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Last Login: May 31, 2008
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Posted in:
Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: May 31, 2008 10:04 am
Help/QuestionI too can relate to your fears. The protocols of my oncologist (at one of the top five oncology centers) also do not include any testing or scanning post treatment. It was very helpful to me when my oncologist responded to my fears by saying that the best advice she could give me was to "wear your seat belt as you are more at risk to die from an accident." Sounds crazy but the statement was comforting. I am 2 years post diagnosis and 1 year thus far of taking Tamoxifen. A book I found very helpful and have reread it many times is: "After Breast Cancer: A Common-Sense Guide to Life After Treatment" by Hester Hill Schnipper. It is available through Amazon. It helped me understand that my fears were normal and also provides some strategies to help move on. Take care,
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Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Oct 6, 2007 09:52 pm
re: Determining recurrence tendency?I just had to respond to this thread. Even though I had bilateral bc with bilateral mastectomies and 4 positive nodes and am Stage II, my oncologist told me at my last visit when I was focusing on reocurrance, "The best advice I can give you is to wear your seat belt!" For some strange reason, this has been very reassuring to me. |
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Support & Community Connections + High Risk of Recurrence or Second Breast Cancer, Created: Jan 15, 2007 05:08 pm
Positive lymph nodesI too had positive nodes with 1 out of 14 on one side and 3 out of 11 on the other side. I am still in the midst of agressive treatment with bilateral mastectomies, DD AC and T, radiation and then onto hormone therapy. These positive nodes really worry me too and I don't know how I am going to deal with it in the future. I have been starting to think about what my new life will be like once radiation ends and am hoping that I can live without worrying and dread but I am unsure too how to accomplish this.
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Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Dec 21, 2006 04:49 am
I just tested Bellisse BrasHi Peggie,
I am so glad they are trying to improve the Bellisse bras. I have bilateral truncal lymphedema and the Bellisse bra does work well for me. I learned through trial and error that I needed to adjust the bra straps so the bra went as high as possible in the axilla area. I find the bra straps thick and are visible through clothing which is a problem for me. If they need another tester feel free to PM me! |
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Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Dec 9, 2006 02:53 pm
Finally got appt. with Lymph massage therapistCathy,
It is great you have found a lymph massage therapist. In many areas they are hard to find. The sessions are so relaxing and educational. I have truncal lymphedema on both sides and it drives me crazy. Thanks to my therapist, the pain and swelling have decreased markedly and I now feel able to help myself cope with this chronic condition. Take care, SusanJean |
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Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Nov 11, 2006 09:50 am
Blood draw from foot--how does that work?This thread is making me pose the question: Can ports stay in indefinately as long as they are flushed according to the manufacturer's procedures?
I ask because I had a bilateral mastectomies in June 06 and am just finishing up chemo. I had a total axillary lymph dissection on one side with the initial surgery. I am now told I need a total lymph dissection on the other side once chemo is done and before radiation starts. My surgery is scheduled in December. I am so scared of lymphedema and actually think truncal lymphedema has started and am seeing a therapist for my first appointment in two days. Like many of you, I will be facing the issue of no sticks in either arm for the rest of my life. How long are ports allowed to stay in place? Are ports ever placed or replaced due to the risk of lymphedema? I have been so impressed with the knowledgeable people on this thread. Hopefully one of you has faced this question before. Best to everyone. SusanJean |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 11, 2006 09:24 am
Is Anyone Starting Chemo In Aug 06RoundTwoinCA,
I am taking Abraxane too but all by itself. The only GI side effects have been diarrhea and excess gas, none of the stomach problems that are troubling you so I don't have any good suggestions. The unpredictability of the fatigue is a problem though. I am finding the fatigue is becoming cummulative and now hitting me up to 5-7 days after the treatment. It is so much different than the A/C was. I am very fortunate to be on STD though so I can just go with the flow and don't have to manage or predict a work schedule. If the fatigue is hitting you later now rather than earlier would changing the infusion day to earlier in the week help? It seems like very few things are predictable with this disease and treatments. It makes me so angry. SusanJean |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 9, 2006 05:59 am
Is Anyone Starting Chemo In Aug 06Hi Erica,
I too need to have more surgery when chemo is done. I have one more chemo infusion and then need to have an axillary lymph dissection done. Uggghh!!! During my initial surgery, bilateral mastectomies, the sentinal nodes were negative for pathology so total lymph dissection was avoided. But then the final path report came back with 3 out of 4 positive nodes so now everyone says there is a 40% chance of cancer hiding out there and they should come out. I am very nervous because I am afraid of lymphedema issues now on both sides as a total lymph dissection was already done initially on the other side. Not to mention that this additional surgery will delay radiation treatments and make this long road to recovery much, much longer. I see that you too are from Mass. I live in the southeastern region but travel to Dana Farber for my treatment. I am confident though that they are recommending the right things for me. I don't want to regret in years to come not having the surgery if mets occurs. None the less, I don't want to do it but I will. Did you have unclear margins? Take Care, SusanJean |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 29, 2006 03:03 am
Is Anyone Starting Chemo In Aug 06Erica, I have finished my second of four DD Abraxane treatments. After the first dose I had neuropathy of mostly my toes and leg with hip and leg achiness requiring a narcotic at night and lots of motrin during the day. The second dose strength was decreased because of these symptoms and the side effects are much less as a result. The neuropathy has improved and the achiness in much less. Other than fatigue I have had no other significant side effects on the Abraxane; it is much easier to tolerate than AC.
SusanJean 51 Stage 2, er+ pr+ her- bilateral mastectomy June |
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Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 26, 2006 05:18 pm
Starting chemo in Sept. 06I didn't like the cold spray that they used on my port. I thought the cold spray was painful. It felt like I was getting frost bite. The cream I use now is called Lidocaine-Prilocaine Cream 2.5%. It is a prescription. Apply a thick paste of it over the port about 1 hour before the port is to be accessed for drugs or blood draws and then cover it with a piece of saran wrap. They will wipe the cream off before cleaning the skin. I have had no port pain at all using the cream and highly recommend it.
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Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Sep 22, 2006 05:29 pm
Is Anyone Starting Chemo In Aug 06I only recently discovered this discussion board and have learned so much from all the posters in all the threads. I am so inspired by this awesome site - chuck full of knowledge and support. I hope it is not to late to join the August group. After starting on August 10th I just finished my 4th AC treatment yesturday.
One of my biggest challenges has been insomnia. Despite a variety of drugs, four hours seemed to be the maximum number of hours I could get week after week. I thought I was going to loose my mind! My oncologist thought maybe hot flashes were causing me to wakeup along with perhaps some depression and anxiety issues. She prescribed Neurontin often used for neuropathy but with BC patients is also found to be helpful with hotflashes. I have taken it for a week now and have been sleeping like a baby!! I thought I would pass this along for any one suffering from sleeplessness to discuss with their oncologist. Diagnosed as Stage2 ER+ /PR+ NEU- and had bilateral mastecomies on June 30th. Chemo started with AC every two weeks x 4 on August 10th and will be followed by a Taxane every two weeks x 4. |
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