Thursday, July 03, 2008
What to Say?
I was going to tell you this morning how the chemo cycle went this time around for it was tolerable till this morning. Some items included a mild headache Saturday morning where 500 mg. of tylenol just took the edge off. Also the constipation was not a problem till the last days. All in all chemo was tolerable for this cycle... except for todays fatigue. I cannot complain.
The LORD is my light and my salvation- whom shall I fear? The LORD is the stronghold of my life- of whom shall I be afraid? . . . Though an army beseige me, my heart will not fear; though war break out against me, even then will I be confident.
Psalm 27 1, 3
I guess taking the boys to the zoo yesterday did me in. I felt fine thankfully just moved slower than normal. I could tell a difference from previous visits. I haven't been to the zoo in about a year. The boys had fun especially Stuart. I am having problems saving my pics to the computer lately so sorry for you and me alike.
Please pray for Cole as his long time fish, Ron Jon died yesterday in a aquarium filled with a bar soap. It was so cloudy I couldn't see a thing while taking the water out. Cole is devastated. This was his first pet. A curious Stuart was involved is all I can say. ...We plan on having a burial for the fish later. My heart hurts for Cole. Long story here.
Welcome to life in the Snodgrass home
k-
Thursday, June 26, 2008
WNL's
Thanks for checking in...
k-
Monday, June 23, 2008
Hello
Last week was VBS week. What a week! Overseeing crafts for three of the days was a hoot. I felt horrible on Monday and Tuesday with what I like to call the chemo cold. I never have had so many colds as I have had in a years time. I think I am at six since February already! Aghhhhhh. Welcome to a compromised immune system.
I have been struggling with keeping up with house duties(laundry, dishes, etc). It is the multi tasking that is difficult. Dave encourages me to rest during the day. I have more energy in the morning compared to afternoons. If I do not rest I will feel it in the late evening with a ache behind my eyes. It happened last night. I had a great time attending a friends bridal shower minus resting during the day(no time). I also taught the pre K Sunday school class at church in the morning which requires energy that I so want to expend for the kingdom. I love being with the kids. God is good.
This week I have my oncologist appointment on Thursday at 11:15 am. I will also have my bloodwork done prior to the appointment as well. We will have the results at the appointment. I am trying to condense my driving due to gas prices. The less amount spent on the road the better. Chemo (350 mg. Temodar) is slated for Friday evening through Tuesday.
Please pray for Dave and I in regards to contacting others hurting with this disease. We have numerous opportunities unfortunately (for their sake). This is one club that should NOT have lots of members.
Kate
Friday, June 20, 2008
Grace & Love
http://www.youtube.com/watch?v=bE2RXTBV8lM&feature=related
k-
Thursday, June 19, 2008
Disappear
"If you disappear would you be missed?" I was troubled with that quote. Are you or I intentional in our relationships?
Just a thought to ponder...
Sunday, June 15, 2008
Saturday, June 07, 2008
God's Love for you
I remember the long drives of quiet Lord time in the van driving to radiation at Siteman Cancer Center (Washington University). It was a special time of conversation between the God of the universe and ME. Me of all people.
I am considering the following today...What kind of God do we have that would love me so tenderly? And that He would give me the ability to have some sort of relationship with Him? Our God is awesome! Don't you think?
Hope you see His love for you today.
k-
Thursday, June 05, 2008
Celebrating the big 10!




As for the chemo update. Cole likes to call it CHEE mo. I was exhausted. On Sunday morning at church I informed Dave that it felt like I would pass out. That was two nights worth of chemo. Tuesday night was my official last night of taking the pills for the five day round. Some constipation occured that was somewhat remedied. I cannot complain for the Temodar wasn't as horrible this time. Thank you for praying. It was appreciated and noticable.
Off to the pool this morning for some birthday splashes.
k-
Tuesday, June 03, 2008
Emma Grace
As always thanks for checking in.
k-
Friday, May 30, 2008
Good, good, not good
Blood work - good
Start chemo tonight at 350 mg. - not good
Well, that is basically it! Thanks!
Thursday, May 29, 2008
Who am I... I am Yours!
Who am I
by Casting Crowns
http://youtube.com/watch?v=VU_rTX23V7Q
I hope to see you tomorrow after my doctors appointment. Depending on my days events.
Tuesday, May 27, 2008
Appreciate
My labs will be drawn at this time as well. If you remember this past cycle was an increase in my chemo dosage. I did 300 mg for four days then 180mg on the fifth day due to lack of pills in the home. Yes, prescription dilemma. I will most likely take 350mg. (already in the closet waiting) the next cycle (Friday eve) deem the doctors approval of my lab findings. My follow up doctors appointment will be on Friday at 11:30.
O the joys of cancer,
Thanks
k-
Wednesday, May 21, 2008
Coming to a close
This afternoon the second graders are having their poetry reading. Cole is looking forward to us attending. He informed me that there will be a surprise. "Can't really tell you but it has to do about you, Mom and a poem." Hmmmmm. : ) You can be sure the video cam will be running.
Sorry I have been delinquent with my postings. It is the same ole story- my lack of multitasking since surgery. I have been distracted lately. I felt it to be unnecessary to be at the computer with things to be done in the home. Dave has been staying up late and helping with the laundry, dishes, etc. I stayed up late with him last night to help. Also for me,resting is becoming more important. It is noticable by the end of the day if I overdo it I just crash by 8:30 pm with a mild headache and good fatigue. Many thanks to my hubby for picking up the slack.
An update on Joe. I received an email last week from his neice, Kay.
"The recommendation is not to do anything at this point since Uncle Joe is not having much, if any pain. They will do a repeat PET scan in 2 months. He said the radiation onocologist expects the lesion in the lung to "decrease" in the next 2 months instead of increase. I do not know where he is pulling that knowledge from (maybe prayers). The family all seemed to be in agreement with the decision." Joe called me as well with an update. He seemed to be in good spirits. Prayer is powerful and effective.
This is the confidence we have in approaching God: that if we ask anything according to his will, he hears us. And if we know that he hears us—whatever we ask—we know that we have what we asked of him. 1 John 5:14-15
FYI - If you read an obscure comment post Saturday eve into Sunday. It was good ole Spam. It ended up being 21 pages ten point font after being deleted forever.
My next MRI is Wednesday, May 28 at 10:30 in the morning. My follow up doctors appointment is Friday, May 30. I start my five day chemo regimen as well on Friday. Most likely I will do the full 350 mg if my labs looked okay from this past cycle. I am assuming they were fine.
Have a great Memorial weekend holiday.
We are so ready for summer days at the pool.
k-
Sunday, May 11, 2008
A Waiter & Chef on Mother's Day

Cole's Breakfast Menu with its own cover 
It was so cute to see the menus. I had a handsome waiter (Cole) in his robe with his specialty tablet. He was told that he is the cutest waiter I have ever had. One side of the tablet read "Hi Mom" for me to view. He took my breakfast choices. I said pancakes he said plain or chocolate chip. I was surprised by the chocolate chip option for it wasn't on any menu. "Well, chocolate chip then - just a few." He did great in serving me my orange juice in our new ice cream sundae glasses from grandpa's house. He said Opps I made a mistake. It was pretty. Though hard to drink out of in my bed. He was the one who was given the opportunity to display the food on the plate since Carter was the chef. The presentation was magnificent. I think you'll agree. 

ON a side note...
Last night Dave and I were discussing what our needs were for a SAM's run later this week. I mentioned Bisquick. His ears perked up and said "We are out of Bisquick?" Yes was my response. He later stated he needed to make a Schnucks run (grocery store). I asked why and figured it out. He and I both agreed to be pleasantly surprised. I am so glad I knew for I was awake earlier than they were this morning and would have gone downstairs to the kitchen for my eats.




Wednesday, May 07, 2008
Update time
On to blog business:
Last night I completed my fifth night of chemo (Temodar). It was thought that I would do roughly 340 mg. of pills. I ended up taking 300 mg. for four nights and 180 last night due to lack of pills. If you remember we have the Temodar mail ordered. It did not come in time for the last days. I am grateful for the "easing into" the 350 mg. dosage. Since the increase dosage I noticed a good headache one night . 500 mg. of Tylenol helped. I also had mild constipation that was somewhat remedied. My first mouth sore arrived. I was given by Stuart's CBS children's leader a cancer specific mouthwash for patients taking chemo and radiation. I have yet to use it till now. With the mouth theme... After 4 hours or so I would wake with a cotton mouth/ dry mouth. I have also noticed acne on the side of my face not clearing up as quickly as it used to. I guess I need to be thankful that I am even getting acne. There has been some fatigue. It wasn't any more noticeable than previous times. I take naps daily so it was just in the evenings when I totally faltered in my energy. Unfortunately, Stuart is growing out of his naps. This has always been a hard stage for me with the older boys. Quiet time has always been enforced in our home. I just am so tired by the time I lay down my head that the enforcement is lacking. Ho hum. He did take a nap the past two days. A time of Halleliuah. (not sure I spelled that correctly)
One night during this cycle I didn't want to take the pills at 10:30 (the correct time for that night). I fell back asleep till midnight and awoken to the thought "I'd better go in and take the pills so I won't get sick due to the Zofran wearing off". I had to pray for courage at the bathroom sink to take the pills at midnight.
I told the above story to one of my friends at Cole's Monday night ball game. I received a postcard in the mail today. It brought me to tears. She was so sweet to send it to me. Her emphasis were in All caps. Thanks Melissa L. for the encouragement.
I eagerly expect and hope that I will in no way be ashamed,
Phil 1:20
Sunday, May 04, 2008
Friday, May 02, 2008
Joe & my pity party
Anyway we have kept in contact with each other. We spoke to each other at Christmas and he left a message while we were in Florida. I returned his call this past Monday finding out he was going to have a CAT scan on Tuesday. He has had some back pain that felt like "pleurisy". The doctor felt it necessary to have it checked out. Since our time together at Siteman, Joe had a second cancer come to his other ear (L) . It was a different cancer than the right side. He called today at noon to inform me of Tuesdays CAT results. A spot was found on his lung. He is to see a lung doctor next Tuesday , May 6 at 8 am. I tried to be strong for him on the phone yet failed. I cried. I could tell he was trying to be strong as well. He is my friend. I feel so bad for him.
Even with his news he was able to tell me the good parts of his day. First being the sale of his home and driving to the bank to deposit the check. (Big deal as you remember driving was not going to happen post surgery at one point) The third good part of his day was that he getting together with his friends at the local Hardees. We have talked about this often- Funny stories. Lastly was that his nephews were coming for a visit/ meal. He even took the time to ask how I was doing. I told him about the chemo increase.
Here I was having a pity party about my chemo increasing today when he called. Life has been put into perspective. I need to be thankful and look for the blessings for what God has and has not allowed me to go through. Does that make sense? I am not trying to dimish Joe's pain. Here he called to give me the news and also his thankfulness of his day. Whew!
I found comfort in the following scripture today.
You are my hiding place; you will protect me from trouble
and surround me with songs of deliverance.
Psalm 32:7
Please pray for me to trust God's ways and also for Joe's new journey.
kate
Also a good quote:
Don't put tomorrows clouds on todays sunshine.
Increase Dosage
I am fearful with the increase. I dread taking chemo. My heart is not in it. I only take the Temodar because I promised Carter long ago that "I would do whatever it took to combat the cancer if that meant chemo then so be it".
I am scheduled to have another MRI prior to May 30 when I see Dr. Needles again.
Thanks for listening to my concerns.
kate
Tuesday, April 29, 2008
On the Cancer Front...
For now I am going to lay it all out. Please know I am not complaining just listing details.
1. Labs drawn today for Thursday oncology appointment.
2. Doctors appointment is a follow up.
3. Start oral chemo (Temodar) Friday for 5 days on 23 off.
4. Rash on both sides of bellybutton due to chemo build up.
5. Some constipation. Early morning pain on lower left pelvic continues. OBgyn checked it out in February. No worries with ovaries. Must be from chemo induced constipation. Lovely.
6. Occasional forgetfulness due to surgery or chemo. Poor Dave has to do follow up.
7. Hair - What do I say? It's not how I would style it...yet this isn't about what I want. Is it? Ok. My hair is slowly thinning out - might be due to chemo or normal life stuff. It is also growing in slowly where the surgery took place in December. I have a good two inches that loves to stick up straight (spike) if not trained in the morning. Scary!
8. Physically & Emotionally- I am getting better since the trauma of post surgical complications (not much usage of left extremities) Ok NO usage of left extremities including the facial muscles. But, by God's grace I am somewhat back to normal. I was downtrodden for a while. Short story comprehension is difficult. I especially notice it with my Bible study. It is slowly getting better. Speech therapy aided in the comprehension. I currently see a counselor. I think everyone should see counselors. It is a broken sin filled world. I also think about not being here for my family in the years to come. The thought is short lived. Please pray that I do not dwell on the "what ifs".
9. Multi-tasking: is difficult but getting better. Cooking has been minimal. Many thanks to the meals still being provided occasionally. Driving skills have improved but, reversing out of a parking spot requires both sides of the brain. Difficult. Not impossible. I really have to focus. I also have noticed when multiple conversations are occuring while I am speaking to someone, I am overwhelmed. Thankfully Covenant Christian School's Field Day is not my respondsiblility this May. Allthough I did oversee the team shirt design and colors. That was fun and DO able. I missed organizing the event but, it was good for my health not to oversee the planning, games, volunteers, etc. Also good to let some things go. Laurie I am sure did a fantastic job. Can't wait for Friday, May 9. She is a blessing.
Thanks for caring...
kate
Sunday, April 27, 2008
Sand in Suit & Trunks 08'
Carter's adventures
Cole looking for shells
Stuart looking onwardFriday, April 18, 2008
happy birthday dave!
I awoke this morning around the 4:30 hour to the bed shaking. I thought it was one of the boys who were shaking the bed. (They've never have done that before so not sure why I thunked it.) Anyhooo...I immediately palmed Dave and woke him up asking him "What is going on?" Not sure what had happened we went downstairs after the rumbling. I checked on the garage thinking it could have done something weird. Turned on the TV. Nothing. Looked outside the sliding door. Nothing. We assumed it was an earthquake. Dave stated lets go back to bed. Back to bed?! How could I sleep after knowing an earthquake most likely occured?
Later it was told that a 5.2 earthquake did occur in southern Illinois. We felt it. I am sure we weren't the only ones. How about you?
Happy Birthday to my rumblin' kind of guy.
Off to purchase some delightful treats for the evening.
kate
Wednesday, April 16, 2008
Remembering grandpa
Carter and Cole were told of grandpas passing Friday evening. Cole immediately cried to my surprise. Carter didn't outwardly express his feelings till later. This was a reverse of what I told you earlier. We are pleased that they are talking to us about the whole situation. Many questions are being asked. To the best of our ability we have answered them openly. It was hard for me after the memorial getting into the car to find the both of them crying profusely. They held it in during the four hour service without crying in front of others yet let it out in the car. I started to cry thinking of their feelings if I were the one who passed away. It was hard. As for Stuart he stayed at home with some friends of ours it was during his nap time and would prove to be too long of a day. It also would be hard to corral a three year old in a small funeral home room. That would of been on Dave's shoulders since I was saying hello to many people. On that front...Many people came that I hadn't seen since childhood. I knew for when they said "Katie" that was when people knew me from early years. I changed to Kate in junior high. It was good.
Busy in the home preparing for Dave's Friday birthday among other things.
Friday, April 11, 2008
Marion Lee
A memorial/visitation will be held Sunday from 2-5 pm in Washington, Missouri. He had already planned long ago to donate his body to SLU.
We decided to tell the older boys after school about great grandpa so they can process the information over the weekend with us. Please pray they process his death well. Cole internalizes things. Carter wears his emotions on his sleeve. I am concerned about both.
I am just sad. Grandpa was like a father to me. He came home early from work to immobilize my arm after I broke it at his home on Purina Farms. I even cut wood with him in the back woods of the farm. I had a competition with him on who could carry the heaviest log to his truck. I have wonderful childhood memories. I am thankful I had so many years (into adulthood) with my grandparents. It is a blessing.
Today has been a day of rememberance. I look forward to digging into pictures for his Sundday memorial later.
Marion Lee Johnson was a grandpa who loved me. He will be missed.
kate
Tuesday, April 08, 2008
Not Much
My grandpa is not doing well. He was admitted in the hospital yesterday. The cogestive heart failure is taking a toll on his body. Thank you for taking the time to pray.
k-
Friday, April 04, 2008
What is love?
It does not envy, it does not boast, it is not proud.
It is not rude, it is not self-seeking, it is not easily angered,
it keeps no record of wrongs.
Love does not delight in evil but rejoices with the truth.
It always protects, always trusts, always hopes, always perseveres.
1 Corinthians 13: 4-7
The above passage has been in my mind. I have been pondering what it means to truly love. I am not perfect. It is difficult to love like Christ but not impossible.
Today is the first of my chemo regimen. I think it is the 3rd series. My weekend retreat starts today as well.
Pondering this as well. http://youtube.com/watch?v=Oad8ov10AjY
I am lost without Jesus.
Gotta run errands & pack!
k-
Tuesday, April 01, 2008
More Info.
After todays visit with Dr. Needles and the unsettled word on the scan I contacted Dr Forget for his opinion and he was able to explain the inconclusive report.
Dr. Forget said not to worry as with any brain surgery like mine there is raw surface of brain that is exposed after the tumor area was taken out. Ok - the whole frontal anterior portion of my brain is gone! That is alot of exposure. He explained that the raw surface of brain is lined with a material called surgicel, a hemostatic agent (like an interior band-aid for my brain - my wording not his). The unexplained "cyst" is most likely a blood vessel, scar tissue or the surgicel material. While he was reviewing my scan Dr. Backer, a colleague asked him what he was looking at. Dr. Backer said that he thought it looked great. There's no tumor there. Dr. Forget said, "I couldn't be happier with the MRI. Now you have two neurosurgeon opinions."
All is well. To think I actually forgot I had an appointment earlier today. Yes, I actually forgot my follow up was for today. I even called my sister, Jean to confirm she was coming over to watch Stu. She said she didn't forget. Whew!
I will wait to hear from Dr. Needles as to what he wants to do from here. I will continue with my chemo regimen this Friday of 5 days on, 23 off. I have bloodwork on the 21st day of the cycle. Another MRI most likely will occur in about two months.
Looking forward to a womens retreat this weekend,
k-
Mixed Review
We discussed to a degree the results of yesterdays MRI. Dr. Needles wants to speak with Dr. Forget about the report. The wording of the scan report is not what Dr. Needles is comfortable with. It could be surgical healing scar tissue . Overall Dave said to me"not to worry about it as we know surgery is not an option".
I might take the time to write out the actual report later. For now, I am waiting on a call from either Forget or Needles as to where to go next. Another test?
If I could... I would write more. My typing is so slow. That is all I can come up with. I will need to write this down manually and look it over prior to coming to the computer to type. Gotta go and pick up the older boys at school. Carter could have a ball game tonight.
My WBC's count is a little low in but, not too concerning at this time.
I will continue with the 260mg of Temodar this Friday. Five days on 23 off.
Sunday, March 30, 2008
Pics pics & more pics

Saturday, March 29, 2008
A Sickly Pair
My MRI at 11:45 this morning was rescheduled to Monday the 31st at 9:45. Can you imagine being sick in a MRI tube? No thanks. This is the second MRI since the December 12, 2007 surgery. My doctors appointment is on Tuesday.
Carter (Dr. or nurse Carter) did a fine job today in our home taking care of everyone. He even made Stuarts breakfast of wafflesand served me pedialyte. That stuff tastes awful.
Stuart is struggling with diarrhea today. He is more stable, though. Pray that his bowels solidify.
I'd take brain surgery over this stomach bug anyday!
k-
Friday, March 28, 2008
The 4 o'clock Flu
Stuart woke up sometime around 6 AM with odd crying and I swept him into my arms held him close as a three year old does not know how to handle vomit. I could care less about my pajama top. It can be washed. Stuart calls his vomiting "I spit up." We ended up training him on the official throw up bowl that the boys carry around the home when sick and away from a bathroom.
It was one crazy morning, Cole stayed up in his room on the third floor while Stu was down on the second floor couch. I was coaxing Cole to come to the couch so I could be with them both and not run up and down the stairs checking on each of them. He was concerned about walking. I think he wanted to bring his beloved bed belongings to the couch so I asked. He did. His special blanket and pillow went to the couch. All was better so I could be with them on one level.
Cole ended up getting over the buggie by noon. Fluids were staying down. Yet obviously rest was needed. Stuart not so blessed. He was concerning me. Dehydration looked near at the noon hour. Fluids were not staying down. When he awoke from his nap I called the pediatrician. We arrived at the office for a peace of mind. Dr. McKinney is off on Thursdays so Dr. Joe took his patients. We ended up "testing" his vomit. Stuart received in the exam room a trial size Pedialyte and was given a tablespoon of fluid every five minutes on the clock. If he could hold it down in thirty minutes we could go home if not...ER would be in the future. His eyes were sucken and he could of benefitted from an IV yet it wasn't absolutely necessary per Dr. Joe. I agreed as Stuart was being more himself in the exam room.
Don't you know? They almost always perk up by the time you arrive to the pediatrician. I didn't mind for I wasn't looking forward to another ER visit.
In the van returning home, Cole expressed his thankfulness of having beds and couches to rest on. I was thankful that the bug came after 4 in the morning so a good nights sleep wasn't hindered as much. Two o'clock would be a different story.
Today was a good day as we had some sweet time together. The older boys have been bummed that their spring break wasn't all that they had desired. We did not go to Nascar Speedpark like we had planned for Tuesday and cancelled a Thursday playdate with friends we hadn't seen in a while. Tuesday was too cold anyway. Oh well, there are other fun days ahead.
Last night didn't lend itself to a post. Go figure!
Almost forgot... I have a MRI tomorrow (Saturday) at 11:45 in the morning. My follow up oncologist appointment is on Monday, April 1 with labs taken prior to that time.
Just being a mom,
kate
Tuesday, March 25, 2008
What A Day
Topping things off...Dave was in Texas on a business trip. I was in a quandary in trying to find someone ASAP to help with Cole and Stuart. I was being sensitive to the possiblity of Carter having the flu and not wanting to expose another family.
OK back to the ER...
We arrived after a fast lunch for Cole, Stuart and myself. The hospital staff questioned Carter about his pain, ailments, etc. He was complaining about a headache and feeling"woosy". His right arm was hurting as well as his stomach ("6" on the pain scale). He so wanted a drink for he was thirsty, yet afraid to throw up due to hurting.
After many questions I asked if they were thinking appendicitis. They said yes, yet no fever is a good sign among other things. His bloodwork showed elevated WBC's which is normal I assume for a virus. He was given Zofran in the IV for his naseau. I also requested the flu test to be performed. We ended with an x-ray.
We came home by dinner time with an exhausted Carter. He went to bed after a bland meal.
The flu was negative. He just had some bug today. Stomach rating by him a "2" by the time we left. Hopefully no one else will get it.
Kudos to Cole for his help in packing a fun backpack for the hospital. Stuart and him were very well behaved. Even the nurse spoke highly of their behavior. I attribute some of it to Cole along with a TV in the room.
It was my first time at the Missouri Baptist pediatric ER and it was wonderful.
So glad Dave is home.
Monday, March 24, 2008
Hello


set your hearts on things above,
where Christ is seated at the right hand of God.
Set your minds on things above, not on earthly things.
For you died, and your life is now hidden with Christ in God.
When Christ, who is your life, appears, then you also will appear with him in glory.
Colossians 3:1-4
I hope you had a blessed Easter. I had wanted to write but, time again did not permit me to do so. Dave has been somewhat fatigued the past few weekends. Family along with work are wearing him out. He will be travelling out of state sometime this week.
I will try to post some pics from Easter service at church with the boys. The above passage was from our service. It was so compelling. I would not do it justice by giving you the notes. I will have to download the sermon to hear it again.
Carter received for the first time last week some eye glasses. I really wanted to post that. It is odd seeing him with glasses. He loves them and protects them. He is wanting contacts prior to baseball season officially starting as he is a pitcher and the glasses feel odd with a hat(so he says).
Spring break for Carter and Cole started on Good Friday and runs all this week. We are hoping for good weather so we can do some outside activities around town. They really want to do Nascar Speedpark at the Mills Mall which is a good 45 minute drive. They have go-carts inside and out along with some games inside. It is difficult to take a toddler to this as I will need a sitter for Stu.
My mom is currently taking care of my grandpa whose congestive heart failure is taking its toll on his body.
Wednesday, March 12, 2008
Not as planned



Tuesday, March 11, 2008
Happy 8th, Cole
Sunday, March 09, 2008
Expelled Documentary
http://expelledthemovie.com/video.php
Like to know your honest thoughts.
Kate
Saturday, March 08, 2008
Fatigue sets in
With this fatigue today, I relunctantly stepped down from chaperoning Carter's upcomingThursday field trip. I sent an email to his teacher.
Today has been a quiet Saturday at home. Basketball season unfortunately has ended. Baseball has started yet, cancelled today. Not sure why, might have been due to weather. Whatever the case, God knew what kind of morning I was going to have.
Please pray for Dave. Holding up the fort is a big task when I am down.
Thanks for hanging with us on this one.
k-
Tuesday, March 04, 2008
Professional Motherhood
http://www.oneplace.com/Ministries/Focus_on_the_Family/Default.asp
Running errands, matching socks,
Fitting lids on bottled bugs,
Yet when I steal a minute Lord,
That you have blessed me all the while,
As I stop to kiss that precious smile.
Monday, March 03, 2008
Round 1 updated results
I will be starting oral chemo, Temodar, this Friday, March 7 for five consecutive days.
k-
Saturday, March 01, 2008
Short & Sweet
1. Cole was able to see by surprise his long time friend, Drew, Friday after school for a few hours.
2. Outpatient therapy for me should be totally complete with a plethora of HEP's (home exercise program) incorporating the usage of the left side hand/shoulder, feet/leg and involving putty,therabands, and a therasponge, some manual balance, also muscles not knowing I ever had. Please pray for time management.
3. It seems evident after the second surgery my ability to divide my attention/ multi tasking is difficult. I will try to give some specific examples later. Please do not hesitate to remind me in a post comment in a few weeks.
4.This afternoon Carter, Cole and I enjoyed the great spring like temperature outside with a long bike ride. I was thankful due to a longing I had a few weeks ago in taking the boys on a bike ride but knowing I would have been unable with my left sided limitations. It was good to be out enjoying the day after a short nap.
5. Had bloodwork taken this morning. The results to be known on Monday at oncologist, Dr. Needles, appointment. Will start 5 day oral chemo, Temodar on Friday, March 7 if he deems necessary. (depending on the blood counts)
Short and sweet,- hope you are doing well.
k-
Wednesday, February 27, 2008
Fever
I have noticed on the cancer front that during the day I experience a headache behind the eyes. Toward evening, I will take tylenol to combat if it is bad enough. I am also tired. I'm not sleeping thoroughly through the night even with the sleeping pill.- Too much on my mind- (or should I say not much IN my mind?)- sorry bad joke.
k-
Monday, February 25, 2008
Graduating
Insurance pays for X amount of visits per calendar year for each therapy session. We are allowing a buffer of five PT /OT visits to be used for the remainder of the year if needed. I can also go in to workout under their watchful eye for a standard fee.
I had a great conversation this morning with a fellow therapy gym patient, Justin, who has had no usage of his lower extremities since November 07, he also was a patient in the therapy hospital during my stay as well. I never had a chance to have a conversation till now. Just a jealous smile of his wheelchair skills. I told him that today! He was such a fast one down the hall while I was not. Here's Kate just tooDaLing in her wheelchair slowly running into the walls getting her insurance worth. Justin told me today he thought I was a therapist. I just laughed and said thanks for I wasn't. Able to share about my left sided weakness being a zero since surgery. It is good to be in the therapy gym as people are real. Hurting like me.
I see oncologist, Dr. Needles early next week sometime. I had some calendar confusion this Friday. Labs will be closer to the dr.'s appointment. The five days of oral Temodar (chemo) pills will be taken later in the week. I'm not in front of the calendar as I write this so I cannot give you the exact date. The 23 days off went by too quickly.
Thankful for today. It was a good day.
kate with a mild headache, cough & needing some rest
Monday, February 18, 2008
Pondering
I am choosing not to tell you her name for privacy reasons. You can pray - for God knows who she is.
I hate cancer!
k-
Tuesday, February 12, 2008
Update Ta Da
I did have my first round of chemo this past weekend and overall it was not pleasant. I will list some of the unpleasantness below:
1. A good headache on Friday evening.
2. Cramping throughout the five days
3. Rash near bellybutton
More side effects were experienced.
The chemo(Temodar) will be doing it's work the remainder of this month. I am to have labs on Thursday the 28th and see oncologist, Dr. Needles the day after.
Thanks for checking in...kate
Wednesday, February 06, 2008
Therapy Evaluation
Pretend this was written on Monday, February 4 -
Today was my one month (30 days) therapy evaluation.
OT (occupational therapy) and PT (physical therapy) have shown improvements with therapist goals reached. I also have noticed improvements.
My outpatient therepay regimen will change from 3x daily one hour each to 2x daily still at one hour. Speech will continue 2x daily at one hour. The speech therapy is working on cognitive processing. I was thrilled to have the OT & PT change for two specific reasons.
1. Muscle improvement is noticeably significant
2. Snodgrass calendar to be simplified
As for driving, I have the written report but, need an oral "Ok" from my rehab doctor, Dr. Ahmad. I called this afternoon to get the ball rolling in hopes to catch him. I was told the report was put on his desk last Friday and he might get back to me by next Monday. I emphasized the importance of hearing from him to the gal. Life would be much easier if I drove. Please pray that the doctor will call prior to next Monday (He called yesterday & I was cleared!) .
I will be starting chemo (Temodar) this Friday. The top possible side effects are fatigue, naseau,constipation and adverse impact on white & red blood cell counts. Zofran will be taken in advance to combat the naseau. Temodar is specific to brain cancers and normally does not cause hair loss. My chemo schedule is as such 5 days on 23 off. Repeat till Dr. Needles, oncologist deems necessary. Please pray as it looks as if I will be on chemo during Cole's birthday in March and our anniversary in May. I obviously prefer the side effects to be minimal. Obsolete Lord willing.
Thankful I am alive and driving, (I need to write to you about a God print while I was driving the other day!)
kate
Friday, February 01, 2008
A Snowy Beach
A view from Mom & Dad's bedroom
Posing for the camera