Help

Two friends today told me they were broken and felt like ending it.  This scared the crap out of me.  What do you say to someone who says this to you?  How do you reassure them that life will be ok and is worth living.  I told them the first things that came to my mind.  You have a family (with kids) that loves and needs you here.  I reminded them of what they do have in their lives to be grateful for…not sure that was right.  However, I wanted to see if I could open the light they have in their lives to help wash away the darkness.

I can’t say I have never thought this way…I have.  I stopped myself and immediately thought of all I have to live and fight for in my life.  Life has dealt me some pretty challenging situations, but I am learning to be compassionate for myself.  You can only handle so much…then it is time to ask for help.  It is ok to say ” I can’t do this today”.  Everyone needs time away even if it is just an hour.  I think we often push ahead because we feel a duty to someone else to keep pushing even if we don’t know who we are pushing ahead for.  So give yourself permission to say not today…I need a break to find my light!

Take care ♥

Waiting

Between the time of my diagnosis and my surgery felt like an eternity.  In all reality it was only a month…I say only now knowing some people wait for monthS before their surgery as they complete testing and see various doctors.  For “only” a month I am grateful; I was at my wits end by the time I had my surgery (many sleepless nights).

I did try to keep my sense of humor through this process…it was a cry or laugh option.  I chose laugh, so I made many inappropriate jokes.  My poor teaching partners and family heard a lot of these jokes.  My first was that I could join the army as my boob could camouflage itself from all the bruising caused by the biopsy.  It was still slightly bruised when I had my surgery. My surgeon got a kick out of this joke.  I loved my surgeon; she presented me with my options and supported me in my choice.  It was recommended to me to have a lumpectomy and radiation treatments.  I talked to and read about many women who went that route and had re occurrences that lead in the end to mastectomies.  I chose to have a double mastectomy ( an extreme) not only for myself, but also my family.  I didn’t want to put myself or my daughter through radiation treatments and a possible re occurrence. My surgeon supported my decision and sent me to a plastic surgeon and oncologist.  I chose to not have reconstructive surgery because I just can’t imagine after having cancer putting some weird chemical back in my body.  I would always be worried.  After seeing all my doctors it was time to schedule my surgery and get the cancer OUT of me!

Lost and Scared

Here is the beginning of my cancer story – I went to my general practitioner on April 22nd where she told me I had DCIS (breast cancer).  As she said if cancer could be good this was the good kind of cancer.  It was stage 0; non-invasive breast cancer contained in the milk duct of my right breast.  I was then sent to a surgeon the following Tuesday to talk options.  I also began telling my family I had cancer…along with close friends.  A friend from work met me at the doctor’s office so I wouldn’t be alone because I am stubborn and chose to go by myself.  I didn’t know I needed this support until we were sitting in her car.  I felt numb and overwhelmed by the news.  So many questions and worries beginning with how to tell family; especially my daughter.

Luckily, my appointment was on a Friday and my daughter would be at her dad’s for the weekend.  I would have time to adsorb the news and begin figuring out how to tell my family. That night I called and invited my parents in for dinner, so I could tell them.  Then, I planned to go out and tell my ex-father-in-law (aka my 2nd Dad) on Sunday before I picked up my daughter.  I would like to say there is nothing harder than telling family members that you have cancer. I spent the weekend laying on the couch, crying and making family members cry…this part of cancer sucks!!  Just writing this has made me cry again remembering the different reactions of family members that weekend and beyond.

This also began a long period of sleepless nights.  I was trying to not lose it at work or in front of my daughter while figuring out what my options were for treatment.  During these long nights I read many articles and looked at a lot of pictures of what women look like after mastectomies and lumpectomies.  I spoke with a few ladies about their experiences with the same diagnosis.  They opted for different treatment plans with different results.  This helped me to make my decision about what I should do, so I would live a long time after this diagnosis.

Another Chapter in Life’s Wacky Journey

I know some people don’t like the word journey, but I use this word to describe the path we take throughout our lives.  There are straight paths, curvy paths, long, short, bumpy -so many ways to describe the events in our lives.  I have even thought of life as a roller coaster at times.  You never know what is around the next corner or hill, but you have to be brave.  This is not always easy and a lot of the time it feels scary and beyond my control.  However, I have learned that I can control how I deal with and feel my way through life.  I want to be brave, loving and inspiring.

I am not sure where to begin, so I will begin at the start. I decided to see my doctor in March due to being tired, maybe exhausted is a better word.  I went thinking of course I am tired; I am a single, working mom.  At the end of my appointment my doctor did blood work and referred me to have a mammogram.  When I asked why she said because it had been a year and a half since my mammogram (my one and only mammogram).  Luckily, I could make my appointment during spring break…woohoo, I wouldn’t have to take any leave or write sub plans (bonus)!

My mammogram was on April 4th.  I took my daughter with me. She got to wait in the waiting room and read – fun way to start her spring break.  After this we enjoyed Spring Break together.  We went roller skating, watched movies, played with Legos, had a visit from her older sister and put in a new garden bed.  It was a good week. The following week we went back to school and the mammography office left a message for me to call back.  I went back on April 15th because they found calcifications that needed to be biopsied.  My biopsy was then scheduled for April 19th.  I was so scared, while friends and family reassured me it would be fine I wasn’t so confident.  I read about what my stereotactic biopsy would entail.  Let’s just say a guy invented this machine – you lay face down on a table with a hole in it.  Your breast falls through the hole and then it is stabalized ( let’s call this what it is PINCHED) in a good place for the technician to be able to use the needle to take samples.  This took an hour, 5 adjustments of my breast to be in the right spot, markers of where they took the sample and to top it off a mammogram to document where the markers were placed.  Then back to work with ice packs in my bra to help with the swelling.  Then the waiting and bruising began – within a week my boob looked as though it could camouflage for the army.  It continued to change colors for quite some time…weird, but a great laugh some days.  Along with the waiting for results not laughable–very nerve raking.   I was told it would be 7 – 10 days for results to come back.

I received a call from my doctor’s office 2 days later; my doctor wanted to see me the next day.  This was no good!  I lost it – it must be cancer and I can’t have cancer!  I have a wonderful little girl to raise, bug, love and life to live.  This begins my cancer story…more to come soon.

Do’s and Don’ts after a double mastectomy

5 things you should not do after a double mastectomy

  1. throw up (it hurts and your pain meds don’t help you)
  2. hiccup ( I know you can’t control this,but wow does it hurt)
  3. cough
  4. sneeze (again you can’t control it, but WOW – OUCH!!!)
  5. laugh – laughter is the best medicine, but a no, no for a week or so

Things I do recommend: eat pudding when taking pain medicine( so it stays down), pain medicine and use ice packs a lot.  That means don’t worry about the heating bill ; turn the heat up and bundle up.  Also, sleep a lot and make sure you have comfy pillows for your head, shoulders, knees and arm pits.  Yep, you read that right; your arm pits. Oh and don’t forget the pillow to hold when you hug your little one(s).  You will also need button up shirts  and pajama shirts for a few weeks.  Along with a lanyard to hold your drains when you shower. I hope this helps!

Stay strong and take care!

Lifes journey is never dull…

I thought I would begin this blog to discuss the ups and downs of daily life as a single mom and teacher.  Then that shoe dropped…  I have spent the last month picking up the other shoe to help find my inner bad@$$.

I was diagnosed with breast cancer in April, which made me rethink all of my choices in life.  My diagnosis also made me wonder what I had done to get cancer.  Logically, I know I didn’t do anything wrong to get cancer.  It happens without any reason or explanation. There are possibly choices that heightened my risk factors, but non that can be directly linked to me getting cancer.  My diagnosis has made me do some soul searching about life and all of the choices I have made during my journey here on Earth.

Overtime, I hope to share my story as I can wrap my head around the whole experience.

More to come….take care and be kind to each other!

A whole new world!

My first post – this opens a whole new world.  The Other Shoe, I have always used this expression in a negative way, but starting today I am turning it into a positive.  In the past when I felt as though life was going well, I would wonder when will the other shoe drop and make life hell.  Now I am choosing to say when the shoe drops I am going to pick up the other foot and kick life in the a$$.