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Thanks, and backattcha ya know* Just sayin. http://www.davita.com/UploadedImages...rStress-th.jpg |
BuMpInG
http://i177.photobucket.com/albums/w...41209/HOPE.jpg http://i332.photobucket.com/albums/m...abob/Faith.jpg My Faith is larger than the Hills -- by Emily Dickinson My Faith is larger than the Hills -- So when the Hills decay -- My Faith must take the Purple Wheel To show the Sun the way -- 'Tis first He steps upon the Vane -- And then -- upon the Hill -- And then abroad the World He go To do His Golden Will -- And if His Yellow feet should miss -- The Bird would not arise -- The Flowers would slumber on their Stems -- No Bells have Paradise -- How dare I, therefore, stint a faith On which so vast depends -- Lest Firmament should fail for me -- The Rivet in the Bands |
this will be the first time I have spoken of this online, hell I don't talk about it much in person. I have stage 3a breat cancer. I have been batteling cancer of one type of another for a few years, first just benign tumors, then uterin cancer, after a hystorectomy I was good for a few years then one day there they where...3 lumps in my left breast.went it for a checkup, then the biopsys...then the 5 days wait...wich I think was the hardest part...then the news that changed everything. they wanna take my boobs, and I know that choosing between cancer and my clevage is a no brainer Im a girlfriend and a mother, but I love my clevage....I finally found a doc that will use my body fat for reconstruction...yayy! tummy tuck and new clevage! went in for per op stuff and my white blood cell count is in the 100,000, for those that don't know thats WAY more then it should be. So now I take pills and wait some more....
I, at first, felt like this was punishment for some awful thing I had done and then I thought about my life and I could't come up with one thing I had done that was that bad, I mean I know I am not perfect but jesus...I'm not that bad either. I made a bucket list...Everyone thoought that was funny, but what if they can't fix it, what if I die? I dont wanna go out feeling like I haven't done anything I wanted to...ya know...now I live in a new place, and I don't have a lot of adult friends...that sucks more cause I feel the depression...So I am seeking new peoples to relate with, people inside and outside my community to laugh with and talk about stuff other then cancer, but I guess I have to talk about this stuff too:hangloose: |
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We are here for you(f) Don't Quit When things go wrong as they sometimes will, When the road you're trudging seems all uphill When the funds are low and the debts are high, And you want to smile, but you have to sigh, When care is pressing you down a bit -- Rest if you must, but don't quit. ife is strange with its twists and turns, As every one of us sometimes learns, And many a fellow turns about When he might have won had he stuck it out. Don't give up though the pace seems slow -- You may succeed with another blow. ften the goal is nearer than It seems to a fair and faltering man, Often the struggler has given up When he might have captured the victor's cup, And he learned too late when night came down, How close he was to the golden crown. uccess is failure turned inside out -- The silver tint of the clouds of doubt, And you never can tell how close you are, It may be near when it seems afar, So stick to the fight when you're hardest hit, -- It's when things seem worst that you mustn't quit. -- Author Unknown -- |
It doesn't knock
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Hi there.. Well, if you were close by, we could chat about that Club we became members of without even asking. That one that makes you realize your mortality, and that makes every day matter. And it's scary. Have you researched ALL your options? Looked for Clinical Studies in your neighborhood. I signed up for one after being diagnosed with Uterine cancer almost 7 years ago. If there is anythiong I can do, holler, write, scream, send smoke signals, or PM me. My email addy is in my profile. This is from NIH.gov website. Stage IIIA (operable) Modified radical mastectomy or radical mastectomy with either radiation or chemotherapy. Radiation could be preoperative external beam radiation or postoperative external beam radiation with a booster dose to primary site. Chemotherapy could be CMF, CA, CAF, CMFP, CMFVP, L-PAM and 5-FU with or without tamoxifen. Here is a link to look at what's new and what's going on in the research and clinical trials. http://www.cancer.gov/clinicaltrials...archid=8960422 So, stay in touch. and PS: I'm glad you are going through with the mastectomy, with or without the reconstruction, the cancer needs to go. Bang Bang:fastdraq: |
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Last week I had my last chemo treatment for Stage 3a colon cancer. I had surgery in early August and then had chemo starting a month later every other week (along with a chemo pump for 48 hours after each infusion). I tend to be a person who researches the heck out of the smallest of things when making a decision (for example, when buying a new camera), but this was the one time I chose not to. I was concerned that I would become overwhelmed with the information I found and I was worried that I would get the wrong information. You have been down this road before, so you probably know a lot already and know what you want to know and don't want to know, so that is a good thing. I found that I wanted to know little about the surgery, but a lot about the chemo treatments. Fortunately, I chose a surgeon who didn't talk, but found a chatty oncologist. Let your doctors know what you need and the pace you want to receive information. I live in an area that has one of the highest cancer rates in the nation. I am considering moving even though I have lived here my whole life. Although I believe that nutrition, exercise, and in some cases heredity, impacts one's chances of getting cancer, I believe the environment does, as well. Hopefully, someone who has had breast cancer will come in here or PM you. However, if you want some additional support from someone else who has had to deal with cancer (although not the same type), please don't hesitate to PM me. Seriously. Anytime. Take care of yourself. |
So I have been away from the site for a few months now. My ex was dx with this in Sept. 1 week later was starting chemo and the 1st day of chemo she found out it had already spread...3 spots in her L5 1 in her hip and 1 in her femur. She in the beginning pushed me away then she wanted me there to take care of her and our house and animals we have together. I am the 1 she screams at...fusses with etc. I feel like I am CONSTANTLY on an emotional rollercoaster to the point of starting therapy next week :(
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One Day At A Time
Cancer doesn't call to see if your busy and have anything planned
Cancer doesn't care that you have other plans. Cancer doesn't knock, it just comes crashing through the walls of your sanity. and then...it disappears. Or does it. Morbid thoughts before a pre-op at 3:30. Raw feelings..me with feelings, wanting to see the sunrise, and hold my tigger while she purrs, and rub Peaches boy till he goes to sleep, and smell the roses. To hear the voices of loved ones near and far that I have failed to call and touch base with. Wanting to plant that 7th rose bush on May 15th. Wanting quiet in my mind. Wanting everyone to be okay. Just for today. I'll deal with tomorrow when it gets here. .:bunchflowers: |
Blessings and Strength
http://i201.photobucket.com/albums/a...t/DSC02256.jpg A Time To Believe To believe is to know that every day is a new beginning. It is to trust that miracles happen, and dreams really do come true. To believe is to see angels dancing among the clouds To know the wonder of a stardust sky and the wisdom of the man in the moon. To believe is to know the value of a nurturing heart, The innocence of a child's eyes and the beauty of an aging hand, for it is through their teachings we learn to love. To believe is to find the strength and courage that lies within us. When it is time to pick up the pieces and begin again. To believe is to know we are not alone, That life is a gift and this is our time to cherish it. To believe is to know that wonderful surprises are just waiting to happen, And all our hopes and dreams are within reach. "If only we believe" Author Unknown |
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Yes, it is understandable that her fear and anxiety may result in irritability, but that doesn't mean that she shouldn't acknowledge it or keep it in check. As a side note, I know that the steroids in my chemo treatment (5FU) causes some BIG TIME irritability in me. My point is, her irritability is not just about having a serious illness, it is also chemically induced. I worked almost full time (72 hours every two weeks). I had been only taking a half day on chemo infusion days, but after noting I was irritable with coworkers, I decided I needed to take the whole day off. In general, I was kind of whacky. In fact, I screwed up and wrote something in a work email that I shouldn't have during that time (and never would have if I was in my "right mind"). There were some repercussions due to it. My point is, understand her emotional state, but don't excuse her behavior. Therapy may be helpful to her. Some cancer centers have therapists trained in working with people who have cancer. Also, there may be some free support group there, as well. At minimum, it may help her to get on some support groups/forums online to talk with others who have the same illness. I know that you and my partner have been PMming, but if you want to talk to someone who went through cancer treatment, please don't hesitate to PM me, as well. I would also be happy talk with your ex via email if she is not on this site. It is a very tough road to travel. For both of you. Take care of yourself. |
Rosie and I are asking for prayers for her one and only sister. She has Barrett's Disease. In fact, she has had this for a number of years, and it has just gotten worse over time. Medicine no longer works, and surgery is a 50/50%. However, she is highly allergic to most anethiesthics (sp?), which decreases her survival rate. We are hoping for surgery in August, but that too is up in the air. She has a tumor growing around her voice box and vocal cords. It is a bad situation no matter how you look at it. Thanks. |
Reminding those that believe., and those that don't. Know what it is all about.
~ If only we believe~ Cherishing today. Thanks SD..
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Just thought I would read, and resend strength and courage from my heart to yours. Hope today is full of sunshine for those in the dark, and warmth for those that are indoors, If only we belive |
Finally got my chemo port out yesterday! Nice to have that reminder, gone!
Soon I will have another colonoscopy and then I will feel completely in the clear! :thumbsup: |
Congratulations Dap. Having lost My Dad to cancer.. and watched My Mom fight and beat breast cancer.. I know this must be a huge relief.. and victory for you. I hope you continue to regain your health.. and remain cancer free. smiles.
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Hey DapperButch, Having that chemo port out must be a reason to Celebrate...:wine: My friend Milana heads to surgery for her second one in on Monday. Infection at 1st port site, and she has only 3 more sessions. Every day is such an adventure, and your upcoming colonoscopy is one of the favorite things you can do, and I KNOW YOU WILL BE THRILLED WHEN IT IS OVER.. :vigil: Had mine several weeks ago, and got the best report. Doc said "Your colon is boring. See you in 5 years." So, keeping my fingers crossed that all the tests, MRI, US, lab work over the last month match the negative colonoscopy results. |
DapperButch, a question about your chemo port...did you ever consider leaving it in or was it a no brainer for you as far as having it removed? My thinking is that it's yet another surgery. :(
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It was a really simple surgery. They don't put you under like they do when getting it inserted. My doc just gave me a local, cut me about 1.5 inches, and then popped it out. Easy peasy. I asked to look at it b/c I was curious. It just looked like a large tadpole! And there really isn't much pain afterwards, either. I had some serious pain for a few days when they put it in b/c they have to push and pull on the muscle, but no pain really after it came out. I don't think I even took a Tylenol. ETA: It is funny that someone posted on this thread today. I have my colonoscopy tomorrow...so I going through the "prep" right now. sucks ass. no pun intended. |
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Positive thoughts for tomorrow's "butt T.V." Oh, how I loathe bowl prepping! :goodluck: |
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If you have any more questions/need support, feel free to PM me! |
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