I visited the oncologist on Monday afternoon. The doctor told me to feel free to call him
Michael. (I sure hope that's his name!) I told him I'd recently seen
Sid, and have an appointment to see
Sam (aka Dr. LePew in mid-Oct0ber). After my echocardiogram, I'll see
Tom. I'm not 100% sure about calling doctors by their first name though I'm not into fighting with Michael over it. On a side note -- I've been seeing Michael for 2 years. Why is he granting permission to call him by his first name at this late date? Is this his way of telling me that I might live?
Michael took my blood pressure -- it was slightly elevated which I said was a result of "white coat syndrome" though Michael doesn't wear a white coat. My last visit with Sam, my blood pressure was quite high. Sam doesn't wear a white coat either. I'm always afraid Sam is going to force me to speak french while performing a rectal exam so it's got to be fear that causes the elevated blood pressure - fear of french and rectums. Why do they call it "
white coat syndrome"? Perhaps
they c
ould call it "doctors who tell you it's okay to call them by their first name after two years of treatment or doctors that request you speak french while performing rectal exams" syndrome? No wonder the blood pressure goes up!
The most probing issue I discussed with Michael was that I'd had an appointment with Sid, and the appointment was pretty much a wash. Sid didn't perform the requisite rectal or the annual pap. Contrary to popular opinion, I am not the norm. Sid needs to go the extra mile for me. Sid needs to treat me more thoroughly than the random vagina on the street. Idle chitchat doesn't cure cancer (and if it did we'd *all* attend support groups.)
Michael advised me to let Sam know that I need someone more experienced with my situation than Sid. Then Michael said to make sure Sam sends any new records to Tom, Sid and himself to keep them all in the loop and handed me paperwork to give to Sam and fax to Sid and Tom. Michael said to make sure that I ask Sam about another CT scan for this year. Michael also said that it looks like I am graduating to the only one CT scan per year -- that it's been 2.5 years since my diagnosis (which isn't true yet -- though I got all excited because I *thought* he was right because he's a doctor and doctors are always right, right?) and that I only need one scan a year unless Sam comes back with a different report.
After I got home, I realized that Michael was wrong. My surgery was almost two years ago the first week of October (next week). The last week of September (this and part of next week) will be my two year cancer diagnosis anniversary (where Sam and Sid both said that I kinda, sorta, maybe had cancer though they didn't really think I did, and if I did have cancer, it would be encapsulated (it wasn't) and not that big of a deal, (and it was) and I wouldn't have to do radiation or chemo and they flat-out lied) and if I did have cancer it would be a cancer that wasn't that bad) (Liars!). (Oops -- wow, calling Sid and Sam both a liar doesn't seem very compassionate -- even to me! I will pay extra attention in class this week.)
So this makes the first week of October my 2nd anniversary of cancer surgery where they took out all my guts and put them in a jar for 'show n tell'. Too bad I'm no longer in kindergarten. I had surgery the day after I returned from an eight day vacation in Hawaii where I spent most of the time hunting for toilets and visiting the
Punalu'u bakery. Which by the way, was the highlight of my life so far though you didn't read that here. 
And because we both found out about our cancer diagnosis on the same day, Lance and I are celebrating this anniversary on Oct 2, 2009 aka LIVE
STRONG Day, a
one-day initiative to unite people affected by cancer in raising awareness of cancer issues on a global level and in communities across the country. And you are part of my community. Please come back to visit us on that day. Fridays are always slow anyway. I'll be highlighting other exciting details about cancer (THOSE tidbits you simply cannot miss!), my life post cancer, and my LIVE
STRONG(
er) life, post treatment, (part of which includes calling my doctors by their first names). Instead of asking for gifts like most young couples (
in love) (
sorry, Sheryl), Lance and I will be giving gifts away to celebrate the occasion.
Read more about
LIVESTRONG and
commit to your own event on Oct 2, 2009. (
Sorry but visiting the Punalu'u bakery is not an official, sanctioned LIVESTRONG event.)
We unite people to fight cancer believing that unity is strength, knowledge is power and attitude is everything
Lance Armstrong Foundation