Thursday, 8 September 2011

Admission Day

Admission to VGH has arrived today. Remission has maintained and the battery of tests has gone well, so the team is going ahead with the transplant, and I am so grateful.

We have had a wonderful August including the trips to Long Beach and Kelowna, and both kids are now settled into University, and Caroline has resumed some semblance of normality with work. It will be a quiet house with  three of us gone, but Rupert the cat gets to come back inside.

I have 6 days of "conditioning" starting tomorrow, and then my transplant, by simple IV infusion, is now planned for Sept 15. I will be largely cloistered from the outside world in hospital for 4-6 weeks because of germ concerns, but family will still be able to visit at times, and even bring food, like my mom's augolemono soup, or Greek chicken soup.

The cobalt radiation machine shown here is the same generation as the one used for my grandmother almost 40 years ago, and cured her of her cancer at the time.  It reminds me of the Starship Enterprise.

I am now at the state where I am totally ready for this journey, thanks to all the time reflecting, reading, and welcoming the love and prayers and good wishes of all the wonderful people supporting me, and again I am so grateful. For me now, it is time to climb a big hill on my bicycle, maybe Cypress mountain;  relax the body, centre the breathing, and focus the mind, and simply find my rhythm and climb the hill. Eventually, you know there is a plateau, with its rewards.

Addendum: Now admitted and settled in to my private room, complete with wifi, cell phone and room service. Sister Michelle is by for a visit on her lunch hour from City Hall.  Will get into my book shortly.






Monday, 29 August 2011

Successful OneMatch Event and the Road Ahead

George Yioldasis
One Match Stem Cell Donor Awareness Event held at the Vancouver Hellenic Community Centre was a great success, with terrific music coordination from Mark Ferris and the Yaletown String Quartet
This was followed by Bouzouki Solo by George Yioldasis, and more Greek Music by Mousiki Parea, and then the Finale by Wanting Qu. Many new donors registered on the available computers, and One Match Reps answered lots of questions. Great Food, and good support from the community all round.
Mark Ferris(left) and the Yaletown String Quartet
Steve expresses appreciation for his family

My brother Andy Larigakis planned and coordinated the event, Claudia Ferris capably MC'ed and rest of family from both sides did a fabulous job of entertaining and informing the the community about this opportunity to save a life.
Mousiki Parea




Recording Artist Wanting Qu

Stem Cell Recipient and Cancer Survivor and Cyclist Rob Nagel and his mom--in-law

Gelato at White Rock Pier with Zoe & Caroline
This week is testing week, where I get poked and prodded to ensure I am fit to tolerate the procedure, and admission to VGH is Sept 8 with my transplant on Sept 14, which becomes my second birthday. I am told to expect to be in hospital for 4-6 weeks and not feel well enough to take visitors except immediate family.

It has been intimated that my donor is a young woman and I will take on her blood type and gender, so I told my daughter to hold me back if I get crazy with the shopping. She said, "Don't worry Dad, I'll just embrace it"


The Road Ahead


Thursday, 18 August 2011

Remission Continues

It is now day 25 on my new medication and I am continuing to enjoy a clinical remission.  I am able to enjoy swimming in the pool and shopping at Costco. Simple things hold indescribable pleasure when they have been denied. Like my first road ride in 3 months when Todd came by:
 My medical team wanted to see a sustained remission prior to proceeding to stem cell transplant, and it looks like we have one, so things are being scheduled for admission to hospital in early September with a week of "conditioning" followed by my procedure in mid September.

I want to acknowledge the deluge of greetings, prayers, cards, books, and gifts that keep coming my way. Every single one of them is received with gratitude and love, and they have all contributed to getting me through to this remission and will carry me on to the next phase of treatment. A large basket of gourmet goods from the Peace Arch Hospital Emergency staff is one of the most recent, and was quickly consumed by family and teenage visitors.

I now see this disease as something that has temporarily occupied my body, and will soon be purged so that my family and I can carry on, much as before.

My chance at a cure for this lymphoma is only possible because of the generosity of an anonymous donor from somewhere in the world. The donor registry includes 300,000 people across Canada and 30 million worldwide. In order to raise awareness and increase the pool of available donors, particularly in the Greek community, my family has launched a donor drive through Facebook. Donation is as easy as giving a unit of blood.

And they have booked a OneMatch Cafe event at the St George's Greek Church Community Hall in Vancouver on August 24 from 5-9:30 pm. I am told the electronic traffic on the OneMatch site has increased 100-fold over the past few days.

Please see the links below:

OneMatch Poster

Facebook Event


Sunday, 7 August 2011

"Clinical Remission"

After a fantastic retreat to Long Beach with friends, we have returned home with body and spirit renewed and good news. The new medication I have been on for the last 14 days has taken away virtually all my symptoms and we are cautiously using the term clinical remission. I have more energy and am able to get out and do things again like shopping and light gardening. It is my 4th line chemotherapy and was provided by special release from Ottawa at a cost of $10,000 per month, and appears to be my salvation.

The other good news is that I have been confirmed to have a match for my bone marrow transplant, and the procedure could proceed as early as a month from now. The response to the public OneMatch.ca has been phenomenal and I thank everyone who has participated so far and those who tried but were denied registry because of age (who says 50 is getting old?). The drive will continue, and although it may not now benefit me, it will benefit many others for years to come and will continue to raise awareness in the community.

                      As my doctor said to me last week, "We were all due for a break!"

Thursday, 28 July 2011

Long Beach!

Well, after suffering a setback last week I have emerged stronger and healthier than I have since the onset of my illness almost 3 months ago. I am tolerating the new medication well, day 4 today, and my rash, fevers, and swelling have all but disappeared, and my blood counts have returned almost to normal. Yipee!



My friend Steve called yesterday and insisted on flying us up to his place in Tofino for a few days and the time is right. I have been dreaming of running my feet through the sand once again!

The family has been incredibly busy organizing and promoting a stem cell drive through OneMatch.ca and CBS and have over 200 donors registered already!


Check out the short video and poster:

                                     http://bit.ly/GiveTIME4steve

                                                                              Poster

Saturday, 23 July 2011

Temporary Setback

A series of events banded together this week to send me to hospital, but fortunately I am now at home enjoying good food, family attention, and reading on the patio.  The effects of chemotherapy, lymphoma fever, and dehydration combined to make me sick, but transfusions and medications combined to make me feel better again. I need go back to hospital tonight but should be fit for discharge tomorrow and resumption of my new chemo drug.

Fun visit yesterday from colleagues; Alan, Martin, and I came up with an escalating series of new and wacky ways to treat patients, which led Yvonne (and Kathie) to comment that we should come up with our own version of the Big Bang Theory TV Series.

Family is organizing a stem cell and blood drive and will send out more information soon.

Saturday, 9 July 2011

Tour de France

Can you imagine winding your bicycle for over 200 km through little villages and climbing to the road summits of the Alps? This is beautiful, but challenging. Imagine doing this at race pace with 200 other cyclists jostling for position, and doing it every day for 21 days. This is the Tour de France. Now imagine having testicular cancer that has spread to your brain and lungs requiring surgery and chemotherapy, and recovering to win the Tour de France 7 times in a row. This is Lance Armstrong.


Every time I complete a course of chemotherapy, I feel like I have completed a Stage of the Tour de France, and am one step closer to completing the journey to recovery. My good friend Steve came by to help me along the journey. The branches of a tree had grown into the Bell satellite dish and prevented transmission of signals including the Tour, and required decisive surgery to clear the trees. Riding friend Al brought me the definitive guide to the Tour and we were able to sit down and watch Stage 6 on TV.


Zoe and Michaela baked me a nice cake to help celebrate an end to a challenging week. Thanks again for all the cards and prayers. For those wanting to do something more you are encouraged to give blood at Canadian Blood Services, or stem cells at onematch.ca.