Member Since: March 11, 2006
Last Login: December 2, 2008
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| Diagnosis: | Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
| Diagnosed: | February 26, 2007 |
| Type: | Invasive or Infiltrating Ductal Carcinoma |
| Recurrent? | Local recurrence (in the breast where it started, or in the skin and underlying tissues where the breast used to be) |
| Metastatic? | No |
| Stage: | |
| Lymph Nodes Removed: | 7 |
| Positive Lymph Nodes: | 0 |
| Tumor Size: | 2cm-2.9cm |
| Tumor Grade: | Grade 3 or high grade |
| Hormone Receptor Status: | Tumor does not have estrogen or progesterone receptors |
| HER2/neu Status: | Tumor has an excess of HER2/neu receptors or genes |
Posted in:
Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 17, 2008 10:13 pm
CMF QuestionGood Evening Ladies, Just got home from my appt. with my surgeon. (only a 2 hour wait in the waiting room) Well the ultrasound I had on Friday came back as showing as a cyst! My surgeon wants to make sure and is trying to schedule outpatient surgery for this Friday. I just hope and pray that it is a cyst. I asked her about getting my port removed at the same time and she wants to wait until the pathology report comes back. Which I'm in agreement with. I will a 3 month follow up PET/CT scan done the following week to make sure everything else is clear. She said that all the lymph nodes feel fine- yeah!! I ask for your continued good vibes and Prayers Please!! Carol- If you and Kent have any free time, Craig and I would love to see you. Thanks again for all your continued support. I don't know what I would do without you!! Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 13, 2008 10:58 pm
CMF QuestionHi ladies, Well things are well. I need lots of support right now. I discovered a small lump on my mast. scar and am scared sh**tless!! i'm scheduled for an ultrasound tomorrow moring and will see my surgeon on Monday. I just have that gut feeling that the BEAST is back!!! I'm trying really had to stay positive but am really scared. Please send all your good vibes my way as I feel Im doomed!! What nexted? It's been a very long 3 year battle and I was going along just fine and now this! Annie- I'm so glad your mammo came back clean- What a great relief!! Rita, Harley, Carol and everyone else. Thanks for all your support in advance. Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 6, 2008 09:03 pm
CMF QuestionHi Ladies, It's been awhile!! just checking in to let you all know that everything is going great. My DH and I were having our midlife crisis and decided to buy scooters! The weather is beautiful now so we've been out riding and about enjoying it and each other. My DD and I also have joined the local gym and been trying to workout 3 days a week. Boy do I feel old and out of shape! We will also be walking in the Susan G. Koman race for the cure this Sunday. I know last year it was very emotional, but had a great time. It sounds like all of us are doing well. Annie- Will be thinking of you on Friday. Hope all goes well. I've been thinking about recon. and have some questions so I will send you a PM. Harley- Sounds like you had a very nice time in FL, I know what youmean about riding on the bike all day, but it's great fun. Rita- Arizona is a great place to live!! Always nice and warm and no snow!! And if you get home sick, it's just an hour and a half away. Carol- Sounds like you're staying busy with your DS and work. Any plans for a trip to AZ? Well time to go see what I can make for dinner. Talk to you all soon, Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Oct 3, 2008 12:44 am
COSTS ? Need to learn costs!Daisyhope, Hang in there!! I've been on this journey for 3 years. I thought I had great insurance when I was first DX. Come to find out I had a $3000 deductible per year! I just pay what I can. I still owe alot, but I don't let it bother me. I found that the doctors and hospital seem to understand what we are going through and have worked with me. Hope this helps!! Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Day to Day Matters + Fitness and Getting Back in Shape, Created: Sep 15, 2008 11:50 pm
any dragon boat members?I attended my irst dragonboat race last year here in Phoenix. There was a team of survivor's racing as well. Looked like a lot of fun and I may look into joining the team for next year. Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Aug 8, 2008 08:04 pm
CMF QuestionHi ladies, Just checking in. We've been busy with DH's brother here visiting from PA with his wife and 4 very active 4 boys. You sure forget how much energy little one's have. Carol- Just wanted to say WHOOHOO!!!!! you are done!!! Time to Celebrate!! Been thinking of you. Sending gentle hugs your way. Will drop in on Sunday, off to the cabin to get out of the heat! Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jul 26, 2008 12:21 pm
CMF QuestionHi ladies, Just wanted to let you know that I AM DANCIN WITH NED!!! This is huge for me being it is the first clean scans that I have had in 3 years!! Thank god for CMF!! It feels like I'm almost a brand new person. A huge rock has been lifted and I can start living again. Thank you all so much for your positive thoughts and prayers. Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jul 18, 2008 04:43 pm
CMF QuestionHello ladies, Sounds like all of us are busy with Dr. appts. Just had my first pet/ct scan after treatment today so the scaniety is setting in. I should have the results next week. Annie- Praying that the lung issue is nothing. Have fun with the wedding favors. Part of my job is plan events and it's alot of fun. I hope it is 'Happily ever after"! Harley- Hoping that your appt. goes well next Tuesday. I will be thinking about you. I totally understand about being online. Just please let us know how you are doing from time to time. Carol- Hope all is well with Rads. Are we half way done? Everyone have a nice weekend!! Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
Posted in:
Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jul 13, 2008 12:15 pm
CMF Hair lossI finished 6 txts of CMF on May 1 and had minimal hair loss. My hair thinned by it was not noticable. It started shedding shortly after my 1st txt and continued until 3 weeks after my last one. Two years ago I had 6 txts of TAC and lost it all. The CMF treatment was alot easier to tolorate. With talking with others on this site I don't think any of them lost their hair 100%, just thinning. Please feel free to PM me if you have any more questions. 2 treatments down!!! Hang in there!! Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jul 10, 2008 11:30 pm
CMF QuestionHi Ladies, Julie- HAPPY BIRTHDAY TO YOU!!! . A good friend of mine always celebrates her birthday by doing something special. Since I turned 40, I really didn't think to much about celebrating mine. The other day she mentioned that I will be having a birthday next month and we should have a big party, I said why do you make such a big deal about your birthday and she said we are not only celebrating our birth day but also looking back on the year and all we have accomplished and been though. It really made me think. So, next month, all of you are invited to my birthday party!! IWill be thinking of you tomorrow. Celebrate Julie Carol- Hang in there with Rads. I was very lucky and did not have the sunburn reaction until after I was done. I used fresh aloe vera and it releaved the itchy feeling. Annie- Congrats- No more Chemo!! Hopefully the SE will pass soon. Harley- Will be thinking of you tomorrow. Hope your appointment goes well. Rita- Thanks for thinking of me. I've been super busy at work and been working in the garden when I get home. Monday I have a 6:30am appointment for my first bone scan. Kinda scared, never had one before. Take to you soon! Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jul 6, 2008 03:23 pm
CMF QuestionHi Ladies, Julie- You have come to the right spot for all your CMF questions. The ladies here are filled with unbelievable love and support and have all the answers!. I was dxt. for the first time in February of 2006 with IDC 2.5cm grade 3 er/pr- Her2+++. I had a lumpectomy, SNB in April 06 followed by 6 txt. of TAC, 35 rads and 11 months of Herceptin. Then the bugger decided to return in November of 2007. Same dxt. had a masctectomy and 4 more lymph nodes removedin December. It was a local recurrance and all nodes are clear. I started CMF in January for 6 months every 3 weeks the IV method. I finished May 1st. Like the others, I did not loose all my hair, but did have hair loss. I had my treatments on Thursdays (total infusion time was only an hour) and I knew that I would be down on Saturday. I also worked through all my treatments. This treatment is very doable compared to TAC. Nausea was very minimal and like Carol I had constipation issues. Please feel free to PM me anytime if there are any questions you may have. Annie- Glad to hear you had a great vacation!!! WHOOHOO for Wednesday. I'll be thinking of you!! I'm with you on taking a break. It sure does help clear your mind a little bit. Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jul 3, 2008 12:20 pm
CMF QuestionHi ladies, Just checking in. All is well on the home front! My dh and I are on our way up north to escape the heat. (114 today). Sounds like we are all busy, busy busy. Also been organizing a food drive for our locate food bank. It's going really well. Carol- Hope rads are going ok. Let me know what your doc says about the removal of your port. Been thinking about that myself. My next follow up is in 2 months. It feels very strange to not have to go weekly. (sometimes scary) I know that sounds kind of strange. My garden is going great. I soon will have watermelon!! We ate all the corn and am able to get a tomato or two every couple of weeks. Squash plants are still going strong. Rita- I love Tennessee!! We drove through there a couple of years ago and I just fell in love. BEAUTIFUL!! Have a great visit with your family. Harley- Your jobs sound like a lot of fun. Oh to be at then beach!! Annie- Hope you are having a plast on vacation! Have a GREAT 4th everyone!! Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
Posted in:
Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jun 16, 2008 12:12 am
CMF QuestionGood Evening ladies, This thread is just so incredible!! The words of encouragement and support are unbelievable. It would have been a huge struggle through treatment without you ladies. Thank you from the bottom of my heart. How do I find out about the road to recovery program? Great idea Rita- I guess I read my pm before your post so I will send you more info. Annie- Hang in there! Thinking of you. The fatigue was huge for me towards the end. I still come home from work and take a quick 15 minute snooze. Carol- Sending out your garden request tomorrow, I will send it 2 day air so you should get it hopefully on Wednesday. Just picked 10 ears of corn with alot more to pick. WhooHoo- No more blue pills! talk to you soon, Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jun 10, 2008 09:26 pm
CMF QuestionCarol-WhooHoo Chemo is DONE!!! Thought about you all day. Glad to hear everything went well. Rads will be a cake walk compared to what you have been through. My girls and I went to see our hometown Diamondbacks play your Washington Nationals a couple of weekends ago. It was alot of fun. Tell your friend that we are thinking of her and she's welcome to join us. Well it''s time for dinner so I'll talk to later. WHOO HOO!! for you Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jun 7, 2008 06:09 pm
CMF QuestionHi everyone, Carol- Sorry to hear about the plumbing issue. Hoping the "draino" will start working soon! I'm with you on the chemopause. Aunt Flo was with me all through chemo but decided to take a vacation after my last treat and now she sent in the night sweats and day hot flashes! This journey is something else. Send me some rain! Todays high is 105. I worked in the garden this morning, but was just to hot by 10:30. I will pm you for your address to send some squash your way. Rita- AWESOME news on your mamo Harley- I know what you mean about the hair. I was very luck not to have lost too much hair on CMF, but it did slow down the growth alot. Also being on Heceptin for a year prior did'nt help either. I'm at the in between stage right now and have an oppointment this afternoon to see what she can do. Congrats on 22 years of marriage!! We will also be celebrating the same in September!! Annie- Hope all is well. July 7th will be here before you know it!! Everyone have a great weekend. Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Jun 2, 2008 10:43 pm
CMF QuestionGood evening ladies, Carol -#11 DONE!! yeah Rita- This is the first I've heard of the Reach to Recovery group. Is there a website for more information? This is something that I would like to be a part of. I don't know how I would have made it through this journey (twice) withhout this group and all the information and support. Annie- I alway love reading your posts. Your words are always so heartwarming. When is your last txt.? Harley- Hang in there!! Going through this journey is no picnic and you are intitled to as many down days that you need. We all understand!! Been staying busy in the garden. If any of you would like some italian squash let me know!! Just got done planting pumpkin seeds and hoping to get a few for halloween!! Have a nice evening, Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: May 29, 2008 08:39 pm
CMF QuestionCarol, I tried posting last night, but was kicked out about 5 times (fustrating).Sorry to hear about your counts. I'm sure they will be back up by Monday. Then #11 will be DONE!! You are almost there girl. Rest, rest and more rest. How many rad txts. will you be having? It's will be a piece of cake compared to the chemo and time sure does fly. Hang in there! Had my 1 month followup with my onc. today and he was in agreement with my decision for Rads. that made me feel alot better. He will just continue to monitor me closely. Will be scheduling a Pet scan to make sure all is well. It was encouraging to hear that the aches and pains that I've been experiencing are just leftover SE's from the chemo. Enjoy your days off! Thinking of you, Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: May 16, 2008 11:26 pm
CMF QuestionHello All, It's been a busy week. Tuesday was my appointment with my Rads. Onc. and my head is spinning! I need to make a decision on having rads for a second time or not. Here are my choices: Being that is the area (right breast) has already had radiation there is a 5-10% chance of skin problems, bone problems and permanent pain but he said he could do it. If I don't have rads. there is a 5-10% chance for a recurrance. When I talked to him in January he had said that when we start rads. he would prefer that I get my port removed (that is where the recurrance was) so I made an appointment with my surgeon and Im scheduled for this coming Thursday. When I had my mastectomy I had clear margins but it was 1mm close to the chest wall! He did say that the surgeon could biopsy the tissue aaround the port to make sure it was clean.I'm really having second thoughts about the port removal. all the what if's are to much! Carol- The festival sounds like alot of fun! We are suppose to hit our first 100 degree day this weekend. I love this weather. My garden is doing great, picked my first chili peppers yesterday. Harley- You're jobs sounds like fun minus the dress portion. Do you get discounts? I have to dress business casual MondayThursday and jeans on Friday. I love Fridays. Annie- Yes, the good ol' dentist. Mine is really great, but I just don't like going. Hope everyone has a good weekend!! Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: May 15, 2008 09:33 pm
Anyone have rads to the same area twiceThanks everyone for their input. Tender- The recurrance was a mass below my port in the same breast. I had 5 axillary nodes removed at the time of my mastectomy and they were all clean. I'm hoping this answers your question regarding the nodes and skin. Thank you for the information. I no long have tattoos (that I can see), they are now somewhere in my mastectomy scar. I had also heard the same about not having rads a second time. I also plan to talk to my surgeon and get her input before next Thursday. Thanks again, Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: May 15, 2008 12:39 am
Anyone have rads to the same area twiceI just finished 6 txts of CMF for a reaccurance under my port and had a visit with my Rads. onc. and hoping someone can help answer some questions. History- Dx Feb 06 IDC 2.5cm grade 3 ER/PR- HER2+++ Lumpectomy-6 txt of TAC 35 rads 11 months of Herceptin. Reaccuarance Nov 08 IDC 2.5cm grade 3 ER/PR- Her2 +++ mastectomy- 6 txts CMF. Dr. said that he is able to do radiation for a second time but wanted to give me the option of also not doing it. If I choose not to have radiation, I have a 5-10% chance of another reaccurance. If I choose to do radiation there is a 5-10% chance that I will have skin, bone and permanent pain and he would prefer that I have my port removed. I have that scheduled for next Thursday. One other option is when the port is removed to have the surrounding tissue biopsied(sp?). This has been a long 2 years and I'm not sure which way to go. Any input would be greatly appreciated. Thanks Jill Dx 2/26/2007, IDC, 2cm, Grade 3, 0/7 nodes, ER-/PR-, HER2+ |
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