Skip to main content

I DID IT!

16 weeks, 8 rounds, 16 shots in the belly, countless days away from the girls, and too many pills to count..but it's FINALLY over! I can't even describe how excited I feel right now!!! Yesterday was a long, pretty rough day. But it's OVER. DONE. I did it!

But of course my body decided to try and resist one last time. After 4 blown veins in my left arm they had to use my right arm for the IV. The nurses said the chemo has just destroyed my veins. Apparently even though using the right arm is a big "no no" because of the risk of lymphedema they say that as a last resort they often have to just risk it. They swabbed me up good with hospital grade antiseptic..and I'm not really worried.

I was so wiped out last night, but today I feel great. Well, the all to familiar joint pain is setting in quickly, but mentally I feel amazing. I think it's silly to say I'm proud of myself...but I am. I am proud of all of us.

I've learned so much during this experience about letting go, admitting I need help, and accepting it from people. I've learned that everyone truly wants to help. Matt never once acted like I was a burden on him, his parents never once complained about having the girls over, and my parents were always willing to drop everything to come be with me. Not to mention my brothers and sisters in law who came through for us in countless ways. And everyone else who made my dark days so much brighter with cards, gifts and kind words.

Even though the "tough" part is over, I still have radiation to face. But I really feel like it will be more of an annoyance time wise than a physical hardship. I honestly can't imagine anything being harder than chemo.

So here I sit with a sore body and a grin from ear to ear. I can't stop thinking about all of the wonderful things we have to look forward too not just this summer but the rest of our long lives. I can't believe how lucky we are that we caught this early on and that I ONLY had to do 8 rounds of chemo. I am so ready to move on and live my life just being ME..not being a cancer patient anymore.

Yay for me!Yay for all of us!

Comments

  1. Hooray, hooray, hooay!!!! Over at last. You are a "survivor". Others have crashed under the burden of chemo - but not you! You and Matt as a team are invincible. Family is always there for you and always will be. It's our way of loving each other. Just think of radiation as sunbathing a part of your body that no one (other than Matt and you) will see. It is a time consuming annoyance and nothing more! Love Mama

    ReplyDelete
  2. Congratulations!!!! You did it!!! I'm so happy for you!!!

    --Jackie

    ReplyDelete
  3. I'm so proud of you too, Melissa. You are so brave, so beautiful, so stunningly real. You win! Much, much love.

    ReplyDelete

Post a Comment

Popular posts from this blog

Beauty in Life and Death

This is Matt unfortunately Melissa did not get finish her last entry so I will take it from here.  I will try not to have any typos or grammatical errors.  Melissa would really not like that, but she was my official proof reader for all important documents. Melissa and I always strived to look for beauty even in the darkest of times.  It is not always easy but it is always there when you look hard enough.  Our situation the last year and half have not been ideal there were lots of tears and dark times, but the beauty was overwhelming. Whether it was a note, meal, flowers, or text a a low point or just the love we felt from family or friends.  The beauty was there.  We had so many people praying for us and for Melissa to beat cancer once and for all, but I also prayed that Melissa would be pain free and if it was God's will that she passed peacefully.  Melissa was in so much pain last year.  She did not let her slow her down but she was hurting.  She packed more into a year with

Sigourney Weaver

Years ago (okay, fine...decades ago) in high school some boy jokingly called me Sigourney Weaver. I don't remember all of the details of how or why that nickname came about, but it's sort of funny that she and I do have a lot in common now. Well, the Sigourney Weaver of 1997 or whenever "Aliens" came out. Bald, badass, and with an alien growing inside of us!! My alien will be removed tomorrow morning though, Thank GOD! I'm SO over having this gross bump that hurts more and more every day. The other day I couldn't even put my jeans on without it pinching my little alien baby. It turns out I'm developing a "day before surgery" routine. I go shopping. Today it was the first ever "Back to School" shopping for Reagan! She starts Kindergarten next month, so I figured we should get her some new clothes before the full effects of radiation kick in and I'm too tired. (Wait.... I don't think anything will ever make me "too tired&qu

It's Baaaaaaccccckkkkk.......

6 years.... that's how long it's been since I finished with active treatment. However, I took Tamoxifen for 5 years to squash any estrogen left in my body. I recently switched over to a "tougher" aromatase inhibitor call arimidex. These drugs provided comfort and faith that I was doing everything in my power to prevent a recurrence. Guess what?! They failed me. Big time. It's back, and it's back all over. After months of hip pain that my NP chalked up repeatedly to muscle pain, she finally sent me to an orthopedist. He took X-rays and did NOT like what he saw. Additional blood work and bone scans have led to the diagnosis of cancer pretty much throughout my skeletal system. Metastases were found in the skull, scapula, multiple ribs, pelvis, both hips, and spine. Definitely NOT the news I was expecting nor wanting to hear. After an afternoon of crying and occasionally feeling like I was going to throw up, Matt and I met with Dr. Adler, my oncologist. He was