Showing posts with label celebration. Show all posts
Showing posts with label celebration. Show all posts

Thursday, October 18, 2012

ONE YEAR CLEAR!



Today marks the one year anniversary of Sammy officially being considered off treatment and done!  It was quite a low key day compared to the end of treatment celebration, but I think it should have been.  We are moving on and growing in strength, wisdom, and understanding.  We are entering a new phase and anxiously excited to be doing it.

Sammy went to the clinic with Brian and weathered the shots he needed.  There are not many more shots left until he is bionic....well, immunized again at least!  Sammy will not be going to the clinic once a month now.  He has graduated to once every three months.

Knowing me, I am going to have my mad moments where I NEED to contact Dr. C and check in about something! Going from weekly to monthly blood draws had given me funny turns occasionally.  I know I will have a day of utter conviction that the cancer might be returning and panic beyond control because Sam won't be going to the clinic for weeks.  That's just me...I'm gonna do it...I know I am....I just have to work on managing it :)

Back to the good news.  (You have noticed, I am sure, that I just ranted on about my future panics which means I am panicking already....darn self-analysis!)  Anyway, Sammy is excited to be invited to a CHAM party in November to celebrate the children who are DONE!  We are celebrating quietly (apart from Facebook and Twitter spreading the word) by having a family dinner at Sam's favorite restaurant over the weekend.  We are happily making less of a deal.

So, what might I wish I had known about the first year off treatment?  Oh my!  There is so much!


  • Families hold together during treatment but fall apart once it is done!  -  We have fought tooth and nail to remain a unit.  It has been incredibly hard.  Communication is key; acknowledging the problems and spending time working them out.  We are coming out of that fog now, but it was a close call at times.  Statistically, cancer does not increase the risk of families splitting up, but the aftermath sure isn't fun!
  • Parents and siblings also suffer from PSPD - I was a MESS for a few months after Sammy was done with treatment.  I fell apart and became lethargic and disengaged from the world in general.  I knew why, but I still couldn't do much about it.  I did visit counsellors and even tried meds...not a good option for me as they actually sent me more squiffy!   I took myself off them and decided to work on picking myself up in other ways.    I'm fine now, but it was hard.  Thankfully I am blessed with an amazing husband, a brilliant mom and in-laws and fabulous friends who took care of me and cut me some slack for being less than I should have been.  
  • It is hard to let cancer go - you would think I'd be glad to see the back of it and just run away from anything that reminded me of those years.  No!  I turned into an obsessed freak!  I had to do WHATEVER I could to beat cancer and find a cure.  I blogged, Facebooked, and Tweeted all the reasons why everyone should be fighting with me.  It was a battle I had to face, my son will be affected forever...and we don't yet know to what extent...so I just kept on going with the cancer thing.  
  • Sometimes, despite having every reason to savor every precious moment of life, you don't!  -  Sitting in the hospital during the very first weeks of treatment back in 2009, I couldn't even read a magazine as it seamed so trivial and, well, useless.  I hated how so many things were taken for granted and misused or neglected.  I noticed all the disparities in the world and resented those who didn't appreciate what they had.  I don't do that so much anymore!  I don't always appreciate what I have.  I am even guilty of brushing Sammy off so I can relax and enjoy some time on the computer or doing 'my own thing'.  I have started taking some things for granted again! 
  • I DO still stare at my child while he is sleeping a weep silently as I think about all he has gone through.  I then do the same with his brother who, as a sibling, had his world changed forever without the 'fame' and support.  I cry for my children a lot.  Sometimes it is with relief ... sometimes regret that things had not been better.  
  • Eventually the crap gets better!  This one is important.  We are not the same family we were back in 2009.  Not by any means.  We have our skeletons and we all probably should see a good shrink...but we are okay.  We are stronger now.  We are ready to look forward and honor the past but not dwell in it.  
ONE YEAR CLEAR means so many things.  We are hoping to be a family that gets to 'five years clear'.  That is the goal.  After that...well, we will enjoy that when it happens.  

Saturday, November 26, 2011

Giving Thanks and Celebrating

We have just had the most amazing couple of days for many reasons.  Firstly, we were able to be truly thankful that Sam and Jack were able to enjoy Thanksgiving in a regular way...no fears about neutropenia, fevers, or admissions.  We were also spending Thanksgiving with MANY family members who were flying in from all over the country as well as driving great distances.  And finally, we were going to host all those wonderful people for the Jack and Sammy Celebration the next day.

Everything was wonderful: great food, company and spirits.  The youngest children, the new generation of cousins, bonded beautifully.  Our generation marveled at our being the parents, and the older generations enjoyed watching the little ones have so much fun.  It really was everything a Thanksgiving should be.  We even got to celebrate Sam and Jack's Great-grandmother Lulu's 90th birthday!!!

The Jack and Sammy Celebration was also fantastic.  Once again the little ones bonded and solidified their relationships.  Cousins and their spouses chilled out with a few drinks, some silly card games, a game of "Shot Checkers" and also enjoyed playing with the kids.  Jack and Sam enjoyed being the hosts...the mimosas flowed (not with the kids) and the party was ON!  I'm going to let the pictures tell you the rest.

Playing football

Sad when you can't run as fast as your little cousins :(

Jack and his cousins

The Lego Tower of Thanksgiving!

Forming the new band

Big cousin makes Sammy a flying Space-ship...much cooler than an airplane

Generations

Lulu looking very good!

My special boy, Jack

Cute!

Celebration cake

Together!

Brothers forever!

Big and little cuz

Our wonderful aunt and uncle

Artistic moment

The boys take a turn

More Space-ship creating....competition about to start

Beer-shot Checkers!!!

The family

Sammy's back!



Sunday, October 30, 2011

We're Done!

"The sun is setting...the sun will rise another day!" (Long Road)  EV


Well, the day for the sun to rise has finally come... Sammy is off treatment.  Strangely, I didn't leap to the computer to share it with you all as soon as it happened.  In fact, I have avoided this blog for quite some time.  I am not sure why...I just didn't want to post anything.

I do have fun moments to share:

We went pumpkin picking at our usual farm and had fun before treatment was over. 










During week two of the last cycle, we journeyed to Maryland for Cousin David's wedding with the beautiful Chesapeake Bay as a backdrop .  



The boys enjoyed the hotel pool!  Sammy perfected his handstands :)




Then came the final dose of Mercaptopurine.  I never thought this would come.  I captured the moment on camera...felling strange for wanting to.  First I had to crush the pills...


This is our box of poisons medicines....the entire drawer is filled!


Once the pills were crushed, I mixed them with coke...once the white powder was hardly visible, it was time to drink it on down.


Nothing like drinking in your sleep.  Sammy actually doesn't remember most nights.


To celebrate, balloons and gifts awaited the boys on the final day of chemo...Sam would be going into the clinic for his final dose of Methotrexate.  Jack wanted to get up early with him to cheer him on.  





Leslie came with goodies:  A big box of donuts and juice to celebrate! 


 Megan  had to have a hug!



The following day, a surprise awaited us....the entire school (and most of the district) donned the orange Superman Sammy t.shirts again to cheer Sammy at the end of treatment.  We walked out to the playground to a sea of orange and chants of "Sammy..Sammy".  Amazing and very emotional!


So now it is over...except it really isn't.  While we feel very lucky, we still have a long time before Sam is five years clear.  We still have to draw blood and hope nothing shows up in it every month.  We still have to force medicine into Sam to protect him as his body is still weakened from the chemo.  We still have to have heart, major organ, and cognitive testing done to see how Sam is doing.

I don't know if I will blog all of this...I hope I do....but for now I just want to put things as far behind me as I can.  Of course I can't do that really....next week is the big Light the Night walk....it means so much to us and raises MUCH needed funds for fighting blood cancers.  I will never stop raising money to find a cure...to beat cancer....to know other children do not have to go through what my beautiful little boy went through.  It has been a LONG ROAD indeed!


Sunday, October 9, 2011

Challenges, Promote Your Blog, Win $100!!





While we celebrate the end of treatment in a few weeks, the picture I took yesterday (see above) clearly shows how much of a toll the chemicals we have to give him to fight the cancer takes on his little body.  This is "Steroid Week" an experience I would not wish on my worst enemy.  Hence the need to continue looking for cures and medicines that are less harmful for patients: Sammy is disabled...hopefully able to recover once treatment stops...and we have to monitor him forever to see if late-effects do more damage as he ages. 

If you want a fun challenge, promote your blog, have the chance to will $100 gift certificate to Amazon AND  help kick cancer's butt, click on over to Shannon's wonderful blog designed to help Sammy and the thousands of others fighting now and in the future.




Or buy something beautiful with 100% of sales on select items going to Sammy's Light the Night Fundraiser by visiting 


PLEASE pass this on to others, whether you decide to purchase, take part, or donate yourself...it is all for an amazing cause.
xxxx

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