welcome

(photo of my sister's backyard fence...all photos are thru my lens)

This is just a way to express my thoughts as I walk this path and journey through as a breast canSURVIVOR.

Make cancer mad, just piss it off by misspelling it..... like "canzer"

In remission ~ December 2012

Invasive Moderately Differentiated Ductal Carcinoma T1cN0M0 Stage 1

Estrogen receptor-positive cancer - Here is how it began



Friday, March 30, 2012

Slow Things Down

Sometimes you have to slow down to really appreciate things.  I think this is my all time favorite video so far in my life.  Enjoy!


Thanks Sally!

Thursday, March 29, 2012

The Color Run

Remember how I was just saying where can I find some color to capture in my lens? Well, I had lunch with Marylee and she has been invited to experience The Color Run in June.  I am captivated by ALL THE COLOR!

Wednesday, March 28, 2012

Creative Juices

This is a "feel good" week finally!

I feel I have the energy to get some things done and I'm leaning towards the area of creativity.  For one, I want to revamp my blog, play with different templates and clean it up.  My sister is coming over this weekend to bounce ideas.

I am just itching to get out there with my camera.  Just trying to think of a place where I can find interesting colors ... interesting subject matter.

Flowers at Springfield Lake

I think it would be neat to find a way to display the beautiful encouragement cards I have received over the past several months.  I found some great ideas for bulletin boards here.

My side effects have eased up considerably and the fogginess in my head as well. 

PS. still got to write many thank you notes, which I plan to do before the weekend is over. 

Tuesday, March 27, 2012

Safer Breast Implant for Women...Research Continuing

New Hope for Breast Cancer Patients that opt for reconstruction thanks to Akron researcher. Watch Video

 

Posted: 03/27/2012
AKRON, Ohio - A University of Akron researcher, who watched a loved one die from cancer, took charge of the deadly disease in her mind.
She couldn't stop thinking of how to beat it, so no one has to go through what she watched her family suffer from.

After years of working closely with big name cancer experts across the country, she is now developing a safer breast implant for women who opt for reconstruction after a breast cancer diagnosis.

During the process of reconstruction following mastectomy, a new kind of implant could actually fight infection, scarring and even cancer.

Monday, March 26, 2012

Follow Up after Chemo #4

Early Spring Flowers poppin thru
This morning was my follow-up with Dr Esther.  It was a tad frustrating as it took an hour to get from the front waiting room to the back.  It took 2-1/2 hours for everything and to get back to work.

Regardless, my blood pressure was 126/78 .... I lost 6 lbs.  I know I'm not suppose to loose weight now, but I can tell you that I'm not complaining about getting some of this chunk-a-dunka-ness off me.  They seemed satisfied with my blood count, took notice of my nose bleeds, did a breast exam and sent me off with some encouragement and hugs.

Q: When will my radiation begin?
A: Three weeks after my last treatment (estimate May 17)

Q: When will my Herceptin (only) begin?
A: I will have 11 more sessions after this chemo round, which will total 17. It will continue on the same schedule as now, every 3 weeks.  Basically, no break in treatment. (estimate Dec 13)

Q: Do I have to have another blood transfusion?
A: Not this time, count looks good. :)

Q: Do I have to continue the Neulasta shot?
A: Yep :(

Q: How is my prognosis?
A: "I plan to fire you in 5 years" says Doc with a hug. "I'm going to make sure you will be just fine."


Got to work about 11:00.  Made it through 5:45! Debbie gave me another set of "ear-bobs" as Grandma Pearl called them....pretty dangly earrings shaped as a flower.  Along with her fabulous Congratulations! Another round behind you! She has been so sweet giving me a gift after each chemo session.  I'm looking forward to the last set, as she let it slip what they are!!!!

This is going to be a good week.  Feeling stronger. Got some "plans of attack" in life.  Looking forward to Easter Sunday service.

Blessings to you ~

Sunday, March 25, 2012

Bonvoyage

Today, we said farewell to another young adult of the family who is moving to Florida ~ nephew, Shane.


I just want him to be happy, enjoy and experience life.  But, I'm telling ya, its these times of losses that will kill me before the cancer does.

We had a nice BBQ at sister's house .... I will miss him greatly.

Garden Angel... Guardian Angel

Carol,

Look!  A garden angel was outside your house. Lucky you. What surprise is waiting for you in the weeks and months to come as summer grows closer?


My sister and her husband (who took the picture and wrote the message), came to my house Saturday and planted some flowers! I have angels all around me!

When she was done, she came in to comfort me.  I had been crying all day (remember that depression I said I was over? well....) Oh my gosh, if I could just pull things together!!  If I could just stop crying!!  It's all stemming from a set of losses in my life.

I'm also realizing that my chemo drug is suppressing my hormones, shot me into menopause, and my emotions are absolutely everywhere.  What a mess.... and did I mention the night sweats? How can I relieve them when I'm not suppose to have estrogen therapy?  My husband is convinced the cancer came when I started taking Premarin. (which I wrote about earlier)

I'm venting again.  Remember, blogging is a way to "get it off your chest". A way to seek help from others.  Which, I'm thinking it might be time for me to find a local support group.

Friday, March 23, 2012

Friday - 1st day back to work

I finally made it to work today and managed 6 hours.  I was still so sick and weak and asked Adam to take me home.  Feeling incredibly disconnected from everything.  I'm sure this feeling will pass at some point.

I'm waiting to Skype with my oldest in Colorado.  Missing her to pieces....
View from her apartment

Resting on Saturday.
Going away party for my nephew on Sunday.
Then starting all over again on Monday.  First stop, oncologist follow up.  Hope my numbers are good.  Telling her I don't want another blood transfusion.  Want to tell her I don't want any more chemo, but I know that isn't going to fly.

Praying for my friend, Marily ... may the birds sing sweetly as you rest.

Wednesday, March 21, 2012

Be Gentle to Yourself, Mind and Body

A friend of mine wrote: Be gentle to yourself, mind and body.  Don’t allow the darkness to come.  Like Paul & Silas did, they started to sing praises to the Lord, when they were bound by chains, after being severely beat up and standing in sewage for days on end.  Sing to the Lord in your mind and out loud as much as possible.  Put your music on and sing with it!   It will lift your spirit, and help your body.

So, as I write this, I hooked into my favorite radio station and it does lift my spirit, body and soul.

With the help of my cane, I'm getting from room to room. Spent a lot of time on the front porch watching the birds come to life in the early spring.  My lilac bush started to sprout its green leaves and we are awaiting the sweet smell the breeze carries to us.  It is great coverage from the street as well ... like our own club house. 
Last year's bloom


The pain is easing from my bones and joints.  I still wonder why it is hitting me so hard. Doc said that chemo attacks weak places and I have a few of those.  Before B.C., I was going to have surgery on my feet for bunions.  That is now on hold.  I also have Raynaud's, which I wonder if the chemo side effects are compounded.  Well, regardless, I only have 2 more sessions .... just 2 more.  For these next 2, April 5 & April 26, please pray specifically that I can mentally and physically get through the "bad" days. 

I'm taking one more day off work, mainly because I know I can't drive.  Matt goes to school on Tuesdays & Thursdays, so I'm holding out for him to take me Friday.  At least for a few hours.  I'm eating away my FMLA and I'm not sure what the rest of the year has in store for me.

Matt has been a real trooper through this.  He is going through the grieving process of loosing his dad and taking care of me.  I wish he had someone come along side him and hold him up.  We usually do that for each other and unfortunately, it has been a little one-sided.  I'm reflecting on my earlier post. He has taken care of me in ways that most people could not.  Private and humbling.  I'm grateful for him.

I'm grateful for my sister & her husband for taking the duty of making sure I'm eating.  When this is all over, I want a BBQ with mom's potato salad!!

Can you tell the fog is lifting? 
Do you know how much you help me?

Beads of Courage

These children are braver than I ~

Tuesday, March 20, 2012

Another New Day

Well, amazing what one writes at 1:00 in the morning.  I've had some very touching messages in my in-box and I want to thank each of you for them.  I also want to be sure that you don't think that I would ever take my own life.  When I wrote so early in the morning, I guess I was baring my soul.  I am a fighter and generally a tough cookie.  It's true though that God called my bluff.  I was always asking to go home and He said, do you really want to?  Okay, deal with cancer.  Now, tell me if you want to fight for your life... See your children marry... See your grandbabies be born. This is some important stuff to me and YES I want that. 

To me, that is how God pulled me out of my depression.  So you see, I never ask "why me?"  I can't put into words how precious all those things are to me and the fact that I don't want to miss one moment of it.

A friend of mine shared this video .... it is so incredibly beautiful.  The way that I want to experience life, adore life, and see life.





Thank you Teri

Getting thru the Dark Days

It's just after 1:00am.  I'm sitting on the twin bed we set up in the spare room ... the one that I'm trying to find a fun, cool name for (Ladies Lounge still #1).   My big guy, Lucky, is purring next to me and Dee-Dee is lying on the floor peaceful.  I feel like I am coming out of my funk.  When I say "bad days", it really means "dark days".  Days when I can barely hold on to my sanity, my reason for existence.  Most folks in my life don't hear me speak like this.  Poor Matt has been subjected to the overflow of my tears and wailing of self pity.  It hasn't been easy for him I'm sure.

Chemo isn't easy.  I have no idea how radiation is going to be either.  In one of my tangents, I cried that if I get cancer again, I'm not doing this again.  Yes, I'm serious. I don't think I can do this again.

I finally shared some of this darkness with my sister today.  I find that telling it like it is  is honest.  I can't be the positive, happy-go-lucky spirit all the time.  That isn't honest.  This is some real hard crap to go through. 

I've not asked the question "why me?" Because I already know why.  2011 was a very difficult year for me and I hit a depression that I couldn't climb out of.  Many times I asked God to take me home.  And then I got the diagnosis that I have cancer.  Well, talk about calling your bluff.  He did. Was I really ready to give up on life?  The answer is NO.  Even when I go through my dark days, I know that as each day passes, the light at the end of the tunnel is brighter.  God has been revealing personal deep messages to me, along with blessings to show me why I'm on this earth and what He wants me to do.

My roller coaster ride definitely has its ups and downs, twists and turns. 

But that is life no matter what situations we are facing. 



I hang on tight to God's promises and I'm so thankful to be His child. As I live in the moment, I can hope for a bright future. I'm also thankful for the love and support from so many people in my life.  Words of encouragement that we give to one another can make all the difference in the world.

Saturday, March 17, 2012

The Friday After #4

Matt took me to work Friday, just in case I got sick or something and couldn't drive back home.  I really thought that the blood transfusion was going to help me feel better.  I had a headache all day and felt queasy.  I barely made it. 

He picked me up at 3:15 to head over to the clinic for my shot.  We were in and out fairly quickly and I just wanted to go home, put my pj's on and lay down.  Which I did.  I got up around 7:00 and lounged on the couch with hubby until midnight. 

The ton of pills I have to take! Yuck.

I'm kinda thinking that Friday's will now be added to the list of days off after chemo.  As much as I want to be at work and keep caught up and not exhaust my leave days, it so isn't worth it.

Thursday, March 15, 2012

Chemo Session #4

Four down - two to go!

Matt is on spring break this week and was able to take me to my chemo session.


I was happy to be able to get the corner suite again! Nice and roomy.



Once we got settled in, I realized that I forgot the numbing cream! I will never do that again! My nurse, Chris, handled it like a pro and helped me through the initial injection. *shew* Nurse Chris is compassionate as well and I am a lucky girl :) Oh! guess what! Nurse Dawn is my sister's neighbor and our kids went to school together....small world ~

I completed my evaluation sheet (gauging pain levels, nausea, fatigue, etc). I felt like a wimp giving most of them a 9.  Matt reminded me of all the times I was crying during the past two weeks .... and not just because of Rickie.  So, 9 it stays.  Nicole (pharmacist) discusses the evaluation sheet and reviews the medications with us.  Since I will have my shot tomorrow, I need to start the claritin again.  Need to work on cleaning my bowels through fluid, fiber and prescription meds.  Not only does it help the digestive system, it helps clear out the chemo drugs.  Ok, I'll do better in that area. Also, since I can't take my pain meds during work, I can take extra strength Tylenol.  It gets difficult with the different meds I am on, especially Coumadin.

I showed my big toe off to everyone ... side effect or something else?  Doc determined that it was something else.  It had "trauma" and I just don't remember how.  Instructions ... keep it clean and wait for it to heal.  It may or may not fall off.  We shall see.

My numbers came back low, but good enough to proceed with the treatment.  Since the neuropathy and pain is hitting me hard, she is "taking 25% off the Taxotere".  Great! I do hope it helps. This one is a 3 hour drip with the ice on my hands and feet.



Doc had a high school student shadow her for the day.  That is very impressive to have one so young interested in doing this. 

As they prepared for my cocktails, the fabulous benedryl was injected and out I went.  I can never keep my eyes open! I only brought one thing to do (read) and never got to it.



By noonish, Christie arrived and the changing of the guards occurred.  She brought me some lunch and I am very thankful for the "extra" duty in getting it (silly girl).  I stayed awake the best I could so we could chat about all the things going on in life. 


Life does go on.
And the world keeps turning.

Then, one more announcement ... I was going to get my first blood transfusion after the cocktails were done.  This should help my energy level and feel like a new woman. (Adam is electing Wonder Woman complete with tights and a lasso) *geeze* ;-) 

My own blood was tested and determined to be A positive.  The unit I received was O positive.  I thank the person who gave their life source to me.


The clear tubes running from the bag into my arm looked like liquorice. Seriously.  The color was very rich and that's what it reminded me of.

I was the last patient to leave.  Everyone was very kind and thorough.  The last thing I want is to be a big wimp about this.  Indicating a 9 made me second guess myself.  But, I felt true to that number.

There is a basket of donated hats and I picked this one.  People are so nice :)


Ended the evening with nephew, Shane, visiting.  Wonderful!

Well, I better get some shut eye for work tomorrow.  May you have a safe St Patty's day out there.  Take care ~

Tuesday, March 13, 2012

I Just Came to talk with you Lord

Sheri had breast cancer and WHAT a TESTIMONY! Let it buffer up and just enjoy it 'cause you can tell it is from the heart.


Thank you Leon!

Monday, March 12, 2012

Man Cave? Woman Cave? Bat Cave?

Today was my first day back to work since my last chemo Feb 23.  Matt drove since we weren't sure how tired I would be after my shift. I'm so glad, 'cause I was tired.  I can't believe my next session is already this Thursday.  I plan to shove the negative vibes off and go in there and fight like a girl. I'm even gonna try not to miss any work post chemo .... grandiose thoughts ...

Got lots of hugs today welcoming me back and for the loss of Rickie.  He made some friends while he was there.  I'm so behind on thank you cards....hoping people are patient and forgiving. 

My brother-in-law moved out of our spare room this weekend.  We decided to rearrange stuff and now we have our "his" and "her's" cave.  Instead of a "man cave", I'm trying to think of a good name for my room. 

Any ideas?

So far: Fem Den, my Rad Pad .... since my brain isn't as witty as it use to be, I'm looking for that special name.

By the way, got a new side effect that looks like it could be from Taxotere. My big toe nail is black & blue and looks like the nail could fall off (see page 2). I don't remember bumping or smashing it.  So, I'll be showing Doc when I see her Thursday.  Actually, I have various bruises all over.  Probably thanks to the coumadin.

I finally picked up the book borrowed from Barb and began reading it.  At times, I felt so overwhelmed with information that I just began making piles.  Now, I feel I want to be empowered and thought reading this book might just help.  I've already experienced some of the items she has mentioned.




  • You will look at life in a whole new way, as something you are lucky to be experiencing.
  • You will appreciate every day, just because it is there and has been given to you to enjoy.
  • You won't take your health for granted, and will take better care of your mind and your body, making yourself a priority (rather than your family, friends, job, or other distractions).
  • You will be calmer ... the little things won't seem to bother you as much.
  • You won't worry about tomorrow as much, but live for today.
  • You will draw nearer to the people who bring meaning and fulfillment to your life, and get rid of those who don't (crises have an amazing way of revealing someone's true character).
  • You will gain extreme clarity ... about exactly who you are and what you want from your life.
from the "Introduction" section

Friday, March 9, 2012

Celebrating Rickie's Life

The calling hours for Rickie were held on March 7.  The photos gave folks an idea of the importance of family, fun and laughter that we all cherished.  His 2 sons and niece wrote about him and we had copies available.  Many stories were shared as well.  Folks from his youth were there, as well as those who just met him on the job. 

Some say that funerals are for the living.  I can see why.

It has been a few days since getting on the computer.  Now that final arrangements are done, grief has begun.  I'm doing my best as my husband takes the steps in the grieving process.  Wish I was physically stronger to care for him.

The flowers are still on the kitchen table.  It is my plan to press and preserve some of the flowers along with the ribbons with the words "father", "grandfather", etc.  I need to pull all the photos off the poster board. Planning to give them to family.

Next on the agenda is taking care of all his financial and personal items.  Probate, etc.

I truly believe that people need to get their affairs in order.  Not just wills, but power of attorney, and every other document that will help families.

Tuesday, March 6, 2012

Monday, March 5, 2012

Love & Support

This afternoon, Katrina hand delivered cards from work and most humbling, money from a fundraiser my co-workers organized and participated in.  We can't even put into words how grateful we are and how much we appreciate the love and support that we feel from so many wonderful people.  How blessed we are.  How honored we are to call them friends.  The waterworks flow easily now.

Food was also delivered too.... me? at a loss for words? ....

If I could climb to the top of a mountain, I would shout to the four corners of earth to proclaim GOD IS GOOD ... ALL THE TIME  and ALL THE TIME... GOD IS GOOD.


Getting Ready

We spent time writing about Rickie to have at the funeral home.  Tomorrow will be spent selecting from all the photos gathered and placing them on poster boards.  CD mix of music. Final touches on the memorial cards (picked out Thomas Kincaid).

Needless to say, a few more days off work ~

Follow-up from Chemo #3

Matt took me to Doc Esther this morning.  I had it in my mind that if she couldn't tell me if the chemo was working, then I was done.  I'm weak and just not really feeling like doing this anymore.  After they took my blood, I sat and waited ... lost in thought.  A few times, the tears flowed of everything that has happened over the past few months.  Then, I began to think about the women I know whose stages are more advanced than mine.  How much more they are going through and I had absolutely no right to sit there and whine.  I'm just tired. No, it's more than just tired ... fatigued.  Not quite right either ... what is a word that can describe being absolutely exhausted?

To her credit, she didn't try to sugar-coat it.  She gave me her full attention and listened.  Because we are not shrinking a tumor, she can not give me the answer to "is the treatment working".  She can only tell me that based on my HER2 protein that statistics say that what treatment I'm getting now can help prevent it from coming back.  Hmmmm, not quite the reassurance I needed to make a decision.  Then, back to the women I have in my mind and in my heart....and back to my daughters and my husband and my family.... ok, I'll stick with it.....

Doc said that there may be a time before all this is over too when I won't be able to go back to work for awhile.  Reduced hours still might be too much.  Ok, looks like I will have to cross that road when I get there.  I reminded her that I'm the only paycheck in the house right now.  She understood.  I was also denied my cancer policy because it became effective Jan 1 and I was diagnosed Dec 7.  She said she would help me appeal it (although I don't know how to change their minds).  Do you?

The blood counts came back and she liked the numbers.  So, the Neulasta is working.  She said that I'm a tad dehydrated, but not bad enough for fluid IV.  (that's good) Doc also told me to eat more junk food (now what doctor would tell you that?) Guess I dropped a few pounds.  She said junk food tastes good and it has calories. ahhhhhh

I asked her again the details for the rest of my treatments.  She is going to adjust next week's chemo .... last chemo should be end of April.  Then 6 weeks of daily radiation.  Then 11 treatments of Herceptin.  Basically, treatments for the remainder of 2012.

What a year ~

Tomorrow, it is my plan to make it to work.  I'm praying for the courage and the strength.

Patchwork of life

Sunday, March 4, 2012

Saying Good-bye for Different Reasons

The past 24+ hours have been saying good-bye for different reasons.

Two Father Figures ~

We celebrated the life of Mr. White and yes, I mean celebrated.  To hear of this man's touch in so many lives was astounding.  He certainly had enough energy to pull a locomotive.  As I battle the affects of chemo, it is difficult to imagine myself with even an ounce of energy.

We then made the final arrangements for Pa. When death comes unexpectedly, a flurry of activity ensues.  There are so many decisions to make and a long list of things to take care of.  Rickie's laughter and caring will be missed and the void in our lives can only be replaced with our fond memories. 

And yesterday, we also said a farewell to my mom as she is going to the Carolina's for a few months with my sister.  They are in transit now.  Unfortunately, I didn't get to spend much time with them yesterday after the funeral ... again, my stupid energy level was too low.  I only get to see my sister a couple of times a year.  And, once again, I had to say my farewells to her and Mel.

Death always brings reflections.  If you remember, I boasted my new year's resolution as "de-cluttering" my piles.  Sad to say that I haven't even started.  But, it MUST be done.  There is no way I want my family to have to sort through all this STUFF. 

And reflections of my own life and how are people going to remember me? What kind of legacy am I leaving?  What kind of legacy are you leaving?

If you want to get to know me, this is one of my top 10 songs.  Enjoy the message ~

Friday, March 2, 2012

Another Day of Trying

I didn't get much done today ~ was in bed most of the day. I really need some energy and strength.

Matt and his brother were at Rickie's place packing up.  There is so much to do.  What do people do about taxes? bills? stuff like that?  I'm sure we will have to go through probate too.

Mr. White's funeral is tomorrow.  And, my sister will be up from S. Carolina for just the day.  Then, mom will be traveling back with her on Sunday. 

We are hoping to know a funeral date for Rickie by Monday.  I've requested that day off as well just trying to get things done.  If we have a choice for the funeral, we are looking at Wednesday March 7.

Aunt Dar and cousin Misty came over tonight and we had a wonderful time of story telling.  I am so glad they were here. 

That's it for now. Good-nite.

Thursday, March 1, 2012

What Happens if You Die on Feb 29?

It is with great sadness to write about the loss of my father-in-law, Rickie.  We received the phone call from work that Rickie had collapsed and CPR was being administered.  The EMTs were frantically working on him all the way out to the squad. 

I got Matt out the door heading to the hospital and I made the calls to family to meet him there.  I couldn't go, as I was way too weak. 

Matt called. He was dead on arrival. 


Only 57 ~ I can tell you that he was with people who cared about him.  They reacted quickly and he was not alone.  He was with people who cared about me and Matt too.  Rickie worked where I work and a few years ago, Matt did too.  A family owned business with a lot of heart. 




The medical examiner called us today and said he had a really bad heart and that there was nothing anybody could have done.  He died immediately.  For me, that is a God send...anytime there is no suffering is a God send. 

Feb 29 - 3:16pm.  I haven't been to work since my last chemo.  If I would have been there, I would have been in the ambulance with him.  How very sad.

So, what do we do next year? What do people do when there is an important event in your life and it falls on leap year?  I have no clue.

We are trying to put all the pieces together.  No will. No power of attorney. No life insurance policy.  Funeral homes want the money up front.  I know God will provide. He always does. 

We did contact Newcomers and think that we will go with them.  And we will definitely make it a time of day that his co-workers can pay their respect. 

For now, we just want to thank everyone for their words of comfort.  We always appreciate prayer.  A friend sent this video today and it is wonderfully moving.

Tuesday, February 28, 2012

It's Tuesday

First Tuesday I missed work after chemo.  I am really hurting so I'm glad I'm home.  I slept most of the day away (again).  Mom came over and made homemade chicken soup, yummy.  The good news is I didn't get that metallic taste in my mouth this time around. 

I'm heading for work tomorrow.  Matt wants to drive and I have no problem with that! My legs aren't working so great. 

Jasmine got a job today! In today's economy, it has been difficult for so many. She is very excited and we wish her the best of luck!

Casey had her first emergency call today.  A husband took his own life.  It is sad when someone feels so desperate that they take this final action.  All life has value.  I know you are valued each and every day.  Our prayers are with that family and with my daughter as she begins this type of journey in life.  God is calling her.

Is He calling you?

Monday, February 27, 2012

Day 4 - After Chemo #3

I'm beginning to hit my low again, I can feel the tears well up inside.  This time, it has to do with changes in my life.  Generally, I can handle changes ~ open my arms and embrace them? ~ not without a lot of questions first.  Plan A, Plan B, what about this, what about that.... What I have to rest assure is that God will take care of me whatever changes come my way.  I know this is cryptic, but since it is a public site, I'm going to leave it like that.

Just got done with another nose bleed.  yuck

Yesterday, the bone crunching was intense.  It's like my knee caps were on backwards.  Reminds me of an alien movie I saw where the alien's legs bent like a grasshopper.  Sort of like how I feel and walk.  The cane I bought last week is helping.  A very cool cane that collapses and fits in my purse.  It gets me up and down the stairs too. 

I didn't go to work today and will probably take Tuesday off as well.  Last time, I wish I had ... so I'm basing it off that. 



Life seems SURREAL.  Pinch me .... am I really here?

Saturday, February 25, 2012

Day 2 - after Chemo #3

I slept most of Saturday away.  Trying to keep the pain under control, which means that I fall asleep a lot taking pain medication.  That's okay. Sleep is helping my body recover too.

Starting the coumadin again .... Just 1 pill! then 1-1/2.  I just took 7 different pills, so you can see how confusing this can be.

My sister/husband made dinner for us tonight.  It was fabulous and I could taste it! I'm spoiled rotten.

I'm so behind on thank you cards and letter writing.  I want to send a note to my Aunt Midge this weekend.  I use to be an excellent pen-pal (before computers).  We moved so many times during my school years and I loved to write my friends.  It is a lost art.  With quick e-mails and instant texting, the rich flavor of words have disappeared.  I use to write short stories and use descriptive words.... I liked the poem I wrote of my sister.  Visual.

Pathway

May God Bless you today ~

Friday, February 24, 2012

The Day After - Chemo #3

Last night after getting ready for bed, I made the decision not to go into work today.  The first Friday I missed after chemo.  I was just too exhausted to think about getting up early and putting in a full day.  I'm ever so glad I made that decision.

I slept on & off most of the day with the company of all my animals (boy, they can sleep A LOT!)  Watched a John Wayne comedy (yes, he made a comedy) called McClintock. Loved it!

Took off for the cancer center for my shot of Neulasta. We braved the high winds today and I wore my leopard hat that is snug fitting ... so windy my hair would have blown off my scalp, if I had any!  The nurse was "petting" my hat because it's soft as a kitty.  Nurse Bev, from yesterday, left a magazine for me of photographs of extreme sports.  Awesome photos from exotic places .... oh, how I wish I could go to places and capture everything breathtaking.  Anyway, (back to the shot) .... nurse had me hold the syringe to warm it up while she was getting things ready.  It was cold and she said it burns going in if the fluid is cold.  Did my best to warm it up!  Easy-peazy, no pain going in!  Continue taking the Clairton to ease the bone and muscle pain that is suppose to last 3-4 days.  Hoping to feel like a new woman!

We stopped by mom's to pick up dinner she made for us.  It was good to visit .... as I haven't seen her much since all this started.  Little sister is picking her up next weekend and taking her south for a few months.  She is so excited and I know that it is definitely time for her to get out of the 4 walls and do something different and in warmer climate. 

Debbie sent over this video that is very worthy of sharing.  Hope it moves you

Thursday, February 23, 2012

It's A Good Day

Teri reading her book

Teri & I arrived on time for the THIRD round of cocktails.  I was hoping for the corner suite like last time .... guess what! I actually have my own room this time! With a door, a sink, and a TV.  How awesome is that, lol ~

Last week during my follow up, my numbers were really low.  Nurse Bev explained that treatment could be delayed if my numbers didn't come up.  So, we had our fingers crossed, said a little prayer and waited.  John, intern from Malone, is on site learning today.  Of course I had to mention my daughter who is graduating from Malone with a masters, where she is and what she is doing, ya-da-ya-da-ya-da. 

Any way, I got all prepped with the IV in the port.

Christina (pharmacist) came in to discuss my pain levels and side effects since the last treatment.  She also explained more about the Neulasta and gave me Clairiton to help with the side effects from it.  More bone pain .... just great :(  My shot is 4:00 Friday and then every time after chemo to boost my white blood cells.

Nurse Bev and John came in doing the happy dance with jazz hands! My levels are good! My liver and kidneys are up for it as well.  Everything is a go!


Signing off for now to get ready for my cocktails ~










It's almost 7pm now and I thought I would write a quick update and then hit the hay for work tomorrow.

My counts did come back at good enough levels to go ahead with chemo today.  But, I really messed up on the coumadin.  The 1-1/2 pill was every other day ... I was taking it every day.  The INR test came back 4.75 - CRITICAL PANIC HIGH.  Normal level is between 2.0-3.0.  oops.  Doc Esther explained again how to take it and I was confused.  Even the nurse was somewhat confused.  But we got it.  Don't take it until Saturday.  Got it.  Then on Saturday take 1 pill. On Sunday, 1-1/2 Pill and then alternate.  I really thought she said 1-1/2 pill every day...plus it wasn't written down at her office. 

I fell asleep right away again from the meds.  Everything went pretty smooth.  I took my dance partner (IV stand) and gave out Purell to my neighbors.  That is always fun to do.

We got done at 3:30 today and made our way to Subway. And, I got spinach on my sub to help lower my coumadin numbers.

Well, my brain isn't working very well so I'll sign off for now.  Good night :)

Wednesday, February 22, 2012

Shot in the Arm

This news story came on today about Tom and Laura who own a coffee and tea shop in Independence, OH.  Their story is heartwarming and if you live in the area, stop by on Wednesday, Feb 29 between 5:00pm-7:30pm.  They are the only locally owned coffee shop in the area.

Take a listen to their story

Brielle's

@briellescoffee

Brielle's Coffee & Tea Room Muffins, Cookies, Scones baked fresh Lunch Entrees, Catering, Box Lunches, gatherings and meetings. (216) 642-9292
6523 RT 21 Independence     

Tuesday, February 21, 2012

Methotrexate Shortage has Ceased!

Response from the Critical Shortage Post

Dear Carol,
We are pleased to share with you that this morning, the FDA reported that the preservative-free methotrexate shortage has ceased.

Based on quick action by numerous pharmaceutical companies, and thanks to your calls and letters, preservative-free methotrexate is being produced and shipped to hospitals and treatment centers in need. Many companies who were not major producers of the drug, or in some cases, were not making the preservative-free version at all, have increased or begun production in order to stop the shortage. The FDA believes that based on new production schedules, the shortage will be completely resolved.
CureSearch, along with the children's cancer community, continues to work with the FDA and Congress to ensure that in the future, such shortages do not occur at all.

Thank you for making your voice heard. You truly made a difference in ensuring that treatment continues, uninterrupted, for children with ALL and osteosarcoma.
Sincerely,
                    Erica Neufeld
                    Vice President of Communications and Advocacy
Erica.Neufeld@CureSearch.org
(240) 235-2201

R.I.P.

The White's Farm - God's Country
We received the news today that our wonderful friend, Mr. White, went home to be with the Lord today.  He fought a courageous battle with cancer but is a testimony of miracles.

Dear Father, I ask that you be with the family right now.  Guide them through this journey of loss.  I pray that Jim's transition to your arms is GLORIOUS where he no longer suffers and is forever at peace. 

One day, Lord, we will have a reunion that will bring down the barn roof! When we will worship YOU and praise YOU for all eternity! 

We have not really lost him, for we know exactly where he is!

More cocktails a'coming Thursday!

I'm SOOOO excited for my next treatment Thursday! Why, you might ask?  Because I'm SOOOO tired! I plan to sleep most of the day away.  PLUS, it will be the half-way point of my chemo cocktail. 

I'll find out what time Friday that I will get the shot to boost my white blood cell count.  Looking forward to that too as I feel so drained.

Family is gearing up for meals during my bad days.  Don't be jealous ... 'cause they are EXCELLENT cooks!  Our Family Recipes are shared on blogspot.

Have a blessed day!

Saturday, February 18, 2012

The Love of Caregivers

Nikki told me about Martina McBride's song about caregivers.  She mentioned how it felt to be a caregiver, because she was for her husband.  This video is amazing, powerful, and true. 

I'm so very thankful ~ every day ~ for the caregivers in my life.  I've never wanted to be a burden to anyone. It is very humbling to ask for help....but in most cases, I don't have to ask.  A helping hand is always there. 

The hugs I get are powerful as well.  I get them daily from many sources.  Sometimes, they come unexpectedly from people I barely know.

I can tell you that to me, knowing that I am not alone makes all the difference in the world.  To know that people are praying for me.  To know that people care ~ amazing.

So thank you.   Please listen to this song and to those who feel this same amazement at the love and support that they received.





Friday, February 17, 2012

TGIF ~

Thankful that today is Friday.  I didn't feel so great today.  My own fault.... Matt drove me to work today and since I was in pain, I decided to take a pain pill.  Breakfast was hours earlier and taking that tiny pill on an empty stomach made me nauseous, dizzy and way off.  Nope, won't do that again.

We had a department luncheon and Debbie was kind enough to get me a bowl of soup.  I sat at my desk for a bit to let it warm my tummy and get me back on track.  Finally, I joined the group in the other room and enjoyed the conversation.  Then, I felt something strange....touched my nose and had blood on my fingers.  Ever so discreetly, I left the room to attend to my bloody nose.  Jeez .... I noticed a bruise on my forearm and can't remember how I got that. Coumadin and cocktails.... Kinda felt like I was falling apart today.

Matt picked me up at 4:30 and I was relieved to go home. Did I mention how relieved I am it's Friday?

On other news, Jasmine moved today a little bit closer to home.  I met the family she is living with and they seem very nice.  We have plans to get Jasmine's license and then make an appointment to get her wisdom teeth removed.  She has been having quite a few headaches and it is terrible if an infection starts in the gums as the poison can travel straight to the heart. 

My friend, Marylee, is leaving for a missions trip to Haiti.  I am so overjoyed for her as this is her heart's desire and she has made several trips there already.  She has a real love for them.  I'm anxious to hear all the wonderful news she will bring back with her....and PICTURES....I am a shutterbug and I love pictures!

Looking Glass Falls
Gonna take it easy this weekend.  May you have a beautiful day ~

Thursday, February 16, 2012

Test Results for #2 Session

Today was my follow-up appointment with my oncologist.  Doc Esther came back from vacation and was running about an hour behind schedule.  Don't you just hate it when you have to wait at doctor appointments?  But, I try to relax and not get overly anxious. 

My INR for my coumidine is 1.7 (needs to be between 2-3).  So, she wants me to go up 1/2 a pill (1-1/2 pill per day).

My white blood cells are low.  So, I will need to get a shot of Neulasta 24 hours after my chemo (Friday).  I'm not liking the side effect list .... man, oh man.  Hoping insurance pays a good chunk of it.

My blood pressure was good :)

I asked her to write a 90 day script for my nausea medicine.  She had only been writing them for 15 pills at a time and it cost $38.50.  I explained our discount plan that it would be $15 for 90 day supply.  I dropped off the script on the way to work only to discover that it had been written for 30 days for $232 dollars.  Oh boy.... it took lots of phone calls to get that all squared away.  Mission accomplished.

Tired ....

It's been nice having Jasmine spend the night yesterday and today.  She made chilie for dinner and has been helping around the house.  I'm glad she has been able to lend a helping hand!

Good night ~
South Carolina

Wednesday, February 15, 2012

That Fogginess

Duct Tape is Wonderful
So there IS such a thing as Chemo Brain !!! I knew it just wasn't ME....seriously?!  Pre-chemo, I use to say I had "some-timerz", not Alzheimer's (hope I'm not offending anyone).

The article states
Here are just a few examples of what patients call chemo brain:
  • Forgetting things that they usually have no trouble recalling (memory lapses)
  • Trouble concentrating (they can’t focus on what they’re doing, have a short attention span, may “space out”)
  • Trouble remembering details like names, dates, and sometimes larger events
  • Trouble multi-tasking, like answering the phone while cooking, without losing track of one task (they are less able to do more than one thing at a time)
  • Taking longer to finish things (disorganized, slower thinking and processing)
  • Trouble remembering common words (unable to find the right words to finish a sentence)
I can certainly attest to it!

I see my oncologist in the morning and my blog helps me keep things in order.  Like most people, I make lists and try to remember it all.

Day-to-day coping

Experts have been studying memory for a long time. There are many resources that might help you sharpen your mental abilities and manage the problems that may come with chemo brain. Some things that you can do are:
  • Use a detailed daily planner. Keeping everything in one place makes it easier to find the reminders you may need. Serious planner users keep track of their appointments and schedules, “to do” lists, important dates, websites, phone numbers and addresses, meeting notes, and even movies they’d like to see or books they’d like to read.
  • Exercise your brain. Take a class, do word puzzles, or learn a new language.
  • Get enough rest and sleep.
  • Exercise your body. Regular physical activity is not only good for your body, but also improves your mood, makes you feel more alert, and decreases tiredness (fatigue).
  • Eat your veggies. Studies have shown that eating more vegetables is linked to keeping brain power as people age.
  • Set up and follow routines. Pick a certain place for commonly lost objects and put them there each time. Try to keep the same daily schedule.
  • Don’t try to multi-task. Focus on one thing at a time.
  • Ask for help when you need it. Friends and loved ones can help with daily tasks to cut down on distractions and help you save mental energy.
  • Track your memory problems. Keep a diary of when you notice problems and the events that are going on at the time. Medicines taken, time of day, and the situation you are in might help you figure out what affects your memory. Keeping track of when the problems are most noticeable can also help you prepare. You’ll know to avoid planning important conversations or appointments during those times. This will also be useful when you talk with your doctor about these problems.
  • Try not to focus so much on how much these symptoms bother you. Accepting the problem will help you deal with it. As many patients have noted, being able to laugh about things you can’t control can help you cope. And remember, you probably notice your problems much more than others do. Sometimes we all have to laugh about forgetting to take the grocery list with us to the store.

Critical Shortage of Medication

Critical Shortage of Medication for ALL: You Can Help

There is currently a significant shortage of the chemotherapy medication preservative-free methotrexate in the United States. This drug is critical to the treatment of children with Acute Lymphoblastic Leukemia (ALL). Unless production of preservative-free methotrexate increases, hospitals will run out of the medication completely in the days and weeks ahead.
I've been reading about shortages in chemo drugs.  Put a face to the need and meet this dear child . Also, read Lil Blue Boo.

Take a moment from your precious time to help save precious time for cancer patients. Here is what you can do

Tuesday, February 14, 2012

Happy Valentine's Day

What is Love?

4 Love is patient, love is kind. It does not envy, it does not boast, it is not proud.
5 It does not dishonor others, it is not self-seeking, it is not easily angered, it keeps no record of wrongs.
6 Love does not delight in evil but rejoices with the truth.
7 It always protects, always trusts, always hopes, always perseveres.
8 Love never fails

1 Corinthians 13:4-8

Monday, February 13, 2012

It's a Matter of Life & Death

This canzer-thingy sucks. It's mean and it does kill.  How long is it going to take before someone finds a cure that is 100% effective?  I followed Lanie's Blog .... and then reality hit once again.

I also follow Lil Blue Boo ... Ashley is amazing and celebrates "Choosing Joy" every day. I can't even begin to compare our diagnosis or treatments (nor should I), but to say that she is a very strong individual who kicks butt.

This disease creeps into our lives and changes us forever. 

If we are blessed to reach remission, we are still looking over our shoulder and wondering if it will return. (as in other blogs I follow listed on the right side of my blog)

REALITY CHECK

A wonderful friend of ours is in hospice.  He is in his final stages of his home-going. We all have an ending story. A beginning, a middle and an end.   I can't imagine facing death without God .... it would be too lonely, too depressing.  I'm thankful that my eyes are wide open now about life in general.  I wasted much of it with stupid stuff.  Now, I get a chance to make things right in many areas of my life.

Colorado

Don't wait to get a diagnosis like cancer ...
make life altering changes
FOR THE BETTER
right now ~

Sunday, February 12, 2012

Pink Glove Dance

Crop Circles

Yesterday after my shower, the stubble on my head looked like crop circles.  No, really, it's true! Most of it was laying down, disconnected.  What a sight! I think I could have just stayed under the shower nozzle and wait for it to all wash out.  Instead, another session with Matt.  This time with lather and a Gillette Mach 3 razor.  I sat on the edge of the tub and let him take his time on my scalp.

Bald and beautiful!  Well, don't know about the beautiful part though, lol.

Saturday, I paid bills and lounged around. 
Sunday, I plan to clean the kitchen and organize some of my piles.
Not too productive, just kinda taking it easy.

The winter snow hit us this weekend in beautiful Ohio. 

May you be a blessing to someone today!

Saturday, February 11, 2012

My Soul is Restored

Above Me
A wonderful friend of mine from my school days in North Carolina has been a great encourager.  He said that through prayer and support that "all bases are covered, but don't forget short stop (your BIBLE)".  He reminded me of Psalm 23, which our family is very familiar with as we have read it at many of our funerals.  But reading it again, brings even more assurance that right here and right now, God's words sustain me.  His promises to us are true.



Psalms 23:1-6(NKJV)
The Lord is my shepherd; I shall not want.
He makes me to lie down in green pastures; He leads me beside the still waters.
He restores my soul; He leads me in the paths of righteousness For His name’s sake.
Yea, though I walk through the valley of the shadow of death, I will fear no evil; For You are with me; Your rod and Your staff, they comfort me.
You prepare a table before me in the presence of my enemies; You anoint my head with oil; My cup runs over.
Surely goodness and mercy shall follow me All the days of my life; And I will dwell in the house of the Lord Forever.


As I listened to a recent sermon, the subject was loving God with all your heart, soul, and mind.  What is the definition of soul?  It is your "personhood"...what makes you, "you"... our "character". 

This journey has many valleys.  I can tell you that right now, my soul (my personhood) has been restored.

Thank you Jesus ~

Thursday, February 9, 2012

The Pickle Jar

A forwarded e-mail worthy of sharing ~

The pickle jar, as far back as I can remember, sat on the floor beside the dresser in my parents' bedroom.  When he got ready for bed, Dad would empty his pockets and toss his coins into the jar

Sleep is Good

Thank you for all the prayers and messages.  I have been in bed by 7:30 each night, so haven't been on top of messages.  It makes my heart smile to read them.

Today, the side effects have lessened their grip.  It is Day 7 post chemo and I'm trying to think of foods that won't make me nauseous.  The vitamin k in leafy greens is a "no-no" because of the coumidine....salads, broccoli, spinach.  I can have it, but if I do, it has to be all the time or none at all because it will spike my blood tests. 

Sleep is good and I can tell it is helping my body recover from the chemo.  I'm going to make it a point to get more of it after treatments.

I'm thinking clearer today.  The skies are bluer today.  God is still holding me.

Wednesday, February 8, 2012

My Pity Party

The last few days have been kinda rough.  I missed all day Monday ... managed to work Tuesday 10:15-4:00.  I have no idea how I drove to work and back. I don't think I'm going to try that again either.  I'll just have to book both Monday & Tuesday after chemo that I'm going to be off work. 

Everything inside of me is getting killed.  I'm feeling it.

I got home yesterday and went straight to bed.  Matt came home from school around 8pm and was distraught that I hadn't taken my medicine or eaten.  Getting hard to eat.  Not hungry and that metallic taste is back.  So, looks like I'll need a babysitter on Tuesday after.

I'm feeling sorry for myself and I don't want to.  I really don't want to do this anymore.  But I have to.

*sigh*

Monday, February 6, 2012

To Believe

Jackie Evancho
To Believe

Express Yourself

When the time comes, I will learn how to make eyebrows.  I had NO IDEA this is how to do it!

Laughter Heals

We've all heard that laughter heals.  I see no reason to doubt it!  Hope you get a kick out of this!

Belly laughs are wonderful for the soul and  Laughter heals

Silly Kitties

Sunday, February 5, 2012

Just another Sunday

Just a quick note to let you know that I'm hanging in there .... although very tired and my bones hurt like last time.  Keeping the pain at bay as much as possible.  Decided to rest one more day and go back to work Tuesday. 

Peace be with you ~

Saturday, February 4, 2012

Sleepy Time ~

I've lost some hours somewhere .... Last I remember, went to work Friday.  Okay day, but got tired before lunch time.  Matt picked me up around 4:00 (glad I wasn't driving) and we went to Sam's club looking for printer ink.  (thank goodness for scooters) They didn't have it so our money went on other "stuff".  Almonds for one.  The nutritionist on my "team" called me to talk about my numbers and even though they looked good, was encouraging me to get more protein and iron to promote healing.  nuts, yogurt, cheese, meats, etc. And, if I'm not hungry for a full meal, snack on trail mix.  Got that too.

Stopped at my sister's house to pick up our yummy dinner. Ate most of it (saving the rest for later) and crashed about 7:30pm on the couch.  I woke up about 4:00am, took my first pain pill and went to bed.  I've been sleeping most of this day away too.  No nausea, pain is under control.  Don't want to walk much though as I can feel it in my feet.

Last time, everything hit me hard on Sunday.  Not sure what to expect, but I'm READY FOR IT and will kick it in the butt this time!