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Old 02-12-2012, 01:57 AM   #20
norkdo
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Join Date: Jul 2011
Location: ottawa canada
Posts: 367
Re: Two beloved voices silenced

amy: many thanks for posting this beautifully written tribute on the passing of those two women who were wise and resourceful and working hard for bc while fighting it themselves.

i havent been on this site for awhile and i just saw this now. bonnie you said it so elegantly: denise, amy, all of you make me so honoured to be in your ranks.

denise: lmao : we are aware already let's get on with it. find a damn cure already.


To get to the goal we want (donated money to be spent on cure not on advertising, and hospital buildings, and building new physical space on hospital campuses, etc) I think we have to challenge, by letter writing, those fundraising campaigns. Fundraisers slap any ole optimistic tripe up to get money for their hospitals. They ain't thinkin'. my friend writes for fundraising campaigns by hospitals. Even if the hospital just needs to build another bldg on campus, they are capable of trotting out all kinds of tripe to support the fundraising drive, cos "hey give this hospital a new building" isn't as heart rending as "Race for the cure for breast cancer". we need to know who exactly gets the dollars donated by the public.

I agree, denise and amy and laurel, we need awareness that does not render the public smug ("honey did u remember to contribute to breast cancer this month? What? Yes? Oh good that's taken care of." and "I do my mammogram every year so I know I will never die of breast cancer.") but to offer a place where grieving children/friends/spouses of b.c. survivors and as many individuals as possible, can focus their compassion and generosity productively, not wastefully. how about we plan a giant march on Gentech? LOL. no but really. how do we get the researchers working on cures higher up the financially important list? Komen, for instance sucks at that.


change of topic
re: Amy's first post above
thank u so much for bringing this up.
there are levels within the appearance v.s. reality weirdness we have all been forced into. worse, i know, in our mothers' days, and grandmas' days for sure. but this weirdness is what u don't know about before getting b.c. and once you do then weird is the new normal. sometiimes i feel like someone in that movie Body Snatchers.


level one, as i call it is superficial appearance vs reality stuff. As we sport our new balding looks during and post chemo, for example, all the other women who went through what we have, sometimes salute us and reveal themselves as fellow survivors.

it happened to me this past week in the plastic surgeon's office. a b.c survivor, six yrs past her reconstruction actually guessed me correctly as a b.c. person by my post chemo hairdo!! or perhaps by my unbalanced chest??? she ended up showing me her entire reconstructed breast in the waiting room! i was glad she did becos i had just remarked that i was going to ask the surgeon what the tattooes of nipples end up looking like. just one example of the weird world we have been dropped into. and i was so honoured by her help. more info is better info.

re: the topless breastless woman who was unfortunately thrown out of the Komen tent

I ask why was she threatening to the Komen women? Komen women should have known better. the topless gesture, being radical, yes, and not particularly "normal" was, I suppose, a challenge to the whole concept of normal.

Those of us with b.c. don't get to choose what is normal anymore. "Normal" is now two large men adjusting my naked torso between them daily on a radiation bed, as if i am no longer a living breathing woman. I still have a nipple on one breast to be embarrassed about. I still feel embarrassed half naked in the hands of two big radiation techs. I don't get to choose. I have become a non sexualized thing now, to them or anyone for that matter. but i am only speaking for the decorum in my particular hospital.

we don't choose our new, imposed weirdness. The ugly deformity of my chest was thrust upon me. We didn't ask to be radically altered, and made newly abnormal. But should we be outcasts when one in eight women will have those weird slices across their torsos in lieu of breasts? My mom chose not to reconstruct so i saw her scar each morning as I watched her make her face up half dressed at her vanity, since i was ten. Even for me, who should have been used to it, I find it traumatic every time I see myself in the mirror after the bath.
when I see other women at the cancer center, now that I go for my thirty radiations, in the same lopsided shirts with the short hair I feel like I am living a science fiction new reality...the one in eight women who are bald and one breasted.

But a deeper level of the Appearance vs Reality weirdness comes when people say "oh b.c. is practically cured now like Aids. It's at vaccine level almost" I have heard that from my sister and from a chemo nurse. You tell them b.c deaths have not improved too much (coupla percent yes) for sixty five years. Billions donated to it. Still no significant change in death rate. they say "that's not what i heard." and they shake it off. but I reply that Linda mccartney died from it. elizabeth edwards died. both women caught it early through mammograms and both women really well connected and rich. as amy says above, the deaths occur regardless of one catching it at stage zero or stage four. hey, this stuff travels, ok? they're called lymph nodes.

Thank you amy for this thread. I really want to thank you for it. Sometimes we have to prepare to dwell on the negative in order to spark change. I will reread all the posts on here over and over in the next few days as they are so thought provoking. amy you are a poet. love reading your wise thoughts.
__________________
fall 2008: mammo of rt breast worrisome so am asked to redo mammo and have ultrasound of rt breast.I delay it til january 2009 and the results are "no cancer in rt breast. phew."
found plum sized lump in right breast the day before my dad died: April 17th 2011. saw it in mirror, while i was wearing a top, examining my figure after losing 10 lbs on dr. bernstein diet.
diagnosed may 10 2011

mast/lymphectomy: june 7 2011, 5/20 cancerous nodes. stage 3a before radiation oncologist during our first mtg on july 15th says he found cancer on the lymph node of my breast bone. Now stage 3b.
her2+++, EN-, PN-. Rt brst tumors:3 at onset, 4.5 cm was the big one
chemos: 3fec's followed by 3 taxotere, total of 18 wks chemo. sept: halfway thru chemo the mastectomy scar decides to open and ooze pus. (not healed before chemo) eventually with canasten powder sent by friend in ny (illegal in canada) it heals.
radiations:although scheduled to begin 25 january 2012, I am so terrified by it (rads cause other cancers) I don't start til february, miss a bunch, reschedule them all and finally finish 35 rads mid april. reason for 7 extra atop the 28 scheduled is that when i first met my rads oncologist he said he saw a tumor on the lymph node of my breastbone. extra 7 are special kind of beam used for that lymphnode. rads onc tells me nobody ever took so long to do rads so he cannot speak for effectiveness. trials had been done only on consecutive days so......we'll see.....
10 mos of herceptin started 6 wks into chemo. canadian onc says 10 mos is just as effective as the full yr recommended by dr. slamon......so we'll see..completed july 2012.
Sept 18 2012: reconstruction and 3 drains. fails. i wear antibiotic pouch on my job for two months and have 60 consecutive days visiting a nursing centre where they apply burn victims' silver paper and clean the oozing infection daily. silicone leaks out daily. plastic surgeon in caribbean. emergency dept wont remove "his" work. He finally appears and orders me in into an emergency removal of implant. I make him promise no drains and I get my way. No infection as a result. Chest looks like a map of Brazil. Had a perfectly good left breast on Sept 17th but surgeon wanted to "save another woman an operation" ? so he had crashed two operations together on my left breast, foregoing the intermediary operation where you install an expander. the first surgeon a year earlier had flat out refused to waste five hours on his feet taking both boobs. flat out refusal. between the canadian health system saving money and both these asses, I got screwed. who knows when i can next get enough time off work (i work for myself and have no substitute when my husband is on contract) to get boobs again. arrrgh.


I have a blog where I document this trip and vent.
www.nora'scancerblog.blogspot.com . I stopped the blog before radiation. I think the steroids made me more angry and depressed and i just hated reading it anymore
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