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"Each day is a gift." ~ Lisa Hartman

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Chemo – Round #3 & PT

June 30, 2006

After much deliberation, it was decided that I would do 2 more rounds of chemo.  Jacque was here to take me but we went thru 2 days of waiting & waiting to get the call!  The wait was awful.  I went into the hospital on Friday, June 16th.  Since I had no reactions to the other 2 rounds of chemo, the process was done faster & I was only hospitalized for 3 days.  I had visitors from PA on Saturday, some of my Sisters & Sister-in-law came & spent the day.  They were so cute because they hated leaving me there alone.  But I was fine.  This was my 4th hospital stay & the medical staff were awesome & attentive.  Plus, I was coloring my Anatomy Coloring Book for Massage Therapy School.  I was occupied & a coloring fool!  Sunday night Sandy came to pick me up & spent the following 2 weeks with me.  Carting me to/fro from appt to appt, etc … I have had a lot of help & support.  More than I could actually use.  NICE position to be in & I am not complaining.

Went to Physical Therapy two weeks after chemo because my counts were down.  I wore masks & alerted the PT Staff of my comings.  They were very supportive in trying to protect my interests.

Filed Under: My Sarcoma Journey

Gaining Strength in Physical Therapy – June 12, 2006

June 12, 2006

I continue to make strides daily with my Physical Therapy.  Last week I was able to lift my leg/foot off the table (Monday), get rid of the cane (Wednesday) and started walking up the steps as you all do (Friday).  It’s been a long time since I have walked “foot over foot” on the steps.  Today I was given the clearance to SIT BEHIND the wheel of my car … not to drive but to practice moving my foot from the brake to the gas, etc.  I also have to practice pressing & holding the brake.  We are working to strengthen the thigh so it can hold the brake for a period of time.  As you can imagine, I can’t wait to drive again & I am very close!

Filed Under: My Sarcoma Journey

June 8, 2006 – life changing appt

June 10, 2006

I had the normal follow-up testing & then met with Dr. Ettinger.  We were to re-evalutate my situation & plan our next attack.  It was an EMOTIONAL visit for Me & I was alone.

We initially talked about the number of treatments I had & then he said, “the question is do WE continue with chemo or stop?”  I was stunned & asked WHY.  He proceeded to tell me that NORMALLY my type of tumor does not respond well to any type of treatment.  He said for reasons he can not explain medically, my tumor did respond to the treatment.  He then said, “You are a lucky person.”  They did not expect me to survive.  (You could have knocked me over with a feather.)  And because I was given chemo & radiation at the same time, they do not know which treatment affected it more.  So now the question is do we do more chemo?  He doesn’t want to give me more treatment than necessary, nor does he want me to have more issues, say a year from now.  He is really struggling w/what to do & did ask my opinion.  I told him my mind set was to do more chemo & keep going, so I can get this all behind me.  With all I have been thru, I did not want to stop now.

Filed Under: My Sarcoma Journey

Physical Therapy & more

June 5, 2006

I started Physical Therapy 13 days after surgery.  I was so tired by this time & was a little surprised the Dr’s wanted me to JUMP into this so soon.  Sue was with me my first week of PT, driving me back & forth, 3 days that week.  I went to JVS Rehabilitation near my place.  Janice and Catherine were on my case, trying to figure out how I was going to learn to walk again.

Alice, Oneida, Janet S, Janet H, Mom, Helen & Barb all helped in getting me to physical therapy & my follow-up appts at Johns Hopkins.  They did very well for not being CITY DRIVERS.

I was scheduled for a CT Scan, blood work & a followup appt w/Dr. Ettinger  on June 8th.  This appt would turn out to be life changing!

Filed Under: My Sarcoma Journey

Home Again

May 5, 2006

I was home trying to adjust to being immobile.  I was using crutches to get around and Mom & Dan were there to help me.  There were a lot of adjustments to be made as I couldn’t sleep in my own bed.  It was too firm.  I missed the hospital bed.  I was able to sleep on the sleeper sofa because there was SOME GIVE on the air mattress.  Getting around was an adjustment.

I went back to Hopkins to have the drain removed but had to wait 3 weeks to get the stitches out.  Since my leg was radiated, they wanted to be sure it had enough time to heal.  The bad part was some of the stitches got buried because my skin starting to grow over them.  It was rough having them removed.

Filed Under: My Sarcoma Journey

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Latest News

  • Follow-up Test Results – May 2012
  • April 25, 2012 – 6 YEAR Anniversary!
  • Oncology GYN Appt – Dec 2011
  • Team Hartman Raised … Oct 2011
  • Joining the ONE YEAR Club – May 2011
  • April 25, 2011 – 5 YEAR Anniversary!
  • End of Year Reflections … 2010

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