More Adventures in ABVD

Another Scan

2010-07-22T15:06:00.000-07:00

I went in for my scheduled CT scan on July 19th. I'll get the results back on Monday. I completely forgot about it until I remembered I had to update my blog. I suppose that shows I really am moving on. Now when I think about my experience, I am more likely to feel like someone who has overcome a challenge than someone who was or is vulnerable. At the same time, I try to prepare myself for the possibility of getting bad news when I get scanned. Surprisingly, I'm not nervous the cancer will return. I'm afraid they'll find something else!

Before I started chemo, my heart was checked. One of the chemo drugs can cause heart damage and they like to make sure everything is OK before they get started. At that time, I learned I had a PFO (Patent Foramen Ovale). The short explanation is that all fetuses have a hole in their heart to speed cirulation. In 75% of people it closes up and in 25% of people it doesn't. It's usually not a problem and most people go their whole lives without knowing about it. However, there is an increased risk of stroke for people who have it.

Before being scanned, I am required to fill out a questionnaire that asked many questions including "Do you have a PFO?" (I suggested they add the words patent foramen ovale to the form and they did.) Since there is a chance that a patient could have a stroke when they inject contrast during a CT scan, they must first get permission from your doctor. And that can take time. It was suggested that I ask my doctor for a SIGNED business card saying that it is OK for me to receive contrast even with my PFO. I'll need to show it every time.

If you have a PFO, they have to make sure there are no bubbles in the liquid. Two people must check the contrast before it is injected into you. Personlly, since 25% of people have a hole in their heart and most don't even know they have it, I think it should be standard practice to have two people check it every time for every patient.

Two Years Later

2010-06-03T14:56:00.000-07:00

May 8th was the second anniversary of finishing chemotherapy. My scans and blood work continue to come back fine and my immune system is strong again. I'm trying to live in the present and keep things in perspective. Like they say, don't sweat the small stuff. With a cancer diagnosis, you learn that almost everything is the small stuff. It's time to enjoy the late spring and summer!

My One and a Half Year Scan

2010-01-29T15:01:00.000-08:00

I got the results back from my latest CT scan and the Dr. said they were "unremarkable". My dictionary says that unremarkable means ordinary and yet I think the results are extraordinary!

Follow-up Visit

2009-09-26T08:22:00.000-07:00

I'm now seeing my doctor every 3 months for follow-up visits where my blood is checked . Each 6 months, I get another CT scan. All is well!

No Mo Lympho

2009-06-09T13:39:00.000-07:00

I just had my one year scan and I am lymphoma free! My doctor advises celebrating and I always follow doctor's orders.

Another Clean Scan

2009-04-28T20:05:00.000-07:00

I had a another scan and got the results back on March 17th. Everything looks great and my ENT says that my adenoid tissue looks better than ever. My next scan is an important one because it will be close to one year. If the cancer remains in remission for a year, not only are the chances of a recurrence reduced but the virulence of the disease would be likely less.

6 Month Scan and Checkup

2008-12-12T06:19:00.000-08:00

I had another CT scan on December 1st and I got the results last Monday. I also went to see my ENT doctor on the same day. The inspection and the scan both showed I was clean as a whistle. The doctor said it was a good reason to celebrate. With each successive clean scan the chances of recurrence are reduced.

I'll continue to have checkups every three months with my oncologist and scans every 6 months for the next 5 years. I'll also continue to see my ENT on a regular basis.

Merry Christmas everybody and a Happy New Year!

3 Month Follow-up Checkup

2008-09-05T18:01:00.000-07:00

I visited my ENT a few weeks ago and everything looked great. I went to see my oncologist this morning and my bloodwork looks good.

I'm scheduled to have a CT scan 3 months from now.

I've been feeling great and my hair has grown back. The color started out blonde but has returned to my original red (at least in my beard). The hair on my head may be a little darker and it is growing on the part of my head that hasn't seen hair in twenty years. Go figure.

I've started going back to the gym and I joined Weight Watchers. Last weekend I went kayaking for the first time.

There is life after cancer!

237 days, 37 doctor appointments, 15 blood draws, 12 infusions, 6 lung function tests, 3 PET CT scans, 1 chest X-ray, 1 EKG and 1 biopsy later...

2008-07-06T08:00:00.000-07:00

I am officially in remission!

My PET CT scan came back with very different results than the previous one. It showed no uptake in any of the places I had shown uptake before. Any swollen lymph nodes had reduced back to their original size.

This news is a big relief. It will be nice to start thinking about plans for the summer.

Drumroll Please...

2008-06-20T13:04:00.000-07:00

I had my adenoid tissue biopisied a week ago on Thursday and I got the results back today. The tissue was benign. Yay!!! It's a big relief and suggests that I am in remission. I'll still get the rest of my body scanned in July.

The biopsy itself went very smoothly. The recovery was fast and I didn't have any bleeding. The nurses were amazed I was up and talking so soon after surgery. The people at Mass Eye and Ear were great and as hard as this is to believe, they even made a good plate of spaghetti and meatballs.

Huh???

2008-06-07T14:20:00.000-07:00

I got the results from my PET CT scan and they were "shocking" in the words of one of my oncologists. The scan showed uptake in 4 different parts of my body: armpit, esophagous, and two sides of my groin. Both of my oncologists and my ENT doctor believe the scan shows a false positive for the following reasons:

1. Nothing showed up in the original site of the cancer, my adenoids. If it were going to show up elsewhere it should also show up here. Had I undergone treatment with radiation it would be possible for it to be gone here but show up elsewhere. I never had raditation treatments.

2. Lymphoma spreads to nearby nodes and progresses toward the spleen. This scan shows uptake in disparate parts of my body.

3. I feel fine and show no symptoms of lymphoma.

I'll need to redo the test on July 1st and I will undergo a biopsy of the tissue surrounding where my adenoids were next Thursday. If the adenoid tissue comes up clean, the rest of me should be OK too. I'm doing my best to stay positive and act like this test never happened.

PET CT Tomorrow

2008-05-29T18:37:00.000-07:00

I'll be going in for a PET CT scan tomorrow morning. During the week the results will be analyzed and I'll find out if the treatments appear to be successful or if the cancer has withstood the chemotherapy and grown or spread. I'm hopeful that everything will be fine. I'll keep you updated!

The 12th Treatment

2008-05-22T15:33:00.000-07:00

My 12th (and I hope final) treatment was on May 9th. It might have been the easiest one yet. Neither the blood draw, nor the infusion was painful and the time passed relatively quickly. Sometimes the Dacarbazine hurts it if is injected too quickly. The nurse seemed to adjust the pace just right and used an ice pack to cool down my arm and reduce discomfort.

Side effects have been relatively mild over the last two weeks. I had the mettalic taste in my mouth and some fatigue. I also had a night of constipation which was one night more than I wanted.

I saw my ENT today and he said that the remaining tissue where my adenoids used to be looks normal. I will have a biopsy in early June along with a PET CT scan next week. These tests will be used to determine if the treatment was successful. Then I'll go for doctor's appointments every 3 months and scans every 6 months for a number of years.

It's been a long six months but the time passed and now I'm done with the standard regimen. Once this round of tests has been completed, I'll be able to focus on moving forward and enjoying life day by day.

The 11th Treatment

2008-05-01T12:04:00.000-07:00

I had to go for a lung function test on Thursday. Every time I go, my lung function decreases but it is not showing the precipitous drop associated with thickening of the lungs that can be a side effect of the bleomycin. The doctors say that over time my lungs should start repairing themselves.

This infusion was a tough one. I was scheduled to get my blood drawn at 8:00, have my doctor's appointments at 9:00 and my infusion at 10:00. After getting my blood drawn, my Dad and I went to get coffee at the coffee shop. When we returned to the office at 9:00 the nurse asked where we had been. The doctor had been trying to reach us since 8:30. She asked why we didn't bring a beeper with us. I asked why I was learning that beepers were available during my 11th treatment and not earlier. Of course, the doctor who wanted to see me at 8:30 was not available at 9:00 so we waited in a room for 30 minutes. The irony is that the doctors have never been on time for any of the infusions.

When it was time to get the infusion I had to wait because the pharmacy had not put the order together. It took 3 trys to find a vein and they weren't sure that the 3rd try was a success either. It turned out to be OK so they continued with the infusion. My arm has been black and blue for the last 7 days and it doesn't look like it's going away anytime soon.

I've felt more fatigue than usual after this infusion. I spend all of my time either working, eating or sleeping. I'm spending so much time in bed that I'm starting to get aches and pains in my muscles. One night I felt pain every time I inhaled. I'm always concerned that it is a symptom of lung damage but my doctors say that it is muscle related. I'm also getting some of the strange arm aches in the arm I got the infusion in. The spots where they repeatedly stuck me with the needle are especially sensitive.

I've been sneezing like crazy. I suspect it is allergy related. Everything is blooming outside all at once. I've also been coughing more than usual. I'm going to keep an eye on the cough. My absolute neutrophyl count is the lowest it has ever been. It's down to 80. A doctor friend told me that this means I basically have no immune system right now. It's really important that I avoid getting an infection right now.

I've been more moody lately than I've been during my treatment so far. I think the ending of treatments brings on a lot of emotions. Some people cry for days after their last treatment. It feels like I'll be in limbo after my final treatment. Am I cured? Am I in remission? Am I living with cancer? What does it all mean? My doctors tell me that my prognosis is excellent and that I'll probably live a long life and this will never come back. Then again who knows what the future will bring. I suppose this is the uncertainty that life holds for everyone. Most of the time we assume that everything will be fine. The truth of life is that nobody knows if they will make it to their next meal. I guess this just proves that we should make the most of every moment and live in the present.

My final treatment is scheduled for 8 days from today.

The 10th Treatment

2008-05-01T11:59:00.000-07:00

Number 10 may be the best treatment yet. The schedule was to have one appointment after another. Getting my blood drawn wasn't too painful and the injection for the infusion wasn't too bad either. I find that one or the other is usually painful but this time neither one was bad.

The only side effect I had after the infusion was the runny nose I get from tears building up and running down my nose. I'm sure my students think I'm sick but I've managed to avoid illness this entire time.

The 8th and 9th Treatments

2008-03-31T13:19:00.000-07:00

I've been busy lately and I got behind on my posts. Let's catch up.

My 8th treatment on March 14th was probably the best one yet. It went by relatively quickly and easily. I suspect the Ativan helped. Remarkably, I didn't experience any side effects afterward except for the runny nose I've had all along. No fatigue. No arm ache. I learned that my nose runs because one of the side effects of the chemotherapy is to produce more tears. The tears then run down my nose.

My 9th treatment on March 28th was long but not too bad. I had to get there at 9:00 for the blood work. My favorite phlebotomist was there but the jab I got wasn't too comfortable this time. The nurse oncologist did a better job of finding a vein without a lot of movement. Then appointments with my oncologists at 10:00. A pulmonary function test at 11:30 showed that my lungs haven't changed from the treatments (that's a good thing). My infusion was scheduled for 2:00 but having my lung tests after my appointments with my doctor seemed to slow up the ordering of the medicine. I had a guest show up during my treatment. It made the time fly by. Thanks Kevin! I got out at 5:00.

I slept after my infusion on Friday as I usually do. I was up early on Saturday and felt great as has also become the pattern. Sunday, I slept all day and night with a few breaks and then most of Monday. If I can get realigned with the clock tonight I think I'll be fine at work tomorrow.

The 7th Treatment

2008-03-13T19:05:00.000-07:00

I received my 7th treatment on February 29th. The day went by smoothly and my absolute neutrophyls went up. In the two weeks following the treatment, I had some fatigue for a few days followed by that creepy arm ache feeling about a week later. It lasted for most of a week. Tylenol helps but I'm not great about staying ahead of the curve. I usually wait until it hurts again before taking more Tylenol.

I'm not really looking forward to tomorrow's treatment but it will be nice to be done with number 8. That will make me 2/3rd of the way through the process.

The 6th Treatment

2008-02-25T14:53:00.000-08:00

I had the 6th treatment on Friday the 15th. My absolute neutrophyl count went up a little bit to 180. The time went by quickly and I had no side effects except for some achiness in my arms. I'm in good spirits and glad to be at the half way mark!

The 5th Treatment

2008-02-06T16:39:00.000-08:00

I had my last treatment on Friday February 1st. It proceeded even though my absolute neutrophil count was low. Neutrophil's fight against infections. Normal is 1,500 to 8,000. A safe level is 500-1500. Mine was 120. Nobody sneeze!

The day started with a Pulmonary Function Test. I have to have one every month to make sure one of the chemo drugs is not thickening my lungs and making it harder to absorb oxygen. If it does they will stop giving me that drug. The tests are performed on two different machines connected to computers. If you want to learn exactly what they test check out http://www.webmd.com/a-to-z-guides/lung-function-tests

The infusion rooms at Mass General aren't depressing the way I thought they might be. The staff tries to make you comfortable and offers you food and beverages and blankets and heat packs. You can choose a chair or a room with a bed. If you choose a chair, you can see two other people. You are close enough to talk to each other if you want. I've met some really nice people. If you prefer, you could pull a screen that provides privacy. The chairs recline.

The needles they use are very thin and pretty painless. Having said that, I've had WAY too many needles lately and I look forward to getting them occasionally again.

Things proceeded normally during the infusion. I made art (watercolor) with the help of the Artist in Residence, Julie Martini. What a great program. It not only made the time fly by but it was fun and sparked my interest in making art. I had to work left handed even though I'm a rightie because I didn't want to move the arm I was receiving the infusion in too much. Any guesses what I was trying to paint?

My mood is good and I'm taking one day at a time. As of Wednesday night, I've had no serious side effects except feeling a little run down. Then again, I just returned from working in Woods Hole for two days.

The 4th Treatment

2008-01-25T12:59:00.000-08:00

I had my 4th treatment last Friday.

I was scheduled for bloodwork at 9:30, two doctor's appointments at 10:30 and 11:00 and then the infusion at 1:00.

My absolute neuts dropped again. Now I'm down to .32. The doctor said that it would be OK for me to proceed with my infusion. When I got to the infusion room, they said that the orders said that I was not to get the insusion unless the levels were above .50. Therefore, they refused to fill the order. It took an hour to straigten out the mess. In the meantime, I convinced them to get me started with an IV and fluids so we moved along once the orders were corrected.

Once we got going, the schedule was as follows:

Adriamycin - 3:10-3:15

Vinblastine - 3:16-3:20

Bleomycin - 3:20 - 3:30

Dacarbazine - 3:35-4:35

After the infusion, I felt great for the rest of the day and good the next day. As usual the next day I was tired and spent a lot of the day resting in bed. I've felt some aches and pains (especially in my arms) but nothing too bad. I've been trying to avoid crowds and sick people but everyone seems to be sick right now.

My mood is a 9 out of 10.

The Night before the 4th Treatment

2008-01-17T20:23:00.000-08:00

Last weekend most of my side effects went away and I've felt great since then. I suspect tomorrow will be a long day since I have to wait 90 minutes between my doctor's appointment and my infusion. Oh well, it's best to expect it to be a long day and just relax through it.

I bought a book by Bernie Siegel called How to Live betwen Office Visits. He writes about cancer patients who give themselves permission to start living the life they want to live after they get diagnosed. As he asks, why do you have to get cancer to live the life you want to live?

By tomorrow night, I hope to be 1/3 of the way through my treatments. I know complications can interfere with the schedule and get treatments postponed but I would really like to be done by the middle of May. Of course this supposes a successful outcome to the treatments - and that's what I choose to do.

I'm going to rate my mood a 10 out of 10.

After the 3rd Treatment

2008-01-07T16:31:00.000-08:00

I had my 3rd treatment on Friday. It turned out my concern about my FEV1 was unfounded. It turns out the DLCO [Hb] number is more important and it was fine. I guess this proves it doesn't make sense to worry about test results when you aren't qualified to evaluate them anyway.

I had an 8:00 appointment to get my blood drawn. I met with the doctor at 9:00 and then I was scheduled for my infusion at 10:00. Somehow things were slow to get started and I got my IV set up and fluids started near 11:00. Then the schedule went as follows:

Adriamycin - 11:05 - 11:15
Vinblastine - 11:15 - 11:20
Bleomycin - 11:20 - 11:25
Dacarbazine - 11:30 - ~12:40

I needed to slow down the Dacarbazine because I could feel it being pumped into me and it's not a comfortable feeling. A heat pack helped. I then got about an hour's worth of more fluids to reduce the chances of my getting constipated.

I got home by 3:00.

That night and the next day I felt great. I went to the gym for a 3 mile walk, I did some shopping and I went to a dinner party until almost midnight.

I went to bed at 2:00 AM on Sunday and slept until 9:00 Monday morning. Yes, you read that right. I slept 30 of 31 hours with only a 1 hour break to eat dinner on Sunday afternoon. At first, bed just seemed like a really comfortable place to be. Over time, I started feeling exhausted and couldn't get out of bed. This morning (Monday) I went to another doctor appointment, came home and, you guessed it, went to bed for another couple of hours until I had to go to yet another doctor appointment in the late afternoon. My doctors think I may have overdone it on Saturday and things caught up with me. My ENT said that I am showing signs of having a cold as well. The good news is that the remaining tissue in my adenoids continues to get smaller.

The last day kind of threw me for a loop. I think when things are going very well it's easy to get discouraged when you have a bad day. Some days will be good, some not so good. Even though I feel pretty good right now (just a little tired), I'm still going to rate my mood over the last 24 hours as a 6 out of 10.

The Night before the 3rd Treatment

2008-01-03T21:06:00.000-08:00

For scheduling purposes, it was decided to move my appointments to Fridays instead of Thursdays. I'm fine with that because it will make it easier to work but I will miss the nurses I've been treated by so far.

I had a pulmonary function test on Wednesday. When compared to the test I had before starting chemotherapy, it showed a reduction in my FEV1 that put it out of the normal range. The FEV1 is the amount of air you can blow out of your lungs in 1 second. I hope it doesn't interfere with my treatment schedule.

I spoke to my dentist today although I know I can't have any dentistry done (including teeth cleaning) until I'm done being treated. He too is being treated for Hodgkin's. He was diagnosed with stage 3 Hodgkin's and now appears to be cancer free after 8 treatments. He has 4 more treatments to go to finish the regimen. His first treatment was difficult and he ended up in the hospital for a day and a half. He also needed to give himself injections because some of his blood counts were low. After the first treatment, things got better for him and now his experience sounds like it is similar to what I have experienced. It is very hopeful to hear that somebody who was diagnosed with stage 3 Hodgkin's is getting clean PET scans already.

I've started thinking more and more about my business. I would like to spend more time on sales but it is hard to focus while health issues have your attention.

I'm scheduled to have my blood drawn in 7 and a half hours so I should probably head to bed.

My mood is another 10 out of 10 tonight. Cross your fingeers that it stays that way after tomorrow!

My Second Treatment

2007-12-20T21:31:00.000-08:00

The second of twelve chemotherapy sessions was scheduled for Thursday. Wedensday night I did a relaxation exercise at a friend's house. We also talked about identifying stressors in our lives and stopping to take a deep breath when we notice them. Then we went to a Qijong class. It was my first time and I found it interesting.

According to Wikipedia, Qigong or chi kung is an aspect of traditional Chinese medecine involving the coordination of different breathing patterns with various physical postures and motions of the body. Qigong is mostly taught for health maintenance purposes, but there are also some who teach it as a therapeutic intervention.

This morning, I had to get my blood drawn at 8:30. At 9:30 I met with my doctors and we discussed my blood counts. I then started my infusion at 11:00 and was out before 2:00.

My blood counts were down again for the second time in two weeks.

Here are the numbers.

The doctors pointed out that my Absolute Neutrophils were very low. They said that we could continue with treatment even if they were much lower but I had to be careful of infections. I was told to call the doctor immediately if I got a temperature over 100.5 degrees.

The infustion itself went well. I had a new nurse because my the nurse I had last week was taking care of one of her sick children. I know one of her little munchkins was sick when I got my first infusion. The nurse that took care of me today was very nice. I'm starting to wonder if Mass General has only great staff.

I started with some pills. They were Andonsetron and a steroid called Decadron for nauseu prevention. It took two trys to get a good vein but once we had one it was smooth sailing. I started with fluids for a short while and then I went on to the Adriamycin (Doxorubicin) I got 46 mg. from 12:19 to 12:33. Next was 18 units of Bleomycin from 12:34 to 12:39. Then we went on to 11 mg of Vinblastine from 12:40 to 12:45. Finally, I got 690 mg of Dacarbazine from 12:50 to 1:50. One of the drugs made my arm itch and feel cool to the touch. The nurse gave me a heat pack that took the chill out of my arm.

I went home and took a nap. Again I've felt no nausea ( as of 1:10 AM) and I ate normally and put up the Christmas tree with my Dad. I'm taking Senna to avoid constipation.

I have a pulmonary function test scheduled for just after New Years. They keep an eye on my lungs to make sure the chemotherapy is not causing any damage.

My mood is a 10 on a scale of 1 - 10.

Follow Up Appoinment One Week After 1st Infusion

2007-12-13T14:38:00.000-08:00

My follow-up appoinment was scheduled for today. I had blood drawn and met with my doctors. As has become the custom, I got weighed and my temperature and blood pressure were taken. Then my doctors and I discussed my blood work and my experience with the first infusion. They were happy to hear that I experienced no nausea and said that my first experience was a good indicator of how future treatments would go. I was told that fatigue was the one symptom that might build up over the course of the treatments but even that was usually temporary.

I was told that my blood work was strong but I noticed drops in categories across the board.

One symptom I have experienced is constipation. When you're used to having no problem in this department it's a real drag when you can't go. I'm now taking Senna and Colace and it's starting to get better. I'm definitely going to try to keep on top of this. I'd recommend asking about medication and taking it at the first sign of trouble.

I'd rate my mood as an 8 out of 10.

My First Treatment

2007-12-07T20:04:00.000-08:00

I had my first chemotherapy treatment yesterday. It went better than I expected it would and I'm glad I didn't worry too much. The first infusion takes much longer than future infusions. They need to perform a test to make sure you are not allergic to one of the drugs and to teach you what to expect and review information for after you go home. Total time for the first appointment: 7.5 hours. Future appointments should take about 4.5 hours.

Here's how the day went:

I arrived at the hospital at 10:00 AM. My blood was drawn by 10:10.

I met with my oncologist at 11:00. We discussed the fact that my blood counts were good and that I could attend the first treatment. Before every infusion, I'll have to have my blood drawn to determine if I can get the infusion scheduled for that day. The doctor answered all of my questions and we reviewed possible side effects and ways of dealing with them. I was given a consent form to sign.

I read the following about blood counts and chemotherapy on the web:

Low red blood count = fatigue, low energy
Low platelets = bruising and bleeding
Low white blood count = susceptibility to infection

My numbers along with the normal ranges were as follows:
WBC - 7.6 (4.5 - 11.0)
HCT - 41.7 (41.0 - 53.0)
RBC - 4.86 (4.50 - 5.90)
PLT - 278 (10 - 350)
Poly - 56 (40 - 70)

My appointment was over by 11:30 and the infusion was not scheduled until 1:00. I had coffee with my dad and toured a new hotel near the hospital.

At 1:00 my weight, height, temperature, blood pressure were measured. Height and weight are used to calculate the dose of medecine you receive.

By 1:20, I had met my nurse, Pam. She was absolutely wonderful. I feel very comfortable with her and fortunate to have her on my team. She seems very personable and professional at the same time.

Pam inserted the IV into a vein and started administering fluids by 1:40.

From 2:15 until 2:30 I received a test dose of 1 unit of Bleomycin. It is important to determine if the patient is allergic to Bleomycin. I suspect people who are allergic can go into shock. I was told that I shouldn't feel anything when the drug was given to me and that I should say if I felt anything immediately. If so, the nurse would ring a bell and a group of people would come running to help me. After receiving the drug I had to wait an additional 30 minutes to see if I had any reaction.

I was then given two anti-nausea drugs in pill form at 3:05, a steroid called Decadron (Dexamethasone) and Zofran (Ondansetron).

The next set of drugs were given via a push method in which the drugs are injected by the nurse into the IV.

I received 46 mg of Adriamycin from 3:35 - 3:45.

I received 10.9 mg of Vinblastine from 3:46 - 3:53.

I received 683 mg of Dacarbazine from 3:55 - 4:02.

The last one was then given via a drip method.

I received 17 more units of Bleomycin for a total of 18 units from 4:03 - 5:03.

Finally, I got a flu shot in the arm. We discussed what I might expect after going home and when I should call the doctor's office or the hospital if I noticed certain symptoms.

I was given a schedule to use to take the prescription anti-nausea pills I picked up the day before the appointment. The drugs are Zofran, Compazine and Adavan. I was told to take Zofran every eight hours for the first three days. This was non-negotiable. I had to take them even if I felt no nausea. The other drugs could be taken if I needed them in addition to the Zofran.

I booked my appointment for the next session and was done by 5:15 PM.

I felt no side effects at all the first night or the day after. I went to the gym for a three mile walk and ate usually. I was told it was very important to drink lots of fluids. I know that there is the possibility of side effects popping up over the next week or so but I feel great right now and I feel relieved that the process of getting the infusion is not painful or scary. The first time is a little tense because you don't know what to expect but I'm not concerned about going back in two weeks at all.

On a scale of 1 - 10 I would rate my mood at 10.

The Night before the First Treatment

2007-12-05T18:39:00.000-08:00

I'm scheduled to receive 6 cycles (12 treatments) of chemotherapy starting tomorrow. The treatments are scheduled two weeks apart for the next six months. Some people receive 4 cycles (8 treatments) of chemotherapy along with radiation. Because the cancerous cells are located in the tissue that was attached to my adenoids, my doctor is trying to avoid giving me radiation. It could permanently dry out my salivary glands. My oncologists seem to be very experienced and I have a lot of confidence in them.

I've learned a lot about the power of positive thought, having a good attitude and prayer over the last couple of weeks. I'm doing my best to focus on the many positive aspects of my situation (such as the share luck of having found this during elective surgery at such an early stage). I'm also very thankful for the support of family, friends, coworkers and healthcare professionals at Melrose-Wakefield Hospital, the Massachusetts Eye & Ear Center and Mass General Hospital.

Now it's time for a good night's sleep to prepare for the coming battle and the path to a healthier me.