“So what are we doing today?”

“What brings you in today?  I know we just saw you in March.”

W E L P …

I met a very nice hospital employee this morning.  I am finding more often I am getting nice ones, which is a huge deal!  When you have to interact with a sucky medical employee it’s such a freaking drag!

As I was in the exam room, I began my story:

  • PTEN mutation
  • Breast Cancer risk
  • Similar to BRCA mutation
  • Brain tumors
  • Surgeries

And the list goes on. I kind of have my “go-to” story when I meet new medical professionals.  She was friendly, and I could tell she has been around the block (but I don’t mean that at all in a negative way).  She says to me, “I have been around over 20 years and I’ve never heard of PTEN mutation.”

GAH THIS IS SO WRONG PEOPLE!

She was nice to let me rant a few minutes about how irritated I am that “everyone” seems to know of BRCA mutation, but no one does of PTEN and it’s JUST AS SERIOUS AS BRCA!  (I would like to add here though that any medical condition that causes a woman to be at high-risk for breast cancer  is serious, whether it is a 10% lifetime chance or 88% lifetime chance.  But, anyway…)

I made it through the appointment with flying colors (haha) and then got dressed and went along my way.  As I was going to my car our entire conversation really struck me:  How thankful lucky I am to have been diagnosed as quickly as I was.  Can you imagine if I had Cowden Syndrome and yet didn’t know about it yet?  Regardless of zero family history of cancer.  What about all these women who are getting tested for BRCA mutation and yet PTEN mutation is conveniently being left off?  I really feel that Cowden Syndrome really isn’t as rare as the numbers say, and that is paralyzing for those who have it yet either aren’t diagnosed with it, or are diagnosed later than they should be, or have had multiple cancers (breast, thyroid for example) and that is not coming up on anyone’s radar?

Gosh, I could go on and on about this of course.  My hope and prayer that at least one person will be educated about PTEN mutations via either my story, or another’s who has found their voice to shout!  (NOTE:  the employee did say, “Thank you for educating me about that” which was really nice.  Those types of conversations really give me strength to keep writing, because validation.)

PS:  Please visit my link and consider supporting if you can.  Every bit helps!  ❤ Thank you.  Let’s all bring awareness for PTEN mutations.

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