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Week 22




Here we are on Week 22 of Kate's fight against Blood Cancer.  Here are all the updates related to whats going on this week.



Bloodwork Results

  • Potassium: 
  • Bilirubin(Liver Function)
  • White Blood Cells (WBC 4.0-10.0): .
  • Hemoglobin (HGB 11.5-16.0): 
  • Platelets (PLT 150-500): 


  • Blood: YES/NO
  • Platelets: YES/NO


  • Lumbar Puncture: YES/NO
  • BoneMarrow Biopsy: YES/NO


  • Methotrexate via IV drip (avg __min infusion): YES/NO
  • Vincristine via IV drip (avg 5min infusion): YES/NO
  • Pegasparagus via drip (avg infusion): YES/NO
  • Cyclosphomine: YES/NO
  • Cytarabine: YES/NO
  • Rituxan via IV drip (avg 4hour infusion): YES/NO
  • Daunorubicin via Syring (avg 5min infusion): YES/NO <--causes hair loss


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Yesterday we found out that short term disability runs out at the end of August and we'll need to pay COBRA to continue the insurance to continue treatments.  It will cost us $1280/month until Kate is able to go back to work.  Not sure how but one way or another we must come up with that.

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On the way home (about 10minutes away from the hospital) Kate got another fever. 

This is the third week in a row.  We were thinking it was a negative side effect to Chi Tea since she had a chi-tea from BigBe on the way down to the hospital (which she loves) but since she got a fever both times we said this week nothing from Bigbe but she still got the fever.

So now we are thinking it has to be one of a few things. 

First it could be the lynacane she rubs on her port to numb the area 1 hours prior to arrival.

Second it could be the heparin they flush kates port with at the end of each blood draw.

Again, the last three weeks all Kate has had done at the hospital is bloodwork (so checking her blood counts) to see if her numbers come up high enough so they can continue chemo treatments which they haven't been able to.

Obviously it can be something more but thats all we have to go on at this time.

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