Any Port in a Storm

For anyone fighting a blood or bone marrow cancer, your treatments will likely include having a port implanted into you.  In two of my cases, the doctors implanted a Hickman Catheter.  You can learn more about them from this good YouTube video: https://www.youtube.com/watch?v=z6dbV8vY1V8

Also: https://en.wikipedia.org/wiki/Hickman_line

It is a long plastic tube that is surgically implanted, usually in your upper chest, and runs into your jugular vein.  Typically it has three ports, or “lumens” that extend from your body and allows medical professionals to either administer medicine, drugs (like chemo) or blood products into you and/or draw blood samples from you.

In another instance for me, they implanted a version of that catheter in the bicep of my arm.

Trust me; you will develop a love-hate relationship with your catheter.  You will love the fact that you will not need to be stuck with needles every day.  That gets really old really fast!  But you will hate having these plastic tubes hanging out of your chest which are a constant reminder that you have freaking cancer and are fighting for your life.  The day they remove your catheter – which is a simple and painless process – is very much a milestone to be celebrated.

The nurses should always be checking your catheter – making sure it is flushed and clean.  In one of my cases, I had the Hickman Catheter in my chest for about seven months.  I guess that was a little long, because I started getting infections that they traced back to the catheter.  So they removed it and put a new one in my collar bone area for the balance of my treatments.  You can’t be too careful about this.  You do NOT want to be getting infections when you have little or no immune system!

I am not a doctor and can only talk about my experiences.  PLEASE do not take my stories as facts for everyone.  Have an honest conversation with your doctor about all of this.

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