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K8 Strong the Journey



This journey I try and capture as much as I can as my wife battles cancer in hopes to help someone else that might be fighting cancer as well will have an idea of what to face which include the good and the bad.

I'm writing this from the ER waiting room at the McLaren hospital in Flint, Michigan but let me explain how we got here.

My wife, Kate (aka K8), has been feeling sluggish (no energy) and she has been loosing lots of weight without even trying.  Lack of wanting to eat which are all signs she needs to see a doctor so she went to her primary care doctor, Dr Winston on Dec 9th which diagnosed Kate as having a cold and she just needs to fight through it with vitamins and rest.

Kate continued to have the same symptoms so in January we went to Urgent Care thinking her doctor just doesn't know since she didn't take any blood or do any testing.  Urgent Care checked Kate over and gave her a vitamin B complex shot which made Kate feel a bit better since she had some energy but that faded after a week and she was back to the way she was previously.

We had a parent from our sons FIRST Robotics team that mentioned she could have Lyme Disease which when looking it up, appeared to possibly be the answer.  We were just in Tennessee and she did lead the way down a trail outside our cabin which had spider webs (could of a wolf spider fell down and bite her giving her this Lyme Disease or a tick?) 

hateBeingSick.jpegKate was having a difficult time standing, having to sit down because she was getting very nauseous and light headed.  Horrible migraines which her Primary Care physician prescribed medicine for that which you supposedly have to take as soon as you feel you have a migraine coming on but it usually made her super sleepy.  Loss of appetite where she didn’t want to eat anything but Tropical Smoothies for some nutrition.  I went to a natural health store and got her some Ginger Shots and some essential oils to help her fight a possible Lyme disease naturally (if it’s even that).  Forced her to take vitamins…. Based on one of my friends (rob) recommendation, I bought some Bovin Colustrum and encouraged her to take that since Indians used it to cure many illnesses and in hopes to beat this as well as several other “remedies” but nothing was helping.

Kate was going to make another appointment with her primary care doctor but her supervisor at work suggested Kate go see her primary care doctor, Bridgett Dyson, since everyone at Kate's place of work could clearly see something was wrong with her health wise.  They described Kate's skin tone as almost a gray color and everyone was concerned, even the stuck up bitches that caused her so much stress.  So Kate figured why not since she wasn't making any headway with her primary care doctor and urgent care.

I told her, if this new doctor says "it’s a cold" we are going to the Emergency Room because I know in my gut it's not a dang cold.

Yesterday Kate went to her appointment with Bridgett Dyson and first site Bridgett had immediate concerns as she confirmed that Kate did not look healthy and immediately ordered three pages worth of blood testing and told Kate if its urgent she will call her that night, otherwise will get with her on Thursday.  

Well guess what, we went to bed around 10:15pm and we got a call which appeared to be spam call (no-caller id) but what spam caller leaves a message?  Kate listened to the message and it was Bridgett saying she is calling right back and please answer.  So Kate answered the second time and Bridgett said, very calmly, that Kate's blood came back with some concerns and that she (the doc) strongly recommends Kate go to the Emergency Room right away (which I overheard since we were both in bed) so before she even got off the phone I’m getting dressed.  I rush her to the ER at McLaren in Flint and of course begin the waiting period which is why I was able to write this.

I'll post more as I get it....


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transfusion2.jpegWe get pulled in the back room they look at what her doctor sent over and they wanted to double check for themselves so they also took her blood.  In a few minutes they came back and said, “How are you walking?”  When her doctor pulled her blood her hemoglobin was at a 5 (normal for women its between 12-15) and her White Blood Cells were at 1 (normal is between 4-11). 

Now in the ER her hemoglobin is down to 4.3 and her white blood cell was down to less than 1.  NOW they are giving her a ton of attention and she immediately gets two bags of O negative blood (since she is O+) at the fastest rate they can perform a blood transfusion which is at 150 in hopes to get her blood levels up. Kate said it felt so cold entering her body and it tasted aluminum in her mouth reminded her of a Pepsi which is disgusting to her.  She asked for the coke version of O- but I guess they didn’t have any.  Did another blood work (checking to see if its raising her counts) and it did slightly but required a total of 5 bags of O-.

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So over the course from Tuesday night when Bridgett took blood (2.4.2020) to Saturday (2.8.2020) noonish my wife had to get bone marrow biopsy so they can determine what blood disease she has.  Initial thought from the hematologist was a-plastic anemia but after the bone marrow biopsy it said it was for sure Leukemia but not sure which kind until results are back from Karmanos Cancer Research in Detroit which we received FINAL confirmation yesterday that it for sure is Acute Lymphocytic Leukemia (ALL) or otherwise known as acute lymphoblastic leukemia which in children under the age of 12 has a good chance for cure and in adults they says there still is a chance to be cured.

What is a Bone Marrow Biopsy?eventguyz_BoneMarrowBiopsy.png

A bone marrow biopsy involves removing a small sample of the bone marrow inside your bones for testing. Bone marrow is a soft tissue in the center of most large bones. It makes most of the body's blood cells. The biopsy is done using a small needle inserted into the bone.


We met with Dr Eilander, Karmanos Flint, on 2.13.2020 and he was fairly confident in the diagnosis and treatment but strongly/highly recommended Dr. Yang located at the Karmanos in Detroit which we have an appointment with him tomorrow (2.14.2020)

I’m sure I’m missing pieces since my head is drowning in knowledge of what this disease is.  I have to apologize that my time is reduced since I am doing everything I can to support my wife while she is going through this without breaking down myself.  It’s insane to think of a time where we were both healthy and just enjoying the day probably stressing about stuff that doesn’t even matter today or involved in drama that goes away.  Everything now seems so minor (except our Health Insurance).

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Acute Lymphoblastic Leukemia (ALL)

What is acute lymphoblastic leukemia?

Acute lymphoblastic leukemia (ALL) is a cancer that affects the white blood cells. These cells fight infection and help protect the body against disease.

Patients with ALL have too many immature white blood cells in their bone marrow. These cells crowd out normal white blood cells. Without enough normal white blood cells, the body has a harder time fighting infections.

ALL affects a type of white blood cell called lymphocytes, causing them to build up in the liver, spleen and lymph nodes.

How common is acute lymphoblastic leukemia?

ALL is the most common type of childhood cancer. It most often occurs in children ages 3 to 5 and affects slightly more boys than girls. ALL is most common in Hispanic children, followed by those of white and African-American descent.

About 3,000 people younger than age 20 are found to have ALL each year in the United States.

Siblings of children with leukemia have a slightly higher risk of developing ALL, but the rate is still quite low: no more than 1 in 500.

What are the symptoms of acute lymphoblastic leukemia?

Symptoms of ALL include:

  • Frequent infections
  • Fever
  • Easy bruising
  • Bleeding that is hard to stop
  • Flat, dark-red skin spots (petechiae) due to bleeding under the skin
  • Pain in the bones or joints
  • Lumps in the neck, underarm, stomach or groin
  • Pain or fullness below the ribs
  • Weakness, fatigue
  • Paleness
  • Loss of appetite
  • Shortness of breath

How is acute lymphoblastic leukemia treated?

Expect your child’s ALL treatment to include three phases:

  • Induction — to kill the leukemia cells in the blood and bone marrow and put the disease into remission (a return to normal blood cell counts)
  • Consolidation/intensification — to rid the body of any remaining cells that could begin to grow and cause the leukemia to return (relapse)
  • Maintenance — to destroy any cancer cells that might have survived the first two phases

Four types of treatment may be used during any of these treatment phases:

  • Chemotherapy (“chemo”) — uses powerful medicines to kill cancer cells or stop them from growing (dividing) and making more cancer cells.
    • Chemo may be injected into the bloodstream, so that it can travel throughout the body.
    • Some chemo may be given by mouth.
    • Combination therapy uses more than one type of chemo at a time.
  • Stem cell transplant — includes replacing blood-forming cells in the bone marrow that have been killed by chemo and/or radiation therapy:
    • A stem cell transplant gives the patient new blood cells from a donor’s blood or bone marrow. These cells grow into healthy blood cells to replace the ones the patient lost.
    • Some types of stem cell transplants may be called “bone marrow transplants” because the cells come from the donor’s bone marrow.
  • Radiation therapy — uses high-energy X-rays or other types of radiation to kill cancer cells or stop them from growing.
  • Targeted therapy — uses medicines or other treatments that target and attack specific cancer cells without harming normal cells.

What are the survival rates for ALL?

The National Cancer Institute (NCI) estimates 5,960 people will receive a diagnosis of ALL in the United States in 2018. About 1,470 people will die from the disease in 2018.

Several factors can determine survival rates, such as age at diagnosis and subtype of ALL.

The five-year survival rate in the United States is 68.1 percent, reports the NCI. However, these numbers are steadily improving. From 1975 to 1976, the five-year survival rate for all ages was under 40 percent.

Although most people who receive a diagnosis of ALL are children, the highest percentage of Americans with ALL who pass away are between the ages of 65 and 74.

In general, about 40 percent of adults with ALL are considered cured at some point during their treatment, estimates American Cancer Society. However, these cure rates depend on a variety of factors, such as the subtype of ALL and age at diagnosis.

A person is “cured” of ALL if they’re in complete remission for five years or more. But because there’s a chance of the cancer coming back, doctors can’t say with 100 percent certainty that a person is cured. The most they can say is whether or not there are signs of cancer at the time.

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Karmanos DETROIT Visit 1

About to go to bed but figured I'd post a quick update about our first visit to Karmanos in Detroit and our visit with Dr. Yang (2.14.2020).  We were given Valet so getting in wasn’t too bad and traffic down from Davison was quick.  Front staff that checked us in was very professional and then a guide brought us to the room on the second floor where we had a pretty brief wait before being called back.

Dr. Yang is another great doctor that is very knowledgeable. Leukemia is his specialty and he is very informed on Kate’s condition.  He mentioned it’s typically found in kids (under the age of 12) with around an 80% success rate of fully cured within three years. If she was 70 years old she would have a 10% chance of survival with treatment.  Dr. Yang said she might be somewhere in the middle being 34 years old but he wants to treat Kate as a child which means it’s more aggressive chemo.

So estimated treatment is:

  • 1-3 months of very aggressive chemo treatment
  • First 4 weeks is induction
  • Then 6-7 months aggressive chemo
  • Maintenance

Kate will have 20 spinal taps over the course of three years to make sure the leukemia hasn’t entered her spinal cord since it wants to get to her brain which would be not a good thing.

Unfortunately she will have to have multiple bone marrow biopsies to monitor the progress chemo is having on the cancer located in the bone marrow.

During this process she will have routine blood transfusions to get her blood numbers up since chemo will bring them down.  Eventually after chemo kills the cancer cells, her bone marrow will hopefully start producing good cells.

How the doctor explained it is the good cells are getting pushed out or over run by all the leukemia cells.  So chemo will hopefully kill this leukemia cells.

Monday Kate’s hemoglobin was 8.8 and then Thursday (yesterday) it was 8.7 and when measured today it was down to 8.3

Apparently when your hemoglobin drops to low you run the risk of bleeding and not able to stop the bleeding. They told us if Kate begins to bleed and we can’t get it to stop within an hour that I should drive her to the ER at Harper Hutzel which is attached to Karmanos and they will admit her then. Scary stuff.

Ran into a little worry.  Tonight (9:25pm) Kate began to have a nose bleed (her first ever).  It luckily stopped within the first 10minutes because if it didn't stop in an hour we would of been heading back down to Karmanos via the Harper-Hutzel Emergency Room.

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Abby Angel Gift

Came home from a tough appointment today to find a care package waiting for Kate. 

one of the sweetest women at Mclaren health plan is always looking out for how she can encourage and help others. One of those ways is through her “Abby Angel’s”. She lost someone and decided years ago to light the path for others struggling by giving these angels when they are needed. It is an honor to be gifted one by Lana because it means that she is now a warrior for your battle. 

We came home today to a package of an Abby Angel from Lana’s personal collection to watch over and protect while we fight this battle. Words cannot express the thoughtfulness and encouragement that this angel and sweet Lana has instantly brought to our home. 

Thank you all for being part of our warrior tribe. With this much determination, there is no way we won’t succeed in our battle.

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Home Care Nurse Visit

Last night Kate called the Support line for the Homecare nurse complaining on how much the bandage hurts after they redid it during our Hospital visit yesterday (Friday).  Kate was complaining of a burning sensation and very uncomfortable.  A homecare nurse showed up and was very polite and helped explain how to clean the pic line with basically salt water and yea, I got my intro on how to do this myself for Kate.  She re-bandaged it up and Kate kept thanking the nurse because it was like night and day difference.  She is no longer after the polite home care nurse re-bandaged Kates pic-line.

Now if I could only get Kate to relax...  I'm trying to restrict her some so she doesn't get her blood flowing.  In my mind, more blood flow means the quicker the cancer can spread since it is a cancer of the blood.  Of course thats my logic and I really don't want to loose my wife.eventguyz_PICC_line.png

What is a PICC Line?  Below is a pretty good illustration but its basically a quick way for doctors to pull blood from within having to re-stab kate with a needle every-time.  It's also a place for the doctor to administer the chemo treatments.  She has to keep moving that right arm so it doesn't get buildup on the line as well as get clogs..  we don't want to get clogs in the line which is why I get the pleasure of flushing the line out daily.

I am glad she is more comfortable now. Kareta had hers in her chest & that seemed constantly uncomfortable. So glad she doesn't have it in her chest. 
So much love & many prayers being sent!

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Fevers are no good

Tonight Kate developed a fever (running 100.5) and whats scary is they say if you have Leukemia and get a fever you must go to the nearest Emergency Room since its more than likely an infection which can prove to be fatal.  So right now we are calling 1-800-Karmanos to find out what they want us to do.

Patients with acute lymphoblastic leukemia (ALL) present with either symptoms relating to direct infiltration of the marrow or other organs by leukemic cells, or symptoms relating to the decreased production of normal marrow elements.

Fever is one of the most common symptoms of ALL, and patients with ALL often have fever without any other evidence of infection. However, in these patients, one must assume that all fevers are from infections until proved otherwise, because a failure to treat infections promptly and aggressively can be fatal. Infections are still the most common cause of death in patients undergoing treatment for ALL.

The doc called Kate and said she needs to immediately get down the the hospital because it means it could be infection.

Loading up the car and heading down as fast as we can since the doctor expressed urgency.


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Arrived at Harper-Hutzel Hospital (it's attached to Karmanos and they address after hours concerns with Karmanos patients)

Just saw Dr.Woolman. Man he was a talker. Not giving Kate a chance to answer any questions.

They asked these questions:

  • when admitted to Mclaren (flint): Tuesday the 4th.
  • When bone marrow biopsy: 2/6/20
  • when was picc line installed: 2/6/20
  • last transfusion: 2/7/20
  • did they give you any medicine: dexatron (2/7/20-2/10/20) 40mg a day for the 4 days.
  • When did you learn for sure Kate has ALL: bone marrow biopsy confirmed Kate has ALL on 2/10/20
  • allergic to anything: no
  • taking any medicine: allopurinol (300mg) because music acid high, norco 7.5mg for discomfort for bone marrow biopsy but hasn’t taken any
  • anything doctor should know?
  • we noticed bleeding from picc Line.
  • mentioned she had a bloody nose

NOTE: We are going to avoid Harper Hutzel Hospital as much as humanly possible....  horrible!


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11:00pm they brought her down for x-ray

Gave Kate tordol at this time for her headaches.

when we came in they gave her via an IV (not using PICC line) cefepime 2gm which is an antibiotic.

we are watching 2.5 men (the era that Charlie sheen still existed)

just had a visit from the Karmanos doctor on duty which did a quick evaluation of Kate. Going to transfer Kate up to a room in Karmanos, just waiting.

So Karmanos doctor on duty came in and did some more checking while we wait for a room. She mentioned Kate’s hemoglobin is down to 7.2 and her white blood cell count is at 1.7, so now we wait for her room 

Got our room (9203) in Karmanos on the 9th floor but was told they may move her to 8th floor.. but not sure when. I'm thinking Kate would really just like to sleep. FYI: room is HUGE.


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What is a Lumbar Puncture - Spinal Tap


During the time you are fighting cancer (especially A.L.L.) you will have to received several Lumbar Punctures or also referred to as Spinal Taps.  So what are they?

Lumbar puncture, also known as a spinal tap, is a medical procedure in which a needle is inserted into the spinal canal, most commonly to collect cerebrospinal fluid for diagnostic testing. The main reason for a lumbar puncture is to help diagnose diseases of the central nervous system, including the brain and spine.

A lumbar puncture (spinal tap) is performed in your lower back, in the lumbar region. During a lumbar puncture, a needle is inserted between two lumbar bones (vertebrae) to remove a sample of cerebrospinal fluid. This is the fluid that surrounds your brain and spinal cord to protect them from injury.

A lumbar puncture can help diagnose serious infections. Sometimes doctors use lumbar punctures to inject anesthetic medications or chemotherapy drugs into the cerebrospinal fluid.


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Induction Phase

It’s 3am on 2/17/2020 and we are in a room on the 9th floor in Karmanos Cancer Facility in Detroit.

This is the beginning of the Induction process which in short means the beginning of chemo treatments while keeping a close eye on Kate during the process.  The doctor believes this will take less than a week this visit but the Induction process is typically a week.

There are four phases to chemotherapy treatment:

  1. The first phase is called Remission Induction. Treatment during this phase is designed to kill the leukemic cells in the blood and the bone marrow, putting the disease into remission.
  2. The second phase is Central Nervous System Directed Therapy. This phase kills cancer cells in the central nervous system and prevents the disease from spreading to the spinal fluid.
  3. The Consolidation/Intensification phase is given after the disease is considered to be in remission. It's designed to kill remaining leukemic cells that may be inactive but could begin growing again and cause the leukemia to recur. This phase usually lasts several months.
  4. The maintenance phase is the final phase of treatment that lasts for two to three years. It's used to kill any remaining cells that could cause a recurrence. Medications are often given at lower doses.

So her hemoglobin dropped to 6.1 overnight (in less than 12 hours) so they are getting everything together for another blood transfusion (#6).  Today she'll also get spinal tap which will inject some Chemo into her spinal cord while they take a sample to test to see if the Leukemia has made its way into the spinal cord..  we are hoping it hasn't.

Dr.Yang is a superstar of a Doctor but seriously all of the doctors that we have encountered have been awesome.  Our least favorite area was the Harper Hutzel ER room (happy to be out of there).

They may take another bone marrow biopsy if Dr.Yang doesn't get back the results from the company they sent the bone marrow biopsy they took in Flint McLaren Hospital.  Dr.Yang doesn't want to delay treatment anymore so another bone marrow biopsy is a possibility and he can get the results next day to find out if she is Philadelphia chromosome positive or negative which dictates what ingredients need to be in the chemo treatment.

Starting Blood Transfusion now... need to get Kate’s blood count up. Only numbers they are really focusing on is hemoglobin (They want above 7 and its 6) and platelets (they want in the 50’s and it’s in 30’s).

Finished transfusion just now and they are now moving into doing a bone marrow biopsy on left side since it was done on the right side.

also adding some platelets

Good news is they didn’t do a bone marrow biopsy but instead they did something where they just extracted some marrow which I think they called aspired.  So Kate earns her hashtag again #k8strong

they mentioned MRD testing, need to look that up.

next they are adding platelets and will do the spinal tap adding chemo in the spinal fluid at the same time taking some fluid for testing

Kate just left to IVR (radiation) for spinal punch. The procedure is roughly 20-40minutes and then there is recovery. They do sedate Kate which she is looking forward to so maybe she could get some sleep.

dr.yang got some news from the bone marrow biopsy and they said Kate is Philadelphia chromosome negative but he wants to double-check since treatment is very important to know for sure. So the test he did earlier will give him those results in 24 hours.  He did say they are trying to get us a room on the 8th floor which is reserved for chemo patients. They do not want to start chemo until Kate gets on the 8th floor since the nurses here on the 9th floor don’t work with chemo.

now we wait for procedure.

Just spoke to Dr.Yang as he made a visit on his way out for the day.

he recommends Kate lay as flat as she can when she gets back to the room for 2 hours preferable but 1 hour minimum.

he said there is no reason why they can not start chemotherapy tomorrow which will consist of two drugs for chemo and she will have to take one pill (steroid) orally. The steroid she will take daily and the two chemo injections she will do once a week. More than likely she will need another transfusion but the current tentative goal is go home Friday and come back Monday. Repeat process for a total of four weeks which would conclude the Induction process at which time they want to get more blood marrow to see if the cancer cells are declining.

Kate got some food in her and now she’s fighting through some pain (with the assist of some pain killers) and maybe one more dose of pain killers before she tries to get some sleep.

im hoping to sleep on a cot or anything besides these chairs which are not comfortable.

i really need to thank our friends And family for helping take care of our dogs while we are gone. It’s a huge stress for Kate and I being so far away but everyone seems to be helping relieve the stress and I seriously can’t thank u enough.

it appear the remaining of our night will be hopefully uneventful so don’t be surprised if you don’t see anymore posts tonight (unless something negative happens).

we just got moved down to the chemotherapy floor (8) so now we are in room 8223

her hemoglobin is down to 7 so they are going to give her a blood transfusion.

Kate got some sleep and woke up on her own at 4am because she had to pee. The nurses then did bloodwork to see if her hemoglobin is back up from 7.4 now that she had a unit of blood last night. white blood cells 1.3 (normal is 4-11) and platelets 35 (normal is 55+).

Kate's fed, she took a tylenol 3 for pain (pill), allopurinol (pill), antiviral (pill), anti-bacterial (pill) and an anti fungal (oral liquid) medicine.  Now we wait for Dr. Yang to give us the game plan for today.


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Internal Medicine (3 doctors) just came in and checked to see how Kate is doing and feeling.  Sounds like Chemotherapy is still on the docket for today but we are awaiting Dr.Yang.  They checked on how Kate is doing with all the procedures she had done yesterday.  She is super sleepy and is passed out now but I think its a good thing.  I see its lunch time and I may sneak downstairs and get something to munch on.  I love chips but because of all the stroke victims in the hospital I lean away from them since its one of the major causes of a stroke.   Actually I have been trying to eat healthy so I can keep taking care of Kate but I may break down and get something non-healthy (meaning something with some flavor) today for lunch like a burger from Wendys.

Dr.yang came in at the this time and gave us more information.  Results of lumbar punture (spinal tap) proved positive results (no cancer in spinal fluid).  He also spoke about treatment which includes:

the following once a week (every Monday as out patient):

daunorubicin (side effect: nausea, hair loss) - Syringe

vincristine (side effect: tingling in hands) - IV bag

*constipation is a worry with treatments so much the nurse and doctors ask every time they come in

the following every day for 28 days:

steroid: prednisone

may add another drug week 2 and another drug that is used on children week 3 (rituxan) which focuses on A.L.L.

he mentioned things to pay attention to while she’s home which is mainly infection (fever of 100.4 that lasts more than 30minutes she must come to ER).

mentioned chemo will reduce platelets which are optimum at 50k but at 30k now and we may notice bleeding when below 10k.


after Induction period (first 4 weeks) the chemotherapy gets kicked up a notch and is unpleasant and this will happen for 6 months and sounds like multiple visits per week.


Kates first chemotherapy treatment is coming soon (sometime this afternoon)

They gave Zofran (for nausea) and Prednisone (the steroid) today at 14:30

at this time (15:12) kate received the daunorubicin via syringe. Nurse mentioned it is important for oral hygiene since it could create sores in your mouth. Also it will more than likely create red urine.  They are also giving the vincristine via IV.

COMPLETED adding the daunorubicin and vincristine at 15:30

Kate is doing good.  She's groggy but doing okay.  Just brought her an ICEE (coke.. uh oh), grilled chicken bits from chik-fil-a and watching TV.

Shes not a fan of how she feels because its different than anything else she felt.  She is homesick... missing her puppies.  I'm saying she's emotional which the doc said a side effect of the medicine.

They just put a bag of cefepime and a couple blue pills which we believe is antibiotics (fungal, bacterial, )

Bloodwork at 3am and then more antibiotics at 4:30am

unfortunately Kate didn’t get much sleep (which is another side effect of chemo). She’s also nauseous and did have tingling in her feet but she was able to work out the tingling.

visit from internal medicine at 7:30am to check on her status.

LABs moved up to twice a day because of Chemo they need to keep monitoring blood counts.

As of now, morning labs came back with hemoglobin 7+ & platelets 33 so no blood transfusion at the moment.  We'll have another bloodwork around 5pm tonight and we'll see what her numbers are then.

We are still on track for going home Friday and we are both hoping that stays true since she is going stir crazy being cooped up in the hospital.

I may leave today to go get a shower and change of clothes since we are here until Friday.  I feel disgusting so need a refresher.  Hoping they validate the parking since we have been there since Sunday.

Nurses helped kate change into a new gown and I got her a breakfast bagel.  They flushed the PICC line to help the machine stop beeping because of blockage.  They also recommended her getting up and walking the floor.

Bandage for PICC line will be changed before we go home which will be nice even though we are only home for Saturday and Sunday and back on Monday for an all day treatment but its suppose to be outpatient so we'll be able to go back home.

She is getting Zofran for nauseous at 9am

Kate got another dose of antibiotics and her daily steroid at 10:15am

antifungal: diflucan

antibacterial: bactrin

antiviral: aciclovir

steroid: prednisone which she'll get every day during the induction phase (roughly 28 days)

And still getting the IV drip of cefepime (2gm/100mL) which is also used to treat bacterial infections.

Kate got about 3 hours sleep last night.  They said the chemo chemicals would cause sleeplessness. Kate is getting headaches but they give her a Tylenol 3 before going to sleep and it helps relieve the pain and allow her to sleep.

They took blood at 5am and Hemoglobin dropped to 7.1 and Platelets dropped to 24k.

She is also still getting some nausea but the Zofran does help relieve it.

So today we walked around the floor with her pet IV stand closely in hand. She decided to wear a gown with an exposed back which proudly displays the lovely bruises from the bone marrow biopsy and lumbar puncture.  We did two Different walks which all together equals about 1/2 mile walked today.

they dropped her bloodwork to once a day instead of the typical twice a day.

No bowl movement since Tuesday so they gave her some Colace.

she should get bloodwork at either 3am or 5am, then blood transfusion. Odd but her hemoglobin has to be less than 7 for her to get a blood transfusion and it was at 7.1 this morning so we all know it will be low 6 probably tomorrow morning which will prompt the blood transfusion allowing Kate and I to go home for the weekend.


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