Ok. I've had a lot of people decide to walk or run the race this Sunday the 12th. I've never done this one so I don't know a good place to meet so I've tried to come up with something. For those of you who want to meet up before the race, Dan, Tristan, Maja, and I will be leaving our house at 6:45 am in order to find parking and get situated with the kids. If you'd like to, feel free to meet at our house in time to leave by then. The 1 mile starts at 7:45 am (after the 5K competitive run at 7:30).
I know there will be tons of people there so if you want to walk with us but prefer to meet there and can't find us, I'll have my cell phone on me.
Also, there was some talk about brunch afterward at First Watch. I think I'm in, but we'll see how I feel after a mile of walking with a 15 pound babe strapped to my chest. I'm so excited to do this! Yippee!!
See you all at the race!
Friday, August 10, 2007
Friday, July 27, 2007
Race for the Cure
I am a runner. That's how I've always described myself whether I'm in shape or not. I ran cross country and track for Ft. Collins High School, Fort Lewis College and Kansas State University. I love to run. I haven't run since I was about 4 months pregnant with Maja. Obviously, I've had some medical conditions and surgeries to recover from which have prevented me from doing so.
Cancer and chemo make me want to detoxify my body; for the most part, I'm only hungry for healthy foods and juice. It also makes me really want to run again, probably because I can't. So, I'm going to take the running out of the race and do the things I can do. I walk every single morning, whether it's around the block or up to a mile. I strap Maja onto my chest and we are silent for the next half hour or so. It provides a time for me to be with nature, observe the rest of the world, and to think about life. It's a good time to meditate.
All of this is fine and good, but I realized that the runner in me is missing something: a race! Now, I know I can't compete in the Bolder Boulder right now, but I think there is another wonderful race where simply finishing is winning, and walking is just as good. The best race for me at this point is the Susan G. Komen Race for the Cure. I don't have Breast Cancer, but this would be a great chance for me to connect with other women with Cancer who are fighting for their lives. I will race for my Aunt Gail who survived Breast Cancer last year and continues to show her support for me. If anyone else would like to accompany me and my family, please join me! You need not be in the shape of your life to compete in this race, but I guarantee it will make you thankful for the health you do have.
The race is Sunday, August 12th at Union Station in Kansas City, MO.
http://www.komenkansascity.org/Default.asp
Cancer and chemo make me want to detoxify my body; for the most part, I'm only hungry for healthy foods and juice. It also makes me really want to run again, probably because I can't. So, I'm going to take the running out of the race and do the things I can do. I walk every single morning, whether it's around the block or up to a mile. I strap Maja onto my chest and we are silent for the next half hour or so. It provides a time for me to be with nature, observe the rest of the world, and to think about life. It's a good time to meditate.
All of this is fine and good, but I realized that the runner in me is missing something: a race! Now, I know I can't compete in the Bolder Boulder right now, but I think there is another wonderful race where simply finishing is winning, and walking is just as good. The best race for me at this point is the Susan G. Komen Race for the Cure. I don't have Breast Cancer, but this would be a great chance for me to connect with other women with Cancer who are fighting for their lives. I will race for my Aunt Gail who survived Breast Cancer last year and continues to show her support for me. If anyone else would like to accompany me and my family, please join me! You need not be in the shape of your life to compete in this race, but I guarantee it will make you thankful for the health you do have.
The race is Sunday, August 12th at Union Station in Kansas City, MO.
http://www.komenkansascity.org/Default.asp
Thursday, July 26, 2007
Let's Get Real
Here is a blog covering the news about another woman with cancer. I don't know her, but it made me very sad to read that she had passed away this week. We share a lot of similarities so it's been hard for me to think about. Please send her family as much positive energy as you can.
http://karincarter.blogspot.com/
http://karincarter.blogspot.com/
Tuesday, July 17, 2007
The Bald Lady
I was taking my daughter for a walk a couple of days ago and feeling pretty down on myself; pretty lonely. I enjoy my walks because I can have silence and move inward for awhile. A couple of blocks into it, I came up on a small intersection where a car had stopped at the stop sign perpendicular to me. It would take me awhile to get to the intersection so the car could have gone but it rested there, waiting for me to get closer. The driver was a bald woman wearing a baseball cap like the one I was wearing, and glasses. She was looking at me and grinning the biggest grin she could. I couldn't help smiling back at her and was suddenly so happy. I noticed a few other people in the car and they turned to look and smile at me too. The car turned the corner in front of me and headed on it's way. I watched it get smaller as it climbed the hill, then dipped out of sight as it passed the crest. I walked faster, subconsciously following the car, still smiling. I wanted her to come back so badly! I really needed that. Sometimes just knowing there are other people like you out there doing exactly what you're doing can make a world of difference.
Friday, July 13, 2007
Cancer Guilt
There is a lot of guilt associated with cancer. For me it seems endless. When I resolve one thing I feel guilty about, I start feeling guilty about something else but there's always something. Sometimes there are many things I feel guilty about.
When I first started thinking about the cancer I thought I must have done something to my body to create this cancer in myself. Maybe it was that cigarette I smoked in 8th grade. Maybe my vegetarianism somehow robbed my body of something it needed. Maybe I was too promiscuous or smoked too much pot in college. Were my maternity pants too tight? I must have used the wrong tampons. Or maybe I shouldn't have used them at all. My self-accusing thoughts abound.
Then I started feeling guilty that I was robbing my children of this time in their lives. Maja hasn't had her pictures taken yet mostly because we don't have the time between chemo treatments and hospital trips but partially because we're spending all our money on prescriptions and medical bills. I feel guilty that almost every dollar we have goes to me and my needs, not to them. I feel guilty that Tristan is so angry lately. I think I've been trying to talk to him about cancer too much. He's having a hard time with it.
Now I'm starting to feel guilty that I wasn't prepared enough for any of this. Perhaps I should have had a cancer savings. I also feel guilty that I can't take some of the side effects like mouth sores. I feel guilty when I have to ask for help. I don't like not being able to do things on my own. One of those things is mowing my lawn. That's just a vanity issue, right? I can live without a mowed lawn. I won't get sicker if my grass is several inches higher. I want my lawn mowed but I don't need it. Same with the mouth sores. I can live with them. It hurts bad but no one can see them and I just have to eat slower and maybe not talk as much. I could use the $25 for the Magic Mouthwash and put it toward getting Maja's pictures taken.
I feel guilty about not working when I can. There are probably five good days between treatments when I could physically function. I should be working. On that same note, I feel guilty about going out or having fun. If I'm capable of having fun, I should be capable of working. And I should definitely not be having a drink and making it harder for my body to bounce back from treatment.
I feel very guilty about not being sick all the time because I know there are other people out there who are very ill during chemo. On the other hand, when I am sick from chemo, I feel guilty that I'm not stronger (insert guilt for not treating my body better pre-cancer) and that I need help taking care of my children/house/self.
It's just a huge cycle of guilt. It's not healthy and is incredibly irrational, I know. It will never completely go away. Guilt should be listed as one of the side effects of cancer.
When I first started thinking about the cancer I thought I must have done something to my body to create this cancer in myself. Maybe it was that cigarette I smoked in 8th grade. Maybe my vegetarianism somehow robbed my body of something it needed. Maybe I was too promiscuous or smoked too much pot in college. Were my maternity pants too tight? I must have used the wrong tampons. Or maybe I shouldn't have used them at all. My self-accusing thoughts abound.
Then I started feeling guilty that I was robbing my children of this time in their lives. Maja hasn't had her pictures taken yet mostly because we don't have the time between chemo treatments and hospital trips but partially because we're spending all our money on prescriptions and medical bills. I feel guilty that almost every dollar we have goes to me and my needs, not to them. I feel guilty that Tristan is so angry lately. I think I've been trying to talk to him about cancer too much. He's having a hard time with it.
Now I'm starting to feel guilty that I wasn't prepared enough for any of this. Perhaps I should have had a cancer savings. I also feel guilty that I can't take some of the side effects like mouth sores. I feel guilty when I have to ask for help. I don't like not being able to do things on my own. One of those things is mowing my lawn. That's just a vanity issue, right? I can live without a mowed lawn. I won't get sicker if my grass is several inches higher. I want my lawn mowed but I don't need it. Same with the mouth sores. I can live with them. It hurts bad but no one can see them and I just have to eat slower and maybe not talk as much. I could use the $25 for the Magic Mouthwash and put it toward getting Maja's pictures taken.
I feel guilty about not working when I can. There are probably five good days between treatments when I could physically function. I should be working. On that same note, I feel guilty about going out or having fun. If I'm capable of having fun, I should be capable of working. And I should definitely not be having a drink and making it harder for my body to bounce back from treatment.
I feel very guilty about not being sick all the time because I know there are other people out there who are very ill during chemo. On the other hand, when I am sick from chemo, I feel guilty that I'm not stronger (insert guilt for not treating my body better pre-cancer) and that I need help taking care of my children/house/self.
It's just a huge cycle of guilt. It's not healthy and is incredibly irrational, I know. It will never completely go away. Guilt should be listed as one of the side effects of cancer.
Tuesday, July 3, 2007
Holy Crap, It's My Birthday!
I'm one of those people who really takes their birthday too seriously. I have a birthweek and a birthmonth that are almost as big as the birthday itself. Anyway, I turned 32 last Monday and I had been feeling pretty good. It was the week after chemo which is when my white blood count tends to be low, but I'm bouncing back after the nausea and achy joints from the drugs.
The thing that happens with chemo is, you get "premeds" which are steroids and tylenol that will help you take the chemo better and not get as nauseated. I really just get tired and sleep the whole time. Then they give you the chemo. I get two different kinds and it takes a total of around 4 hours for the whole thing. Then I get a bunch of steriods (two different pills to take several times daily, and one to take on the onset of nausea). I also get a lot of drugs to help with the side effects of chemo and the side effects of the drugs that help those side effects, like hydrocodone or Lortab for my achy joints. The Lortab and chemo make my, uh, "plumbing" malfunction, so I have to take Colase which is a stool softener. TMI, I know.
Well, to make a long story short, most everything I take has it's own side effect that I can go ahead and take another pill for until I get to a side effect I can deal with. This last time I ended up just having too many problems with the plumbing issue and a lot of vomiting. If you're not on chemo I don't think it's a big deal, but since I am, I had to head to the hospital at 6:00 am the day of my birthday. Now, I'm not wallowing in self-pity (well....not really). I had a really great nap, some good drugs in the hospital, and I even got a little cupcake that said "Happy Birthday" on it from the hospital cafeteria.
The point is, sh*t happens. I felt like crap from the chemo anyway. It's not like I was going to go on a bender and hit the strip clubs anyway. I have to admit I was pretty down on myself while in the hospital. I finally got out in the afternoon. Dan and I walked down the hall of the cancer ward and some people had their doors open. I looked in at a few patients and realized how freakin' lucky I am to be having a birthday for goodness sakes. At least one of those people I looked in at was on their death bed and would not live to see another birthday, but they all peered out at me and smiled. So from here on out, my birthday will still be a fabulous day that I celebrate endlessly, but for a different reason: because I AM ALIVE.
The thing that happens with chemo is, you get "premeds" which are steroids and tylenol that will help you take the chemo better and not get as nauseated. I really just get tired and sleep the whole time. Then they give you the chemo. I get two different kinds and it takes a total of around 4 hours for the whole thing. Then I get a bunch of steriods (two different pills to take several times daily, and one to take on the onset of nausea). I also get a lot of drugs to help with the side effects of chemo and the side effects of the drugs that help those side effects, like hydrocodone or Lortab for my achy joints. The Lortab and chemo make my, uh, "plumbing" malfunction, so I have to take Colase which is a stool softener. TMI, I know.
Well, to make a long story short, most everything I take has it's own side effect that I can go ahead and take another pill for until I get to a side effect I can deal with. This last time I ended up just having too many problems with the plumbing issue and a lot of vomiting. If you're not on chemo I don't think it's a big deal, but since I am, I had to head to the hospital at 6:00 am the day of my birthday. Now, I'm not wallowing in self-pity (well....not really). I had a really great nap, some good drugs in the hospital, and I even got a little cupcake that said "Happy Birthday" on it from the hospital cafeteria.
The point is, sh*t happens. I felt like crap from the chemo anyway. It's not like I was going to go on a bender and hit the strip clubs anyway. I have to admit I was pretty down on myself while in the hospital. I finally got out in the afternoon. Dan and I walked down the hall of the cancer ward and some people had their doors open. I looked in at a few patients and realized how freakin' lucky I am to be having a birthday for goodness sakes. At least one of those people I looked in at was on their death bed and would not live to see another birthday, but they all peered out at me and smiled. So from here on out, my birthday will still be a fabulous day that I celebrate endlessly, but for a different reason: because I AM ALIVE.
Saturday, June 23, 2007
Welcome to the Club
You see the women banded together, arm in arm, with their pink t-shirts, bald heads, and baseball caps with ribbons on them and think, "wow, now that's a group of courageous women". You kind of envy those women and their camaraderie. I know I did.
I've always felt like I needed to be a member of some kind of group and had trouble finding it. I'm so embarrassed to say this, but I almost wished something big would happen to me so I could have something to be motivated by; something to identify myself with. Do you ever hear about those people who get in horrific car accidents and then they all of a sudden have a greater respect for life, or some purpose they may not have had before? I think I was looking for that purpose.
After my surgery, I went into the Cancer Institute where my oncologist's office is and we talked about what was going to happen next. She told me I was in Stage IC Clear Cell Ovarian Cancer which is an epithelial cancer. Stage I is when only one ovary has cancer, II is when both ovaries have cancer, III is when it has spread to other areas of the abdomen (uterus, fallopian tubes, etc.), and IV is when it has metastasized to other areas of the body like the lungs. The C part is the grade of cancer. "A" is a very slow-growing, non-aggressive cancer, and "C" is the most aggressive and easily metastatic. My tumor had grown very large in such a short period of time and was so close to rupturing but was only on one ovary.
During my office visit, I was taken on a trip around the chemo ward for introductions. It is a very quiet place, with people sleeping in large La-Z-Boy chairs while hooked up to bags and bottles of meds. I walked in, fully aware of my long, hair-sprayed hair, and gazed upon all the women and men receiving chemo. Most had some kind of headwrap or hat on. One lady had a turban, one a scarf. There was a man with a full, bushy head of hair. The nurse brought me over to meet a woman in her mid-50's who was also bald with a baseball cap on. She looked rather sporty and energetic. She was connected to her meds through her chest using a port which is a catheter inserted under the skin above the collar bone to administer chemo. The nurse wanted me to see her port because she wanted me to have one as well. I asked all sorts of questions about it; one of which was "does your bra-strap get in the way?". As soon as the words left my mouth, this confident woman looked slightly embarrassed and I realized she had no breasts and was probably not wearing a bra. She sheepishly said, "No."
After leaving the chemo ward I felt almost evil. I was secretly excited to be a member of this group, even after meeting the woman with no breasts. I guess I felt like I could some how feed off these people's confidence and motivation, something I was lacking, and that was more important than worrying about my body parts. I would use this energy to my advantage and make it through this with a new outlook on life, a new purpose, and be just like all those women who do that Susan G. Komen race with linked arms. I almost couldn't wait to lose my hair even. I wasn't really looking forward to it, but I wanted people to know what I was going through and I felt like a faker with just a t-shirt or a ribbon citing my impending fight. Losing your hair is a visible mark that you have cancer.
What I didn't know is that later in the process I would feel much, much different about it. I would feel more alone at times than I did before the cancer diagnosis. I would need much more help. I wouldn't even be able to trudge through a cancer walk on my own. Luckily, I wouldn't have to.
I've always felt like I needed to be a member of some kind of group and had trouble finding it. I'm so embarrassed to say this, but I almost wished something big would happen to me so I could have something to be motivated by; something to identify myself with. Do you ever hear about those people who get in horrific car accidents and then they all of a sudden have a greater respect for life, or some purpose they may not have had before? I think I was looking for that purpose.
After my surgery, I went into the Cancer Institute where my oncologist's office is and we talked about what was going to happen next. She told me I was in Stage IC Clear Cell Ovarian Cancer which is an epithelial cancer. Stage I is when only one ovary has cancer, II is when both ovaries have cancer, III is when it has spread to other areas of the abdomen (uterus, fallopian tubes, etc.), and IV is when it has metastasized to other areas of the body like the lungs. The C part is the grade of cancer. "A" is a very slow-growing, non-aggressive cancer, and "C" is the most aggressive and easily metastatic. My tumor had grown very large in such a short period of time and was so close to rupturing but was only on one ovary.
During my office visit, I was taken on a trip around the chemo ward for introductions. It is a very quiet place, with people sleeping in large La-Z-Boy chairs while hooked up to bags and bottles of meds. I walked in, fully aware of my long, hair-sprayed hair, and gazed upon all the women and men receiving chemo. Most had some kind of headwrap or hat on. One lady had a turban, one a scarf. There was a man with a full, bushy head of hair. The nurse brought me over to meet a woman in her mid-50's who was also bald with a baseball cap on. She looked rather sporty and energetic. She was connected to her meds through her chest using a port which is a catheter inserted under the skin above the collar bone to administer chemo. The nurse wanted me to see her port because she wanted me to have one as well. I asked all sorts of questions about it; one of which was "does your bra-strap get in the way?". As soon as the words left my mouth, this confident woman looked slightly embarrassed and I realized she had no breasts and was probably not wearing a bra. She sheepishly said, "No."
After leaving the chemo ward I felt almost evil. I was secretly excited to be a member of this group, even after meeting the woman with no breasts. I guess I felt like I could some how feed off these people's confidence and motivation, something I was lacking, and that was more important than worrying about my body parts. I would use this energy to my advantage and make it through this with a new outlook on life, a new purpose, and be just like all those women who do that Susan G. Komen race with linked arms. I almost couldn't wait to lose my hair even. I wasn't really looking forward to it, but I wanted people to know what I was going through and I felt like a faker with just a t-shirt or a ribbon citing my impending fight. Losing your hair is a visible mark that you have cancer.
What I didn't know is that later in the process I would feel much, much different about it. I would feel more alone at times than I did before the cancer diagnosis. I would need much more help. I wouldn't even be able to trudge through a cancer walk on my own. Luckily, I wouldn't have to.
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