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Kate Eckert

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Kate Eckert"I have learned to trust my gut feelings and to be my own advocate."

I was diagnosed with stage I breast cancer back in 2006. I was 32 years old and had recently decided with my husband to start trying to have a baby. My mother is a breast cancer survivor but I still was unaware of some of the warning signs and risk factors for the disease. I believed it was something that happened to older women. I just happened to find a lump when I was in the shower. I went to my doctor in Portsmouth NH and they referred me to a surgeon who did an ultrasound and biopsy that confirmed cancer. I had a lumpectomy and sentinel node biopsy. There was no lymph node involvement. My surgeon referred me to an oncologist who I went to see right after my surgery. He recommended that I complete chemotherapy and when I asked him about getting pregnant post treatment he responded " There is always adoption". I felt sick. I have always wanted to be a mom.

I just did not feel right being at that office so I did some more research and found that Dana-Farber Cancer Institute in Boston, MA had a program for young women with breast cancer. I was able to get an appointment with the head of the program and she was amazing. She explained that my cancer was hormone positive and that I would not reduce my risk of recurrence that much if I opted for hormone therapy. So we chose a treatment plan that included radiation and tamoxifen. She understood my concerns about starting a family and was really supportive of the idea after I finished my treatment. She understood that young women who are diagnosed with breast cancer have unique concerns and really made me feel like she was treating me as an individual. I have been taking tamoxifen for the last three years and I am cancer free and excited to try and start a family in the next few years after my treatment with tamoxifen ends. I have learned so much throughout my cancer journey. I have learned to trust my body. I have learned to trust my gut feelings and to be my own advocate. I think that the Early Act is so important not only to save lives through early detection but also to educate healthcare providers on the concerns of younger cancer patients and their quality of life.

Posted by BUILTIN BUILTIN at 10/09/2009 12:05:38 PM | 


Hi Kate, How are you. I'm so proud that you took action and became your own advocate. I was recently diagnosed with ductual carcinoma. I lost a sister to this monster a little over 1 year ago. Although, I'm older and have a family, each of us share a bond that only a breast cancer survivor can truly understand. When my sister was diagnosed, She was 36yrs old. Unfortunely her cancer was aggressive and found late, but she fought a brave 5yr battle. She always said to me that I was her rock. I thought I knew this illness inside and out. It's different when you are diagnosed. I strongly believe that women should be their own advocates and fight for their choice fo treatment. Sometimes its a tough battle. I do not have insurance, but my local cancer society helped me with my journey, and if it wasn't for them I may not have gone as often as I did for screening and a few biopsies.This last mammo showed a suspicous lesion and the rest is history. My breast surgeon is very hopeful and believes that I caught it early. I had the brac1 gene test, but because my medicaid is not complete the lab is putting my test on ice until my medicaid is completed. I'm on a mission more then ever to fight with any legislature that will listen that without these free screening centers for women without healthcare many will go undiagnosed or will just not go for their mammos. I'm confident that as a strong network of compassionate, courageous, beautiful women we can make a big difference. Good luck in kyour journey, I will pray for you. Warmly, Sue
Posted by: Su Foxman ( Email ) at 10/9/2009 6:38 PM


This was truly inspirational... thank you for putting your story out there!
Posted by: Olivia ( Email ) at 11/3/2009 10:51 AM


Hi Kate. Thank you for sharing your story. I am in the early process of something similar. If there was no spread to the lymph nodes, can I ask why your oncologist felt you needed chemotherapy, and your second oncologist felt you needed radiation and tamoxifen? I am trying to understand the rationale of different oncologists.
Posted by: Judy ( Email ) at 11/20/2009 8:45 PM


Hi Kate. Thank you for sharing your story. I am in the early process of something similar. If there was no spread to the lymph nodes, can I ask why your oncologist felt you needed chemotherapy, and your second oncologist felt you needed radiation and tamoxifen? I am trying to understand the rationale of different oncologists.
Posted by: Judy ( Email ) at 11/20/2009 8:49 PM


Hi Kate, thank you for your story. I just posted my story today too. I am 41 and just 4 months ago had a bilateral mastectomy. I had stage 1 DCIS-MI. To help the Judy with her question- I think that you probably had a lumpectomy and this is why you needed adjuvant therapy (to protect remaining breast). If you have a mastectomy as I did- and have no lymph involvment- and are stage 1- they are less likely to recommend any further treatment as there is no breast tissue left to protect. Congrats on being cancer free Kate and we all hope to hear about a baby soon!
Posted by: Scarlett ( Email ) at 12/17/2009 2:38 PM


HI KATE, HOW R U, now how r u feeling after operation. i think that your condition is so good. i really impress with ur story.


from
vipul jain
Posted by: vipul jain ( Email ) at 1/11/2010 4:17 AM


Hey! Thanks for sharing!
Posted by: John ( Email | Visit ) at 6/28/2010 5:41 PM


Hi Kate,

Thank you for sharing. I hope that everything turned out well!
Posted by: Tina ( Email | Visit ) at 6/28/2010 7:02 PM


Thank you very much for sharing your story.
Posted by: Nina ( Email | Visit ) at 7/10/2010 10:46 AM


Thank you. Hope that everything turned out well.
Posted by: Cathy ( Email | Visit ) at 7/15/2010 7:05 PM


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