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  • Ozguy32
    started a topic Australia


    Hey Fellas,
    How are you going?
    Just sending a message to see what you think this group could do and suggest some ideas. I have been disappointed in some ways about the level of help with cancer survivorship specifically to TC. Instead of expecting the help to come to me I have gone out to find it and there is basically no cancer groups that relate specifically to TC and the general cancer survivorship groups are few and far between. TC is also a cancer that relates almost specifically to younger people, that is rare in the world of cancer and gives some of it's own challenges to overcome.
    Obviously everyone with TC is a bloke and I think blokes would rather just meet up in pub somewhere for the most part as well as email/phone support. This does not help with getting people to join this group though. I think this forum is the best site on the internet to attract people from Australia but there is also Cancer Councils, notice boards at hospitals, other cancer groups that will also spread the word. Another internet site may also be an idea but there is already this one and a wealth of knowledge and experience to go with it.
    Everything has to start from somewhere, any other ideas?



  • Darwin2015

    Hey Everybody ,
    My name is Gary , Irish bloke living in Darwin the last 4 years , diagnosed with TC 2 years ago , had a relapse in September , just finished 3XBEP . Like alot of you guys , really struggling to get some proper advice , I’m starting to question my oncologist and his experience with TC . Not sure if anyone has being in similar position . I’ve just put together a brief history of the past two years & where I’m at right now .
    Basiclly I just finished chemo , it’s had no effect on my AFP markers or the enlarged lymph nodes , not sure what to think now .

    Feeling slightly confused but more frustrated . I could really do with some advice , I'm starting to lose faith in my Doctors decisions regarding my treatment .
    Today was supposed to be the day when the good news started , the results from my post chemo (3xBEP) CT Scan & Bloods .

    AFP 13.7

    CT LYMPH NODES : There is a chain of abdominal lymph node in the left para-ortic region just inferior to the left renal artery. they measure up to 11mm in short axis which is stable .

    My AFP has always being slightly above average since i had my left I/O(7/9/2015) , its always fluctuated between 12-15 , its never being below the magic marker 10 .

    Its being 4 months since i had my initial CT followed by PET scan , there has being no change in Lymph node size since then. My AFP is slightly elevated which has always being the case since 2015 .

    I just get the feeling from my Doctor today , that he might of rushed me into Chemo , maybe we should have watched the AFP , then had another scan in 2-3 months . Which is exactly what he wants to do now , hes asked to come back in 6 weeks with new bloods and then decide on our next step Biopsy/RPLND.

    Thats why I'm feeling confused about the whole situation , did i just complete 3x BEP for no reason , should we not have went ahead with the Biopsy before Chemo rather than after chemo ?

    SEPT 2015 Left I/O . No Invasion .
    Tumour Size 17x15x12mm
    confined to the testis
    Embryonal Carcinoma

    Followed survelliance protocol till 7/8/2017 two enlarged lymph nodes found on CT Scan sent for PET Scan
    Lymph Nodes had increased from 7x7mm to 9x9mm

    The known enlarged retroperitoneal para-aortic lymph nodes are F D G avid consistent with metastases . No scan evidence of F D G avid malignacy elsewhere .

    9/10/17 Started 3xBEP
    9/12/17 Finished 3xBEP

    Today 15/12/17) Post BEP CT &Blood , no change in lymph nodes , slight change in AFP

    07/8 14.7
    16/8 14.7
    06/9 14.1
    20/10 11.9 ( Finished 1x BEP)
    27/10 11.3
    17/11 12.9
    11/12 13.7 (3xBEP Completed )
    Back in 6 weeks to check AFP , and to decide the next step in my treatment . feeling very nervous now .

    Sorry guys i tried to explain everything as best i can , any advice would be really helpful . My Doctor is starting to make me feel nervous about everything .

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  • Mikestar
    Hi Guys,
    G'day from Bendigo Victoria. Been cancer free for 5 months now. Another mate and I have set up a campaign/foundation called BlueBall Foundation ( ) to raise awareness of TC and Men's health. We made it to the front page of the local paper and alot of opportunities opened up for us to get our story out there.

    Mike Elliott

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  • lozmac
    Hi guys! Not long found this site, and being new and not quite with the lingo yet, having trouble, so glad to meet some local lads and ladies.

    My hubby was diagnosed four months ago with stage 3c tc. Abdo involvement, lungs were chockers, and a 3cm brain tumor were also detected. First day of BEP and he heamohraged and was flown to the Austin in Melbourne. We're in bendigo. One month in ICU on the ventilator, a stroke, and a dose of shingles nearly got the better of him, but he's a tough bloke and got through it.
    They started the chemo again 4x etopiside and cisplat. At diagnosis his beta HCG level was 2.3million, a the end of the four rounds, it was 11. This week he started the first of four rounds of VeIP treatment. Some scary stuff. We are collecting stem cells next week if things go well.
    That is our story in a nutshell. Anyone in a similar situation? Desperate here to hear some positive news of a comparable case.
    Regards, Lauren

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  • Kiwi
    Hey Andy

    Welcome - the groups here are hard to keep up with as you do not appear to be able to subscribe to updates, anyway there are a few guys here.


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  • Andy B
    Gidday fellas, I'm in northern NSW, just finished my 1st cycle of BEP , so far so good, no major side eefects, starting to lose a little bit of hair.
    Getting my treatment at Lismore base hospital in the new Chemotherapy unit, which is great, people are good and friendly and always willing to help.
    Flash recliner chairs, disgital TV, free tea coffee biscuits sangas etc,.
    I was diagnosed when I went for a 45 yr old health check, I had a vasectomy about 18 years ago and recently remarried, so had a reversal 08' , so when I went for a check up my doc referred me to a urologist who was the doc who did the reversal and he had a look at his handy work ( I now have an 18month old boy!!) he detected a lump in my left testicle, had scans , CT , ultrasound etc, saw doc on a thursday arvo and was in hospital having an Orchidectomy the next day.

    Op went well up and about the very next day, hardly any pain at all.

    will update when I start my 2nd cycle next week.

    Cheers guys hope you are all doing well.

    Leave a comment:

  • pete_qld_au
    Hi guys
    Im in qld here, to get help i have found is near impossible, as im 4.5 hrs west of brisbane, so if you woud like to chat about anything, n everything feel free to contact me. Im 30 here n only have me orchidectomy 4 weeks ago so its all new to me, and depressing, me msn is
    Talk soon guys

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  • TGlover
    Thanks for pointing this out KiWi.

    I am a 31yo guy in Sydney had cysts since I was a kid, which was diagnosed as possible TC with high hCG markers. I/O done (recovering) and following up with oncolgists. Stage 1b with vascular intrusion. Initial operations done at St Vincents but going to RPH in Camperdown for followup with the Sydney Cancer Centre.


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  • Paul54
    Unless anybody has an objection, I'd like to add myself as an honorary member having spent some time touring and learning. We have offices in Sydney and Melbourne. And I shall return!

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  • Kiwi
    Hi Trent

    Like you I am in QLD and with TC#1 7 years ago I did look for some support but there was nothing specific for TC guys. I always was going to approach the QLD Cancer to see if I could help and after being so slack approached them earlier after TC#2 this year and asked about the way I could help. They have one person on their list for TC support and while they would like help they will note take you into their program until after 18 months out of treatment, they said they would be in touch with me next year.

    This local web site popped up a few months ago linked to the Broncos/Titans but does not appear to have been updated.

    I guess its opening up guys to talk about it that is the biggest problem and I find it frustrating that the Cancer Council does not promote an awareness program.



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