Cancer Stinks!

On October 5, 2011, I went into the McKay Dee surgical center in Ogden to have my tonsils removed. Instead, the doctors found a cancerous tumor growing behind my tonsils. It's called "Nasopharyngeal Rhabdomyosarcoma" and I'm told it's curable about 80% of the time for someone like me. It's going to be a long road, but I think it's going to be 100%.

Wednesday, October 19, 2011

Jeremy's treatment plan


Many have asked what Jeremy's treatment plan is so here it is for those who are interested.

Chemo is a 3 week cycle.  Jeremy's chemo day is Tuesday. He will receive chemo for 42 weeks.

The first week he receives three chemo medications and we call it the VAC (Vincristine, Actinomycin-D, Cyclophosphamide) week.  All chemo meds are given through an IV.  Jeremy has a "port" that was surgically placed on his chest for easy access for IV, medications, and blood draws. On VAC weeks Jeremy is hospitalized for 24 hours at Primary Children's Hospital.  This week is sever nausea (there is medication to help with this, and it did help Jeremy), loss of appetite and tired.

The second week Jeremy receives one chemo med.(Vincristine)  This is done at the Oncology Clinic at Primary's and is out patient.  The second week his ANC (blood test that shows Jeremy's ability to fight infection) count will be the lowest and he will be extremely tired.  His ANC count was 400 yesterday.  On chemo 500 is best.  A normal ANC count is about 3,000-5,000.  This is why it is so very important that we protect Jeremy from germs and avoid contact with individuals who are sick.

The third week Jeremy receives Vincristine, out patient.  This week his body has had a chance to produce more white blood cells and his ANC count will go up a little.  He will also start to feel less tired.  Just when he starts to feel a little better, it will be time to start the cycle again with the VAC meds.

Radiation will start sometime in November.  We will make the daily drive to the Huntsman Center for radiation Mon-Fri for six weeks.  Jeremy will continue his chemo while on radiation.

1 comment:

  1. Wow Russels! We are praying for you. Every meal and family prayers my kids make sure to include Jeremy in our prayers. If it is forgotten then both Savoy and Cash remind us. You are so loved and am sure you can feel all the love and prayers sent your way. Hearing your description of what you are doing for treatments sound very close to what Laylas treatment plan was. I know she had the Vincristine and the Actinomycin. I can testify that only through prayer, fasting, and lots of priesthood blessings did Layla survive it and so well. We wanted to bring a care package for Jeremy, something he can do while doing his chemo. Or even the days that he is not up to doing anything (I know Layla watched Aristicats and Monsters Inc, over and over) If there is anything specific that he has been wanting please let me know. We love you and always keep you in our thoughts and prayers. Jeremy you are so lucky you have such a wonderful family and doctors! Love the Knight family

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