Wednesday, March 11, 2009

MARCH 11, 2009


I think I mentioned recently that while at The Wellness Community the other day, I found out that there is a similar organization in England called Maggie's Place. It's a place for patients, survivors, and caregivers to go to get some of the emotional support that they need while dealing with cancer. My experiences with TWC here have been so positive and uplifting, and I thought it would be such an amazing experience to visit Maggie's in England.

So, I went to the website for this organization (www.maggiescentres.org) and got in touch with some people from their sites in London and Oxford. Lo and behold, I got an email back. From two people. I am beyond excited. I will be meeting with someone from the Oxford location next Friday, and I am hoping to be able to have the time to meet with someone on Monday in London (Jim & Tom - let me know what you think of this).

I don't know what I am expecting, if anything. I am excited to see what their locations look like. What they have there. I want to meet the people there, and to just make a personal connection. My goodness, what an amazing opportunity this is. How can I be more honored to be this sort of impromptu ambassador between these amazing organizations?

When I told Paula, the Executive Director at TWC here in Phoenix, about my connections, she was so excited. This is a wonderful relationship to build, and I can only begin to imagine the things we will learn from their group, and them from ours. My goodness - this could become a new job for me. :-) Michelle, cancer ambassador. I like the sound of that.

Comments:

Carol Urban said...
Love it! Girl, you are too COOL! Awesome! High Five!

Do you promise to post info to your blog while you're in Britain? I can't wait to read about the goings on there.

I am so frikkin proud of you!
March 12, 2009 at 7:48 AM
Blogger Tina said...
Michelle,
I was recently diagnosed with colon cancer, and did a blog search for others who have gone thru this, and that is how I found your blog.
My tumor was found on Feb 6th, and my surgery was the 20th. I see my oncologist this coming Tues. the 17th.
I have read your entire blog (some of it more than once!) and am so grateful to you for writing about everthing you've gone thru! You are an inspiration to me, and I hope to get thru it all as well as you have. I started my blog hoping to help others in the future who are diagnosed with colon cancer, and I will do my best to keep it up to date and be honest about everything I experience.
Thank you for getting the message out about colon cancer awareness.
And thanks again for your blog! I hope it will be ok if in the future I write again with questions I might have.
I can't wait to be a survivor!!
Tina
March 14, 2009 at 10:10 AM


Monday, March 9, 2009

MARCH 9, 2009


I was speaking with my brother this weekend. He's the one I am heading to England to see next week (NEXT WEEK!!!!). He has a friend there that is having difficulty dealing with her own personal battle with cancer, and he has asked that I speak with her. I am excited for the chance to meet with her, and hope that I can, in some small way, help her.

In talking with my brother, I was expressing how hard it is for a cancer patient to live life after a diagnosis, and how difficult it can be to have to make some changes. It's not the large, life-changing things that most people talk about. It's some of the smaller, less obvious things that have to change, and that have an effect on your emotions. Things like having to check "YES" next to the question on a form that inquires as to whether you have had cancer. And then, having to fill that information out. It changes how you view yourself, and it's certainly going to change how other people view you.

Jim brought up a good point - it's not just the people that are dealing with the cancer that are affected in these ways. It's the family of the cancer survivors that are also affected. Now, my entire family has to check "YES" in the space that indicates that a close family member has had cancer. They are forced to answer the questions, forced to endure the testing, all because of something that I had to go through.

I have mentioned before how I am dealing with some survivor guilt - it's the gratefullness of being alive that fights with the question of why I was allowed to live. And, along with that is knowing that my illness, my disease has had a rather profound effect on my family. My parents have to live the rest of their lives knowing that one of their kids had cancer. My brothers will have to live with this. My kids will have to live with the knowledge that Mommy had cancer. It's a frustrating feeling. You all know how proud I am to be a survivor - one of my favorite moments of post-chemo-dome was at the luncheon on Friday. I was looking at the table that had all of the name stickers on it, and there was mine, standing out from everyone else's - "Michelle Hastings, Cancer Survivor." (I don't think Cancer Ass-Kicker would have been appropriate.)

Along with that pride comes a sense of shame. A sense of indignity. A sense of failure. Did I do something along the way that made me sick? Did I give the cancer the fuel to grow? What could I have done differently to make sure that I wasn't a statistic? There's the sense of shame, in asking myself how I could have put my family and friends through this? Why couldn't I remain a healthy wife, mother, daughter, sister?

So, my conversation with my brother definitely gave me some food for thought. While I have been so focused on how I am personally handling the emotions, the feelings, the struggles, I have to ask myself - what have I done to make sure my family is being taken care of emotionally? What have I done to make sure that my friends and family are okay?

Have I been selfish? Is that okay? I don't know the answers. It's a tough question to ask. As a patient, one of the first things that is drilled into your head is that this is the time to take care of yourself. This is especially true with mothers, because we tend to ignore our own needs to take care of everyone else. And, it's pounded into our psyches over and over by everyone - this is your time. This is time for YOU to take care of YOU, so that YOU are around to take care of everyone else later on.

When does that point stop? It's a tough line to walk - I know I still need to take care of me. I need to make sure that I take the time to allow my body to heal, to allow my feelings and emotions to process. I need to make sure that I provide my body with the tools it needs to beat the cancer. But, where do I draw the line. I am a caring person - I want to take care of everyone. I want to nurture my family and be the best mom I can be. I want to nurture my husband and make sure that whatever time we have together is cherished. I want to spend time and make memories with my parents, my brothers, and their families.

But, how do I help them through the cancer ordeal? Can I? How do I ask them - hey - how are you doing, now that your daughter/sister has/had cancer? I know that they are proud of me - I'm as sure of that as I am my kids names. But, I wonder if I have done enough to take care of them. Did I ask enough questions about their feelings? Did I think enough about how this was affecting them?

I just don't know. I really just don't know.

Comments:

jnwhiteh said...
Although it's on a completely different scale, it's something that we as the family have to internalize and integrate into who we are. I may not have been able to come home to see you when you were first diagnosed, but I've been over here championing your cause as much as I possibly can.

Anyone I meet who is having issues, I ask them to please get it checked out. There are talks about breast cancer or testicular cancer in schools, but no one seems to mention the other things that could indicate an problem. I go out of my way to pester people who are shrugging things off in order to get them to actually go and speak to a doctor about it.

I'm sure we could have a really productive therapy sessions with each of us sitting down and talking about how cancer has changed our lives. Although none of us will have anything quite as drastic as you have, I'd wager pretty heavily that we've all had some sort of change in mindset, outlook or behavior.

"Did we do something when she was younger that helped contribute to this?"

"Should I have come home and helped her through everything so the burden didn't fall solely on her husband and my parents?"

In the end what matters the most is something you've said over and over again. We must all find our new normal, and recognize what goes into making it.

My sister is a cancer survivor, and I am incredibly proud of her. I am incredibly proud that her friends rallied support around her so quickly. I am incredibly proud that my parents were able to make such a drastic change in their lives to provide direct support for her, even when it was difficult. I am incredibly proud that my brothers were able to continue living their lives in the midst of so many drastic changes and continue to improve themselves.

I can't say the experience was difficult for me, because almost all of my time was spent thinking about how it was effecting YOU. But I think I can say that we've all taken something important away from the experience that we'll carry with us forever.
March 10, 2009 at 2:40 AM
Blogger Amanda: said...
Not being a survivor myself, but being the parent of a survivor, I think what you feel is absolutely normal and completely ok.

There are times when I wonder why Joshua was spared when I have to watch other kids that I've come to love lose the battle. Don't get me wrong, I'm so thankful my child is ok, but what about all those other parents? Why were they chosen to endure the worst hardship EVER imaginable?

The only thing you can do is KNOW that there was a reason why you were spared. I know Joshua's battle brought SO MANY people on their knees to God, praying and begging that this small child would be ok. What more could I ask for? Through my family's pain came SO MUCH GOOD.

Of course, hindsight is 20-20 and I'm not sure I was so confident of all of this when we were walking down that path, but now, I can see the "why". And yes, everyone who knows my child has been affected. But mostly for good. And they have all adjusted to the "new normal" and are more thankful than they were before.

I do know what you mean, though, about having the little things become big things. Whenever I have to fill someone new in on Joshua's history, it's like reliving it all over again... not necessarily in a bad way, but it's something I will have to do for the rest of his life.

If you want to talk, feel free to get ahold of me :)
March 10, 2009 at 7:48 AM
Blogger Carol Urban said...
Ah, you don't know this about me but I am the most IMPATIENT person in the world! Yes, that sign belongs to me. I am working on being patient. I need to work harder.

I absolutely HATE filling out papers or telling the nurse for the umpteenth time what my history is. I mean, for godssakes, doesn't the computer you are typing into save anything???

I check the cancer box and I check the surgery box but I am not for the one millionth time going to write down all the surgeries I've ever had in my life along with the dates, hospitals and who what where and why! That's in that dam computer somewhere and you better go locate it because I am not telling you yet AGAIN!

Ah, but I rant and I am trying so hard to be a patient and kind person so I better run along and take my Zoloft before things get outta hand.

Thank goodness for cancer because I appreciate life now and am trying so hard to be a good, kind and patient person. You should have seen me before. Well, no you wouldn't have wanted to. :)

Did we do things to make ourselves have cancer? Heck no. Like I told my family doctor who didn't want to sign off on the colonoscopy; shit happens, let's just deal with it. Colon cancer runs in my family so I knew somewhere down the line I would get it. My mom's baby sister, Wanda Jean, died at age 29 from Colon cancer. If I hadn't have been diagnosed my sister, Kim, may have. She got her colonoscopy checkup right away and had precancerous polyps removed.

I can honestly say I'm glad I got the cancer because I would NOT have wanted anyone else in my family to get it. They might not have been as strong as I am. I'm another ASS KICKER just like Michelle!

My mom stayed with me the entire 6 months I was undergoing Chemo. She said there wasn't anywhere else in the world that she needed or wanted to be. I thank my dad for letting her stay. I could not have gotten through it without her. Cancer drew my mom and me closer together.
March 10, 2009 at 9:04 AM


Saturday, March 7, 2009

MARCH 7, 2009


I had an opportunity to speak yesterday at a luncheon called a "Friend-Raiser" at The Wellness Community. What an honor - this event was a way to tell about 30 women who TWC is, what they do for patients, and what services are available. I was asked to speak to give them a patient's view on how TWC has helped me, and continues to help me, get through this battle. This was an amazing event, and I am so proud to have taken part.

While I was there, I was given yet another amazing gift. Back in August, I was asked my TWC to be in a photo shoot that was to be used for an upcoming fundraising event. The book that they released is called "Voices of Hope", and is a spiral bound, classic collection of stories of survivors, patients and caregivers. There are about a dozen of us featured, and on each open page, there is a picture of the person featured, a formal blurb about TWC, and a "daily journal" entry from the featured person. In my case, they had me write what TWC provides to me, and what hope means. When I was writing this, and when the pictures were taken, I was right in the midst of chemo. It was August or September, and I was really in the depth of everything. I remember that writing one entry wasn't possible for me - I am a pretty vocal person, and I had many different views of what hope meant, of what TWC meant to me.

They took my ideas, and combined them into a wonderful journal entry. The best part of this book - my kids and I are the first entry. How cool is that?!?! We lead off this book. So, you open the book, and there's a picture of TWC house, which is a house that was built in 1908. On the next pages, on the left is a picture of the kids and I, laughing and smiling. As I remember it, Kevin was being pretty pain-in-the-butt-ish, and I had to tickle him to get him to sit still and smile. The result - a very informal picture of the kids and I, loving each other and having a wonderful time. (I am pretty bummed that Levi wasn't here with us - he was travelling for work at the time.) The journal entry reads as follows:

"My six-year old Julia and two-year old Kevin are my reason for living. They help me fight when I edon't think I can go on. There are weeks when the only thing that gives me a sense of hope is my support group. I NEED to be with other cancer patients, if only to know that I am not alone."

Following us are more patients, caregivers, etc., their journal entries and gorgeous pictures. It's a heart-wrenching book, and the pride I feel in being a part of this cannot be captured in words. TWC will be using this book as a way to try to persuade businesses to provide funding to their organization. They also used our picture on the invitation for yesterday's luncheon. What an honor.

I am so blessed to be involved with so many wonderful, amazing, giving people. While I wouldn't wish cancer on anyone, I can only hope that others have the kind of life-changing experience that I have had. I can only wish that others can feel the same kind of fulfillment and purpose in their lives. Being involved with TWC, with the Colon Cancer Alliance (our Central AZ chapter application has been submitted....), with I'm Too Young For This (an org that supports young cancer patients.....I am working with their CA chapter to try to establish a local group in Phoenix....)......I am just so damned blessed. It's an amazing life I live. Really - how in the hell did I get so lucky to have these amazing things happen to me? It makes me feel guilty - there are other wonderful people that suffer from atrocities such as cancer, illness, etc., that have wonderful traits that they can give the world. Why aren't they given a second chance at life, to be able to provide for the human race? Why is it me that was chosen?

These are questions I ponder everyday. These are some of the things that go through my mind. I recently learned of a school friend whose brother passed away from colon cancer. At age 34. He left behind his wife (a high-school acquaintance of mine) and his 4-year-old daughter. All because some doctor didn't think that his family history of colon cancer was enough of a reason to have a colonoscopy, in spite of ten years of pain and suffering. Why was I given the chance to live, to survive, when Dan had to lose his battle with this beast? Why does his daughter have to grow up not knowing her Daddy? It just seems so unfair to me that his doctor didn't do this simple test, which might have saved Dan's life. It pisses me off so much, and yet bothers me on a personal level that I live while he doesn't. Why me? What do I have that needs to be shared with others?

Interesting thoughts for a Saturday morning, eh?

Comments:

Matthew Zachary said...
We're here for you. Thanks for the mention and we are very excited to have you on our team working with Sarah to get Phoenix off the ground. Stupid Cancer! Matthew Zachary
March 7, 2009 at 6:30 PM
Blogger Carol Urban said...
I'm crying reading this. Crying burns. Still some effects left from the Oxalyplatin(sp?).

Such an amazing write up on the speaking engagement. I am so proud of you! If you have the gift of public speaking I say go with it!

We have to be our own advocates when it comes to dealing with doctors. Mine wanted me to wait until I was 50 for a colonoscopy. I told him I'd be dead by then. After the colon cancer surgery he came in to apologize to me. I doubt he'd ever make the same mistake again with another patient.

Keep up the good work girl! You are such a blessing to the rest of us.
March 8, 2009 at 2:32 PM


Thursday, March 5, 2009

MARCH 5, 2009



This is the text of an email I sent out to all of the people in my contact list. Please, consider copying it, and sending it to all of the people in YOUR contact list. How many people can we hit with this? Imagine the sea of blue you could see at your school, office, hangout, etc. tomorrow. Imagine knowing that you touched that many lives, as you have mine. Please, imagine yourself living in a world where colon cancer is something people dont suffer from, don't have to worry about......

Please - wear blue tomorrow, and make people ask you WHY you are wearing blue.

************************************************************************************
To my family and friends....

Tomorrow, March 6th, is the first annual "Dress in Blue" day, to help raise awareness for colon cancer. As you well know, I battled this disease last year, and am currently enjoying my status as colon cancer ass-kicker and survivor. I ask that you participate in this event, and that you spread the word. Colon cancer effects more people annually than breast cancer and AIDS combined. This number is staggering. Even more alarming? Every nine minutes, someone dies from colon cancer. And, this year alone, they estimate that 150,000 people will be diagnosed with this disease. Think about those numbers.
Then, think of this. This disease is 90% preventable through routine colonoscopies. When caught in the early stages, this disease is treatable, and beatable. I am the perfect example of that. I am also the perfect example to prove that colon cancer doesn't just affect older men. It affects more and more young people daily, and raising awareness of the symptoms and the need for testing is the only way we are going to be able to beat this monster.

So, please consider wearing one article of clothing tomorrow that is royal blue in color. Proudly wear this, and please voice your reasons for wearing blue to all that you encounter. Give them my blog address. Spread the word. Help me to eradicate this disease, and to make sure that no one else in the world has to go through what I, and my family, have endured over the past year.

With love, well wishes, and hope for the future....

Monday, March 2, 2009

MARCH 2, 2009


March is Colon Cancer Awareness month. Please take a few moments to remind yourself, your friends and family, your colleagues, and anyone else that you come in contact with that it's Colon Cancer Awareness month. This is so important - only by raising awareness will we eradicate this disease forever.

This disease is preventable. It's treatable. And, it's beatable. PLEASE know that the testing for this isn't difficult. Yes, I will agree that it's not fun. But, you know what's less fun? Chemo. Surgery. Cancer. So, get tested. I did - and, I'm a big baby!

REMEMBER TO DRESS IN BLUE ON FRIDAY! Friday is our (CCAs) first annual Dress in Blue Day - make people ask you why you are wearing blue, then tell them.

This is going to be an amazing year - I get to celebrate simply being alive, and one of the perks of living is having the opportunity to spread the word about this awareness. It's so important. A few statistics to leave you with:
  • Every nine minutes, someone dies from colon cancer.
  • Colon cancer kills more people each year than breast cancer and AIDS, combined.
  • 150,000 people will be diagnosed with colon cancer this year.
Think about those things. Then, help me spread the word. Please.