Blog for a Cure - A community of cancer survivors supporting each other. Log in

avatar

Vitals


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 2 – Lump was 2.4 cm. – 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 1 – Lump was 1.6 cm. 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

August 27, 2008

ANSWER TO LISA'S (LITTLE PRINCESS) QUESTIONViews: 516

THIS POST IF IN ANSWER TO LISA’S (LITTLE PRINCESS) QUESTION ABOUT THE ANTIBOTICS THAT I WAS TAKING FOR MY EYE CONDITION.
Yes, I remember in 1994 how BAD EVERYTHING TASTED. The only thing I could stand was pretzels and milk. I worked in the office for Pepsi-Cola from 1973 to 1974 and I have ALWAYS LOVE PEPSI. Well, my Pepsis that I always loved so much tasted awful. I could not stand to drink them during the chemo. I completely quit drinking Pepsi or Coke several years ago and replaced them with water.
Ok, back to your question about my eyes. I was on Vigamox antibotic eye drops during the surgery and for the past 2 weeks to clear up the inflamation of my eyelids but I am off that now. I am on Predniselone Acetate Ophthalmic Suspension 1% and have been on it since June 2006. I have used it anywhere from once a day to four times a day. I also use Optive 3 or 4 times a day for my dry eye ondition. My eyes were very bad before the surgery but my eyesight didn’t fluctuate the way it does now. My doctor just prescribed an oral antibotic Doxycycl Hycl, 20 mg, for maybe 6 months to see if that helps the Blepharitis condition. You said they told you to expect the changes for a year. Well, I have until next June and July to deal with the changes if that is the case. I hope yours soon begins to improve. I like my eye surgeon and I think he is good. What really bothers me is that he did not tell me to expect this and he doesn’t appear to know why it is happening.

Hi Joyce; Glad to see you back. I posted a “Where Are You”, alert cause I hadn’t seen you for a while, so I’m pleased that you have landed. So sorry to hear about your eyes not working out the way you thought it would. These damn Dr.’s never really tell all, so it is hard to know whether they are surprised about the outcome or it is usual stuff. Perhaps with time you will find that your eyes will adjust more. My stepmother went through both too, after chemo and she found it difficult for the first 8 months. So hang in there it might just get better. Hope eveything else is fine with you. Guess you had a great visit with your daughter and grand kids. What a lovely summer to do this in. Take care and see you on the blog again, no doubt. Weezie

Good to see you up and about. Hope all is well and healthy

Hugz
Mac




Joyce's Stats

Posts: 21
Photos: 24
Events: 0
My Supporters: 23
I Support: 61
Comments: 98
Views: 14256



Become a Supporter



Blog for a Cure Info

Blog for a Cure spends about $200 a month to keep this site up and running.

If you wish to become an advertiser or want to read more about the company please see our advertising page.

All proceeds, if we ever have any, will go back into building a better system.

Thanks for your support - Jill, Founder, Cancer Survivor

p.s. If you have any suggestions on how to improve Blog for a Cure, please send me some feedback. The last thing I want to do is offend anyone with too many ads. Please keep in touch & let me know how I can make this the best system possible for you.