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Last Login: November 22, 2008
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| Diagnosis: | Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
| Diagnosed: | March, 2002 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | |
| Metastatic? | |
| Stage: | |
| Lymph Nodes Removed: | 8 |
| Positive Lymph Nodes: | 3 |
| Tumor Size: | |
| Tumor Grade: | Grade 2 or medium grade |
| Hormone Receptor Status: | Tumor has both estrogen and progesterone receptors |
| HER2/neu Status: | Tumor does not have an excess of HER2/neu receptors or genes |
Posted in:
Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: 17 hours ago
HAPPY BIRTHDAY FIT CHICK MARIN!Marin, Just joining in to wish you the happiest of birthdays! Hope you get the BIG ONE (that means whatever you want it to mean in a good way!) Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: 20 hours ago
Scans, Scans and MORE scansWings of Hope, Sending you lots of good wishes that the rest of your scans are clear and that chemo blasts away those lung mets. It's my understanding that the PET does not include the brain, at least not when I had it. Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: 20 hours ago
stress testRooni, Sorry you have this on top of everything else. ER's seem to be the luck of the draw but I'm dismayed to hear that apparently they did not pay attention to your heart problem in a timely manner. In 2006, I also had a heart attack (not fun!). Had one stress test since. It did involve a treadmill and as I recall was about four hours long. I was injected with something (???), told to go sit and wait (the four hours mostly involved waiting!), then go back and be scanned, and so on and so on. It was a very long morning, but honestly, there wasn't anything freightening about it and I am the number one sissy on the planet. Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: Nov 19, 2008 07:51 pm
post lumpectomy painHi Jen, Glad your lumpectomy is over! That's a step in the right direction Pain/numbness two weeks later is very normal for most. The numbness may last quite a while. It's best to use an electric razor to shave underarms while numb. I remember going back to work after a week and still being in pain and I had numbness for quite a long time. Of course, we're all different and pain/numbness differ from person to person. As Lainey suggested, it also depends where the incisions are located. I was quite surprised (in a bad way) that I was in so much pain afterwards and had numbness, but eventually, it did subside. I had lumpectomy, SNB and AND, so perhaps that was the reason. My initial tumor was at the "2:00" position and the scar was large. It is best to speak to your doctor and get his take. If the pain is bad and you have pain meds do take them. I was a total dope and refused to take the pain meds and suffered neednessly. My best to you for a full recovery, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Not Diagnosed but Concerned + Waiting for Test Results, Created: Nov 19, 2008 08:54 am
Worried about metsTomatoJuice, First, my suggestion is to find an Onc that meets your needs and that you are comfortable with. It's most important to have trust and confidence in the doctors' who are treating us for cancer. As far as scans go, some oncs do and some don't. Generally, a baseline bone scan is taken in the beginning, so there is something to compare to down the line. A lot also depends on the type of insurance you have. Pet scans are expensive and need good justification to be approved. Just recently read an article that insurance companies are dilligently trying to reduce the number of scans to cut costs. In the future we're going to see many less scans receiving approval unless we have symptons (pain, high TM's, yellow eyes). Whether you do or don't change oncs, I would push for a bone scan at the very least. Also, some docs run tumor marker blood tests and for some (about 75%) they are telling of spread. You may also want to check w/your onc about your TM's, but be aware, once again, not all oncs use them. Most scans emit radiation (for instance, CT scans emit 20x the amt of radiation than an xray) and it's my belief that the less scans the better, but I agree with baseline scans. Of course not everyone shares this sentiment. Wishing you the very best, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 18, 2008 03:00 pm
Now I have liver metsThe swift trajectory of it is quite a shock. I'm so sorry this is the news you got. Fortunately, there are treatmens and I hope they're very successful and in ten years you'll be writing your story for others to read. Hugs, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: Nov 16, 2008 07:42 pm
I don't understandYes, it does happen to many of us and it's normal. I've never been in actual combat, but the BC experience is combat (to me) and definitely affects us emotionally. You're newly diagnosed and have had both of your breasts removed - that's enough to bring anyone to tears. It's good you're on effexor, but if you find it's no longer working for you then ask to change to something else. Happy that your nodes were clear, that's definitely good news. Take the very best care of yourself, mentally and physically. Wishing you continued good health, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 16, 2008 07:22 pm
Jodi (Jodian)Another young woman taken in the prime of her life by this ruthless killer. Condolences to her family. This is a tragedy beyond words. Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 15, 2008 10:16 pm
fatigue or depressionFatigue is a by-product of anemia, so to speak. Your doctor can determine anemia through a simple blood test. If in fact it is anemia, there are drugs or a blood transfusion that can give you back your energy. Check with your doctor about this and ask about options. Depression often comes with breast cancer for many. For some it's only temporary and for others it lasts much longer. There are many drugs for depression and it may be wise to keep trying until the right one is found. Also, if it is something feasible for you, adopting a dog can have a multitude of benefits. A dog will provide you with unconditional love and be your constant companion. Megan gave you good suggestions - joining a support group may prove beneficial for you and get you out of the house. It's important to talk to your GP or oncologist about your fatigue/depression and ask what can be done. Sorry you're in this position, but as Megan said, we're here for you. Hope this is a very temporary thing and you'll be feeling good real soon. Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Nov 14, 2008 07:12 pm
Where to buy?Hi Rose, Andrew Lessman has the purest vitamins that I know of, however they are expensive. You can check out his site for info. When I do buy I wait for sales or free shipping, it helps a lot. He also sells on Home Shopping Network and they also have sales and free shipping (on different products than his website). In not Andrew's, then choose a vitamin with the least amount of fillers that you can afford. As far as calcium goes, there are different types and some are difficult to absorb. You may want to do some searching online. You can also check out Willner's Chemists website: You can call Willner's and speak with a knowedgeable person about vitamins. All-in-all, don't break the bank but buy the best quality you can afford. Good luck, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 13, 2008 06:18 pm
Masectomy after lumpectomyShellyJo, I'm a big believer in peace of mind. It would be best to discuss your thoughts with your breast surgeon and explain to him that YOU will feel better removing both breasts (it's not about him - it's about YOU). If you don't like what he/she says, do seek another opinion. Also, your insurance company would have to approve. Honestly, it isn't about what we think - it's your body and your decision, and it's best to go with your feelings. I would suggest reading about mastectomy and looking at online pictures. Get info about reconstruction as well, if you choose to go that route. You look very young by your photo and I'm sorry you're dealing with this horror. All the best to you, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Stage III Cancer, Created: Nov 12, 2008 09:10 pm
How do I respond....This question, I have found is a common one. Is there a "right" answer? Dont know. Obviously, it does depend somewhat on prognosis. My answers to this question are varied depending on my mood and who's asking: "Whatever God wants it to be" "There is a lot of uncertainty with cancer and we hope for the best" "I'm alive and breathing today and that's all I care about" "The doctor hasn't recommonded me for hospice...yet" I do wonder why people want to know. If it is a bad prognosis, do they quickly want to convey that info to others? Oh geez, ran into Jelly today and she says she's dying soon. I just don't get the gist of that question, but I don't let it bother me anymore. All the best to you. Hope tomorrow is a better day. Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 12, 2008 06:40 am
Totally Great News!Such fantastic news! Prayers for everyone that all goes well. Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 12, 2008 06:37 am
Another AngelDear Michelle, My sincerere condolences on your Mom's passing. Yes, she is now an Angel and will look after you. You were a wonderful daughter and took such good care of her. Prayers and hugs to you, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 10, 2008 06:38 pm
Me, tooLisa, Wishing you extreme success with your treatment, but I'm very sorry these are the cards you've been dealt. As some of the others have said, "IT SUCKS". Hugs, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 10, 2008 06:34 pm
Overwhelmed!!!Carmen, What a shock it must have been for you today. Did you have an opportunity to speak with the onc and ask questions about your markers (if h/she does them) and other tests? What about other chemos that haven't yet been tried on you? These are questions for the onc to answer and not the nurse. I'm so sorry to hear you're in such distress. At least the oxygen is helping. Hugs and prayers to you, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Nov 10, 2008 06:27 pm
Brain Mets - Me Too #2CalGal, I'm sorry your facing this horrible condition. No one on the planet should have to endure mets to the brain. I have no words of wisdom, just prayers that the WBR will do its job and it will be the last time you'll be dealing with this. Prayers and hugs to you, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Nov 10, 2008 05:58 pm
AI versus mistletoeElisabeth, Good luck with your appointment and I hope h/she is the right doctor for you. I did find this page from the NCI on mistletoe: http://www.cancer.gov/cancertopics/pdq/cam/mistletoe/healthprofessional Come back and let us know how you are. Good wishes to you, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Nov 9, 2008 08:34 pm
AI versus mistletoeIt is well known that Suzanne Somers went the mistletoe route but I'm not aware of anyone else who took this. I believe it's expensive and am thinking it's not available in the US. You may want to check out PubMed for any studies. Good luck, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Nov 9, 2008 08:29 pm
Need help - what am I doing wrong?CP, You may want to call into a Dr. radio show and ask Dr. Hoffman this question. He is most knowledgeable about supplements and can most likely give you reasons/suggestions. He is one of the very few who has been into CAM for more than twenty years. Just an FYI...I've never met the Dr (his prices are waaay out of range for my wallet) but have listened to his radio show for years. Just wish I could retain all the good info he disseminates. Here is his website with his radio schedule: http://www.drhoffman.com/page.cfm/53 Good luck, Jelly Dx 3/2002, IDC, Grade 2, 3/8 nodes, ER+/PR+, HER2- |
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