Wednesday, November 18, 2009

Test Results Are In

Well, definitely not the results I was hoping for. I found out today that I did test positive for the Cancer Gene BRCA1. A mutation or alteration in the BRCA1 causes most cases of hereditary breast and ovarian cancer (HBOC). HBOC syndrome increases the risk of various cancers (and recurrences) but primarily attack breast and ovarian. The kids also have a 50% chance that I have passed it down to them. My next step is to consider my options of a mastectomy as well as a hysterectomy since the risks of recurrence now are very high. Not sure I am willing to do nothing and risk the cancer coming back with a vengance. Looks like I won't be able to "save the Ta-Ta's" after all. So much to think about and so many other unanswered questions. Unfortunately, I was too upset at the Dr's office to think of the questions that I now have.

Labwork today was really good. Overall, the best it has been since I started the chemo. Got the thumbs up to start round 3 tomorrow. Few minor tweaks again and hoping the nausea won't be as bad this time. Dr. Rosenfeld told me that I am doing the hardest regimen of chemo that there is and he is very pleased at how my body is tolerating it all. Not sure I agree with him but I guess other people don't do so well. I am hoping to be up and recovered by Thanksgiving because my entire family is coming into town.

Friday, November 13, 2009

Another Round Over

I am finally well enough to post again. The treatments this round made me sick most of the week. I did not get the other side effects from the first round (thanks to the tweaking) but I have been nauseated and felt yucky all week. I got out yesterday for the first time and was able to watch Kaitlyn ride her horse during Horses For Healing. It was such a beautiful thing to see. Unfortunately when I got home, it kicked in again and I was down the rest of the day/night. I'm hoping for additional tweaks on the next round because I am not good with the sick feeling all the time. Luckily, Bryan was home most of this week so my mom was only here for a day. Dinners are still being provided 3 days a week and that has been a huge help and one less thing I have to worry about. Thanks again to everyone that has helped out and have come by to hang out with me "in the bed" even if I am sleeping.

I also decided to get the genetic testing done to see if I am a carrier for the cancer gene (mutation as it is called). I will have those results Wednesday. If I carry the gene, it will help determine what steps will be taken next in order to ensure there wont be a re occurrence. If I test positive, I have a 67% chance that this could happen again and the kids have a 50% chance that I have passed the gene to them. I am hoping for the best and preparing for the worst.

Today is my 11th anniversary. Hard to believe that 12 1/2 yrs ago I met my husband in a Dale Carnegie Class. Very ironic as we celebrate this year that I remember the vows we took to love honor and cherish, in sickness and in health, until death us do part. I am so thankful he meant it.

Wednesday, November 4, 2009

Reality sets in

Today was the day that confirmed the reality of what I have been going through for the past 3 months. Today is the day my hair started falling out. Through this entire process, this was the hardest for me emotionally. I have waited anxiously for this day and thought I was fully prepared for what was about to happen. I thought I had come to terms with the hair loss and was ready to just get it over with-then it happened and I don't feel so ready.

Since I started my meds last weekend for all the infections I had, I have felt great. I have had 4 days of feeling somewhat normal again other than just being tired. I took advantage of those days and enjoyed the little things that I would normally take for granted. I actually braved the outside world yesterday and went to hang out with a dear friend and even went out to lunch.

I went to have my lab work done today and to meet with the oncologist to talk about the side effects from my last treatment and see what we would do differently for the treatment tomorrow. Luckily, my White Blood Counts were back up to 7.2 which is normal. They were at a 2.2 last week when I was sick. They are going to make a few changes to "my regimen" and use less steroids which they are hoping will decrease the side effects I had last time. They are also hoping my counts wont drop so low and that my immune system will stay up.

keeping my fingers crossed!