Thursday, September 28, 2006

Game Plan













Ok...now I have some great news for me.


I am STABLE again with NO drug changes...had all my new scans done at my new treatment facility, MD Anderson last week .....they compared with scans ordered from my former onc in June.

NOTHING has changed... My Ca27-29 has stayed at 90 for 4 months....SOOOOOOOOOOOOO....they want to reserve the Tykerb/Xeloda for when I really need it.

So after mets came back in June...I have waited all this time to find out they are unchanged. By the way...MD Anderson ROCKS!

Game plan: Stay on Herceptin and Zometa...change out femara and replace with faslodex. Improve QOL by managing pain in chest better (related to surgeries last year NOT tumor progression) with gabapentin (for nerve damage) Drink a gallon of water a day, light exercise, and live my life!

WHEW!!!!!!!!! I like that plan!!!!

Thank You SO much for all the encouragement, cards, emails, good wishes and holding my hand during this Roller Coaster Ride....Namaste. Posted by Picasa

Tuesday, September 26, 2006

Monday, September 11, 2006

SO Happy it's College Football











Watched the last 2 games PPV....when are we going to play a real football team?


Couldn't bear to watch one NFL game this Sunday.

Football is always played on Saturday as far as I'm concerned. (Unless it's a Bowl Game of course).

I am hoping to get to a few games this year. Would love to see the ol' ball coach when he shows up with the Woodcocks in the Swamp. That's gonna be one emotional game. Posted by Picasa

The last 6 weeks have been CRAZY

So much has happened since the last time I posted. I know I promised to keep this up....but it has been tough. Part of the reason is because of the Roller Coaster I have been on emotionally.

Some of the things 'of note' since last my last post:

In August I spoke in front of about 300 people at a breakfast kick-off for American Cancer Society's Making Strides (5k) event coming this October. It was very nerve wracking (sp?).

And a big thanks to Cindy and Suzie and Jeff for coming to the event to "hold my hand". It looks like I did ok becuase I have been asked to speak at another event at the Citrus Club in front of yet another large group October 5th. If I could just figure out a way to get paid speaking about Breast Cancer I'd have it made.....

I STILL, as of this date, have NOT started any new treatment for my rediscovered mets (back in early July?) SOO....it's been a long, long wait and it's made me nervous as hell. A little too nervous.

I found out I qualified for a new drug Tykerb (see earlier post) but my Oncologist's office has taken MONTHS to get into the program. The waiting has made me borderline NUTS....alright, if you talk to Jeff he will correct me and say CERTIFIABLY NUTS. Of all the thing I have been through in the last four 4 years....this waiting has got to be one of my worst experiences.

I finally made the decision to switch Oncologists (HUGE UNDERTAKING)....and as of today I am now a patient of MD Anderson. (Ranked 2nd in Nation for Cancer Care behind Sloan Kettering)

I had my first consultation today with the Oncologist and got the full dog and pony of the facility.

I am going away this Wednesday-Sunday with a bunch of girlfriends to San Destin. (Never been there before and now have been twice in one year!) Once I get back..starting on September 18th I begin practically a full week of tests and scans. Seems like every day that week I will be at Doctor's. By Sept 22nd I will get instructions on my new treatment....whatever it may be. I am just relieved to be MOVING in any direction.

This so called summer of fun and surfing was spent mostly hand-wringing and waiting and being very anxious and irritable. I NEED this vacation. I'm sure Jeff could use a vacation from me too!

ALSO big news: I am taking a break from work for a few months. It was something I needed to do primarliy so I could focus on getting my treatment in the right direction....which turned into a full time job.

It was tough to pull away from the job and the company I work for. I have been with the same company for 2 1/2 years and they have been great to work with. I miss the "action"....but I'm starting to relish the free time.

To anybody out there in blog world who actually reads this damn thing...sorry I have been so remiss.

I will have tons to talk about when I get back from my trip to San Destin....also will have tons to talk about with my new Doctor's and treatment...... AND don't forget it's almost PINK RIBBON MONTH (I used to love the color pink) October was my favorite month and pink was my favorite color. Can we turn BC awareness month into like November or March and make the color yellow or something else.

OK mostly being sarcastic....October can be overwhelming when you're not only a survivor but still a patient. BUT I am involved in umpteen fundraising and BC awareness events in October. So you will be hearing more from me....probably directly too...to hit you up for some type of participation!!

And I am sure by October I will be hitting you up for job leads too! Something that pays a ton of money with great benefits and no accountability. :)