how to treat an ulcerated (breast) tumor
Comments
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piper's dream,
Lovely story about your grandmother. She sounds like she was a special person. That being said, I really find it difficult to "respect" anyone who joins a message board because they have decided that they have a particular disease, without actually knowing if they do. I can't imagine posting on a forum, where women are dealing with life and death issues, and saying, " yes, I have that disease too, even though I haven't been dx'ed". And, despite understanding why Abigail won't see a doctor, it is not respectful to those of us who really do have bc.
As for honoring her "belief" that she has bc? I guess my feet are too firmly planted in reality to understand how we can honor such a thing. Because I think something or believe something, doesn't make it true.
Caryn
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"we" don't have to deal with it, I do. I've described it & described how I treat it.
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If someone clearly has a solid ulcerated tumor on their breast that is growing in size, and they don't want to get it smashed and radiated, and poked numerous times w/ large needles leaving seedlings and more of what is likely cancer all around it, I can respect that, and I do respect that. Everyone deserves respect.
To repeatedly insinuate, that a member on the breast cancer site doesn't deserve to be here, is disrespectful. You don't have to agree w/ her choices. You don't have to believe she has breast cancer. But you most certainly do not know that she doesn't have it. The likelihood given her symptoms is that she most definitely could. She's made her choices, she's given her reasons for making those choices, and it has been decided that she is allowed to be here, and to post on the alternative forum because that is what the alternative forum is really for, not for arguments w/ people who don't like, nor understand alternative choices, so why not just accept that?
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Reminding members again to please be respectful of others experiences and choices. Our community is an inclusive breast cancer/breast issues community and therefore we acknowledge that there will be diversity within the community but that people can still come together to support each other within the forum/s to which most relates to them and their experience.
Thanks again for your understanding and for the support you offer to each other.
The Mods
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I guess that since I have dx'ed bc, as does almost everyone else on these boards, and as I have watched many, who have been dx'ed, struggle and pass away, it pains me that someone who may or may not have this disease, is considered in the same light as the brave women who know that they do. Ultimately, the lack of acceptance of Abigail's self dx is my problem. IMO, it dishonors and disrespects people who do. I have no qualms with alternative choices, just never imagined that self dx was one of them and that just because someone says they have a disease we should honor that.
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biopsy, exrays & such are toxic. if I could be diagnosed by a look-see I'd pretty much have no problem though there's no "treatment" I've read about here that I could stand still for so I see no need. to get the ins I want, perhaps. stay tuned
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Caryn, I do hear you and I've heard you several times now. You are insisting on taking another's own very personal choices personally. You feel disrespected, and feel you must lash out by disrespecting them in return.
I too have grown close to people who have suffered and died from this disease and I certainly do not feel dishonored or disrespected by Abigal or her choices..and I had a diagnosis by a doctor.
Maybe you could start your own thread on another forum about your feelings regarding self diagnosis, and alternative choices, rather than taking up this space on the alternative forum?
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While I respect people's choices, I do have to say that it's very hard to encounter such blatant self-delusion, knowing that it's going to end in the most spectacular train wreck. I find it exceedingly painful that people are enabling such self-delusion in the guise of "respecting another's choice" and supporting it. It's like watching a child playing in traffic. Not to step up and say- or do something is irresponsible. I cannot support abigail in such a path. I could not support anyone in such path. And those who keep insisting that I must... well, I have no words for the damage being caused.
abigail. Go to a doctor. Get a diagnosis. Get treatment. You DON'T have to live like this, you really don't. If this is breast cancer, you need treatment to help with the pain. If it isn't breast cancer, you need to know what it is, so that it can be treated properly. Please, I beg you. You don't have to live like this.
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I don't believe conventional is proper treatment. I don't post for you or the others, I post for members who may have the same symptoms, I've come across some, one not here, had a "risen" lump as I did & was diagnosed with an inoperable cancer. shes had an infusion to shrink the tumor, but it didn't shrink. she is in pain & her lesion (s?) gives off she says a quart of liquid, orange, a day. she's also tired. my trouble is so much less. but I wouldn't like to make it worse as it seems she may have with conventional chemotherapy
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I'm reporting your post Selena because it disrespects the rules of this forum.
People who take the conventional route who have ulcerated tumors do not typically seem to have good outcomes either. Quality of life and yes quantity can often result from a non-conventional choice.
Someone on here argued that Steve Jobs, because he didn't do chemo for his pancreatic cancer died as a result. He still lived for 8 years as a result of his choices. Patrick Swayze died w/n 2 years of his diagnoses when he used chemotherapy from the start.
You do not know that Abigal choosing your path instead of her own would not result in more suffering, and quicker death.You do not know and cannot determine the result of her choice and compare it to the result of a choice that you would make. That is disingenuous to say that you can. Abigal is "not diagnosed but worried" and she is suffering too.
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On some level I feel disrespected by anyone who self-diagnose's their own cancer. In this particular case I didn't read too deeply until Abigail mentioned she'd had what appears to be a fungating breast tumor for "many years" (although it is unclear to me just how many). I witnessed the horror that another member endured back in 2011/2012 when I first arrived here, as she was trying to cure her fungating tumor with an alternative treatment (I won't go into details here because this isn't about the treatment but about this person's experience). I call it a horror because she was in excruciating pain, desperately attempting to save her life, and she died what was likely a horrible, painful death. She honored us by sharing her journey even when she knew it would not be a positive outcome. She didn't survive "for years" with this tumor, but rather died within a few months.
I gave no quibbles with the choices others make for their own treatment, be it conventional, alternative, complementary, whatever. My concern is the message we leave behind in our posts here, for those who come after us looking for answers, who are Not Diagnosed But Concerned - you don't need a doctor, it's perfectly acceptable to self-diagnose, then create your own treatment plan. Just because you believe you have cancer (or anything else) doesn't make it true.
More importantly for me, Abigail, is that I wish you would care enough about yourself to at least learn what you are dealing with so that you could use the best alternative and holistic treatments for your situation. Any reputable doctor should be able to confirm a fungating breast tumor without invasive procedures. Without those you wouldn't know the receptor status or type of BC - but you've made it clear you don't necessarily care about that. And frankly, if you know more about what you're dealing with and you find alternatives that help you, we would want to hear about that. It is hard to know if what's working for you would work for me if I don't know what you're truly treating. I read this thread to educate myself about alternatives so if something makes sense to me, I might try it. I appreciate having options.
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I have hesitated to post in here, but NancyHB has summed up my exact thoughts on this:
I gave no quibbles with the choices others make for their own treatment,
be it conventional, alternative, complementary, whatever. My concern
is the message we leave behind in our posts here, for those who come
after us looking for answers, who are Not Diagnosed But Concerned - you
don't need a doctor, it's perfectly acceptable to self-diagnose, then
create your own treatment plan. Just because you believe you have
cancer (or anything else) doesn't make it trueWomen coming to these forums are often scared, and vulnerable, and I truly worry about what some of them may choose to do after reading threads like this, when they don't know the backstory, like about how abigail has never been diagnosed though I recall her saying she has had what she calls breast cancer for decades; that is either one very slow growing breast cancer tumour (that has not turned metastatic) or it is not breast cancer at all. They also don't know all of her "treatment" and may be too scared to do anything if they believe a fungating tumour is inevitable for them too. I too remember that forum member with a fungating breast tumour (I was still lurking then to find more information on my mother's diagnosis, and my own high risk status). And yes, it was horrifying and heartbreaking to witness, especially near the end when she knew that she was out of options.
I also don't believe that just because someone has a belief it deserves automatic "respect" without comment or judgment. That is not true in the offline world, and ought not to be on here, not when those beliefs have the potential to harm others. I can respect a person's individual autonomy, without respecting or honouring their harmful, dangerous, and/or uneducated beliefs.
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I had what I'm pretty sure was a cyst 50 years ago, from the "birth-control" tablets, it was said to give them & mine was the first generation & mexican, from sheep there. then 10 years of america-type. one docktor when I was trying to get a re-fill her face changed when she pressed that breast. I said "cysts", & never went back to planned parenthood. it went bad only after a year of juicing fennel )'08-'09. early on ''10 I got my first laptop. in march the cyst, began coming through the skin, kept growing (slowly), & now is a great deal bigger. what ever it is it takes a lot of time to manage. I'd like to see the thread about the ulcerating tumor here, I've not found such
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Abigail - your experience with this cyst or tumor is *real* - regardless of whether of not it's breast cancer. You will find little information here about fungating tumors because very few people will get to a point where their tumor is breaking through the skin and ulcerative. Even in alternative-therapy circles, surgery is typically considered acceptable practice; removing the cancer keeps it from fungating. You may find information on the interwebz about treatment - but that, too, usually includes surgery. Please be cautious when critically researching treatment for your current situation.
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appreciate your post, Nancy. I'm currently nervous about the artemisia topical use. I read the chilipadi posts a while ago, hadn't realized she used the "black salve" internally. I havn't used much that way, but still. I think the artemisia oil must be estrogenic. I'm gearing up currently (3 days of use, not concecutive) I think I'll start gearing down, then up again. one site said to use it for 3 weeks , that was internally. it's very dark colored & smells strong.
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not cancema?? bloodroot what I've known to call it
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light and wind,
I have no problem with alt tx, but self dx is another thing. I am not talking about any type of tx, Steve Jobs or anything else. I am speaking only to the idea of supporting someone in a self dx of bc. Encouraging and asking for respect for that is totally beyond my realm of comprehension. I agree with Selena. If I see someone walking in to an inferno, I'm not going to ignore it and respect their choice.
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Fell teknique used blood root for breast tumors in the 1800's but I can't find more about that. but if chilipaddi used the other stuff it seems very not good. blood root? don't know. know it grows here but is endangered
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please recall I'm now 77 years old with no lover or children.
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The woman with the ft had chemo. It didn't help her. Drs refused to operate. she had no conventional options. She tried salve which didn't work. Saying that she died as result of using the salve isnt accurate.
Should all the women who have died after all the chemo be blamed for their choices? Should I post research on how chemo harms more than it helps on the chemo thread?
Why are we enabling all of these women to choose a quicker death by chemo?
Caring about onesellf does not have to mean subjecting oneself to debilitating tx that may harm them even more.
Caryn I can't comprehend why someone chooses chemo in many instances when it has been shown to provide little if any benefit and a lot of harm. That is why I post my altetnative views on the alternative forum.where I thought they were not to be judged.
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I still respect any person who makes any choice. I respect that it is theirs to make. I respect people who see things differently than me, but I don't like it when people gang up and judge a person especoally when that is supposedly not allowed here.
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actually, if you re-read my post you will note that I never said she died because if her alternative treatment choice - in fact, I specified that I wasn't talking about treatment but rather her journey.
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You know, I've never reported a post.....ever, but if you all don't let my friend rest in peace, I'm going to start. I know exactly what she went through. Seriously presumptuous and kinda ignorant, I might add, to insinuate she died because of her choices.
Edited to add: there is absolutely no reason to bring up her suffering in this thread again and again. Two totally different situations.
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Its not a pretty horrifying journey with toxic chemicals ?
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Steve Jobs had a curable type of pancreatic cancer. Swayze did not.
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came across your moniker the other day: you then are what can be called, not a hindue, but a god-person?
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lightandwind,
I am not speaking of chemo or any tx for that matter (I've never had chemo myself). I just can't fathom supporting the dx of bc or any other disease just because a person decides that's what they have.
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no, I decide I have something on my rt breast which probably is some kind of trouble, a tumor probably certain,
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As for the woman who had IBC that became a fungating tumor. No one will know for certain what she died from, save breast cancer in the end. At the time of dx, she chose to have no conventional tx, not even surgery. Later on, when her disease was quite advanced, she did try chemo. Her doctors would not operate because it was not feasible at that point. Ultimately, she died from bc and we don't know what might have resulted if she had made different choices. Pointless to speculate.
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the domain name of this site is misleading. It should maybe be renamed "breast dot org" to reflect the confusing part of this topic (for me). Then, I think all women should help a member be responsible in her choices if it is apparent that what she is doing is possibly harmful.
I wish I had not had my one chemo infusion and believe I can be cured by alternate means but not if I get so obsessive about all means being "alternative" that the stress does me in.
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