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Mason_avatar

Member Since: July 5, 2007
Last Login: November 22, 2008
Birthday: May 27, 1956
Location: Canton, NC United States
Occupation: school bus route data manager

Biography

dx 07/07 with Stage 1 IDC, lumpectomy plus re-excision with clear margins; SNB with negative nodes; body scans clear; ER/PR negative, HER2 positive

Diagnosis

Diagnosis: Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Diagnosed: July 26, 2007
Type: Invasive or Infiltrating Ductal Carcinoma
Recurrent? No recurrence
Metastatic? No
Stage: Stage I
Lymph Nodes Removed: 4
Positive Lymph Nodes: 0
Tumor Size: Less than 1cm
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

Recent Posts by bluewillow

Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Nov 18, 2008 02:59 pm

Venting: freaked out about post-tx mammo results

hI CP418,

Although my onc surgeon did not mention an MRI or US, my radiation onc did say that he often did MRIs and USs for some women where there might be a doubt or if it would ease their mind, and he did add that he was "totally confident" that what was showing up on me was scar tissue.  If I pushed the issue, I am sure he would agree to send me for the MRI.  Right now, I think I am ok with his decision, mostly because he had examined me four days after the mammogram and told me I was still having radiation-related skin changes and was still healing.  At least I know that if I change my mind and want an MRI, I should be assertive in requesting it, and will do so in the future for sure, as you suggest.  Thank you so much for reading and replying!

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Nov 18, 2008 01:29 pm

Stupid things people have said since I was told I have cancer!

I have already posted here earlier, but I just though of another "Stupid Thing"--

I work in a state government job where I have colleagues all over the state (we are all friends and communicate regularly).  When I first got my diagnosis, I sent out an email to them giving them a short summary of what was going on.  I was overwhelmed at the out-pouring of thoughts, prayers, blessings, cards, etc. EXCEPT for one, who happens to be a male, and who I still speak to but not as often.  He told me that he "would rather have Alzheimer's than cancer-- at least he would die happy and not know what was happening to him and not have to suffer".  That just floored me and really hurt-- I had an aunt that had Alzheimers and have known so many others stricken with it and I know first hand what an a cruel and awful disease it is.  Though I have tried to forgive, I will never forget his words.  Some friend, right?

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Nov 18, 2008 01:14 pm

Venting: freaked out about post-tx mammo results

Thanks, ladies-- I am much calmer after your replies.  Brenda, my port removal was scheduled back in September, so it sounds like they were confident that I could have it out, and I am so ready! Smerf, thanks for reassuring me-- I will know now that the scar tissue will likely show up.  Does it ever get small enough to have a "normal" mammo?  Sflow, glad to know yours was scar tissue and it makes me feel better knowing the ultrasound option is available!  Wow, ICanDoThis, you really had to suffer some crap-- that is scary knowing they messed up your results.  I hope they offered you a profuse apology at least.

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Nov 17, 2008 04:49 pm

Venting: freaked out about post-tx mammo results

Hi ladies,

Thanks so much for your replies-- you've given me a lot of reassurance. Tender, I didn't know about the MQSA, and that makes me understand the letter's wording.  The onc nurse did tell me it was a form letter and I guess that's why. But a more thorough explanation from my dr. would have been nice.  Brenda, thank you for sharing and telling me not to freak out, and I'm glad you got some thorough attention wth yours. Another big concern of mine was whether my port removal was still on schedule-- I guess they would have said something if it weren't-- maybe I've blown this all out of proportion, but after all that we've been through, I guess that's normal, right?

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Nov 17, 2008 02:23 pm

Venting: freaked out about post-tx mammo results

Hi- this is long, but I need to know if anyone else has had similar problems and would like advice on what to do and think:

I just had my final herceptin treatment this past Monday, 11/10 and am eagerly awaiting my port removal December 8.  I had my six-month mammogram the previous Thursday, 11/06.  While I was in the chemo room getting my last Herceptin, I inquired about my mammogram results and was told it was fine, no recurrence, with a follow-up recommended in six months.  I was fine with that and on top of the world just knowing my treatments were over with!  Then, 3 days after my final tx, I got a letter from the breast center about my mammogram results.  It said "Your mammogram shows a finding that we think is benign (not cancer), but to confirm that this area has not changed; we recommend follow-up diagnostic mammogram in 6 months."  After reading that, I felt like I'd been kicked in the stomach!!  The next morning I was on the phone with the cancer center, asking for an explanation.  My onc surgeon's nurse explained that it was "probably" nothing and said she would fax me the actual lab report from the radiologist.  It said "Multiple views of the right breast show an area of scarring in the upper right breast from previous surgery.  It is not well demonstrated on the films of June 2008.  I do not, however, see evidence to suggest any tumor recurrence.  I would, however, recommend a six month follow-up mammogram."  I feel like I have been stressed out unnecessarily. I don't even think the breast center should have sent out that letter.  And it didn't help matters that the mammo tech was very rough while doing my mammogram.  I have lost a lot of confidence in the breast center, which is part of the women's cancer center.

To me, the breast center letter and the lab report said two different things and to say the least, I am pissed!!!  I feel like I was needlessly upset and this has not been conducive to my good mental state.  I told the onc nurse that I am not happy with the wording on the breast center letter and she said "yeah we've tried to get them to change the wording on the letters but they haven't done it yet".  And I thought, Well, duh, why the heck not? I also consulted with my radiation oncologist about this and told him how it upset me and he said he was confident that I had nothing at all to worry about, that what showed up was scar tissue and no recurrence.  All my exams and previous post-tx mammos have been fine and I trust his opinion.  Has anyone else had this happen to them?  Also, I might mention that my BIRADS score on my post-rads mammo in June was 2 (benign), and on this last one the BIRADS score was 3 (probably benign).  Is this a significant change and should I just stop freaking out? 

Also, how long do you all normally wait for results?  I wonder if it would be possible to find a mammography center that gives immediate results... anyone know?

Thanks for listening!!

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Nov 16, 2008 07:41 pm

CANCER CURE FOUND BUT.... FOR THOSE WHO HAVE NOT SEEN THE VIDEO

Wow. 

Graceths and Barry, my husband has been saying the exact same thing for years about a cancer cure not being lucrative for the big business, especially after I was dx'd with breast cancer.  He has had several family members with cancer, so he knows first hand that cancer is a huge money-maker-- an industry, and I'm pretty much with him in that thinking.  Look at what a marketing opportunity breast cancer has become.  Look at all the pink crap that is being sold-- heck, Ford has even built a Mustang with a pink ribbon on it-- looks like they could fund the real cure.  If there was a cure for cancer, my insurance company wouldn't be out $200,000+ and the cancer center where I go could not have added the multi-million dollar addition, in which each and every room is decorated with its own color and theme...  makes me want to puke everytime I go in there, because we're still struggling to pay off what the insurance didn't cover.  Whew, I have to get off this subject...

Thanks for bringing it to our attention.

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Day to Day Matters + Fitness and Getting Back in Shape, Created: Nov 12, 2008 02:48 pm

questions about Strength Training

Hello there!

THANK YOU, everyone, for all the great advice you have given me!!  I plan to print out your posts and put them in my fitness/weight loss notebook/journal so I don't forget anything.  I am anxious to get started.  I had my last treatment of a year of Herceptin on Monday and I feel SO RELIEVED!!  I feel free and ready to get my poor body back in shape.

Again, thanks so much and best wishes to all!

Mary Jo 

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 11, 2008 04:56 pm

PORT REMOVAL-can anyone describe it for me?

Hi again!

Moody, mine is under the skin too and I was told it was farther down than most-- a trademark of my surgeon so that the scar won't be as visible in a bathing suit, tank top-- how "kind" of him! 

Brenda, I wondered about the scar tissue-- I have a tendency toward that and I guess I'll just expect it-- not so bad though compared to all the other crap that's gone on.  And I've had mine since Aug. '07 and wonder if it's "grown" in there too..

Thanks, Miss S - I do think I will ask for mine, even tho my husband thinks I'm nuts.  He so kindly took photos of the nurses yesterday at my last Herceptin, even one of the needle being pulled out for the last time!  I plan to freak out some people with it, like my adult children-- mean, aren't I?

Katiejane, did you remember anything from the procedure with the twilight sleep?  I had that with a colonoscopy and couldn't recall anything... really a strange feeling!  Thanks for the heads up about the Ativan-- I still have some and I will take it just in case.

Donna, wow, the world is getting smaller Smile  My brother-in-law lives in Candler, and I know where Otto is!  We camped in Macon County last weekend up on Wayah.  How neat that you were reunited w/your birthparents-- what part of Florida?  My aunt lives in Melbourne and a cousin in Naples, and I vacationed at Jax Beach as a child- wonderful memories!  My doctor is David Hetzel at Hope A Women's Cancer Center in Asheville.  Good luck on your last treatment!!  BTW,  I KNOW the port removal will be better than the drain removal-- those things are baaaadd!!

Hugs and thanks to all for your advice and encouragement!

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 10, 2008 08:33 pm

PORT REMOVAL-can anyone describe it for me?

Wow, Nancy, what a small world it is!  My mom was born in Hendersonville and lived in Asheville until she met my dad.  My dad retired from the paper mill in Canton.

Actually my hubby took me out to dinner just so I wouldn't have to cook tonight-- that was a big enough celebration.  I think the big party will come when my port comes out on December 8.  I too am a little afraid, but at the same time, I feel really free!!  It was a bittersweet end of the day at the chemo room-- got lots of hugs and I felt sad to leave-- does that make sense?  I had some fantastic nurses in that room keeping me going.  I want to do something special for them, maybe a donation to the Cancer Center's fund for uninsured women.

Congratulations to you too on finishing Herceptin!  We'll be fine!!!!!

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Nov 10, 2008 09:33 am

hair coloring after BC + hairstyle sources

Hi there Tina!

Thanks for your advice!  Yes, my daughter is quite the fashion critic-- she is 28 and has great taste and a very classic style-- not sure where she got it from Laughing   She has told me many times that she is trying to get me on the show What Not To Wear-- boy that would be awesome!

Now you've got me excited about a change!  I'm so glad you mentioned Loving Care-- I was thinking about it the other day-- is it permanent or does it wash out in a few days?  I'd much rather do it at home since salon color is so costly.  What other brands do you use and recommend?

Thanks again for your encouragement!

Mary Jo

ps-- I'm still reading your decluttering thread, and still being inspired! Wink

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Nov 10, 2008 07:44 am

hair coloring after BC + hairstyle sources

Hello all you nice fashion conscious ladies!  I need help...

Now that I have hair, I am ready for a cut (okay, trim) and a new look.  My "default" hair color is a mouse brown with just a bit of gray. (I have less gray now than before-weird!)  My daughter has suggested I have red/auburn highlights in my hair, instead of the blonde/frosted look that I had before bc.  I am just a little hesitant about using hair coloring now that I've had bc, I guess because it's something artifical and chemical.  Anyone have any thoughts on this, warnings from drs. or nurses, and am I being silly?  Any suggestions on brands, colors, etc.?

And, can anyone suggest websites for short hairstyles where the photos are actually large enough to see?  I have found some that have pictures of styles, but they are so small I can barely see them.

I would love to hear what you all have done with your new "do's".  Mine was straight and fine before bc, and it has come back the very same way, no curls at all.

I am 52 and often dream of having a new look all the way around.  My daughter tells me it's time to lose my jeans and flannel shirt/old hippie look, so maybe the hair will be a start!

Thanks and hugs,

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 10, 2008 05:30 am

PORT REMOVAL-can anyone describe it for me?

Thank you so much for your help, wonderful ladies!

Adrienne, I'm glad yours went well even tho you were under general anesthesia and thanks for the heads up about the muscles adjusting... hadn't thought of that. Barb, I had wondered if I would feel a pulling and only took 15 minutes-wow, I hope I'm that lucky. Kerry, what an awesome idea to make jewelry out of yours-- I would love to see pictures of it if you could post them when you get your creation finished! Heck, we paid $$$ for them-- we oughta get to keep them! Wendy, I am so glad to hear you don't have much of a scar. Not that I ever wear anything revealing, I just feel scarred up enough right now. Nancy, it sounds like yours was as easy as my oncologist has promised me it will be.

I am so grateful to hear that it is a simple procedure, and it sure sounds much more pleasant than drain removal.  Cry That was sure no fun!

YAY for everyone for getting that port out and again, thanks and hugs for helping me out!

Have a great week,

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Nov 9, 2008 05:09 pm

Stupid things people have said since I was told I have cancer!

Moody, you should make the shirt-- you could sell thousands right here Wink.

I actually had to apologize to my hubby today for being such a "w"itch lately-- my nerves are on edge because of a bad mammogram experience last week plus still waiting on the results-- then right after I said "I'm sorry", I thought to myself, 'why am I apologizing, I had breast cancer...' but really, so did he...

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Day to Day Matters + Fitness and Getting Back in Shape, Created: Nov 9, 2008 04:58 pm

questions about Strength Training

Hi ladies,

I have a question about strength training, and I'm hoping to get some advice from the fitness experts here-- like FitChick and Felicia and others who are more "in the know" than I am... (which would be a lot of people)...

I am at the end of my treatments (Herceptin), have about 25 pounds of chemo weight to lose and I'm ready to get on a regular fitness/weight loss program. The only real workout I have gotten lately is on the weekends out in the woods hiking and hunting. Before I was diagnosed with BC, I was in good shape and could lose weight fairly quickly just by cutting back on eating and moving more, but now that I am 52 and in menopause, I know I'm going to have to take a very aggressive approach to getting this weight off.  I have a desk job and am flabby due to loss of muscle tone.  To put it better-- I feel like a marshmallow!  I enjoy strength training, so I just ordered several ST videos to get me started (using 2-5 lb weights).  My first question is: can I do a strength training video each day or do I really need to skip a day in between workouts?  I will also do cardio at least 3x a week on a treadmill or walking outdoors.  I would like to do the videos each day just to get into a regular routine-- it seems when I skip a day I get lazy, slack, etc.  BTW, I have a lot of upper body strength and don't fear getting muscles, etc. 

Second question:  is it best to eat a snack before a ST workout?  is so, what foods are best?  am thinking I'd like to work out in the mornings before breakfast.

Thanks to anyone who can offer me advice!

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Hormonal Therapy - Before, During and After, Created: Nov 8, 2008 08:36 pm

Too much calcium is a warning sign

Hi Susan,

I had high calcium levels for many years and my family dr. and my oncologist both said it was nothing to worry about.  Funny thing is, it is normal now, and I have been taking calcium supplements too, when I wasn't before-- maybe the chemo/rads had an effect on it?  who knows?!

Love the kitty typing!!!!!!!!

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Nov 8, 2008 03:57 pm

Stupid things people have said since I was told I have cancer!

Wow, in reading this great thread, I am blown away by some of the awful stuff people can say Surprised

My experience definitely pales in comparison with most everyone's here, but I will never forget it.  Because I had a fairly "easy" time with chemo, I continued to work through my treatments.  My job involves computerized school bus routing and I deal with all levels of people from school administrators to school bus drivers (my favorites!).  Other than this one incident that I am about to describe, I had lots of support, love, and help from my co-workers and administrators.  One day, the lady in charge of our exceptional children/special education program came into my office for some bus stop information.  She knew of my bc and after a quick and insincere "how are you?", she asked "so, when will your hair grow back?"  I calmy told her "I'm not worried about my hair growing back as long as the cancer doesn't" and she quickly exited my office. And to think she is in charge of our exceptional children's education and welfare...

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Nov 8, 2008 12:50 pm

PORT REMOVAL-can anyone describe it for me?

Hello to all,

I have one more Herceptin treatment left to go this coming Monday and am scheduled for my port to be removed on December 8. (have a Bard port) Can anyone please tell me what to expect for the port removal, is it painful, recovery time, etc.  The nurses at my cancer center tell me it's a breeze, but I'd like to know what to expect.  I do know they will do it right there at my oncologist's office.

I hesitated posting this on the chemo forum, but wasn't sure where else would be a better place,  mostly because I don't want to scare anyone! Laughing   In case anyone who is in active chemo treatment reads this, please know that there IS life after chemo, and a wonderful one!!!!  I did the A/C for four DD, had my last one (Taxol) January 2008 (continued until now with my year of Herceptin), rads done in April 2008, and I made it through just fine, have hair again, feel great-- just like all of you will!! If I can ever help anyone, just send me a personal message! 

Best wishes and thanks to all!

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 8, 2008 09:39 am

"Cure" or "Remission"?

Hi! 

On this beautiful crisp Saturday morning, I'm decluttering and throwing out stuff, thanks to inspiration from Abbadoodles' Making Do With Less thread under the Moving Beyond Cancer forum -- check it out, it's great!  

I just found this clipping of an ABC News transcript from an interview with Dr. Susan Love, M.D. entitled "Can Breast Cancer Be Cured?"  (copyright 2007 ABC News Internet Ventures)  It follows:

Question: Can breast cancer be cured? 

Answer: Breast cancer can be cured.  In fact we cure three-quarters of breast cancer; the problem is when somebody is diagnosed with breast cancer, we can't tell that woman that she is cured, until she dies at 95 of something else.  So, we know we cure breast cancer, but we never know if any one particular person is cured at any one time.

It pretty much says what all the combined responses here say.

For some strange reason, I found great comfort in this quote, and this is one thing I will keep. I found it a week after I was diagnosed and I found it very uplifting and encouraging. Have a great weekend, all.

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Day to Day Matters + Humor and Games, Created: Nov 7, 2008 08:42 pm

Movies

An American Carol.   (has anyone seen this one yet-- good or bad?)

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Nov 7, 2008 04:49 pm

I don't want to be a "survivor"

Susan, I understand perfectly what you're saying.  I too have mixed feelings about the term "survivor". (but like Obama said, it's better than the alternative!)  All you ladies gave the greatest responses here!  Otter, like you, I've never heard the term "heart attack survivor", or "diabetes survivor", etc.-- tho I'm glad for those who are!  I do know now at this point, I feel like I want to help others by what I have experienced, so those who are going through the awful treatment times will know that they too will "survive" and there is life after treatment.  By the way, Harley, good for you on being a RFR volunteer!  Tina, I agree that we should hang around this site for those who need us! Farila, you are such a wonderful inspiration to us all! 

Although pink has always been my least favorite color, right after I was diagnosed, I absolutely despised anything with that damn pink ribbon on it-- and I mean anything and everything.  Now, I don't feel that strongly. I even have a pink magnet on my office door that says "early detection saves lives", and that is my mantra.  I do hope when people buy pink stuff, the sales will benefit somehow in finding a cure and better treatment.  And sometimes I think the media makes it harder on us trying to move on.

Hugs to all!

Mary Jo

Mason's Granny
Dx 7/26/2007, IDC, <1cm, Stage I, Grade 3, 0/4 nodes, ER-/PR-, HER2+

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