Middle of the Night

"It's 3am and I can't sleep standin' on the edge of something much too deep."                                                                                                Sarah McClachlan

Actually It's "Dex week"  This steriod messes with my nerves, sleep, and patience.  But it does crazy things to cancer cells and the proteins they live off of.  So my family puts up with me.

         

        In the middle of the night here is what I think.

We are all lined up in heaven watching earthly gifts being handed out as people leave for earth.  Up ahead someone says, "Who wants cancer?"  I mistakenly hear "who wants answers?" I jump up and down, raise my hand high in the air and say. "I do, I do, Give me a big one!"  

P. S.  My hair is growing back!

Back in the High life Again?

 Today I am sitting on a beautiful green mountain top feeling a slight breeze while the smell of wild flowers wafts across my face and blows through my long, thick, curly, blonde hair (hey it’s my daydream!) The white puffy clouds dot the blue sky.  

    Today is a day of rest and reflection. My family and I have been looking forward to this moment for over nine long dark months.  It is a day to peer down off this steep mountain peak and realize how far I have climbed.  I am tired.  I am thirsty.  I have blisters and battle wounds but today, “I made it to this mountain peak and the mountain’s under me.” 

    We met with Dr. Tricot yesterday. I “aced” my tests and scans! All the results indicate that there are no signs of any active myeloma cells. I am in complete remission! 

    Now I wish I could dance through the field of daisies like Julie Andrews in the Sound of Music and say this is the end of my journey.  It is the end of days and weeks living away from the family.  It is the end of aggressive, high dose chemo, and two stem cell transplants but it is not time to retire my hiking boots yet.

       I will still be undergoing maintenance therapy for the next year.

This involves four chemo injections a month of Velcade, along with a steriod drug, Dexamethesone, and Thalidomide an “anti-cancer” medication. The Doctor explains that   this regimen will kill off the “sleeper cells” lurking in my body and give me the possibilities of a much longer remission.  

     I haven’t felt “normal” for over a year. I told Dr. Tricot that I would love to go off all the medication for a couple weeks to see what I feel like without any side effects.  He laughed and explained in his Belgium accent,  “You must remember what our objective is, you haven’t reached the finish line yet, but you are doing everything possible to get there and the rest is out of our hands.”

     These words brought me comfort and assurance that this dark, difficult journey for our family has been worth it.  That I have scaled this steep, sharp, rocky mountain knowing that I am doing everything I can possibly do to reach the top and to extend and improve my life.  The rest is in God’s hands.  

      I am tired.  I am thirsty.  I have blisters and battle wounds but today, “I made it to this mountain peak and the mountain’s under me.” 

Test Day

    Tomorrow is test day.  Joe and I will head up to Huntsman to see exactly how much progress has been made through chemo, two stem cell transplants, and specialized drugs.

     I will have lab tests run first, and bring in a 24 hr. urine collection (fun :0)  Then a bone marrow biopsy and aspirate.  If you want to see what this involves, there are some great videos on Youtube.  None of my sons were brave enough to watch, but my daughter and I watched them twice.

   I will also have a combination PET/CT scan.  This procedure takes about three hours, because first  they must inject you with a small tracer quanity of radioactive material that is attached to a sugar which goes to the metabolically active parts of your body.  You have to sit in a recliner in a quiet room for 45 minutes to give the sugar time to get where it needs to be before the procedure.  

   One time I brought a book to read, but the nurse told me I couldn't read because then all the particles would go to the brain. interesting.

    After a peaceful rest,  you are lead to the room with the big tunnel machine.  The nurse shows you where to lay down.  The blanket covered "bed," is abut 12 inches wide.  So you lay down with no place for your arms. Do I lay them across my chest or let them dangle to the floor? Then the nurse steps in with big black velcro straps.  She straps your legs together below the knees.  Then straps your arms closely to your body.  "snug as a bug in a rug!"

     That's the easy part.  "Let the magic show begin!" Now you must lie perfectly still for 45 minutes to an hour as the bed moves through the tunnel.  

    What do I do?  Do I sleep?  What do I think about?  The first few times I went through this procedure my objective was to try  not to think about anything.  Because one thought would lead to another and ultimately end up rather quickly back to cancer.  Bringing fears and fighting back the tears.  

   Now my mind wanders all over during the scan.  Last time I could not get a John Denver song out of my head.  "Country Roads take me home to the place I belong...  The problem was I forgot most of the words, but kept starting over, ugh! very frustrating!!

    When the test is over and the straps are removed from "the Magic show," they point the way down the hall to the waiting room.  The only good thing, I've decided, about this whole day, is I don't have to worry now (since I've lost my hair) of getting up and walking out the door with "bedhead!"

    Well there is no last minute cramming for me.  We will get the results of the tests from Dr. Tricot next Wednesday.  Wish me Luck.  We are expecting the best.  I will keep you posted.

                                Love, Kris

Me and Myeloma facts

I have been pretty slack about writing-sorry.  I have been sooooo busy  what with summer gardening, painting my house, and training for my next marathon-not!

   Actually I have been enjoying the rainy weather, trying to do what I can around my house and trying harder to ignore the things I can't do, and considering a walk through the grocery store as my "marathon" training.  

   So now for the long anticipated update.  How am I doing?

Well that is a loaded question and the answer is prone to change hourly.  I am regaining my strength ever so slowly.  I guess I was getting a little too cocky last week thinking how lucky I was that I had not had any infections after this second transplant.  Alas that was not to be the case.  Last week Joe had a conference in Park City for two days and I was so excited to go with him.  Instead of spending some quality time together, I spent most of the time in the bathroom kneeling at the toilet.  I couldn't blame it on chemo so I assume I had picked up a stomach infection.

    The last few days I have been developing a sinus infection.  It's been a doozy and has really knocked me down physically.  There is nothing like getting sick to remind me that I need to be more careful with this weakened immune system that I have.  That is the nature of this beast multiple myeloma.  It is a cancer of the plasma cells within the bone marrow.  The cancerous cells crowd out the healthy plasma cells that help fight disease and infections.  

   Since we are on the subject of multiple myeloma I wanted to give you a few facts about this cancer because I have never really explained much about it and very few people even know what it is.

     Like I mentioned multiple myeloma is a cancer of the plasma cells.  It represents only 1% of all cancers.  It is most commonly found in older men.  It is called multiple myeloma because it affects multiple parts of the body.  The acronym CRAB helps me remember what they are.  The C stands for hyperCalcemia.  Calcium from the bone leaches into the blood stream.  If enough of it gets into the blood it can damage the kidneys or Renal system. The A stands for Anemia a common problem with mm. The B stands for Bone.  As the myeloma cells begin to multiply they start to eat into the bone causing lesions, and repeated fractures.  I was very lucky to not have any broken bones which is usually how mm is diagnosed. However I do have numerous lesions or weak spots throughout my body.  I have an infusion once a month to harden the bones.

   Multiple Myeloma is treatable but is not curable yet.  There are several different approaches to treatment.  My Doctor takes the "hit 'em hard and hit 'em fast" approach.

Thus the high dose chemo and two stem cell transplants.  We were able to knock off most of the myeloma cells through this, but my doctor explains that there are "sleeper cells" lurking which we have to get rid of through maintenance chemo shots and anti-cancer drugs and a steriod throughout the next year. 

   So the question is How am I doing.  Well I made it to the top of this first mountain range but I am not done mountain climbing yet.  Every step through this journey has been hard.  It has affected every facet of my being. It has made me grieve for the life and body that I had, but truly appreciate the many good things in my life I still have. I look forward to renewed health and a happy future.

My Life Preservers

 After reading my previous blog,  I realized that I had failed to mention one of the greatest blessings in all of this.  My parents!  I don’t know what we would have done without them.  Luckily they live just 20 miles from Huntsman; a true blessing while I am required to be close to the Hospital during testing, treatments and recovery.  I can not even imagine how we would have managed without them. Having them live conveniently near the hospital has been wonderful, however they have done so much more than that.

    My parents have given me life twice.  Once when I was born; the only girl in a family of four boys. (ironically just like the family I am raising) And now they give me life again through the many sacrifices they have made to get me through these last several months. 

     They raised me in a home filled with love.  They taught us life skills I am grateful for now.  Both teachers, they worked hard to care for a big family and made sure we knew how to work hard.  We spent many happy summers in my favorite place-Star Valley, Wyoming, working and playing in the hay fields and woods.

     They have been with me every step of the way.  From the moment we found out the plan, they have adjusted their lives to help my family and I manage all of this.   My dad bought a new car that would be easier and safer to drive into Salt Lake everyday for appointments and treatments.  He  made sure it had good snow tires and was heated before I got in during December when I had to be at the hospital by 7am every morning for over a week.  My dad has taken turns taking me to appointments-He takes the shorter ones :) and gets things done around the house when my mom is with me.  

     My parents just bought a trailer home in St. George last year and were anxious to get down their and enjoy it. They put all their plans on hold without a second thought.  My dad is one of my life preservers!

    My mom has spent her life caring for her children. She cooked, canned, sewed and worked full time.  Although she was a 4th grade teacher for many years,  I think her second career has been that of a nurse. She has spent countless hours in hospitals over the years attending to the needs of our family with broken bones, health problems, and serious life-threatening accidents. Well her experience comes in handy once again as she takes care of me.

     She has spent many, many hours in the waiting room and infusion room by my side.  Her life has been completely consumed with me and my needs.  She probably knows more about my disease than I do as she researches and stays on top of what I should be doing each step of the way.  She spent everyday of my ten day hospital stay with me even though I wasn’t good company and manages to whip up healthy meals for me even  though I could only take a few bites.  My mother has given her life to give me a second life.  She is one of my life preservers!

     How can I ever express the love and gratitude I feel for my parents.  I ask the Lord to bless them everyday for the sacrifices they make on my behalf, and hope that I can be there for them whenever they may need my help.

      I Love you both and am so grateful to be your daughter.  Thank you for all you have done for me now and throughout my life. You have supported me every step of the way.  You are my life preservers in every sense of the word.  Love, your daughter, Kristine

Doggy Paddlin'

I have lots of time to think lately. I try to avoid it as much as possible but sometimes as the hours and days drag by I find myself stuck in a thought or idea with nothing to do but pursue it. 

    Before I had cancer. I was very good at avoiding such scary and difficult topics. It was too depressing to think of what it would be like if something like that ever happened to me or someone I loved. In fact I doubt I would even read a blog like this one unless it was someone I was very close to. Much easier to avoid such a sad topic.        I compare it to an icy cold lake. I would walk near the water’s edge and maybe dip my toes in the cold water but I am not a very good swimmer so I would only swim near the shallow area where I can still touch the bottom. Never think of venturing out to the deep areas too distant from the safe shore.       Well seven months ago someone came and threw me out in the middle of the lake. I spluttered and thrashed and doggy paddled trying to come to grips with this new reality and not drown in the overwhelming circumstances I have been thrown into. I am not superwoman and there are times when I come close to drowning in self pity. In fact today I made a list in my journal of all the things I have lost because of cancer. As my list grew the tears begin to flow. In fact, I think that lake is made of the tears I have cried over the last seven months. Sitting there looking at my list a thought came to me like a light bulb turning on. I wasn’t left alone in the deep waters of the lake. The Lord had thrown out some life preservers before I even got there. He had prepared some things in my life before cancer became my reality.       I can look back and see things being orchestrated in a way that makes this journey more bearable. I think of the timing. If I had been diagnosed a year earlier, I would have been going through treatments during preparations for my sons marriage. I would have missed my daughters High school graduation. Because of the circumstances this year, my daughter was able to arrange her college schedule so she could help more at home.      In September we moved our Martial Arts studio from a studio in our back yard to main street. Eventually making it easier to rearrange my preschool after my diagnosis. My oldest son has been able to help run the studio. I was able to hire a preschool teacher who would eventually count on the income when her husband lost his job several months later. Also for the first year ever, there is an assistant principal at the school where my husband is principal. Thereby lightening his load. And probably the biggest one is the fact that my Dr.- Dr. Tricot a top Myeloma Researcher and Specialist in the country moved from Arkansas to Huntsman a year and a half ago. Those are just a few examples of the little miracles or life preservers that were put in place before I even got thrown out in this lake.       I am still out in the deep, and the water is still cold, but I have a life preserver and the Lord is watching out for me. I have to quite thrashing around so much and trust in the Lord. He has a plan for me and He makes preparations on my behalf before I am even aware of it.       I am a terrible swimmer and a slow learner. I am sure there will be days ahead where I will still be doggy paddlin’ and “cryin’ a river” in my cold lake, but for today I am going to make another list in my journal of some of the life preservers I have been given and practice the back stroke.

One day at a time

Well here I am 33 days out from my second transplant. What a journey it has been. Harder than I ever dreamed it would be. I am gaining my health back ever so slowly! Last Wednesday I was able to go home for a few days. It was Joe's birthday so my daughter came and got me and snuck me home. Joe was completely surprised when he walked in the house and saw me there. It was so good to be home. I was able to get a few things done while I lay in bed. It was tempting to stay, however after a couple days we knew I was not yet ready physically, emotionally, or mentally. So I am back up to my parents home. I am trying to be patient with myself. Every morning I want to just jump out of bed and move doing the normal routines in a day. Instead I slowly shuffle around the house and spend most of my time resting as my body continues to regain it's strength. Joe reminds me to just take it one day at a time.

Preschool Plug

I am starting to think beyond one day at a time and beginning to plan my future. I have put serious thought into my plans for preschool next year. I am told that my immunities as well as my energy level will still remain quite low for another year. So with that information I have made the decision to hire one of my past preschool teachers to run my preschool for me next year.  Hopefully after the new year I may be able to help.  Teresa has taught for me for four years and I have great confidence in her abilities to take this ball and run with it. So If you or anyone you know is interested please let them know. Here is a little information about my program Kris Kelly-/teacher/owner  Certified Teacher-BYU graduate Taught at BYU's Preschool Lab.  Has over 16 years experience teaching  and developing preschool curriculum. Several of her teaching ideas have been published in a national educational  magazine. Loves finding innovative ways to teach young children and seeing them progress as they learn new skills.

Teresa Veater-teacher

Veteran Preschool teacher with over 22 years experience working with preschoolers in the classroom as well as Nebo School District's Transistional Kindergarten program. Her organized yet gentle approach will help your child to gain independence and educational skills for future success.

Country Kids Preschool

is an established preschool in Spanish Fork for the past fourteen years.  We offer a full academic program in a unique preschool setting.  A classroom as well as a large gym area provide many opportunities to educate the whole child.

We offer;

*Developmentally appropriate activities with a hands on approach.

*Small class sizes, 8-10 children per class.

*Thematic units organized to teach basic skills while learning about the world around us.

*Monthly parent newsletter and calendar.

*Alphabet introduction focuses on using all the senses to explore recognize, and remember the letters and sounds.

*Math and number exploration through manipulatives, patterning, sorting, and calendaring.

*Large and fine motor skill practice through games and activities.

Two and three day sessions available

Contact Teresa 801-423-1888

or Kris 801-798-6146  for more info.

(Thanks for letting me share and advertise this important part of my life)

99.9%

I met with Dr. Tricot this morning. All my lab work came back with great results. The myeloma cells are 99.9% gone and my white blood cells, hemoglobin, and platelets have recovered significantly. If I had more energy I would be jumping for joy. I am now set to begin maintenance therapy for the next year. Hopefully I can recover quickly enough to begin enjoying it. Strangely enough my biggest issue right now is food! I just have no appetite. I have been on anti nausea medication but it makes me so tired. Now I am trying medicine to increase my appetite. How I ironic! I've spent my whole life trying to lose those last ten pounds and now I have to force myself to eat and gain weight! This afternoon I was pleasantly surprised by a visit from my husband. I didn't think I would get to see him and the kids until Sunday, but he drove up and spent a few hours with me today. He always lifts my spirits and gives the best back rubs. I could not ask for a better husband, father to our children, and best friend. I know this year has been so hard for him. Having to juggle responsibilities as a school principal, running a martial arts studio, being there for our kids and just making sure everything keeps running smoothly. I always knew he was amazing but now I know he is definitely my super hero! All my Love Joe, Love, Kris

I Can See Clearly Now

So much to express. So Little energy to do so! Yesterday-Saturday May 2nd, I was released from the U of U Hospital. I was there ten days. It is all a blur now-of pain, side effects, Trying to eat when my mouth is too sore to swallow. Trying to get up and move when I am too weak to stand. Trying to stay connected to my family when I can't remember anything. I feel like I have been in a big black hole that I am just now starting to find my way out of. Into sunshine and coherency. I have been told that I had about every side effect possible-Lucky me! One crazy one began right after the stem cell transplant when my hands and feet began to swell and turn red. They felt like when you freeze your hands out in the snow and then come into thaw them out and get that prickly pain feelng. I figure it felt like that for 30 hours without much pain relief. As soon as that began to subside and the skin began to peel off in big sheets than I was blessed with different side effects. This is all so crazy! I have always been very healthy. When I go to the hospital, I bring home a new baby! This time I bring home a new perspective, and new hope for a long remission and opportunities for a new life. I am so grateful for all those who have prayed for me. I know He listens to those prayers even when I am too weak to pray for myself. I am humbled by the kindness, concern, and love of others. Thank you.

Faith Will Get Us Through

I recently was reading in the scriptures and found a great quote the I believe fits Kris and our family. 2 Corinthians 4:8-11 8 We are troubled on every side, yet not distressed; we are perplexed, but not in despair; 9 Persecuted, but not forsaken; cast down, but not destroyed; 10 Always bearing about in the body the dying of the Lord Jesus, that the life also of Jesus might be made manifest in our body. 11 For we which live are alway delivered unto death for Jesus’ sake, that the life also of Jesus might be made manifest in our mortal flesh. Kris and I have discussed many times the strength of the spirit at this time in our lives. The Lord has not abandoned us. He is with us stronger than ever. Kris is slowly gaining strength. Her white blood cell counts are slowly on the rise. Today is day 10 since the stem cell transplant. This is a milestone day for her. Your comments and prayers are felt and appreciated. I was able to take our kids to see Kris yesterday. It lifted her spirits greatly. People ask what they can do for us and I simply say: "Pray for Kris." Thanks again for all of your prayers and thoughts. Kris will be back soon to write on her blog. Joe Kelly

Another Tough Day On The Mountain

This is Joe writing again. Sorry to disappoint the fan club but Kris is still out of commission today. I have spent the entire day with her. She is still in a lot of pain from the chemo. The pain is general and spread over her body. There is only so much that pain meds can do. I want everyone to know that she has world class care here. The BMT unit is very impressive and she has great nurses and doctors. She is in a private room and comfortable as she can be under the circumstances. She is on day + 5 since her stem cell transplant and received her last major dose of chemo today. By day +10 her stem cells will be ingrafted into her bones and will begin to produce red and white blood cells and platelets. Currently, her white cell count is at 0 and she is nutripenic which means she has no resistance to infection. She is on IV antibiotics and IV pain meds. I was able to read her all the comments from the blog and it lifted her spirits. God Bless everyone who is reading this blog and supporting her. I know many of you read and do not comment. That is ok. The prayer that you carry in your heart is helping. I met a man today in the cafeteria who was in a much worse place than we are as a family. We were able to talk and comfort each other. He is two thousand miles from home and his wife is pregnant and very sick in this hospital. We are still counting our blessings. Kris and I actually realize them and savor them more at this time. Family and friends like you are the greatest blessings of all. In the end it is the gospel of Jesus Christ that keeps us going. The spirit is very strong in our family right now and very close to Kris. Thank you all for everything, hug your spouse and your kids and keep praying for Kris. I was able to serve that man in the cafeteria today in a very small way and it made me feel great. When we are down we need to find someone to serve, it will make us feel better. Take care and God Bless. Joe Kelly

We Can Feel Your Prayers

This is Joe writing on April 21. This round of treatment Kris was given new drugs, more stem cells than before, and stronger doses of chemo drugs that she received last time. The infusion of stem cells make it possible for her to receive doses that are up to 10 times greater than a regular dose of chemo. There have been some tough side effects this time around and Kris is in alot of pain. She was admitted to the Bone Marrow Transplant Unit at the University Hospital today. What she needs more than anything right now is all of your prayers and faith. You are all so wonderful and have been so kind to Kris and our family. When I say we can feel your prayers we do. I know its a hard thing to understand unless you have had so many people at once praying for you, but it is a very powerful experience. We really do feel your faith and prayers. Kris is doing better tonight and has the pain under control. We will keep everyone updated on the blog. She loves the comments you write. This means the world to her and they really are her contact with the outside so please continue to post comments. Thank you so much and God Bless. Joe Kelly

The Climb

Early Thursday morning I woke up and seriously considered calling everything off.  “I think I will just just sit down in the dirt and slide down this mountain on my butt!”  I did not want to walk into that hospital and start another round of chemo! This is seriously not very fun anymore!!  The first time around I did not know what to expect, now I know too much.  But I guess there is no way out of this--but up so it is time to start climbing again.

   I had several high dose rounds of chemo on Thursday and then went in this morning for my second stem cell transplant.  The procedure is fairly simple.  After receiving a short saline IV, I was given a transfusion of my previously stored stem cells, then two more hours of saline.  The cells are stored in a DMSO solution as a preservative.  The minute it hits your body, you get a metalic, garlicky taste in your mouth and an interesting odor-which my family did not enjoy.

    My husband, my daughter, and one of my sons came with me to celebrate this second “Stem Cell Birthday.”  It will take several days for the cells to begin working, and my body is beginning to slow down.  This afternoon my face, hands, and feet began to swell.  I look like a pink lobster. 

    I have probably had cancer for several years.  I have know about it for over five months.  I am still in shock about it everyday.  This mountain is very steep!! and some days this climb is on my knees, but I still have lots of life to live and enjoy, lots of family and friends to love, and many lessons and blessings to receive from my Savior.  

The Big Week

Well this is the big week.  Yesterday-Monday I started the first regimen of Chemotherapy.  I was at Huntsman from 8am to 3:00pm. It began with blood tests then we waited for the pharmacy to mix up my personal chemo-cocktail.  The first drug was a high dose of Carmustine given through an IV, a quick run of Velcade.  Then finally a two hour infusion of Gemcitabine, a new drug which my insurance doesn't cover! This medical adventure is not cheap, but we feel very blessed to have good insurance which does cover most of the costs.  I guess it's one more year of driving our old red van!

    I have had little reactions so far-just enjoying it for as long as I can. I know the side effects will eventually come.  I go back in for another round of chemo on Thursday replacing the Carmustine with Melphalan the happy high dose drug which causes mouth sores.  I had it during the first round with few side effects of the mouth because they have you pack your mouth with ice for over an hour before and during the transfusion.  I am really looking forward to that!

   Friday is the stem cell transplant.  A transfusion of 8.27 million of my own stem cells which had been previously harvested and stored.

Well here I go-so far so good.  Wish me luck.  Thank you for all the good thoughts, the many prayers and the kind deeds for me and my family.  I love you all!!

Happy Easter

   Sorry I am a few days late.  I was busy enjoying a great weekend and feeling somewhat normal.  My treatment schedule was put off from Monday April 6th to Monday the 13th due to a bad cold.  It took the whole week to feel better.  Saturday I got the family rounded up to clean the house,  helped my daughter sew a dress, and helped prepare food for easter dinner. I made rolls, a fruit salad and Great Grandma's famous Easter Chocolate Roll for desert. My husband took over the ham and potatoes. It felt so good to feel so good!   Sunday I went to church and listened to my son give a talk in Sacrament meeting.  Then my parents came down for dinner and drove me back to their house to begin treatment on Monday morning.  Here we go again!

Good News, Bad News

I have Good news and Bad news. The Good News first-We met with Dr. Tricot on Friday and found from all the test results that the chemotherapy and my body have been doing what they are supposed to. There is no sign of cancer in the bone marrow and the overall cancer has decreased by 90%!!! After telling the Dr. that I was so frustrated with how slow my recovery from the first tranplant had been, he replied this meant that my body had been working extra hard to kill the cancer (and I thought I had not done a thing for last two months!) I always feel better and more hopeful after meeting with Dr. Tricot. The Bad News is not that bad after such great news. The plan was to begin the next round of treatments on Monday the 6th, however I caught a cold and possible sinus infection over the weekend so everything is postponed til Friday. Plan B is to get over this cold and get healthy enough by Friday to begin chemo then. I am leaving my bags packed and thinking healthy thoughts til then.

Gearing Up for Round Two

Monday and Tuesday were test days. I hope I passed! First was the biopsy-not fun! They take bone morrow fluid, and bone from the hip bone by the lower back. You are given the option of having pain killer or just a local. I always opt for the drugs but it still hurts! I also had an EKG, heart scan, and PET/CT scan. It is hard to lay still on your back when they just drilled a hole in you. I also had a Pulmonary function test. I am always a slow learner on this one. You have to do certain breathing exercises correctly into a tube. It took me seven tries to get it right! I go to see Dr. Tricot tomorrow. I think we are getting smarter at this. The first time we didn't know what to ask now I have a list of questions to ask him. If everything from the tests I had this week look good I will probably begin the next treatment on Monday the 6th. This is round two. The first round knocked the cancer down. We are counting on this next round to knock it into a long, long remission. This has been quite the journey-one that I would not wish on anyone. However I do wish everyone to have the opportunity to feel the love and support that I have felt. I have received so much love and encouragement from so many friends, family, and aquaintances. I am so blessed to have had such good friends throughout my life. It is very humbling to know that so many are praying for me and my family. May you each have the opportunity at some time to feel the overwhelming love and support of others in your life. Thank you and may the Lord Bless you, Love Kris