GREAT NEWS ON MY JOURNEY

15 Oct

As i am trying to convince you out there about your trip with cancer i thought it only appropiate that i keep you up to date with mine.
There is several ways in which the doctors will advise you to take depending on the type of cancer you have. They start from chemo to radiation to surgery. As I have postate cancer it’s the only one i can tell you about from my own experience. I know a lot of men now who have this disease and are doing or done totally different things. Most have been convinced to have their postate removed which does not mean that the cancer has gone away others like me have chosen limited intervention, by this i mean i was having a slow release horemone drug put under the skin which lowers tetosterone levels which slows the cancers growth rate.
As i have mentioned i was given a dodgy gene from my dads side to do with clotting, my body clots bad if my PSA readings get up over 100 so was having to have blood thinning tablets as well. I went off the horemone drug and the thinners a year ago and started getting clots again after three months. The PSA sky rocketed up to 144.
Horemone drug back in and on thinners again till the PSA reading came back down again.

I have been taking the human worm tablets now for three months and my PSA done monthly is at 10. My last hormone insertion was in April this year and needing redone in July, I decided to see if anything has changed so didn’t have the hormone put in again and kept up with the monthly PSA tests (self monitoring).

And the great news is I had another PSA test done on the 15th of October and it came back at 11, that’s 3 months after the hormone has worn off.
Which means the cancer in my postate has gone (positive thinking) but i’m sure the PSA reading is coming from the cancer in my spine. As I still have no pain in my spine means that the cancer isn’t growing.
So the moral of the story is take your time (if you have time) to look at all the options before you make a move. I didn’t have any options apart from the doctors but still decided to do my own thing, which some of my mates say it takes big balls to do this when under the pressure of dying from cancer.
I hope this blogg helps those of you out there with making rational decisions when the life threatening decision has to be made.

5 Replies to “GREAT NEWS ON MY JOURNEY

  1. Hi as ricky70,
    20 years ago I had a PSA.READING OF 7.My doc a lady suggested I go to a Urologist for a check. He did fingers and samples, said BPH BENIGN PROSTATIC HYPLASIA. DO NOTHING Every year the doc sends me prescription and I get a check, and my level this year reached 21.He said wait for a month or go to Urologist now? I will go for another check now.
    I have been studying selenium for 20 years. [I’m now 87] .I’ve been taking 200 mcrogm. Se/day giving me a reading of about 1.6 umol/lt. Prof M Rayman of Surrey Uni. published in the Lancet 31/3/12 the optimum range for Se is [1.6-1.9 ]for cancer prevention. The 2 urologists, I know are ignorant of Se.I agree take it slowly, best wishes.
    .

    • thank you for your comments. As i have stated before information is the key, I’m not sure where your from but most uroligists here panic when the psa gets to 10. I have decreased the amount of mebendazole I have to 1 100mg tablet per day for 3 days then 4 days off as the slight twinge in my spine has totally disappeared and feeling great.

  2. Hi Stewman, your Blog came to my attention whilst researching Fenbendazole availablity in NZ.
    I discovered you are using Mebendazole, initially 250mg daily but have recently reduced to 1 x 100mg tablet daily – do you have a particular reason for this change of dosage ? Do you have any side effects from consuming Mebendazole ?
    I am diagnosed CLL + 17P depletion cell so am participating in a trial of a new treatment being developed but will finish in 6 months. I am looking incorporate fenbendazole/Mebendazole in my daily regime at that point after finding and reading http://www.mycancerstory.rocks.

  3. Hi Stewman,
    I note you previously had a daily dose 250mg Mebendazole.
    Is there a particular reason for reducing the dose to 100mg daily dose ?
    The http://www.mycancerstoryrocks website details 222 mg daily Fenbendazole as an assist for my cancer.
    Currently I am in a Clinical trial of a new treatment being developed which will finish in six months but want to incorporate Mebendazole in my daily regime to reduce lymph node size.

  4. Hi Terry I have been away for the last week, hense the late reply. I have tried all sorts of dosages but found the same one that Joe Tippens is the better option. I am taking 2 x 100 mg mebendazole 3 days on and 4 off, I also have 10 apricot kernals on the 4 days. As the oncologist told me I wouldn’t see 2017 out is proof that something is working. I have found a web site that is dealing with research into the benifits of using fenbendazole compared with mebendazole. They have found the fenbendazole is more effective for most cancers. I had issues getting panacure into the country and found a company selling 222 mg of fenbendazole. I will put this website and info on the blogg. It’s a good idea to swap treatments around.
    Kind regards Stew

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