...Or maybe an entire wing. Stephanie has been re-admitted to the hospital. She started Radiation on Tuesday and Wednesday. Then on Wednesday night we drove to Waco for Thanksgiving and her grandmother's birthday party. The trip seemed to really wipe Stephanie out, she was in a lot of pain, sleeping most of the time, could barely walk, and was pretty confused. After seeing everyone and enjoying the party on Thursday we packed up and headed back to Gonzales so Stephanie could get her next two treatments on Saturday and Sunday. Sunday evening she started getting even more confused and weaker. When we went to the doctor on Monday he immeadiately suggested the hospital because her calcium was so high. Hypercalcemia is relatively common in people with solid tumors in the lungs, and causes most of the problems she was having. On Tuesday, after recieving some anti calcium drugs she was still pretty loopy, so the doctor decided to scan her brain just in case. The scan was thankfully clear, but it was still a scary few days. Today she is mostly lucid as the effects of the calcium are wearing off finally. Hopefully she will be discharged early next week.
Saturday, December 5, 2009
Sunday, November 29, 2009
Update: One Month Later
It's been a while since I've updated, even longer than the month it's been since Stephanie did. And what a month it has been. After her last update Steph started complaining about the Taxol and significant numbness in her hands and feet (a common side effect of the chemo). The third week of her three week cycle her blood counts were down and she didn't recieve the Taxol, only the Erbitux and later two units of blood. The next week was an off week, towards the end of the week she began complaining about a sharp pain in her left arm and hand. On Monday when she saw the doctor we discussed this and he determined he would like to scan her and see if there was a reason for her pain. She had treatment that day as well since we were in the bulding. At the end of the week we traveled to O'Fallon IL to visit my family, surprise my sister as she was in a play, and celebrate my mom's 56th birthday. Unfortunately there was a reason for the pain that showed up on the scan. The Taxol/Erbitux combination was not being effective and the large tumor in her left lung (the only one that showed any activity a month before) was growing somewhat significantly. It has begun eroding the chest wall and is pressing on nerves in the let shoulder blade area, which is causing the pain in the arm and hand. He switched her to another new drug to see if it would be effective. She felt good in the beginning of the week, but again towards the end the pain became unbearable. When we saw the medical oncologist on Monday and told him about the pain he suggested we consult with the radiation oncologist and determine if the tumor could be radiated to more quickly relieve the pain in the shoulder. The RO decided that he could and Stephanie started her second round of radiation on Tuesday before Thanksgiving. She recieved two treatments before Thanksgiving and then we headed out to Texas for Stephanie's grandmother's 80th birthday. It was good to see her extended family and celebrate such a long life. Stephanie was of course the second center of attention at the party. Unfortunately all the traveling has pretty well done her in. She slept the entire day Thursday, except while we were actually at the party. We had to return to Gonzales on Friday so she could receive her next two radiation treatments today and tomorrow. She has slept all day today as well, she even missed the Razorback game and slept through all my hollering. Hopefully tomorrow she will get some energy back.
We are still planning on moving back to Tulsa. The date is currently set for traveling on December 18th, and staying in our house for Christmas. The MO is researching cancer centers for us and will make a recommendation, probably sending Stephanie to an academic center in order to participate in a clinical trial.
Grace and Peace
Posted by warner at 12:21 AM 5 comments
Wednesday, October 21, 2009
Can't A Girl Just Get One Step Ahead?
Can't I just have a normal life for a day? I mean seriously I'd settle or an hour if that would be possible. On the 19th (Monday - when I had my treatment I was feeling pretty good, tired though. So I had my chemo, and got that shot to boost my red blood cell count again - yeh the one that hurts unless they push it in fast enough and not all of them do that. Everything was all hunky - dory. Well, at some point during the afternoon I did something to the mid - left section of my back and as the night went on it got worse and worse. Yesterday I barely got out of bed and it was killing me to even breathe because of the pain. Today was a little better, but not as much mostly kicking me in the - it just . I can drink a few small sips at a time - like 2 - and I haven't even attempted to eat so we are using the feeling tube. I've mainly been sleeping the day away with the drugs. Does anyone have any back /injury fixes?
Posted by Stephanie at 6:59 PM 7 comments
Monday, October 12, 2009
Have You Forgotten About Me Yet?
Long time no post! Well, I guess it's been a week or two, which isn't toooo bad. I finally have some news to post about - see, good things Last week I had the week off from chemo and had my PET/CT scan. It was definitely nice not having to get up early for chemo on Monday. Today we got the scan results and they were definitely positive. The only scans he had readily available to compare them with were the scans from April and I've had several other scans since then during my hospital stays.
Posted by Stephanie at 8:04 PM 9 comments
Monday, September 21, 2009
Somebody Listen To Me!
Story Time!
Posted by Stephanie at 11:09 AM 6 comments
Saturday, September 12, 2009
Fatigue At It's Finest
Posted by Stephanie at 6:44 PM 5 comments
Tuesday, September 1, 2009
There's a Hole In My Belly Dear Warner, Dear Warner
So, today I got my drainage tube taken out. You would think this would be no big deal because I had my PEG tube taken out last year and it was a piece of cake. Well, except for the whole confusion in the pre-op area and no one being able to find me, and yeah, no big deal. Well, turns out they put in a different type of tube this time - one with a non-deflatable stopper in it. NON-DEFLATABLE. Last time, my PEG tube had a balloon on the end of it and the radiologist just deflated the balloon and slipped the tube out. Then he butterflied the hole with tape and threw some gauze on there and we called it a day. This time, after waiting in the waiting room for an hour and a half (they were super behind) I went back to the room only to find out that the G tube had the mushroom stopper on the end of it and that was going to be pulled through the hole in my belly - I wanted to start crying right at that moment, but I didn't. Then he pulled the tube out and let's just say I screamed some and then my eyes got quite watery. Warner's hand is probably broken in about 20 different places as well. So, he pulled the tube out in two yanks, yeah, not one, but two, and stomach content went everywhere. I soaked through tons of gauze in about two seconds. My tshirt and jeans did a good job of soaking up the stomach stuff as well. I'm still leaking a good bit tonight so I've got a stack of towels and gauze nearby and Dr. Warner is doing a great job by keeping me doped up on some pain meds for now.
Posted by Stephanie at 7:48 PM 6 comments