Blindsided

An American tourist visiting London tries to cross the street.  Instinctively, he looks to the left first.  Finding it clear, he steps off the curb, looks to the right, and is immediately flattened by one of those double-decker buses they have over there.  Whoops!

I’ve been feeling a little bit like that lately.  For a long time now, my multiple myeloma journey has been sailing along on cruise

Many Moons

It’s been many moons since I last blogged.  Actually, there has been only one full moon since my last blog…August 18th, but there have been two new moons…August 2 and September 1.  So maybe it has been two moons since I last blogged.  Whatever.  Who’s counting?  Anyway, it’s been a really tough month, so I haven’t been up to blogging about it until now.

I’m very sorry to report that our

Pushy People

You may have noticed that I haven’t updated my blog in quite a while.  I apologize for that, but I do have a bit of an explanation.  This blog is supposed to be about me, but although things have been going well for me lately, they haven’t been going so well for my sister-in-law, Kathy, or Gretchen.  Kathy has advanced lung cancer and Gretchen has esophageal cancer.  Gretchen goes in for surgery

Belated Update

Okay, it’s May 31 and I haven’t updated my blog since right after the amazing 5K event.  I didn’t want to miss another opportunity to post in the month of May, so here goes.  This will be short, since there is not a lot of news about myself to post.  My visit to the Farber last week went well, as I still seem to be in remission, thank goodness.  However, as I posted last month, there are some

Race Day

Team Epic for Bill Tent

The night before the big MMRF 5K run/walk race, we were a bit nervous, as we were about $450 short of our fundraising goal of $10,000.  But our son, Jason, was a savior.  He drove up from Connecticut Saturday night and dumped donations on the kitchen table that he had collected from his co-workers that day at his restaurant, Joey Garlic.  It came to $602 in cash!  I

Latest Results

Monday I paid my my monthly visit to the Farber.  The news is still good!  My blood work came out fine and I got the printout of my annual bone marrow biopsy pathology report.  In my last post, I mentioned that the bone marrow aspirate contained 7% plasma cells.  I lied.  Actually, it was 8%.  Last year it was 6%.  I asked Mary about this, and she said that Paul Richardson had reviewed the report

Florida Trip

Last weekend, we traveled to Fernandina Beach on Amelia Island, Florida to attend Pat Killingsworth’s Myeloma Survival School.  It was a beautiful setting and what a wonderful time it was!  About 140 people attended from various parts of the country for this weekend event.  It was an awesome tribute to Pat’s life.  Pat’s wife, Pattie, was amazing!  She was so outgoing, upbeat and cheerful, and

Birthday

Today marks the fourth birthday of my stem cell transplant on March 20, 2012, when I received my brand new immune system.  I now have two birthdays, December 2 and March 20.  I share the honor of having two birthdays with Queen Elizabeth, whose actual birthday is in April but whose official birthday is in June.  How many people can say they have two birthdays?  I feel so regal.  I think Liz and I

This and That

Last week at the Farber, everything came out normal again, thank goodness.  I’m very lucky to still be in remission at cycle 45 of my maintenance therapy.  Believe me, I don’t take this for granted.

We are getting ready to head to Florida at the end of March to commemorate Pat Killingsworth’s death at a memorial celebration for him at Amelia Island.  I’m still not over the shock of Pat’s passing

Cancer Sucks – Part 2

In my previous post with this title, I was worried about Pat Killingsworth, who tragically passed away last week.  I feel like I have lost a real friend, though we have never met.  However, I also had another reason to worry that is closer to home.  My sister-in-law, Kathy, has just been diagnosed with lung cancer!  By the way, she doesn’t smoke and she is only 56 years old.  Our whole family is