I can't find the source info) I read that green tea extract was thought to be beneficial to myeloma patients. No pharmaceutical business was going to make money out of it, so the US Government started a clinical trial. It was abandoned after more patients died taking chemo + green tea compared to chemo alone.Why? Because the green tea extract stopped the Bortezomib from working!

    Likewise some supplements MUST NOT be taken if you are on Bortezomib, like Vitamin C.

    This is part of what Chat GPT says on essiac tea:

    "Essiac may affect how your body metabolizes medications.
    Some of its herbal components (like burdock root or rhubarb) can impact liver enzymes or kidney function, which could:

    Interfere with how bortezomib is processed

    Increase toxicity or reduce the effectiveness of the chemotherapy"

  • I have all the meds , why I’m not sure, I stopped all meds in hospital and said I’d rather die at home than take any more meds , so it’s just the tea n vits. 

  • Assiac has been proven non toxic and can be taken with chemo check out Rene Caissy

  • I’m not on meds so I’m ok , loads of testimonies on cures with assiac and treatment along with just assiac