Thursday 22 February 2007

Dancing, visiting and the 90s


This week I've seen that time and age mean nothing. On the weekend, I flew to Regina for my great Aunt Marj's 90th birthday. Saturday afternoon we visited another great Aunt, Emelda, who is also in her 90s, but still living independently and offering jam jam cookies to us guests. Saturday evening was a great party - Aunt Marj's 90th included a dinner and dance and over 90 guests. She stayed until midnight and danced several times to the band Carnival (two of my old elementary and high school teachers played bass and piano!). Truly a day of young ladies in their 90s. It even inspired me to dance a few songs (with shoes off!) which was a remarkable event given my fairly recent inability to walk!

Mom, Colleen, Bob and I stayed at Ellen's house, which allowed lots of visiting with Ellen, Amy and Amy's fiance Ryland. I lived with Ellen and Amy for a while about 10 years ago, so it was wonderful to have the "girls" back together again!


Sunday I visited yet another young lady, Grandma Antonini, who will turn 90 in January. Her hair still naturally red and curly, and dimples still smiling, she seems to me to be younger than she was 15 years ago. I was lucky enough to visit with a bunch of the Antonini's that morning and afternoon as well - Holly and her family (Jamie, Eddie, Mia, Lui and Ellie), Heather, Ed, Deanie, Tony, Carol, Sonia, Len, Kelly, Therese and Christine (A). It was fantastic to see everyone and I look forward to the reunion in August to see everyone.

After a quick dinner visit with the Boyd's and Ellen Sunday evening, we arrived home late that night to Calgary. I had definitely done as much visiting as possible in a 48-hour period and was basically exhausted. Monday and Tuesday I had really significant bone pain and nausea, which kind of wiped me out until last night. It was worth it though!


Last Wednesday I started "day 1" chemo again, and the doctor mentioned to me that the transplant team still reviews my case each week to decide if the chemo I am on currently is the best path. He said there is still talk about revisiting more toxic chemo (as I missed most of the two toxic rounds when I had the infection last summer) at some point in the future, depending on my strength and continued recovery. It seems uncertainty about the plan for the near future will continue. I feel it just confirms that making my "lists" and trying to knock things off of the lists sooner rather than later is the right move.

Yesterday I started physiotherapy to try to improve my muscle strength and overall range of motion that I lost while hospitalized. I haven't really had formal physio since I left the hospital, so it will be a slow process, but I'm excited to start. This afternoon I go to the hospital for a monthly inhalation of an anti-viral drug, which will give me "coverage" for another month.

On a non-health note, Dad and I are going to the Rascal Flatts concert tonight. I may need to nap tomorrow, but again it will be worth it. If Aunt Marj, Emelda and Grandma A can do it, I can!

Cheers

Monday 12 February 2007

Lists and things

It's cold and snowy outside today...apparently warmer weather is coming in a few days, so the snow should melt soon!

I start chemo "day 1" again later this week. I continue to be feeling well, with mainly fatigue and stamina being my greatest challenges lately. Last week I had another CT of my chest - that, combined with pulmonary functions tests later this week, should give me a picture of what my lungs are doing. They feel pretty good to me, but I am anxious to see what the numbers look like, as I confidently told the PF technician in December that "I'll bet you those numbers improve by the next test"!

Physically, I am miles ahead of where I was only a few months ago. Mentally, I still struggle with the uncertainty of my short-term and longer term life, as well as adjusting to everyday life again, after leaving my life as an independent, happy, busy woman living in Manhattan.

Struggles aside, I've had a number of good days since my last post...I went for a few lunches and dinners with some good friends and coworkers who I hadn't seen for a while. One one lunch, a wise friend asked me if I had made a list of things I wanted to do, especially in this "limbo" period, where I am well enough to do some things but not healthy enough to return to work. The truth is, I've had an informal list ever since my diagnosis almost 10 years ago...it prompted me to turn to my acting again and it was certainly why I accepted the New York position. I haven't ever formalized the list, but now I am thinking I should. From experience, I know if I write something down it is far more likely that I will do it! I'm still working on it, but will share some of it when I am ready. What's on your life list?

Since that day at lunch, I've made a few plans. Some of these were in the works before, but it seemed that I moved into high gear! I had already planned to travel to Regina this coming weekend, to attend Great Aunt Marj's 90th birthday and see my Grandma Antonini and many others, with Mom, Colleen and Bob. In March, I am going to Grand Cayman for a few days with Dave and his parents, who I haven't seen since the day I went into ICU. That will also be my first visit to the Caribbean. In early April, Dad and I are going to fly to Las Vegas to sit in the 10th row of the Elton John's Red Piano concert (this is the one concert I've always wanted to see). Mid-April will be a return to my previous home, New York, to see all the people I never got to say goodbye to when I disappeared last July. Mom is accompanying me reluctantly (ha ha). Finally, at the end of April, my long-time childhood friend who is soon to be Dr. Shelley Boyd, will travel with me to South Beach, Florida. Neither Shelly nor I have been to Mexico or Florida and we have a lot of celebrating to catch up on while lounging by the pool.

I realize these trips seem a bit condensed in terms of timing, but all were based on different date demands and just happened to run into each other. So don't be concerned, as Tasha asked me "are you sure everything's alright?" after I told her the schedule. All will include a few "life firsts" and knock off a few things on my list. I will still do chemo the entire time, arranging the "day 1" days in between trips to get my IV chemo. I can do blood work from any of these places, as most are in the U.S. and Cayman was "approved" by the bone marrow clinic.

There are many more things on my list, many of which don't require travel! What's on your list?

Cheers

PS To any of the Antonini's who will be in Regina this weekend, I am going to Grandma's Sunday afternoon for a visit, so if you feel like popping in, I'd love to see you!