Sunday, January 17, 2010

"Wishes do come true"

Good evening,


I just have time for a quick entry tonight because we are a very busy household these days. Dane's "wish" to watch a San Jose hockey game and meet "big" Joe Thornton has been granted and we are on a plane to California later this week. As you can likely imagine, the excitement factor is kicking into high gear and everyone is really looking forward to this trip (ok, so Clare isn't sure what is going on but that's kind of been the story of her life thus far).

We will be staying in Anaheim for several days (lets hope the torrential rain forecast for this week ends before we arrive) and then we'll move to San Jose. We plan to take in as much of Cali as we can, including Disneyland, Universal Studios, shopping (this is MY part of the trip), hockey, the ocean and general sightseeing. This experience has been a long time coming and it will be very nice for Ashley as we will be away around her birthday.

Dane gets to spend "one-on-one" time with Joe T. and we're pretty sure the Sharks have some neat stuff in store for him. It will truly be a once in a lifetime moment and many photos will be taken to capture it for his "fan base"!

The after effects of his Jan 5 chemo treatment & steroid boost have worn off and he's feeling great. Although his team had a tough outing against a very strong team this past Friday night, he played what was likely his best game of the season. He skated hard and fast and carried the puck more than he has all year. It was wonderful to see. Aside from the pills he takes at home every day, he is "med" free until early February and this bodes well for the trip.

A catch-up item from my last post ... I forgot to include the link from the story that ran on CTV on X-mas Eve re: the Believe in the Goal Foundation. So if you missed the story, please just click the link below and it's the second story.

http://winnipeg.ctv.ca/sports/

So, until we return from Cali, take care everyone ... Janie, Dirk, Ashley, Dane & Clare

Wednesday, January 6, 2010

"365 Days"

Today is the day. January 6, 2009 - Dane's oncologist confirms he has leukemia and our lives would never be the same again. As is the case with most traumatic events, I have been having "flashbacks" to this time last year. Although it has been 365 days, I can still vividly remember meetings, phone calls, procedures, needles, medical explanations, visits from family and friends, and lots and lots of tears. Fortunately I can also remember many tender moments shared with Dane and Ashley - lots of hugs and kisses and reassuring words. So in the spirit of the"glass half full (vs. empty) philosophy", I have compiled the first "top 10" list of Dane's blog. Here goes ...
Top 10 Highlights of the Past 365 Days (in no particular order because that would be way too difficult)
#10 - Dane's oncologist tells us that although Dane has leukemia, it's the "best" kind to get - very common (as common as childhood cancer is) and very treatable.
#9 - Children's Wish Foundation. Everything about this organization is fantastic and our entire family has been treated very well. As of earlier today it seems like some progress is occurring on Dane's request to meet Joe Thornton so we'll keep folks posted (Ashley is sooo looking forward to a warm trip this winter to make-up for cancelling Disney last year).
#8 - Ongoing and amazing support of our family and friends. People in our lives have been outstanding this past year and as we have said many times in this blog - thank you so very much!
#7 - After a mere two weeks of treatment, Dane's body kicks the leukemia's @#*# and he is declared an "Early Rapid Responder". This means he is in remission and his prognosis is even better than when first diagnosed.
#6 - After an eight month hiatus from the sport he loves, Dane steps back on the ice in September for camp. After a slow start, he gains speed, strength and stamina and is successful in his attempt to play 8A1 Hockey. Halfway through the season he is passionate about the game again and asking to go on our backyard outdoor rink on a daily basis.
#5 - CancerCare Manitoba. The doctors, nurses, child life therapists, pharmacists and Foundation staff are wonderful. Our family has been treated with nothing but care and compassion throughout this difficult journey and we are so grateful. We "give back" by agreeing to be the face of the Holiday Appeal campaign and this leads to many great things - CTV Sports Star and NHL Experience.
#4 - Dane's body puts up a very good fight and infection germs are kept at bay all year long. This results in zero re-hospitalizations in 2009 and that is great news for everyone.
#3 - Believe in the Goal Foundation. The surprise news on Christmas Eve that Dane has been chosen for the NHL Experience was an exciting day for our entire family. We are very grateful to Shawn Churchill (CTV), the Believe in the Goal Board and Bob & Barb Davison (Todd's parents).
#2 - The gem amongst the pokes, prods, nausea, blood transfusions, etc. of our visits to the Clinic are our new and dear friends. To the following kids and their families - Hayden, Jessie R., Jessie L., Nick, Zoe and of course our special Kendra - thank you for friendship and kindness.
#1 - May 11, 2009 - Clare Avery Hantscher is born healthy & very happy. Not much more to say about this event as it speaks for itself. It was a real highlight this past year and even though I said at the beginning that these are in no particular order, this one is hard to beat!
Here's to hoping the 2010 highlight reel is filled with many great moments, stories and memories.
Take care - Janie & Dirk
p.s. I just about forgot the darn medical stuff. Dane had his monthly IV chemo yesterday and all went well. His neutrophils are just high enough to stay at 100% of his pill dosages (they were .82 yesterday) and the doctor figures they are borderline because he is fighting yet another cold (he just can't seem to stay away from them right now). His hemoglobin is at 130 and that's great news for energy & attitude!

Friday, January 1, 2010

"Welcome 2010"

Happy New Year! We hope that you enjoyed your evening last night. We celebrated the beginning of this new decade with our very good friends "The Martin 5". It was casual and cozy and just the right pace for our family. One of the highlights was watching Canada beat USA 5-4 in a shootout - it was a very exciting game.
The past holiday week has been filled with lots of activities - special times spent with friends and family and many hockey games. Dane's team ended up coming 5th out of 14 teams in the X-mas tourney and they even won a trophy. The last game featured a tight score and a victory lap by all the players. Dane was a bit behind the pack as he was too busy trying to find his new hockey gloves in the pile in the middle of the ice. It was quite funny to watch him pick up gloves and throw them back into the pile until he found his pair.
The "Believe in the Goal" euphoria has subsided for a bit. I'm sure it will pick up again once the trip planning begins. We are still waiting to hear from the Wish Foundation re: a trip to San Jose ... we are hopeful an answer will come soon because we are hoping to go away later in January. The story that aired X-mas Eve is no longer on CTV's website but I am trying to get an electronic copy soon so I can post it on the blog.
The past few days have been pretty tough. Kendra's funeral was Wednesday and it was very emotional. It was a beautiful service - a fitting tribute to a young woman who was beautiful inside and out. I think I've found it particularly tough because even though it's been 11 years, I can still vividly remember the intense sadness we felt in the days, weeks and months after Cole died. My heart aches that her family has to feel such sadness and I find my mind drifting to them often. Dane's next appt at the Clinic is on Tuesday and it will be hard to see the construction on "Kendra's Room". When it is finished though it will be a wonderful legacy.
The kids are calling because we promised we'd play a game to end what has been a very lazy Jan 1. It is exactly one year ago this week that Dane was diagnosed with leukemia - what a year it has been. It has been filled with many hard and scary moments, but at the same time, much joy (aka Clare of course). As a family we are relieved to say good-bye to 2009 and welcome what we hope and anticipate will be a gentler 2010.
All our best - Janie and Dirk

Thursday, December 24, 2009

Dec 24 - "What a Christmas Present!"

The "Believe in the Goal" event went off as planned this morning. Dane had NO idea what was in store for him and wondered why I was rushing him into the shower at 10:00 am. He met Todd's family and friends at 11:00. They are all wonderful people and we are so very grateful for what they are doing for Dane and our entire family. It was evident today was bittersweet for them, as it was three years ago this month that Todd passed away.
CTV captured the entire meeting on camera and there will be a story on the 6:00 pm news tonight. It should run during the sportscast, which generally starts around 6:40 or so. We will of course post a link to it on the blog after it airs.
We are in last minute preparations for Christmas Eve dinner tonight with Dirk's family. The kids are very excited but doing a good job of holding it together.
Until next time, take care - Janie and Dirk

Wednesday, December 23, 2009

Dec 23, Part II - "Believing is Magic"

Yes, I am still typing tonight. I promise, this entry will be very short compared to Part I but I have some news I must share quickly.
To make a very long story short, we received a phone call today from the President of the "Believe in the Goal" Foundation. This Foundation was created several years ago by Todd Davison. Like Kendra, Todd battled a rare sarcoma. He lost his personal battle with cancer on December 2, 2006 at the age of 20. He created the "Believe" Foundation to make a difference in the lives of those who continue to battle cancer. One element of the Foundation's work is to provide children with cancer an "NHL Experience". I'm sure you can see where this is going ...
For this year, Dane has been selected as the child who will receive the "NHL Experience". There are still many, many details to be sorted out but something exciting is happening tomorrow. Todd's parents want to tell Dane about the "NHL Experience" as a Christmas present so they are coming to our house at 11:00 am to meet him. Shawn Churchill of CTV is on the Foundation's Board and he is the person who nominated Dane. Of course he was introduced to Dane by the CTV Producer who shot the TV commercial for the CCMB Foundation's campaign. So if there was ever a story about "paying it forward", this is it!
Apparently CTV is coming to our house as well tomorrow as they want to feature this great news on the Christmas Eve newscast. So I will post a quick update tomorrow afternoon advising when it should be airing. And when I'm not so sleep deprived, I will provide more details regarding this wonderful opportunity for Dane. He knows NOTHING about it so tomorrow is going to be quite the day!
Merry Christmas - Janie and Dirk
p.s. There was a short story about Dane in the Winnipeg Sun last Saturday. The link is not being cooperative but if you are interested, just go to the Winnipeg Sun website and search under the heading "Unmelancholy Dane". It should come up right away.

Dec 23, Part I - "A Beautiful Life"

It is two days before Christmas and I have just put all three of my children to bed. Logically I know I should be right behind them, but tonight my heart is in charge. It is a very sad day as we just learned earlier tonight that Kendra McBain, the beautiful young woman I wrote about a few months ago, has lost her hard fought battle with cancer.
Kendra turned 18 just two months ago. She was diagnosed with an extremely rare form of cancer when she was 15. For the past three years, she and her family have waged a war against this terrible disease. It is so very unfortunate that a cure did not exist for the sarcoma that invaded her body.
Kendra had a maturity beyond her years. In the midst of her personal battle, she organized "Kendra's Walk for Kids" this past May. Through her efforts, over $100,000 was raised to renovate the teen's room at the Cancer Clinic. Apparently the teens haven't been all that keen on sharing their space with toddlers and school-age "punks" like our Dane and I can't say as I blame them. The renovations are currently underway and I understand that Kendra was receiving regular photo updates of this wonderful work in progress.
Kendra was kind, compassionate and from what I saw, very positive in the face of adversity. Although I understand that "punks" are not always high on her list, she seemed to bond with Dane. They shared stories during chemo treatments and on a particularly rough day for Dane, she put her new two pound puppy in his lap to ease his stress during an IV insertion. The puppy and Dane never moved for an hour and we all talked like we'd known one another for years. Even when she knew near the end there was no cure for her cancer, she was bright and forthright.
Although you don't know Kendra except through my description, please believe me when I tell you she is a symbol of many important life messages. Our family is privileged to have known her and although I hate cancer, I am thankful she came into our lives. Dane and Ashley shed many tears tonight when they heard she died, however only as children do, they were able to park their sadness. I suspect though there will be many moments over the next little while when one or the other talks about Kendra.
For our family, it has been exactly a year since Dane first showed signs of being ill. Although I try not to think about it too much, it is very evident looking back now that he was so not himself last December. He really just went through the motions during the holidays because that's all his little body could handle. This Christmas he is "fired up" - at home, at the rink, at friends, etc.. And although his attitude still drives us over the edge at times, we are so very grateful his quality of life is back.
If it hasn't become evident yet, I am writing tonight because I need to. It's my therapy once again, as it was in the early days of Dane's journey and at the very anxious times in his treatment. And for those individuals who know me "like a book", you will read between the lines and realize this is a very hard day. Hard because I am the mother of a child with cancer and as much as I can rationalize that leukemia is so very treatable and Dane should never relapse, I would be lying to say losing Kendra isn't traumatic. Hard also because I am a mother who has grieved the passing of a child and that is a heartache that cannot be understood unless you have walked that path. Hard because even though we said good-bye to Cole long before we ever wanted to, we did not really know him like we do Dane, Ashley and Clare and I can't imagine the anguish that Kendra's parents and brother are feeling right now. So hard because I wish I could DO something for the McBain's that is more productive than banging away on my keyboard, but I know that although they are likely surrounded by loved ones right now, this is a journey they ultimately have to make very much on their own. So very hard because embarking on parenthood is a leap of faith and although we hope with all our hearts that our children will be healthy, this is not always the case. Kendra's parents had the same hopes and dreams for their special daughter that we all do for all our children.
As I close Part I, I do so with a story from last January when I was still "reeling" from Dane's diagnosis. It was late at night and I was restless so I sat down and wrote. I wrote a letter to a FP columnist about Dane and our family. In the moment, I really didn't know exactly why I was writing him but it was something I just needed to do. He contacted me right away and was going to publish our story. During our back and forth correspondence, I told him I was ok with the story being told, however I would never want people to read it and feel that I thought we were the only people facing adversity or worse, seeking their pity. Some time went by and he never wrote the column. A few months ago I made contact with him for another reason and told him I appreciated that he never wrote the story. Just knowing I could write to him had been enough for me. I was able to say out loud that "this is a tough, lonely walk" but we were "so thankful we had so many wonderful people supporting us" and we asked that those who believe in a higher power "say a prayer for Dane because we really needed a good outcome this time around". My mom knew about my letter and recently she commented that it was fate that he kept our story private, because it was likely meant to come out as positive as it did in the CCMB Foundation campaign. The Foundation's "ask" for us to be involved came out of the blue and it has truly been a wonderful experience for our family. I share this story because for me it shows how far we have all come this past year. At the beginning I could have jumped out of my skin and shouted at the world. And although I knew we were not alone, I was very lonely. So even though I still have these thoughts and feelings, they don't dominate my days and that in my view is progress.
Thank you for your patience tonight and I hope that most of you don't read this until after Christmas. I'm starting to unwind a bit now so after I post a very quick Part II, I will call it a night.
From our entire family, our heartfelt wishes for a wonderful holiday season.

Warm regards - Janie and Dirk

Saturday, December 12, 2009

"Crazy time of year"

Hello everyone,

My apologies for the lengthy delay in posting this update, life has been crazy busy the past few weeks. What a difference a few months makes though, because if I'd gone this long in between blogs earlier this year I would have had many emails asking "is everything ok"? Now folks realize my "tardiness" is due to our activities and not Dane's health.

I've got quite a bit of ground to cover so I'll dive right in ...

Medical "stuff"

The best news, Dane has been feeling great these past few weeks. He takes his meds at home like a trooper and if we ever forget a dose, he reminds us. On Monday he completed cycle 1 of too many cycles to count over the next 2 1/2 years. He started cycle 2 on Wednesday. This is a heavy week for meds as he had his once every three months spinal tap, plus IV chemo and his five day steroid pulse. He looked very tired on Thursday but has since bounced back. His hemoglobin continues to rise - it was up to 129 on Tuesday. This is a far cry from the days when it hovered in the 80/90 range. There is one downside though and I mentioned it to his oncologist. We see a corresponding increase in Dane "bad" attitude the higher his hemoglobin gets. Hhmmm, if only we could solve this dilemma!

CancerCare Manitoba Foundation Holiday Appeal "stuff"

Whether Manitobans like it or not, we Hantschers are everywhere these days. We've been on TV, in the newspaper and in mailboxes. I taped a radio spot this past Monday so starting next week we'll also be on CJOB (Dirk said he can't believe he's going to have to listen to my voice on his peaceful drive to/from work every day). The CancerCare MB Foundation has indicated the response to the campaign has been very positive thus far so that makes it all worthwhile. If you live out of province and can't watch CTV or you just haven't seen it here yet, I've attached the video file for your viewing - just hit play. As I reported a few weeks back, Dane was also the Sports Star of the week in late November. If you missed that piece, log onto CTV Winnipeg, click sports and then sports star. He will be the third story from the top. The piece is excellent - Dirk, Dane and the Sports Director all did a wonderful job.

Sister "stuff"

Dane's big and little sisters are doing pretty well these days. Ashley is skating up a storm at ringette. She netted five goals in our last game and has developed quite the natural skating stride. She's VERY anxious for Christmas and we will all be thankful once the present suspense is over! Clare continues to be a wonderful and happy baby, however these past few days have been pretty challenging because she has a bad cold. She's been pretty clingy (a relative term for Clare) and not sleeping well at all (like her newborn days). I've had three nights of being up every hour or two so I'm whooped. She seems to be feeling a tad better today so I'm hopeful we will all get some much needed rest tonight. She was seven months yesterday and I'll post a few new photos in my next entry. Her weight gain is slowing down, however she has surpassed the twenty pound mark already. She is as big at seven months as Ash & Dane were at a year!

Hockey "stuff"

As I've been typing, Dirk has been phoning me every 20 minutes with updates on Dane's game. They were playing the #1 team today and usually I'd be a loud fan but I didn't want to take Clare out in this brutal weather with her cold. It was a "barn-burner" ... 3-3 after the 1st period; 8-6 for us after 2; and an 11-9 victory for Dane's team when it was all said and done. It was killing me to know I was missing such a great game - yikes, he is only 8, what will I do in a few years? He's playing with a great group of kids and they are well coached. After today they are sporting a 7-1-1 record and are tied for first in their league. He is LOVING hockey this year and that is so very rewarding for all of us.

For next time "stuff"

We are quickly closing in on the one year "anniversary" of Dane's illness and diagnosis. In my next entry I will reflect on how it feels to hit this milestone.

Take care everyone and don't let the December madness get the best of you.

Janie and Dirk