Wednesday, December 31, 2014

Bye Bye 2014

2014.12.31

New Year's Eve

365 days ago, we lived in Sweden and celebrated with dear friends, watched the fireworks in our neighborhood and face timed with my parents at midnight. It was to be a year of many exciting things to come - 2014.


January 2014
  • Taught Lego classes and held Lego Birthday Parties, 
  • Cleaned out house to style it and put it on the market, 
  • 31st - Peter and I to London so he could start new job

 
February
  • 15th - discovered large mass on my neck
  • 15th -House offer accepted and contracts signed
  • 15th - spent 8 hours in the ER with no results
  • 17th - headed to a private doctor and got the ball rolling with tests to get an answer
  • 20th - Mia went with me to demand the results - IN SHOCK as it is non-hodgkins lymphoma DLCBL. 
  • Life is forever changed
  • 21st - trip to Gran Canaries cancelled
Smiling with cancer bulging from my neck.

March
  • 10th -CHEMO R-CHOP #1
  • 17th -Parents arrive to help out
  • Haircuts (heads shaved - all of us)
  • 25th -CHEMO #2
Chemo #1

Chemo #2






April 
  • 1st- Mom and Dad back to NY
  • 9th - CHEMO #3
  • 10th - Marcus turns 14.
  • Quick trip to London to check out houses.
  • 23rd - CHEMO #4
  • 29th - I turn 49. Yippie! (bald and 49 what more can someone ask for?)




May
  • 3rd- my sister Kris arrives for one week visit
  • 5th - toenail removed due to infection, chemo delayed a week
  • 5th - afternoon trip to ER with Eric - admitted to intensive care unit for DIABETES.
  • 14th - CHEMO #5
  • 16th - Nicole and Jackson arrive for one week visit
  • 28th - CHEMO #6
  • 29th - MOVERS PACK UP THE HOUSE
  • 30th - MOVERS PACK UP THE HOUSE








June
  • 2nd - House contracts exchanged.
  • 13th - last days of school for the boys
  • 16th- CAT and PET scan for me
  • 19th - doctor visit to hear the results: REMISSION
  • 21st - Celebrate Midsommar in Sweden
  • 22nd - Trip to America to celebrate my parents 50th Wedding Anniversary
Kevin's last American Fottball Game


July
  • 1st- Eric turned 11
  • Visited Charlotte-Bluffton-St. Augustine-Ft. Lauderdale-Key West-Charlotte
  • 14th - Back to Sweden
  • 25th - London Exploration




July 8 (our 19th wedding anniversary) Key West







August
  • My hair is growing back
  • Kevin turns 17
  • Filmaking camp for Kevin
  • Drama camp for Marcus
  • Boys start new school 
Hair on August 1st

Sending Sophie to London
September
  • Visit Nikki in Malta
  • Doctor visit in Sweden - 3 MONTHS ALL CLEAR 
  • 25th - Personal shopping day. A great day!
  • Met and made many new friends here in London
  • Eric starts karate, Marcus starts drama classes, Kevin starts Parkour





















October
  • 3rd - Start at G14 with my personal trainer, Ben
  • Saw Canterbury Cathedral and Whitsable Beach
  • Mia and her family visit us
  • NFL games in London. FUN FUN FUN

















November
  • Girls Weekend in Lisbon
  • 14 workouts in Gym with cardio and strength training
Blood Red Seas- November 11th
Lisbon - Torre de Belem






December
  • Christmas Fayre in Burnham-on-Crouch
  • 16th - Mom and Dad arrive for a 3 week visit
  • Art of the Brick Exhibit
  • Christmas and New Year in London



Art of the Brick



Globe Theatre

The majority of these points above are positive, wouldn't you agree? 

It has been a long year and I feel like I lived every second of it in slow motion. Luckily my chemo brain forgets that fact sometimes and I can reflect on how blessed I am to have so many dear family members, great friends (new and old). I got to see so many things this year even though I was totally exhausted after chemo. I did most of these things at a much lower activity level and that is the new me.

My children have matured and tried many new things. My husband is happy with his Christmas presents.......as I am too. Just happy to be alive. YES, ALIVE. 

So happy to say goodbye to 2014. It was a bumpy ride but I came through on the other side and I have now taken control over my eating, exercising and I focus on living here and now. 

Battling cancer has changed me and I am focused on embracing that change. The cancer will not define who I am, I am more than just a survivor of cancer. I will live my life to the fullest and I am grateful that I can do that.

Tonight will be celebrated by eating well, enjoying dessert, watching the fireworks on TV and hugging the nearest and dearest that are gathered here. Sending big hugs to all the rest of you that have been a part of my life in 2014. 

Please feel free to comment below in the comment section.

I look forward to new adventures in 2015 with all of you. 

HAPPY NEW YEAR! 

LOVED. GRATEFUL. 
KICKED CANCER'S ASS. LIVING LIFE. 
BE BRAVE. LOVE LIFE.


Thursday, December 4, 2014

CHEMO BRAIN sucks.

2014.12.04

So, I have been sitting here for 15 minutes and all I wrote was this sentence.


The definition according to cancerresearchuk.org of CHEMO BRAIN or MCI (mild cognitive impairment) is when cognitive changes occur after chemotherapy. Cognitive is the way you process information or understand the world and how it works.


Excerpt from Cancer Research UK: Most people who have cognitive changes are able to do everyday things. But they may notice they aren’t able to do some things quite as well as before they had cancer. 
Symptoms can include (I HAVE ALL OF THESE)
  • Memory loss – forgetting things that you normally remember
  • Difficulty thinking of the right word for a particular object
  • Difficulty following the flow of a conversation
  • Trouble concentrating or focusing on one thing
  • Difficulty doing more than one thing at a time (multi tasking)
  • More difficulty doing things you used to do easily, such as adding up in your head
  • Fatigue (tiredness and lack of energy)
  • Confusion
  • Mental fogginess
The changes are often mild and very subtle. But if you have them they can reduce your quality of life. Doctors now know that people with different types of cancer may have these problems. 
Tips for coping with chemo brain (I AM USING ALL OF THESE)
  • Try to keep your life as simple as possible
  • Avoid trying to do too many things at the same time
  • Think about writing list about what you need to do, things you need to buy and where you left things
  • Writing people's names down with a brief description to help you remember them may be helpful
  • Repeating things back to people, for example, the names of people you meet for the first time can help
  • When arranging to meet someone or organising an event it may be helpful to write the details down and repeat them back to someone
  • Try to talk to people somewhere quiet with few distractions
  • Many people find it useful to keep a calendar on your wall
  • It may be helpful to write yourself notes and stick them up where you can see them to remind you to do things
  • Try to follow a healthy diet, and get some exercise and plenty of rest - try to avoid becoming over tired
  • Keeping your mind active may help -for example, doing crosswords, sudoku and puzzles

Those that knew me before cancer know that I was able to focus on a task for long hours and complete it. I could be counted on to follow through. I was amazing (even though I didn't know it) at multi-tasking and seemed to thrive on on having many balls in the air at the same time. (figuratively not literally - I am terrible at juggling). I started my own business and at the same time oversaw the building of a new house that I had designed. I kept track of appointments, remembered birthdays (didn't always send the card though), I was always prepared and even sometimes a step ahead for every event. I worked my butt off in everything I did.


The new me is going to take some getting used to. My attention span is like a goldfish. It doesn't bother me until I realize that my attention span is so short. I can't finish a task- especially if I can't start it. Just one of the many things that suck with Chemo Brain.

I have too many things on my mind and they are too many for my brain to handle. I become paralyzed with my actions and end up not being able to get anything done and only getting more frustrated. I make a list in my notebook to get these things out of my head. I try and do one or two of these things on the list. Frustration again because there are 10 new things to do every day.

So, here I am now 5 hours later, stopping and starting to get this blog post finished. 

Frustration comes and goes. This week it has been high as many things are happening at once. It is kind of overwhelming. I try and get myself out of my funk. Break the pattern. I am again so blessed to have friends here in London that I only met a few months ago that care. The girls are great listeners and have excellent ideas how to cope with all the varying consequences of having chemo brain. THANKS GIRLS.

If chemo brain sucks, then me getting in better physical shape is at the other end of the scale. Working out 3 times a week in the gym and then walking at least 3 miles a day means that my hip joints are sore just sometimes and not all the time like they were before. Exercise is keeping me sane. Thank goodness for that or I would already have been checked into the loony bin.


Recovery and living life after cancer always comes down to the support and encouragement of friends and family to get through it. I am truly blessed and grateful.

FRIENDS. GRATEFUL. CHEMO BRAIN SUCKS. FAMILY. RAINY LONDON. 

MAKE A LIST. START AND FINISH IT.

LOVED. BE BRAVE. LOVE LIFE.