TEN years in stage 4 metastatic breast cancer!

10 years ago today, I was diagnosed with breast cancer.

WOW… that statement ALONE is noteworthy… TEN YEARS! But even more noteworthy is that initially I was told “we caught it early” and that I was in stage 2. Later, after several scans and tests, I was told I was in stage 4 and the cancer had metasticized to several areas of my body – although, thankfully, not to any organs – and was given months to maybe a few years to live depending upon whether I had chemotherapy and radiation or not.

The American Cancer Society (ACS) states that the five-year survival rate after diagnosis for stage 4 breast cancer patients is 22 percent. This percentage is considerably lower than at earlier stages. At stage 3, the five-year relative survival rate is 72 percent. At stage 2, it’s over 90 percent.
According to a site I saw on the internet, “There is a small subcategory of people with Stage IV breast cancer (about 2%) who beat the odds and live for years. However, it is difficult to predict who will fall into this group.”

WOW…. TEN YEARS in STAGE FOUR metastatic breast cancer!!! I guess you can consider me a walking, talking MIRACLE!!

For those that might be going through what I have gone through, or have a friend or family member who is going through it… I would like to relay some ideas as to why I feel that I have fallen into that “2%” of diagnosed survivors.

1. The grace of God.
2. Powerful prayers.
3. Great doctors with innovative, up to date treatments
4. Wonderful, loving, supportive family and friends
5. Positive attitude and supreme will to live

1. The grace of God.
First, let me say, I have no “illusions of grandeur” that I am any more special to God than anyone else. Quite the opposite. I certainly do NOT feel deserving of His grace! I see others who have passed on from and are still surviving with breast cancer that were/are, in my opinion, MUCH more deserving of God’s grace than I will ever be. That being said, I truly feel that it is only by the grace of God that I am here typing this today! Almost every night, when I go to bed, I thank God for His grace and for giving me even just one more day to be with my family.
When I was first diagnosed, I was 48 years old. I had been married to my wonderful husband, Tom, for almost 20 years. Our children, Tommy, Stephen and Marianne were 19, 16 and 13 years old respectively. My husband told me I HAD to fight this, that I was the “glue” that held our family together. While I truly love God, and want to be in heaven with him some day, I could not stand the idea of leaving my husband and children! I honestly do not know how anyone could survive this dreadful disease (or any other for that matter) without having some sort of faith in a higher power. I suspect there may be some out there somewhere… but I know that I, personally, would never have survived this long without my faith and belief in God and His grace.

2. Powerful prayers.
I realize this ties in with #1 – grace of God – but I believe in prayer so much, that I feel it needs to be separated and highlighted. I was raised by a very spiritual Mom and Dad and I thank God that they raised me to believe in the power of prayer. From a headache to a fever to breast cancer… God answers prayers! I had friends, family and people all over the US and internationally that said they were praying for me. How could God possibly not hear all those prayers and respond?

3. Great doctors with innovative, up to date treatments
I was lucky enough to be led to go to Cancer Treatment Centers of America in Zion, IL where they deal with MANY victims of latter stages of breast cancer. The local oncologist here could count on one hand how many patients she had treated that were in stage 4 of breast cancer. Three of them did not live very long. The other two had not yet made it to 5 years. It only makes sense that, if you can, you go to a place that has a high success rate in treating people in the latter stages of any disease.
One of the many things I like about CTCA is that they incorporate natural supplements into your protocol. Supplements the doctors here at home scoff at, but that TRULY help! I totally believe that God, in his grace, led me to CTCA because of their innovative approach to treatment of cancer. I actually take more supplements than I do prescription medication. And, believe me when I say, I take a lot of prescription meds.

4. Wonderful, loving, supportive family and friends
I know that my husband of 20 years (at that time) and our children were probably scared half to death at the thought of losing me. But they are all so STRONG and supportive of me and my battle with breast cancer! Yes, they broke down and cried – just like I did.. but they were so strong and helpful. When I could not even lift a suitcase to go out of town to CTCA, someone was always there with me to help me. Our daughter, Marianne, probably went with me the most times while I was undergoing chemo and for the first few years.

5. Positive attitude and supreme will to live
I have been told by many people, including doctors, that my positive attitude and sense of humor has played a major role in my survival. From as far back as I can remember, I have always been a jovial person, full of humor, joy and love. I was determined (and still am) that I was NOT going to let having breast cancer take me down.
I have to admit, there are some days that the pain from the tumor that metastisized into my L4/L5 region of my spine is so debilitating I have feelings of wishing I could be out of pain and in heaven. I have a nice little pity party for myself on those days. But in the depths of my painful despair, I think of my family, and I MAKE myself change my attitude. I’m not saying it is easy… its not. I realized very early in my life that it does no good to whine and cry about something bad that has happened to me. My attitude is… it happened… there is no changing what happened, no going back in time and doing things differently….. so pull yourself up by your bootstraps and move on. You can either cry your eyes out about it and be down and dark and make everyone you love around you depressed, or you can laugh, learn and live with it.

I know that I don’t make posts on this blog like I really should, but I can only hope that what I have shared here will help SOMEONE in their journey!

Part One of My Breast Cancer Journey

Because this is a new blog, and will now be my preferred method of getting information out to those needing it, I am going to give a recap of what I call Judy’s Journey!  All of this info (and even MORE!) can be found in the forum.  The forum will remain, but has been locked for several years because of spammers attacking it.

Here we go!

June 13, 2007 – x-ray of lower back and mammogram because I had a lump on left breast that showed up two weeks prior, and also had been having severe back pain for a year or so.

June 15, 2007 – diagnosed with breast cancer by Internal MD, who said it appeared to be in stage 2.

July 3, 2007 – underwent surgery to have mastectomy of right breast.  Surgeon could not find mass, so he sewed me up and scheduled me for a mammotome

July 20, 2007 – Mammotome biopsy

July 30, 2007 – modified radical mastectomy of right breast.  Removal of 24 lymph nodes, 14 with cancer in them

August 10, 2007 – saw local breast cancer oncologist who said it looked like I was in stage 3 and ordered a port to be put in, a MUGA scan, a bone scan and a CT scan.  She also scheduled me for chemo to begin on 8/28/2007.  Aggressive treatment with four cycles of Adriamycin and Cytoxan, followed with 4 cycles of Taxol on dose-dense regimen every 2 weeks.

August 14, 2007 – had CT scan

August 16, 2007 – bone scan

August 27, 2007 – CT and PET Scans

August 30, 2007 – drains removed from right breast from mastectomy

August 31, 2007 – local breast cancer oncologist went over scans with me and husband Tom.  She said I was in stage IV of metastatic, ER Positive invasive ductal carcinoma of the right breast.  She said it was not curable and the median life expectancy was 2-3 years.  Bone scan showed cancer in L4, left 6th & 7th ribs and right femur.  Also showed “at least 4 adjacent hypermetabolic lesions in the left middle to lower abdomen” within the omentum.  Scheduled in one week to start chemo – Adriamycin and Cytoxan every 3 weeks.

September 2, 2007 – My dear friend Marilyn, called and told me to check into Cancer Treatment Centers of America.  I called, liked what I heard and set up an appointment immediately.  Now… watch how FAST things go from this point forward in comparison to up until this time!!

September 10, 2007 – Meet with Dr. Neelam at Cancer Treatment Centers of America in Zion, Illinois (CTCA) with my sister, Patti

September 13, 2007 – MRI of lumbar spine ordered by CTCA

September 14, 2007 – First cycle of Taxotere – also put on Tamoxifen – CTCA

September 25 – October 11, 2007 – 13 treatments of radiation locally

October 12, 2007 – Second cycle of Taxotere at CTCA with my husband, Tom

November 9, 2007 – Third cycle of Taxotere at CTCA with our daughter, Marianne

November 30, 2007 – Fourth cycle of Taxotere at CTCA with our son, Tommy

December 11, 2007 – Met with therapist for lymphadema – fitted for specialty german made sleeve

December 21, 2007 – Fifth cycle of Taxotere at CTCA with our son, Stephen.  Dr. Neelam said chemo was working and no cancerous activity seen!!