The Kim Connection

Thursday, August 09, 2007

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Welcome friends and family!             

This site was set up so you can check up on the latest news about Kim.                            

MANY THANKS FOR YOUR PRAYERS, THOUGHTS, AND SUPPORT!  

 
Check out the Newspaper Articles section to read about Kim and her donor!

                 Latest News                

 
Thursday August 9th, 2007

       Hi, All is well here. Sorry for such a gap in information. We had an enjoyable summer. We were able to get out of the heat and go up north. We went camping at Woods Canyon Lake, Christopher Creek and then up to the North rim of the Grand Canyon. At the rim we were able to stay in a rustic cabin a short walk from the edge. It was a very relaxing summer. Kevin was able to get his "Man Cave" (garage) organized and painted. The summer went by too quickly now to get ready for another school year.

        I was released to go back to work and will be starting this year out at Pioneer Elementary working part-time. Pioneer is right down the street from where Megan and Aaron go to school so it will be a convenient location. I've had a busy week of meetings and moving my classroom. I am making sure that I don't over do it !!

      Can you believe that I'm already having my 2nd year birthday of having my transplant on the Monday August 13th ??? Amazing how time passes so quickly. I thank God for all he has done in my life!!! I also would like to thank all of you for your continued support and prayers may God give you little delights to let you know he's there.

 

Monday, February 12th, 2007

        Isn't it amazing at how quickly time passes when you're not busy keeping track. Two years ago today I was initially admitted into the hospital with anemia.  I've experienced quite a bit since then. What a truly blessed time it has been!!

        I'm now feeling much better and reducing medications at almost every doctor visit. I really enjoy the rainy weather we've been having as I can't go out in the sun. I'm sure that it won't last too much longer though.

       Now let's see if I can fill in some of the gaps in this journal.

        The holidays were busy. Aaron and Megan took turns getting sick the two weeks before and the two weeks after Christmas. I got a sinus infection right after Christmas and it feels like it's finally getting better. I go to the ENT on Thursday afternoon to discuss the progress. It's been almost three weeks since I've had to go to the clinic. My next apt. is for Thursday morning and hopefully we can reduce some more medications.

        Oh!  I forgot ---Christmas vacation we took a day trip to Flagstaff. It was like experiencing winter in New England for a day. The kids were really excited. Before we got into town we experienced some fog which scared the kids but that all changed once they saw snow on the ground! I should have audio taped them. They were so funny saying "look snow, look snow, there's snow there and there etc." They have seen snow before but this time they were also able to experience a snowstorm and not just seeing it on the ground with the sun shining brightly.  The snow stopped when we got to town but started up again when we were leaving. Needless to say we had a snowball fight at a park. It was a funny change to say the least. We also went to the Science Museum to see the Toyland Exhibit. We all had an enjoyable break resting at home.

        Lately I've been busy doing motherly things, staying away from crowds and out of the sun. I pray that you and your family are healthy and enjoying quality time together.

May God richly bless you and you loved ones. -Kim

Wednesday November 15th

I met my donor, Terry and his wife Robin on Sunday evening!!

It was an evening of emotions and gratitude. Believe it or not we were the first ones there as guests at the dinner!!! I guess I'm on time for the life changing events!! (LOL)

Being early I had plenty of time to be nervous. I spoke with the coordinator of the event, Janet and she introduced us to her staff along with an outline of the evenings events. When it was my turn to speak I was really nervous but I did ok, a little too serious. Then Janet spoke for a little while and then called Terry from the crowd. I wanted  to jump off the stage area and run to him but I couldn't. I patiently waited as he climbed up the stage to me. We hugged and I thanked him and he said "your welcome". We were both in tears along with the rest of our families and probably most of the other dinner guests. Then Terry said a few words to the dinner guests and we went off the stage area so our families could meet. Terry and Robin received hugs and words of appreciation from my family. We enjoyed a BBQ dinner together and talked so much I had to remind myself to eat. Afterwards, Terry and his wife joined us at our house for more conversation. We had a very enjoyable evening getting to know each other. Terry and his wife Robin treated me to breakfast Monday morning and we spoke for another two hours. They are very giving and generous people. I foresee us keeping in touch for a long time. I am very blessed to have had the opportunity to meet Terry and his wife and thank them.

Please consider being a donor if you haven't already signed up! It's a life saving act!!!www.marrow.org

This week has been busy trying to recover from the weekend. Monday, I spent the morning with Terry and Robin and then had to take Meg to the dentist. She's a trooper. She wanted to go back to school after so I let her. Tuesday, I slept in and rested along with some light chores around the house, like fighting with the computer to send out emails. Today, I finally finished up with  painting the back living room. I just have to do the trim around Aaron's bedroom door left.

Health wise, I'm still putting drops in my eyes for dryness and my toes still tingle. The Dr. is reducing the steroids and I'm at 5mg a day now. We added a medicine called Lyrica for the neuropathy in my feet. I really haven't noticed any changes yet. Last visit the Dr. did a bunch of hormone testing because the MRI showed that my pituitary gland was small. I spoke to him today but they didn't have the results yet. I don't go back for another clinic visit until the Monday after Thanksgiving.

Well, I think I filled you in on just about everything I can think of. I hope that you and your families are doing well and healthy. Live each day to the fullest.

God bless - Kim

Saturday November 11th, 2006

Excellent News: I get to meet my bone stem cell donor tomorrow!!! 

We will be guests at a recognition dinner for donors and volunteers where I will get to meet my donor for the first time. I'm nervous and also full of indescribable joyful emotions. The evening is sure to be a memorable one!

A reporter for the Californian in Bakersfield, California contacted me on Thursday. He wrote an article in 2005 about my donor and is eager to do a follow-up article about our meeting this weekend.

Thursday October 12th, 2006

Hi, Everything is going well here. I have a touch of allergies/hay fever that's bothering my nose but other than that I'm doing well. We reduced my steroids again last week. I guess the MRI looked fine. I forgot to ask the Dr. last week. I'll e-mail him tonight and find out.   I've been tired and taking naps a lot but I've been sleeping well at night.

Oh, I almost forgot to tell you!!! I was contacted by my donor and we've been e-mailing. I might be able to meet him in Nov.!!!

 I've been enjoying the time with Aaron and Megan. They had Monday off from school and we took them roller skating. No, I did not skate. I'm not quite up to that kind of physical activity yet. We let the kids try it on their own. They did really well and even wanted to stay the whole time. They fell a lot but they kept on going. Aaron surprised us with his determination. Megan has quite a few bruises on her knees.

All for now. God Bless -Kim 

Wednesday September 13th, 2006

Hi,

 I have some great news for you!!! I had a bone marrow biopsy and the test results indicated that there are "NO SIGNS" of Leukemia!!! PRAISE GOD!!! The results also indicated that engraftment is occurring which means that the transplant process is proceeding as it should. All very good news. I still need prayer for the side effects of the meds I'm on (sleep, muscle cramps, numb feet (neuropathy) etc..) I've been dealing pretty well with everything. I'm going to be having an MRI done on my brain to see if there's one in there!!! LOL. I've been having some odd sensations in the back of my head and I can hear on occasion my blood swishing through my head.  It's kind of weird. I just want some peace of mind that nothing is going on other than higher level thinking skills in my brain. The Dr. has reduced some of my steroids which I appreciate greatly. Hopefully, my face will thin out soon. The redness in my face has diminished. Medically that's about all that's new.

I've been enjoying the afternoons with Aaron and Megan. We've gotten into the school routine. They really like going to school and believe it or not doing homework. It's finally starting to cool off (90') time to get the jackets out --LOL. The kids can now go outside in the evenings and ride their bikes etc.. and I can join them when the sun goes down. I still have to stay out of the sun. Kevin is doing well, he is busy this week with progress reports.

I hope you have a great week and are blessed with many delights from God. -Kim

Wednesday August 9th, 2006

Hi, Things are going well here. It feels weird not getting ready for students this year. Last year I didn't have a chance to think about it as I was preparing for my Bone Stem Cell transplant at Good Sam. Hospital. Wow, what a year !!! On August 13th it will be an official year since day "ZERO". A huge THANK YOU to all of you for your support and prayers. God has blessed me and my family more than words can express.

I went to school on Monday to unpack and clean up a little bit before the new therapist comes in to take over. It was great to be back on campus again. I hope all of the teachers /staff reading this are having a productive week getting ready for another year. I know Kevin's been busy.

The kids and I have been enjoying our last week of vacation. Yesterday, we went school clothes shopping. Today, we might go bowling. Aaron and Megan are ready and anxious to go back to school. We get to meet their teachers on Friday.

Health wise, I've been having some leg and hand cramping still but it has definitely decreased in severity and frequency. My blood pressure is getting better but my pulse rate is still high. I go to the Clinic on Thursday and maybe they'll reduce some more meds for me.

All for now -- look for the little delights that God gives us!! Love, Kim

 

Thursday July 27th, 2006

Hi, I spent a lovely morning at the clinic. I forgot to not take one of my meds so they weren't able to determine one of my med. levels. Oh well. I'll take that pill out next week so that I don't forget. My blood pressure was high so I have to take some more medications once again two more new ones!!! Yippie!!! On a good note, one of them should allow me to start reducing the steriods, which I am thrilled about. I hate the round look of my face and the weight gain from them. I head back to the clinic again next Thursday. All for now, God Bless-Kim

Wednesday July 26th, 2006

Hi, I had a relaxing day today. I slept really well and stayed in late this morning. We had a storm last night that woke me up once but I feel rested today. I went to the clinic on Monday and my blood pressure was high so I have to go back again tomorrow. My face is still a little red but at least is doesn't hurt like a sunburn would. I went out to lunch with Kevin and then did some shopping at the book store. I've been reading a lot more with all this free time.

I went to school to check out the new classroom and rummage through my things that I've left there. I didn't have as much of mess as I thought but I haven't been through all of the boxes yet. I figured I'd go through some things so that It's set up for the other therapist to come in and just get to work with the kids. The kids are excited to be changing schools. I still want to enjoy this rest of the summer and not rush it, less then a month left. They start school on the 14th of August. All for now I'll let you know how things go tomorrow with the blood pressure. Take care and God Bless- Kim

 

Wednesday July 19th, 2006

       Boy the summer is going by quickly. Only a couple of more weeks and then school again. I went to the Dr. and they increased the anti-rejection medication. My face is still really red, it looks like a bad sunburn but it doesn't hurt. My arms have a little marbleized rash to them. I'm feeling good except for some muscle cramps in my legs and hands. The Dr. says it's from the steroids that I have to take. I take another medication and they go away in about five to ten minutes. My feet are still numb feeling from the neuropathy but I've been used to that for a while now. 

Well with all the latest increase in medications, I won't be going back to work in August. I guess God wants me to do other things right now. I was really hoping to go back to work but I don't want to rush it if my body isn't ready yet. Kevin and I decided to transfer Aaron and Megan to their home/ local school that they would go to. It's also the school I worked at. This way they can meet friends in the neighborhood and I don't have to drive so far to get them. This year they will both be on the same schedule 8:00-2:00pm. I'll even be able to walk or ride my bike to get them (once it cools down a bit that is!!)

     I've been staying out of the sun and doing some scrapbooking. I recently purchased the Scrapbook Factory Deluxe 3 computer program to help with scrapping. Kevin's hoping that now I'll start finishing some of my projects in work. I've also started a new bible study at church "Lord, Teach Me to Study the Bible in 28 Days" by Kay Arthur. The first week has gone well. I'm also going to be helping the quilting group at church and start learning to make quilts. I think I can sew in a straight line!! LOL That's the latest here. Take care and God Bless- Kim

Tuesday July 4th 2006

What a hot summer we're having here!!! We've been pretty busy. We had a great week of vacation bible school at our church. I helped out in Megan's class. It was a lot of work but the kids had fun. Megan accepted God into her heart and was baptized. Praise God!!!

The next week,  I woke up with  a fever and sore throat. I visited the Dr. and it turned out that I had strep throat. I took the mediation and the next day I felt 100% better.  Last week we went camping from Sunday to Thursday at Woods Canyon Lake north of Payson.  It was about 30 degrees colder there. It felt great except it rained almost everyday. We went fishing and boating. We inflated our boat and Kevin rowed around with the kids and one day we rented a row boat with a motor and took a spin around the lake. Aaron caught one fish and Kevin caught two. All of the fish went back into the lake. I'm not quite ready to skin a fish. However, I did put the worms on the hook and those guys like to move around a lot.  The kids really enjoyed playing in the woods and feeding the chipmunks.  

Yesterday, I went to the Clinic for my regular appt. and I have Graph vs. Host which is when my body shows signs of rejection of the transplant. I basically have a skin rash. My face looks like I have a sunburn. I have a white spot on the inside of my mouth and my eyes are dry. It doesn't bother me much at all. I put lotion on my face and eye drops in my eyes. The Dr. increased all of my medications and I'm back on steroids. Hopefully this will be a small bump in my road to recovery. I was hoping to go back to work in August. Well that is all for now.  I hope you're having an enjoyable time with your family this summer. Happy fourth of July!! God Bless -Kim

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Kim's Diagnosis

 

In February Kim was diagnosed with Acute Lymphoblastic Leukemia with Philadelphia Chromosome positive. This is considered a "high risk" category Leukemia and Kim had a bone marrow stem cell transplant on August 13th, 2005. She was in the hospital recovering for about a month. She is home and in the recovery stage which could last for months, possibly years.  

 
         

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