Showing posts with label Grange. Show all posts
Showing posts with label Grange. Show all posts

Thursday, October 13, 2011

I am done with Chemo!!!!

I am happy to report after 5 months, 16 sessions and countless hours,  I finished my last chemotherapy session this afternoon at 4:40 p.m.!!! Yay! I have not been this excited in years. To know that the worst is over and I only have radiation and one more surgery left puts a HUGE smile on my face. Normally I need to take a nap after chemo (because the drugs they give me before the chemo knocks me out) but today I can't sleep. I want to celebrate! I could not have gotten through chemo without the love and support from all my family and friends. Chemo drivers...THANK YOU so much for taking time out of your busy schedule to take me to and from chemo. You know who you are!  My advice to anyone going through chemo:  If you are fortunate enough to have the love and support of friends and family ask them to be your chemo driver.  It was so hard to go out of the house after chemo sessions because of fatigue, nausea and the fear of getting sick.  Because I had a new chemo driver every week I got to see friends I hadn't seen in a while.  Instead of dreading chemo, I looked forward to it because I knew I would get to hang out with friends and family.  I do have to give a special shout out to three people:



Chemo Session #15- October 8, 2011
Deb Bothof took me to a few chemos and stopped by my house every week to see how I was doing.

Chemo Session #15 - October 8, 2011
Lyndsey Foster signed up for my second chemo session but came to 14 sessions!
There is one thing that I learned about Deb and Lyndsey...they are caretakers and all they wanted to do is take care of me.  I never expected them to go above and beyond but that is who they are as people, kind, loving and generous....angels sent,  to get me through chemo. =)  Love you both! 



Chemo Session #15 - October 8, 2011
My mom - Doesn't she look great?!
My mom has been there for me since day one of diagnosis. 
She watched the kids when I couldn't up until she was diagnosed with
cancer.  We talk on a daily basis and she is doing fantastic!
 Maybe our twins (aka: our ta ta's) will be born in the same month?
I will have 33 radiation treatments (Monday - Friday for 6 1/2 weeks) that will start on Halloween. The side effects do not compare to chemo so it will be a breeze! These past two weeks have been busy. I am working on a business plan for my non-profit organization.  "Auntie Em's Angels" will educate cancer patients on the importance of eating healthy and exercising during and after cancer treatment. I want to create awareness for everyone to prevent cancer. What you put in your body and how you take care of yourself can and will prevent cancer from starting in the first place.

I met with Tonee Gay, Executive Director with Midlands Community Foundation and we will be partners. They take care of the accounting and some of the marketing pieces and I can focus on fundraising and creating the programs that need to be in place. Hopefully I will have the website up in the next few weeks so you can see what we are doing! =)  My friend Lyndsey Foster is going to help develop some of the programs too!  I am looking forward to my new journey and hope to help as many people as I can! =)

Here are more pics from the past couple of weeks.


My sister added to her family!
Meet Lulu, isn't she cute?
She is a maltese / yorkie


Komen Walk - with my nieces and nephews
Cullen, Avery, Sully and Addison

My sister Angie with the kids

My general surgeon was there...Dr.Grange
I was suppose to be at a breakfast the day before for cancer survivors
I missed it and Dr. Grange informed me that I won $150 Gift Certificate
to a clothing boutique...but I had to be present to win....=(
Darn it!  I shouldn't have slept in!

My friend Sasha ran while I walked around the venue.
Sasha runs for her Aunt every year who passed away from breast cancer 2 years ago.

Vala's Pumpkin patch
Paxton and Olivia

Me, Olivia and Steve

Travis, Paxton, Olivia and Michelle




Thank you to my Aunt Vicki for the new cup and nail polish!

Thank you to the nurses of Midlands Cancer Center!


MY LAST CHEMO SESSION - #16 is my new favorite number!
Lyndsey, me, Deb and Steve

Thank you to my husband Steve for taking care of me and Olivia, you do such a great job and I could not get through this without you.

Thank you to all our friends and family for your love and support - We are truly blessed!

Saturday, June 25, 2011

one...twO...THREE.....KNOCKOUT! (Chemo #3)

Oh what a week this has been!  I have been extremely, fatigued, nauseous and angry to write.  I thought if I give it a day or two so I could clear my head .

I will start from the beginning....

My index and middle finger have been completely numb since my first surgery in April.  When Dr. Grange put my chemo port in my right arm it hit a nerve knocking out feeling and movement.  This makes it extremely difficult to do everyday tasks I use to take for granted.  Writing, typing, opening jars, slicing food...you get the idea.  Let's just say I have adapted to my new life style.  Since then I can now crack eggs with my left hand, but that doesn't mean I don't want my right hand back!  I WANT my right hand back!

Since then I met with Dr. Tiedemann a hand surgeon with GIKK who then referred me to a neurologist Dr. Weber.  We need to find out if my nerve will come back on it's own or if I will need another surgery to repair it.

Thursday, June 16, 2011

12:00 p.m

I met with Dr. Weber a neurologist who did a series of tests which included electric shocks and needles going in and out of my arm and hand.  OUCH!  Let's just say when I left his office I didn't want to go back.  Dr. Weber said he would have my results at the end of the day and I would find out once I met with Dr. Tiedemann.

2:00 p.m.

Chemotherapy #3



My good friend Gretchen took me this time.  I have known Gretchen since junior high but we became much better friends the summer before we started high school.  We would enjoy long afternoons in her swimming pool, taco and pizza night when I would stay with her family when my parents were out of town.  Gretchen and I were also on junior varsity cheerleading our sophomore year in high school.  I paid it forward and trained Gretchen since I had one year under my belt.  In return Gretchen found us our new coach Jenna who was a former dance teamer.  She trained with us everyday for metros in which we placed first in our division and first place overall winning the entire competition which included varsity squads.  We were the #1 squad in the Omaha Metro area.  That was such a fun year! 

From there we went to college and when I met my husband Steve, we all found out Gretchen's family was related!  Steve and Gretchen are second cousins.  Gretchen's mom Nancy (Pottebaum) Ballard's dad and Steve's Grandpa are brothers!  It was funny because when I first started dating Steve I kept forgetting his last name so I would always call Gretchen and ask. When I did forget I would always say Steve's last name was Potterybarn.  =)

Gretchen is expecting baby #2 a Boy!

Our friend Lyndsey stopped by to hang out too!



Friday, June 17, 2011    

Happy 39th Anniversary to my parents! 

Happy Anniversary to Lyndsey and Jerid Foster!

1:00 p.m.  Get my nuelasta shot
3:00 p.m.  Get my ta ta's filled

4:00 p.m.  Down for the count

Saturday, Sunday and most of Monday I was sawing logs.  I could barely lift my head, eat or drink anything without dry heaving.

Tuesday, June 21 , 2011

I thought I was back for the week to spend with the kids.  Today we spent the entire day indoors because it was raining.

Wednesday, June 22, 2011

Started getting sick with cough and sore throat.   Thank God my mom is on call she came to relieve me for the rest of the week so I don't get sick.  I called the nurses line at my oncologist and it took an entire day of me calling back at least 6 times to get an antibiotic.  LONG story here but lets just say the nurses line at my oncologist needs a lot of HELP! 

Thursday, June 24, 2011

12:20 PM

Met with Dr. Tiedemann to get my results for my hand.  Of course he said my median nerve in my right hand has a partial cut so I will need surgery.  UGH!  As he was talking about the procedure I was fighting back tears.  How in the heck am I going to be able to do chemo and have a surgery thrown in the mix.

4:30 PM  I was feeling awful so I went to my oncologist to get fluids and nausea medicine.  Dr. Thome' said I could have the surgery.  He would just administer a 1/3 of the dose on my 4th round. 

After sleeping on it I made the executive decision to not do chemotherapy next week.  There is no way my body is going to handle chemotherapy and surgery within hours of each other.  I am taking CONTROL.  My body...My decision!

I am also researching alternative treatments outside of chemo and radiation.  If you know of any doctors, books or websites to alternative treatments send them my way!

I know chemo is suppose to work but I hate feeling like crap.  I want to feel healthy and energetic like I use to! =)

Friday, June 24, 2011

Scheduled my hand surgery with Dr. Tiedemann for Friday, July 1, 2011.  I tried to cancel my chemotherapy with Dr. Thome's nurses and once again no one called me back.  So when I don't show up for my session next Thursday I might get their attention!

Please pray for my hand to come back and for a safe and successful surgery.

Don't forget!  Today is the last day you can vote for my friend Melissa G. to win $2500 to donate to Susan G. Koman! https://www.mkmakeovercontest.com  There are 9 Melissa G's so here is a picture of Melissa.  I couldn't get the one from the website to work...I am sure you all are smart enough to figure it out!  =)  I have known Melissa since high school.  We were on dance team my junior and senior year and were roomies in college my sophomore year.  Please support Melissa on her quest to win $2500 for Susan G. Komen! 



This is Melissa G!

Thank you to:

Jeff, Traci, Mia, Sam and Ava for the Papa Murphy's pizza, the adorable hat and sign!

John and Joan Allen for the delicious ribs and potato salad.

Sara Rogers for the delicious dinner!  Tomatoes with feta cheese and Chicken pitas!

Deb Bothof and Matt Edstrand for the organic produce and rice crispy treats.

My sister-in-law Jessica for the generous donation to Susan G. Komen of Iowa in my name.

Melissa Gregory for entering a contest to win $2500 to donate to Susan  G. Komen in my name!

My sister for watching Olivia Wednesday night.

My Mom for always watching the kids when I am to sick or weak.  Love you Momma!

Thank you to all our friends and family for all your love, support and prayers!

Monday, May 2, 2011

Thank You pt. 1

Tuesday, April 26, 2011

Thank you to my sister who drove and stayed with me for another unexpected surgery.  I had to go back to Midlands Hospital for surgery to remove my chemo port.  Dr. Grange came to the conclusion I would need a pediatric port because my arms are so small.  They are going to wait until I get all the feeling back in my fingers and my hand is completely functioning before they put in the pediatric port.  It will go back in my right arm.  For the anesthesia for surgery they had to put in an IV but they couldn't use my right arm, because it was already in pain and they couldn't use my left arm, because they took out almost all of my lymph nodes from my mastectomy the week before.  So they had to put the IV in my foot.  I am not going to lie...it hurt!  Of course I could not shower for two days after surgery...but at least it wasn't a week like the first surgery I had.  I stayed at my sister's because Steve travels for his job and he was going to be gone this week.  Thanks to my sister for taking on the additional duties of taking care of Olivia and me while Steve is out of town.  You are the best!

God bless my mother who is watching all the kids until I am recovered from surgery and the days I have chemotherapy and radiation.  Thank you to my dad for helping out by driving the kids to and from school.  You have helped me so much during these last few weeks.  Thank you will never be enough.

After my first surgery I received so many phone calls, texts and gifts.  It is so overwhelming as I am hearing from friends that I have lost touch with over the years and their generosity has sincerely touched my soul.  I get so emotional when I think the time and effort friends and family have put in.... all for little ol' me.

I have so many thank you's and I dedicate this blog post to all of you who have reached out to me with your kind words, cards, phone calls, flowers, gifts and meals.  There are so many I hope that I don't forget you.  I tried to write them all down post surgery.

THANK YOU to:


My Aunt Linde and Uncle Terry for bringing over the first meal with beautiful flowers. 
Home made chicken noodle soup always hits the spot.

Joan and John Allen for our second meal.  Mexican, fruit and brownies

Jen and Matt Fehringer for the enchiladas, salad, muffins and cookies.

Katy Bode and Deanna Wolf- The Steak salad and soup were delicious!

Kathy Knickrehm Your Chicken and rice was wonderful

Kelly Robson - LOVED the fettuccine Alfredo the kids loved your Easter themed cupcakes.=)

Thank you to my sister-in-law Rebecca for the adorable necklace! 
Thank you for taking the time to make it.




Thank you to:

Mary Jo Ellis for the whole foods gift card.
Barb O'Brien for the gift card to Target.
Kay Bataillon and Barb Jackson for the gift card to Target.

Monday, April 25, 2011

Post Surgery and Cancer Diagnosis

The days that followed my surgery I was never in any major pain.  I stayed on top of the pain medications and did what the doctor's told me to do, rest but try to get up and walk as much as I felt comfortable.  I can't lift my arms or pick up anything over ten pounds.

For five days after surgery I had brought some books to the hospital to read but I could not see or read anything up close.  I thought I would have to get bifocals because my friends and family would shoot me text messages and emails and I could not read or respond to any of them.  The doctors said anesthesia does have short term effects on eye sight. 

My only complaint is my right arm and hand.  Dr. Grange did say it was difficult putting in my chemo port because I am so small and don't have much meat on my bones.  Either the swelling or the port itself is sitting on a nerve which makes my index and middle finger completely numb.  It wouldn't be a major issue but it is on my right hand.  I can't physically write anything.  I have been wanting to write thank you notes for a week now but I physically can not do it.  Steve left me for an hour one day to go grab a sandwich.  I thought I could handle Olivia's lunch a simple peanut butter and jelly sandwich but the jelly jar was brand new and I could not open it.  I can't do my hair or make up, use a fork or cut up fruit.  It is so frustrating!  Dr. Grange wanted to see if it was the swelling that was pushing on the nerve but I know it is not the swelling because it is getting worse.  I couldn't sleep at all last night because any which way I put my arm a sharp pain shoots up to my fingers.  Other then that my all my drains were taken out a week after the surgery and my body is healing quickly so they moved my chemo date up to start May 5th.

Steve and I met with Dr. Grange this past Thursday to get the results from the pathology report.  This will finally give me my stage of cancer.  I learned through this process women have 30 lymph nodes each on the right and left side of their breasts.  Lymph nodes are small bean-shaped parts of the lymphatic system that drains fluid outside blood vessels which is called lymph.

Lymph nodes produce immune cells to help fight infection. They also filter the lymph fluid and remove foreign material, such as bacteria or cancer. Common areas where lymph nodes can be felt include the armpit, behind the ears, and sides of the neck.

When breast cancer spreads, lymph nodes in and around the armpit are some of the first places it travels, and surgeons often remove some of these nodes to determine whether the cancer has spread.

Dr. Grange removed 27 of the 30 lymph nodes and all 27 tested positive for cancer.  My tumor a month ago when I met with my OB GYN Dr. Dan Kirsch was 3-4 cm in my left breast. In one month it grew to 6 1/2 cm.  That is huge tumor!  Dr. Grange tested the tissue on my right breast and said she found the beginnings of cancerous tumors on my right breast.  If you are diagnosed with breast cancer at a young age cancer is much more aggressive.  If I had gone through with the second opinion I was seeking at the time it could have been an extra two weeks and I could have been at stage IV.  I am so glad I went with my instincts this time.  I stopped my second opinion early because I just knew I didn't have much time based on my first opinion.

To get the stage this is the chart they go by:  If you scroll all the way down to IIIC this is my stage and diagnosis.

Stage 0
Stage 0 is used to describe non-invasive breast cancers, such as DCIS and LCIS. In stage 0, there is no evidence of cancer cells or non-cancerous abnormal cells breaking out of the part of the breast in which they started, or of getting through to or invading neighboring normal tissue.

Stage I
-Stage I describes invasive breast cancer (cancer cells are breaking through to or invading neighboring normal tissue) in which:
-the tumor measures up to 2 centimeters, AND
-no lymph nodes are involved

Stage II
Stage II is divided into subcategories known as IIA and IIB.
Stage IIA describes invasive breast cancer in which:
-no tumor can be found in the breast, but cancer cells are found in the axillary lymph nodes (the lymph nodes under the arm), OR
-the tumor measures 2 centimeters or less and has spread to the axillary lymph nodes, OR
-the tumor is larger than 2 centimeters but not larger than 5 centimeters and has not spread to the axillary lymph nodes

Stage IIB describes invasive breast cancer in which:
-the tumor is larger than 2 but no larger than 5 centimeters and has spread to the axillary lymph nodes, OR
-the tumor is larger than 5 centimeters but has not spread to the axillary lymph nodes

Stage III
Stage III is divided into subcategories known as IIIA, IIIB, and IIIC.
Stage IIIA describes invasive breast cancer in which either:
-no tumor is found in the breast. Cancer is found in axillary lymph nodes that are clumped together or sticking to other structures, or cancer may have spread to lymph nodes near the breastbone, OR
-the tumor is 5 centimeters or smaller and has spread to axillary lymph nodes that are clumped together or sticking to other structures, OR
-the tumor is larger than 5 centimeters and has spread to axillary lymph nodes that are clumped together or sticking to other structures

Stage IIIB describes invasive breast cancer in which:
-the tumor may be any size and has spread to the chest wall and/or skin of the breast AND
-may have spread to axillary lymph nodes that are clumped together or sticking to other structures, or cancer -may have spread to lymph nodes near the breastbone
-Inflammatory breast cancer is considered at least stage IIIB.

Stage IIIC describes invasive breast cancer in whichTHIS IS MY STAGE
-there may be no sign of cancer in the breast or, if there is a tumor, it may be any size and may have spread to the chest wall and/or the skin of the breast, AND MY CANCER DID NOT SPREAD TO MY CHEST WALL
-the cancer has spread to lymph nodes above or below the collarbone, AND
 MY CANCER DID NOT SPREAD TO MY COLLARBONE
-the cancer may have spread to axillary lymph nodes or to lymph nodes near the breastbone

Stage IV
Stage IV describes invasive breast cancer in which:
the cancer has spread to other organs of the body -- usually the lungs, liver, bone, or brain

"Metastatic at presentation" means that the breast cancer has spread beyond the breast and nearby lymph nodes, even though this is the first diagnosis of breast cancer. The reason for this is that the primary breast cancer was not found when it was only inside the breast. Metastatic cancer is considered stage IV.

After Dr. Grange told me my stage I kept thinking thank God it wasn't stage IV and it did not spread.  It really didn't sink in how serious my condition was until after I got home and did a little research.  I know I am not a statistic but the statistics show 49% of people who are diagnosed with Stage IIIC breast cancer live up to 5 years after they are diagnosed.  I am praying now that the chemotherapy and radiation kills off all the cancer cells that could have been left behind after surgery.  I also pray that after 2012 I never have to hear the words "You have cancer" again! 

I hate cancer more then ever.  It took the life of Hannah a 5 year old girl who passed away Easter morning.  She is in my Auntie Em Prays section.  Two out of three have been killed by cancer since I did the Cancer walk down in Lincoln.  Hannah's story was introduced to me by my friend Kathi.  It makes me angry that her life was cut short.  The other two people Kathi was walking for was her boss Bob who passed away last year from cancer and me.  I don't plan on going any where with out a fight.  I am determined to come out of my situation cancer free and help other women who find themselves battling with breast cancer.

Ladies, Please do your self breast exams  two to three days after your period.  It saved my life and it will save yours!

Friday, April 15, 2011

Surgery Day!

Friday, April 15, 2011

6:30 AM  Steve and I arrive and check in at Midland's Hospital.

I am introduced to my nurse as she takes me back for a urine sample, wash down with surgical wipes, change in to my hospital gown, surgery tights, stockings and surgery cap.  Holy cow did I look ridiculous!  My mom and dad arrived for a last good bye and of course my dad was trying to get a picture of me.  Needless to say I won..there were NO Pictures!

I was starting to get anxious as there was a clock right in front of me and I found myself staring at the seconds.

7:15 AM
The anesthesiologist came in and asked me a LOT of questions and said I was going to be his easiest client.  I have been healthy my entire life, he laughed when I told him I never had a cavity, so there were no major concerns.

The nurses put in my IV and Dr. Grange (the general surgeon) came in to brief us before surgery.  The surgery lasts at least four hours so Dr. Montag (the cosmetic surgeon) wouldn't arrive for another hour when Dr. Grange needed her to start with her part. 

7:45 AM...now I am starting to get really nervous....only 15 minutes until surgery.

Dr. Grange is doing double mastectomy and a biopsy on my lymph nodes. If they test positive for cancer then she removes those nodes and several ones around them to make sure she removes all of the cancer.  Dr. Montag will move in after Dr. Grange and insert expanders under my breast muscle.  They look like deflated balloons and once I heal from the surgery (3-4 weeks) I will go in every week to have them filled with saline solution to help stretch my skin to my desired size. (This could take 3-6 months) I am going for a B cup this time... a gift to myself!  Once I get to a B cup then the expanders are removed in another surgery then an implant will take its place.  When it is all said and done I will look like a barbie.  Ta Ta's with no nipples and they will move with me.  Another bonus, when I am eighty my boobs will still be perky!  =)

THANK YOU Midlands Choice Insurance for my new Ta Ta's! =)

I remember one of the nurses say I probably won't remember much of the conversation because they started to administer the anesthesia.

8 AM

I remember the nurses rolling my bed past Steve and my parents going to the surgery room and then darkness....

9 AM, 10 AM, 11 AM,

12 PM (Steve said Dr. Montag came out and said everything was going fine, Dr. Grange was finishing up and should be done around 12:30 PM,

1PM.......

1:30 PM They finally got me to wake up from the anesthesia.

All I remember is seeing my mother and father-in-law and saying thank you for coming and then I was out for the rest of the day.

I don't remember this but Steve said when I woke up I was complaining of a pain in my arm. (from my port for chemo)

I am not sure when I woke up again but it was later in the evening and Steve was in a reclining chair next to me watching TV.  At this point I met my night nurse Megan who promised me to give me the much needed pain medications every 4 hours.  She brought me some water and did bring me my medications every four hours.  I had no pain. =)

Thanks to Marv and Annette my in-laws who drove all the way from Remsen, my friend Lyndsey who sat with my family and Steve while I slept, my parents who waited patiently for me to come out of surgery.  Thank you to my husband who was by my side through out today, Saturday and Sunday.

Thank you to my sister-in-laws Rebecca and Jessica who sent me pink roses.



Thank you to my Aunt Vicki and Uncle Denny who sent a bouquet of flowers.


Thank you to Ruth, Scott, Grant and Kyle who sent flowers.



Thank you to Leah, Chad and Charlie for the beautiful Tulips.


Thank you to my Aunt Linde, Uncle Terry, Leah and Chad for having cleaners come to our house.  It was spotless!

Thank you to Crystal for coming to visit me the next day, for the flowers, magazines for Steve and gift for Olivia.



Thank you Lyndsey for coming to visit me the next day.

Thank you Sasha for my get well kit! =)





Thank you Louise for my support pillows.



Thank you to my mom and sister for coming to visit me the next day.

Thank you Travis and Michelle for watching Jake and Elwood.

Thank you to my sister for watching Olivia the entire weekend.  I am sure she had a blast hanging out with her cousins.

Thank you to Dr.Grange and Dr. Montag and the staff of Midlands Hospital.  You made my stay very comfortable and helped me to get on the fast track to a complete recovery.

Wednesday, March 30, 2011

My Team of Doctors

MY SURGERY IS FRIDAY, APRIL 15, 2011 8 A.M.

MIDLANDS HOSPITAL, PAPILLION, NE

20 WEEKS of CHEMOTHERAPY STARTS
THURSDAY, MAY 19TH AT 2 P.M.

Chemotherapy Schedule
Weeks 1-7 are every other week so (week 1, 3, 5, 7)
I lose my hair after week 3 =(
Weeks 9-20 are every week

Followed by:

5- 6 Weeks of Radiation (Will know for sure after surgery)

YAY!  I WILL STILL HAVE HAIR FOR MY BIRTHDAY! =)

General Surgeon
(She is taking my (non existent -A size) Ta Ta's Off!
 I wish her luck trying to find them =))

Everyone wants to know how we chose our doctors.  To be honest, I went with facts and my instincts.  Dr. Grange specializes in ONLY breast cancer.  Instead of inserting the port for chemo in a separate surgery under my collar bone (which will leave a visible scar) she will put it under my arm.  She does this surgery while I am under during my reconstruction.  Instead of being awake for the sentinel lymph node biopsy  which sounds extremely painful, Dr. Grange has the radiologist to do this while I am under for the double mastectomy.


Aesthetic Surgical Images
(She is going to give me new Ta Ta's! =)

I chose Dr. Montag because she was referred to me by Dr. Grange and we just hit it off!  She is giving me my B cup....that is if my skin can stretch that much! =)  YAY!

Stephan D. Thome', M.D. Ph.D. (hem), F.A.C.P.
Medical Oncology/Hematology
Nebraska Cancer Specialists
(He is taking my hair!)

I chose Dr. Thome' because he knows his stuff! Good Lord! This is probably the smartest person I have ever met. He also gave me a lot of facts to help choose my general surgeon. He answered ALL my questions and gave it to me straight - no dancing around topics. When I left his office I felt like a huge weight had been lifted off my shoulders.

I AM IN GOOD HANDS!  =)

All I can ask for you is to pray the surgery is successful in removing the cancer and the chemotherapy and radiation will get rid of it FOREVER...........
AND...pray that my skin stretches so I get my B cup! =)

Monday, March 14, 2011

Auntie Em is getting New Ta Ta's

First off I would like to say I think my phone almost broke today from all the texts, phone calls, emails and face book posts.  Holy cow!  THANK YOU for all your support.  Thank you to Leah who brought us dinner this week.  You know the way to my heart. =)  Delicious!

Today's report is the best news I have heard in 7 days.  I have breast cancer but it has not spread.  ALL YOUR PRAYERS WORKED!  I can't begin to tell you how relieved I am right now.  I am not saying it is going to be a breeze after this but at least we can just focus on one area.  Dr. Grange did say that she is questioning my lymph nodes.  If it has spread to 4 or more then I will have radiation in addition to chemotherapy. 

I have always wanted a boob job but I would never have the guts to get one. BE CAREFUL WHAT YOU WISH FOR!  I am having a double mastectomy and instead of my A cup I asked if I could go up a size to a B.  I figure if I am going to feel like crap for the next 6-8 months why not give myself a gift and have our insurance pick up the tab.  Steve just requested a C...hmmm....I am going to have to think about that one.  This surgery is 4 weeks of recovery...UGH!  Thank you mom, dad, Angie and Dave for offering to help me with the kids.

It gets better...I get a new hairdo too!  After I have the double mastectomy it will be followed up with 2-6 months of Chemo (depending on what they find with my lymph nodes).   So, yes all my hair will fall out.  THANK YOU Brea for referring me to a place who offers free wigs to cancer patients.

If 4 or more lymph nodes are affected then it will be 5-6 weeks of radiation after the chemotherapy.  If they are not infected then we get to skip this step.

I met some great people up at Lakeside.  Thank you to Collette, Patty, Katie (CT Tech) and Jaymi (Nuclear Medicine Tech).  Jaymi was diagnosed with breast cancer a year ago in May and I grilled her on the experience she had with her chemo treatments, mastectomy and how she feels today.  She has short hair now, looks and feels great!  My goal is to be where she is one year from today....new hair, new ta ta's and cancer free!

Thank you to my husband Steve for all your love and support.  It was fun spending time with you today. 

Love you! XOXO

Saturday, March 12, 2011

Auntie Em has Cancer

After meeting with Dr. Grange for my biopsy results my biggest fear is coming true.  I do have breast cancer and although she is not able to give me a stage of cancer she already knows I am going to have chemotherapy.  I am all for getting rid of the cancer and doing what ever it takes but I am scared to death of chemotherapy.  I am afraid of how it is going to make me feel and losing my hair.  I know it is just hair but unless I get a wig (which I plan on doing) I can't imagine myself without hair.  It is such a big part of me and every time I think of losing my hair I burst in to tears.  You would think a possibility of losing my life would be the bigger deal...right?  It is a big deal but I don't plan on going any where without a fight first! =)

I am going to the hospital on Monday for CT scans to see if there is any other cancer in my body or anything wrong with my bones.  Dr. Grange finds it suspicious that I could have breast cancer so early in my life (32 years old today as I write this) if there wasn't something else at the root of the problem.  To rule it out I need to have a lot of tests done to get my complete diagnosis and stage of cancer.  So for now I am praying that the only thing wrong is my breast cancer and every other inch of my body is healthy.

Thank you to my family and friends for your support during this difficult time in my life.  I plan on fighting this disease until it is gone and your support will give me the strength to do this!

We found Cancer

March 8, 2011

If you are my friend and you are reading this and you haven't heard from me...I think writing this down is going to be a lot easier for me at this point and time.  This is not something I thought I would share online.  But what the heck!  My life is an open book and if I can reach one person my job is successful.  A little over a week ago I found a lump in my breast.  I checked my breast from the advice of a Brea Nelson who I met a month ago on February 10.  She told me and everyone else in the room "give yourself a breast exam"!  I took this to heart and I found a rather large lump a couple weeks later.  Right under my nipple.  I called my doctor and went in to see him yesterday.  He tried to extract it and nothing came out but he did get a little piece of tissue.

March 9, 2011
We scheduled an ultrasound today because they wanted to get a better look at what was going on.  I thought it was going to be a 20 minute ordeal.  They would tell me that it was a cyst and send me on my way.  After an hour and fifteen minutes and being checked by an ultrasound tech and the head of radiology they were not so optimistic.  They said it could be cancer but they were not sure so we needed to schedule a biopsy asap.  At this point I hear the word cancer and I can't help but think nothing but the worst.  I don't remember much of what they said after this point. 

I had to take the girls to dance right after my ultrasound and at one point of watching them dance I got a little teary eyed.  What if I never get to see Olivia dance? 



Right after I scheduled my biopsy I got a call from my doctor late in the day.  Dr. Kirsch didn't have the best of news.  The tissue he extracted from my breast tested positive for cancer.  Of course he didn't know what stage or any of the specifics that a biopsy can read but he was almost positive I had cancer.  My mind went blank and tears started to fall from my eyes.  All I could think about was Olivia and Steve.  Then I thought about Cullen, Avery, Addison, Sully and the rest of my family.  How was I going to break the news to them.

I was actually composed when I called my sister and started to explain what was going on but when I tried to spit out the words "I have cancer"  I was almost to the point of hyperventilation.  She got off the phone and rushed back home.  The second person I called was my mom and she was shocked but calm and said we can fight it!  The third person and my most dreaded call was Steve.  I was actually composed, very positive and was thinking a little more clearly at this point.  I had some time to digest what was happening.  Of course he was shocked and reassured me that he would be by my side every step of the way. 

March 9, 2011
Steve drove home so he could be with me for my biopsy with Dr. Grange.  I like Dr. Grange because she has completely focused her career to breast cancer after losing her sister to breast cancer over 20 years ago.  She is attentive and answered all our questions.  She explained everything she was going to do before and during the procedure so I was comfortable the entire time.  She even said she would have our results by Friday so we wouldn't have to wait over the weekend.

If you are a female reading this or a male with a mother, sister, wife, daugther, aunt...PLEASE tell them to get a mammogram.  If not right away give themselves a self breast exam to find any lumps.