Member Since: January 3, 2008
Last Login: November 7, 2008
Location: Cincinnati, OH United States
Occupation:
| Diagnosis: | Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
| Diagnosed: | June 7, 2007 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | No recurrence |
| Metastatic? | No |
| Stage: | Stage IIIa |
| Lymph Nodes Removed: | 20 |
| Positive Lymph Nodes: | 9 |
| Tumor Size: | 2cm-2.9cm |
| 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 |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Oct 22, 2008 09:00 pm
Scalp pain from Arimidex?Wishiwere, I was on Arimidex from May until early Aug. and had the exact same scalp pain and tenderness that you described. My onc switched me to Tamox in Aug. because my periods started again. melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Stage III Cancer, Created: Aug 14, 2008 04:18 pm
AvastinHi, I finished 6 months of weekly chemo treatments this past May. I received Navelbine weekly along with Avastin every other week. I can honestly say that I had very few side effects. Like others have mentioned I had very dry nasal passages and a little bleeding when I would blow my nose. I got tired more easily, but I think it was a combination of chemo treatements, rads, and surgery. I was getting pretty severe headaches on the premeds (Aloxi) so my onco took me off them and I didn't have any problem with nausea while on the Avastin. I hope this helps. Best wishes to your wife as she begins treatment. Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Aug 14, 2008 04:01 pm
Weird Arimidex SE? Hair?Wish, I've been having the same problems with my scalp since starting Arimidex in May. Although I haven't noticed considerable fall-out, it seems like my hair is thinning in one spot just above my forhead. I don't know if that area just hasn't really filled in yet from the chemo hair loss, or if it's indeed getting thinner. I keep asking my dh, mom, and friends if the area looks thinner. I know they think I'm crazy!! My eyelashes haven't really recovered completely from the chemo either. And my scalp is SOOO tender!! It hurts to brush it! Unfortunately the hair on my legs and face seems to be growing like a weed. :( Back to daily shaving! Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jul 26, 2008 07:17 pm
Anyone started Arimidex in 2008?Hi Tym, I had vision problems similar to what you're describing, but it happened before I started Arimidex. I finished 6 mos. of Navelbine/Avastin in May, but near the end of treatment both eyes got progressively blurry and cloudy. It was horrible! I couldn't read print or see the computer screen. I normally only wear glasses for reading. My optomolgist said I had an inflammation on my corneas, but he had never seen anything like it before. My onc was puzzled as well. I even went to a corneal specialist and he wasn't sure what is was. He put me on steroid drops. I'm convinced it was a SE from all of the chemo, even though it's one that has not been associated with the drugs I was on at the time. Putting all of these drugs and such into our bodies definitely takes a huge toll. We are all so different in how our bodies respond to treatment. The good news is that my eyesight did clear up on its own over the course of 2 weeks. I went in for a follow-up a few weeks ago and my eyes are completely back to normal. I hope your eyesight clears up quickly. Let us know how you are doing. Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Connecting With Others Who Have a Similar Diagnosis + Stage III Cancer, Created: Jul 22, 2008 11:51 pm
5 yearsMary, I'm so sorry for your recent diagnosis. I was initially diagnosed as Stage 2 in June 2007, but after surgery in Nov. (I did chemo first) the docs discovered my cancer had spread outside my lymph nodes so I immediately got bumped to stage 3. Not at all what I was expecting! I agree that it's very overwhelming to think about. I'm 44 and my children are still fairly young-10, 8, and 6. I made the decision right after I was diagnosed to not even think about how many years I would have to live. My onc has never recited stats to me either and has been very optimistic and hopeful that I will beat this cancer. I really appreciated that! Like so many others have said, this site is such a wonderful place for encouragement and support! I read these boards for so long before I joined the community--I wish I hadn't waited so long! The road before you will be difficult and bumpy at times, but you will get through it. Surround yourself with those who are positive and love you and allow yourself to receive help from whomever offers it. Take care of yourself, Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jul 18, 2008 08:07 pm
Anyone started Arimidex in 2008?Wish-I'm sorry your symptoms are worse this week. Does your scalp tenderness come and go? Mine seems to. I got my hair cut today and it hurt like the dickens when my stylist was brushing out my hair! Now that I finally have hair again I'm so fearful that it's going to start falling back out. :( I also started spotting a little bit this week for the first time in a year. Something else to worry about! Tym-I pray that you are one of the fortunate ones that have minimal SE's. This is my second month on Arimidex and (so far) my SE's are not too bad. Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Jul 18, 2008 07:43 pm
What is"cording"?Ladies, Thanks you so much for all of the great info and for sharing your experiences! It gives me a clear idea of what to look for. I'm 8 mos. out of surgery and last month I experienced some tenderness and pain in my right arm. I didn't have the range of motion that I had prior to this happening and it hurt to stretch my arm. I didn't have any swelling and I didn't notice any cording as you described. I stretched daily and have been doing yoga and it cleared up on it's own, thank goodness. Like many of you said, doing the exercises and stretching seem to be important. I had an ALND so I know I'm at a greater risk for LE. Kira-thanks for the links to the references! Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Jul 17, 2008 05:02 pm
help for newbie to topicBinney, Thank you so, so much! The study you quoted is excellent! I will definitely use that as a resource to show my docs. I felt in my gut that I should probably seek the help of a LE therapist right away, but, of course, my docs were saying "wait and see." It definitely makes more sense to be proactive, especially when dealing with something as serious as LE. :( Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Jul 17, 2008 04:49 pm
What is"cording"?Hi Ladies, I've been reading the boards regarding LE recently, as I'm at risk to develop it, and I've noticed that several women have mentioned that they've experienced "cording" in their arms. Could someone please explain to me what this is and what to look for? Thanks so much!! Melissa Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Lymphedema After Surgery, Created: Jul 17, 2008 12:00 am
help for newbie to topicHi Binney, My situation is similar to MBpetit. I had a right mast. in Nov. with ANB and 9/20 nodes. Overall my recovery has been good, but in June I had some tenderness/stiffness in my right arm for about a week that I have never experienced before. I mentioned it the PA when I was at my onc's office for a follow-up since starting Arimidex. She didn't seem overly concerned--just told me to keep a close eye on my hand/arm for any swelling. You offer such wise counsel for all of us on these boards and I would value your opinion as to whether or not I should make an appt. with an LE therapist at this point in time. I'm so worried that what I experienced in my arm is the beginning of LE! My arm feels fine now. I have been doing daily stretches and try to do yoga 3 - 4 times a week. It really seems to help with the stiffness. I, too, really appreciated all of the information you posted above! Thanks so much for taking the time to listen and share! Melissa Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Jul 11, 2008 06:40 pm
Is Sugar a link to Cancer?I'm totally confused about the sugar/cancer connection! It certainly makes a lot of sense. I presented the sugar question to my onco right after I was diagnosed. Basically his comment was that if sugar fueled cancer cell growth then people with diabetes would have a higher incidence of cancer than the general population, and he hasn't seen any studies to support that. That seems to make sense too, although I'm sure the science behind it is much more complicated than that. I'm truly starting to believe that there is no rhyme or reason as to who will get BC. Sure there are things that can increase our risk, but even women who are strict vegetarians, exercise regularly, and have no family history get BC. During that same visit my onco told me not to blame or second-guess myself for the BC. It was just what I needed to hear! I had this running tape in my head wondering if it was something I ate (or didn't eat), or did (or didn't do), or stressed about that could have caused my BC. His comment helped me focus instead on getting better and getting rid of the cancer. I do think we should try to avoid refined sugar and processed foods and strive to eat healthfully, but I confess I still have to have a piece of dark chocolate each day and an occasional ice cream cone! :) If any of you have come across some helpful studies regarding the sugar/cancer link I'd love to read them. thanks! Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jul 7, 2008 11:16 pm
Arimidex BeginnerOmahaGirl--Like you said, "whewwww!" Your body has been through a lot in just a short period of time. Allow yourself the opportunity to rest and heal and ease slowly back into things. I know after each treatment I often felt as if I had been run over by a truck. I just had to give myself permission to take naps and not feel guilty if something didn't get done. Sometimes it's so hard to know whether an ache or pain is normal or if it's a SE. I've been on Arimidex for over a month and had a few hot flashes at first, but haven't noticed any recently (makes me wonder if the drug is working!). Like WishIwere mentioned, stiffness and aches in the muscles and joints seems hit most of us on Arimidex. And my brain has definitely suffered from the chemo and drug treatments. Very frustrating. I find myself making more lists and writing notes to myself to remember things. :) Take care of yourself! Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jun 29, 2008 10:57 am
Anyone started Arimidex in 2008?I'm wondering if any of you have experienced bloating or feeling like you're full since starting Arimidex? I've been on it for a month now and just always seem to feel bloated, like I felt right before starting my period. I haven't noticed any significant weight gain, maybe a pound or 2. I've had a few hot flashes, tender scalp, and the usual stiffness in the AM, but at this point my body seems to be tolerating Arimidex pretty well, thank goodness! Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jun 20, 2008 08:04 am
Anyone started Arimidex in 2008?I'm also questioing whether or not I'm really in memopause for good. I'm 44 years old. I haven't had a period since last summer after I started chemo. Blood tests showed that I was indeed post-menopausal so my onc started me on Arimidex. I experienced a few hot flashes initially, but haven't really noticed any in the past few days. I've also had extreme vaginal dryness, plus my face is breaking out a bit. I've noticed a little bit of a discharge (not bloody) which I haven't had in months! I feel like my hormones are going crazy! I guess I'll wait it out to see if I start my period again. But it IS frustrating waiting and wondering if I'm taking the right medication. Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jun 17, 2008 08:07 pm
Anyone started Arimidex in 2008?Wishiwere-- It's SO nice to know that I'm not crazy either!! Every time something feels different I wonder if it's an SE or if I'm totally imagining that an ache, pain, tenderness exists. I've read that other women have experienced hair thining as well and I'm truly praying that that's NOT the reason that my hair hurts! I guess I can add hair aches to the ever-growing list of BC side effects!! Princess--I experienced vision problems during the last month of treatment while on Navelbine and Avastin. Both eyes became totally blurry and cloudy, like I had a thin veil over my eyes. My onco and 2 optomologists were totally baffled and called it an "inflammation on the corneas." It gradually cleared up after 2 weeks on steroid drops. I'm convinced it was a SE from chemo, but the docs weren't so sure. So far I've had no problems with vision since starting Arimidex. I hope your eyes heal completely on their own as well. Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jun 17, 2008 06:41 pm
Anyone started Arimidex in 2008?Wishiwere, You mentioned "hair aches" in your last post and am wondering if I'm experiencing the same thing. I've only been on Arimidex for a little over 3 weeks and I was noticing that my scalp feels tender in some spots--similar to when my hair fell out on chemo. I was thinking it may have been from being out in the sun over the weekend. Is that what you've experienced? I, too, love these threads for the much needed emotional support. Many of us have chemo and surgeries behind us, but we still fight this disease daily, and the Arimidex is a reminder of that. I have an amazing, supportive family and community of friends who blessed me tremendously through treatment and surgeries. But now that I've made it through those things and "look good" I think many people think that I have completely won the BC fight and can now move on with my life. I certainly don't fault them for their thinking because most have never had cancer and have experienced what we have. But it's so nice to have a community of sisters who understand and are so willing to share and listen. Thank you!! melissa Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jun 5, 2008 10:00 pm
Anyone started Arimidex in 2008?I, too, started Arimidex on June 2 and so far have not noticed any changes or SE's. I did wake up with a headache on the second morning, but don't know if the Arimidex caused it--I'm prone to headaches. I'm trying to exercise daily (doesn't always happen!) and keep active with my children. I also started drinking 4 oz. of a seaweed supplement called LIMU each day that was recommended by a friend of my mom's. Maybe that's helping in some way??? I'm praying hard against SE's and am trying to take one day at a time. It's too overwhelming to think about 5+ years of Arimidex and potential SE's. Blahhhh! :( melissa Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Jun 1, 2008 11:08 am
Anyone started Arimidex in 2008?Hi ladies, I will be starting Arimidex this week and am very nervous about taking it. I just finished 6 months of Navelbine and Avastin. I started treatment last July with 8 rounds of AC/Taxol, then lumpectomy, right mast., and rads. I'm celebrating the fact that I made it through a year of treatment and just don't want to put anything else into my body right now. But I'm also afraid to NOT take it! Blood tests confirm that I'm post menopausal. I'm so glad that this thread was started!! I'm looking forward to being a part of this community! Melissa Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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Tests, Treatments & Side Effects + Breast Prostheses and Reconstruction Alternatives, Created: Mar 10, 2008 09:19 pm
Bathing suit came todayCarol, I just received a Nicola Jane catalog, but have also been looking at suits at Land's End. I like the Nicola J. styles better and am wondering if you're happy with the suit you ordered. Thanks!! Melissa Dx 6/7/2007, IDC, 2cm, Stage IIIa, Grade 2, 9/20 nodes, ER+/PR+, HER2- |
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