All of Chad’s updates are here — all in one convenient little place in reverse chronological order.


March 20, 2009:
Dr. Stephen Tatter successfully removed the majority of Chad’s primary tumor. Radiation to follow in about a month.

February 24, 2009:
Consultation with Doctors Shaw & Tatter at WFUBMC. We learn that the smaller tumor is nearly gone, and surgery is now an option! Details to come as they are available.
February 11, 2009:
Dr. Campbell called with results; tumors still stable but there are a few areas of concern. We are being referred to Wake Forest University Baptist Hospital for a second opinion.
February 10, 2009:
Met with Dr. Campbell to discuss MRI results, but she had not yet received them. Blood work within normal range.
February 4, 2009:
16 month post-op MRI.

December 5, 2008: Results of biopsy showed no malignant cells.
December 1, 2008:
Fine needle aspiration of thyroid.

November 25, 2008: Chad had an ultrasound of the thyroid mass. Dr. Meehan (primary doctor) recommends a needle biopsy.
November 13, 2008:
CT Scan results don’t show blood clots, but does show a 9mm mass on his thyroid.
November 11, 2008:
Chad had a chest CT scan to rule out blood clots from the chest pain he had with the last two rounds of chemo.
November 10, 2008:
MRI shows tumors are still stable. Dr. Campbell & Chad decided to take a Chemo Holiday for 3 months and then reevaluate after a 3-month MRI. Also met with PA Kovacks – neuro eval still normal. We took our hot air balloon ride today – it was beautiful, but the combination of heat (from the burner), heights, and sudden movement left Chad feelings a little anxious.
November 3, 2008:
12 month post-op MRI.

October 17 – 21, 2008: Round 10 of Temodar. The toxicity seems to have built up over the course of treatment. Chad was too nauseous to take the final dose of this round. He again experienced severe chest pain.

September 19 – 23, 2008: Round 9 of Temodar. Chad experienced severe chest pains he felt were similar to Pulmonary Emboli. They resolved themselves quickly.
September 17, 2008:
Attempted another EEG to invoke a seizure. Didn’t work.
September 9, 2008:
Neuro eval with Dr. Glenn was normal. Suggested another EEG.

August 23 – 27, 2008: Round 8 of Temodar.
August 11, 2008:
MRI reports no change. Chad & Dr. Campbell decide to stay on Temodar. We’ve found research that notes the median range for response is 12 months.
August 4, 2008:
9 month post-op MRI.

July 21 – 25, 2008: Round 7 of Temodar. The effects seem to be lingering longer, as Chad didn’t feel well enough to return to work until July 30.

June 23 – 27, 2008: Round 6 of Temodar.

May 26 – 30, 2008: Round 5 of Temodar.
May 19, 2008:
MRI showed no change. Continue Temodar.
May 14, 2008:
Six month post-op MRI.

April 29 – May 3, 2008: Round 4 of Temodar.
March 31 – April 4, 2008: Round 3 of Temodar.
March 18, 2008: Chad was granted permission to drive by Kitty Kovacks, PA to Dr Glenn.
March 3 – 7, 2008: Round 2 of Temodar. Chad discovered that taking Kytril is necessary for combating nausea.

February 8, 2008: Ended Round 1 of Temodar. No major complaints, and he handled it fairly well.
February 4, 2008: Met with Dr. Campbell to discuss our different options and opinions from different doctors. Chad decided to start with Temodar, and a chemo cycle that will last for 5 days out of every 28. Chad started Temodar that night.

January 31, 2008: Had EEG at Raleigh Neurology. They were unable to induce a seizure to locate the propagation site.
January 29, 2008: Finally hear from Duke, Steve Silverman. They suggest forgoing treatment for now, and monitor with MRIs every 3 months. We don’t feel comfortable with that.
January 24, 2008: Met with neurologist, Dr. Glenn. She recommended an EEG for a baseline.
January 15, 2008: Another Keppra increase due to increased anxiety levels. We are also referred to a neurologist from Dr. Koelevled since Chad is having a few symptoms.
January 14, 2008: Wake Forest consult with Dr. Lesser & Dr. Tatter. They recommend standard chemo & radiation.
January 9, 2008: Wake Forest consult with Dr. Shaw. He told us the tumor had been there approximately ten years.
January 2, 2008: 2-month follow-up MRI at WakeMed.

December 28, 2007: Chad was taken to the ER again due to a large seizure. Dr. Koeleveld recommended going in because he obviously needed a medication change.
December 27, 2007: Talked to Dr. Henry Friedman from Duke. He wants all of Chad’s medical records & biopsy sample for analysis.
December 21, 2007:
Met with Dr. Campbell again, to discuss most recent pathology report from Dr. Berger at Johns Hopkins University. His expert opinion is a clearly defined Grade II Oligodendroglioma. We’re very skeptical about this – there is a vary vast difference between High Grade Mixed Glioma & a Grade II Oligo. (We continue to question this – and have been told that it’s subjective to the pathologist’s perception of cells. Frustrating!)
December 13, 2007: Consultation with Dr. Reilly (radiology oncologist) at Cancer Centers of NC. He agreed to getting more opinions and set up appointments for us with Wake Forest to explore other treatment options.
December 7, 2007: First consult with Dr. Campbell (oncologist) at Cancer Centers of NC. Discussed chemotherapy options, and recommended starting aggressively and immediately.
December 3, 2007: Chad started working from home 20 hours per week.

November 29, 2007: Released from hospital. Continued Lovenox injections at home.
November 27, 2007: Went to Urgent Care for back/chest pain. After an x-ray and exam, we were told to go to the ER. Turns out, Chad had several Pumonary Emboli. He was again admitted to the hospital and put on blood thinners.
November 26, 2007:
Staples removed (26 in all) at Dr. Koeleveld’s office. We mention the back spasms again, and are told that it’s probably anxiety.
November 22, 2007: Thanksgiving. Rash & chest pain develop (believed to be back spasms from lack of activity). Allergic reaction to Dilantin, put on Keppra for seizure control.
Novmber 21, 2007: Released from the hospital with the diagnosis of Grade 3 Mixed Glioma. It was the day beofre Thanksgiving.
November 17, 2007: Craniotomy performed to debulk tumor and get a sample for biopsy. Dr. Koeleveld could not remove any of the tumor. Preliminary histology graded the tumor at a mid-to-high grade mixed glioma.
November 12, 2007: Chad was rushed to the ER after a series of seizures. A few were tonic-clonic (losing consciousness). A CT scan showed a large mass in left frontal lobe of his brain, and a follow-up CT showed a smaller mass in the temporal lobe.

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12 Responses to “Chad”


  1. 1 aunt Donna February 16, 2009 at 4:33 pm

    Chad

    Keep danceing!

  2. 2 Chad February 17, 2009 at 1:09 pm

    Thanks for giving me my own page. I feel special. Matter of fact, I am very special according to my doctors!

    Donna, I will keep dancing but I think I will switch to slow dancing.

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    Chad,

    Your too young just to slow dance. We enjoyed your dancing and singing. Slipknot rules!!!!

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Look what you missed….

Coming up

April 3: Happy Birthday to Chad!
April 7: Cailyn's 37th dentist trip
April 8: Happy Birthday to Faith!
April 12: Happy Birthday to Landon!
April 23: Carys' field trip
April 30: Chad's 1-mo post-op eval

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