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Joyce (joyce)


February 19, 2008


Click here.


jmhinnant41


Scotland Neck, North Carolina


November 7, 1941


Breast Cancer


January 1994 & November 2005


Stage 2


03


Positive


Positive


Yes


Lymph Node Removal, Mastectomy


Fluorouracil, Methotrexate, Cyclophosphamide (brand name: Cytoxan), Adriamycin (chemical name: doxorubicin)


Tamoxifen


Cancer Survivor


The Chemo


Be Thankful For Every Day You Have


Pray for me and donate to this site and to cancer research if you can.


I really had no symptoms that I noticed. I accidentally found the first lump in 1994 myself. The second one in 2005 was detected during my annual mammogram. I would never have found this one because it was in the center of the breast at the back wall.


January 1994 – Stage II - 2.4 cm lump… a second 0.3 cm lump found in breast after surgery. Left modified radical mastectomy with removal of 9 lymph nodes…1 (3cm) lymph node positive. ER/PR both positive.

November 2005 – Stage I – 1.6 cm lump. Right modified radical mastectomy with lymphatic mapping and sentinel lymph node biopsy. 2 lymph nodes removed…both clear of cancer. ER negative(1%) and PR positive(7%).


None either time.


6 treatments from March 3, 1994 to June 29, 1994. Started with Taxol Study. Received high-dose Cytoxan 3980 mg and Adriamycin 74.6 mg for 2 cycles. Except for the 1st and the last, blood transfusions were required after every treatment due to low hemoglobin. I developed a blood clot in my right arm shortly after the first blood transfusion in April and had to be hospitalized and put on coumadin for 3 months. Had to be taken off Taxol Study because I could not take high-dose Cytoxan/Adriamycin and Coumadin. I was given Cytoxan 995 mg, 5-FU 995 mg and Adriamycin 99.5 mg for the next 4 treatments. Other side effects were nausea, some vomiting, sores in mouth, diarrhea, heartburn, fatigue and complete loss of all hair.

6 treatments from January 20, 2006, to June 2, 2006. I was given a CMF combination of 1200 mg of Cytoxan (Cyclophosphamide), 80 mg of Methotrexate and 1200 mg of Fluorouracil (5-FU). This bout with chemo was much easier than the first. I also had a blood clot in my lung in February, 2006, and was hospitalized for 7 days and put on coumadin for 18 months. Only other side effects were minor nausea, fatigue, sore mouth, minor diarrhea and only thinning of my hair.

The worst thing to happen was the death of my husband and my boston terrier dog in May during this bout of chemo.


Tamoxifen – July 1994 through July 1999
Hot flashes were the only side effect I remember.

Arimidex – June 2006 through January 2007
No side effects that I noticed. I was taken off Arimidex because my oncologist was concerned with damage to my bones. I was diagnosed with low bone mass or osteopenia on 02/20/06


None


Injections of G-CSF 10 mcg/kg until my ANC recovered. No side effects that I remember.




joyce's Cancer Blog

July 8, 2008

ANSWER TO WEEZIE'S QUESTION ABOUT MY CATARACT SURGERYViews: 136

Weezie asked me a question and this is in answer to her question about my surgery last month on my right eye. I decided to enter it also as a post in case anyone else had ever had the same problem and could offer any suggestions.
The surgery helped the sight in my right eye quite a bit. Colors are so much brighter. At times I can see very, very clearly even without my glasses and other times during that same day things are fuzzy and I can hardly see at all. My eye surgeon said these changes could be due to damage done by my last chemo taken two years ago or it could be just my age. He thinks it probably is coming from the chemo because it has only been happening since that last chemo in 2006. If I stop the high strength steroid eye drops I have been taking for 2 years, my eyes get all red and start mattering up like they do when you have pink eye. It also hurts to use them or keep them open. They are very sensitive to any light. I also have Glacoma. He wanted to get me off the steroid eye drops because he says they make the pressure in my eyes worse.
He wanted me to try a new eye drop called AzaSite (azithromycin ophthalmic solution) or an oral drug called Allodoy but my prescription drug plan does not cover either of these. They cost so much I cannot afford to pay for them myself. I plan to call my drug plan and appeal to them to PLEASE cover me on one of these prescriptions. I don’t know yet what answer I will get from them. At the present time I am using lower strength steroid eye drops and the doc is watching carefully the pressure in my eyes.
I still want the surgery on my left eye because of the times during the day that I can see very well and the brightness of colors. I feel EVERY LITTLE BIT helps. When the surgery is done on July 14 and is healed then we will work on the other problems and hopefully find something that will help without causing the Glacoma to get worse.
THANKS SO MUCH FOR ALL MY WONDERFUL FRIENDS ON HERE AND MOST OF ALL THANKS SO MUCH FOR YOUR LOVE, CONCERN AND YOUR PRAYERS.
GOD BLESS All Of YOU.

Prayers are always a good start to the treatment of any condition.

Be well
Hugz
Mac

so glad you are part of this amazing group joyce! Thanks for being so supportive to everyone. ;-) Hope you have a wonderful day.

Wow Joyce, you have had quite an adventurous ride. I admire your strength and positive attitude. Those two things take us very far. You go girl!

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Joyce's Stats

Posts: 14
Photos: 19
Events: 0
My Supporters: 18
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Comments: 65
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