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May 30, 2006

Moratorium

Just so you know, you will not be reading any more cancer news on this website for at least 5 weeks. Yes, that is right. I won't be writing another word about it until I have had my scan, and maybe then I will have something to say. I feel as though I have inundated you with my disease and everyone has just had enough -- me included. So, I will be posting, but not about cancer. At least, for a while. Watch for more interesting things, more fun things. The clematis is blooming. Photos to follow.

May 29, 2006

Graduation Day

I promised you photos, but I am going to start with Daddy's graduation. I will post photos of the Grand Canyon in a few days. So watch this space for more.

Graduation Day.JPG
Notice the gold chord (summa cum laude) and the bling-bling around the neck (Outstanding Student-Respitory Therapy).

Graduation 3.jpg
Notice the proud Mother. Notice the please wife. Notice the proud and pleased graduate. It was a good day for all.

May 27, 2006

Please forgive me

I was not totally honest with you in my last entry. I have my reasons, but I will clear the air first and then justify.

The reason that Dr. Pelley discontinued my chemo is that it seems to be destroying my ability to make white blood cells -- to the point where it is endangering my health and putting me at too high a risk of infection. It took three weeks this last time for my ANC (the part of my white blood cells that fight infection) to come back up to the bare minimum level. This is what they expect to happen in one week, which it never has for me. But it has happened in two weeks before and now took three. He doesn't know if it is from the radiation or if there is something else going on. Remember that the original reason that we started on this search was that my white cell count was low. This has been going on for over 3 years now.

What we are going to do is wait. I find that very hard, just waiting and not knowing anything. In July I will have my baseline scan. Why July and not June, I don't know. I think it may have to do with Dr. Pelley's vacation schedule, but I don't think it will make a big difference. At that point he will run a bunch of blood tests. If things haven't improved by September, then I go back to Dr. Silver, the hemotologist/oncologist who originally did the scan that found the pancreatic cancer. I would be going for a third bone marrow biopsy.

This really leaves me hanging and, I have to admit, a bit worried. So, that brings me to why I didn't tell the whole story in my last entry. I wanted to go on vacation myself and not be thinking about what is coming next. It didn't work very well, but I really did enjoy the trip (more in a later post). The other reason is that we just don't know what is coming next. It seemed pointless to worry everyone for maybe nothing.

May 18, 2006

Graduation

This is not Daddy's graduation that I am talking about here, but mine. Yes, it is so. No more chemo! Isn't that wonderful? I am so thrilled. So going to the Grand Canyon can be a true graduation celebration for both Daddy and me. I'm sorry I haven't posted any pictures of Daddy's graduation. I haven't even had time to look at them yet. I Promise that when I get back, I will post both some graduation photos and some Grand Canyon photos. Really, I will. I bought a 1 gig memory card for the camera yesterday to make sure I don't run short of memory while I am there. Off to pack. I love you all and good night.

May 7, 2006

Today is a day of celebration

Six months ago today, I was headed in to surgery. And I am still here. That is a victory.

May 6, 2006

Not So Bad

Well, I rode my bike to Gloria's yesterday. I thought it would be about 2 miles. Daddy thought it was closer to 3-3.5. He was right. It was 3.9. Each way. So I rode almost 8 miles. And lived to tell the tale. I guess I am pretty healthy.

I felt like I was riding up hill both ways, though. (I think it it perfectly level, to tell you the truth.) It turns out that my back brake is maladjusted and was rubbing on the wheel the whole way. Whew! When I got to Gloria's, I wasn't sure that my knees were going to hold me, but other than that, no ill effects. Today I am not even sore.

Except for me knee. I got my wheel caught between the sidewalk and the grass and couldn't get back on the sidewalk, so spilled. It just so happened that a nice policeman was driving down the street at that time so he pulled over and offered to call me an ambulance(!). I politely declined, while slightly panicing inside. The last thing I wanted to do was go the the emergancy ward! They are too familiar with me. I don't want to get a rep as a frequent flier. And I only had a skinned knee.

May 4, 2006

Loser. Flunky. Failure.

That about sums it up. That is what I am. I am setting up for a major whine, so if you aren't up for it, move along. I won't take it personally.

Yes, I feel like a major failure. I flunked my blood test again. This is the first time it has been two weeks in a row that my white blood cells were too low. Usually, one week is enough for my body to rebuild those cells, but not this time. And there is nothing I can do or eat or take to build up my white blood cells. It just takes time. The doctor will call me next week to decide if I should come in next week or just skip it.

Now for the major whine: I'm tired. Just plain tired. I don't have as much energy as I think I should. Yes, I know that it has been just over a month since my radiation ended and it can take up to a year to get it all back, but I feel discouraged.

And I am tired of smiling and saying, "Fine" when people ask me how I am. For crying out loud, I have pancreatic cancer. How do they think I am? I have good days and not so good days, but I feel one of two ways when people ask me how I am. Either they are just being polite and no more hear the answer than if they were to say, "have a nice day." Or I feel they are looking at me very closely to see how I really am, as if what they see isn't the truth, or that I am really suffering underneath, but being stoic. And maybe they are right; maybe I am. But I just want to be normal, to forget that I have a potentially deadly disease with a poor prognosis.

I'm tired of the pinch that I feel in my side all the time. It makes it difficult to ever get comfortable, to go to sleep, to forget that I had major surgery, and, well, that I have cancer.

I'm tired of the medical professional going over a list of symptoms, then when I admit to one, moving on down the list. If they don't want to address it, why do they bring it up?

I'm tired of buying a zillion different drugs, both prescription and over the counter. I feel as though I have turned into some little old lady with a million ailments. And I only get them because the doctors tell me to. And I may use them once and then there they sit, cluttering up my counter, my life.

I'm tired of taking 'neutropenic precautions.' That means staying out of crowds, especially if there are children, washing my hands as if I had OCD, and in general, admitting that I am sick. I am tired of being sick. I want to be well again, like before I got this diagnosis.

Okay, enough with the whining. On to the dangers of looking healthy. I was at the office yesterday. I share my office with a student worker. I said that I was feeling sort of in the dumps. She asked what was wrong, to which I asked if one could be depressed without a cause. She thought not, unless you were clinically depressed. I said, 'Well, I do have pancreatic cancer.' To this she said, 'Oh, I thought that was all gone.' If only it were so easy.

Thanks for listening and being here for me.

On to a more positive note. Merry advocated for me and re-arranged the budget, and generally finagled to get my position approved for full-time. She has decided to leave in January (on her birthday), so is leveraging to have at least one full-time position in place. I am very grateful for her efforts, though I wasn't too sad at the thought of some time off, even if it was without pay.

May 1, 2006

Well.

Where to begin, where to begin? Five years ago (it doesn't seem that long ago), when Morris Beverage became president of Lakeland, he started his tenure by having seminars on the book, Who Moved My Cheese.

I should have figured out from that that he was planning on doing a far bit of cheese moving. And so he has. The handwriting has been on the wall for quite a while that the Women's Center was not a highly valued, or even understood, part of the college. It was started as a pet project under the previous president, so was fair game.

Then came budget cuts from the state. And reduced marketing budgets. And flat enrollments due to many factors, like reduction in Pell funding from the federal government, on-line enrollment, etc. Cheese moving all over the place! The Women's Center was shifted from one department to another, each not quite knowing what to do with us or even what we did best.

So where am I going with all this? Well, today I found out that my job has been reduced. It is now a 10-month position, rather than all year. I can still keep my benefits (Thank God!), but won't be working so many hours. Yes, this will affect my pay, but, fortunately, Daddy had a job interview this very afternoon, and it looks like they will offer and he will accept. So, it could all work out rather well. I can take my time off whenever I want so if anyone comes to visit me, I don't have to use vacation time to be with you. I probably won't take 2 months at one whack, but spread it out over the year.