Member Since: April 10, 2008
Last Login: November 14, 2008
Birthday:
Location: NJ
Occupation: 1st Grade Paraprofessional
| Diagnosis: | Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
| Diagnosed: | March 27, 2008 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | No recurrence |
| Metastatic? | No |
| Stage: | Stage IIa |
| Lymph Nodes Removed: | 13 |
| Positive Lymph Nodes: | 1 |
| Tumor Size: | Less than 1cm |
| Tumor Grade: | Grade 1 or low 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:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 12, 2008 07:31 pm
Starting Chemo May 2008Jen, Would you like a chocolate wig? Would that help? Check this out. http://www.smh.com.au/ftimages/2003/11/14/1068674353606.html If it doesn't post as a link just copy and paste Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 12, 2008 07:26 pm
Starting Chemo May 2008 |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 12, 2008 06:34 pm
Starting Chemo May 2008Otter oh wise one, I knew you would know something about the facial hair. Maybe there is a bit of hope for me. As I said before I had the facial hair going on before chemo but it came back with a vengeance. Maybe some of it will leave and will just be the annoying fuzz I had before. Linda I don't have any food aversions but do have smell aversions. During chemo I loved the smell of Dial kitchen hand sanitizer soap, Olay body butter ribbons with jojoba butter (body wash) and Lysol Spring Waterfall scent. As a matter of fact you might remember me telling you that the Lysol smell took me back to a happy time in my life. Now the smell of these will make me sick and start to gag. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 12, 2008 04:57 pm
Hair Hair Hair - Another questionEyebrows and Eyelashes I am now 15 weeks to the day since my last chemo. I NEVER did loss all my eyebrows. They first thinned out at the insides. I used powder to fill in. By the time the outside started to thin the inside had grown back. As for the eyelashes they came out in cycles so I never went lash less. I think it was somewhere between weeks 5-8 that they started to fall out about 3-6 each eye every weekend. By the time the next week rolled around the ones that left before had already grown back. If I start to loss them for a second time I hope they go and come like they did before. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 11, 2008 09:06 pm
Hair Hair Hair - Another questionOtter, You said "but curling and wavy and fairly thick." When did it start to curl? The picture you posted last month it was straight. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 11, 2008 08:52 pm
Starting Chemo May 2008Facial Hair I hate to be the bearer of bad news but I think this might be. If my understanding is correct, doesn't chemo and or Tamoxifen throw your body into early menopause? The peach fuzz facial hair is acquired during menopause. I already had it before chemo. It was the last of my hair to leave and the first to reappear with a vengeance. I hope for your sake I'm wrong but if I'm right don't plan on it leaving. Oh and Rock don't shave again. It will return thicker. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 10, 2008 05:12 pm
Starting Chemo May 2008It's good to be back. Still haven't had time to read and catch up on what I missed. Sneaking a few minutes now to check in before hubby gets home and I have to do the diner thing. Update on me. My right breast almost looks normal again. Only skin still left to peel is at the boost area. Last treatment was a month ago. I bought a blow dryer for my hair. The towel no longer dries it. Side burns are starting to peek through my wig. Don't know what I'm going to do. I don't want to get another wig but it is still too short to go topless at school. Last year when I had long hair the kids would laugh when I took off my glasses because they said I looked like a guy. Then again the kids could just call me Mr. Karin if they want. Will post a new hair pic soon. I have been on Femera 3 ½ weeks and so far so good. Have noticed a few hot flashes or Flush-flash as Rock calls them. Usually during the evening or at night while sleeping. Can handle these with no problem. When going through menopause I suffered real badly with Funeral-pyre flashes (Rocks term). Back then the only thing that gave relief was soy protein powder mixed with milk. Drank it daily for over a year. As the song goes, I wish that I knew what I know now, when I was younger. If I suffer from those again I will have to deal with them or ask onco for something. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 9, 2008 02:21 pm
Starting Chemo May 2008All, Sorry you haven't heard from me in awhile. Thought I would pop in before you start worrying about my absence again. I have been really busy and haven't had time to use the computer. Will try and get on later tonight and catch up on what I've missed. Hope all is well for all of you. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 20, 2008 03:40 pm
Starting Chemo May 2008Too much catching up to do and no time to do it now. My step father passed away last Wednesday night. I have been with my mother since Friday and just got home last night. I wasn't near a computer. The service and internment are tomorrow. Don't know when I will be online again because between my sister, mom's friends and myself we are keeping vigil over her. She is still not ready to be left alone. Don't know if I have another shift to pull. Just wanted you to know I'm still around and haven't left. Randie - my thoughts and prayers are with you. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 14, 2008 06:09 pm
Starting Chemo May 2008Eddie - Happy Anniversary! I was on Taxotere. Tomorrow will be eleven weeks out. I never had the burping thing but I do still have slight tingling in the ball of the left foot. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 13, 2008 04:55 pm
Starting Chemo May 2008Jen, I forgot to answer your question about the wig. Before going I had touched base with Mary Anne the person that did the make over. I had sent her the photo of me that used to be my avatar so she had an idea of my face shape and coloring. At her shop she specializes in Curly Hair (has something in common with our own Noelle) and Hair -Loss. She told me to bring my wig but she had one that she thought we could have fun with. At the make over she didn't seem to care for my wig and wanted to try hers. I warned her if she put it on my head and I liked it she might have a hard time getting it back. She said she kind of suspected that and it was alright I could have it if I liked it. Well I did and I brought it home with me. The American Cancer Society also brought one of their Look Good...Feel Better make up bags for me. Since we used Mary Anne's make up and didn't use it I gave it back so someone that needs it can have it. I already have one from when I attended one of their class. I didn't want to be greedy. As I mentioned early the greatest thing I brought home with me was the experience and memory of meeting with Dr. Weiss and letting her know the bond she had enabled to be created among our group here. Sue - Enjoy your time of silence Adrienne - Your eyes look gorgeous Everyone else - Love you gals P.S. Jen, Sue, Adrienne your included in the Love you gals, LOL Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 13, 2008 11:38 am
Starting Chemo May 2008Beating the Odds Against Breast Cancer update I still haven't seen the broadcast myself. As of yet there is no link on ABC for a video. I am still waiting to hear if there will be. My family told me that on the first shot I looked very nervous. I knew this before they told me. Because it was a live show we did a quick run through before hand. During the run through the camera was only on me for a little bit. During the live show the camera stayed on me longer while they introduced me. Rock called my smile a Million Dollar smile. My husband calls one of my smiles a dumb grin. I know which one he is referring to because it is a dumb grin. So when the camera didn't move off of me I was thinking am I doing the dumb grin or am I OK? Thank God the only time I had to talk was when the host asked me "So Karin how do you feel? I wanted to be creative and respond with "Thanks to the American Cancer Society and Mary Ann I now Look Good and Feel better". After all that was the reason for me being on the show, to promote the Look Good...Feel better program. Instead my nervousness took over and I gave a quick either Fine, thank you or Good, thank you reply. I don't even remember which one it was I said. To sum it all up I am a little embarrassed of myself on air. My family told me I also did my nervous twitch thing. I wear dentures and sometimes when I am nervous I suck my dentures back up tight. They told me I did that but I still looked fine and not to worry about it. Oh well I wasn't on to look glamorous anyway. I was on to give hope to those getting ready to go through hair loss and show you can look normal and not like a cancer victim. I did manage to accomplish that. The highlight of my day was meeting Dr. Weiss. I still can't believe I got to talk with her. You never know how much things you do can touch the lives of others. I let her know and see (through our pictures) how she is responsible for bringing us all together. I gave her a big teary eyed thank you from all of us. Dr. Weiss was wearing the Breast Cancer logo necklace available for purchase on this website. If you don't know about it you can find it by going to the Breast Cancer .org homepage. Go to the bottom and click on Visit our gift shop. I would proudly wear this necklace because it is a reminder of all of you and what got me through my ordeal. I wish they made it in silver so I could afford to purchase one. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 13, 2008 10:02 am
Starting Chemo May 2008Posting Pictures You can not upload a photo from your computer to post in the thread. It must be online somewhere to post. This is why many will use photobucket. I upload mine to my MySpace page. Once the picture is online somewhere all you have to do is Right-click on it and then click copy. Once in post a reply box when you get to where you want to add photo right click again and then click on paste. If a small Internet Explorer Box pops up asking Do you want to allow this webpage to access your Clipboard?, click on Allow Access. Some times you will have to click 2 or 3 times before it will paste. Hope this helps. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 13, 2008 09:44 am
Starting Chemo May 2008 |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 12, 2008 07:03 pm
Starting Chemo May 2008OK, first I will add to the hair growth update.
Don't have time right now to go into detail about my TV appearance. Will fill you in later. All I will say now is I met Dr. Marisa Weiss, founder of this site. I almost teared up when she walked into the room. I thanked her for this site and told her that her site and the great bunch of women I met here is what got me through chemo. I showed her our pics and she loved the IV Pole Dancing thing. Here is a picture of me after the make over and a picture of Dr. Weiss and myself.
P.S. - Dr. Weiss if you see this I'm sorry I used the photo with your eyes closed but the other one was a terrible picture of me. Even though your eyes are closed you still look great. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 10, 2008 05:09 pm
Anyone on just Taxotere and Cytoxan?Speaking of Insurance issues I just have to share what I told my Rads Onc Cigna representative. They keep charging me out-of-network for him and he is in-net-work. He gave me his representatives name and told me to email her to complain. In my closing this is what I said "I never in my wildest dreams would have thought the excellent Cigna coverage I have would turn into one of my worst side effects of Breast Cancer." Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 10, 2008 08:48 am
Starting Chemo May 2008PERMISSION REQUESTED Jen and To all in Jen's Graduating Class of May 2008 photo I would like to copy and print out the photo to take with me on Sunday. I respect each of you here and will not do it if there are any objections. Please reply and let me know your feelings on this. Karin Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 10, 2008 08:36 am
Starting Chemo May 2008Rads advice Mary I too used the Remedy Skin Repair Cream. My center used to give the Aquaphor but found better results with the Remedy so that is what they give out now. I never had to buy it they kept me supplied with it. I loved it because it is not greasy like the Aquaphor plus it smells good. You said you are starting to get pink. Once that pink starts to turn red I would stop wearing a bra. I didn't and because of it the bra band made my skin peel off before it was ready to. I had raw skin. Once I stopped wearing a bra the rest peels with new skin under it so no rawness. I am waiting for the under arm area to heal before I start wearing a bra again. To help with the healing process I have been wearing tanks or T shirts under an opened shirt or blazer. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 9, 2008 08:46 pm
Starting Chemo May 2008I just did a search and maybe a video will be available on-line. Here is the link I found on the show. http://chat.go.com/abclocal/postMessage?event_id=356 Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
Posted in:
Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 9, 2008 08:25 pm
Starting Chemo May 200815 minutes of fame. Yesterday was my last radiation treatment. Today when I got home from work there was a phone message from my rad nurse. She wanted me to call back because she had a question to ask me. Turns out she had recommended me to an American Cancer Society person as a good candidate for a model she was looking for for an ABC show airing this Sunday. Because of Hippa laws or whatever it is called she could not give her my name or number but could call me and ask me to call the representative, which I did. I will be on a local Philadelphia show this Sunday morning. Sun, Oct 12, 11:30am - 12:00pm ABC's channel 6 WPVI Take Action: Beating the Odds Against Breast Cancer Patients, breakthrough treatments and a panel to answer questions. From what I understand Robin Roberts will be part of the panel. As for me at this point all I know is I will be the model for the American Cancer Society's Look Good...Feel Better program. They will start with me bald (semi bald, it is starting to grow) and with no make up then show how make up and a wig can transform you into not looking like a cancer patient. Don't know if I will get a chance to speak but I am taking my pole dancing picture with me and if the opportunity arises they will know about all of my friends here that have helped me through this. Randie - hope your recovery is going well. Enjoy the day, Karin Dx 3/27/2008, IDC, <1cm, Stage IIa, Grade 1, 1/13 nodes, ER+/PR+, HER2- |
© 2008 Breastcancer.org. All rights reserved.