Updates on Kathy's battle with breast cancer.

Friday, March 22, 2013

The Gift that Keeps on Giving


 Friday, March 22, 2013


It’s been seven weeks since my last treatment, and about five weeks since my last post.  So many wonderful things have happened in the mean time.  I’ll start with the health updates. 
I’ve seen my surgeon and oncologist for follow-up appointments.  They both gave me a clean bill of health and said to come back in three months.  The surgeon told me things to watch for.  He said that when breast cancer travels to other areas of the body, it usually travels to the brain, bones, lungs, or liver.  I thought the things to watch for could be helpful to anyone keeping watch over their bodies for any signs of illness, so I’ll tell more about them here.  Any medical professionals reading this will likely have more detailed information to add, but in lay terms, this is what I gathered from the conversation:  sudden extreme change in vision or bad head aches can indicate a brain tumor, very painful bones that hurt even when you aren’t moving them can be a sign of bone cancer, constant unexplained coughing or shortness of breath can indicate lung problems, and sudden weight loss without explanation or yellowing of the eyes can indicate liver problems.  So, in addition to self-exams of the breast tissue and related lymph nodes, I need to be watchful for other signs. 
I read on a chat board where someone commented that breast cancer was the gift that keeps on giving.  I enjoyed that comment.  There seem to be several things that no one tells you about until afterwards, which is probably wise, since you don’t really have a lot of choice about it anyway, and knowing everything might be too much to carry at the time.  But, for those that might be curious, I’ll go ahead and talk about a few.  If you really want deeper details and know me well, then give me a call and we can talk further.  Part of my armpit and about half of my under side of the arm, from the elbow to the pit is still numb.  Feeling may return to some of it at some point, and some of it may stay numb forever.  It doesn’t limit my mobility, so it is mainly just an odd left-over reminder.  The connective tissue from my forearm to waist is constantly trying to tighten up.  Twice a day I do stretches to keep it loosened up.  The major shrinking will continue for about a year, but after that I will need to stretch that area daily forever, because the shrinking will continue, but more gradually. 
Another thing that took me by surprise, was that my surgeon said I was now starting the most difficult part of the entire breast cancer journey……what???  I’ve been elated, and celebrating that the hard things were over with, and that is definitely how I feel.  But, it was interesting to learn that for most women, after all of the treatments are over with, depression is a common challenge.  In thinking about our several cross-country moves, I could relate to how this could happen.  You’re in full action gear, lots to do, so many things to take care of that there is no time to really think about what is actually happening to you.  It’s usually about two weeks after settling into a new place before there is time to sit down and let it sink in that you’ve just left so many friends behind and you’re in a new place where you hardly know anyone.  In those situations, I’ve learned the hard way, that it is best to reach out to others from the get go.  Instead of sitting in a class at church waiting for someone to come and sit by you, it’s best to look for someone sitting alone and go sit by them and introduce yourself to them.  I’ve often found a new friend who has also just moved in by using this strategy.  I’ve learned to invite someone over, instead of waiting for someone to invite.  I’ve also learned that I’m happiest once I’m busy serving someone else.  All of these things have helped me get over the blues when I’ve moved.  Maybe there are too many things keeping me busy for depression to set in, but it was good to have a heads up from the doctors to watch for this challenge.  I also appreciated knowing this as a friend, when someone I know is given a cancer challenge, I’ll know to check in even after the treatment is complete, to make sure all is going well.  I’m doing great, so this isn’t a shout out for inquiries.    
            Another cause for the high occurrence of post-cancer depression for women is the hormonal drugs some of us need to take.  The hormone blockers, like the one I’m on, can throw lots of things off.  Thankfully, the biggest side effects I’ve experienced, so far, are hot flashes (usually at night) and “chemopause.”  Again, in case you or a friend ever experience any of this, you’ll have a better idea of what to expect.  With no warning, you’ll go from cold and bundled up, to throwing off the covers and removing layers of sleep clothes, then about 15 minutes later, you’re freezing again.  This process seems to happen two or three times a night.  It has to be considered as comical, allowing you to keep a positive attitude about it.  Chemopause as opposed to menopause is a great way for a woman to go through “the change.”  It gets it over with quickly.  Chemotherapy stops menstration, and if you’re getting close to “the change” anyway, 90% never have to worry about the monthly meanies again.  Weight gain is another challenge with the hormone blocking drugs, and I’m trying to prevent that part, which they say can cause ten to twenty pounds of weight gain.  Joy. 
            My hair continues to grow at a rapid pace.  It doesn’t appear to be much longer, but that is because these curls continue to coil around and around and around.  I’ve always had straight hair, so this is all a new adventure.  It’s fun to experience a different look and feel.  I’m learning about hair products that keep everything in place.  If I brush through the curls and let them go wild, I get an afro look.  If I pat my hair dry, apply gel, and let it dry naturally, then the curls tend to stay close to my head and seem less out of control.  For now, I’d like to grow it out to shoulder length or so, so in the mean time, it means I need to be patient for these coils to grow long enough to give me some additional options.  I’m VERY thankful to have hair again.  I appreciate bad hair days over no hair days.  It’s a lot warmer! 
            So, I’m obviously feeling much better, because I’ve rambled on and on and on.  My energy is returning, but I’m also glad to know that it takes several months to hit 100%.  I feel like I’m probably at 70% of my previous energy levels.  Exercise makes a huge difference.  I am definitely more energetic on the days I exercise.  I feel so much better.  At the time, I didn’t realize how crummy I was feeling, especially during chemotherapy, which was a blessing.  But now, it is exciting to feel so much better and have more energy. 
 Sorry that the health update was so very long.  So many exciting things have happened since my last update.  I’ll try to be brief. 
Garrett has a new position in Chicago, only 3 ½ hours away!  I was able to drive up and help him get settled in his downtown apartment.  He is now one of two correspondents covering the upper Midwestern states for the Fox News Channel.  He works with a camera operator and a producer as they travel around to cover stories in several states.  His first story aired this week (click to view, watch for the very end--my favorite part).  I'm so proud of him!  I'll try not to brag in future posts.  
I went on a trip to Santa Barbara and met some mom friends from when I lived in California.  It was my first airplane trip anywhere in ten months.  It was really fun.  We talked, exercised, shared ideas for volunteer work, sewed baby blankets for a cardiac unit at Children’s Hospital L.A., saw a chick flick, and ate great food.  
    On February 27th, we sent Heath off on his 2-year mission.  He was so excited and ready.  His blog is ElderHeathTenney.blogspot.com  We had some really sweet moments together as a family before he left, and gave our last hugs for two years at the security checkpoint at the Indianapolis Airport.  Kirsten and Weston picked him up and delivered him to the MTC.  That last hug before a mission is still one of the hardest things I’ve ever done, even when I’ve done it before.  You have to love the Lord and strongly believe in His message to part with your child for that long.  It gives a parent just a tiny feel for what it must have been like for God the Father to send his son Jesus down to earth to be our example and to die for each of us so we can all live again.  I can’t imagine how that must have been, knowing what all would happen to our Savior, but I’ve felt a tiny bit of that love and sacrifice with sharing sons for only two years, and it makes me love and appreciate the Father and the Son even more.  I do deeply believe in the message Heath will be sharing, that the gospel of Jesus Christ brings us joy, that after Christ and his apostles were killed, over time there was a falling away and loss of priesthood authority, and that Christ’s full gospel has been restored, along with a living prophet and apostles, to guide us through the current issues and challenges in the world.  I’m thankful to share Heath for two years so he can bring this message and joy to others.  If you'd like to hear his message, let me know and I can send some sweet missionaries like Heath to your door, visit lds.org, or I can have my niece who's serving a mission on Temple Square give you a telephone call!  

Thursday, February 14, 2013

For Valentine's Day, a Marriage Proposal--from 1841


It’s been two weeks following my last radiation treatment.  The fatigue has been minor compared with chemo.  I’ve done computer work or reading for a few hours each day, but it’s not been for the entire day, as it was at the end of chemo.  I’ve had no burning, blistering, or pain.  I’m very thankful that radiation went so smoothly.  I thought I was scheduled for multiple doctor visits the week following radiation, but after arriving for the first appointment of the day on Feb. 4th, learned that all of my appointment were in fact on March 4th—chemo brain again, I guess.  I will start Tamoxifen, the hormone blocker, on Friday.  Since my cancer was fed by hormones, this drug will cause any remaining cancer to starve.  I will take it for the next 5-10 years, maybe longer as they continue to track and study it’s effect.  

I’m adjusting to my new hair.  I’ve never had short, or curly hair before.  Bad hair days are definitely better than no hair days.  I’m experimenting with different hair products to keep it all under control.  It’s growing fast!  Today I was able to run my old route, slowly, but that was very exciting!    

I’ve enjoyed working on family history while I’ve rested.  I’ve come to enjoy the search for relatives in my family tree—especially the challenge of finding married and maiden names.  This past week, I came across a marriage proposal to a cousin on Scott’s side of the tree.   It’s sweet, socially awkward, sincere, and successful.  I thought it would be fitting to post on Valentine’s Day: 

A MARRIAGE PROPOSAL March 24, 1841   

To my dear Miss Ann Bourland

Dear Miss, permit me for the first time in my life to make known my love to you. Having come to the conclusion to marry soon, I have selected you out of a large number of my aquaintance for my intended bride. To you Miss I promise that I have never loved before, but I can say so no longer. To you Miss Ann I offer my hand and my heart with the hope that I shall have yours in return. My writing thus to you may somewhat surprise you, but rest assured I am in earnest. It may be the least of your thoughts of receiving such a document as this from me, but Miss be not surprised. I will acknowledge that I have acted rather strangely for a lover, but unfortunatley I was not intended to be a ladies man.  Should I be so fortunate as to win your consent to a holy alliance, I can not promise you at what time we would be united in a holy state of matrimony, but Miss, if you like another, or think another man is more worthy of your affections, I am in hopes you will tell me so. Believing in your good judgement and that you will deal with me honestly, I leave the subject with you for your consideration. I will call upon you next Sunday for a positive answer, and at that time, if an opportunity affords itself, to hear from those little lips of yours my future happiness.

Yours in haste,
Manion

They were married 2 months later. He was 23, Ann was 16.

I’m so thankful to have had the same valentine for the past 36 years.  When we were 15, I bravely decorated a heart shaped cake for Scott and wrote on it, “Knock, Knock.”  I’m sure it made the entire cake thing even more embarrassing for Scott when everyone asked what it meant.  He probably didn’t share the rest of it:   “Knock, knock….who’s there?  Olive.  Olive who?  Olive you!”  I guess I was a little shy, socially awkward, sincere, and definitely successful!  Who would have thought at that time that the biggest crush I’d ever had would be my biggest crush forever!  It’s been a joy ride.  I’m so thankful to have found my best friend at a young age.  He is always my biggest fan and supporter. 

We have loved having Heath home for a little while before he leaves on his 2 year mission to Buenos Aires, Argentina.  We’ve completed all of the tasks and purchases on his lists.  We’ve seen a lot of miracles from heaven along the way.  Family starts arriving tomorrow.  He will speak in church on Feb. 24th at 1:00, if you’d like to come, and that evening from 6-8 he’s having an open house and we’d love to have you stop by.  He enters the missionary training center on Wednesday, the 27th

I’m sure you were all thinking this blog was finished, since I’ve crossed the finish line; but I’ll continue to leave updates along the way.  Thank you for your love and support.  It has made such a huge difference.  Each individual kind word has combined into a great source of strength.  Thank you!

Saturday, February 2, 2013

The Finish Line


“Celebrate good times, come on!!”  This was the imaginary music playing in the background on Friday, the wonderful day we crossed the finish line!  The night before, my friend Mark, who does hair, trimmed and shaped my 2 inch long hair, adding a bit of color to camouflage the skunk stripe.  



I decided to leave the wig behind as I started this new chapter.  My friend Christi picked me up for my last radiation treatment.  When we got to her car, it was filled with friends coming along to celebrate.  They were all very complimentary about my short hair, saying that pixie cuts were all the rage these days, and how they all wished they had one.  It was really, really nice of them to say such kind things, since I was very unsure and insecure about my first public appearance without a wig. 

My last radiation treatment was fast.  Next, I saw the doctor. She said my skin looked great.  I was just a little pink, but have had no burning.  She said to continue the skin care routine for the next two weeks, and come back in 6 weeks for a follow up.  She gave me a big hug and told me "Congratulations."  

I see the chemo doctor and physical therapist on Monday, and the surgeon next Friday.  In a few weeks I’ll start Tamoxifen, the medication I’ll be taking for the next 10 years.  It’s a med to block the hormones that feed my type of cancer.  I’ll find out next week what the rest of my schedule will be.  I know they’ll watch me close, and at least every 6 months will do mammograms or ultrasounds. 

So, back to the celebration.  After finishing with the doctor, I walked into the waiting room and let out a big “Woo hoo” with my arms up in the air.  My cheering section stood up and started clapping.  We then had the friendly receptionist take our photo, before we headed off to lunch.   

Gretchen, who knows every patient by name
and always greets with a big smile.

At the restaurant, we were met by a huge crowd of friends.  It was so fun being surrounded by many of my church family sisters and kids not in school.  They have been an amazing support through this whole process, and helped make each step along the way into a party. 

































My day was filled with numerous texts, Facebook well wishes, and phone calls.   When the party bus dropped me off at home, I was greeted by a decorated front door with fun messages, and then a decorated room inside.  Heath made signs, purchased flowers, and decorated my bathroom mirror.  That night, we celebrated with dinner at a Mexican Restaurant—one of my favorite kinds of food. 














It was a wonderful day, and a wonderful way to celebrate the final step of this adventure.  The fatigue will continue for the next couple of weeks, but the adrenalin from crossing the finish line will carry me through!  My heart is full of thanks!  We can do all things through Christ.  I’m so thankful for His help, comfort, and strength; and for his earthly angels that have been by my side this entire time.  Scott, my favorite angel, has been amazing as coach and team captain.  Life is a joy ride!      

Monday, January 28, 2013

A Lethargic Slug


I have 4 radiation days remaining!!  I will finish radiation on Friday, Feb. 1st.  Radiation has gone well.  I have not had any burning, so far.  My neck is a little pink.  I’m now using the cream on that area 3 times a day, with 2 times a day application to the rest of the radiation field (my front left side from about the waist to the shoulder).  I spray the green tea spray about 4 times a day, take the turmeric twice a day, and vitamin B-50 once a day.  Together, these things have helped prevent burning.  I’ve been seeing a physical therapist once a week that specializes in lymphedema prevention.  Since my doctor’s group and Indianapolis University Medical are the only practices in this area using the green tea spray (that I know of), patients from other practices that my physical therapist sees have significant signs of burning.  I’m so thankful to have found this doctor that uses a mix of medical and herbal treatments. 

I feel like a lethargic slug.  Thankfully, until the middle of last week, an hour of reading in bed in the middle of the day was about all I needed to recoup energy for the evening.  It was hard to get going in the morning, but once I was up and at it, I was fine until mid-day.   Now, I’m back to the point of waking up and feeling just as tired as I did when I went to sleep.  I’m thankful that the finish line is in sight!  I’m excited about dragging myself across it this Friday!!!  They say the two to four weeks following my last treatment are when the fatigue will be the strongest, as my body works at repairing the damage done by the radiation.  So I have 3-5 weeks to embrace and enjoy this time for reading and lounging. 

This weekend, I was again reminded of the miracle of the enabling power of the atonement.  In this lethargic, sluggish stage of treatment, I was blessed with a needed burst of energy so I could attend and enjoy our stake young women’s volleyball tournament on Saturday, and a stake youth fireside on Sunday night.  They were both wonderful events.  I loved spending time with the youth in our stake and watching their amazing examples as followers of Christ. 

Recently when visiting a nearby LDS congregation, our stake president (church leader over several local wards/congregations) shared a message that felt like it was written just for me.  It referenced Psalms 24:3-4  “Who shall ascend into the hill of the Lord? or who shall stand in his holy place?  He that hath clean hands, and a pure heart; who hath not lifted up his soul unto vanity, nor sworn deceitfully.”
Often in the scriptures, mountains are used to represent the Lord’s house, His temple, a place where we can return to Him, and prepare for when we literally return to Him.  But here, the term “hill” is used.  The speaker referred to Mount Everest, and the limited number of people who are successful in climbing it.  I looked up some of this information and share it below.  (Skip past this for the rest of the story, if you’re not interested in additional facts about this mountain) http://geography.about.com/od/specificplacesofinterest/a/mounteverest.htm: 
Expeditions to the Top of Mount Everest
Despite the extreme cold, hurricane-force winds, and low oxygen levels (about one-third of the oxygen in the atmosphere as at sea level), climbers seek to successfully climb Mount Everest every year. Since the first historic climb of New Zealander Edmund Hillary and Nepalese Tenzing Norgay in 1953, more than 2000 people have successfully climbed Mount Everest.
Unfortunately, due to the hazards and rigors of climbing such a dangerous mountain, over 200 have died attempting to climb - making the death rate for Mount Everest climbers about 1 in 10. Nonetheless, in the late spring or summer months, the climbing season, there can be tens of climbers attempting to reach the peak of Mount Everest each day.
The cost to climb Mount Everest is substantial. The permit from the government of Nepal can run from $10,000 to $25,000 per person, depending on the number in a group of climbers. Add to that equipment, Sherpa guides, additional permits, helicopters, and other essentials and the cost per person can be well over $65,000.    

        So, to continue with the message from church, he shared that God wants all of us to seek Him, not just a limited few.  He doesn’t want any of us to fail.  Perhaps Psalms 24:3-4 refers to “hills” because they are achievable and not over-whelming.  They require consistent work, but it’s a gradual process with variations in difficulty.  President then talked about taking a 50-mile hike in Southern Indiana, at first thinking, “It’s Indiana, how hard can this be?”  But, it ended up being very challenging as each day passed and muscle soreness and fatigue increased.  He later learned that with the constant changes in elevation, this 50-mile hike was equivalent to having climbed Mount McKinley, the tallest mountain in the United States. 

This whole reference to mountains, hills, and hikes was so similar to my journey with cancer.  I’m nearing the end of this breast cancer hike.  It has felt more like a series of hills, rather than a majestic mountain that is over-whelming to look at.  By taking one day at a time, one hill at a time, and with the help and support of family and friends, constant prayers, and help from above, this entire mountain climb, or rolling hills hike, has brought us all closer to God.  We’ve seen His miracles, we’ve felt His peace, and we’ve come to better appreciate the daily strength the Lord provides for us as we seek Him.  It’s been a hike of learning, a hike of faith, and a hike of gratitude.  I know the Lord wants us all to ascend the hill.  It’s do-able, one step at a time, and one day at a time, helping each other along the way.    

Monday, January 7, 2013

Birthdays in Heaven



Happy birthday in heaven to my dad.  He left us three years ago today.  In celebration of his birthday in heaven, for his gift, we enjoy doing service for someone else in his honor.  His advice for a happy life was to do something to serve someone else each day.  He actually said you're wasting the Lord's time if you don't do this.  We have this family poem we say after singing happy birthday to a family member:  "Many happy returns on the day of thy birth, may sunshine and gladness be given, and may the dear Lord prepare you on earth for a wonderful birthday in Heaven."  This poem has taken on new meaning as family members have passed over to Heaven.  So, it's nice to think of the celebrations that must be happening every time someone arrives in their heavenly home, and as their birthdays occur.   The photos below were from when I was bald.  I wondered if we looked alike, since he was bald the whole time I knew him.  Now that I'm NOT bald, I'm comfortable posting these:  
My favorite picture of my dad.
Photoshop fun--when I was bald.  Look alikes?


           





















I’ve had 14 of 33 radiation treatments!  Things are going well.  They said starting treatment #11, I may find some pinkness of skin.  I’ve been doing all of the preventive skin care and so far, my skin is healthy and normal.  I see the doctor once a week so she can monitor how I’m doing.  My eye brows and eye lashes are growing back!  My hair is about one inch long all over and it's keeping my head warm at night without wearing a hat.

I had my first visit with a physical therapist that specializes in lymphedema—a condition I’m at risk for due to the lymph node removal.  As long as I’m careful to avoid infection in my left arm, I should be fine.  If I get an infection, the arm can collect fluid and swell.  I’m to carry anti-biotic ointment and band aides in my purse in case I get a cut.  I will meet with her 5 more times, as she works with me on exercises to strengthen my left arm and also stretches to ease the “cording”-- tightness of connective tissue.  It looks like there’s a tight cord running from my wrist to my waist.  I will need to stretch that area daily for the rest of my life to keep it from tightening up and to keep up my flexibility.  

They say the fatigue starts to set in at about the half-way point, so we’ll see if I start to feeling later this week.  So far, things have been great.  They also say the rebuilding of energy takes longer with radiation than chemo.  The two to four weeks following radiation are supposed to be the hardest, and then my energy rebuilds, but I should give myself a year before I feel like I’m 100%.  So, we’ll see how it plays out.  Friends who have been through it say it took them 4-6 months, so I’m hoping for that range instead of a year.  Right now, I’ve loved feeling like I’m at 80% after the chemo.  It’s great!

Christmas Eve, Indianapolis




I really enjoyed Christmas and New Years.  It was so nice having everyone home.  Heath, Kirsten and Weston hit a bad blizzard on their way home, delaying their arrival for a few days, but thankfully they were able to arrive safely—plus enjoy two nights in Kearney, Nebraska while the freeway was closed off due to snow.  Garrett, Kirsten, and Weston left on January 2nd.  We have Heath home with us until he leaves for his mission in February. 

I’m thankful for 2013 and the adventures it will bring.  I’m also thankful for 2012 and the lessons we learned through our adventures.  We grew closer as a family, and also grew more appreciative of the spiritual blessings life provides us.  We could feel of the strengthening power of so many prayers in our behalf.  We came to better recognize and appreciate some of the many tender mercies that the Lord continually blesses us with.  We also learned a lot about serving others—lessons we learned from so many who served our family in so many different ways.  We plan to pay it forward this year and in the years to come.  It is exciting that the finish line is within sight!  Deep thanks to everyone who has climbed along with us and cheered us on along the way.   

Monday, December 17, 2012

Day 1 of Radiation

I just returned from my 8:00 a.m. first radiation treatment.  It was painless.  I hold still on a table, they line the markings on my skin up with the laser beams for the machine, and then apply radiation from I think 4 different angles.  It was like having about 4 x-rays done.  Two lasted for about 40 seconds, the others were maybe 10 seconds, according to the specialists running the machine.  But, there was no pain.  I applied the green tea spray beforehand, the prescription cream afterwards, and will apply the green tea spray 3 more times today, and the cream one more time before bed.  So far, so good!

I just read the paperwork about fatigue.  It said if you have radiation following chemo therapy, the fatigue that occurs towards the end can last up to a year.  Yikes!  I hope that's wrong, or that it means a year until you're at your full energy levels.  I've loved this past 6 weeks of gradually-building energy.  It's been a really nice reprieve.  

The rest of the treatments will be at 10:45 a.m., lasting only about 20 min. in and out the door.  So, if I'm feeling up to it, I can treat my drivers to lunch afterwards.  So, one down, 30 to go!    

Friday, December 14, 2012

Radiation


These past 2 weeks I’ve had doctors appointments with the oncologist (the cancer doctor that does chemotherapy and meds for long term prevention) and the radiation oncologist (3 visits).  I start radiation on Monday, and will every weekday for the next 6 weeks except Christmas Day and New Years Day.  I will make one of those days up by going twice the day after Christmas or New Years (it has to be 6 hours apart, and I can only double up for one of those missed days—more than that would be exposure to too much radiation).   

Things are going well.  I feel like I’m at 75-80% of my previous energy levels, but it’s hard to tell for sure.  I’m feeling the best I’ve felt since this all started in May!  It’s been a welcome few weeks off!  My surgery has healed well.  I’m amazed at the range of motion for my arm.  After surgery, it was hard to imagine ever being able to raise a straight arm up to the side of my head.  I can now put my arms straight out in front and then raise them up totally over my head, though it still hurts a bit until I’ve stretched it several times.  I can do the same thing starting with my arm out to the side.  My hair is growing back at a rapid rate now, but I have a Cruella Deville stripe that has to go before I toss the wig, plus it’s still pretty thin on top.  My nails are like the rings of a tree trunk.  You can look at them and literally see the passage of time—the chemo part of my nails gradually being pushed out by the new healthier nail.  I’ll post a photo.  I can run for a mile without stopping, then walk for a bit, and run some more.  My walking/running friend Denise has been so helpful, consistent, and patient.  We go at 6:10 a.m., and some days it looks so cold out, and so warm inside, that I choose the lazy warm bed and opt for going with Joey the dog once it’s warmed up a bit.    


Radiation machine, tilted on its side.


CAT scan machine for 3D imaging in radiation prep.

Chemo damage growing out from nails.











I’ve been learning so much about radiation and ways to lessen side effects.  In the past, they would use small tattoo type markings for lining up the machine.  I had been trying to decide what I wanted those tattoos to be—a flower, “Scott,”…. Since it was a medical necessity to have the tattoo.  But, now, they don’t do tattoos.  Instead, I’m all marked up with a paint pen.  They touch up the markings each time I go in, and they used a green pen to stay with the holiday spirit.  If the tattoos were anywhere near the size of the paint pen marks I could have chosen both flowers AND Scott as the designs! 

There are a lot of foods, vitamins, and products I need to avoid, and there are also things I need use on my skin or eat/swallow.  In the Word of Wisdom, which is the health code Mormons live by, we are taught not to drink tobacco, coffee, or tea.  It says tobacco is an herb that can be used to heal bruises.  My doctor, who is not Mormon and probably hasn’t read about this health code, is involved with a group doing a study on green tea, and how using a fresh green tea spray—sprayed on clean skin before radiation (after radiation I apply a prescription cream and let it soak in), after arriving back home, (I again spray the entire quadrant and let it dry before putting clothes over it) and then again 2 more times each day (4 total), reduces reddening and blistering of the skin during radiation.  I purchased a Costco box of 100 packets of green tea, for spraying, not drinking.  Every evening, I will make a fresh batch of concentrated green tea using 2 tea bags to 1/2 cup (4 oz.) of water.    I’ve never made tea before, so hopefully it’s easy to figure out.  Each morning, I’ll refill my spray bottle with the fresh batch, to use for that day.  (I thoroughly clean a Bath & Body Works spray bottle--it makes a very fine mist).  

Another thing they’ve found that helps reduce side effects is Turmeric.  In studies, they found that women from India had less reactions to their skin.  They first researched Curry, which is made up of multiple spices/herbs, and then narrowed it down to Turmeric.  So, I take a capsule of Turmeric each day, and also a Vitamin B-50 (making sure it does NOT have vitamin C, which I need to avoid).  I can’t take multi-vitamins during radiation.  So, those are some of the new things I’ve learned recently.  

It was so nice having my mom here for 3 weeks.  She worked like crazy and had to have been exhausted when she returned home.  She went through many of my drawers, cabinets, and pantry, organizing things and making everything look better.  She also spoiled by making Scott’s favorite cake—Oatmeal cake (recipe at the end, if anyone’s interested), and healthy meals that tasted great.  The night before she left, we had our church women’s Christmas dinner at our house.    It was really fun having her here for that, and also helpful having her help on it. At first, they had made other plans for the dinner, not wanting to add any stress; but after telling them how much I loved doing it, they gave in.   Eight women came over the day before and helped set the tables, cover the chairs, tie sashes, and make everything look festive.  The next night, we had 12 men and young men serve dinner to 54 women.  The clean up crew was huge, and it was all put away so quickly.  It was a wonderful night! 














We’re preparing for our college kids to arrive next Wednesday.  As of today, all of the college kids are finished with finals!  I’m trying to finish up Christmas preparations before radiation starts and the kids arrive.  I love this time of year!  I’m so thankful for Jesus Christ.  I’ve grown closer to Him this year.  I have felt His embraces so strongly.  He is the Prince of Peace.  He is there for each of us, waiting for us to reach out to Him.  He’s also counting on us to watch out for each other.  I’m so thankful for and appreciative of the love and kindnesses that have been shown to our family.  We have felt peace through our storms, and joy in the journey.  It is exciting to see the finish line!!  This next 6 weeks will go by really quickly.        

P.S. Here's the Oatmeal Cake Recipe:

Combine & let stand:  
1 1/2 cups hot water  
1 cup dry oatmeal

Cream together:

1 cup brown sugar
1 cup white sugar
1/2 cup shortening
2 eggs

Add the softened oats to creamed mixture, then add:

1 1/2 cups flour
1 tsp. cinnamon
1 tsp. soda
1/2 tsp. salt
1 tsp. vanilla
(if desired, new add in we loved, 1/2 to 1 cup coconut)

Pour into 9x13 greased pan.  Bake 350 for 25-30 min, until toothpick comes out clean.

Frosting (the best part!)

1/2 cup butter
4 Tbsp. canned milk
1 1/2 cups brown sugar, packed
1 cup pecans
1 cup dry oatmeal
1/2 cup coconut.

Boil butter, milk, and sugar 1 minute.  Remove from heat, stir in pecans, dry oatmeal, and coconut.  Pour and spread over warm cake and brown under broiler until golden (watch closely, this happens quickly).  This results in a sort of crunchy yummy topping.