tag:blogger.com,1999:blog-1203763377570564372024-03-13T03:39:12.322-07:00Lisa Huffman's Cancer ExcursionLisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.comBlogger42125tag:blogger.com,1999:blog-120376337757056437.post-21713280886232235962016-06-10T17:24:00.000-07:002016-06-10T17:24:40.446-07:00RhabdomyolysisA friend texted me this reminder: "The hotter the fire, the harder the steel." Isn't that the truth, and I know that God is with me through yet another trial.<br /><br />
Although Rhabdomyolysis isn't related to cancer, breast reconstruction or my recovery, it does seem to be a part of my journey.<br />
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I'm not quite sure exactly what caused my Rhabdo, but do have some suspicions. With having had breast reconstruction surgery in October, a breast revision in January and another breast revision in April, I haven't been able to exercise like I'm used to doing. Finally finished with all of those surgeries, and with school out for the summer, I decided to jump back in last week and begin a regular workout schedule. I started with my usual 3-mile treadmill walk since I still can't quite run yet and added P90X 3. Friday I completed the workout called Challenge with 100 pushups and 70 something push-ups (assisted). I felt pretty good through most of the workout, but pushed myself to finish strong. I felt great and proud of myself for knocking out 100 pushups!<br />
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Saturday I was a little sore with arms like Jell-O, but that was to be expected. I did a light workout and walked on the treadmill. I spent a fabulous afternoon with friends and family. We went to Nitro Circus and I felt pretty good, just a little tired.<br />
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James and I went for a mountain bike ride on Sunday. We rode the single track Mighty Bikes at Kincaid and completed about 6 miles. I felt really sluggish and sucked wind, but just contributed it to being tired. I hadn't slept well because my arms were sore. <br />
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On Monday I completed a 3-mile walk on the treadmill and a P90X that didn't use arms. Still feeling sluggish and having sore arms, I felt like I could push through and would start feeling better by Tuesday. After Tuesday morning's workout, I knew that it was more than just some sore arms from working out. I couldn't really bend my left arm to touch my nose and definitely couldn't straighten my arm. I looked at my arms in the mirror and thought Pop-eye!<br />
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<tr><td class="tr-caption" style="text-align: center;">No funny mirrors were used for this picture!</td></tr>
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I Googled "swollen and sore arms after workout". What came up was "Rhabdomyolysis". After a quick read of the causes and symptoms, I was pretty sure that was what was going on and I headed in to see a PA at primary care. The PA said she'd seen Rhabdo before and was sure that all I did was strain my muscles. She sent me home and told me to take 500mg of Naproxin every 12 hours. I went home and took the Naproxin, but after two hours, knew that there was more going on than strained muscles. The pain reliever wasn't really touching the pain either. With that, I called James and then had Jared take me to the ER.<br />
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The ER is always such an adventure. There's such a range of medical needs: someone intoxicated, another lady with some nerve damage causing half of her face to go numb, a young girl miscarrying, a kid arriving by ambulance with a broken limb. Made me feel like my medical needs were minimal, so I waited patiently for 2 1/2 hours before they got me back to evaluate me.<br />
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I let the doctor know right away that I thought I had Rhabdomyolysis, and that it probably drove him nuts that patients Google their symptoms and diagnose themselves, but he didn't seem to mind. He did however give me an ultrasound of my arm to make sure there were no blood clots and an x-ray of my arm before taking a blood sample. The blood sample came back an hour later with creatinine kinase levels over 20,000 which meant they were admitting me to the hospital. Normal CK levels should be nearly undetectable. <br />
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What have I learned? Rhabdomyolysis is the rapid breakdown of muscle caused under extreme conditions, usually from trauma to the muscle like an accident or by chemical means like toxins or drugs. The breakdown of the muscle causes the protein myoglobin to leach into the bloodstream. The kidneys try to clear the harmful protein out of the bloodstream, however they can clog the kidneys causing damage or kidney failure. Although Rhabdo is considered rare, exercise induced Rhabdo is considered extremely rare. <br />
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The symptoms that tipped me off that I had Rhabdomyolysis were<br />
<ul>
<li>weak muscles</li>
<li>intense pain at the affected muscles on my arm</li>
<li>swollen arm</li>
<li>inability to straighten my arm </li>
<li>fatigue</li>
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There are many other symptoms such as bruising, tea-colored urine, fever, vomiting or nausea, and confusion or agitation. I didn't experience any of those, unless you perhaps ask James and he thinks I was agitated. <br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com2tag:blogger.com,1999:blog-120376337757056437.post-70986190032027114862015-10-28T08:20:00.000-07:002015-10-28T08:20:49.805-07:00Tuesday, October 27, 2015<br />
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Finally, heading home to Anchorage! <br />
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I had a great weekend visiting family and friends. James, my designated drive for the past two weeks because I can't move my arms, was able to drive us up to Bellingham on Saturday to visit James' parents and his brother's family. While there, Colleen was able to pull the right thigh drain that was ready - loved that! I love visiting Jon, Colleen, Anna Corinne and Emily. We have lots of fun together and they've got a little farm which I enjoy. Loved meeting the llamas!<br />
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<tr><td class="tr-caption" style="text-align: center;">Isn't she cute?!</td></tr>
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Sunday we were able to drive down to Tacoma and visit some long time friends from Fairbanks. It was great to see Diana and Mary. They made us a delicious lunch which we needed to get us through the I5 traffic as we headed north in the afternoon. We stopped in Issaquah to visit Jennifer and Jon, James' sister and brother-in-law. While there I went to the restroom at the restaurant and returned uneventfully. Jennifer then went to the restroom and returned asking if I'd seen the picture of David Lee Roth. Nope, I missed it. I returned to check it out with this selfie as evidence. What a laugh we all had!<br />
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<tr><td class="tr-caption" style="text-align: center;">No caption needed...</td></tr>
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Yesterday, I had an appointment at UW with the Physician's Assistant. Ann checked for infection, checked stitches and checked breasts. Everything looked great. She was able to remove the doppler wires from each breast. She explained that they have a dissolving rubber bulb on the end where it is connected to the vein or artery. The longer they are left in, the more the bulb dissolves, the easier it is to pull out. She removed the tape covering the exposed ends and gave a tug to the wires on the right breast. Came out like a breeze! She removed the tape covering the exposed ends and gave a tug to the wires on the left breast. Not so easy peasy, which made me a little queazy as blood came running out. She patched up the hole and I was ready to go. Unfortunately, I still had one drain in my left thigh still draining over the 30cc allowed per day. On the bright side, because everything looked great, I didn't need to follow up with Dr. Said today.<br />
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This morning James was able to pull the final drain. The PA suggested pulling it before flying and then wearing compression stockings for the flight home. In addition to the compression stockings, I've continued to need to wear my compression sleeve because of the Lymphedema in my arm. I'll follow up with medical providers in Anchorage. <br />
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After 4-6 weeks I can resume activity, taking it easy athletically. In December I have a follow up appointment with Dr. Said where he'll outline the second part of the reconstruction. This ends part one of four for this next part of my journey. More to come at that time...Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com0tag:blogger.com,1999:blog-120376337757056437.post-13587862352121501952015-10-24T09:45:00.000-07:002015-10-24T09:45:07.776-07:00<div class="separator" style="clear: both; text-align: center;">
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Friday, October 23, 2015<br />
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Since surgery and being released from the hospital, it has been a week of ups and downs. The first hurdle was waking up in the hospital with a severely swollen right arm, Lymphedema. Lymphedema is not curable and results from damage to or loss of lymph nodes. Lymph nodes are a part of the immune system and not having them prevents lymph fluid from draining well, and the fluid buildup leads to swelling. Lymphedema is a life long problem. Because I had so many lymph nodes removed during the bilateral mastectomy, I've had to be cautious with my right arm. I wear a compression sleeve when I work out, run, mountain bike, do strenuous activity around the house, fly on an airplane...you get the idea. <br />
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When James first realized I had Lymphedema and pointed it out to medical staff, they seemed a bit unconcerned. The thing with Lymphedema is that not only is it uncomfortable, but it restricts the range of motion in my arm and it is painful. So painful that I couldn't straighten my right arm without sharp, intense pain - while on pain medication! The medical staff didn't know anything about Lymphedema and were unable to help. Fortunately, I brought along 2 compression sleeves and James ran home to get one. A week later and the swelling is about gone and there is little pain when I straighten my arm. The Lymphedema specialist at UW is out of the country so I'll follow up with a doctor when we get back to Anchorage.<br />
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A second little scare was when my right flap lost color and felt cool on Monday night. We called in to the medical staff who asked us to watch it overnight and call in the morning if we were still concerned. Tuesday morning, the flap was still white and cool. They asked us to come right in, however when we got into the examination room and Dr. Said looked at the flap, it had color and was warm! He assured us that he believed us and we weren't crazy. He explained that with the new veins and arteries in the flaps, blood would sort of clot and slow causing the flap to go white and become cool. When the "blood clots" broke free, the color and warmth would return. He had me add an aspirin daily to thin my blood. Since taking aspirin on Tuesday, I've experienced no further flap complications. While there, they pulled one of the four drains. <br />
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<tr><td class="tr-caption" style="text-align: center;">A Monday evening walk along Golden Gardens Park.</td></tr>
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The third, and I hope final scare was when I woke up on Thursday to a red, warm, swollen inner right thigh just above the drain and around the donor site area. After waiting for a call back, we were finally able to be seen at 3:00. It was in fact an infection and they started me on antibiotics. On a positive note, they pulled another drain. Now just two drains left!<br />
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Thursday night we went to see Owl City at the Neptune Theater next to UW. Another really cool theater and the band was amazing. I did have a small episode of, "James get me a chair quick before I pass out." When he got me to the hallway, he said I was as white as a ghost. I guess the infection was taking a little bit of a toll. After sitting for a few minutes I felt much better. I really wanted to see this band, so we went back inside the theater where James found me a barstool to sit on and we were able to enjoy the rest of the concert. I woke up Friday feeling much better!<br />
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<tr><td class="tr-caption" style="text-align: center;">"Flowers" on NE 43rd St and University Way NE before Owl City.</td></tr>
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<tr><td class="tr-caption" style="text-align: center;">Beautiful view from our VRBO.</td></tr>
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Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com0tag:blogger.com,1999:blog-120376337757056437.post-12435415657539045542015-10-22T18:13:00.001-07:002015-10-22T18:13:54.849-07:00Thursday, October 22, 2015<br />
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I was in ICU until Saturday. The first 24 hours are most critical, so the nurses checked the blood flow in each flap every hour. They check it by listening to a doppler machine connected to some metal wires coming out of the flaps. First listening to the right side and then flipping a switch to listen to the left side. They also have a small stitch on the right flap where they can hold a doppler tool to listen to blood flow in the artery. They leave the machine running day and night.<br />
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They also monitor all of the usual vital signs. Even though I had a third IV in an arterial vein near my wrist to monitor blood pressure, they still took my blood pressure each visit. They also gave me antibiotics through an IV and I could use patient controlled morphine pump through one of the IVs. They ended up taking the morphine pump out on Saturday morning, as I wasn't using it. <br />
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I shared the room in ICU with Mr. Pfefferkorn. He had been in ICU for 16 days when I arrived. I couldn't wait to get my own room as I could hear him at night crying "get me outta here" over and over again along with the names of family and friends. Unfortunately, I had to spend a second night in ICU but I was only being woken every 2 hours to have my flaps and vitals checked and I was able to get up and out of bed by myself, with a bit of a struggle. <br />
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I forgot to mention that when Dr. Said went over the pre-op information two days before the surgery, I learned of my restrictions: can't lift over 10 pounds (a gallon of milk is 8 pounds), can't lift my arms to the side more than 45 degrees, can't reach behind me, can't reach in front of me higher than 90 degrees and....can't drive for 4 weeks! So getting out of bed means all abs and James' help because I can't push myself up. I also can't lift my legs out sideways which means I'm sitting and spinning to get in and out of the car and bed. Doesn't feel so hot on a bottom full of stitches!<br />
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Saturday evening I was hoping to leave the hospital, but because discharge was going to take so long and they had a private room on the surgery floor, we opted to move. I was no longer hooked up to any machines or IVs, however I still had in two IVs and the doppler wires. Those were all finally cut loose on Sunday morning when we were able to leave the hospital. <br />
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Fortunately, James' job is allowing him to stay with me the entire two weeks, and Jared and Caleb are being taken care of by family and friends. Thank you to everyone for the calls, texts and prayers. <br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com0tag:blogger.com,1999:blog-120376337757056437.post-46142735535172982532015-10-21T10:48:00.000-07:002015-10-21T10:48:01.498-07:00Wednesday, October 21, 2015<br />
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Surgery day was Thursday, October 15, 2015. <br />
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When the alarm went off in the morning, it was straight into the shower for an antibacterial cleansing then off to the University of Washington Medical Center. We checked in by 5:45am and were back in the pre operation room five minutes later. The room was a revolving door of nurses, doctors and anesthesiologists from my surgical team introducing themselves and getting me ready for surgery. One of the anesthesiologist placed the first of my three IVs with ease. James and I enjoyed talking to him about Africa, a place I would someday love to visit! He had just returned from visiting his family there. James tried to get his mom and dad's name so we'd have a place to stay, but no such luck. :)<br />
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Dr. Said came in with Dr. Miller and they sketched out the incision sites on each of my upper thighs. James said it wasn't pretty. They marked along my bikini line from the middle back of my thigh to the front of my groin, about 12 inches and then a vertical line about 6 inches long from the middle of my groin down towards my knee. That's about what I've got for stitches right now - Yikes! <br />
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One of the nurses from the surgical team stopped in and introduced herself. James asked her what the doctors do for lunch and breaks...10 hours is a long time to be in surgery. She giggled and assured him that they go in prepped with everything they need and it isn't a big deal. As Dr. Said told us, it is just another day at the office for him, although he also said he understood that it wasn't for us.<br />
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It wasn't too much longer and the anesthesiologist asked me if I wanted some valium before heading back. I told him no, as I was completely at peace knowing that God is at my side. James gave me a kiss and I was on my way down many back hallways to the operating room. When he wheeled me into the room, the surgical team was gathered around a large monitor looking at what appeared to be the CT scan of my upper legs. They were looking at the veins and arteries. They slid me over to the operating table and everyone from the team of 15 greeted me and shook my hand. They strapped me to the table, put a mask over my nose and mouth telling me to breath deeply. I was out for 10 1/2 hours.<br />
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James received updates from the head nurse every two hours. What a long day for him. About 6 1/2 hours into the procedure, the microsurgery portion was about complete and they were monitoring the newly transplanted tissue for blood flow while they began sewing up the donor sites.<br />
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Dr. Said came out after surgery letting James know that everything went well and then I was taken into ICU where they monitored my newly placed skin flaps every hour. They watch the flaps very closely the first 12 hours as that is when 80% of the complications occur.<br />
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<tr><td class="tr-caption" style="text-align: center;">Waking up in ICU.</td></tr>
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If you're wondering what a TUG Breast Reconstruction Surgery is, check out this site: <a href="http://www.breastcancer.org/treatment/surgery/reconstruction/types/autologous/tug">http://www.breastcancer.org/treatment/surgery/reconstruction/types/autologous/tug</a><br />
<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com0tag:blogger.com,1999:blog-120376337757056437.post-83768007475168316512015-10-21T09:02:00.000-07:002015-10-21T09:02:41.057-07:00Wednesday, October 21, 2015<br />
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In preparation for the TUG breast reconstruction, last week I had a pre-op visit with the surgeon as well as a CT scan on Tuesday. The contrast CT scan is used by the surgical team to map my veins and arteries, planning how they'll stitch the flap together. Absolutely amazing!<br />
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We spent Tuesday evening and Wednesday enjoying concerts. The Wind and the Wave was a small concert at the Sunset Tractor Tavern in Ballard. They were a fun band in a small setting. Here's one of their songs.<br />
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Wednesday night we went to the Paramount Theater in downtown Seattle. This theater originally opened in 1929 and seats about 2,500 people. It is absolutely beautiful inside this venue. We were fortunate enough to get seats up front right outside the standing room only section to see Chvrches. They were another amazing show, and another Scottish band. We saw the Scottish band Of Mice and Men this summer in Seattle. <br />
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Then it was home to bed and set the alarm for 4:30am so that we could be at the University of Washington Medical Center at 5:45am to check in for surgery.Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com0tag:blogger.com,1999:blog-120376337757056437.post-46795372637817864062015-10-20T20:25:00.000-07:002015-10-20T20:25:15.317-07:00<div class="separator" style="clear: both; text-align: center;">
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Tuesday, October 20, 2015<br />
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A lot has happened in the 2 1/2 years since I last wrote this blog. There were many times I thought about writing and wished I had kept up with it. I finally decided that it isn't too late to jump back in and now is the perfect time. <br />
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About six months ago I began pondering breast reconstruction. I wasn't unhappy with my body, but there were definitely times when I was disappointed I couldn't wear a certain shirt or dress. And putting on prosthetics was certainly a reminder of Breast Cancer. Not that it was a good or bad thing, just that it was. <br />
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During these past months, I spoke with a friend who recently underwent breast reconstruction and consulted with two surgeons about my options. My friend was open and honest about the process. I appreciated her willingness to share and admire her greatly for the light she sheds on cancer and all that she does to support the American Cancer Society. Thank you, Becky!<br />
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When I consulted with the surgeon in Anchorage, she shared the process she'd recommend which was inserting expanders and then implants. She used words like probably, likely, might, and possibly. Those made me a bit uncomfortable. Going through a major surgery to possibly get an "A" cup just didn't seem like something worth the risks. <br />
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James and I celebrated our 20th Wedding Anniversary in Seattle a few weeks after the consult with the Anchorage surgeon. I decided to seek a consultation with a doctor at the University of Washington Medical Center. Within the week that we were traveling, I was able to get an appointment with Dr. Said. When we met with him, he asked how I was able to get the appointment at the clinic off campus. I just emailed, they called and voila! I had an appointment. It was a God thing. <br />
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While at the appointment, the plastic surgeon explained the various options and the success rate and data for each type of surgery. He explained that trying to stretch my radiation damaged skin and insert implants was maybe a 50/50 percent chance. He said he would not recommend that surgery for me. He then looked at the second option which was a DIEP Breast Reconstruction where they take muscle, tissue and skin from the abdomen to build breasts. He said that also was not a good option as I didn't have enough abdomen tissue to build two breasts. He then talked about the latissimus dorsi flap which uses muscle and tissue from my upper back. He didn't like this option for me either because it uses a "good" muscle. Are there any bad muscles? <br />
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The next two options were the gluteal free flap which uses muscle and tissue from the buttocks, and the TUG or transverse upper gracillus which uses muscle and tissue from the upper thigh. Of the two, he explained the TUG would be my best option. Success rate for this surgery is above 95% - much better odds than the 50/50 for expanders and implants. All of the benefits included higher success rates, using my own tissue for the entire surgery, long-term higher satisfaction among patients, and never having to mess with the site again as I would with implants. After the consult, I immediately knew that I was going to have a TUG Breast Reconstruction with Dr. Said. James was 100% supportive and the next part of the journey began. <br />
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<tr><td class="tr-caption" style="text-align: center;">A trip to Mexico after completing a year of cancer treatments.</td></tr>
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<tr><td style="text-align: center;"><a href="http://3.bp.blogspot.com/-ZlNkdKck1q0/VicDwD-jCaI/AAAAAAAAAkE/vXhNz4Gg8uc/s1600/James.jpg" imageanchor="1" style="margin-left: auto; margin-right: auto;"><img border="0" height="320" src="http://3.bp.blogspot.com/-ZlNkdKck1q0/VicDwD-jCaI/AAAAAAAAAkE/vXhNz4Gg8uc/s320/James.jpg" width="289" /></a></td></tr>
<tr><td class="tr-caption" style="text-align: center;">James & Lisa</td></tr>
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<tr><td class="tr-caption" style="text-align: center;">We had our picture taken here 20 years ago!</td></tr>
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Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com0tag:blogger.com,1999:blog-120376337757056437.post-60246037727826748812013-03-17T15:22:00.002-07:002015-10-22T10:55:21.444-07:00Sunday, March 17<br />
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I can't believe it has been almost one year since I first found that lump. March 30, 2012 was the first of many doctor appointments - the one appointment which James pestered me to make for a week. I'm glad that he did too.<br />
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Since the hysterectomy, I have recovered well. I've been back at work full time since January 31, two weeks after surgery. My apologies for not blogging sooner about how the surgery went, but I've been swamped with work and I am trying to keep my big rocks a priority. The surgery went well and the doctor said that it did in fact look like my ovaries were beginning to work again, and he also commented that it was a good decision to remove my uterus as it was full of fibroids and needed to be removed. My six week post surgery check up went well. I haven't experienced any real hot flashes or menopausal symptoms so am very blessed in that regards. I am officially graduated from Gynecology. <br />
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<tr><td class="tr-caption" style="text-align: center;">A note from the school greeting me in the entry upon my return.</td></tr>
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I began taking the AI the day after surgery and haven't noticed any side effects. It is a small pill I take daily in the morning for the next five years. I'll have my next Oncology appointment on April 8. I don't anticipate anything much at that appointment other than a check up. From here on out I'll be monitored every 4 months with an Oncology check up.<br />
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I have noticed some real set backs with my right arm movement and armpit since I haven't been doing yoga or other exercise. Everything is very tight, and sort of numb and sore. I did go to yoga yesterday and will make an effort to go at least once a week. I'll also get my butt up and moving every morning too. I have really felt tired, sad and/or depressed lately. I went to acupuncture on Wednesday which helped tremendously, but I still don't have the stamina I used to.<br />
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<tr><td class="tr-caption" style="text-align: center;">A little friend greeted me one morning when I was feeling a little blue. Cheered me right up!</td></tr>
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I don't plan on doing reconstruction at this point. The process involves several surgeries to stretch the skin and place the implants. Stretching the damaged skin is a painful process, and although the pain doesn't really scare me, I'm not thrilled about the idea of more surgery. With implants, you also need to do follow up replacement surgeries every ten years. <br />
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I have enjoyed time off for Spring Break - it was filled with Jared, Caleb and I volunteering for Citiserve this week while James worked. We delivered furniture for Love Inc., bagged potatoes for the Food Bank, played with kids at the Boys and Girls Club, chipped ice at the Rescue Mission and helped at Kids' Kitchen. There are so many needs in Anchorage and it was nice to be a part of helping our community.<br />
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The best part of spring break was just being together. We spent yesterday skiing at Alyeska; it was beautiful and fun! We are so blessed to live in such a spectacular place and have time together as a family.<br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com3tag:blogger.com,1999:blog-120376337757056437.post-49718881113809478612013-01-16T20:50:00.000-08:002013-01-16T20:50:04.381-08:00Well, tomorrow is the big day - last surgery! I am so excited, which might seem a bit strange, but it marks the last major hurdle in this breast cancer journey. I know I'll have follow-up care and medication to take daily, but that is all so manageable.<br />
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Since completing radiation two weeks ago, I am amazed at how quickly my skin has healed and I've recovered. After one week, all blisters had healed up and this past week the redness has really toned down. You can definitely still see the radiation fields and it is still a little tender - I don't want to wear a bra yet, but it is such a vast improvement over the last two weeks of radiation that I'm thrilled. James laughed when I said I couldn't wear a bra yet - what do I need to wear one for? For the prosthetics of course. Although I really only wear them if the outfit requires some shape and nothing I'm wearing right now really requires that. It has really been a blessing that I have not been working and have been able to recover completely for this surgery. <br />
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<tr><td class="tr-caption" style="text-align: center;">Blood draw?</td></tr>
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After prayer and consultation with the gynecologist, the conclusion is to remove my ovaries, uterus and cervix. The procedure will be laproscopic surgery, three incisions in my abdomen with the organs being removed vaginally. Any complications would result in a cut in my abdomen and organs removed through the incision.<br />
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Had some more blood taken today, and I miss the Oncology nurses! This nurse has drawn blood twice and both times left me bruised and bloody, and I've got great veins! I am anxious to see the result tomorrow as my last draw on December 27 had low white cell, red cell and absolute neutrophil counts. I was surprised - my white count was at 2.2. <br />
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I've continued with hot yoga which has helped tremendously - not only with sweating out all of the chemo drugs, but it has helped the range of motion in my right arm and shoulder. I can feel the skin, muscles and ligaments stretching in the intense heat. I love it! I can't wait to get back to it after surgery. I did get some great advice from a nurse friend of ours who said to get up and get walking right away - so that's my immediate exercise plan.<br />
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<tr><td class="tr-caption" style="text-align: center;">Salmon with roulade</td></tr>
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We enjoyed a wonderful family dinner this evening - Salmon Roulade. It is one of my favorite recipes and I want to thank our friends in North Pole who first gave us the recipe. The boys have a hockey tournament this weekend and will take on some additional responsibilities once again. I'm hoping to get to make their finals on Monday. <br />
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Please keep our family in your prayers. <br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com4tag:blogger.com,1999:blog-120376337757056437.post-3066593533139360292013-01-08T16:03:00.000-08:002013-01-08T16:03:53.495-08:00Relieved! I am so thankful to be finished with radiation. Thursday, January 4, 2013 was my last treatment. The daily treatments left me tired, but the last two weeks really took a beating on my skin in spite of the prescription cream, medicated bandages, supplements and other lotions. I ended up blistered on my right side under my arm which was a most inconvenient location because my arm either rubbed the area continually or I had to hold it out like a scare crow. I ended up holding it out scare crow style without even thinking about it. I have a new empathy for burn patients as I found my little burns uncomfortable and painful - I can't imagine what some people must go through. <br />
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There were three or four days during the 33 treatments when the machine was down and I had to be rescheduled later that day or evening. I found myself hoping that the machine would stay broken so I wouldn't have to go. The last day of treatment, the machine was down and I again found myself wishing they'd just tell me I really didn't need that last treatment. But they squeezed me in on their second machine and I'm glad I completed the treatments. I even received a graduation ceremony complete with music, a rose, certificate, t-shirt, water bottle and bubbles!<br />
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I've been attending hot yoga for the past month and have really enjoyed it. I think it has helped with detoxification - the first couple of classes I had a chemically kind of stinky sweat. Aren't you glad you weren't next to me in class? I'm still going about five days a week up through my surgery next week - in between all of my doctor appointments. <br />
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I met with the Oncologist and Surgeon today. The Oncologist is pleased with how well I've done through my treatments and will start me on the AI the day after surgery. My bone scan showed minimal loss in my spine with my hips and shoulders looking good. I'll start a calcium supplement and he will do a bone scan every two years to monitor bone density. My echocardiogram also looked great. I'll get the results from the blood work next Tuesday when I meet with the Gynecologist. When I met with the Surgeon today, she explained the process for removal of the medi-port; they simply make an incision on the previous incision, cut the two places holding the medi-port in place, pull it out along with the tubing which connects to the vein and then close everything up. Side effects may include bruising. She told me I couldn't keep the medi-port, but why would I? I guess some people have wanted it for a souvenir, ornament...no thanks.<br />
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When I meet with the Gynecologist next week I'll have to have made a final decision as to whether or not I'll just have my ovaries removed, or if I'll have ovaries, uterus and cervix removed. The Oncologist said it was a matter of preference as I don't have any genetic information showing I have a gene which predisposes me to uterine cancer. I'm on the fence and still have a week to decide. I've talked to people who have said I should take it all out and others who say keep what I can - each for good reasons. I'll pray about it.<br />
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I'm still receiving acupuncture and massage weekly and will continue with those, and supplements, through the end of January. I'm looking forward to surgery next week, as it is the last hurdle. I plan to return to work on January 31. In the mean time, I'm trying to recover from radiation and get healthy before surgery. I've had a head cold for the past two weeks. <br />
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Although I had to go to radiation every day over Christmas break, our family really had a nice time together. The boys had a little bit of hockey; they enjoyed skating and skiing with James (I couldn't manage it with my burns); my mom came to visit; and we had several family movie nights. We celebrated the end of radiation with a weekend of dates: a concert, a cooking class and pizza with friends. In spite of all of the challenges this past year, I feel blessed. I'm so thankful that God has seen me through this experience with the
help of outstanding physicians, nurses, friends and family. Thank you again for your encouragement and support - with much love, Lisa<br />
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<tr><td class="tr-caption" style="text-align: center;">Date night...A cooking class!</td></tr>
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com4tag:blogger.com,1999:blog-120376337757056437.post-42913031246875450802012-12-12T22:31:00.001-08:002012-12-12T23:20:40.026-08:00<table align="center" cellpadding="0" cellspacing="0" class="tr-caption-container" style="margin-left: auto; margin-right: auto; text-align: center;"><tbody><tr><td style="text-align: center;"><a href="http://2.bp.blogspot.com/-4BJ5pGu_avg/UMlj444gmUI/AAAAAAAAAdo/RqCIOnKJGgo/s1600/photo%5B7%5D.JPG" imageanchor="1" style="margin-left: auto; margin-right: auto;"><img border="0" height="239" src="http://2.bp.blogspot.com/-4BJ5pGu_avg/UMlj444gmUI/AAAAAAAAAdo/RqCIOnKJGgo/s320/photo%5B7%5D.JPG" width="320" /></a></td></tr><tr><td class="tr-caption" style="text-align: center;">Finally! Great weather for building a snowman.</td></tr></tbody></table><br />
<div class="" style="clear: both; text-align: left;"><a href="http://1.bp.blogspot.com/-yL6NDAq5udU/UMl1JiKTsGI/AAAAAAAAAe8/pCZdVlR_7wI/s1600/photo%5B10%5D.JPG" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="150" src="http://1.bp.blogspot.com/-yL6NDAq5udU/UMl1JiKTsGI/AAAAAAAAAe8/pCZdVlR_7wI/s200/photo%5B10%5D.JPG" width="200" /></a><a href="http://4.bp.blogspot.com/-AT3mJjLYhhg/UMl1NrCndkI/AAAAAAAAAfE/vGO0_zXhZDw/s1600/photo%5B11%5D.JPG" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="200" src="http://4.bp.blogspot.com/-AT3mJjLYhhg/UMl1NrCndkI/AAAAAAAAAfE/vGO0_zXhZDw/s200/photo%5B11%5D.JPG" width="150" /></a>Where to start? I've been thinking about writing for weeks and the time just seems to get away. I've just completed treatment 19 out of 33 - over halfway finished with radiation! Other than fatigue and extreme redness/burn, I've been doing well. You can now see very clearly the fields that they are radiating. I've been keeping a variety of lotions on the area and have prevented anything too painful at this point. My only pain this evening is a self-induced twisted ankle. I rolled it when I missed a step this afternoon and now it is swollen and stiff. </div><div class="" style="clear: both; text-align: left;"><br />
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</div><div class="" style="clear: both; text-align: left;"><a href="http://4.bp.blogspot.com/-luFHjq0p_uU/UMllhoAsGKI/AAAAAAAAAdw/LRK7ytSYxVE/s1600/IMG_6542.jpg" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="150" src="http://4.bp.blogspot.com/-luFHjq0p_uU/UMllhoAsGKI/AAAAAAAAAdw/LRK7ytSYxVE/s200/IMG_6542.jpg" width="200" /></a>One of my newest observations is that my eyelashes are growing back, but now my eyebrows are falling out! I've never been fond of the drawn-on eyebrow look and have never understood why someone would pluck all of their eyebrows just to draw them on. I have new understanding and empathy...maybe they never had control of losing their eyebrows? </div><div class="" style="clear: both; text-align: left;">In the past month I've had an echocardiogram, bone scan and an appointment with the Gynecologist. The Gynecologist told me I would not need a hysterectomy, however after consulting with the Oncologist he called back a few days later to say that yes I would. I will also have my blood drawn this next week to gather baseline data prior to starting the aromatase inhibitor in January. I'll go over all of those results with the Oncologist at the beginning of January when I'm about finished with radiation.</div><div class="" style="clear: both; text-align: left;"><br />
</div><div class="" style="clear: both; text-align: left;">I started a detoxification regimen. I was tired of feeling so crappy, and tired. In addition to the formula that I blend up and drink each morning, I'm not eating any dairy, gluten, wheat, red meat and a few other things. It helps that the whole family is now moving in that direction, although not necessarily by choice. Jared's anemia and allergies to fruit led us to do some follow-up allergy testing. He has food sensitivities to wheat, gluten, cow milk, coffee and a few other items. I'm quickly learning a lot about cooking wheat and gluten free. I've made a few loaves of bread that flopped and purchased a few "yucky" tasting items, but am figuring things out pretty quickly. Today I made a delicious loaf of bread that served as our dinner - the menu called for french toast with hot cocoa. I also made some chocolate chip cookies with sea salt that I had a hard time staying out of. I got a thumbs up from the entire family. Although trying to switch to gluten and wheat free cooking has been a little bit of a challenge, I think it is contributing to my feeling better. </div><div class="" style="clear: both; text-align: left;"><br />
</div><div class="" style="clear: both; text-align: left;">I tried hot yoga this week; I went to an hour class at Anchorage Yoga and really liked it. It was another suggestion by the naturopathic doctor - a way to detox, as chemotherapy drugs will stay in fat cells as long as a year. I'm trying my best to flush and sweat them out!</div><br />
<div class="" style="clear: both; text-align: left;">My favorite things to do while being at home - spending time with the family and cooking. I appreciate all of the prayers, emails, notes and phone calls. </div><div class="" style="clear: both; text-align: left;"><br />
</div><div class="separator" style="clear: both; text-align: center;"><a href="http://1.bp.blogspot.com/-t9OFLG6tLoo/UMlqsdojSsI/AAAAAAAAAeM/joAm9Vt3QAk/s1600/photo%5B3%5D.JPG" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="200" src="http://1.bp.blogspot.com/-t9OFLG6tLoo/UMlqsdojSsI/AAAAAAAAAeM/joAm9Vt3QAk/s200/photo%5B3%5D.JPG" width="149" /></a><a href="http://1.bp.blogspot.com/-wnOMcPRAbEE/UMlqwbTQt1I/AAAAAAAAAeU/ftrmqmJ4odo/s1600/photo%5B2%5D.JPG" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="200" src="http://1.bp.blogspot.com/-wnOMcPRAbEE/UMlqwbTQt1I/AAAAAAAAAeU/ftrmqmJ4odo/s200/photo%5B2%5D.JPG" width="149" /></a><a href="http://3.bp.blogspot.com/-u_1eUfw4mHY/UMlqxdC-S7I/AAAAAAAAAec/WKS517krDYg/s1600/photo%5B8%5D.JPG" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" height="200" src="http://3.bp.blogspot.com/-u_1eUfw4mHY/UMlqxdC-S7I/AAAAAAAAAec/WKS517krDYg/s200/photo%5B8%5D.JPG" width="150" /></a></div><br />
<table align="center" cellpadding="0" cellspacing="0" class="tr-caption-container" style="margin-left: auto; margin-right: auto; text-align: center;"><tbody><tr><td style="text-align: center;"><a href="http://3.bp.blogspot.com/-mPBkRHw5zmw/UMl1OONlZ_I/AAAAAAAAAfM/S3od0Y7FQio/s1600/photo%255B12%255D.JPG" imageanchor="1" style="margin-left: auto; margin-right: auto;"><img border="0" height="240" src="http://3.bp.blogspot.com/-mPBkRHw5zmw/UMl1OONlZ_I/AAAAAAAAAfM/S3od0Y7FQio/s320/photo%255B12%255D.JPG" width="320" /></a></td></tr><tr><td class="tr-caption" style="text-align: center;">Cow bells, cow bells - no more cow bells! At an Aces game.</td></tr></tbody></table><br />
Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com2tag:blogger.com,1999:blog-120376337757056437.post-18951089522169028562012-11-14T21:32:00.000-08:002012-11-15T09:11:36.424-08:00I was originally scheduled for 30 radiation treatments, but found out yesterday that I'd have 33 treatments with my last treatment on January 4. What is a couple more treatments you ask? A downer. I was really hoping to be finished on December 28. I plan on asking the radiology oncologist what difference those 3 extra treatments will make when I see her next week. What does the research show? That's what it is all about. And if I opt not to do the extra three treatments and I have a recurrence, then I'll always wonder - what if I'd done those last three treatments? Okay, I'm over it now; I'll be finished with radiation on January 4, 2013.<br />
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Yesterday during my radiation appointment, the technicians had me lay on the table, lined up my tattoos and then took multiple x-rays of the areas they planned on radiating. They also drew lines showing the perimeter of the areas they were treating. The doctor came in to look at the area and made a minor adjustment which meant that today when I went in, they had to redraw the area on my chest, take a couple of x-rays and have her check the area a second time. With her confirmation, they gave me my first treatment. The machine is quite interesting in that it is located in a room with a metal door about two feet thick and as it rotates around the patient a "window" or collimator adjusts the radiation beam to a flexible shape. The machine is quiet. It moves into position and then for 7-15 seconds radiates an area. It did this seven times radiating basically my right chest wall, lower part of my neck, right armpit, and right side/back. I immediately followed the treatment with lotion which I'm supposed to do three times a day, but not three hours prior to my treatment. I've got lanolin, an aloe plant, BioOil, lotion...a little bit of everything to combat the possible damage to my skin. I'm not to swim, use a hot tub or be in the sun. The swimming and sun won't be a problem, but I'm bummed I can't use the hot tub.<br />
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After radiation today, we met with my oncologist. My blood work looked fine and he was impressed with the amount of hair I was growing and its length. I guess I'm at the top of the list of cancer patients for hair growth, really. He then talked to James and I about the next two months. First, I'll have an electrocardiogram which will be compared with the one I had last February to make sure my heart has not suffered any damage. I'll need to have a bone density scan in the next couple of weeks. I'll also meet with the gynecologist by mid December to discuss the hysterectomy. The oncologist will want the hysterectomy completed immediately following radiation, so that means I'll need to have surgery the first or second week of January. Following that surgery, I'll begin taking an aromatase inhibiter which prevents estrogen from being produced. Aromatase inhibiters can increase the risk of bone loss and fractures, thus the previously mentioned bone scan. When an AI is taken for 5 - 10 years, it reduces the risk of relapse by half.<br />
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Today was a bit overwhelming with all of the information and appointments, but now that I've processed it and prayed about it, I'm planning next week's menu. Caleb had taken on the menu board and planned this week's meals. We're pretty much on track and in addition to what is on the menu, I made some delicious rosemary pretzels with rosemary cheese dip. I've also tried to make sure I stick with daily exercise, as I put on five pounds pretty quickly (and have since taken it back off). In addition to great family time, exercise and cooking therapy, I've been working on Apple iBooks for each year of Jared and Caleb's life. After several days, I have two years worth of pictures, artwork and schoolwork scanned in for Jared and one book completed. Jared is 13 and Caleb is 10...hmmm - I've got a lot left to do!<br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com5tag:blogger.com,1999:blog-120376337757056437.post-92029378139568190602012-11-10T15:03:00.000-08:002012-11-10T15:03:46.253-08:00<!--[if !mso]>
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My first chemotherapy treatment was on May 30 and
November 8 was my last. James calculated that I've had approximately 2.25
gallons of chemicals run through my body over the past six
months. Even so, my blood work looked good this week and has held
stable for the past several weeks. </div>
<table align="center" cellpadding="0" cellspacing="0" class="tr-caption-container" style="margin-left: auto; margin-right: auto; text-align: center;"><tbody>
<tr><td style="text-align: center;"><a href="http://4.bp.blogspot.com/-KaBJ0lGrxH4/UJ7OG_aj-wI/AAAAAAAAAbY/EqFJBj-iCx0/s1600/photo.jpg" imageanchor="1" style="margin-left: auto; margin-right: auto;"><img border="0" height="264" src="http://4.bp.blogspot.com/-KaBJ0lGrxH4/UJ7OG_aj-wI/AAAAAAAAAbY/EqFJBj-iCx0/s320/photo.jpg" width="320" /></a></td></tr>
<tr><td class="tr-caption" style="text-align: center;">The absolutely amazing group of nurses who delivered my weekly chemo. I won't miss chemo, but I'll miss them!</td></tr>
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<br />
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<tr><td style="text-align: center;"><a href="http://4.bp.blogspot.com/-4l6P3RgppBA/UJ7OPpfP7jI/AAAAAAAAAb4/MKBoBh4TzWw/s1600/photo%5B4%5D.jpg" imageanchor="1" style="margin-left: auto; margin-right: auto;"><img border="0" height="320" src="http://4.bp.blogspot.com/-4l6P3RgppBA/UJ7OPpfP7jI/AAAAAAAAAb4/MKBoBh4TzWw/s320/photo%5B4%5D.jpg" width="245" /></a></td></tr>
<tr><td class="tr-caption" style="text-align: center;">My last chemo nap. Yea!</td></tr>
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<span style="font-family: Times;">This past week I met with the radiology oncologist
on Monday and again on Wednesday. The soonest that she would
consider letting me start radiation was a week after my last chemo due to the
individual intensity of each treatment. With that being said, my first
radiation will be on Wednesday, November 14 and my last radiation on Friday
December 28. I’ll have Saturdays and Sundays off in addition to
Thanksgiving Day, the day after Thanksgiving and Christmas Day. 
<o:p></o:p></span></div>
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<br /></div>
<div class="MsoNormal" style="font-family: Consolas;">
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out on the CT scan table for over 30 minutes, hands above my head holding a
bar, legs straight and rubber-banded together, top off. They marked the
areas on my right chest wall with metal markers along my scar and points where
the drains were located. They also made bulls-eye marks with sharpie
markers and in the center of those marks they gave me a freckle tattoo with one
in the middle of my chest, one above my belly button, and one on each side of
my chest near where the drains were located. They took two scans and
photographs, which will be used when mapping and planning my treatment. Tuesday,
they’ll have me laid out again taking x-rays to confirm the exact location of
the radiation. <o:p></o:p></span></div>
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<span style="font-family: Times;">Although Thursday was my last chemo treatment, I’ll
be back for blood work and an oncology visit on Wednesday. I’ve met
with the naturopath doctor and he has changed my supplements slightly; I’ve had
those okayed with the radiology oncologist. I’ve also picked up some pure
lanolin and have an aloe plant on hand to help with any fried skin from
radiation. I’ll continue with acupuncture and massage throughout
radiation and will taper it down once I’ve completed my treatment. <o:p></o:p></span></div>
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<span style="font-family: Cochin;">"Do not be anxious about anything, but in every situation, by prayer and petition, with thanksgiving, present your requests to God."<o:p></o:p></span></div>
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<span style="font-family: Times;">A friend sent me this verse this week and I found it so appropriate. Throughout diagnosis, surgery, and chemotherapy, I have really been at peace knowing that God will see me through this experience - but it has really been thanks to all of the prayers on my behalf that I have truly done so amazingly well. When I was diagnosed with breast cancer on April 10, I had no idea what to expect, but I wouldn't change a thing. Not that I would want anyone to ever have to go through any type of illness, but it certainly has been a positive change for me and my family, and maybe even my friends. And I know I'm far from finished, with radiation starting on Wednesday, detox from chemo in January, a hysterectomy soon after and years of medication. But with my last dose of chemo behind me, I feel blessed.</span></div>
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<tr><td class="tr-caption" style="text-align: center;">One of my projects this week: pickled veggies!</td></tr>
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<tr><td style="text-align: center;"><a href="http://1.bp.blogspot.com/-rDeh6UKkEHU/UJ7OQuKAvPI/AAAAAAAAAcA/oB3GRJzoZBM/s1600/Pee+Wee+Novak.jpg" imageanchor="1" style="margin-left: auto; margin-right: auto;"><img border="0" height="253" src="http://1.bp.blogspot.com/-rDeh6UKkEHU/UJ7OQuKAvPI/AAAAAAAAAcA/oB3GRJzoZBM/s320/Pee+Wee+Novak.jpg" width="320" /></a></td></tr>
<tr><td class="tr-caption" style="text-align: center;">Caleb's hockey team from last year went to Fairbanks to play - the kids taped their sticks in pink and wrote Huffman on the blade to support Caleb. Awesome kids!!</td></tr>
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<tr><td style="text-align: center;"><a href="http://1.bp.blogspot.com/-YgIII1kQdRE/UJ7OR6Nf0DI/AAAAAAAAAcI/N9xoJXRVQwI/s1600/Halloween.jpg" imageanchor="1" style="margin-left: auto; margin-right: auto;"><img border="0" height="274" src="http://1.bp.blogspot.com/-YgIII1kQdRE/UJ7OR6Nf0DI/AAAAAAAAAcI/N9xoJXRVQwI/s320/Halloween.jpg" width="320" /></a></td></tr>
<tr><td class="tr-caption" style="text-align: center;">Having some fun with friends for Halloween. Jared is wearing black and Caleb is wearing green.</td></tr>
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<!--EndFragment-->Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com4tag:blogger.com,1999:blog-120376337757056437.post-65078342580480368772012-10-23T21:33:00.000-07:002012-10-23T21:33:37.852-07:00God has certainly showed me who's in control. And it is not me! Not that I really ever thought that I was, but I am strong-willed (not stubborn) and it has taken awhile for it to sink in that I need to take some time off from work. The past two weeks have really solidified that decision with stresses hitting our family from all different angles. <br />
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My cancer treatments are going well - the oncologist said today that he has never encountered anyone doing as well as I have been doing throughout chemo. My blood work both last week and this week have held steady - thanks to three shots in the rear from James each week. My liver numbers are elevated, however not so much to change the chemo treatment and the oncologist said that he really doesn't want to do that. Besides the fatigue, the only new side effects I've noticed are a tremendous amount of spider veins on my legs, which the doctor said is probably due the Paclitaxel - it is hard on the veins, and fuzzy hair on my face. Did I mention that before? Sometimes I substitute words and forget things easily. Another little side effect that I don't attribute to age.<br />
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The treatment plan at this point is to finish the final three rounds of chemo over the next three weeks. The oncologist thought that I could jump right in and start radiation immediately following chemo. I have an appointment to meet with the radiologist on 11/9, a day after my last chemo. That should last six and a half weeks and then I'll meet with the oncologist again to discuss follow up treatment which may include Tamoxifen for five years with Lupron shots every three months for two years. We'll talk with him more about that after radiation.<br />
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Not being at school, I don't have as many great kid stories to share, but I do have one that deeply touched me. Alba and Jessica Brice's son goes to Sand Lake. Zak insisted that his mom get some pink hockey tape so that he could tape his stick for a game that night. When his mom did not come home with the right color of pink, she had to call his dad to get pink tape. Not only did he tape his stick pink, but he wrote Lisa on the blade. My hope was that he would play well and he did - even though he was playing Caleb's team. What an inspiration Zak is to all of us.<br />
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<tr><td class="tr-caption" style="text-align: center;">School Picture</td></tr>
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One final update...I emailed the Las Vegas Wranglers hockey team after the ceremonial puck drop. This was the general manager/coach's reply. It was a pleasant surprise. <br />
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<span style="font-family: Arial; font-size: x-small;"><span class="116060116-16102012">Lisa</span></span></div>
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<span style="font-family: Arial; font-size: x-small;"><span class="116060116-16102012">First off let start by saying I have you in my thoughts as you battle..I remember you dropping the puck and you cant believe how disappointed I am in Adams behavior.</span></span></div>
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<span style="font-family: Arial; font-size: x-small;"><span class="116060116-16102012">Being a Principal I can only imagine the thrill of hearing one of your students doing well and the disappointment in hearing one of your students not doing the right thing. That being said my players are a reflection of me, I cant begin to tell you how deflated I felt reading that this morning.</span></span></div>
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<a href="http://2.bp.blogspot.com/-L_B5ipxrp_E/UIdi6XsMRPI/AAAAAAAAAas/rIgNnMDn7XM/s1600/photo.jpg" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="200" src="http://2.bp.blogspot.com/-L_B5ipxrp_E/UIdi6XsMRPI/AAAAAAAAAas/rIgNnMDn7XM/s200/photo.jpg" width="150" /></a><span style="font-family: Arial; font-size: x-small;"><span class="116060116-16102012">I can ensure you Adam will be dealt with this morning as I m a huge believer in protecting the culture in our room and our community. I apologigize for Adam making the wrong choice. He is a I kid who is always on the edge and is a constant example of me trying to have patience, again its no excuse and I will deal with Adam 's behavior.</span></span></div>
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<span style="font-family: Arial; font-size: x-small;"><span class="116060116-16102012">Lisa , please don't hesitate to fire me a line if there is anything I can do, even though you are Alaska Aces fans, I would love to see the boys donning a Wrangler hat next time we are up there...well maybe for there protection not a good idea.</span></span></div>
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<span style="font-family: Arial; font-size: x-small;"><span class="116060116-16102012">My thoughts are with you and your family...</span></span></div>
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<span style="font-family: High Tower Text; font-size: x-small;">Ryan</span></div>
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I am so appreciative and thankful for all of the prayers and support. James and I could not manage without it, and these mere words can't really express how much it has meant to us. Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com2tag:blogger.com,1999:blog-120376337757056437.post-49976265968244836792012-10-11T21:15:00.001-07:002012-10-11T21:31:42.642-07:00<div class="separator" style="clear: both; text-align: center;">
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We had an exciting evening Tuesday, October 9. I was asked to do the ceremonial puck drop for the Alaska Aces Paint the Rink Pink game against the Las Vegas Wranglers. There were so many things about the night that made it remarkable. One of them was the behind the scenes work by James to get many family and friends to attend the event. Even though I'm the one with Cancer, he is truly the one carrying the majority of the stress: caring for me and worrying about me; taking care for the kids and getting them to school and hockey; and taking care of all of the routine chores around the house, not to mention the stress of his work. I have many dear friends who remind me how important family is and to put the stress of life and work on the back burner. I'm fortunate that my staff understand that and have been supportive. Next week I plan on working half days Monday - Wednesday and then take Thursday and Friday off.<br />
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The night held some surprises as well. As we were waiting, we were able to get a family picture with Scott Gomez prior to the game. James had a conversation with him regarding the lockout. He is so kind to his fans. We're hoping the NHL lockout ends soon so we can watch him play. After our picture with Scott, the boys and I headed out on the ice for the National Anthem and then the red carpet. Things on our end went off without a hitch, however #17 from the Wranglers had other things in mind. He refused to back up when the photographer gave him several motions to do so because he was blocking me and Jared, and then he said, "I dont' take orders very f____ well." The Aces player looked at him like, you've got to be kidding me dude - have some class. He did not. I wish I would have had the nerve to throw him out of the face off circle! <br />
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<span class="Apple-style-span" style="color: #444444; font-family: arial, sans-serif; font-size: 11px;"><a href="http://youtu.be/41XMJVYlsqA">http://youtu.be/41XMJVYlsqA</a></span></div>
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After the ceremonial puck drop, we headed up to watch the game and received a warm welcome and surprise from Caleb's hockey team. When the doors to the elevator opened, there they were - the Mighty Moose Squirt B team and coaches each holding a rose which was then given to me. I was overwhelmed. They are an amazing group of kids, parents, and coaches and we are blessed that Caleb is skating with them this year. Jared's team is another amazing group of kids and families. They are skating with special hockey jerseys for the month of October. Each jersey has the name of a family member or friend on the back - Jared is wearing Lisa Huffman. Like the pink hair?</div>
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With all of the support, it makes it easy to forget how tired I am and all of the other horrible aspects of cancer. A few I forgot to mention last week, I have a continual bloody nose that fortunately doesn't run, my mind is fuzzy, and with my hair coming back - I've got peach fuzz hair for side burns! Now doesn't that just make you laugh. I did Google it and it is one of the side effects of chemo. Some women suggest shaving, others using cream hair removal, others say it will go away with time and some use electrolysis. I'm going to give it some time. I'll keep you posted. </div>
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One final video clip...Port access: <span class="Apple-style-span" style="color: #444444; font-family: arial, sans-serif; font-size: 11px;"><a href="http://youtu.be/-NAdJWh1myU">http://youtu.be/-NAdJWh1myU</a></span></div>
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And a final note. I received this note from a student this week. With all of the challenges with my job and life, there are also many blessings. Kids, family, and friends are definitely at the top! I thank God every day for each and every one of you. Much love, Lisa</div>
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Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com1tag:blogger.com,1999:blog-120376337757056437.post-45015836981512430642012-10-06T10:56:00.000-07:002012-10-11T19:52:22.208-07:00<div class="separator" style="clear: both; text-align: left;">
This past week was a bit challenging, but I was thankful that James was off and able to take care of me and everything else around the house. I experienced some intense hip pain last weekend and was hoping it wasn't due to the Nuprogen shots. It lasted for an evening and was gone by mid morning Monday. I haven't experienced any further joint pains and the doctor said that it usually occurs in the smaller joints so I am optimistic that I just tweaked something and all is well. I still have some annoying nasal congestion, but at least it is out of my lungs. </div>
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With the continual rain and wind, we had a bit of excitement when our trampoline took flight - James tried to stop it but ended up having to run. I spotted him through the kitchen window running across the lawn. The boys and I quickly joined him and we ended up disassembling the final pieces without getting too drenched. </div>
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Chemo went well on Thursday, however I was much more tired than usual. I went to bed at 8:00 Wednesday night, slept after chemo on Thursday, and went to bed early Thursday night as well. I've been trying to drink lots of fluids, but can't seem to drink enough. Tell tale signs - dry skin and lips, although it is that time of year. My counts were stable this week with my white count at 4.2, red at 12.4, and neutrophils at 2.8. The number which measures my liver function was elevated, so no alcohol. I don't drink much, but will miss a glass of red wine with dinner. With the elevated number, the doctor will watch my blood work closely to see if my chemo medications need to be altered. </div>
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Thursday evening my heart was beating irregularly and it continued into Friday. James contacted our nurse which resulted in an EKG Friday afternoon after acupuncture. It was a short snapshot which showed that everything was fine with my heart. I was told that it was probably due to stress, to slow down and take some time off work. I'm going to work Monday and then take the rest of this coming week off. At least I won't go in to school - I'll still work a few hours from home each day. </div>
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I love kids - while in the lunch room at school this past week, a fourth grader named James said, "Mrs. Huffman, your hair is growing!" I asked him what color he thought it was. He replied that he thought it was the same color it was before. The boy next to him interjected that no, he thought it was gray. James looked a bit saddened by the boy's comment. The next morning I came into my office and found the following note and three 4-leaf clovers. I don't know that they are helping my hair grow, but they sure made me smile.</div>
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com2tag:blogger.com,1999:blog-120376337757056437.post-53494212916528498202012-09-29T14:10:00.002-07:002012-09-30T12:46:03.474-07:00<div class="separator" style="clear: both; text-align: center;">
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This morning we woke to a beautiful blanket of snow covering Anchorage. We weren't prepared. Snowblower is in the shed, lawnmower is in the garage, and lots of other summer/winter items need to be swapped. Our strategy, wait to see if it melts and then get a move on it. Jared had a team 5k run this morning and Caleb had hockey practice. Hockey doesn't stop for a little snow - six inches at our house. </div>
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<a href="http://3.bp.blogspot.com/-9ohsyf-On5g/UGcyOjAKs2I/AAAAAAAAAXQ/TBHFghLA1zc/s1600/Cupping.jpg" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="200" src="http://3.bp.blogspot.com/-9ohsyf-On5g/UGcyOjAKs2I/AAAAAAAAAXQ/TBHFghLA1zc/s200/Cupping.jpg" width="149" /></a>I'm so thankful to be at the halfway mark of this 12 weeks of chemo. This past week was marked by a cold that moved into my chest, so I am taking antibiotics for 5 days. My acupuncturist also did cupping to help with my chest and cough. It seemed to help, but left some interesting marks on my back. (No, it isn't my wedding dress - it is a cami I wore beneath my suit jacket.) I'm still trying to eat foods to improve my qi and I took last week off from working out just to sleep. It felt good, but now I think I'll try to thrown in a few walks or workouts this week.</div>
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<a href="http://3.bp.blogspot.com/-w-TvLdv5lPk/UGihJQiWgwI/AAAAAAAAAYE/toGqUd7OGKQ/s1600/photo.JPG" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="200" src="http://3.bp.blogspot.com/-w-TvLdv5lPk/UGihJQiWgwI/AAAAAAAAAYE/toGqUd7OGKQ/s200/photo.JPG" width="149" /></a></div>
<a href="http://3.bp.blogspot.com/-yyguVTCL3UE/UGcyKNAi_ZI/AAAAAAAAAXI/hzpMGzYIRdo/s1600/photo%5B1%5D.JPG" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="200" src="http://3.bp.blogspot.com/-yyguVTCL3UE/UGcyKNAi_ZI/AAAAAAAAAXI/hzpMGzYIRdo/s200/photo%5B1%5D.JPG" width="149" /></a>My counts were all similar to last week's counts and seem to have stabilized a little low, but high enough to have my treatments. James will continue giving me shots for three days after each chemo treatment to keep my counts up. I was "dry as a bone" according to my oncology nurse and was given the bonus bag of fluids via IV. It could be the result of hot flashes, loss of heat through my bald head, or just not drinking enough fluids. </div>
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<a href="http://4.bp.blogspot.com/-vqJcFvF9HCY/UGcyGGCzoSI/AAAAAAAAAXA/PoDXAv4td9o/s1600/photo.JPG" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="149" src="http://4.bp.blogspot.com/-vqJcFvF9HCY/UGcyGGCzoSI/AAAAAAAAAXA/PoDXAv4td9o/s200/photo.JPG" width="200" /></a>The day of chemo still pretty much wipes we out. I'm thankful for wonderful friends who have brought by food on Thursday so we don't have to cook. After sleeping all day, it has been a treat to wake up to a wonderful meal. I haven't felt any nausea to speak of, however occasionally the smell of someone's food can turn my stomach. The day following chemo has been difficult emotionally. I'm not sure if it is the Paclitaxel or menopause, but it is typically a very sad day for me. Each day following Friday improves. </div>
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Although I probably work too much, I do love my job. I was visiting classrooms this past week and stopped in a kindergarten class. I was kneeling down talking to a little girl on my right about a picture she was drawing when the little boy on my left said, "Mrs. Huffman! Your hair is growing!" Then he gave me a quick rub on the top of my head. The little girl behind him asked if she could rub my head too - of course. </div>
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Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com1tag:blogger.com,1999:blog-120376337757056437.post-9738329346186225302012-09-15T11:07:00.001-07:002012-09-15T11:07:26.434-07:00You never really realize how much you love something until it is gone. We had to put our wonderful St. Bernard down yesterday due to severe hip dysplasia. Tucker couldn't get up and walk, and when he tried, his hips gave out from under him. He was in a lot of pain. James and I took him to the vet while the boys were at school, and although we all knew it was going to happen, it has been a difficult week. Not only is it difficult because I miss Tucker, but it is so difficult to listen to the heartache when your child talks about how much they love and miss their dog, how they miss vacuuming up Tucker hair, scooping Tucker poop, and how Tucker was supposed to be there until they moved out of the house. He was only 4 1/2 years old. Those of you who know James and I well, know what a change we had to make to welcome that furry friend into our home - dog hair and slobber is not something that either of us tolerate well. I will miss walking downstairs each morning to a warm welcome from Tucker; our morning walks; the head shake with fur flying everywhere; the slobbery dog dish; the muddy paws from his water hole; and feeding him carrots, apples, and peanut butter treats. <br />
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I'd like to think that I'm doing well, but the stress this past week took a toll, making it more difficult to keep the tears from flowing. My counts dropped before Thursday's chemo treatment so I'll need to continue the Neuprogen shots for three days following each chemo treatment. The good new is that the doctor thinks I'm doing extremely well and inquired about acupuncture so that he could refer others in treatment. He also said that I wouldn't need a blood draw or doctor visit for three weeks. And hair? I have hair growing on top of my head! I'm not sure if I should let it grow or keep it trimmed. Wondering if it will stay with this type of chemo treatment and if it will stay when I start radiation. I have an acupuncture appointment on Monday and will see the naturopath on Friday, with chemo on Thursday as usual. <br />
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Knowing that stress can be a leading health problem, I'm trying to keep the stress from work from invading my recovery. I'm thankful that I'll have a substitute once a week to help my assistant principal. And I'm thankful for my husband, family and friends that keep me grounded, remind me to take care of myself, and show me they care in so many thoughtful ways. Thank you...<br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com6tag:blogger.com,1999:blog-120376337757056437.post-50553838359282863452012-09-07T19:48:00.000-07:002012-09-07T19:48:03.006-07:00Yesterday was my third round of Paclitaxel. Three down and nine to go. <br />
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The staff at ANMC is fabulous. Since the beginning of this journey, I've been so impressed with the staff, nurses, and doctors. The dread that I get every week having to go to the infusion room quickly changes when I see the staff. They know the right things to say and do. It must be a challenging job, but they all do it with such ease and care. <br />
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My acupuncturist is amazing as well, and she too is part of the ANMC system. She knows exactly what is ailing me and is able to place needles so strategically. She always asks how I'm doing, and like a kid asked what their day at school was like, I answer, "Fine." She probes with specific questions about my mood, or stress, or pain, and she's always right about the ailment I hadn't thought to mention. Amazing!<br />
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This weekend I'm going to try to eat foods to help my Qi. I play Qi in words with friends all the time, but didn't even really understand what it was. Qi is the energy in our bodies, and mine is lacking. <br />
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The other thing lacking in our house is healthy bodies. Caleb had been sick with a chest cold for several weeks, then Jared got the germ, and now James is sick. We couldn't decide who should wear a mask last night, so we both wore it to bed. I'm not sure how long it actually stayed on after I fell asleep, and if I fell asleep before James, I'm not sure if he kept his on. :)<br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com3tag:blogger.com,1999:blog-120376337757056437.post-40952248160360017442012-08-29T19:38:00.001-07:002012-08-29T21:40:53.154-07:00July 26! I can't believe it has been a month since I last posted. Believe me, I've thought about it. My last round of AC was on August 1. I had the typical week of not feeling well and had I posted then, you would have heard more about the negatives of cancer and chemo. I try not to dwell on those things, or even ponder them, as they will pass. I might not even be honest about all of the affects it has on me. What good would it do?<br />
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It has been a little harder more recently to keep up the pace. I went back to work on July 26 and have hit the ground running ever since. Working ten to twelve hour days, seven days a week was difficult when I was healthy - now it is pretty much impossible. Beyond all of the side effects, I think the inability to maintain the family, house, and work schedule is the hardest for me. That's what brings tears to my eyes, not my hair falling out.<br />
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But, I am over half way done with chemo. I had my first round of Paclitaxel last Thursday, August 23. I'm scheduled for 12 treatments, one every Thursday until November 8. My blood count has been low, but high enough not to delay treatments. Today's white count was 1.8 and red count was 10.2. A little lower than last week's 2.9 and 11.6. My absolute neutrophils were 1.9 last week and 1.8 this week. After this week's treatments, I'll probably need to resume neuprogen shots to boost my count since they continue to drop. Other than a headache the day after treatment and increasing fatigue, I haven't experienced any of the other side effects. Things to watch for with this drug: allergic reaction, lower blood counts, neuropathy, joint and muscle pain, heart problems, vomitting, diarrhea and constipation. Hmmm...<br />
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Speaking of allergic reaction, when they did the first Paclitaxel infusion last week, a nurse watched me closely, along with James, to make sure I didn't have a reaction. They had a kit ready to go - just in case. I did leave staggering, as always, but thankfully had no reaction. After getting home, I slept for four hours. That's the plan tomorrow - infusion at 8:00am until 11:30 and then home to sleep.<br />
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I'll be working part time from here on out taking sick leave every Thursday and Friday until the end of my treatments. Although I still keep up with work at home, the doctor has advised that I need to reduce my work load.<br />
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Speaking of work, I love my job. The honesty of kids and the joy they bring to a challenging job. I've heard things that make me smile each day. "Mrs. Huffman, why did you shave your head?" "Mrs. Huffman, are you supporting cancer?" "Mrs. Huffman, are you okay?" "I don't remember what you looked like last year." (Then I showed the student my id badge from last year.) "You're the first bald principal I've ever met!" "You look nice without hair." "We made this for you." (As a group of fourth grade girls handed me a lei made of clover flowers.)<br />
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Next time I won't wait so long to post and you won't have to read so much! Here are a few pictures taken over the past month. Thank you for your prayers.<br />
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<tr><td class="tr-caption" style="text-align: center;">A beautiful bike ride up powerline pass from the parking lot at Flat Top.</td></tr>
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<tr><td class="tr-caption" style="text-align: center;">The office staff asked me to Take it Off.</td></tr>
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<tr><td class="tr-caption" style="text-align: center;">Lovely head wrap.</td></tr>
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com4tag:blogger.com,1999:blog-120376337757056437.post-57100960197866663522012-07-26T21:09:00.001-07:002012-07-26T21:21:15.322-07:00One of the lessons God's been teaching me through this process is to keep my priorities straight: to cherish my family and friends, to enjoy each moment and live in the moment, and to take care of myself. It is easy for me to get caught up in the business of work and day to day routines. As I head back to work today, I know that I need to avoid falling into that trap.<br />
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Fatigue has been the predominant side effect I've noticed most. There are some funny things like "prickly" hair stubble on my head and inconsistent bowel movements, but fatigue is the hardest for me to deal with. I don't rest well. I stopped by the Oncology department to ask if they thought I should do a blood check - they told me it wasn't necessary, fatigue is a part of the game. I am still taking my supplements and going to acupuncture.<br />
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I had an appointment with the naturopathic doctor today who thinks I am doing well - no joint pain, no mouth sores, no neuropathy - lots of things to celebrate (and I'm not being sarcastic). After reviewing the supplement list, he asked me if I minded adding one more pill and I paused before answering. He picked up on my lack of enthusiasm, but explained the benefits of taking alpha lipoic acid and I was on board. I left with a updated list of supplements as my chemo regiment will be changing after the fourth treatment on Wednesday. <br />
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I have thoroughly enjoyed my summer with family and friends - what a blessing each and every one of you are to me. We just finished another trip to Homer with James' brother and even though there were some rough seas, we were finally able to get out and fish, enjoy the scenery and have fun. <br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com6tag:blogger.com,1999:blog-120376337757056437.post-53685282434346890192012-07-13T11:59:00.002-07:002012-07-13T11:59:49.029-07:00<div class="separator" style="clear: both; text-align: center;">
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It has been a fabulous week with family visiting from Kansas City, MO. We were able to enjoy the outdoors including hiking Flat Top; mountain biking (for the boys) and Saturday Market for the rest of us; and a trip to Homer and Seldovia to fish for halibut. My energy level has stayed pretty good with lots of help from family and friends.<br />
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<tr><td class="tr-caption" style="text-align: center;">45 Pounder</td></tr>
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Fishing out of Seldovia was a lot of fun with calm seas and plenty of fish. Our largest fish was about 45 pounds but most were around 20 pounds. We kept the fatties and threw the rest back. Everybody caught fish - we even caught a few rays and cod. The halibut were fun to watch as they followed up their hooked buddies in schools. I was even able to lean over the boat and gaff an unhooked halibut.<br />
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My blood work Wednesday was good showing my red count had climbed to 12.2 and my white blood cells were at 6.4; everything else looked good. With that being said, I had chemo Thursday morning and followed the usual routine: 7 anti nausea pills, hook up to the medi port, steroid iv, anti nausea iv, Adriamycin iv, Cytoxan iv, and a final flush. Everything went well and I had some great company and a fabulous nurse who kept me smiling and laughing for 3 hours. I was pretty tired, so came home and slept for over 3 hours, but was able to enjoy some deep fried halibut for dinner. <br />
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Looking forward to acupuncture today so she can address the nausea that woke me up last night. I'm still taking all of my supplements which seem to be helping a great deal. I did start my menstrual cycle Tuesday, however the flow was only heavy one day and night so that's an improvement. Wednesday night I woke up covered in sweat - so maybe menopause started and that was my first hot flash. But probably not.<br />
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<a href="http://3.bp.blogspot.com/-hAA7KA6npIA/T_-Fw1mz29I/AAAAAAAAASY/qDWrkiPgKcY/s1600/Jared+Flat+Top.jpg" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><br /></a></div>Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com5tag:blogger.com,1999:blog-120376337757056437.post-11240418567880439552012-07-05T21:47:00.003-07:002012-07-05T21:54:45.546-07:007/5<br />
I haven't blogged in awhile and have been feeling kind of blah for a couple of days. I can't quite put my finger on what it is. Could it be all of the chemo drugs running through my body? I forget about that. My request for acupuncture tomorrow - stick the needles in where ever they will make me feel happy and full of energy!<br />
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<a href="http://4.bp.blogspot.com/-sxbH_dwWQe8/T_Zl4EXHXJI/AAAAAAAAARs/mLE1XFinPXI/s1600/Buns.JPG" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="200" src="http://4.bp.blogspot.com/-sxbH_dwWQe8/T_Zl4EXHXJI/AAAAAAAAARs/mLE1XFinPXI/s200/Buns.JPG" width="149" /></a><a href="http://4.bp.blogspot.com/-MENPgIcmE_Q/T_ZgBnTrPEI/AAAAAAAAARU/5i58_W81c8s/s1600/Cookies.JPG" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="149" src="http://4.bp.blogspot.com/-MENPgIcmE_Q/T_ZgBnTrPEI/AAAAAAAAARU/5i58_W81c8s/s200/Cookies.JPG" width="200" /></a>My therapy has been cooking (and Pinterest). The boys love it. Chocolate chip cookie batch number 2. Vitamin waters - my favorite is pineapple, lemon grass, ginger, and mint. Spicy smoked salmon and barbequed ribs were on the menu this week. And home made hamburger buns for moose burgers tomorrow. <br />
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<a href="http://2.bp.blogspot.com/-cu_AT5Euxco/T_Zf8NrBJpI/AAAAAAAAARM/UsmmHGT9Qus/s1600/Bear.JPG" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="320" src="http://2.bp.blogspot.com/-cu_AT5Euxco/T_Zf8NrBJpI/AAAAAAAAARM/UsmmHGT9Qus/s320/Bear.JPG" width="239" /></a><br />
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I took a few days off from working out and this morning while running, I ran into a black bear as a rounded the corner. He was "looking into" mailboxes, basically getting on his hind legs and looking at the closed box. He was about 100 yards down the road and I didn't get a very good picture of him, but I did turn around and backtracked the way I came. I was still able to get in 3 1/2 miles and didn't run into him again. James' reminder - run with the bear spray - which I usually do. This was the first time I didn't have it...really! <br />
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<a href="http://2.bp.blogspot.com/-f13CxQ3qCl8/T_ZgCcUEDwI/AAAAAAAAARc/qto-XYPzKDw/s1600/Hat.JPG" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="200" src="http://2.bp.blogspot.com/-f13CxQ3qCl8/T_ZgCcUEDwI/AAAAAAAAARc/qto-XYPzKDw/s200/Hat.JPG" width="150" /></a></div>
Thank you for all of the notes, emails, phone calls and prayers (and hats). They really lift my spirits. James, Jared and Caleb are very understanding and patient, but often aren't sure what I need. I often don't know either. So thank you!<br />
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Much love,<br />
LisaLisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com3tag:blogger.com,1999:blog-120376337757056437.post-24927138165323005352012-06-29T17:23:00.000-07:002012-06-29T17:23:14.580-07:006/29<br />
Had acupuncture this morning and a blood draw. Both went well. My white blood cell count was 4.3 and my panel looked like a healthy person's blood work, except for a low hemoglobin count. A normal count should be between 12.3 - 15.3. Before starting chemo, my count was 13.3, after the first round it was 11.3, and today it was 10.4. Nothing alarming, but I picked up an iron supplement to help give it a boost.<strong> </strong>With a low red blood cell count I need to watch for any of the following symptoms: fatigue, weak, short of breath, increase in my heart rate, dizzy or lightheaded. I'll try to monitor my activity level - I've got several good books to read, so this is a good excuse.<br />
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I've been enjoying feeling good this week and have been doing a few things on my "to do" list. One goal this week was to make a new recipe each day. Yesterday I made pretzels - they were delicious. I also made maple glazed salmon with pineapple salsa. Yum! <br />
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<a href="http://4.bp.blogspot.com/-0hV6msfCFCc/T-4sph0UiXI/AAAAAAAAAQ0/G8-69FUgxX0/s1600/Vitamin+water.JPG" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="149" src="http://4.bp.blogspot.com/-0hV6msfCFCc/T-4sph0UiXI/AAAAAAAAAQ0/G8-69FUgxX0/s200/Vitamin+water.JPG" width="200" /></a></div>
Last night and today I made some vitamin waters. They are delicious, although I might be the only person to drink them. The strawberry, watermelon, rosemary water is "stressless"; the pineapple, ginger, mint water is "digestion"; and the grapefruit, lemon, lime, and orange water is "power C". Great to mix half and half with mineral water to make the pitcher last longer. After the water is gone, I think I'll use the remains to make a smoothie.<br />
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<a href="http://3.bp.blogspot.com/-UcyGtdi9IoY/T-4we8f5qII/AAAAAAAAARA/0Tx5XPuiDGE/s1600/Menu.JPG" imageanchor="1" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="200" src="http://3.bp.blogspot.com/-UcyGtdi9IoY/T-4we8f5qII/AAAAAAAAARA/0Tx5XPuiDGE/s200/Menu.JPG" width="149" /></a>I've got chicken caesar salad with homemade croutons and grilled avocado with melted cheese and hot sauce on the menu for tonight. I love cooking! That would be my second career if I could make it happen. I put together this menu board to help plan meals for the week. It was super easy to make and the boys will love helping plan meals. We used to have a night a month where they chose the meal, cooked it for James and I, AND cleaned up. We haven't done it for awhile and they are quite anxious to start it up. Jared loves to choose involved recipes; Caleb loves Hamburger Helper.<br />
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My next plan of action - I'm going to scan all of Jared and Caleb's tons of school work and saved stuff by year. Then I'm going to make an Apple iPhoto book for each year and pitch all of the paper work. Maybe save a few cute projects to frame and add to the collection in my office.<br />
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com4tag:blogger.com,1999:blog-120376337757056437.post-9492221409222514882012-06-26T21:11:00.002-07:002012-06-28T09:37:35.390-07:006/26<br />
This round of chemo really knocked me out on Thursday and
Friday. I felt miserable both days and had a headache all day Friday. I
was able to relax around the house with ever so helpful boys, and
friends who took the kiddos overnight. By Saturday I started feeling
myself again, and was feeling good by Monday. I had acupuncture Monday
and the only request I had for her was to help
with my digestive system. The acupuncture session on Friday did a
fabulous job of alleviating my nausea - I didn't even need to take any
of the anti-nausea medication after Friday. My next appointment - a
blood draw on Friday to check my white blood cells. <br />
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I have two wonderful boys who are ever so helpful. Jared
has taken over as lawn boy this summer and is doing a fabulous job. I
trim it out and Jared does the rest of the mowing. Caleb chips in
whenever he is asked too. Scooping Tucker turds is probably their least
favorite job.<br />
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<a href="http://3.bp.blogspot.com/-_au0aZdpju0/T-qCJxtYuiI/AAAAAAAAAQo/fVPz2enpJYY/s1600/Lawnmowing.jpg" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="150" src="http://3.bp.blogspot.com/-_au0aZdpju0/T-qCJxtYuiI/AAAAAAAAAQo/fVPz2enpJYY/s200/Lawnmowing.jpg" width="200" /></a><br />
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<a href="http://4.bp.blogspot.com/-yXQZV2uez9k/T-qCF6_OOMI/AAAAAAAAAQg/Mj4PFqzheRk/s1600/Helpers.jpg" style="clear: right; float: right; margin-bottom: 1em; margin-left: 1em;"><img border="0" height="240" src="http://4.bp.blogspot.com/-yXQZV2uez9k/T-qCF6_OOMI/AAAAAAAAAQg/Mj4PFqzheRk/s320/Helpers.jpg" width="320" /></a><br />
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After
a few days off from exercising, we all went for a mountain bike ride
through Prospect Heights Trail Head off of Upper O'Malley on Monday. It
was some tough terrain with a little mud, roots, rocks, and running
water. We all made it - something I couldn't have said 18 years ago
when James took me for my first mountain bike ride. Sunday was our 17th
Anniversary! I'm a blessed girl to be
married to such a wonderful, supportive man. It
sure makes going through this a lot easier. We had a great anniversary -
church, family time, and friends.<br />
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<table align="center" cellpadding="0" cellspacing="0" class="tr-caption-container" style="margin-left: auto; margin-right: auto; text-align: center;"><tbody>
<tr><td style="text-align: center;"><a href="http://2.bp.blogspot.com/-outFle8tPGc/T-qB6IZaHhI/AAAAAAAAAQU/0aPcnj3BBXE/s1600/Biking.jpg" style="margin-left: auto; margin-right: auto;"><img border="0" height="240" src="http://2.bp.blogspot.com/-outFle8tPGc/T-qB6IZaHhI/AAAAAAAAAQU/0aPcnj3BBXE/s320/Biking.jpg" width="320" /></a></td></tr>
<tr><td class="tr-caption" style="text-align: center;">Smiling, because it is all downhill from here!</td></tr>
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<br />Lisa Huffmanhttp://www.blogger.com/profile/13148319327384099179noreply@blogger.com6