Skip to content
Forum IndexCommunity Member List → Profile for deem

Member Since: January 25, 2006
Last Login: February 19, 2008
Location: elkton, fl United States
Occupation: hospital administration

Biography

stage IV, bone mets, mets in Jan 02, her+, estrogen +

Diagnosis

Recent Posts by deem

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Feb 15, 2008 12:12 pm

I need info on plural effusion

MJ

I have had bone mets for 6 years now.  After I had chemo for a year with radiation to my mid back and sternum area.  I developed pleural effusion on my left side.  They drained it twice checking the fluid and it never showed any signs of Ca.  After about 3 years, it went away on its own (or the grace of god!)  I had started excising more and believe that may have help it heal.  But there is many reasons for pleural effusions not just cancer.  Hope that helps!

Posted in: Connecting With Others Who Have a Similar Diagnosis + HER2/neu Positive Breast Cancer, Created: Mar 2, 2007 08:09 am

Herceptin & hair growth

Karen,

I have been on herception for 5 years and I have talked to many women about this. Yes, it does slow down your hair growth and my hair is not as thick either. However, Denny is right and good diet and exercise will help!
Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Mar 2, 2007 07:43 am

14 years with stage 4 this month

Hi all and Kathy,
Kathy, thank you for taking the time to post, I know how busy life can get. I have not posted in over six months because I moved and started a new job. I just celebrated my 5 year anniversary for metastatic bone and I am doing great. Nobody at my new job has any idea that I have cancer much less bone ca. But we always have the 'fear' in the background so to hear of a 14 year survivor is just plain 'cool!'

Please take care and thank you!
Posted in: Support & Community Connections + Get Togethers, Created: Mar 5, 2006 06:50 am

MI Survivors

Ladies,
Thank you for sharing the pictures. It looked like you all had a great time.
Irene, I live just north of Imlay City (about 10 minutes) so that would be great but I can drive with no problem. I will keep an eye on this site now and hope to met all you ladies soon.
Dee
Posted in: Support & Community Connections + Get Togethers, Created: Mar 3, 2006 11:19 am

MI Survivors

hey Michigan ladies,
I wanted to thank Nancy for contacting me about this site, I have only been on line since January and had not explored this forum yet but I will now! I am so sorry I can not join you all tomorrow but we have plans in Windsor for a 85 year old birthday party. But I look forward to joining all of you next time and I will remember to look at this site as well. I hope all of you ladies have a great time and thank you again for thinking of me, I really appreciate it!
Dee
Posted in: Recovery, Renewal, & Hope + Biographies of Breast Cancer Survivors, Created: Jan 29, 2006 12:25 pm

Bios of BC Survivors

Hi all,
Just found this site last week so wanted to give my bio. I was first diagnosed at age 34 with in situ ductal ca. Had a left masectomy and reconstruction with saline. 9 1/2 years later, I kept having mid chest pain and they were treating me for inflammed cartridge between my ribs and sternum for over 6 months. Then I found a lump in my neck. Immediately had a biospy only to find more cancer. After the bone scans and cat scans, we found out it was mets to bones including the sternum, ribs, spine, hips, scapula and left humerus.
I use to do Radiation Therapy so I made out my will! I had taxatere, herception and zometa for 12 straight months every week with herception then every 3 weeks with taxatere. Plus radiation to my chest and back for six weeks. Man was I sick. My son was graduating in June when we found out in January and I prayed everyday to make it to his graduation.

I just had my FOUR year anniversary and I just met my son's girlfriend (pretty serious!) from college. I could go on and on but I guess my point is, Never give up! They are coming out every day with new mediation. I know some of us are in clinical trails so we seem like the little lab mice but if it will save one more life down the road, what do we have to lose! Hang in there ladies and God bless.

© 2008 Breastcancer.org. All rights reserved.