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Ilovetherain

Member Since: June 12, 2007
Last Login: March 21, 2008
Location: In the Moment
Occupation:

Biography

breast cancer survivor/thriver, living life and making the most of each day.

Diagnosis

Diagnosis: Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Diagnosed: May 4, 2005
Type: Invasive or Infiltrating Ductal Carcinoma
Recurrent? No recurrence
Metastatic? No
Stage: Stage II
Lymph Nodes Removed: 27
Positive Lymph Nodes: 1
Tumor Size: 2cm-2.9cm
Tumor 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 EachDay

Posted in: Recovery, Renewal, & Hope + Growing our Friendships After Treatment, Created: Dec 27, 2007 10:18 am

Getting lost in ETSY!

I belong to etsy as a seller and a buyer.  The safest way to make any payment on etsy is through paypal.  If you don't have a paypal account, you can set one up while you are browsing/shopping through etsy.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Growing our Friendships After Treatment, Created: Oct 29, 2007 06:57 pm

The New Season Of House

I love the show but I'm still not sure about how this season is progressing.  Might be more interesting now that Foreman is back with House...but we'll see.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Connecting With Others Who Have a Similar Diagnosis + HER2/neu Positive Breast Cancer, Created: Oct 28, 2007 11:20 am

Her2 Positive with Estrogen negative Surviors Stories wanted:

Count me in this group.  I'm her2+ and er/pr -

Diagnosed in May 2005, lumpectomy, axillary node dissection (1 node with traces discovered in SNB during lumpectomy...no other node involvement).  2 cm. tumor...did 8 rounds chemo, 30 hits of radiation, 1 full year of herceptin (which finished in May 2007)...and I am currently NED...living and loving my life.  Taking it just one day at a time.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Oct 22, 2007 11:58 pm

TREATMENT ENDS-NOW WHAT?

Cydnee, first of all...congratulations on completing all of your treatment!  That is a monumental achievement!  As for where do you go now?  All up to you.

I'm only 6 months from finishing all my tx (chemo/rads/herceptin) and going through the process of reclaiming my life, rediscovering who I am.  Some days aren't so great, most of them are good.  It takes time, and patience and there is much to be said for getting to know yourself.  I've done support groups, I've talked with my primary care physician.  I read a lot on subjects I didn't know anything about, I have done some cognitive thinking/work to help me understand what I want, where I want to be.  If you think it took you 35 years to get where you are now, you can see moving forward doesn't happen overnight.  It can be a very rewarding time in your life and if you are feeling good about yourself and excited about life that has got to carry over into relationships, sexuality, etc.

Embrace it if you can and I'll be sending you many warm thoughts.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Oct 22, 2007 04:51 pm

I forgot to tell you a funny from my surgery

Well wasn't it a good thing you happened to look at your chart?!?!  AIDS from Eight??  Okay, I can "see" the similar sound.  But if you had said AIDS, wouldn't she have had other questions for you?  Or shouldn't she have?  And I guess that also explains the looks she was giving you but even that is highly unprofessional!!


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Oct 22, 2007 04:48 pm

skaky

Glad you are feeling a bit better.  Anything really unusual or not covered in list of side effects they have told you to expect don't hestiate to call the doctor or nurses.  If you didn't experience this with the first treatment, remember you are building up with each treatment so your body is absorbing more and more of the AC (and then the taxol when that happens).  Listen to your body...if it's shaky and feeling weak, make sure you are resting.  The first 2 weeks of a 3 week cycle are usually the worst, with the 3rd being the one you feel more like yourself.

I like how you ended your last post...that you hope you can look back on this and see how strong you were.  I'm here to tell you that I'm betting money you will...and I hope you'll come here and tell us just that when all the treatments are over.  It is by no  means easy, but if you keep up your spirits as best you can and keep that attitude, it is amazing what the body and the mind can do with the spirit.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Oct 22, 2007 04:44 pm

just so TIRED!!!

I always mention anything out of the ordinary that seems to have no connection to anything else, to my doctor to rule out anything I should be bringing to her attention.  At the same time, remember that this fatigue lasts for a long time, there is no time restriction on it.  Sometimes you are feeling energetic and full of your old energy and then "wham" it hits you like a brick wall.  To me, that's a sign for me to slow down, I've been doing too much...not just physically, it could be psychologically or emotionally.  I was talking to a woman the other day who is 6 years from a Hodgkin's diagnosis and she still suffers fatigue which she described as "fatigue right into her cells" which I thought described it perfectly.

Hope you find an answer to this soon and in the meantime, pamper yourself, be good to yourself and do your best to put the worry aside until you have talked to your doctor.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Oct 22, 2007 04:41 pm

Has anyone lost their faith?

I think this is an excellent question of valid feelings, worries and fears.  Issues such as breast cancer, and all the other things that seem to hit us with this (or the cancer comes after other life changing, traumatic events) disease.  And we question our faith.  I think this is normal and perhaps even necessary.  If we have become complacent our faith is shaken so that we can re-examine and re-evaluate our lives, our belief system.  There are times when we seem to be left on our own and abandoned.  It has been my experience that those times are when I am meant to look inward instead of looking out...to find what I have, what I can do, where I fit and what I am made of...so that spiritually and through faith I can reconnect with better understanding.  I'm very much impressed with Joel's response.  He and I are on the same path here but he has said it so much better.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Growing our Friendships After Treatment, Created: Oct 22, 2007 10:15 am

Just for fun...What is everyone reading??

I just read "Undressing the Moon" by Tammy Greenwood.  The main character has breast cancer, though the story is not "about" breast cancer as such.  It was dark and I wouldn't recommend it to someone newly diagnosed or even those of us who are moving beyond.

Also read Joan Didion's biography/memoir "The Year of Magical Thinking".  While this was mostly about the grief surrounding her husband's sudden death, there were elements of this book that would apply to breast cancer suvivors...loss and grief are universal.


Dx 5/4/2005, IDC, 2cm, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Oct 8, 2007 02:25 pm

re: Determining recurrence tendency?

Juli, it's true that when a doctor says "just live your life" and you're waiting for answers, having more tests...you wonder "is this a subliminal message?"  "are you telling me something?"...the thing with doctors...they don't always think before they speak.  So they say something and it can be taken out of context (naturally) by us.

If you are doing all that you can, then do try to relax, live as if you have only today...(regardless of how many you do have) and do your best to put worry and stress on the highest shelf (the one you need a ladder to reach!).


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Oct 8, 2007 11:20 am

Aches/paines 2 yrs after IDC

I finished radiation in February 2006 and my breast, chest, shoulder are still tender.  I feel it when I roll over in bed and adjust as needed...so many great things have been said here already.  Just know..it's not just you and it's all part of the journey.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Oct 7, 2007 12:23 am

Do you talk about losses...?

I talk about all of it with my non-bc friends/family.  This is part of my journey, what my life is about.  Those who are closest to me are interested and know why this involves me, why this is what my world is.  And they "get" it.  Last year, this very weekend was my MIL's 90th birthday.  There was a party for her and just as I was to leave to go to that I learned about a woman I knew who had passed away from her cancer.  I was late to the party because I needed to have some time to absorb this, grieve it and assimilate it.  And everyone understood because it is the "what if" if our lives.  So I just do it, and if others don't get it, or react like there is something wrong with me, too bad.  It's part of what my life is now as a part of the breast cancer society.

Excellent question by the way.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Oct 7, 2007 12:18 am

re: Determining recurrence tendency?

boofey,  your doctor is remarkable.  And I love the comment about wearing the seatbelt!!  Does that sum this up or what?  Totally brilliant!!!


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 5, 2007 01:09 pm

I Regret To Inform You That Pixie Dust Has Left Us.

My heart just breaks to read this news.  You had come to tell us about the pneumonia and we all hoped and prayed that she would overcome this.

My deepest sympathies to you and your family.

My prayers to the angel that Stacey was and is, and may your "pixie dust" gently guide you.  Her beautiful smile will stay with you for always.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Just Diagnosed, Created: Oct 5, 2007 01:06 pm

TIME mag focus on breast cancer link

This is an excellent link Dotti.  I'm glad you shared it.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Radiation Therapy - Before, During and After, Created: Oct 2, 2007 03:55 pm

Cried all through 1st pre radiation

Oh Janet, please do not cancel!! I had one node and needed rads too.  I cried and I was upset the first day of rads, not when I had the markings, it was the first day I had to go and be "zapped".  I was fine with chemo but rads threw me for a loop.  I was panicky and upset and I almost ran away from the hospital while I waited.  Not exactly sure why other than, looking back over a year ago, maybe I was feeling that the rads was "specifically" hitting the breast, whereas the chemo "went into my arm".  It meant being at the hospital every day, 5 days a week for 6 weeks.  Being constantly reminded day after day that this is breast cancer I'm coping with.  Chemo was once every 3 weeks.

Just hearing you say "I DO NOT want to do this" sounds just like me a year ago February. 

Know that you aren't the only one who has felt this way and hopefully you can hang on to that and get yourself on the table.  The zap takes a few minutes only.  The entire time the zapping was going on I pictured cannons going off, blasting inside my breast.  It helped me to feel more in control and empowered.

Looking back now, I'm glad I did the rads.  I felt like I had conquered a small mountain of my own fear.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Oct 1, 2007 08:28 pm

It's my 2 year cancer-versary today

Life is now about risk, taking chances, doing the thing that screams out to be done.  If you feel it in your heart Deb...go for it.  What is stopping you?????  Smile

Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Recovery, Renewal, & Hope + Moving Beyond Cancer, Created: Oct 1, 2007 06:03 pm

Totall O/T: Britney

I feel the same way you do Beth.  I'm old enough to be her mother and I feel like taking her under my wing and helping her to pull it together.  Living life in the lens all the time she's a cross between wanting attention and not knowing what to do with it.  She needs help and she needs people who care about her helping her get it.  To lose her children?  A blow most assuredly, but for now, lets hope it is the right move for the children first of all and for Britney to get her lifle back into order.  It's really heart breaking.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Tests, Treatments & Side Effects + Help Me Get Through Treatment, Created: Oct 1, 2007 05:57 pm

Terrified but grateful

I think everyone is just that little bit afraid of chemo, mostly from what we would have heard about it from others or seen on tv...and rarely, if ever, is having chemo portrayed as something positive.  Your experience with it will be your own...go into it with open eyes and an open mind.  Know that it is going to be strong, it will kill cancer cells and healthy cells and that you are fighting this disease with a very strong armful of ammunition.

 That said, you have very long hair and have been told to cut it off before chemo.  The fact is, with AC you will lose your hair.  It generally starts to come out around day 14.  As hard as it is to lose your hair, do your best to remind yourself that these drugs are working to give you the best possible chance at more years of life.  And hair will grow back.  You can play around with great wigs, you can discover a "face" you haven't seen for awhile and discover the woman who is behind the hair.  And if you make the decision to cut most of the hair before it comes out on it's own, there is a sense of ownership and empowerment about it, rather than feeling "victimized" about the loss.

It's a really tough road to walk down Kristina...but know this.  You can do it.  And you will.

If you want to talk to others who are going through chemo at the same time and what they are experiencing, go to the forum about chemotherapy in this "section" of the board. 

Positive thoughts to you my dear.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+
Posted in: Not Diagnosed but Concerned + Waiting for Test Results, Created: Oct 1, 2007 05:51 pm

nervous

It's a pretty scary place to be right now, hearing the new words in your vocabulary like "mass" and "consultation".  Your mind goes all over the place and you find it hard to focus on any one thing.  Seeing the surgeon this week will give you and your mother some answers.

Right now, breathe deeply, focus on your mom and help her get through this week.  You can be her strength and her support ~ but only to a degree.  She will need a lot of different support as no one person can do it all. 

Once you have definite information, one way or the other, than you can proceed and if you need to come back here and ask questions or vent or just worry and be concerned, that's a good thing for you.

Positive thoughts to you tonight and through these next few days.


Dx 5/4/2005, IDC, Stage II, 1/27 nodes, ER-/PR-, HER2+

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