Posts by Ellen Harris-Braun

the 5th floor

On my way up and down the elevator from Nuclear Medicine the day before my first surgery, the doors kept opening on the 5th floor, where there was a big bright cheerful sign:

Morrell Center for Childhood Cancer and Blood Disorders

Every time, I kept thinking, thank goodness this is about me and not them.

telling people is the worst

I don’t like being the center of attention. I don’t like giving people bad news. This is not a good recipe for someone who has to go around announcing that she has breast cancer again. Silver Bay, where there were maybe 50 people who needed to be told, was getting a bit agonizing.

Hi, how are you? Oh, I’ve been better.

Eric told a few people. I told a few people. Spee and Sandy mercifully went around telling some of our friends so I wouldn’t have to…what a relief! I felt so taken care of.

timeline (july-august 2006)

Here is a timeline of this summer’s breast-cancer adventure:

Late May: found lumpy area in left breast. This was only the second time since my first breast cancer in 1995 that anything had worried me–and the first was in ‘97 or ‘98.

Early June: went to midwife for annual exam, she agreed area felt worrisome, said to wait a couple of weeks and then (if it didn’t go away) get an ultrasound and a surgical consultation. Waited 6 days, didn’t want to wait anymore (I’ve never had cyclical lumpiness), scheduled ultrasound

what am I doing here? (said Persephone)

Good question. Given my reaction to blogging, nothing but something unusual and prejudice-shaking would bring me here. That something seems to be breast cancer, for the second time in my life, just before my 40th birthday. Though I have been sending out periodic e-mail updates to a large list of family and friends, there are some musings I haven’t wanted to deliver to peoples’ In boxes yet still thought some people would want to hear. Not sure yet what exactly I am up to, but capital letters are sure making me self-conscious.

So one thing I realized I’m feeling, overall, is that there are these two worlds–the world of the well and the world of the sick–and I slip from one to the other all the time. Maybe slip down into one from the other in a big way, too, with this scary diagnosis, and emerge later…next February?…back to the regular world again. Maybe the cycle is bigger–every 10 or 11 years?

Everything is chugging along in life and breast cancer is far behind me, making me an interesting and maybe more evolved person, but certainly not part of my personal day-to-day life, and then suddenly the ground opens up and I’m back in the hospital-doctor-surgery-Vicodin-recurrence percentages-chemotherapy drugs world with all the other scared sick people.

Here is where my reaction is kind of interesting. When I’m in the world of the sick, I feel relatively well and lucky, especially to have the partner I have and the family, friends, and community we both have holding us up. Not to mention having a curable disease, and being smart enough to learn what I want to learn to feel like a part of my own care. And finding good doctors who will talk to me and answer my (sometimes overly intellectual) questions, and perhaps even enjoy doing so. So it is somehow less complicated and less depressing to be in the world of the sick. Plus, priorities are pretty clear there.

Then I surface back into the world of the well where I am Greatly Impaired all of a sudden. Have I just had surgery and am on painkillers and have no energy? or am I just tired, distracted, worried, and wanting only to either Fix Things, Learn Some More, or read an escapist novel? Either way, I’m feeling Not Normal and being around normal people, living their life in the world of the well and not even being conscious of the world of the sick, really makes me feel pitiful. I feel like I don’t fit in at all anymore and have nothing to talk about–at least with people who don’t know what’s going on with me. And with the people who do know, sometimes I want to talk about it and sometimes I just want them to know, so we don’t have to talk about it.

This slipping back and forth is hard to handle. It’s also hard to explain why a trip to the oncologist is easier to deal with, for me, than an afternoon at the beach.