September 2023
Hi there Ankrhealth,
Thank you for your post and for providing information to our online community members.
Unfortunately, your video link will be removed as it is not information, or research approved by Cancer Council.
Kind regards
Susana
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May 2023
Hi @Azjoetrucker We haven't heard anything from you in a while so thought I would checkin. Hope everything is well.
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April 2022
great to see your still kicking,I am 59 too had melanoma tumers...not sure what RET+ is,how did they figure that out....I guess for two years on keytruda,I was napping 2-3 hours a day,after it effected my brain was more like getup coffee then back to sleep...now 3.5yrs I stay up all day but dont do much (funny enough sleeping is hard now)...might try Iron tabs,nothing to lose....
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June 2020
4 Kudos
I think how you feel is the important thing. For me it's worth a think about where the things that make us feel good come from, and are they ultimately healthy or unhealthy - but in general, chasing what makes you feel good & happy is seldom wrong. (Sorry, I don't want to side-track you, but mate I do think your a very fired up and resolute individual - and that can come at the cost of acceptance & perspective. I think there *is* a new you, and although I never met the old you, I personally am confident I'd find the new you a lot more impressive as a human being. I'm just writing this gibberish because I think it's important to respect that and not overly measure the future by the past) You want to battle the side effects ? Great mate, I'm impressed by courage and fortitude. You mentioned paranoia and fear of death - those two are MASSIVE, and such elusive, tricky enemies to try and fight. Honestly, I'm regularly failing in that regard, but for me the best strategy is a kind of sideways forgetting, distracting myself with fun and love wherever I can. You want to look better ? Cool mate, especially if that makes you feel better. You look good to me. I'm not a gay man, but hey, I'd pause and think about it (he says with a joking smile) You're winning each day, and that's great. But what happens if you stop winning ? What happens if you have a setback ? Buddy, I just wanted to offer these words to you - you ARE the new you. Like it or not. You're changed. Your life has changed. Let's not bullshit and say "cancer makes you stronger", cancer is absolute dogshit on the shoe of the universe, it's a kick in the guts crap-fest. BUT .. the way you've overall battled it is extraordinary. I've noticed your remarks across the forums, invested with a strength and dignity that can't be ignored. Are you a warrior ? Absolutely. But you're more than that, man. I have a friend who's a great fighter. professional athlete, mixed martial artist. Throughout his life, he's tackled every challenge like a bulldozer. Built like a brick shithouse. But cancer would destroy him. He wouldn't have the tools to take it on. He's a mad viking. but he isn't the warrior you are. You've faced adversaries that many couldn't, and you continue to face them. Yeah man, you're winning. But you're winning more than you think. Sorry buddy, I just wanted to comment about perspective. I applaud the courage and vigour that you have in your attitude, mate - it's fantastic. I just wanted to say that you should weave these victories into that overall picture. Because you are a new you, even if you refuse to accept it. And that new you is strong as all hell. Strong enough to accept the things he cannot change, and fight fiercely for the things he can. I guess it's that "I cannot/won't accept" language that freaks me out a little bit. The take-away to research is phenomenally important, anybody dealing with cancer or it's side effects needs to read up and understand the treatments and some of their vicious side effects. But if you're suffering and looking for courage, I think the key is to find ways to feel better, find ways to be happy - for Viking Joe that's making war against the things that make him unhappy (and more power to him), but if someone else is here looking for strength - it's OK to take up the guitar or fart arse around with learning to paint landscapes. Try to minimise your symptoms, and sure - don't worry so much about a 'new you', there is a lot of bullshit language amongst cancer survivors (and the professionals who try to help them!) , and accepting the 'new you' is kinda one of them, bandied about like 'find your new normal'. You sort of do need to do that - but do it your way. My humble opinion There's this concept of a "Cancer Warrior" which is also, in my opinion, dripping with bullshit. Suffering cancer doesn't make you a warrior. Joe already was. I think I am, actually. But you don't *need* to be a warrior. Just have the courage to take things on as best you can, try and remember to love and be happy wherever you can. Cancer tries to steal that from you. Sorry, I think I failed to articulate a point that on reading felt quite important 🙂 Oh well, stupid me. Congrats Joe, you're a legend, even on days when the cancer shit gets to you more than it should, don't lose sight of that, you're inspiring in your approach. Good luck, mate.
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February 2020
1 Kudo
Sch- To answer your questions- aside from the Joe Tippens protocol, my lympho program is an amalgamation of established lympho massage techniques, swallowing exercises, upper body calisthenics (to promote circulation) and two days using Red Root tincture believed to help detox the lymph nodes. I seem to max out at 10 drops of red root twice per day for two days...more seems to overload my liver. Hope this helps. Joe
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January 2020
1 Kudo
Thank you Joe. I intend to reach back out today. You are certainly right about this new stranger I now am
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January 2020
1 Kudo
Hi Yas- One thing that took me 8 months to come to grips with was the realization that both the cancer and the treatment...pretty much eradicated the person I used to be. The person I was and too many of the people who associated with him...now had different priorities and outlooks. Again, this realization is all too recent but what brought this epiphany to my mind is the fact that I sought new groups and new environments. You see, i found that by being a stranger had the advantage of making friends who simply accepted me, my "new look" and "new interests and priorities" as well as limitations. Seek out new venues and you very likely find new strengths as well as acceptance...and personal usefulness. You will be amazed how your experience can make a positive difference in other people's lives. Cheers, Joe
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January 2020
1 Kudo
Hi Russ... Hope all is well. I am curious how you are getting along post treatment. I am still working my way through lymphoedema of face and neck, searching for a way to at least minimize the discomfort and damage. Still unsure as to the degree of success, but seem to have made some progress stalling the swelling from rearranging my face. Cheers, Joe
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January 2020
1 Kudo
Seven months after last chemo another new Radio Gift reared its ugly head-Face and Neck Lymphoedema. It was interestesting to discover first hand what people meant by "woody neck" and "moonface" (oh, did I mention "Turkey Chin?). Having run out of insurance and no access to medical people...I had to turn to research on the internet. By now the left side of my face had ballooned, my chin had disappeared under swelling and my neck was not only swelled to one side but also disfigured. Came across a tincture called Red Root which was said to clean up lymphatic system and of help to people whose lymph nodes and channels were insulted or plum fried by Radiotherapy. Tried a measly 10 drops in water the afternoon it came in and 15 drops that night before bed. The results the morning after were amazing-the swelling was noticeably reduced, my ability to rotate my neck was less painful. This is only the second day (15 drops this morning and 15drops at lunch time) and already my jawline is almost visible, most of my turkey chin has been refuced and the arc of swing my face from side to side is increased. This stuff is pretty incredible. If you or someone you know is suffering fom Lymphoedema due to radio...have them research this. It's working for me.
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January 2020
1 Kudo
Anyone out there come against Head and Neck Lymphoedema months after cancer? I'm now looking into ways to fight/alleviate the condition and am looking to benefit from your experience with this as well as share my own experiences. Cheers, Joe Aristy
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