Tuesday, October 15, 2019

You won't believe how my app is encouraging me!

I've been asking for others to pray that my strength, energy, endurance and stamina come back full force. Well, my app sent me an update today that says I am +45% more active this week versus last week. So out of curiousity I looked down at last week's update and it said I was +105% more active last week than the week before. Well praise God for that. Prayers are being answered and there is real proof "because my app says so"! LOL! Honestly, though, I feel that these things are coming back. I'm not fully back, and have to pace myself, but I'm so grateful that God created our bodies to recover and heal like they do.

Along with the above prayer, I just have to ask you to add that when I have scans again on 11/01, they will show the radiation and immunotherapy combination has done its job perfectly and cancer is not active and shrunk or gone. Oh how this would revive my soul and encourage me. I'm ready for a break from this every other week treatment I've been doing since June 4, 2018 (16 months).

I believe that God can heal me of this cancer once and for all. This November 9th marks 9 years since my first surgery to remove some growing episiotomy scar tissue that turned out to be a rare rare cancer. I remember then my gyn told me this was going to be a long hard road. Little did we know what that would really look like, yet praise God, here I am alive and still in the fight. We didn't know if we'd make it to this year, let alone be hopeful for a good scan in a couple weeks.

Today in my bible study Lysa TerKeurst, Christian author said, "The enemy is vicious, but he is not victorious!" Praise God for that. I'm counting on it. I hope you will too.

"Though a thousand fall at your side, though ten thousand are dying around you, these evils will not you." Psalm 91:7

Wednesday, September 18, 2019

I am not depressed, but I am depleted.

After feeling poorly for a couple weeks, I ended up on the couch for the last 6 days sleeping my life away. I began radiation on the one spot in my right lung that continues to grow and since then I’ve been going downhill until I’ve just slept, became mentally foggy and physically bed-ridden. It’s an extremely difficult place to find myself once again, but my body isn’t as strong as it used to be to stay in the fight. We are closing in on 9 years since this cancer battle began and today I awoke weary in every way.  Fully depleted of all self-strength and human will. As I made myself keep one eye open and push toward getting ready for today’s appointment I became so angry, but not with God - but Satan. I yelled out loud like an angry lion. I’m not sure where it came from, but it was deep within me and felt good. I yelled again and said Satan go away! And then fell into a puddle crying and blubbering to Jesus, begging him to carry me as I have nothing left, I told Him. 
My sister came to pick me up and brought her sweet Evelyn Grace. I couldn’t be fun Aunt Kee Kee today. It made me sad and I told Jesus I need to fully live. I’m not depressed. I am depleted. It’s in this place where I meet Jesus face to face. Where I weakly give Him all my pain and weakness and frailty and ask Him to carry me. I admit I cannot do it anymore. I’m done in. 

I told my nurses and doctors I felt like I needed to go to the hospital. Not that I wanted to, but I needed help now. I guess they know me well enough to know I don’t ever want to go to the hospital and put their heads together reviewing bloodwork etcetera etcetera and determined I have Pneumonitis (like pneumonia, but without the infection). Radiation can cause this down the road a ways, but coupled with Immunotherapy that can also cause it, they decided to treat with a steroid regiment. This means no Immunotherapy infusion next week, but did allow me to continue radiation today. I also have a bad Urinary Tract Infection, which always presents different since I have a urostomy. Plus regular physical strain from radiation and Immunotherapy treatments. I’m been so mentally foggy, but I can tell the iv fluids, multivitamins and antibiotic, coupled with steroids is helping in this area or I couldn’t focus more than two seconds on this update. 
Please pray that I will rest in the wings of my Savior and my body will respond to these meds and quickly so I can get back to fully living and serving. 
And thank you to my sister, Katy, who gave over half her day and got me to the doctor today. Without help I would have not gotten there at all. 
         When I am weak, He is strong.

Wednesday, August 14, 2019

The crazy life stories continue....

Praise the Lord, I do not have cancer in my brain.  Why would I think I did? Well it's quite a traumatic story, so I'll have to start from the beginning.

July 3rd I was shopping with my daughter for a couple items before we left town on the afternoon of the 4th for her to compete in the National American Miss State Pageant.  We stopped at a stoplight and I stretched back against my seat and was suddenly struck in the back of the head with a huge amount of force. I screamed as I thought we'd been hit from behind and something had come through the car and hit my head. My daughter looked at me like I was crazy until she realized what happened.  She took a picture of my headrest and showed me that it had exploded toward my head.  I was so confused and it was very painful.  We've now learned this is supposed to be a safety mechanism that deploys when you are hit hard enough your body would jolt forward.  However, mine just deployed for no reason at all and it has caused a series of painful emotional and physical events.

I pushed through taking 3 IB Profin twice a day for the pageant, but by the time I got home on the 7th it was worsening and I knew it wasn't healing on its own.  I told a PA at my cancer treatment appointment that I could barely turn my head and it was causing me to not be able to sleep or function well because of the pain.  This is a big deal because I'm pretty used to pain and discomfort nowadays. The PA ordered a CT Scan of my neck to ensure there wasn't a fracture.  They did not see a fracture so I planned to schedule an appointment with my MD.  Before that could happen I began throwing up randomly and my Oncologist became concerned that I had a concussion from the headrest deploying so called me in for an immediate CT of my brain. He told me right away that it looked like I had a brain hemorrhage and that the neuro surgeon he consulted wanted me to go the ER for better imaging. I could not believe this was happening! When I arrived they were very concerned that I may have an aneurysm causing this bleed.  They labeled me as a fall risk and put me in a bed.  They told me this was urgent because if I had an aneurysm I would have to be flown out to have a surgery immediately. They prepped me quickly to do a CT with Contrast (which requires steroids and Benedryl as I've had a previous reaction) and then rolled me in my bed down to get the CT Scans.  Thank the Lord they came back fairly soon to tell us it was not an aneurysm, but they didn't know what it was so needed an MRI. I had the MRI and finally around midnight the doctor came in and asked if anyone should leave the room.  Billy, Isaiah, Alyssa, my sister and brother, Amy and Joshua, all wanted to stay and hear the news together, so he proceeded to tell me that I had metastatic cancer in my brain.  That they were going to give me a big dose of steroids to keep me from having seizures, but this is a side effect to be aware of.  He also told me this could progress into mental confusion and then into speech problems.  He said he was sorry and that I should see my oncologist the next morning first thing.  We were traumatized, in shock and disbelief. My brother kept saying they didn't know if this was really cancer or not and Alyssa asked me on the way home if that was just her uncle's coping strategy. I think God was giving him a Word!

The next morning Billy & I walked the familiar stairs up to see my oncologist after a very restless night. When we saw my doctor he said he was thrilled with the news it was not an aneurysm or an active hemorrhage.  We agreed, but were a bit confused by his upbeat mood.  I told him that the ER  doctor had told us it was definitely brain cancer and he immediately said that was not true.  He said he looks at brain scans all the time and this is not indicative of brain cancer.  No edema, no swelling, nothing aggravated, no symptoms.  He told us to go do something with our kids and not worry about seizures.  He would be thorough though and take my case to the neuro cancer board for review, which he did, and they have also agreed this is not cancer.  It could be fatty tissue, a mole on the brain, a calcification.  They aren't sure, but will watch it with my regular scans.

So, back to my car headrest, they referred me to an Orthopedic Doctor and sent my scans to him. After seeing him he said he can see how this caused real pain and damage and it won't heal quickly.  He gave me a numbing shot in the top of my shoulder to numb the muscle spasm and prescribed muscle relaxers and PT 2 x per week for a month.  Plus exercises at home and ice therapy. I will see him again in a month.  I am a week into my PT and wow, it makes me sore, but I am getting a small amount of mobility back in my neck.  My Physical Therapist agrees that this is going to take a while to heal as his tests show there is nerve response down my right arm and down my left leg from this injury also.  This is because the nerves are inflamed and run through the body.  I'm taking prescription pain meds at night to sleep for 4-5 hours without waking up due to pain and taking 3 IB Profin twice a day and using ice and heat to try to get through most days.

Isn't this a crazy story?!?  I would have never had a brain scan, a brain cancer scare or any of this additional pain and extra appointments and therapy to deal with if that head rest hadn't deployed.  It is unreal!

Plus, in the midst of this I learned that I cannot stay in my clinical trial because my cancer in the top of my right lung has grown over 20% since we began the trial, so I'm kicked out.  However, my good doctor has a plan and we are going to radiate that one growing spot, releasing my cancer "essence" back into the body for my immunotherapy to recognize again and go attack.  My doctor was able to apply for these meds himself through the pharmaceutical company and they were approved.  His opinion is that it is working, but needs more time.  2 of my spots have totally disappeared, many are smaller, some are stable and just one is growing.  And symptomatically I was finally feeling really good, until the crazy headrest blew up!

So, please pray that this PT and home therapy works and I don't have to have anything else done to heal my neck and shoulder and nervous system. Pray that the radiation added to the immunotherapy kicks this cancer once and for all.  Pray that I can stay positive and patient when in pain every day right now.  I still desire to live fully and enjoy everything that is coming this next year with our business, with Billy & I and with our kids' lives. It's hard to live fully when at medical appointments, under stress and in pain.  Thanks for reading and praying.  God is still writing this crazy life story of mine and I'm doing the best I can to live it out still smiling.  XoXo

Monday, December 31, 2018

We stood together in prayer and the Lord answered.


Thank you friends for standing with us in prayer! We have gotten our answer and it was a YES! I just finished my trial treatment of Opdivo Immunotherapy! My bloodwork was very close to normal on all liver functions and Potassium. And God took it one step further, along with getting treatment approved on the last possible day, before getting kicked out of the trial, he also gave me good news about my scans! 

Dr B. says that he did a formal review/report of my scans for the trial research company and his finding were better than previously reported. When the radiologist measures the cancer spots horizontally it may show that the spot shrink from a 2.4 cm to a 1.9 cm, for example. This is accurate, but in addition the spots are also shrinking vertically so they look more like a pancake. This is AWESOME! 

Here’s an example. 

I feel like I can let out a huge sigh of relief.  Thank you Jesus! May this single drug work and continue to shrink and destroy this cancer until it’s gone and may it be easier in my body with less “itis” complications. ✝️🙏🏻🙌🏻 

Thank you Jesus for saying YES to my requests. Selah. 

Thursday, December 20, 2018

Sometimes life just gets tough; gotta kick Satan out

Last Tuesday Billy & I went to Fayetteville and had blood drawn and a check up again to make sure the high dose prednisone is doing its work on my inflamed liver. They called it auto-immune hepatitis, which is liver inflammation, but it’s all temporary caused by the trial meds only. We were a bit deflated last week when they said my liver enzymes were so high (over 8 x normal levels) that I cannot continue on the Yervoy medicine any longer. Dr B said that With melanoma patients they only give 4 rounds of Yervoy and then continue on with the Opdivo med. PTL they verified I had 4 rounds so got in a good amount to gain momentum and continue with Opdivo on 12/31 if I’m healthy. I believe I will be if i can avoid all viruses spiraling around. Yesterday, I had blood drawn again and they said my liver enzymes were at the high end of normal again so I am weening down on my steroid medications. This date of 12/31 is my 1 day window to accomplish treatment because I will have gone too long without treatment according to the trial requirements. I cannot do it before because I have to ween off prednisone first. PLEASE PRAY that everything will go smoothly to be healthy on 12/31 and over our Christmas together with my family. We are gathering in a new location in Colorado, so we still get our Colorado white Christmas, but a little different than in Meeker as our precious mom would have hosted. A hard first Christmas without Mom, but looking forward to this time together with Dad, siblings and our families. 

Last Tuesday when we left Fayetteville still processing my appointment, Billy’s dad called and said his mom was very ill and had an ultra sound. They believe they saw cancer in her liver that appeared as metastatic, coming from elsewhere. She was dehydrated and malnourished. My father-in-law got her to the hospital to be admitted Tuesday night for fluids and anti-nausea meds. We got Billy packed and he left for Oklahoma. Slept 2 hours in his truck that night as they didn’t want to keave her, she was so miserable. Wednesday proved to be a bit better and she ate and drank a little bit. Thursday she had a biopsy and an MRI, but slept all day, so miserable. Shortly after midnight on Friday her heart stopped and she went to be with Jesus before we even got a diagnosis. 💔 We are heart broken to have lost both of our moms in 6 months time. We had several days with Billy’s side of the family, planning, crying and reconnecting as we honored my mother-in-law’s life. 

When life gets so hard, I’m so grateful to know that I don’t rely on my strength. We are sheltered by the Master, carried by the Savior and led to a place of peace by the Holy Spirit. 🙏🏻❤️✝️



Tuesday, December 4, 2018

Answers aren’t what we hoped, but God’s still Greater!

Well after 5 hours at HOG today we know why I’ve been so sick once again. The Colitis seems to be taken care of after 4 weeks of steroids. But they do think I have an upper respiratory infection of some sort, caused by a virus originally. My flu test was negative, which I almost wish was the problem. But now I also have what they call auto-immune hepatitis, also caused by my trial meds. It is a temporary condition treatable by more strong steroids, which I’ve already begun tonight.  Basically inflammation of the liver. 
This is found tgrough high liver enzymes in my blood tests. They were slightly high a week ago, but much higher today. It causes the nausea, vomiting, extreme fatigue and overall not feeling good.  I’m sick of not feeling good, so I can’t pretend to feel anything good about this, other than we are glad to know what has been causing me to feel so sick. I am reminded how cancer robs us of LIVING fully as I’ve just been laying in bed so much of the last 10 days. 

I’m only aloud 56 days, which I’m not sure how they count exactly, to go without treatment and still be part of this extremely important trial for me. My clinical trial nurse is like my little angel friend that goes before me and makes sure I am well taken care of. 
She counted and eased my nerves saying we have until January 1st to get a treatment done. I’d sure like to get it done where it doesn’t mess up our Christmas trip to Colorado with my family. Please pray for this. Also, pray my liver has responded really really well to the steroids when I go back in on Friday to retest. 
And lastly, pray that my body can go back on this trial and handle it ok. It was working and boy do we believe God planted this trial in my lap as a life-giving treatment. 

Satan would like to discourage us and make us feel afraid, but God is greater than Satan. God is greater than illness like auto-immune Hepatitis. He is greater than cancer. Sometimes our faith is fully a choice when things look bleak, but we just need a mustard seed of faith! 
Thank you for going to battle with us in persistent and Jesus-empowered prayer! 

This is more than I’ve been in my phone in days, so I’m wiped out and must go, but our family genuinely appreciates everyone who stands with us in this journey. ✝️💜 Thank you. 

Tuesday, November 27, 2018

Celebrating 8 years of life; WITH CANCER.

I am sharing my recent post written in my sisters & I’s ministry page, called Sisters4Christ. Please feel free to follow us and keep our ministry in your prayers and we step out in faith as God calls each of us. 
You can find us on Facebook, Instagram and our web page.