SomeDay,SomeWay-A-C-CURE, Part 3, The Radiation Therapy

Radiation Therapy begins:

April 16th: last day of radiation-Yippie, I am so glad. My nipple is fried to say the least. I'm soooo ready and glad to be done!!!!My follow up is June 3rd.

April 6th:Apt:4:15p.m. @ TMH Rehab. Ctr.This is the last visit with my rehab therapist for Lymphedema. Ms. Marylynne said I no longer need therapy as I'm doing my home exercises quite well. She said my arm movement and the range of movement was back to 95% complete.

April 6th: Apt:3:45p.m. @ T.M.R.M.C. Radiation therapy from now until I'm done on the 16th will be what is called a "BOOST". They concentrate on the area that had the tumor, whereas before they done the entire breast area and where the nodes under the arm where as well.

April 5th:Apt:3:45p.m. Last regular radiation therapy. Thank Goodness as the burn is beginning to set in. I was given "Special Cream" to use by Dr. Newman, and I believe it has helped. She said I actually look great compared to most people. I only have what looks to be a sunburn. (But, it hurts) She said some get so bad their skin breaks down and tears and blisters, so I know I am blessed with only a tan.April 3rd: Attending Tonya's Hope, A Benefit started in Lanark Florida and that has now been extended to all in Franklin County that are dealing with issues at hand from cancer. They have mad my journey a little easier and I am blessed for that. Looking forward to the day to honor Tonya and to be at the benefit. I am blessed to be here and able to make the event.April 1st April Fools Day wasn't NO JOKE, I found out I needed 1 more week of radiation.So, my last day will be April 16th, 2010. This is the week I'll get my 9 boosts, which are directed to where the surgery was performed on removal of the tumor. I don't know why, but I just cried like a baby over just one x-tra week. I was so ready to celebrate on the 12th and to get this journey over with. BUT~~ I need to do whatever is necessary to be strong & healthy.

March 27th: I was able to make a RACE Event Motocross I love it. I went to Jacksonville and spent time with my grandchildren as well. At the race, Pro Racer Davey Millsaps signed my head for the cause, just because. He is a wonderful young man and one awesome Motocross Rider. I will try to upload the picture of my head! Davey Millsaps # 18 Thanks Davey!!~~~~

March 12th: I went to a Lymphedema Specialist per advice of my surgeon because of the 23 lymph nodes I had removed from my cancer surgery. Marylynn Gordien is a specialist who does rehabilitation on Lymphedema patients. I will do rehab with her twice a week. She will order a compression sleeve for me that I have to wear during any plane flights or during any aggresive exercises to keep my arm from swelling. I was told I had to be careful of this for the rest of my life~~

March 4th, #3 TX thru April 09th, #34 TX: Radiation TX each day after work

March 3rd, 2010: Radiation #2 at 3:10 TMRMC with Dr. Sheiliah (Ramsey) NewmanThe hardest part of radiation therapy so far is the drive from Carrabelle to Tallahassee and then back home to Carrabelle again. This takes approximately 3 1/2 to 4 hours of my day just in the drive. The therapy itself takes a very short time. I would say 20 min. including undressing and checking in. They are very prompt with their apt. times for the patients at TMRMC. I'm quite impressed. So, I work till 2:00, drive to therapy TX, by 4:00 I'm done so we drive back home. Then there is still dinner to cook. I must say it is exhausting~~~ All I need is a personnel chef and someone to clean at the house~~~Also I have noticed although I try not to let on to most that I am somewhat depressed with the radiation more so than I was with the chemo. Maybe because most feel like oh well, she is done with chemo, all is good now. Just radiation, no big deal, BUT it is a big deal and I'm tired of the whole ride now. Let alone, you also just lie on a table like a slab of meat all alone kinda spread eagle like just waiting to get radiated, zapped!~~~~~~ I am just so ready for this journey to be over and get on with my life.

March 2nd, 2010: Radiation scheduled at 10:45. !st Tx took approx. 45 min. all together. I don't know why for sure, but directly as they finished the radiation, I began to ball like a baby. I think just realizing I now have to go through this for the next 6 weeks is breaking me down a little. The drive everyday from Carrabelle to Tallahassee is exhausting. 3 hours round trip. I still am working till 1:30 ish. to make my 3:300ish daily appts. The regular routine will begin tomorrow.

February 22, 2010: Seen Dr. Shaw my Radiology Oncologist and I had a CT Scan and they done temporary tattoos to get me ready for my radiation therapy. My first Tx will be next Tuesday.They will begin my daily treatments for the following week each day around 4:00
(I hope) as I am still trying to continue to work until at least 2:00 before my drive to Tally.

February 17th 2010:Consultation w/ Dr. Shelileah Ramsey. I have met with her once before and she is very sweet and understanding. This will give us a chance to follow up since my Chemotherapy is completed. She will set me up with a 5-6 week program of radiation to be given each day. I will drive daily Monday - Friday from Carrabelle to Tallahassee. Approximately a 1 1/2 hour drive. BUT, the drive is well worth the outcome~~~~Let it begin so as to end!~~~

February 15th 2010:My Oncology nurse called today, they ran a special test last Wed. once I finished my chemo and I got news today that all my blood work came up really good. NO CANCER showed at all. I go this Wed. for a consultation, the next week I go for a simulation
(dry trial run) and then by 1st week of March I'll begin. In six weeks my nightmare on -C- Street will be over!~~

Love Davey Millsaps

Love Davey Millsaps

Love Davey Millsaps

SomeDay,SomeWay, My -C- Journey Continues, Part 2, The Therapy.

As I start Part 2. of My C-Journey, I will always have the newest post on top.

THANKSSOMEDAY,SOMEWAY, -A-C-CURE, My -C- Journey Continues, Part 2,

The Therapy.

Feb. 10th:Chemo - The last one!!!!! 2:00 appt. w/ Dr Snyder. It went very well. During his consultation he said to me, "This is something I can't say, -0- zero!" I said 0-0 what? He said that I like many others where on a regime of Adriamycin and Cytoxan, yet he added I was on a very high dosage of this toxic medication in addition to the FU-5, and that I will have radiation starting in about 3 weeks and I will follow up with Aroma-base Inhibitor (I think tis is the one he said) for the next 5 years following. Point being he said i believe in all my heart you are one of the few I can feel comfortable saying you have a zero percent chance of this recurrence. Then added i can't say zero so I'll say 10% chance recurrence. I feel so totally blessed. I want to thank all my family and friends that have supported me throughout my journey on this roll a coaster ride. It has been quite an experience. Part 3 to come:Radiation Therapy

Jan 22nd: Still not feeling up to par and wish I could go home again. Jan 21st: Went home early from work, totally exhausted, heart racing, and very flushed feeling.Went straight to bed when I got home. Jan 20th: Chemo 10:00am appt. Dr. Bandari, Start with weigh, blood pressure, chat with onc. Today they begun as usual with checking my white blood count all was well. So, the drip of the pre med began.I took my ativan to calm my nerves, then took my "Emend" once I knew my WBC was good. Then started the usual drip of the decadron, the zofran (they upped this amount) and also this time gave me pepcid in a drip as well. Then I was administered the dreaded "Red Devil" pushed in the Adriamycian. Once that was done they then gave me the Cytoxan drip, which was also a boosted amount from the normal amount I have been receiving. He prescribed me some extra compazine because my stomach has had more problems the last go round. So, to ensure no nausea he prescribed this for me. Jan 17 - 19th: Anticipation of Wed TX# 5 is beginning to close in on my train of thoughts. Again the worry, the pre chemo jitters as I call it, are setting in. I dread another 2 Chemo TX's.Jan 7th - 15th: Still feel just slightly nausea (down to one compazine a day) and I tend to get tired very easily. I am sleeping well, thank goodness for that and I have lost the dizzy feeling for now, YEAH. BUT, now I have noticed my fingers and shoulders and joints just seem to be kinda achey all the time and I have now lost all my eyelashes and most of the brows! This go around has had more downs than ups!Jan 4th - 6th 2010: Still feel under the weather. although I have returned to work after 10 days off I feel so depressed because I just can't shake the aches this go round. Besides the Emend, I now have to take my nausea pills twice daily, Tylenol every 6 hours, antacid meds every day, and depression meds to boot!~~~.I hope soon to feel better. Please Sweet Jesus, heal me ~ SomeDay,SomeWay,A-C-CUREJan 1st thru Jan 3rd: Still at home recouping from the TX on Thursday. I am having a more difficult time after each TX. The build up of the chemo is beginning to take its toll on my body. I feel very weak and tired all the time. My skin is drying and cracking and the headaches and dizziness continues to get worse. I still THANK Sweet Jesus, as I still feel so blessed. My heart knows this could be so much worse~HAPPY NEW YEAR'S EVE 2010Dec. 31, 2009:Thursday at Chemotherapy 10:15 am. Happy New year's Eve to me~I also received the results of my ECHO from Dr. Mabry and he said i was doing quite well. He also said that he was going to stop my chemo after 6 TX's rather than at 8. So, good news there. I'll be done by Feb. 2010 and I'm so happy for that. This also means my 6 weeks of radiation will be over by March. (I hope and pray)I celebrated 2010 by drinking a couple of glasses of champagne and soaking in my new JACUZZIEDec.16th 2009: Beginning to feel alive again and come out of the FOG. The sun is beginning to shine. My head is clearing~I am still dizzy however. Dec 15th 2009: Woke up still a little green around the gills. Managed to make it through the day. I noticed a few slight chest pains kinda like indigestion~continued to be dizzy and had only a slight headache. By after work I was beginning to feel a smidge better, just still in a FOG.Dec.14th 2009: I had a really hard time going to work today. I had to call the boss to let him know I was under the weather and would be late. I made it in about an hour late. I had to wait for the sun to rise, Somehow the vertigo worse while driving when it is dark~~I remained in a sick FOG all day~ when I got home at 5:00ish ~ I took a compazine, a meglazine, a couple of Tylenol X-tra Strength, an Ambium, and then I went straight to bed~slept till 5:30 pm~Dec. 13th 2009; Still feeling pretty good other than the dang migraine headaches. Drove our son back home, he lives 4 1/2 hours away~I won't do that again~Too much vertigo with the long ride~ got home about 6:00ish, started getting nauseated and still very dizzy.Dec 12,2009: Woke up pretty refreshed after a good nights sleep. I took 2 Tylenol and an Ambium CR before bed at 9:00ish. Got up at 9:00am. Fixed a nice breakfast. Fixin to catch a nap now. Till later.I am so blessed!!Dec.11,2009 eveningCooked a wonderful dinner. Grilled Porterhouse Steak,twice baked taters, a wonderful tossed salad, bake dinner rolls. Then baked 3 dozen cookies. I feel amazingly well.Dec.11,2009 @ 2:15pm:#3rd TX First take my"Emend" then she inserts my "Power Port" and OH MY I cried and cried. I don't know why I got very emotional. I felt like a baby. My RN said I was doing well considering I was on one of the very hardest concoctions. I said I had thought I had it very easy. She said NO WAY, I am just dealing with it excellent. My WBC was AWESOME, even better than the last counts next they began the Dexadron and Zofran dripping after they gave an ativan to calm down my anxiety . The started my drips. First the (FU-5) Then came those HUGE RED VIALS of COLD TOXIC Adriamycin, this injected by hand by my RN (Ms Aaron) she is so sweet!Into my PORT in goes.Aaron just chats with me the whole time keeping me calm. Then next the final drip of the Cytoxan DONE!My Cocktail(CA-FU-5) Cytoxan,Adriamycian,and Fluorouracil, drips again. When she Dec.11,2009 @ 11:00am meet w/ surgeon follow up on surgeries. Sue suggested I start a regimen of exercises to prevent lymphedema. She is sending for an approval for me to be seen for a sleeve. I will do rehab myself. I will get the required exercises on line!I CAN DO IT YES I CAN!!!!!

Dec. 7-11 had a little nausea issue. Took. Compazine once a day to help.December 2009-The vertigo continues. I will have to deal with this the rest of my journey.--Nov 19, 2009: 2nd Chemotherapy TX - All went well. I met with Dr. Bhanderi, and was told NO BRAIN METS!!!!!!!!!! YEAH!!!!!!! I had a reaction to the "Zofran" This is one of the drugs given to me to help reduce nausea. So, he cut back on the amount of this medicine to help alleviate the vertigo!!! Dr. Bhanderi was also kind enough to give me a prescription for some Ambien CR. Only 30 he said to use them wisely, he didn't want me to get addicted to them. I was very happy though to have these 30 which I will use for my first 3-4 nights after my chemo. the steroids won't let me sleep on those days and I need my rest to get better. Hopefully my side effects will be as gracious as they where the last 3 wks.

Nov. 17th 2009, Tallahassee Diagnostic received an MRI lasted approx. 2 hours. Will get results when I go for my second round of "Chemotherapy"

November 19, 2009Nov 16th 2009:Called my oncologist and they made an appointment for an MRI. Suggested I could have brain mets and they needed to do this to rule it out, therefore the brain scan. I was scared to death and my hands where shaking like a leaf. OMG. How much more can one take!!!~~~~~~~

Nov. 9th-16th, 2009: Began to almost feel normal then, UTTOH. I started to get vertigo really bad. I called my onc on Thursday the 12th because I was still dizzy,and so the RN called me in a prescription for anti-dizziness. She said if I still had vertigo come Monday the 16th, to call he.

Nov6th- 9th, 2009: I ate like I had never eaten before. I seen a picture of a CAKE and that is all I wanted. I bought (NO LIE) Twinkles, ring dings, Devil dogs, Banana Nut Bread, Snowballs, then I baked a Carrot Cake had to have it, and then an Angel Food Cake. I ate some of each that day. My hubby went shopping on the 6 th, when he came home I just devoured the bags of food. Them steroids are something else. If I eat like this he whole time OMG, what a rolly-polly I'll be.

Nov. 1st - 6th: Headaches lessened some, but I had some kind of gas problems going on. Nothing that hurt, just was burpy and gassy. Appetite improved quite a bit. Then I started by the Nov 6th HUNGER!!!

Oct. 29-31, 2009: My experience with my "Chemo Cocktail" Days 1-3 extremely tired, kinda like being in a fog. I was very fortunate not to experience any stomach problems, no throwing up. I was on a very good medicine called "Emend" I did however experience dull headaches and could not sleep the first three days as well. The steroids keep you wide awake and a sense of feeling good while in this fog. Not much of an appetite either. The headaches where easily controlled with Tylenol X-tra Strength.

October 28,2009:FIRST DOSE of Chemotherapy Scheduled @ 2:00 @ Dr. Mabry's office.To be administered, Cytoxan - 1 hour, Fluorouracil - 15 minutes, Adriamycian - 15 minutes.This is my regular regimen, unless there are unforeseen problems, then they will adjust the dosage.October 28th,after hair/pick up personnel things needed as well, all my prescription meds at Walmatt's on West. Tennessee St.Tallahassee"Emend,Prevacid,and the Zoloft"

October 28, 2009:Early morning appointment with my personnel hair dresser. I am cutting all my hair off to have it sent off to (Hip-Hat-Hair). They will create a cap w/ my own hair attached to it. This should be more comfortable to wear than any wig I've tried. Bless those that have tried to help me with offering a wig. BUT, my CHOICE is my own hair. I also prefer to have it done this way, rather than it suddenly start falling out 2 weeks after chemotherapy starts, in clumps at night in bed or perhaps in the shower, as I'm shampooing my hair. I'm not sure I would deal well with that situation, so this is my CHOICE!

October 23,2009 @ Dr Kent's,(my primary care health physician), received influenza shot during exam to ensure my health before starting chemo on Wed. The 28th. Ms.Kay Fin Law renewed all my regular prescriptions for my Zoloft and for my Prevacid. She said to continue back w/ all my regular meds. They will not interfere with Chemo TX.

October 19,2009: @ 6:00pm: Chemo Class for all new patients diagnosed with Breast Cancer. Dr. Mabry, my chemo oncologist strongly suggested myself and my husband to attend this class to make us well informed of all the in & outs, ups & downs and all side affects of receiving chemotherapy.We choose to attend class.

October 15, 2009:Scheduled for Surgery at TMH w/ Dr. Snyder to have a "Port" placement. This will allow them to give my chemo and any other drugs needed, as well as draw blood, All from the port that is placed surgically just below the collar bone and a bit above the breast., right below the skin's surface. This also is a MUCH safer way of receiving some of the chemotherapy treatments as some are very TOXIC. If any where to escapes into the skin it would cause a BAD reaction and could lead to a very serious infection. Having the "Port" will be a better way to receive the treatment versus the "pic" or by intravenously. Therefore my choice was the "Port"

October 14, 2009:Attending @ 1:30pm Look Good, Feel Better Program, put on by "The American Cancer Society" to help women restore their appearance and self image, held at TMH 'A Women's Place'October 09, 2009:Appointment with RN @ my surgeon's office, Dr. Snyder's. To evaluate the infection caused from the drain tube after my "Axillary Dissection" I must be careful of infection before I continue. I feel confident that the infection is clear.

It's OK! It'll be back! Maybe just not my BLONDE Chicken feather Colour

See Ya Oct 28,2009

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Day to Day on my -C- Journey

THANKS FOR THE breastcancer.org SITE SO I CAN KEEP UP WITH WHAT'S GOING ONE FROM DAY TO DAY MINUTE TO MINUTE, AS I NEED, THANK YOU SOOOO MUCH!

This is my journey on the biggest rollacoaster ride ever!!!!

July 23, 2009 Check up with primary heath care, because I noticed a lump (Dr. Kay Fin Law)
July 30, 2009 Complete physical, pap, blood tests, sugar diabetes, cholesterol, eyes,etc.

August 5, 2009 Dr. Kay scheduled a mammogram & an ultrasound, and a vaginal ultrasound, which I did not like at all!!! (Women's Imaging)

August 12, 2009 ultrasound guided "core biopsy" L. Breast took two samples (painful as Hades) IT HURT I CRIED, A LOTThis test felt like I had a branding iron sent through my entire breast, and stayed painful for quite some time thereafter!!!

August 13, 2009 confirmed diagnosis cancer L. Breast

August 17, 2009 M.R.I. to check R. & L. Breast for futher diagnosis purposes. Now they want a biopsy for the R. Breast as well. OH NO!!! I freaked out and cried, because of how bad the first one was. I received notice of this by voice mail. I was driving and had to pull over because I almost lost it on the road!!! I was so frigging scared.

August 19, 2009 ultrasound guided "core biopsy" R. Breast, not painful this time :-) YEAH August 19, 2009 meet surgeon Dr. Snyder - discussed my diagnosis some. 2.5cm lump, estrogen positive, invasive, how they will check my guardian nodes, what would happen, etc.

August 20, 2009 Recieved diagnosis on R. Breast, it was NEGATIVE!
August 20, 2009 Set up appt. for pre-op Sept. 2nd, & surgery for

Sept. 3rd.Sept. 01, 2009 Requested anti-depressant from my health care physician, I will pick them up and start them on Wed. This is my scheduled pre-op day.Dr. Kay Fin law>Zoloft

Sept. 02, 2009 Scheduled for pre-op @ 11:30 am (I have my questions & recorder ready)

Sept. 03,2009 Scheduled Surgery???????? Talk to y'all later, much later!!! to fill in the blanks!Went to TMH for my surgery. I was a little anxious and my 8:30 scheduled appointment turned out to be about 1:00 that afternoon. I was being prepped for the lumpectomy, and I was watching the core needle for the surgery being put into my L. breast. Then as it touched my cancerous mass, the pain was again unbelievable. He told me to breath, I started breathing like a woman does as she goes into labor, and he said one last push. He had to get it into the center of the affected area. As it entered, I SCREAMED loudly. He said to quickly get me up to the surgery area and begin meds immediately even if surgery was still going to be a while. I believe they thought I was going into shock. My area of cancer was sooooooo painful, unlike anything seen before. Just like when they performed the biopsy, the pain was like a branding iron piercing into my breast and then doubled with the feeling of an electrical shock.~~~~~~~~~~~It's now time!!Dr. Snyder began the surgery. Lumpectomy, followed by removing three sentinel nodes. When I came out of my sleep in the recovery room, my husband turned to me and said, "Baby, Dr. Synder took out three sentinel nodes and they where all negative." I was so relieved by the news I instantly felt like I was better. I was given my instructions to return Friday Sept. 11, 2009 for my post-op follow up appt. released and went home. I recouped for 4 days, I must say I felt pretty good for the most part.I have returned to work
Tues.the 8th. I have light duty work so it is not a problem for me being there. My treatments should JUST be radiation and hormone blockers, but my surgeon said it's up to the oncologist. So, until Friday I won't know for sure.Sept.11th:follow-up was bad news,turned into rediognosis because one of the sentinal nodes had a 2mm Cancerous node! I know am scheduled for anothber surgery and possibe chemo now in addition to the rads treatments. I'll speak to Sue Fishara about the onco DX even though it's in the NODE! 2nd opinion!My NEW surgery date again is Sept17th. Complete auxillary disection, the removal 2/3's of my lymph nodes I will KEEP FIGHTING!!!!

Sept. 16, 2009 Happy Birthday to my mom.

I'm getting things packed and ready to go for my overnight stay. As well getting mentally ready for tomorrow's surgery. Axillary Dissection of 2/3rd. Lymph Nodes, say a prayer & hold my hand Becky!!!! (This is my sissy she passed away from cancer but was a brave girl)

Sept. 17,2009; Surgery by Dr. Synder for a complete Axillary Dissection of the Lymph Nodes. Stayed overnight in the hospital. This was much more painful than the previous surgey. I felt as if my arm has been broken again, I will have to do serious rehab! I have a drain tube coming out from under my arm, uncomfortable and hurts as well. I take readings of the fluids that drain 2-3 times a day. When they level out to 30ML per day for two days in a row I can have them taken out. I can not wait!!!

Sept.18, 2009:Released from the hospital by choice. I choose my husband to be my caretaker, and thank the Lord Sweet Jesus I did. He has been a wonderful nurse!!!! Took excellent care of me, feed me, clothed me, washed me. He didn't even hurt me when he had to strip my drain tube each time. (Unlike a med at the hospital) So, my choice to go home was good for me.

Sept.20, 2009 Feeling MUCH better since the surgery. I'm Soooooo, ready to get on with my life!

Sept. 21, 2009: Feeling much better, returned to work. I have light duty type work and can handle it OK. Dealing with the drain is a nuisance however. But, I guess I need it.

Sept.23,2009: spoke with Sue, this afternoon the ARNP and she said my drain tube will be taken out next Thursday and I will see my Radiology Ongologist also on the same day and then I will (should) know how the path of my journey will continue.

Sept. 24, 2009: Recieved call that I had 21 more nodes removed during the surgery, only had one more that was positive. It was not one of the end ones that where special marked, which is a good piece of news. GOT my appt. for my hemotologist today with a Dr. Mabrey and is scheduled for tomorrow!! Finally, this is the oncologist who decides what type of chemotherapy treatment I'll be given.

Sept25,2009:Dr.Mabrey@11:30am,my prognosis was that I WILL receive chemo + radiation+ hormone therapy. Exact dosage + time frame will be decided when he and the radiologists and my surgeon get together and we will all discuss the path reports. I will most likely start the chemo end of October.

Sept.28,2009, My drain is still producing over 30ML and appears a little red around the opening of the drain, so I need to call Dr. Snyder's office for an opinion on status.Oct. 1, Sue remvoed the drain,slightly painful. I do have an infection, so I was put on antibiotics for the next two weeks.She has also scheduled me for my port placement in two weeks with Dr. Synder at TMH, as long as my follow up next week is good and my infection is gone.I'm researching different type of chemotherapies I can discuss with my hematologist to know what is best for me, so when I see Dr. Mabrey next week I'll be ready!
Soooooo many Dr's
Soooooo confusing!!
To be continued ,SOMEDAY,SOMEWAY,A-C-CURE

SomeDaySomeWay A-C-CURE

Biography I still don't know what the HELL is going on! I've been confused since this ride started. Just trying to understand the lingo, chemo-brain, rads, DX,blah,blah,blah. Appointments out the kazoo.I don't know if I'm coming or going, maybe sometimes both at the same time.It's been a whirlwind, a spin, a roller coaster ride. BUT, I still don't have enough answers. Everyone else says everyone else will tell you what is going on. Then I still know nothing! I don't know an oncologist, from a surgeon, to a whatever specialist, it's all a new language. I truly am just freaking out!!~~

Diagnosis: 8/13/2009,

ILC, 2cm, Stage II,

Grade 2, 2/24

NODES: 1=1mm +1= 6mm,

ER+/PR+, HER2-

Diagnosed: August 13, 2009

Type: Invasive or Infiltrating Lobular Carcinoma

Recurrent? No recurrence

Metastatic? YES

Stage: Stage II

Lymph Nodes Removed: 24

Positive Lymph Nodes: 2

Tumor Size: 2cm-2.9cm

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

SomeDay,SomeWay, A--C--CURE__