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Biography

Diagnosed 10/5/06. At that time I was 53, married for 27 years, the mother of two fine young men in their 20s.

Diagnosis

Diagnosis: Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Diagnosed: October 5, 2006
Type:
Recurrent?
Metastatic?
Stage: Stage IIIa
Lymph Nodes Removed: 17
Positive Lymph Nodes: 4
Tumor Size:
Tumor Grade: Grade 3 or high grade
Hormone Receptor Status: Tumor does not have estrogen or progesterone receptors
HER2/neu Status: Tumor does not have an excess of HER2/neu receptors or genes

Recent Posts by JanClare

Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Dec 1, 2008 01:58 pm

Port Placement

I have had my port for 2 years.  I had it put in under "twilight sleep" at the hospital and was immediately taken to my oncologists for my first chemo.  It's a Power Port, so they can use it for contrast solutions, etc, as well as chemo and blood draws. Yes, it was, and still is uncomfortable (I can't sleep on that side, well, I can't sleep on either side now, but the right side is because of the port), but I really feel like the port was a good thing.  No IVs, no damage to my arm veins, and very little pain for blood draws.  No bruising. 

I'm finally getting it removed Dec 23rd.  In a lot of respects, I'm going to miss it.  It was a little security blanket for me, ya know??  

I will say that it's very wrong that the doctor/ or his staff did not fully explain the procedure.   I received very detailed instructions as to what was going to happen. 

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Dec 1, 2008 11:46 am

Illinois ladies facing bc

 

YES, IT IS WINTER!!   ACK!

 And we still don't have our shingles installed!

I have to go pick up my son at the airport sometime today- but I don't know when, and I don't know where! He's flying stand-by and may come into Milwaukee, not O'Hare. I sure hope he gets on a flight to O'Hare! They are predicting MORE snow this afternoon.

And my dog must have a urinary tract infection, even though she acting the same. She is peeing dark red blood (which is easy to see in the snow) and I'm now wondering how long this has been festering! I have an 11:30 appointment, so we shall see...

I ending up working until midnight yesterday. Didn't feel that well, but managed to avoid the start of a CVS episode. Don't ask me why sometimes I can control the symptoms, but 80% of the time, I can't.

Got some sleep last night, but woke up at 8 am to the carpenters ripping out the last of the old kitchen floor. So at least something is getting done.

Off to see if I can get a "clean sample" of the dog's pee. Hard to do with so much snow- I've tried this before. Even if I can get something under her, I end up scooping up some snow as well! 

Hugs to everyone!

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 30, 2008 04:21 pm

Illinois ladies facing bc

Hey everyone- checking in to see how everyone is doing. Looks like we all had good Thanksgivings. Even without a kitchen, we managed. We cooked turkey breast (along with stuffing) in an oven bag in a pan on the grill, garlic mashed potatoes made in an an electric stock pot, microwaved veggies, bakery rolls and pies, various salads and relishes, etc. Everything turned out great and I ate too much!

Unfortunately, I had a bad bout with my Cyclic Vomiting Syndrome last night, and, from how I am feeling, I may be having another bout tonight. That's usually how it works.

They are predicting 2-4 inches today with more tomorrow. Looks like my roof shingles are not getting installed any time soon.

Karin, your house light decorations sound neat!  I'd love to see it- maybe you could get a video up on Ytube??

Rita, all my good vibes are being sent towards you!  I'm sure everything will be alright, but it sure is hard not to worry??  

Elfsong- ((Hugs)) to you, sorry that chemo is being so rough on you.  I've heard that it's often that way when you are younger.  But I agree with Wendy, your doctors should have lots of options to offer you! I sure hope you can make it to the lunch- if you feel up to it.  If I have my car that day, I'd be more then willing to come down and pick you up, if you'd like. I would not know until about Saturday if my husband needs my car or not, but you probably won't know until Sunday how you may feel??

Laura, love the trinket tree.  You are one crafty person, that's for sure!

Ginny, sorry to hear about your lymphedema.  I have truncal LE, but so far my arm has been spared.  Manual drainage massage has helped with my chest.  

Have to go to work- just hope I make it to 10 pm and get home before I have a CVS episode!

Waves and hugs to everyone!

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 25, 2008 09:51 pm

Illinois ladies facing bc

YAHOO!!!  Just wanted to let you all know that my scans were clear.  WHEW!!

And let me say how much I love my breast surgeon, Dr Rosen- I went to see him about setting up removal of my port, and I told him that I still didn't have my results from the oncologist.  He immediately got his nurse to get on the phone to the hospital and within 5 minutes he had the results with copies for me to take home.  Seriously, I like my oncologist, but I wish Dr. Rosen was my main doctor- instead I don't have any reason for follow-up except for stuff like this port removal.

My port removal is scheduled for December 23rd, plus he is also going to remove some scar cording/ lumps on the right side that is painful.  Hard to believe that after 2 years, I'm going to be port free!

Wishing everyone a Happy Thanksgiving and looking forward to our lunch on the 8th!

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 23, 2008 04:37 pm

Illinois ladies facing bc

Just wanted to send everyone a quick wave and ((hug)).  Special hugs to those in treatment. 

Christmas already??  I think I'm on the opposite end of the spectrum, I'm ENJOYING the fact that I will put up NO decorations this year.  I rather wish that I could fly to somewhere warm and spend Xmas on a beach.  Wink

OMG...... I just remembered that I was supposed to sign up for and run a Turkey Trot with some friends today! Ack! Chemo brain strikes again. I can tell that I'm going to have to do some groveling..

I haven't gotten my test results yet. Hoping that no news is good news, ya know?? Oh, and I still have not decided on the Zoloft or not. I've been feeling more upbeat in general, so thought I would hold off for awhile.

Have a great week everyone!

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 19, 2008 03:50 pm

Illinois ladies facing bc

Thank you all.  I'm still sitting here with the Zoloft script, but I think I will take it to be filled tomorrow. 

Sorry that you can't see the photos.  Don't know why they are not showing, since I did everything the same as with the other photos. 

Here's the link to the gallery (go to the end pages to see the most up to date photos):

http://www.smugmug.com/gallery/6456009_B8bWb/1/409382939_gbZ4H

password is: mortgage buster

(be sure to put the space inbetween the words)

another try for a photo: 

 The CT and MRI went alright.  I should have the results in about 48 hours.  

Funny story- the tech for the CT was a 12 year survivor.  When she found out that I had no reconstruction, she went on and on about how she thought the same thing, but that 4 years after her surgery she decided on reconstruction and how much happier she was.  I'm kind of amused because one thing I really don't care about is my lack of boobs.  Anyway, she insisted on showing me her 'set' after the scan was done- she dragged me into the women's dressing area and gave me the "show"- even had me feel them up!  They were just okay as far as I was concerned, but there I am behind a curtain feeling up another woman's foobs, while she tells me about her nipple tattoos. I then show her my scars and she tells me how nice they look.  I come out from behind the curtain to run into a little old white haired lady, just standing in the dressing area with her jaw down to her chin!  She was so shocked, especially when the tech walked out, adjusting her clothing and boobs.  I just started giggling about the whole thing.   

And no, still not currently interested in foobs.  *shrug*  I may change my mind in the future, who knows.   

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 18, 2008 10:32 pm

Illinois ladies facing bc

Oh, for those who are just starting this journey- thought you might like to see that life can become sort of normal again-  just a "new" normal.

Before the chemo:

Head shaved:

The Wig:

Bald, but beautiful? (LOL!)

The last picture of "the girls"- and the extra weight brought on by the chemo and steroids:

Four months later- the "new" normal.  Hair back, weight lost- just a little more flat chested *cough* Smile

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 18, 2008 10:21 pm

Illinois ladies facing bc

 Big hugs to everyone.  I'm sorry I've been MIA again, well, I'm just having some problems with a lot of different things. 

Julie, I'm so sorry to read about your cat.  (((hugs))  It's so hard to lose our fur babies, especially one that has been so special in your life. 

Wendy, WOW!  So glad you survived the pill mixup.  And I'll keep your niece in my thoughts- good thoughts and vibes.  

EJ-  so sorry to that you had to join this fight.  I know it's hard to believe now, but you will find strength that you didn't know you had.  It may be a long fight, but it will eventually be over.  (((hugs)) to you as well. 

Sharon, good luck with the surgery.  I hope everything goes well and that maybe you can be with us on the 8th.  

Rene, good luck with the PS.   So glad that you can meet with the one you wanted. 

Rita, glad you and Wendy TY had a good time at the boat- even if you didn't win.  Keep up with the walking!

Jule, I have to admit that I hated rads- just because it was cold, hard, and impersonal.  But Rita and Wendy are right, in general you just bop in and bop out. The weeks will go fast.

Well, I'm still alive, but I'm having job, home addition, and health issues. Yes, all at once. On the job front, it's really just the matter of actually working two jobs- it gets old and draggy, ya know?? And I'm tired all the time, well that could be related to how I've been feeling.

I'm having chest discomfort (seems like swelling under my clavicle), headaches, and my blood pressure has suddenly decided to go up slightly. (Borderline high now, where it always was normal before. ) So today I had a CT scan to check out my body, and tomorrow I will have a brain MRI.

And, this is hard for me to admit, I finally am facing that I'm suffering from depression from my whole bc experience. I thought I was handling it well, but I've actually spent a lot of time hiding out from everyone. My doctor has diagnosed me with a kind of post traumatic distress disorder. He's given me a script for Zoloft, but I have not been able to bring myself to fill it. Another thing that I feel I have to research to death, or maybe just another avoidance? Who knows.

For the addition, we kept having so many delays from the inspectors that our schedule just changed and now we are not going to finish until April!  ACK!! It's mainly the fact that they won't be able to pour all the concrete, for the driveway, and for the deck supports, etc. Too cold.

So here is where we are at: (actually, the roof is on, as shown in the 2nd photo)

And here is the dishwasher and sink that my husband set up in our extra downstairs bathroom:

Isn't that cool??  

Well, I have to get up for work at 4 am!!  so off to bed..

Oh and, believe it or not, I feel better now that I've opened up to you all...  

 

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 15, 2008 05:49 pm

Bi Mam with a port? Has anyone had this

I have had a power port since 10/06 and had a bilateral in March  2007.  I still have the port and have had no problems. 

 Don't worry- the port probably isn't really embedded in your breast tissue.  It's under your skin and then the tubes probably go up and through by your clavicle before inserting into your vein.  They will be able to work around it for the surgery.

But if you have concerns, please discuss with your surgeon- he should be able to reassure you and explain how it all works.  

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 10, 2008 10:32 am

Illinois ladies facing bc

Only time to wave "Hello" and say that YES, I will be coming to the holiday get-together in December!  Just let me know where! 

Is there a November meeting?  

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 5, 2008 04:57 pm

Milwaukee/WI people?

I'm sorry you are not getting any answers right now.  Just wanted to let you know that we have a pretty strong Illinois group, many of us from the Chicago area, and you are more then welcome to join our Illinois thread.  We give support and strong shoulders to any who need it!  Just jump in at the end of the thread and let us know about you. 

We also try to get together about once a month- if you are feeling up to it maybe you could join as in person as well?!  

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 5, 2008 06:42 am

Illinois ladies facing bc

Hi Kater- here's a link I found on google:

http://www.medicalnewstoday.com/articles/123682.php 

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 4, 2008 09:34 pm

Illinois ladies facing bc

Oh, can you take one more?? 

Here is my halloween costume:

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 4, 2008 09:28 pm

Illinois ladies facing bc

And remember...

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Nov 4, 2008 09:18 pm

Illinois ladies facing bc

Wasn't it a beautiful day??  I didn't have any work to do for my husband's business, so I had all day off.  Worked out, voted, shopped, took the dog for a long walk- it was great. 

Jule- I've been where you are- the day of my surgery, 8 weeks after my chemo ended, I lost my eyebrows and eyelashes! (which had thinned from the chemo but were still hanging on)  Weird, but it was only the once and I have known some gals who lost both multiple times.  I also had a lot of fatigue for almost a year, plus I still have some nerve problems from the Taxol.  Good luck with the radiation!

Michelle- I have what's consider truncal lymphedema and I do manual drainage all the time.  I was taught by the therapists at the Lymphedema clinic at Good Shepherd.  Rita,  they also used the Kenesio tape on me, but I didn't find that it worked that well.  The manual drainage and massage worked the best. 

Oh and for those who are interested, here is a link for the Fashion Alert bracelet like I wear.  The Lymphedema tag I wear says simply"Lymphedema Alert This Side".  There are other sites out there that also sell the Fashion Alert, you might be able to find it for cheaper, but this site has a large selection...  http://www.colonialmedical.com/product.php?productid=20895&cat=545&page=1

To all the Julies, looks like you are all in recovery from some type of surgery!  LOL.  Hope you are doing well! 

Carol- big hugs and best wishes for your healing as well.  

Well I promised some photos a LOOOOONNNNGGG time ago, back before my computer angst, so here's a few!

LOVELY JULIEA ON HER WEDDING DAY-

Lovely Julie's Wedding Photo

 RACE FOR THE CURE: 

 

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 31, 2008 07:45 pm

Illinois ladies facing bc

OMG- I just remembered that two years ago TODAY on Halloween was my first chemo treatment!   Wow, what a difference 2 years makes!

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 31, 2008 07:42 pm

Illinois ladies facing bc

Wanted to stop in and wave hello. HELLO!! Things are finally moving with my construction and not only do we have foundations and basement walls, but we actually have the framework for walls on the garage! Yeah!!! Electricity and water have been off and on for the last couple of days, as they work on various areas, which is why I have not checked in before.

Today was a beautiful day but, with all my construction, we had NO trick or treaters.

Karin- I wanted to let you know that I don't yet know about the Day of Sharing.  As soon as I do know anything, I'll post it here.  

Oh and a big thanks to the "lunch bunch"- thanks to your encouragement, I've made an appointment with my oncologist to discuss having a full battery of tests before having my port removed. Next tuesday.  Bless you all.  It's been 2 years now and it's time to get this port out, but on my terms!

 I'm way behind on everyone, so I'm confused as to who is who, but I wanted to mention to someone out there that I'm a triple negative who did her treatments at Good Shepherd and was very happy with the outcome.  I think there was someone asking about Good Shepherd??   

 Tomorrow I should have time to finally post some of the photos I have been collecting.

My husband has torn apart most of our kitchen (we are reusing and re-coating a lot of our cabinets so he's taking them out rather then the construction crew), so I'm off to go out to dinner.

Big hugs and waves to everyone! Special prayers and hopes to those undergoing treatment and surgery. I hope everyone is doing well. I'll try and stop by tomorrow!

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 28, 2008 09:18 pm

Illinois ladies facing bc

Oh my gosh, I'm BACK!!! (don't fall over now!)  My life has just been filled with so much lately and a balky computer made it just that much worse. To the point where I could read somewhat, but it took too long for everything to load and I had to spend my time online doing mostly research for my husband's business and our addition. I never seemed to be able to just sit down and post.

My son said he would fix it, but he was working on a project at work so that day after day it seemed that my tech problems were forgotten.  Well, I threw a major hissy fit and got my son to finally, truly FIX the computer. (I paid thousands for his computer degree, I figured I should benefit some how!)

So big hugs to you all!!  I'm so glad to be back. I've been struggling with a lot since starting this addition process (which is making me tear my hair out!!  It's currently on hold while our contractor and the village inspectors come to some sort of agreement about underpinnings and plumbing for our foundation- it's been SIX WEEKS of back and forth. I swear, I think the inspectors don't have enough to do because of the economy and they are using our project to justify their jobs!! )

I'm off to read the thread and catch up a little. Doing a happy dance! (((HUGS, HUGS, HUGS)))

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Sep 28, 2008 09:14 am

Chemo Port Questions

I have had my port for almost 2 years (yes, two years!).  I was triple negative, grade 3, stage 3, and my doctor feels strongly that I needed to keep it at least that long since triple negative is more aggressive then most bcs and more likely to come back in that time period.  So even though I have been done with chemo for almost 18 months, I still have the darn thing and get it flushed every 8 weeks.  They also take all blood draws through it.  It's a pain, but I decided that I could stand the discomfort since my doctor felt so strongly about it.  

 It's a "power port" so that contrast solutions for things like CAT scans or MRIs can be put through the port, as well as blood draws and chemo.  (Springtime, that may be why they couldn't use your port for your MRI- an ordinary port can not take contrast solutions.)  It does require a special needle and I have had to stop some techs who were going to use any old port needle and have them send for the proper one.  

In my opinion, it's been a GOD-SEND just for not having the sticks for IV or blood draws. In some ways it's like a security blanket to me, something I know the nurses can easily use (if they get the right needle!).

I don't really notice the port during the day, and I no longer have breasts and don't wear bras anymore, so the strap thing is not a problem.  I agree that it would be a good idea to make sure it's not in the way of your strap before the insert.  I do have some problems with it at night- I can't sleep on my back or on the side that had the lymph node removal because of discomfort, so I sleep on the port side and I have to use a series of pillows to prop my arm up and cushion the area.  Some nights are better then other.  

I think the benefits outweigh the discomfort and risks.  Hope this helps.   

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Sep 13, 2008 03:20 pm

Illinois ladies facing bc

Girls, I'm so sorry, I've been MIA. It's just that I'm officially overwhelmed. I almost wish for the relative peace of chemo treatment.

I think my computer problems are over, but I'm so far behind, I just don't know what is even happening with you all anymore. Let me just tell you what is up with me, and I'll try and catch up with everyone.

I still don't feel very well, but they can't find anything wrong. It's entirely possible (and my belief as well) that it's just all stress. I'm not sleeping well, I still have the CVS, so add that in. Oh, and my truncal lymphedema is flaring, and who has time for physical therapy these days?? I'm trying to deal with it just with manual lymph drainage.

The whole thing with my FIL was fine down in South Carolina, it was all just family. There wasn't even a funeral- just cremation and his ashes to be brought back to Illinois. We spent a week helping my mother sort through and pack up stuff, because they already had plans to move into a smaller house, which MIL will do next week.

But now we are trying to help with a memorial party up here (they used to live here) and tip toeing around my mother in law, who, no other way to put it, is being extremely cheap about the whole process. My FIL was a past trustee of our town, a past commander of the local American Legion, a past district governor of the Lions Club, on the school board, etc...in other words, generally well known and liked. There could be a lot of people, but my MIL keeps shooting down all ideas for a service, or even just a real party. I'm trying to get across the idea that this service is as much for my husband who is still super involved with people in this town, as for MIL. My husband is feeling like not enough is being planned to acknowledge his father. And I feel (yes, being selfish here) that this whole thing will reflect more on us, then on MIL, who will blithely go back to South Carolina when this is over.

More stuff- My garage has been knocked down, they pulled out the water service right out of my house doing it! It was a very understandable accident because they were trying to move the root ball from a 200 year old oak tree (we had to cut it down for the addition), but we were without water for 2 days, and the excavation company lied to me and the contractor about sending out a qualified plumber and the guy they did send almost contaminated the water supply with the products he was using- Luckily we know the utility inspector here in town and he stopped by just in time to prevent this worker (turned out he was an employee of the excavation company, not a plumber) from hooking my drinking water up with pipe that had been soaking in paint thinner for some unknown reason!! He kicked the guy out of my house, and the contractor got a plumber in. I'm really not blaming the contractor because I know that the excavation boss lied to my face as well about sending out a qualified plumber.

Oh, and they also ripped up my sewer line while the plumber was still here, so he had to fix that as well. But that was for only about 3 hours- so I just had to use the jobsite port a john out in the backyard.

So, now my garage is gone, they finally moved the root ball and replaced the water lines and sewer line, I have a giant hole in the ground and.... THE RAINS CAME! It's been raining hard for the last 24 hours and they are trying to keep the water out of our basement using portable sump pumps.

My entire house, but especially the back entrance and kitchen, is a mud pit. I'm furious with my husband because I have a $1000.00 rug in the dining room that is basically being ruined because he would not move the table and roll it up. Drop clothes just move around and shift on top of it, it's hard to keep the dog off it.

My husband is stressing about this entire renovation project now. Even though we are headed for our best year of business ever, and have been steadily doing better year by year, AND NO LONGER HAVE BOYS IN COLLEGE- he's convinced that we are not going to be able to keep up with the new payments. The payments that are going to be LESS monthly then what we were paying out for 3 years of two kids going to college! He's hyperventilating about the economy and I have no way to help him get over it. Especially since there is not much we can do about it now, we are committed to a contract to do this project and we have to pay for it.

I'm not exercising and I miss it so much- I barely get in walks with the dog and Sharon- maybe about 3 times a week. My office has been moved into the living room and my exercise room is about 1/3 of the way through being turned into a bathroom, so not much room to exercise indoors anymore. I belong to the YMCA, but I'm just so bushed, I never want to actually spend the time to go there!

You know, I think I'm just emotionally drained. And this house project just started!

Sorry, this turned into a novel! Hugs and healing vibes to all those in treatment. I'm planning on coming to the lunch next week, and I am signed up for the Race for the Cure, so I hope to see a lot of you in the next few weeks!

Once you choose hope, anything's possible. -- Christopher Reeve
Dx 10/5/2006, Stage IIIa, Grade 3, 4/17 nodes, ER-/PR-, HER2-

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