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 23, 2008

Update On My EyesViews: 578

Hello everyone. I am sorry I have not been around much in the last month but my eyes have been bothering me. I have also been feeling kinda down and I know I shouldn’t. Most of you have much bigger problems than I have. As I told you earlier my cataract surgery went very well. My eye sight is doing something that I (or the eye surgeon) don’t really understand. It fluctuates all during the day. When trying to get a reading for my eyeglass prescription the eye surgeon got 2 completely different readings within a 30-minute time frame. This happens all the time. At times I can see 20/20 without my glasses and then an hour or so later things are more like 20/50 or worse. Last night at one time my right eye seemed almost as bad as it did before the cataract surgery. This morning I can see good again.
I also have a condition called Blepharitis which I have had since my last chemo in May of 2006. Blepharitis is inflammation of the eyelids. This condition is a lot like Pink Eye but is not contagious. Dr. Robertson says he thinks this happens because the fluids in my eye are not working properly and are not washing the irritants out of my eyes. I have been on 1% steriod eye drops since June 2006. He has been trying to get me off this eye drop because it raises the pressure in my eye which caused me to have Glacoma. Every time I stop the eye drops my eyes get red, irritated, matted up and it hurts to keep them open or to be in daylight or a bright light. My right eye was so bad last week that he had me use antibiotic eye drops and he also prescribed an antibiotic in pill form for the next 6 months.
I think about all of you and says prayers for all of you but it is just hard to answer everyone when my eyes are bothering me. All I want to do is just close them and rest.
Please remember you are in my prayers even when you don’t hear from me.
GOD BLESS AND BE WITH ALL OF YOU, MY FRIENDS.
Love and hugs,
Joyce

Good to hear from you, young lady. I will keep you in prayer.

Feeling kinda down seems to be a theme here lately. I hope you feel better and find a positive way to dump the blues.

Hugz
Mac

Good to hear from you! Those eye problems would get me down too! Its interesting about the vision changes throughout the day. I had lasik done about a year ago, and sometimes I get that too. I’ll wake up and see fine, then later in the day it will get all blurry, then back to fine. They told me that would happen. I hope you find relief soon!

XOXO

Glad to hear from you. Eye problems would get anyone down so don’t feel bad I believe we all understand. I hope they can work it out for you. My 94 year old dad has Macular degeneration in both eyes it drove him crazy when it happened but he has adjusted well. I sure things get better…
Cheryl

They told me to expect the vision changes for at least a year. Well, its a year now…I hope it stops soon! My changes don’t sound as severe as yours. It happens a lot when I’m on the computer too much. lol Or when I get tired. Which antibiotic are you on? Hopefully that helps, because I’m sure a lot of your vision changes are caused by the pressure changes. Keep us posted!

Thank you Joyce. I am near the end of my treatments My Dr. took me off the Xeloda I don’t know about the chemo yet I see him on Weds. of this week. It is hard for me with my family both my sisters are older then I am and neither one is in good health them selves. My daughter is very busy this time of year and she has a new boy friend she hasn’t seen my feet since they got this bad. I am hoping they will start doing better now that I am off the Xeloda.. You hang in there also
Cheryl

Joyce thank you again for caring it helps to know I am not alone. I was reading your bio. I am so sorry to hear of your losses. I am also a widow my husband died in 1990. I have one daughter who lives with me. She struggles with her life can’t seem to get it together oh well. My feet seem a little better this early am so I will be going to work in about 2 hours. I am glad your cancer seems to be gone. I wish mine would go away for awhile give myself a rest. It amazes me how much the body can take. I will know more come Weds. this week I see the Dr. and my CT scan results should be in… I feel pretty good about this one I hope I am right. Take care and I will let you know what happens
Cheryl




Joyce's Stats

Posts: 21
Photos: 24
Events: 0
My Supporters: 23
I Support: 61
Comments: 99
Views: 15025



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.