Thursday, November 13, 2008

Welcome Friends and Family

Well, here is the first entry in our blog. Most of you are already aware but here is little history for those who may not know...

Cynthia found a lump in her right breast back in June of this year. It was very high...about 3" below her collar bone. She saw the doctor in early July and was then scheduled for a mammogram and ultrasound. They could not see the tumor on the mammogram because it was too high. They did the ultrasound and that is when they saw it. She was then scheduled for biopsy at the end of July. The biopsy unfortunately was positive. It was a Stage 1 tumor (under 2 cm in size and had not spread as far as they knew).

Here she is the weekend before the surgery enjoying a cool beverage at Water Buffalo.















She had lumpectomy surgery to remove the tumor (the remaining breast was left in tact) on August 18th. The surgeon got clean margins on the tumor site and the lymph nodes were all negative (whew). However, the tumor was a grade 3 tumor (very fast growing and aggressive). It was also hormone resistant. These factors have determined the remainder of the treatment...both radiation and chemotherapy.

Radiation is always recommended for lumpectomies. Normal protocol for women under 50 is whole breast radiation for five weeks. This is typically performed after chemotherapy. However, Cynthia elected to participate in a clinical trial for partial breast radiation. This involved two treatments twice a day for five days. She was selected for this protocol so she had the radiation first. She started Monday, October 6th and had two treatments a day for five days and finished on the 10th. Although there was some difficulty getting her positioned just right each time, she made it through without major difficulty.

The doctors had her wait four full weeks before she got to start chemotherapy. Prior to starting, she needed to have a port surgically inserted in her chest. They use the port to administer the drugs. She had this procedure on the 30th of October. Which brings us to this week. Her treatment schedule is Monday and Thursday, every three weeks for four rounds. This will take her into mid-January. After that, she will start a new drug that she will get every week for 12 weeks. This will take her into mid-April. If all goes well, that will be the last of the treatments.

Her first two treatment this week are complete. She had the first treatment on Monday and seemed to tolerate it well. Her only real symptom now is fatigue. She went to work on Tuesday and Wednesday. Her Thursday treatment went well but she is feeling tired.

So that is where we stand. It is expected that she will lose her hair about the time of the second treatment although she is really pissed to learn that she will not lose the hair on her legs. She has a cute blond wig and is ready for that adventure when it comes.




14 comments:

Anonymous said...

Wow! Great idea. Love the pictures. Now we miss you even more. Hugs, kisses and prayers.

Anonymous said...

AWWWWWWWWWESOME!!!!!

Thanks, its on my quick-launch bar now!

Great seeing you guys last nite!

Tom & Keith

Anonymous said...

If anyone can show cancer who's boss, its Cynthia!

Sounds like its time for a wig party. I've always wanted to try being blond.

Marianne and David

Unknown said...

Aqua man has done it again! Taking things to the next level of coolness. Good job, Bobby!

Cynthia - we're sending you lots of love, hugs and prayers. When you are ready to have a cocktail or three - call Flower Blossom and I pleeeease. Love Soch & Todd

Betsy said...

Go get 'em Cynthia!

Anonymous said...

Hi Cynthia and Bobby,

Haven't seen you guys forever!!!! We need to get together when you are up to it. Hugs and kisses, my prayers are with you.

Love,
Lisa

Anonymous said...

Bob,this is great. Glad to hear the first two chemos are done and over! You are both gifts to everyone around you.

Christy Schwan

Anonymous said...

This is a great idea to keep us up to date on what is happening. You are both in our thoughts and prayers.
Brad & Jenny

Anonymous said...

CYNTHIA!! Sweetie! Miss your cheery smile. I have a little present that will be in the mail today. Love you much! Lynn Steinle

Anonymous said...

Bob, thanks for giving updates on Cynthia. It is always uncomfortable specifically asking about her, so this is a great way to keep everyone up to date. We trust that Cynthia will follow all the necessary protocols to get through this process. Al and Ann

Anonymous said...

Great pictures and blog idea!

Hope the treatment goes better than expected. If you're ever having a bad day, just think it could be worse....we could bring our 3 cats over along with an extra bag-o-cathair for good measure! ;)

We're thinking of you, let us know if there's anything we can do.
Love,
Jane and Bob (and Watson, Biscuit and Mr. Mustache)

Anonymous said...

You guys are constantly in our thoughts (and sometimes I giggle over some of those thoughts)and we are happy to have access to this great communication tool. Even computer illiterate l'il ol' me can figure it out. Thanks for setting it up and keeping us up to date. Love you both. karen and joyce

Anonymous said...

We can appreciate the recommendation to not drink and kudos to you Bob for joining her BUT we just discovered a new line of wines - "Cleavage Classics" - with 10% of the price donated to breast cancer research. Perhaps something to celebrate with when all this is beyond you - and Cynthia is truly well. Thinking of you and praying for you daily - love and more love, Cindy and Dave

Monkey said...

To My Dear Brother,

You missed your calling. I think you should be a writer! What a great idea and it is such a wonderful thing to be able to keep up with Cynthia's progress without bothering either of you with the same questions and conversations. Kuddo's to Steven for the tree!! I'd love to hire him for our place. We have a huge palm tree that needs some light!

PS Good catching up with you the other night. Have a great Thanksgiving!

As always, you are both in our daily thoughts. Love to both of you.

Sara and Bob