Monday, February 20, 2012

Quick Post

Seriously... This will be quick.

Radiation is going fine. So far, so good. Thank God for Magic Skin Balm! I put it on every night before bed and wear a t-shirt to bed. My skin is darker but it is holding up. I have this week (4 more days), next week (5 days) and then my last day on Monday, March 5. Then I am DONE, baby! DONE!

My hair is really starting to grow back. I have an actual wave going on in the back and a bit of curl here and there. I know in about another month or so it will probably look like a poodle's butt. haha!

I'm feeling really good. I have a lot of energy. I even lost a couple of pounds. I cannot complain.

Sorry to cut this so short... It's past my bedtime.

Nite, nite!

Sunday, February 12, 2012

Celebrating My Husband's Birthday


Here I am keeping my resolution to enjoy my life by celebrating my husband's birthday at Morton's Steakhouse last night with our good friend Terry. It was a fun (and expensive) evening!

Sunday, February 5, 2012

New Skin Cream + Working Out + Going "Au Natural"

Several women on the Crazy Sexy Life website have written glowing reviews about Magic Skin Balm by Brigit True Organics. They used it during and after radiation and claim that it really helped alleviate their radiation dermatitis (i.e., radiation burns). Many of them continue to use the product well after treatment.

I did a little research and lo and behold - these organic products are made about 1 hour west of me in Charlottesville, Virginia. Talk about coincidence... Anyway, the good news for me is that it is widely available at health food stores in the Richmond area. Today, I picked up a small jar at Ellwood Thompson's. My skin is holding up fine so far but I plan to use the Magic Skin Balm from here on out. I will keep you posted on how it goes...

In other news -- I actually worked out today. I guess you could call it a workout. It certainly wasn't what I was used to in my "former" life but hey, I have to restart somewhere. I did 30 minutes of cardio on the treadmill then used dumbbells for squats, biceps curls and triceps. I also did some pushups and crunches. I think it was a good start. I am also tracking all my food on Weight Watchers. I lost two pounds last week. I would love to lose another pound or two this week. *fingers crossed*

And finally, I went out "au natural" this weekend - no scarf, no hat, no wig - nothing! My hair really isn't long enough but I just didn't care. I decided to run some errands without anything on my head and guess what? No one stared. Babies did not scream or cry. No one laughed and pointed at me. Basically, no one cared. Yay! I am pretty close to going au natural at work. Maybe another week or two...

My next goal is to scope out some yoga studios and actually join one. I would love to start taking a class on the weekends.

Okay - it's almost time for kickoff... Happy Super Bowl Sunday!

Thursday, February 2, 2012

Some Words From the Wise

I know that many of us who are currently undergoing treatment or just finishing up treatment are experiencing an unnerving side effect: The constant worry of whether or not our cancer will come back.

I would like to share with you some words of wisdom that a friend and breast cancer survivor emailed to me yesterday. It is a little "trick" that she uses to shut out the negative worry from overtaking her.

She tells herself: "I do not have cancer TODAY. I do not have a doctor appointment TODAY so I cannot be diagnosed. This may all change TOMORROW but TODAY I am cancer free."

She says this mantra helps her manage one day at a time.

Words of wisdom for us all.

Thank you, P!

Monday, January 30, 2012

26 Points

I have gained just over 20 lbs. since my diagnosis. I thought most of that weight was due to water retention and bloating from chemo. My doctor and nurses all said the weight would come off a couple of months after I finish chemo.

Well, it's been almost two months and guess what? They were wrong. I still weigh exactly what I did on December 7 when I went in for my last round of chemo.

I was one of those rare people who didn't get sick during chemo. If anything, my appetite increased due to the steroids I was on. I also gave myself permission to eat anything and everything that appealed to me. After all, I had cancer and I felt like I DESERVED that piece of chocolate cake! Now I am paying the price.

A few weeks ago I decided to take action and joined Weight Watchers. I joined online, set up a profile, answered a bunch of questions and was told I could eat 26 points per day. How much is 26 points, you ask?

- A packet of unsweetened instant oatmeal is 4 points.
- An egg is 2 points.
- A peanut butter and jelly sandwich is 12 points.
- Most fruits and veggies are less than 2 points or no points.

You can swap food points for activity points. It's simple - the more you work out, the more food you can eat. For example, my 90 minute hike yesterday earned me 7 points to swap out for food. woo.

So what's my point? (Yes, the pun was intended.) 26 points is not a lot of food.

And here's a newsflash: Just because you join Weight Watchers doesn't mean the weight is going to magically come off. You still have to do the work!

I am ready to take this seriously though. I stocked my fridge at work with all kinds of good snacks - fruit, hummus, yogurt. I need to fit in a minimum of 30 minutes on the treadmill every day. That's going to be tough because I am doing radiation every day, too.

But I will get there. I must get there. I have my 30th high school reunion to attend in June and I absolutely cannot show up looking fat, bald and sick!

Saturday, January 21, 2012

Radiation and Livestrong at the YMCA

I started radiation this week with my first session on Thursday afternoon. It was relatively easy and definitely painless but for some reason, it bothered me more than chemo. It seemed scarier than chemo.

Laying on the table with this giant machine circling me, it almost felt like the machine had a mind of its own. It zooms in and out to target the spots on my body that it needs to zap. Obviously the radiology technicians are operating it, but it seems like a bad science fiction movie to me.

At my session on Friday night, I decided to just close my eyes, relax and visualize positive healing. I visualized the machine treating all the right spots and the radiation zapping any lingering cancer cells. This technique definitely helped me get into a more positive frame of mind.

In other news... I forgot to mention that my oncologist recommended a program to me called Livestrong at the YMCA. It is a 12-week program to help adult cancer survivors successfully transition from treatment to wellness. The program is offered at three YMCAs in my area but none of them are very close. The only facility that offers the program in the evening is 25 miles away. I may do it anyway after I finish my radiation treatments. A few miles of driving every day would be worth it if it helps me regain my health.

Thursday, January 19, 2012

First Follow Up Appointment

I was back at the hospital a few days ago for my monthly lupron injection. I happened to notice some new reading material in the magazine rack. These were my choices:

“Living with Advanced Cancer”

“When Cancer Comes Back”

“Looking Forward: Life After Cancer Treatment”

Any idea which brochure I chose to read?

“ I will take ‘Looking Forward’ for $500, Alex.”

Which leads me to today’s post…

I saw my oncologist yesterday for my first follow up appointment since completing chemo. The appointment went well. She was pleased with how I handled chemo and felt quite certain that radiation would go just as well. We discussed hormonal therapy and agreed that I would start Tamoxifen as soon as I complete radiation.

Here’s the kicker… There is absolutely no way to tell if my cancer is going to come back. There are no tests to run, no indicators, nothing. I will have a mammogram every six months for the next couple of years. I will also see either my oncologist, my radiation oncologist or my radiologist once every three months. They are a tag team (or triumvirate) – one of them will see me and report back to the others.

Of course, I am to let my oncologist know if I experience any abnormal bone pain, difficulty breathing or headaches as these symptoms could indicate metastasis to my bones, lungs or brain. This is every breast cancer patient’s worst nightmare.

I would be lying if I said I didn’t think about it every day. Some days are worse than others. When I talked to my sister about it, I explained that it was like background noise. It never goes away. Some days it is louder than others but it is never peaceful and quiet. The worry is always there. At least it is for me at this point.

My oncologist tried to be reassuring by telling me that I have done everything that is recommended and medically available in 2012. Then she told me the rest is up to me and I need to start looking forward. I need to get on with my life.

When I asked my husband for his take on the appointment, he said it was the best possible follow up appointment given my situation. And his 100% correct.

Still – there are no guarantees and that leaves me feeling very vulnerable.

I have a lot more to say on this subject but I will stop here. It is well past my bedtime!

Nite, nite.