August 10th, 2010

It has been an interesting few weeks. While the news that my cancer has been subsiding has been good, I continue to deal with small niggling issues. One of them is odd intermittent pain in various places. It never lasts long and rarely occurs in the same place over periods of time. However, the painful headaches I had in succession, albeit briefly, last week were a bit disconcerting given their intensity. They took my breath away. I mentioned it to my oncology nurse, like I have a whole succession of pains over the last few months, which have generally been acknowledged and shelved by the doctors.

I guess to some extent with metastatic cancer, pain is simply a given. It is a question I get asked every time I go in.  They seem to be looking for the cases of excessive on-going pain to see if it is indicating new growth and to deal with the pain if it’s bad — but that’s it.  In any case, this time they insisted on an MRI and wouldn’t let me leave the building or give me my chemo until this was done.  Bottom line — the MRI took place pretty quickly (and was cake) and the results showed that while the brain tumor has shrunk further, there is some swelling, which may explain the pain.

Apparently, the brain is not crazy about any changes in the brain (OK, I guess I understand) and so swells when anything moves around. For those of you around me, you should be forewarned that the solution for the next few weeks will be steroids! Yikes! I should be on over-drive and hope to get lots done though! My apologies in advance for any untold behavior on my part that may seem out of line. I really don’t mind (and would welcome) input if I’m not really being “me.”  :) It’s kind of interesting because I can be pretty self unaware in terms of the drug impacts.

In the coming month I will be getting a whole host of tests to ascertain whether I am ready to get off regular weekly chemo. Although things look good, please keep your fingers crossed. Even if I am able to get off chemo, even if the tumors all disappear eventually, even if my life is blessedly less stressful, even if I’m healthy otherwise and feeling optimistic, the chance of recurrence is very real for those of us who are metastatic. In addition to my current  life prognosis of 5-10 more years, the oncologist is very clear that once you’ve gotten to this point, the risk of  recurrence is always there. It’s just a persistent reality. It may sound crazy but I can deal with that. It helps me live in the moment which is something I am trying to do any way.  The fact that there will be unknowns is a known. OK. I will take it a day at a time and live each day like it is precious. I want to make the most of what I do have and to love it while I have it.

In the meantime, things are pretty hopeful. The drugs I’m on are obviously working pretty well. The issue is the long-term and how that works out.  As I’ve noted before, the oncologist sees this as a very strategic process. You have to keep using the drugs that do work  until they stop working and try to keep some options up your sleeve.  She is very optimistic about having the Herceptin hold the cancer in check for a while. It’s worked well for some others. However, Herceptin can be tough on the heart and a time will probably come when either my heart can’t take it or it’s no longer working to keep the cancer at bay.  The real hope is in the development of new drugs over the next 5 to 10 years that can replace it.

I can’t underscore the importance of funding for new breast cancer research. It really, really makes a difference. To be very personal, it could make the difference between whether or not I (or anyone else in the same situation) can be there for the key moments in my life including milestones such as watching the girls grow up, birthdays, graduations, trips and just the joy of being with friends and family and feeling like  I’ve given and gotten everything out of life that I feel I can. You understand.

There are so many opportunities for making a difference in cancer research and you have heard of many of them already. I just want to acknowledge two specific efforts under way that are personal to me and might be of interest to you. I would be most grateful to for your support in helping these two friends in making a difference in this area that is so critical to me and others in my situation. Thank you Jamie and Todd for all you’re doing and thanks to Chris, Carolyn and many others who contributed $14,000 to the Komen Race for the Cure here in DC in June.

  • Jamie Schreifels-Corbett – My amazing sister in law who has run and walked to raise funds many times and who works in the medical field specifically with women with breast cancer so sees cancer first hand regularly

Yes, I’m doing it again – I signed up for the 2010 Susan G. Komen 3-Day for the Cure! I had such an incredible experience doing the Komen 3-Day for the Cure last year. I’ll walk 60 miles over the course of three days with thousands of other women and men. This event isn’t easy, but I promise you, I wouldn’t be doing it if I didn’t believe 100% that it was worth every muscle ache, weary night and training walk! I’ve agreed to raise $2300.00. If anyone is able to donate please visit

http://www.the3day.org and visit my participant page listed under Jamie Corbett.”

  • Todd Wilson — Our wonderful neighbor who has inspired  us by running multiple marathons to celebrate turning 40!

“As some of you may know, a few months ago I signed up to run the Marine Corps Marathon to raise money for Susan G. Komen for the Cure to help fight breast cancer.  This marathon will be my third (and, as I realized the other day, my third in a year), but it will be my most important one so far because of the people it will benefit.
The Susan G. Komen foundation has helped me set up a fundraising web page with information about why I’m running this race (there are some people very close to us who are our inspiration) and what the foundation does.  Please visit my page at the link below, learn, and please contribute if you can. Every donation helps!
Thank you very much!
Todd ”
http://www.info-komen.org/site/TR/MarathonfortheCure/MarathonFortheCure?px=7085184&pg=personal&fr_id=1914&refresh=1

Thanks for your support!!

XXOO, C

This entry was posted on Tuesday, August 10th, 2010 at 3:03 pm and is filed under Advocacy. You can follow any responses to this entry through the RSS 2.0 feed. You can skip to the end and leave a response. Pinging is currently not allowed.

3 Responses to “The Need to Keep Fighting for a Cure!”

Margaret Poethig Says:

Constie–I will keep my fingers crossed that you can get off weekly chemo. That will give you more time to focus your steroid-induced energy on a project, like building an addition onto your house or something. :-)

Margaret

Doreen Sterling Says:

Hi Constie. Just got back from 2 weeks in Maritime Canada so checked in on your blog. I hope you can get off the weekly chemo. Sorry you are having pain. Your positive attitude is an inspiration to me. Hugs!

Karen Seevers Says:

Constie,
To start at the beginning….It was wondeful seeing you in Tokyo, albeit under sad circumstances. After I learned of your laspe back into cancer, I was sadded beyond belief. How could this girl, looking so healthy and so lovely have to face this…again. I have thought of you so often, sent many many prayers up and asked of you often. I just saw the clip on the Susan Komen walk for cancer piece you and your friends recently participated in (9NEWS NOW). I am asked every year to walk in these fund raisers: for American Cancer, Susan Komen, and others. I am not home in the states long enough to participate, but not sure I would if I were. I made a decision to long ago, to help in other, more quiet ways. Your blog entry “The Need To Keep Fighting for a Cure” has stopped me in my tracks and made me look at this in a different light. It is NOT that I don’t give, or that I don’t support these and other causes…it is that I don’t want to be reminded, I have “moved on”. But now, after reading your post and seeing your efforts … this now seems so unfair. I can ‘move on’ but so many can’t …(at least not yet). You are by far one of the most courageous woman I know. You are a shining light into a whole realm of possibilities. You are a fighter and a realist. You are the reason I will rethink the stance I have taken for not wanting to be ‘out there’ walking, with other cancer survivors.
Constie, I send you love and all the good, positive healing energy out there to send. Know you have touched me in ways that has moved my heart.
Keep up the good fight knowing, without a doubt, that all things are possible.
hugs and hugs, Karen in Tokyo

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