Hospital launches program for survivors

I wrote this yesterday for my newspaper blog. It's another in an occasional series on my breast cancer journey.

Griffin starts cancer survivorship program

Cupcakes add festive air to kickoff reception at Center for Cancer Care. Photo by Patricia Villers

DERBY - My daughter and I attended a reception Thursday to kick off a free survivorship program at the Center for Cancer Care at Griffin Hospital.

What better time to launch the initiative than during October, National Breast Cancer Awareness Month? 

I was among almost 20 breast cancer survivors there who learned about participating in the program.
Griffin will be scheduling workshops on topics such as rehab, pastoral care, nutrition, and exercise.

I'm looking forward to being a part of it, and sharing my experiences with readers here on the blog and in the newspaper. 

Labels: Center for Cancer Care at Griffin Hospital, Derby, kickoff, survivors

A Christmas miracle ~ for moi anyway

I found out today I only need to have 25 radiation treatments instead of 35. Woo hoo!

And today's was number 24, which means on Monday I'm all done. 

Not that it adversely affected me; and not that I won't miss the four awesome radiation therapists I've gotten to know. 

They're all wonderful women who made me feel great about myself.

My radiation oncologist said the blood work and the skin in the affected area both look good. So again I say woo hoo!

In a few weeks I have an appointment to learn more about the next step: pills. 

~

This is yet another in my continuing cancer journey saga..thanks for reading! 

My online cancer journey journal continues...

It's almost 5 p.m. 

I'm tired and I've caught a cold (boo hoo) but I'm still planning to attend a support group meeting that starts at 6.

I always enjoy my time with the ladies. Our group, Circle of Friends, meets every other Thursday but in two weeks we won't meet, because it will be Thanksgiving already. (gasp!)

I can't believe how fast November got here and how fast the month is flying by us. It has been one of my crazier years, it's safe to say.

Tomorrow I go for a dry run of sorts for my radiation treatments, which start Monday morning. 

Thanks for reading!

I'm all about medical appointments these days

I had a mammogram yesterday before I start radiation.

Dare I make a joke and say the screening only took half as long as it used to take? Or would that be unbecoming of me?

Anyhow, I waited all afternoon for the results but no phone call. So today I wait again.

{My online cancer journey journal continues..thanks for reading!}

I do believe 'tis better to give than receive

...but receiving lots of support since my cancer diagnosis from family, friends, and even from folks I don't even know is almost as good!


On Wednesday I received some unexpected recognition from a group of wonderful people, and I'm trying to figure out how to thank them for their thoughtfulness.

I'm purposely being vague here...need to think about what to do to show my gratitude.

~ ~ ~ 

In other news, Ralph and I are taking part in "Haunted Lantern Tours" tonight in downtown Derby, Ct. 
The cool thing is we're not attending, we're two of the presenters. 
He and I will be at one of the stops on the tour to tell a story about the former inhabitants of a (haunted?) Victorian house that is now a funeral home. 
We'll mention the sudden death of one them inside the house ...

Spooky!

Last 'chemo light' treatment delayed a day

... but tomorrow it will finally be here!

The doctor had a day off today so I must wait until tomorrow to have the 12th and final treatment.

That's OK. Time flies anyway. I don't wish it to go any faster than it does.

{And so my online breast cancer journey journal continues. Thanks for reading.}

Steroids + coffee = a hyper me

Up, down, up, down. What a week. Blame it on the steroids I got Monday, I suppose.

On Tuesday I felt like I was in perpetual motion. I covered two live events, wrote a third story, and did some other stuff for work.

On Wednesday that "energy" was gone, but I did cover a live event first thing in the morning, and also filed a second story.

By Thursday I was "mezza-mezza" energy-wise, but managed to cover yet another live event at night.

Now it's Friday afternoon, I filed a story. And I'm hoping that's it for this week.

Before I know it I'll be back in chemoland, and the cycle will begin again.

Only two more treatments and I can get off this roller coaster for now.

{Now it's Sunday. Thank you for reading my online journal about my breast cancer journey ~ I don't like to complain but was urged to post what I had written Friday, so I did.}

Back to the grind...the chemo grind, that is

It's Monday morning and I'm all set to go back for treatment #10.

Only two more after today! Yay!

I always get hungry while I'm sitting there, so once again I'll bring my peanut butter and jelly sandwich for a snack. This time on multi-grain bread instead of whole wheat. Exciting, eh?


I'm going to wear my new long-sleeved T-shirt that I got for participating in the walk on Saturday. I'd take a picture of it but my rechargeable batteries aren't recharging any more. And I can't seem to find any AA batteries. Must buy some. I hate to be without my camera.


I guess that's it for now. Thanks for reading my online cancer journey journal!

Walkin' in the rain

We'll see how this goes...getting ready to leave for a walk/run (I'll be walking, not running) to benefit the Center for Cancer Care at Griffin Hospital in Derby, Ct.

And it's pouring out.

Being part of a group with the same goal of raising funds and awareness will keep me inspired, I hope!

Happy to report I raised $155 for the cause.

More later...

Only three more to go!

Yesterday was my chemo day again...Happy to report I feel fine. Just tired. 

Three more chemo treatments left, then at some point after that (hopefully there will be a bit of a break) I'll start five weeks of radiation. 

That will be five days a week. Woo hoo!  I'm guessing it will be a tiring experience..

On Saturday I'll attempt to walk 3.1 miles in a fund-raiser for the Center for Cancer Care at Griffin Hospital in Derby, Ct. It's the third annual event and the first one in which I'm participating.
I plan to take it easy...the second half will be the hard part, since I'm so out of shape. 

Maybe I'll ask Ralph to ride along nearby in the van so he can pick me up when I'm losing my energy. (just kidding) 

My friend Linda suggested I amble. I agree ambling is good!

My (sometimes hurty) knee and I did fine Sunday walking in an event along the shore in West Haven, Ct. to raise funds for the Center for Disability Rights. 
Ralph works for the nonprofit, which gives college scholarships each year to students with disabilities. They said the route was 1.5 miles. It felt like more, but maybe because it was so muggy out.

As you can see in the photo it was an overcast morning.

Meanwhile my oncologist said yesterday he'll be making some brief remarks at Saturday's event, as will several other health-care professionals. He jokingly asked me if I wanted him to mention me.

No thanks, Doc, just wave. I'll see ya. ;-)

{That's about it today for my online journal about my breast cancer journey. Thanks for reading.}

Out of my comfort zone

I've never asked anyone for money but I've decided to take a step outside my comfort zone to ask for sponsors (any small $ amount would be much appreciated) as I participate in next week's third Annual 5K Walk/Run to benefit the Center for Cancer Care at Griffin Hospital.

That's the facility in Derby, Ct. where I'm currently getting chemo and will soon be getting five weeks of radiation treatments.
 
The fun never ends! 

The state-of-the-art facility (below see photo of the healing garden outside the treatment room) opened three years ago. 

 

I took this photo in August. It's such a peaceful setting.

I guess I never dreamed I would be a patient myself in 2011. Goes to show one never knows.

Anyhow, I wrote a story for the paper about the walk/run that you can read here. I hadn't planned on blogging about the event, but I decided to give it a go. 

It's always a good idea to raise awareness of breast cancer. It seems to affect so many people.

The walk organizers' goal is to raise $75,000 this year. I set a goal of $200, to do what I can to help. 

To make a donation click here. Thanks so much!

Kemo brain kicks in

Methinks the kemo is kicking in big time. I feel like I can't keep up with anything.

I really could use a mental health day. 

Looks like I'll have to wait until Saturday ...

P.S. I spelled chemo wrong just because I could. ;-) 

{And so my online cancer journey journal continues.} 

Chemo light #7 turned out to be #8

Time sure flies when one is having fun! Looks like I lost track of time.

Yesterday I wrote here that it was day number 7 - glad to learn that it was number 8! One less to go until I get to the magic number 12. 

The chemo kinda messes with my sleep, but I much prefer that side effect to others I won't bother mentioning.

I came home exhausted yesterday afternoon and slept for more than two hours to recuperate. Then this morning I woke up after a less than full-night's sleep. :- (

Maybe it's because I skipped a week, and my body has to get used to it again.

{Thanks for reading my online cancer journey journal}

Back to chemoland today

I missed a treatment last week because the doctor was on vacation and the other oncologist in the office is not authorized by my insurance or some such thing,

I was given the option to see a different oncologist in the medical group in another city, if I didn't want to miss a treatment. 

But they said it would be OK to take a week off, so I did.

I believe this is number 7, but who's counting?

I feel fine, and for that I am grateful. 

{Thanks for reading the continuing saga of my cancer journey.}

It's almost worse than losing one's hair

Eyebrows. 
I never thought much about them until I didn't have any. : (


I realize there are worse things.
And I know there are artificial ones I could get, or I could use eyebrow pencil. 

But I prefer the real kind.

And they're not there any more. 

At least with my head I can find a variety of chapeaux and scarves to cover up the few remaining strands of hair I have. And the wig option is still there.

But eyebrows and for that matter eyelashes (they are mostly gone too) are so visible, unless one wears large sunglasses to cover the blank areas.


Oh me, oh my. 

OK, done whining for today.

{My online journal about my cancer journey continues.}

Tossin' and turnin'

... it's not something that I normally do.
I'm blaming my insomnia  on yesterday's chemo light treatment #6.


I woke up after only four hours of sleep. Wasn't happy.
Finally got back to dreamland after about two hours of tossin' and turnin' thanks to a soft and furry heating pad we call Linus. He snuggled up to my back, I was able to relax, and all was well.

Awww ... what a helper he is.  And what a sleeper! He's asleep as I type this. What else is new? Tee hee.

{And so my online journal about my cancer journey continues ... thanks for reading!}

It was a beautiful day in the neighborhood

This is how the courtyard outside the area where I get chemo looked at noon today. It's a beautiful setting. 

This was taken through the window. Unfortunately we can't go out and play in the courtyard. 

Today is Chemo Day again...the weeks fly by

Gimme a c - C!

Gimme an h -H!

Gimme an e - E!

Gimme an m - M!

Gimme an o - O!

And what does that spell?  Exhaustion.  

Well at least it's 'chemo light,' as I prefer to call it.



Must be Monday.  ;-)


{And my online cancer journal continues..}

Time for 'chemo light' again, tra la, tra la

Actually I joked to a friend last week that going for the treatments is my only break! My days seem to get pretty busy. So it's relaxing to just sit there and veg out.

My mother is there with me, and she goes to the snack bar in another part of the building and gets us a roll or something to snack on, and there is free coffee...

The doctor will even get it for you! How cool is that.

He seems to get miffed if you don't want any!

 

{And so my online cancer journey journal doth continue. Thanks for reading.}

Building up a tolerance? Could be

Yesterday was "chemo light" day number 4, and miraculously when I got home I was not ready to go to sleep.
I actually stayed up for two and a half hours and worked before taking a nap.

When I told Ralph he said I must be getting used to it.

Maybe my body is building up a tolerance to it or something.

All I know is eight more treatments to go! Or as the doctor said, I'm one-third of the way there. The weeks are flying by.

~ ~ ~

My online cancer journey journal doth continue...

Thanks for reading!