Thursday, February 25, 2010

Back In the Chair






It's Tuesday. Feb. 23. 6:30 pm. I'm sitting in the clinic with my husband, reading a magazine, getting a dose of chemotherapy through an IV line. I have nothing but time so figured I'd just start writing whatever comes to mind. Chemotherapy is a test of patience. It sluggishly drips from the bag, falls into  a long, narrow tube and then flows into the catheter in my chest. It takes hours to complete a dose. I never thought I'd be here at a cancer clinic - especially not now, right when I was hoping to build our family and my career. I feel like we were just getting comfortable with the direction of things. And then suddenly, boom, cancer. I've been here at the "infusion center" for more than 6 hours. And at least another hour to go. Starting to feel the medicine.  I don't feel nauseous so maybe the anti-nausea medicine is working. But I'm drowsy. My joints are stiffening. And I'm so dry all of a sudden. Almost immediately, my lips have become chapped and cracked. My hands too. I'm drinking tons of water to stay hydrated and to help prevent the chemo drugs from harming my uterus and kidneys. "Drink lots of water and empty your bladder frequently," the nurse warns, reminding me of how toxic this stuff is that's dripping into my veins. I didn't expect to be here today. I was supposed to be starting my stem cell transplant but somehow the stem cells they collected from me are contaminated. Go figure. Contamination only happens 1% of the time. This is exactly why I have no respect for probability. Just because something is not likely doesn't mean its impossible. Now that I have a rare cancer, I don't feel any comfort from statistics that show that something is unlikely. Unlikely happens! I feel like I need a T-shirt with just that on it.  Its unlikely that I'd have plasma cell leukemia. In fact, those were the words of one of my doctors before my diagnosis. He said: "You need a bone marrow biopsy today because you could have multiple myeloma, a very rare blood cancer." But he added that "It would be highly unusual if you actually have it." And for some reason that kinda comforted me. Well, let's just say "highly unusual" has happened. Not only do I have multiple myeloma but I have it in a flavor called plasma cell leukemia, which is even more aggressive. Fast forward a couple of months to this week.  It was unlikely that my stem cells would be contaminated. But that's what happened. To have to switch gears mentally and come back to this chair in this clinic waiting for this IV to finish is upsetting. But slowly, I'm starting to think, or hope, that maybe there's a reason and this is all part of the plan. My friends tell me that a setback is a setup for success. So I'm searching for the positive...My doctor today told me that while they are trying to determine the next step for me, it makes sense for me to be in this chair, starting up another cycle of chemo.  The thought at first made me sick. Just like the transplant, I don't want chemo but I know I need it. The mental conflict is nauseating. They don't have pills for this kind of nausea. But I'm still searching for a positive to all of this. My doctor did note that I'm responding well to treatment. The cancer-related proteins in my blood are falling. If the numbers got to zero, I'd be in complete remission.  Maybe I'm back in this infusion center because God wanted to rid me of more cancer before proceeding with the transplant. I don't know. Either way, I'm still certain I will be okay. My cancer is lethal. The statistics are scary. But the good thing about knowing the unlikely happens is that I know the unlikely can happen for good as well. I know there's a solid reason to keep the faith. The unlikely happens! T-shirts coming soon.

Saturday, February 20, 2010

Transplant postponed. Just got the word on Friday, just days before I was planning to go to the hospital. I was packed and getting ready but now things have to be rescheduled. The stem cells the hospital collected from me last week may be contaminated. It'll take more tests for them to know for sure. Right now, I'm just on hold.... 

Wednesday, February 17, 2010

Psalm 91

This is wild. I was cleaning up, listening to my Ipod - to that Richard Smallwood song I just wrote about in the last blog post, and I stumbled across a daily devotional that I haven't started reading yet. A church in Pennsylvania sent it to me after a friend mentioned my situation to her college buddy who is the associate pastor there. Well, I got curious and opened it up to give a look at what today's scripture is. And Guess what it's about - Angels. I couldn't make this stuff up if I wanted to. This is more than a coincidence. I feel moved to share. I guess I just stumbled upon my scripture of the day: Psalm 91: 11 - 12. For he will command his angels concerning you to guard  you in all your ways. On their hands they will bear you up, so that you will not dash your foot against a stone. 

Angels

This song gets me every time. My parents use to play this Richard Smallwood CD out, blasting it in the car on the way to church. It's touched me since I was little. I'm so blessed to have been raised by parents that gave me a strong foundation in the church - a strong, Georgia baptist church at that, the kind in which you had no choice but to absorb and soak up the pastor's message because they would scream it, sing it and shout it the whole service. You would leave feeling exhausted. Some folks don't need all that shouting, but I'm grateful because when you're 9 and you think you'd rather be at home in your PJs watching TV with a bowl of cheerios, you need somebody to shout a message until you finally get it and understand it and can carry it with you over the years. My pastor didn't shout for nothing. He could speak quietly. He could whisper as he told a story. But when he was making his point, rest assure he was going to let out a shout or two. I have a lot of growing to do spiritually, on my own. I need to make room for what I'll call be-still time to meditate on the bible and my own personal relationship with God. I  need to learn the bible. I'm actually excited to see how far I can grow. I think this is what I'm supposed to do as I fight this illness and recover. But at least I am starting with a strong foundation and a heart that's acutely aware of God's love and healing powers... and at least I have this song to remind me that "unseen hands are guiding me through my storm." I might vent every now and then but honestly, I have no worries.

Interesting article in today's Washington Post about a woman who needs a lung transplant but was reluctant to have a necessary blood transfusion due to religious reasons: http://www.washingtonpost.com/wp-dyn/content/article/2010/02/16/AR2010021606057.html?hpid=topnews.

Tuesday, February 16, 2010

Just when I'm trying to feel down and sulk a bit something lifts me up. I just got word today that I won a journalism award at work for a story I did this time last year on the government's financial bailout. A nice little unexpected pick me up. The blessings keep flowing.

Gorgeous and Bald: Pics of Brandi Maxiell - (NBA player's wife)

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Basketball Wives


I was watching E! today when a documentary called Basketball Wives came on. Pretty interesting. I focused in on Brandi Maxiell. She just married her high school sweetheart Detroit Pistons player Jason Maxiell. Brandi had ovarian cancer and lost her hair while undergoing treatment in 2007. Jason shaved his hair bald too as a way to make her feel better about her hair loss. Sweet!  

Countdown

Heading to the hospital in six days. 6 days! And I can't stop thinking about it. It's like there's a clock ticking in my head, distracting me from thinking about anything else. I could be in the hospital for weeks. I'm hoping not more than three. My son isn't allowed to visit, and I've never gone that long without seeing him. I'm trying not to get anxious but  this whole transplant thing is a little frightening. I don't even feel like going into the scary details because I know everything will be fine. Everything so far has been fine. And I'm strong enough to handle this. I keep reminding myself of that. This is the meat and potatoes of my treatment. I need this and I will get through this. This is what I need to move on with my life. It's just daunting to know that it'll have to lose so much to get there. My mind won't stop running. Hair. My immune system. Both will be wiped out this time next week. I'll be tired and sick. Stuck in bed. No son. No hair. No energy.  Fragile. It'll take 3 months for me to recover at home. 3 months!!!  Vomiting. Nausea. Wearing a mask to prevent infections. And no hair??!!! This is when the Why Me's creep in.

Thursday, February 11, 2010

Snowblivion

What a week. Despite the historic "Snowblivion" here in the D.C. area, I made it to the cancer center in Baltimore not just once, but twice, for two critical procedures. And now my doctors have collected enough of my stem cells to move on with the transplant at the end of the month. This is yet another blessing - mainly because it took a lot to get to the point in which my doctors could collect my stem cells. I got a super dose of chemotherapy last week that made me sick to my stomach. I also had to start injecting myself with a special medicine, and I had a catheter placed in my chest. Each of these steps had to be done within a strict timeline. So if the blizzards and icy roads had prevented me from getting to Bmore this week, I would have had to redo most of those steps and probably postpone the transplant. That would have been crushing and a huge setback. But thanks to two dear friends ... (and their white, magical, Hummer,) I made it to Baltimore on Monday in the aftermath of one of the worst snow storms ever for the DC area. Other people could barely walk down their driveways, let alone drive anywhere. That night, my moms - my mom and my husband's mom - made it in town after several cancelled flights. The next day, they took care of my son, while my husband and I hit the snowy roads again so that I could have my stem cells collected. To collect the cells, I was hooked up to a machine that withdrew my blood. The procedure is painless. I just laid on a hospital bed. But it can take two days for the technicians to successfully collect enough cells. Our goal, however, was to try to be home before the second blizzard got underway. We only had hours, not two days. We were able to leave the hospital around 4, right as the flurries started to come down. Soon after, we got good news from the hospital: in that one day, they collected twice as many stem cells as they had expected. Looking at all of the snow outside now, I smile with comfort because I can't believe I'm still on track for my transplant. I can't believe I made my appointments.... I can't believe I'm here, relaxing, spending time with my moms - cooking, laughing, talking. Things could have easily been derailed for me. But that wasn't the case, largely due to friends, family .. and that big, white magical Hummer.... And I'm still not sure how my moms made it here in all this snow.... And I can't believe I have such peace. I have cancer. I'm not supposed to feel this happy...I just smile and shake my head. What a week.

Swiss Chard, Anyone?


Had Swiss Chard for the first time a couple of weeks ago and meant to write a post. It was high on my list of new veggies to try, especially because they remind of collard greens. According to "Cancer-Fighting Kitchen" Author Rebecca Katz, swiss chard is a powerful cancer-fighting food. She says Betalain, a pigment in Swiss chard is also being studied for potential anticancer properties. Some experts believe certain foods - mainly vegetables - make your body less hospitable to cancer, while others, such as white flour and sugar help it thrive. All I know is swiss chard was tasty and quick. I simmered some olive oil, garlic and onions in a pan and threw in the chard and some Worcestershire sauce and a bit of cumin. Ready in no time. And then for dessert, I had ... ice cream. But at least I coated my stomach with that "Betalain" stuff first. Sigh. Baby steps.

Wednesday, February 3, 2010

Charm City


Up early again. Body is tired, but my mind is racing. So will spend some time counting blessings. Always helps. I think I'm on blessing #6. And since Baltimore is on my mind, that's what I'll write about, mainly because it's just a sign that this journey is bigger than me. I was born there. Decades later, God has led me back for life-saving treatment, so that I can heal and continue to live a wonderful life. I think that's by design. Riding into Baltimore for treatment reiterates how this whole journey is bigger than me, how there is a plan for each one of us. Despite its troubled schools and notorious crime, I've always had a fondness for "Charm City." Now, I greet this town as the place God has chosen for not only my birth, but for my healing. There's something to that. When I got my diagnosis, the doctor referred to my current oncologist in Baltimore, praising him as one of the best in the world for treating multiple myeloma/plasma cell leukemia. Not many cancer doctors have seen patients with myeloma because it's so rare. But up the road, just about 40 minutes from my house, I'm not so rare. And that's truly a blessing.

Tuesday, February 2, 2010

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After spending 10 hours in Baltimore for a super-dose of chemo, this picture sums up how i feel. Intoxicated. Drunk. Super-Drowsy and Silly. So I'm hitting the sack...after American Idol.

What I'm Reading Now

Cover ImageAnticancer by David Servan-Schreiber: Book Cover
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Monday, February 1, 2010



I hadn't seen the clip of Robin Roberts ditching her wig during her cancer battle. So dug it up and here it is:  http://abcnews.go.com/GMA/BeautySecrets/story?id=4694536&page=1

And another: http://abcnews.go.com/GMA/OnCallPlusBreastCancerCommunity/story?id=3869529
Here's a profile and short video of a 26-year-old Nigerian-born athlete who is battling cancer and working to get more African-Americans to sign up for the bone marrow registery. All it takes is a cotton swab, folks. I never knew that.
http://www.thegrio.com/black-history/thegrios-100/thegrios-100-seun-adebiyi.php

And here's a link to his blog: http://nigeria2014.wordpress.com/2010/01/

He just graduated from Yale Law School and is working to become, in 2014, the first Nigerian delegate to compete in the Winter Olympics, all while battling  stem cell leukemia and lymphoblastic lymphoma. Also, he went back to Nigeria to help get more people to sign up for the bone marrow registery.Whew,  makes me feel lazy. I only have one cancer to beat and I fret over that. I'm taking notes, though. I like the way he sets long-term goals despite the obstacles he's facing currently.