Five hundred twenty five thousand six hundred minutes
Five hundred twenty five thousand moments, oh dear
Five hundred twenty five thousand six hundred minutes
How do you measure, measure a year?
Five hundred twenty five thousand moments, oh dear
Five hundred twenty five thousand six hundred minutes
How do you measure, measure a year?
In daylights, in sunsets
In midnights, in cups of coffee
In inches, in miles, in laughter, in strife
In five hundred twenty five thousand six hundred minutes
How do you measure, a year in the life?
In midnights, in cups of coffee
In inches, in miles, in laughter, in strife
In five hundred twenty five thousand six hundred minutes
How do you measure, a year in the life?
Seasons of love
Five hundred twenty five thousand six hundred minutes
Five hundred twenty five thousand journeys to plan
Five hundred twenty five thousand six hundred minutes
How do you measure the life of a woman or a man?
Five hundred twenty five thousand journeys to plan
Five hundred twenty five thousand six hundred minutes
How do you measure the life of a woman or a man?
In truths that she learned
Or in times that he cried
In bridges he burned or the way that she died
Or in times that he cried
In bridges he burned or the way that she died
It's time now, to sing out
Though the story never ends
Though the story never ends
Let's celebrate
Remember a year in the life of friends
What an amazing feeling to be able to look back and realize that I am soon able to measure my remission from Hodgkins Lymphoma in years. As I approach July 2015, it will be one year that I arrived back in Wiarton with K and K - bottle of champagne in hand to celebrate a PET scan that showed I was in remission 3 months into chemotherapy. This past week there were many reasons to celebrate. I received a letter from Long Term Disability confirming that my official return to work date is September 1, 2015. I enjoyed a very full week orientating myself to my new position for next year, participating in several meetings, signing for my laptop/cell phone. A tour of my new office. A very emotional send-off party with my staff at Lackner. I felt like a young girl in university who was leaving home for the first time. While I would be in new surroundings, I still do feel like I will be able to call Lackner Woods home and return for support and solitude in my new position. Our extended yurting family enjoyed our traditional celebration of the End of Year Foo Fah Party. A celebration of our children's successes. And the ever favourite tradition of burning their notes from the previous year. A symbol of the amount of work and pressure our kids today in the classroom. How amazing is it to learn how many of our children were recognized for Citizenship awards, Art awards, Honours distinction, Valedictorian, Athletic and Music awards. A testament to the wonderful adults our kids are supported by. We are so very blessed for our extended chosen family. As I reflect on the past year and the challenges our family has so humbly and successfully met, I am in wonder of what we are able to rise above. We have much to look forward to this summer. A quick trip to Grand Bend, Tragically Hip concert, Huether patio remission celebration, a month of leadership camp for Cam, a long-awaited trip to Calgary for Jordan and I, the Stampede, girls horse camp, road trip to Jasper, massage/spa day, cottage weekends, Darien Lake, Southampton family weekend. Before we know it, 8 weeks will have passed and we will be ready to embark on new adventures of Itinerant DST role and Grade 10-11. How quickly the days, months and years pass. Those 525 600 minutes fly by, thankfully bringing me minutes, days and weeks closer to what the medical profession considers a cure.
I had a good appointment with my family doctor this week. Thyroid testing comes next. As well, I do continue to have complications of mild Lymphedema from the lymph node surgery I had on my right arm. I have swelling and tightness in my hand/wrist from lymph node fluid not properly draining. A very common side effect from that surgery. Unfortunately, according to my doctor there isn't much that can be done outside of elevation, Ibuprofen, exercise. I will see what Dr Stevens recommends in August when I have my next appointment. Word of caution for those with a similar diagnosis to myself reading this, I have found that having bloodwork done or blood pressure taken from that arm to be a trigger for increased swelling, I have been told to avoid this to assist with minimizing the swelling. Something I wasn't immediately told.
Aside from that mild annoyance. I feel absolutely great. We enjoy much joy and gratefulness in our life. Thank you to everyone from my Lackner staff to my new Developmental Ed team. I appreciate the varied caring, friendship, wisdom, guidance and support you bring to our lives.