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Ta_in_truck

Member Since: May 1, 2008
Last Login: October 7, 2008
Birthday: July 11, 1975
Location: Oakland, CA United States
Occupation: student-mommy

Biography

Diagnosis

Diagnosis: Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Diagnosed: April 23, 2008
Type: Invasive or Infiltrating Ductal Carcinoma
Recurrent? No recurrence
Metastatic? No
Stage: Stage IIa
Lymph Nodes Removed: 17
Positive Lymph Nodes: 2
Tumor Size: 1cm-1.9cm
Tumor Grade: Grade 2 or medium 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

Recent Posts by hotsyta

Posted in: Tests, Treatments & Side Effects + Chemotherapy - Before, During and After, Created: Oct 7, 2008 12:20 am

Anyone starting chemo in Aug. 08?

Hello All,

 Another bald beauty here, I started in August as well.  AC X4.  I tend to get too absorbed on these boards so I come when stuff gets too overwhelming, like now.  But I may bounce out after a few weeks if it gets too overwhelming.  I am scheduled for my last AC tomorrow.  #3 was soo bad and I am really scared.  Still not throwing up, but horrible heartburn.  My mouth was so sore I was in excrutiating pain from thursday until today.  Deanna--I have really bad joint pain in my right knee.  I guess it's from the chemo cause I was in bed for almost a week and then it just started hurting, so I know I didn't injure it.  The Dr. said she didn't know why.  Any way I just wanted to know if there are any ideas for what to eat when you have mouth sores, cuz it hurts to even talk.  I was thinking something cold but no spice or salt and not liquid cus the thought of using a straw is too painful.  The magic mouthwash is really gross and doesn't work that well. anyway I am now rambling.  Help!!

Tennille 


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Alternative, Complementary & Holistic Treatment, Created: Jul 30, 2008 04:37 pm

Choosing No Chemo

I have a friend who is pushing me to refuse chemo and try Essiac tea.  I just don't feel comfortable doing this.  I wish I could find information that would support this treatment, especially since I am 33 and I have "heard" that there is not a lot of data that demonstrates the effectiveness of chemo for younger patients.  I looked on the Amazon group and it was a huge site.  Not sure where to look.  So much information is out there and I feel so overwhelmed with it all.  Onco says "if it tastes bad don't do it, no compelling evidence shows effectiveness of alternative therapies"  Seems like a big gamble to me.  Does anyone have a comment?  Ta


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Support & Community Connections + Get Togethers, Created: Jul 30, 2008 04:22 pm

PINKSTOCK 2008

Sounds like so much fun, just found this site today!!!  Hope to be in on the next one!! Have too much fun!!  Ta


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Just Diagnosed, Created: Jul 22, 2008 07:28 pm

Be Positive!!!! (shuuut up!)

Quickly, I will say I am so glad you have started this thread!!  People seem to get so offended when you even suggest that it is difficult to stay positive all the time.  I too have a family members (that I live with) who insist that if I continue to live my life as it was before the dx I will be fine.  Only I don't feel the same, I am exhausted both physically and mentally.  I haven't even started chemo yet, maybe after they will give me a little slack.  I am not positive, in fact it seems that every day getting closer to chemo I feel even more out of control, and anxious, and pissed that I can't make decisions for myself and my family.  I am so independent and I HATE to have to depend on others that will turn around and throw it in my face.  I am glad to hear you set a boundary with your father, I have had to do the same with my Aunt.  The first conversation I had with her post op started with her telling me how mad she was at my Husband, when I defended him she got really mad.  My chest tightened up every time I was involved with a conflict--literally the muscles contracted--painfully.  I had to tell her I would not argue with her any more because it was physically painful and if she insisted I would just not talk to her.  She has really eased up, but I think she know she has to because she is all I have, both of my parents have passed.  We did get into a doozie this morning, but it was probably my fault due to pent up and not expressed frustrations.....I hope your Dad will feel the sting of losing contact with now two of his children and perhaps will ease up too.  Thanks Heidi

Ta 


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Support & Community Connections + Young Women with Breast Cancer, Created: Jul 19, 2008 12:52 pm

Who's the youngest?

 Beth-You probably hear this a lot, but you are wise beyond your years...or just you give really wise and comforting advice!!  I am so glad to read your conversation with Sandy about the journey you have made with your emotions.  I too have felt angry and selfish at being 32 at DX. I really appreciate what you said about no matter what age we will feel angry at "what might have been"  I think the most important thing I have to keep telling myself is that is "it still can be!"  I am so thankful I didn't wait to have children and that I did get to breast feed.  I THOUGHT that was my ticket to NOT getting BC, but I was wrong.  Despite my anger at my losses my heart goes out to others as well, it seems that no matter how bad your situation is there is always someone that has it worse.  Beth your posts, even when I haven''t responded, have been so helpful to me and I am glad you have turned your bad situation to a helpful and healing one.  This is my goal as well, but at this point I still feel very self-centered.

 Sandy-- I too have treated my DH so terrible at times that I am surprised he sticks around.  Thanks for being honest.  I will keep your comments in mind the next time I feel like giving him a good ribbing.

I grew up without my Mom and just 2 months after moving 20 minutes from her she was Dx with BC.  She passed 6 months later, we barely even found out what stage she was by the time she passed.  She was only 54.  Immediately after her Dx I went and had a "baseline" mammo, I never thought the lump I found only a year after her passing would be cancer.  I always knew I would get it based on our history, (ggma, gma and ma same BC in the same side, all same grade and type) but I never thought it would be when I was only 32!  I never wanted to put my little ones through this!!  They are so young (5 and 7) and it just breaks my heart to see the fear on their faces, it's all I can do to try to figure out the best way to help them through this.  I wish there was a magic formula to prevent permanent damage!!  We are BRCA neg, but they have found a genetic abnormality (polymorphism) in our family that is shared with 80 other families that is as of yet unidentified.

Jenny--I had a bi-lat mx for two reasons.  To be honest, it is hard to say which one was the most important.  1.  To KNOW that I would not get BC in the good side, (There was a mass on the gs which they assured me was NOT BC, but I felt uncomforted by their assurances). 2.  When reconstructing PS told me and I read everywhere that symmetry is easier to achieve when reconstructing both at the same time.  I wish I could say that the health risk was my #1 concern, but I am pretty vain.  I loved my big busty chest and I was really upset that I was losing my "best asset" as I always termed them...I know the brain...I know.  I was really stuck on getting a flap surgery so I could turn this bad surgery into a good PS experience.  When two PS told me I was not a candidate I was so pissed.  I felt cheated.  Now that I have had the surgery w/ immediate recon w/implants that had to be removed due to infection. I am so glad I listened to my docs, you don't want any added risks based on vanity.  I will have recon again after chemo, but I will not get my heart set on a particular procedure or even outcome.  I have learned--or am learning--to love myself despite what my body looks like.  Sometimes I feel so silly for being so caught up with body image, I mean it's not my fault I lost my breasts.  It's not like I could diet back my breasts or diet away my BC.  So this is my journey right now, hope it is helpful to you as well.

Ta 


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Breast Reconstruction, Created: Jul 18, 2008 07:10 pm

Thinking about flower tattoo.No, 2 flower tattoos

Hello!!

I am so excited by your almost decision to get a flower, I will also be doing "traditional" tattoos instead of "nipple" tattoos.  I am really into tattoos and I hate the idea of wasting a good tattoo session!!  My biggest problem is that I want one from someone that I will never run into on the street.  

I am not a dropout and I don't have any diseases--other than BC.  Almost all of my friends have tattoos and I have never in my life met someone that has contracted a disease from a tattoo parlor. Considering the fact that I worked in a blood bank, where our business was to assess risky behaviors, I think that is pretty good.  I think most of the reports you hear nowadays about people getting diseases are hyped up.  Any time you choose to be in a place that deals with blood and body fluids your risk for infection is increased and unfortunately these reports really give reputable parlors a bad name and scare people.  Maybe things were worse a long time ago, because now--at least in CA, by law, parlors have heavy regulations concerning hygiene.  I see parlors taking the same blood borne pathogen precautions we used in the blood bank.  Such as covering all surfaces that can receive spatter (like in the dentist's office), disinfecting all uncovered surfaces (like the chair you sit in), using an autoclave sterilizer on all reusable items such as the tattoo gun, and using disposable ink cups and needles that they open right in front of you.  If you go to a shop and you don't see this happening--run, because it shouldn't be that way!

I would look for a place that has a long standing reputation, you can check with the better business bureau and look for an artist with a substantial portfolio.  Many artists post their work online so you can see what they do first.  You can bring in a photo, or copy, or sticker or whatever and all artists will draw what you would like--or you can choose from "flash" on the walls.  Also it is always good to visit shops to see how comfortable you are in the shop, I have found that some are not that "friendly".  I want to be welcomed and feel as if my business is appreciated--I will be wearing it forever!!  I also want to feel comfortable with my artist so I can ask for changes if I don't like the original design.

I hope this information is helpful, I would be scared too if all I had to go on was the fact that my deadbeat students went into tattooing, as well as stories of disease-ridden tattoo parlors.  You certainly aren't the only one that feels this way about tattoo--my Auntie feels the same way...and she lets me know about it every chance she gets!  I can't convince her but maybe I can ease some of your fears, any how it's worth a try!!  Good luck with your choice!

Ta 

One more thing--there is a lady at Triangle Tattoo in Fort Bragg--where I got my first tattoo, that specialized in mastectomy tattoos.  I even saw her profiled in a documentary on the Discovery Channel.  I forgot her name, but her partner was Mr. G.  He had 30 years experience and was very understanding when I asked to see his autoclave and to know about his sterilization practices.  Fort Bragg, CA is a long way from Colorado, but just a suggestion for a place I knew about!  


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: Jul 18, 2008 01:14 pm

More than one grade/type in Lump?

I did have more than one type of cancer, but not in the same lump.  The lumps were smaller than anticipated so that accounts for the growth in the short amount of time.  I had two tumors sized 1.7 and 1.1 that were IDC as well as DCIS in four quadrants of my breast.  Thanks for the input!!

 Ta 


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Breast Prostheses and Reconstruction Alternatives, Created: Jul 18, 2008 01:10 pm

Bras and breast forms you love

I am interested in purchasing a set of prostheses.  What a daunting task!!  I have "tried on" the amoena Contact Lite, Natura, Climate, as well as the tria plus.  I like the tria plus the best because the sales person told me I would get better ventilation.  I live in a hot climate and I think ventilation would be very good.  I have some issues with plastic tape--it breaks me out.  Paper tape does not.  I really wanted the contact type because I am active mom of two under 8 years and I HATE worrying that someone will be able to see my scars down my shirt when I bend over--as they can now!  So I wanted to know if anyone with slightly sensitive skin has been able to use the contact type products and if anyone with the non-contact type forms have had good experiences with bending over and not having the forms show.--Like when you are playing pool.  Also if you have the contact type and start to sweat profusely, because it's 114 degrees, does the form fall off?

Thanks!!

TaLaughing 


Dx 4/23/2008, IDC, 1cm, Stage IIa, Grade 2, 2/17 nodes, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: Jun 4, 2008 01:59 am

Surgery in May?

Hello All,

Jax...Thanks for the advice. The residents came around the day after the surgery and asked me why I wasn't elevating my arm, and I said I didn't know i was supposed to. I was so out of it when they released me I didn't really remember much and I thought they were sending home the papers the nurse was reading from.

Manda--I am so sorry to hear about the pain. Some days are better so far for me and that's what I am clinging to. BTW I just had the chest xray last pm to check for fluid, and the metal from the expander it in the direct center of the breast area, but there was metal mesh all the way across my chest, maybe the mesh is what is what is irritating you...idk.

Kathy--The drains yeah, my paperwork says 1 week but I doubt it cuz mine are about 60cc each daily. $54 per tube!! When do you start using this? No one has mentioned scar cream. I guess I should ask.

Sheila--Q-man? I assume it's your son? How old and where has he been? Sorry I am so behind, didn't keep up for two weeks, sorta-denial-like.

So here goes, I went to the ER last PM to have stuff checked out since I had been feeling so crappy and fever and all that and they told me slight bronchitis, but mind you this is not the ER where my surgery was performed. I just saw the NP tonight and she said maybe bronchitus, but you definately have cellulitus (sp?) so now I am on my way home to Oakland (was recovering at a family member's home, where we are moving for the summer) got some different antibio onboard and hoping to see someone tonight or tomorrow am. I was feeling so good and we went out and had lunch today and went to the wig shop and I just thought the tight hard feeling boobies were normal, guess not. Booooo!!!

I will let you know how it all turns out tomorrow.....

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: Jun 2, 2008 07:08 pm

Surgery in May?

Phyllis--I saw that you had expander exchange, how did that go? Much better than the mx and snb?

Ta

Did anyone have blisters on the reconstructed boobs?


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: Jun 2, 2008 01:23 pm

Surgery in May?

Hello Girls!!

Manda--Sorry to hear about your wound opening. That is so scary, when will you find out about your expander? This whole situation feels like getting to know your body all over again, then to find out that you will be losing another part is so devastating. You have probably already thought about this but if you place a towel then a ten gallon garbage bag then another towel then the sheets with another towel over where you sleep, this will protect your bed. hope it helps.

Jax--Hopeing only one node is positive!!!!! That is something to hope for!! I think they said I would start chemo in August or like 6-8 weeks after my surgery. Boy...that was not something I was looking forward to. My two little ones know about the cancer, but If I could have not told them I would be a lot happier about that. My mother died of BC Feb 2007 and my dad of diabetic complications in April 2005. I was really afraid they would think I was dying if i didn't tell them what was going on, so they seem to be a bit standoffish. They don't want to hurt me which I appreciate, but I just want stuff back to normal for them. We are moving back to Stockton, our hometown, so that is another big upset. I just have to pray for them, cause I just don't know how to protect them from all of this. Deep down I feel that I just need to be there and answer any questions they have and like I said just pray.

Kathy--I hate the drains too and since almost everyone has already had them out I will join you in complaining. They are the worst part of this whole thing. well the most uncomfortable definately.

Pam--Hoping for good reports for you too--thanks for your good wishes as well!!


What are things that we can do to prevent LE? They said I could have a shower when I came home, but that was way too soon, so I did today. I am feeling kinda bloated, have had my BM's but still feeling kinda nauseaous and bloated any suggestions? This is a long one I know..but I just wanted to get back into the swing of things!! love you guys,

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: May 31, 2008 11:22 am

Surgery in May?

Hey all,

I am home to stockton now and very dizzy. Surgery went well, I was in major pain the first night, but by the second day it was tollerable. Now I am taking darvoset and motrin. makes me very dizzy. I think I might cut down to half of he darvo. I haven't had time to read all of the posts from the last time, but I am working on it. I am very sleepy, I have been reading about 1 hour now and I think I am ready to go back to sleep. I wasn't to sleepy on the morphine drip, but very itchy. Kathy, did you get the drains out yet? I have two and they suck!! I ready you got two out, that's good!! I forgot to mention that my sentinel node was positive, so they did the full dissection. I will find out thoses results next week. Definately chemo, Jax i like that hat party!!! I told my friends to start collecting good wigs for me. I am scared too! and also mom of 2. Gotta Jam, I will be back and hopefully caught up too!!

luv,
Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: May 26, 2008 11:26 am

Surgery in May?

One more thing--an update my surgery will be bi-lat skin-sparing mastectomy w/ immediate expanders and a large fill as well as SNB. My internet is down in Oakland, so I can't go online when I am there. I will try to stay in contact when I am in Stockton.

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: May 26, 2008 10:52 am

Surgery in May?

Hey All it has been a while, I have been trying to stay away from the boards for a while and trying to not focus on the breast cancer, but my time is coming quick and I can't focus on anything else, I hope everyone is doing well. I couldn't figure out how to post the pics of Big Sur, but we had so much fun. I hope everyone is doing well. I am scheduled for wed and BS says only 1 day!!!!!! I can't believe that I hope I can stay longer if I want to. I am having bi-lat mx with immediate expanders plus a large fill d/t the fact they are doing the skin-sparing mx. Was everyone discharged that soon? I am kinda worried. My surgery is in Oakland and I will be returning to Stockton for recovery, which is an hour away. There is a hospital 1 block away from my house here in Stockton and they said they could coordinate care if there was an emergency, but I am still worried. Does anyone know how to make sure I am really ready to go home, the breast care coordinator said the worst pain is on the 3rd day and I would be in the hosp for 3 days, but the bs said nope only 1. help!!!!

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: May 16, 2008 11:11 am

Surgery in May?

oops!! I got mixed up! C-ya when I get back!!

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Breast Reconstruction, Created: May 16, 2008 10:19 am

Overweight but "not enough tissue" for DIEP...bummed

I have Kaiser insurance and they are notorious for not paying for stuff. Colleen you had all of your dx done with photos? Does this mean that almost everyone will be a candidate? I am 20 lbs heavier, a smallish 18 and about 1/4 inch shorter. I guess it can't hurt to send some pics yeah? I'm gonna give it a shot!! I feel so down about asking Kaiser for ANOTHER referral, and I know I shouldn't feel that way, but part of me feels like I may be making a big deal just because this is such a difficult process and I really just want it to be over with. Implants are much easier to recover from....ol' flip floppy me, can't make up my mind..

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: May 16, 2008 10:13 am

More than one grade/type in Lump?

Wo that just adds a whole new level of confusion to the mix don't it? Did you have chemo or rads? My BS estimated the the lump that was biopsied (sp?) to be 3cm. It seems big to me.

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Tests, Treatments & Side Effects + Surgery - Before, During, and After, Created: May 16, 2008 10:08 am

Surgery in May?

Good Morning Party People!!

Jax: I wish you could go shopping too!!

Pam: That sux that you had to have all the nodes out. My BS said if the SN is pos then she doesn't know how many she will remove till she sees how close the rest are to the SN. Scary to me. You just had SNB? If they are pos then you will go further with tx?

Kathy: We just had a heat wave where I am and I think I would be happy for a little rain, but the good news is we will be spending the weekend in Big Sur CAMPING!!! It's my 10 year anniversary!!

Sherry: You probably already said this, but why didn't they place anything? And they still left the skin? My docs made it seem like if I wanted to keep the skin I HAD to have some type of immediate recon, but I almost think I'd rather wait till after I find out if I have to have chemo or rads. I don't look forward to waking up flat, but I really wanted to have the flap surgery and I don't have time or energy for another opinion before the surgery, I would rather just get the implants if I have to.

I am feeling much better today, but it could have something to do with the fact that I am kid free and going on a beautiful drive for a super great camping trip!! We will be driving down hwy 1 which goes all the way down the CA coast!! I will post some pics 4 you after I get back!!

Love

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: May 15, 2008 09:07 pm

What are the chances like?

http://www.AdjuvantOnline.com

This is the website, I got it from another thread. Supposedly it's just for the DR.s but lots of people use it. God luck I am going there now.

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-
Posted in: Connecting With Others Who Have a Similar Diagnosis + IDC (Invasive Ductal Carcinoma), Created: May 15, 2008 08:39 pm

More than one grade/type in Lump?

Has anyone been told they have more than one type of cancer or perhaps more than one grade in the lump?

I had an "excellent" mammo last year and now have 3 lesions in the left and 1 lesion in the right. My BS only biopsied one lump and it is grade one, very slow growing, but I have so many masses....I don't get it. She said maybe there might be more than one type. I am 32 years old, but my breast tissue is not dense, so if the cancer was there, it should have been seen--yeah?

Ta


Dx 4/23/2008, IDC, 3cm, Grade 1, ER+/PR+, HER2-

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