Monday, April 19, 2010

2 years later


Picture: Callum and my brother at the AC/DC concert in Las Vegas, April 9/10.

Here it is over a month since the last post - not a few days as promised! I think I really just could not write much more about Callum's hospital stay. The "Reader's Digest" version is that he made it through a real rough time. We were really fortunate to have so much family around - everyone travelled for hours just to come and be with him. He had a few ups and downs after that, but with some major antibiotics he recovered. And both of us learned we could trust me to give him an IV antibiotic and flush an IV line!


- The IV pump and antibiotic tube.







Lately I have been thinking more of the past 2 years and all that has happened. It was 2 years ago on April 10 that we first learned the cancer had spread to both lungs and there was to be no cure. I remember some very tense filled days as we tried to fight hard to see an oncologist and get the treatment he needed as soon as soon as possible. April 14 was the 2 year anniversary of the lung biopsy. Another long, stress filled day - well, week, I suppose. April 15 was the 2 year anniversary of my job at SSEA. And coming up April 27 it will be 2 years since Callum was given the 18 - 24 months prognosis for life expectancy (which was later reduced to 6 - 12 months in Sept/08). Well, he showed them! Recently there has been some growth in the area where his one remaining brain tumour is. It is most likely still some swelling from the gamma knife procedure he had in Dec. But as a precaution, we went to see his fabulous neurosurgeon, Dr. D. Fourney. He said that Callum has done remarkable with the metastatic disease. He recently was told by an oncologist that if he were to say how things were going just by his clinical exam, he would say he is great. I am sure they are wondering why his physical appearance just doesn't match his file!

So, over the last 2 years, these are some things that have happened:
- lung biopsy
- chemo
- brain metastases
- blood clot
- gamma knife surgery
- whole brain radiation
- change in chemo drugs
- more gamma knife surgery
- sepsis infection
- 11 day hospital stay

And:
- trip to Ixtapa
- trip to Scotland
- day trip to Carnousite and St. Andrew's golf courses
- bought Porsche
- 30th wedding anniversary
- trip to Ireland
- birth of the sunshine of our life - Cade
- trip to Vancouver Island for a 60th birthday party
- another trip to Ixtapa
- trip to Las Vegas
- celebrated parents' 50th wedding anniversary
- many, many, many wonderful moments spent with family and friends

We certainly have made the most of the last 2 years. And we continue to set goals and make plans. We are planning to see George Thorogood in Saskatoon in May, and go to Toronto to see U2 in July. We are most thrilled to be invited to our nephew C's graduation in June. Callum is really looking forward to his golf match: our son Jamie and nephew Chris versus Callum and Chris's father-in-law. Those young guys are in for a wild time!

And of course, we always enjoy our time with Cade (and his parents!). He is growing up so fast and is just a wonderful boy.























We never know how things will turn out. We are very lucky to have had this wonderful time with Callum. He continues to do well and he is an amazing inspiration to many. He is my hero.

“I am only one, but still I am one. I cannot do everything, but still I can do something. And because I cannot do everything I will not refuse to do the something that I can do.”
Hellen Keller

TTFN
Lorna

Monday, March 8, 2010

WARNING! Emotions involved -discretion is advised! part one.

Yes, discretion is advised. I have not blogged in about 7 weeks. And now I will start again. Emotions will be a big part of this blog. We have had a rough road, but thankfully things are now better. I started this blog so that I could have an outlet for my feelings, a way for me to cope, somewhere to make sense of the senseless. If any of those things are truly possible.

So, if you don't like emotions, if you have experienced a similar thing in your life, you might want to skip this blog entry. Callum, that might mean you. At times I have tried to keep things very positive in these blogs - to focus on the good things. We have travelled this journey together, step by step, the good, the bad, the uncertain. In January we experienced the same crisis, but in vastly different ways. I do not want to cause you more worry or distress. You are welcome to read this, to take a "walk" along this part of my journey, but I understand if it is difficult.

So, now that I have everyone's attention.....

My last blog was Sunday, Jan. 24. We had just had a wicked winter storm. Callum had just recovered from a flu or something. He was feeling better. And then came Tuesday.

Callum woke up at 4 am with a headache and vomited. He took a gravol and went back to sleep. He started shivering afterwards and when we got up to get ready to go see Dr H he was still not well. We headed to the ER where they monitored him for the day. His temperature starting going up, they gave him Tylenol, the temp went down, his heart rate was fairly high and his blood pressure fairly low. By the end of the day they asked to keep him overnight - mostly for observation. We found out the next day he had sepsis, which they thought was caused by some form of E.Coli.
Wednesday went pretty good. He was moved into an observation room on the oncology ward and started bantering with the nurses, L and P. We knew he was sick and were expecting a 4 - 5 day hospital stay.
Thursday, he was sitting up in the chair for breakfast, and looked quite a bit better. I went back to the hospital about 2:45 pm that afternoon. They had started giving him Lasix to help get rid of the excess fluid in his body. They had been pumping him full of fluid to try and flush out the infection. He said he had been sitting in the chair for lunch. Somewhere around 3, he suddenly said he was feeling cold, shivering and I gave him another blanket. He asked for the oxygen mask so I let the nurse know what he wanted. He had just finished a blood transfusion and they thought he was having a reaction to the blood so they gave him some bendryl.

The next thing I remember I had nurse S.'s arm around my shoulder asking me if Callum wanted to be intubated, if we got to that point. Up until then I absolutely believed they would be able to get him through this crisis. I had no idea that we were now faced with something so serious. Intubation, that means he can't breathe on his own. They are asking me if I want, if he wants, to have life saving measures, if it comes to that. The words were so hard to comprehend. What were they telling me? I had to ask if I needed to make this decision right now, and was told that yes, they need to know Callum's wishes, just in case. My first thought was that V. was only a few hours away from leaving on her vacation to Mexico. Should I call and tell her not to go? I don't know how many times I asked that. And each time I was told that they strongly suggested I call. That I call all the family. It was too early to tell if it was really needed, but it would be the safe bet to call them in.
My head started swirling. Medical professionals filled the room - one, two, three, four, five...I lost count how many white coats surrounded his bed. I heard someone ask for ventolin. I remember thinking that means he is still having trouble breathing - they had to keep him breathing. I went into the hallway, pulled my pink blackberry out of my pocket, looked at the screen and tried to figure out how to dial V's number. I have no memory of exactly what I told her - I am pretty certain I said they told me to tell her she had to come to Saskatoon. My heart broke to tell her- not only because we were facing a crisis I didn't yet truly understand, but because she was just hours away from heading to the beach, a vacation that she and S. so much deserved.
Fog continued to fill my brain. One of the nurses saw me on the phone, tears streaming down my cheeks, and gently guided me to the unit clerk's room to finish phone calls. I tried so hard to concentrate, but time after time I misdialled. Who do I call? What do I say? Is this really happening? I managed to reach nearly everyone, or at least someone who could call the rest. The family was on its way. I popped into the room to check on how things were going. There were many doctors, nurses and I don't know who else. I remember hearing wheezing, loud wheezing - how long could he wheeze like that?
The room was full, I swear every square inch held the feet of a nurse, doctor or technician. The calmness in the room betrayed the serious of the situation. They were busy. Very busy. Fear started to creep in. But mostly, it was surreal. How does he go from looking so well to being this critical? It made no sense to me. This could not be the end. It just couldn't. I didn't believe it. But everything they said to me contradicted my thoughts.
When people say you may forget what people say, but you don't forget how they act, I now understand. At least on some level. I remember few words. But I remember my heart sinking when Dr H said "Come with me, let's go for a walk". And then he put his arm around me, for a brief moment. It can never be good news when the doctor, who you have only really seen once, puts his arm around you and takes you away from the room where your husband is fighting for his life. The arm of comfort did little to stop the lump from forming in my throat, and feeling like my heart had just dropped into my stomach. This could not be happening!
I suddenly felt very alone, with an emotional force field trying to protect me. "He has Acute Respiratory Distress Syndrome" he told me. "Does he want to be intubated? How far do we go with life saving actions, if we get there." My face must have told the story of how much I disbelieved what was happening. Dr H said "Do you understand what I am saying?". I insisted that Callum deserved a chance - after all we had gone through we couldn't give in that quickly. Dr. H kept saying - "as long as it's reversible. You want us to do everything, as long as it's reversible. " I had to ask - "when do we find out if it's reversible?" Within a few hours, I was told. And then he said he really felt I made the right decision. So, the fight for life continued.
And I was still alone. I think. I called some friends to come and sit with me until family could get there. Were our friends there at that time? I don't think so. The fog in my mind was thick. Some things are not in logical order in my mind anymore.

I am sure Callum knew things weren't great when he saw our friends in his room. But nothing was as scary as the look on his face when his brother G came in the room. When Callum looked at him I could see extreme fear on his face - that he was now really afraid of how serious was his condition. Oh, how I wanted to take it all away, to just "kiss and make it better.". Again, my heart fell into my stomach. He had many visitors that night. The nurse on duty in his room was so patient and understanding, but by 3 am he was emphasizing the need to let Callum rest.

Thank goodness by that time we had made it through a lot of the major crisis.

I never thought that things could end that way. We are not ready for that. It likely seems like a contradiction that after this length of time to say we are not ready to face that final journey. But we aren't. We are to have more time. Things are to happen in stages. We are to have warnings before we were having to make those decision. As I told people that night, and the days following, "I am writing a book and this is not how it ends.".

There is much more to say, but that is enough for now. For those who are reading this but don't know, Callum is home now and on his way to a great recovery.

That is enough for now. I will continue in the next day or so.

TTFN


Sunday, January 24, 2010

Oh the weather outside is frightful.....


We have had a cosy weekend staying indoors from the large winter storm going through Saskatchewan. Lots of blowing and drifting snow!

We have had a pretty uneventful couple of weeks. Both Callum and I had little colds a couple of weeks ago, but we managed to get rid of them with no major problems. Callum did have a bit more of a crash than usual after chemo last weekend. I imagine it was likely from having had a cold - just harder to handle the chemo. And then he picked up a bit of a flu. He slept quite a bit and hardly ate for a couple of days. It was a little scary to me - it can be hard to tell the difference between what is just a normal flu or cold and what might be the dreaded cancer starting to grow again. However, he is quite back to normal this weekend so we are sure now it was nothing more than the flu. He had his regular follow up CT scan on Friday, and we see Dr. H on Tuesday so I am sure if there is anything happening we will find out then. It is just good to see him back cooking and eating. We even hung a couple of pictures yesterday!! And he is talking back to the TV golf commentators so is as normal as ever!

We are excited to head down to Medicine Hat on the 31st to look after Cade. I am sure Vanessa and Stuart are counting down the days until they head to the beach! We will have so much fun that week! It will be quite a time looking after a 7 month old baby again. :-)

“There are those who work all day. Those who dream all day. And those who spend an hour dreaming before setting to work to fulfill those dreams. Go into the third category because there’s virtually no competition.”
- Steven J Ross

TTFN

Thursday, January 14, 2010

Happy Birthday Callum!

HAPPY BIRTHDAY CALLUM!







We are just thrilled to be celebrating Callum's 49th birthday. Nothing exciting planned as he is on chemo. I know, it isn't fair to have to have chemo on your birthday. The sad and ironic thing is, without chemo, there are fewer birthdays. So, we must really celebrate every birthday (and say a little thanks to chemo)!
I do believe he has had an incredible year. He started 2009 in Scotland, and had a great trip to Carnoustie and St. Andrew's Golf Courses - a celebration for Jamie's birthday. Callum celebrated his 48th (2008) birthday in Glasgow. Lots of travel, the exciting birth of our grandson, Cade and here we are, a year later.
This birthday is a little bit quieter. A day spent at home, cooking his own birthday supper! He made the most fabulous oven ribs. They definitely rival BBQ ribs! Some good chocolate fudge cake and an evening of watching TV and we'll call it a day! Thank goodness for some good old SNL stars' TV shows tonight - I have turned into the biggest 30 Rock fan!
so, here we are, heading into Callum's 50th year - we look forward to some great concerts, seeing our grandson grow, a bit of travel - and writing one year from now "Happy 50th Birthday, Callum". Isn't that something to look forward to!

"Inside every older person is a younger person -
wondering what the hell happened. "
- Cora Harvey Armstrong

Friday, January 8, 2010

A hardy prairie winter!


Ahhh....the memories of warmth, sun and no socks! After a few weeks of very cold weather in Saskatoon I am trying hard to remember what those days in Ixtapa were like. Temps of plus 30 and nearly never ending sunshine. Oh, why can't we just pack it up and bring it home??!
And how Canadian am I - talking about the weather!


Today our first baby turns 30! I don't know how I can have a 30 year old when I am only 35! Oh well, I like to think we are only as old as we feel! We wish Jamie a very Happy Birthday and many, many, many, more!

We had a pretty good week this week. How lucky are we to see Team Canada play in the World Junior Hockey Tourney! Callum saw 3 games and I saw 2 - both of the Canada - USA games. While the gold medal game gave us nearly a thrill a minute, we, like the rest of the country, were hoping for a different result. It was a great atmosphere to experience and so exciting.

Both of us are doing quite fine. A little cold to make us a little more tired, but maybe it is just time to slow down for a while anyway. We are planning to be home for January and will head to Medicine Hat in early Feb to look after that sweet little Cade while his mom and dad get to fly away and get a much deserved break. I have accomplished some important things like cleaning my fridge! There are a few more things to sort out (ugh! pantry!), throw out, organize. Isn't that what January is all about?

Callum is doing quite well. He continues with the chemo treatments and each treatment comes with the surprise of steroid side effects! It is an adventure! He has a CT scan on January 22 so at his doctor appt on the 26th we should find out whether there has been any new growth in the chest, abdomen or pelvis. I am a little anxious about this test result since there was new growth in the brain. It is important to remember, though, that the chemo doesn't go through the blood brain barrier so the chemo doesn't stabilize anything in the brain but could still be working to keep the lungs stabilized. His new oncologist, Dr H, has been getter better acquainted with his file and we have every confidence he will be on top of things just like Dr A had been. We do have positive thoughts and expectations that the status quo will be what takes us into February!

I will endeavour to write more often, even if it is just about our boring life in the middle of the prairie!

"Courage and perseverance have a magical talisman, before which difficulties disappear and obstacles vanish into air. " John Quincy Adams

TTFN
Lorna


Friday, January 1, 2010

HAPPY NEW YEAR!!




Cade and Grandad watching Canada play Latvia.







Happy New Year everyone!

I am sitting at the computer uploading some music so Callum can change the songs on his iPod. So, I thought it would be a good time to update the blog.

We had a great Christmas in Medicine Hat with Vanessa, Stuart, Cade, Jamie, my Mom and Earl. We squeezed in a dinner with my nephew and family too. It was a busy few days but wonderful time spent with family.

Callum had his last chemo treatment bumped a week. His neutrophils were too low. They were just fine this past week so he carried on with treatment this past Wed.

Many of you know that there were a couple of suspect spots on his brain. The MRI in November showed some growth so he headed off to Winnipeg for Gamma Knife surgery (see Aug 2008 blogs for more information on this amazing procedure!). The MRI in Winnipeg in mid-December showed a tumour around the same spot as the last one in the right cerebellum, and a new, very very, tiny (3mm) one on the top of the brain. Both spots were treated and we can only assume it will be as effective as the last gamma knife treatment. The spot at the front of the brain that was treated last year no longer shows up on the MRI's! The CT scans of abdomen/chest/pelvis have shown no change to date. Overall, quite remarkable to keep things stable this long! What a guy!

It is a very interesting time. When I think back to a year ago, I know we were all really hoping that Callum would see another Christmas, but I don't know how many of us honestly thought he would - or be doing so well! After such a busy 2008 with new medical issues monthly, we have had an amazing and wonderful 2009! We started the year by taking our kids to Scotland for 2 weeks. After a bit of a lull, Callum picked up his Porsche in Winnipeg in May, we had a baby shower for Vanessa in May, went to Medicine Hat in June for the exciting arrival of our first grandchild, who decided to keep us waiting until July! We were so thrilled to be there on the arrival of our grandson, Cade Scott Bonneville.













In August we helped my Mom and Earl auction many of their belongings on the farm and had a trip to Ireland so that I could attend the LIVESTRONG Global Cancer Summit.













We headed to Vancouver Island in September to celebrate my brother in law's 60th birthday. We had a great time and were able to visit many old friends! September and October were quite busy as we had the launch of Saskatoon Supporting LIVESTRONG (a group I founded) which included The Giant Colon Tour, an educational exhibit of the Colorectal Cancer Association of Canada. Our group was busy fundraising and had an amazing day!









In November we headed to Ixtapa, Mexico to visit my sister for a week,













and then to Manitoba to celebrate Callum's parents 50th anniversary. What a milestone and it was a great party!

















We spent Christmas in Medicine Hat spoiling Cade a few other people there.

Along these many journeys we were able to spend time with many old friends, meet some new ones, and enjoyed the company of our family. Thank you to each of you for helping to create so many wonderful memories!

All in all, it has been a very memorable, exciting and busy year!

Want to keep the spirit of Christmas all year long? Try this:

Recipe for Christmas All Year Long

Take a heap of child-like wonder

That opens up our eyes

To the unexpected gifts in life—

Each day a sweet surprise.

Mix in fond appreciation

For the people whom we know;

Like festive Christmas candles,

Each one has a special glow.

Add some giggles and some laughter,

A dash of Christmas food,

(Amazing how a piece of pie

Improves our attitude!)

Stir it all with human kindness;

Wrap it up in love and peace,

Decorate with optimism, and

Our joy will never cease.

If we use this healthy recipe,

We know we will remember

To be in the Christmas spirit,

Even when it's not December.

By Joanna Fuchs


TTFN
Lorna

Thursday, December 3, 2009

I'm back.....

Hi everyone. Just a quick note tonight. I have had many people say they have been checking the blog and there have been no recent updates. No problems, just "making hay while the sun shines".
Fall is a busy time for me at work, with art educator retreats, finishing up year end, follow up reports to funders, conferences, and all the other stuff!

I was also very busy with LIVESTRONG Day, October 2, which was also the public launch of Saskatoon Supporting LIVESTRONG Cancer Corp. It has taken a while for me to catch my breath.

In November we spent a few days in Medicine Hat, a week in Mexico, and a few more days in Manitoba. You could say we did the M&M&M tour!

I finally got the tree decorated tonight, and ready to get the rest of the Christmas decorating done this weekend.

Callum has been doing quite well. The fall has been quite typical with chemo every 2 weeks, along with follow up tests. So far there is nothing new to report. He has been feeling quite well with the exception of those 5 - 7 days after the first chemo day.

I promise to fill you in on the the past few months in a day or so.

Thanks again for everyone's best wishes and positive thoughts. We truly believe they make a big difference!!

TTFN
Lorna