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Posts with tag collarbone
Posted Mar 28th 2007 9:00AM by Jacki Donaldson
Filed under: Breast Cancer, Prevention, Daily news, Thought for the Day
More than 200,000 American women are diagnosed with breast cancer every year. And about six percent of all invasive breast cancer cases involve a condition called inflammatory breast cancer (IBC), the most aggressive and often undiagnosed form of the disease.
IBC does not present itself in the form of a lump or mass and is typically not detected by self-examination, mammogram, or ultrasound.
IBC is a misunderstood disease. But if women learn to recognize some of the symptoms, there is a better chance for better diagnosis, treatment, and survival.
Think about this, a list of early symptoms of IBC:
• One breast rapidly becomes larger than the other
• Breast has a rash, redness, or blotchiness
• Breast and/or nipple persistently itches
• Breast tissue thickens or feels lumpy
• Breast becomes sore with sharp pains
• Breast is warm to the touch or feverish
• Lymph nodes under the arm or above the collarbone become swollen
• Breast dimples and may look like the skin of an orange
• Nipple retracts or flattens
• Color of the areola (the dark skin around the nipple) changes
Contact your doctor immediately if you detect any of these symptoms.Posted Sep 14th 2006 10:00AM by Jacki Donaldson
Filed under: Breast Cancer, Cancer Survivors

On January 14, 2005, my sister drove me to the hospital for my port placement -- a minor surgical procedure to implant an
Infuse-a-Port® underneath the skin on my collarbone. My port -- used steadily ever since that January day for the infusion of breast cancer chemotherapy drugs -- is about to be removed.
Tomorrow -- September 15, 2006 -- my sister will drive me to the same hospital where another minor surgery will result in the removal of this same port and its accompanying parts. I will come home with a scar that will mark the spot symbolic of my cancer travels. Along with my healed lumpectomy incisions and my head full of new hair, this scar will remind me of where I've been and will not ever let me lose sight of where I'm going -- full steam ahead into a life I am blessed to have in front of me. A life that was never promised to me for any specific amount of time. A life I am going to wrap my arms around -- for every second, every minute, every breath I am lucky enough to take.
Posted Aug 24th 2006 9:00AM by Jacki Donaldson
Filed under: Breast Cancer, Chemotherapy, Cancer Survivors

And so the countdown begins -- 22 days until my port comes out. On September 15 at 9:00 AM I will report to the basement of Shands Hospital at the University of Florida where I will be doped into a semi-conscious state and wheeled into an operating room. Doctors and nurses will open the skin near my collarbone and while watching their own procedure on a monitor hanging overhead will remove my port and all connected tubing. They will close my skin, leaving an incision that will quickly become a scar -- and a physical reminder of the cancer than once settled into my breast and the drugs that ran through my veins in search of it. It will be my battle scar -- second in importance only to the marks that criss cross my stomach and mark the spot where two big baby boys stretched my skin to unimaginable proportions.
The state of my port has plagued me for some time now -- ever since I knew chemotherapy was fast approaching its end. I have wanted to keep it in place just in case I need it again. And I have wanted to get it out just in case I never need it again. And when it came down to making a decision, I decided taking it out was best. So I can move on. So I can move forward. So I can move away from cancer. I know I'll never move completely away from it -- and that's okay. I don't want to forget my journey. I just want to live beyond its reach. Beyond the port that pops out from under my skin. The port that if needed again, can simply be put back in place.
And so my soul searching -- chronicled in the following two posts -- is over. My port is coming out.
Posted Jul 27th 2006 9:00AM by Jacki Donaldson
Filed under: Breast Cancer, Drug, All Cancers

My port -- that thing that pops up from under the skin on my collarbone, that thing that by default stays in place because I can't decide whether or not to remove it -- is now officially in maintenance mode, now that my treatment for breast cancer is complete. My last Herceptin infusion was on June 28. And my first port flush was today. For as long as I keep my port -- and for as long as it has no real use -- I must have it flushed one time each month. So today, I strolled into the cancer infusion center where I've spent many hours and this time spent just a few minutes -- enough time for my usual chemo nurse to puncture the skin on top of my port, push through a rather large needle, and inject a dose of blood thinner into the lines of the port to keep clots away. The whole procedure was harmless, painless, no big deal at all. And I will return one month from today for a repeat performance.
One day these once-a-month visits may become a hassle. After all, I have to find a place for this appointment in my already-busy schedule and find childcare for my kids and find a place to park. I have to numb my port and endure a needle stick and sometimes fight traffic to get home. And the whole trip to and from the cancer center takes longer than the procedure itself. Clearly, this may be a waste of time for a port I don't even need right now. But at the moment, this visit is just what I need while I sort out the details of my post-treatment world. I need to go back to the infusion center. I need the comfort of the drive. I need to feel part of the chemo community. I need medical people swirling around me. I need a bit of hand holding. For now anyway.
Posted Jul 25th 2006 7:30AM by Jacki Donaldson
Filed under: Breast Cancer, All Cancers
I can't decide what to do about my port now that my breast cancer treatment is over. It's been an on-going internal battle. I don't know whether I should leave it in place -- tunneled underneath the skin on my collarbone where it is available and accessible should I ever need further infusions of cancer-fighting drugs -- or whether I should have it removed since there is no real purpose for it right now. There is the issue of superstition and safety -- leaving it right where it is allows for easy use if cancer returns and prevents another surgery to implant a new one. But there is also the issue of moving on -- and removing it because I don't need it, because I may never need it. One doctor told me recently that it should come out because if it remains in my body, I risk infection. And anything foreign in my body for an extended period of time is not completely safe. But a cancer survivor told me that she had hers removed immediately after treatment and had to get a new one because her cancer recurred three months later.
I am accustomed to wrestling matches like this one -- like my stand-off between treatment with Taxol or without Taxol, between anti-depressant or no anti-depressant, between vegan diets and traditional diets. Sometimes I can make a good call. Sometimes I just can't decide. Like right now.