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Showing posts with label LLS. Show all posts
Showing posts with label LLS. Show all posts

Thursday, September 18, 2014

LLS Light the Night Walk 2014

Greetings Friends :)

Team Invictus will once again be lighting up the skies of San Francisco next week as we participate in this year's LLS Light the Night Walk. If you would like to join us or donate, please visit our team page here
pages.lightthenight.org/gba/SanFran14/TeamInvictus

Thank you so much to everyone who has already donated!!!!

Thursday, September 19, 2013

Light the Night Recap: Part 2

The Light the Night Walk started with a VIP reception in the Giants' dugout that Jonathan and I were invited to attend.  It was VERY cool to be there.  
In the bullpen!
With the World Series trophies
Bullpen "stance"
the walk route took us along the warning track inside AT&T ballpark....pretty cool!

After the reception, we headed back to our tent, where our team was gathering.....
the team tent!

Nic getting a little pep talk prior to going on stage for mama's speech....
the team!
Thank you to all of our supporters who very generously donated to the LLS.  We've raised almost $5500 (a top ten team!) and sincerely, every penny counts.  One of the newest treatments to the Hodgkins game is a drug called Brentuximaub--a therapy I received prior and post-transplant--and some of the research/trials prior to its approval the were funded by the LLS.  Because of donations like yours, I was able to participate in this walk!  THANK YOU THANK YOU THANK YOU!!

Wednesday, September 18, 2013

Light the Night Recap: Part 1

After months of anticipation, last night was the Light the Night Walk!  As the Honored Hero, I had to give a 3 minute speech right before all the walkers headed off.  Jonathan and Nicholas joined me on stage.  My speech is below!

Hi everyone!  I am Caitlin Mullinix and this is my husband, Jonathan, and our son, Nicholas.  Nicholas will turn 2 years old this weekend.  And I am so lucky to be here to celebrate, because he was only 4 weeks old when I was diagnosed with Hodgkins Lymphoma. 

I went from pregnant and glowing to tremendously ill quite quickly.  The early days at home with Nicholas were full of the typical baby-related challenges, as we had expected.  But things didn’t get easier as the days passed.  I experienced what I thought were post-partum symptoms and possible complications from my c-section….fevers, night sweats, shortness of breath.  And boy, was I tired.  But I had a newborn, and I figured, “so this is what everyone is talking about!”  

After several visits with my OB, my symptoms eventually landed me in the emergency room.  A battery of tests ensued, which revealed an enormous mass in my chest. No wonder it was so hard to breathe when baby Nicholas rested on my chest.  The mass was biopsied immediately, but the procedure was too stressful for my already strained system.  I wasn’t breathing well during biopsy, so I was placed on a ventilator and stayed in the ICU for a week. 

Doctors began chemo immediately – my first treatment actually took place when I was asleep under the power of the ventilator.   When I woke up, reality sunk in.  I had cancer. What a frightening word.  Cancer is something that happens to other people, not to me.  I was only 32.  I had a new baby that needed me.  I had to return to work.  I had plans.  This was not my plan.  But, everyone emphasized that this was a good cancer to get.  It was highly treatable.  I’d be free of it in a short period of time and would be able to move on with my plans.  

For the next 6 months, I underwent the standard chemotherapy treatment for my disease.  Maternity leave from work became disability leave.  Family and friends came from all parts of the world to take care of me, and my husband, and baby Nicholas.  The switch from doing the caring to being cared for was emotionally very difficult.  I was supposed to be the nurturing one.  For nine months, I had been “becoming” a mom.  Now, I was back in the arms of my own mom.   

After six months of standard chemotherapy, it became clear that my disease was unusually aggressive.  It turns out that my Hodgkin’s wasn’t the easy kind to get rid of.  During the next six months, my excellent team of physicians attempted three more chemo regimens in an effort to reduce the amount of disease in my body, but nothing proved to be “the cure.” 

Finally, in October of last year, I had a stem cell transplant at UCSF.  My younger sister was a perfect match and donated her stem cells to me.  I am so happy to say that the transplant was successful.  Approximately 6 months after the transplant, the graft started working and her healthy cells starting killing the wicked Lymphoma ones in my body.  By the beginning of the summer, scans revealed that all those previous areas of disease that had been so resistant to chemo were now gone!    

This last year since transplant has been one of recovery.  I was in the hospital for a month during the transplant, and after being released, I was under house arrest for a few months.  My immune system was as fresh as a newborn’s and the exposure to germs in the outside world was just too risky.   I have experienced a range of side effects from the transplant and medications and graft-vs-host disease.  Also, there were two little diseased nodes in my lung that my sister's cells just couldn't get to that were surgically removed two weeks ago.  Which means that today, as I speak with you, I am officially cancer-free.  I am finally seeing a light at the end of this long, crooked tunnel.  So, this weekend we are not only celebrating Nicholas' big day but also my remission! 

Facing cancer opened my family’s eyes to the fact that it can really happen to anyone—even when you are 32.  When you are healthy, cancer is just something that you hear about, read about, and see in movies.  But when you yourself get sick, you find out that cancer actually all around.  Although I may be in remission, our fear of cancer will never fade away.  Until there is a cure, there will always be uncertainty that the cancer will return.  For everyone who may be touched by blood cancers, the research enabled by events like Light the Night is essential to eliminating this uncertainty.  The funds we've raised will hopefully mean that a cure will quickly be a reality.   
Thank you to the LLS and all of its generous supporters for the help in finding therapies that saved my life.  Because of you, I am here to celebrate.

Monday, July 29, 2013

A Couple Firsts and a #2

On Saturday, we attended the LLS Light the Night Kickoff for Team Captains, followed by a Giants baseball game.  Nicholas' first game!
Nicholas ate more than his share of garlic fries at the event (an SF Giants ballpark specialty!)
Nicholas loved throwing peanut shells on the ground.  And his hot dog.  And his chicken fingers.

 
Proud new owner of a SF Giants baseball!
There is a Muni (light rail) stop just outside the ballpark, so after the game we treated N to his first train ride.  He was so excited!  (The other day we had been walking around the city and he saw a train, and pointed to himself and said "nicholas...train".....so, it was time!)  We rode it one stop (approx. 3 blocks) to our car.  It capped off a really great San Francisco day.  

 

Also just had to share these post-bath pics from Sunday.  Nicholas was running around before we could get him suited up and he accidentally let out a little poo poo on the kitchen floor....
"Nicholas, what happened?"
"oops!"
PS If you'd like to join our Light the Night team and walk with us on September 17, please click here!  It's time to start FUNdraising and there are lots of great prizes for top fundraisers :)  And we're also looking forward to a really fun evening starting on the Giants field with a great group of friends and family!  We have a VIP tent!

Monday, July 15, 2013

KOIT Interview

Feel free to CLICK HERE to listen to the radio show, Today's World on KOIT, in which I was interviewed!

Friday, July 12, 2013

ON AIR!

I was invited by the LLS to do a radio interview with them on KOIT (96.5 FM) in San Francisco.  On Tuesday, I went to the station with Nicole Chapman Wilson, Campaign Director of Light the Night Walk, to record the show.  We are guests on the public affairs show "Today's World," which airs on Sunday mornings, and we were there to promote the walk and LLS in general.  Thank goodness it was pre-recorded; live would be very intimidating!  It's a 30 minute show, and if you happen to be awake at 6:30am PST this Sunday, you can tune in here!  (click on the Listen Live button)  And if you aren't awake yet,  I am sure I'll be able to figure out how to upload the show in the future :)

Tuesday, June 25, 2013

Let's Light the Night!


On Tuesday, September 17, 2013, Team Invictus will be participating in the Bay Area LLS Light the Night Walk.  Our team page is now active, so if you'd like to join us for the walk or support us by making a donation, please visit this page:  http://pages.lightthenight.org/gba/SanFran13/invictus

This year is particularly exciting for many reasons!
  • Caitlin will not be receiving a stem cell transplant and will be able to participate!
  • The walk originates at AT&T ballpark (home of the SF Giants) and a portion of the walk takes place on the field itself!
  • Caitlin is a 2013 "honored hero" for this event, so our group will have a VIP tent and special attention!
  • Nicholas will be an almost-two-year-old (omg!), so we'd like to plan a BIG CELEBRATION for him and for his whole family for persevering through these staggering last two years!!

Invictus

Out of the night that covers me,
Black as the pit from pole to pole,
I thank whatever gods may be
For my unconquerable soul.

In the fell clutch of circumstance
I have not winced nor cried aloud.
Under the bludgeonings of chance
My head is bloody, but unbowed.

Beyond this place of wrath and tears
Looms but the Horror of the shade,
And yet the menace of the years
Finds and shall find me unafraid.

It matters not how strait the gate,
How charged with punishments the scroll,
I am the master of my fate:
I am the captain of my soul.

-William Ernest Henley

Sunday, June 9, 2013

Weekend Things

I LOVE Chipotle burritos.  Jonathan really likes them as well.  So naturally, when we heard that they were hosting a festival here in Golden Gate Park, we were very excited.  We headed there on Saturday.  Nicholas got to make a t-shirt and draw with chalk, and all of us enjoyed a rice bowl from Chipotle's new Asian-themed chain (ShopHouse Kitchen, which is currently only in DC but is expanding!).  We also got a couple coupons for free burritos, who hoo!

On Sunday, we went to a picnic in Golden Gate Park for the LLS honorees.  Nicholas had tons of fun, despite the chilly and cloudy weather!

Jonathan's doing his usual Sunday evening cooking as I type, so there will hopefully be another food post soon! 

Thursday, May 23, 2013

LLS Corporate Breakfast

As this year's Honored Hero, I was invited to give a speech this morning at the Corporate Breakfast for the Leukemia and Lymphoma Society.  I was so glad to be out of the hospital and able to attend!  This breakfast hosts potential local corporate sponsors for the Light the Night Walk in September, in the hopes that these companies will form teams (these teams are usually very successful fundraisers).  I was asked to share my experience with Lymphoma and my speech is below:

I am Caitlin Mullinix and I am probably not that different from you.  I grew up in the suburbs of New York, went to a small liberal arts college, got a graduate degree in hospitality (and met my husband in the process), and we moved to the Bay Area to start our lives.  In 2011, we felt like life was really beginning for us…..we were going to have our own little family.  I was pregnant and due in September.  I had an unproblematic pregnancy and, even though it ended in a c-section, we had a healthy baby that we named Nicholas.  The early days at home with Nicholas were full of the typical baby-related challenges, as we had expected.  But things didn’t get easier as the days passed.  I experienced what I thought were complications from the c-section and pregnancy….fevers, night sweats, shortness of breath.  And boy, was I tired.  But I had a newborn, and I figured, “so this is what everyone is talking about!” 
After several visits with my OB, my symptoms eventually landed me in the emergency room.  A battery of tests ensued, which revealed an enormous mass in my chest. No wonder it was so hard to breathe when baby Nicholas rested on my chest.  The mass was biopsied immediately, but the surgery proved to be too stressful for my already strained system.  I wasn’t breathing well during surgery, so I was placed on a ventilator and stayed in the ICU for a week.
Nicholas was four weeks old when I found out I had Hodgkin’s Lymphoma.  Doctors began chemo immediately – my first treatment took place when I was asleep under the power of the ventilator.   When I woke up, reality sunk in.  I had cancer. What a frightening word.  Cancer is something that happens to other people, not to me.  I was only 32.  I had a new baby that needed me.  I had to return to work.  I had plans.  This was not my plan.  But, everyone emphasized that this was a good cancer to get.  It was highly treatable.  I’d be free of it and move on with my plans. 
For the next 6 months, I underwent the standard treatment for my disease.  Maternity leave from work became disability leave.  Family and friends came from all parts of the world to take care of me, and my husband, and baby Nicholas.  While I had this beautiful little boy to adore during this really tough time, we did have to hire a nanny because I didn’t have the energy to be a full-time mommy.  I also had to spend lots of time at the infusion center. 
The switch from doing the caring to being cared for was emotionally very difficult.  I was supposed to be the nurturing one.  For nine months, I had been “becoming” a mom.  Now, I was back in the arms of my own.  And even though I had all this support around me, I couldn’t help but feel alone.  Although Lymphoma is the most common cancer among young adults, I felt so isolated because of it.
After six months of treatment, it became clear that my disease was unusually aggressive.  It turns out that my Hodgkin’s wasn’t the easy kind to get rid of.  I transferred from CPMC to UCSF and met with Dr. Andreadis.  During the next six months, we attempted several more chemo regimens in an effort to reduce the amount of disease in my body, but nothing worked very well.
Finally, in October of last year, I had a stem cell transplant at UCSF.  My sister, who is three years younger than I, donated her stem cells to me.  Life stopped for all of us, not just me.  She had to leave for a week from her final year in law and business school (not easy), to come out West.  My mom came for the month that I was in the hospital and was with me there every day.  My husband became both mommy and daddy to Nicholas.  My in-laws came from Singapore to help.  And my mother-in-law came for several months and moved into our home to be my caretaker after transplant.  After being released from the hospital, I was under house arrest for a few months.  I really only left to go to the clinic twice a week.  My immune system was as fresh as a newborn’s and the exposure to germs in the outside world was just too risky.    
The transplant was successful in that my body has, so far, accepted my sister’s cells. Some disease did manage to rear its ugly head in the months afterwards, so Dr. Andreadis has me on a brand new drug to the Hodgkin’s game in an effort to keep the disease under control until my new cells are strong enough to fight on their own.  The hope is that in these next few months, my sister’s healthy cells will take over and kill those wicked Lymphoma cells that are left in my body. 
Personally facing cancer opened our eyes that it can really happen to anyone.  And in July of last year, it happened to our family again.  My dad was diagnosed with bladder cancer, and is now himself battling the disease.  When you are healthy, cancer is just something that you hear about, read about, and see in movies.  But when you yourself get sick, you find out that it’s actually all around. 
I am hopeful that my cancer will go away completely.  And that my dad’s will too.  But our fear of cancer will never fade away.  Until there is a cure, there is always uncertainty. In the meantime, we’ve learned that life does go on.  Cancer just becomes part of it, some days more than others. 
We always talk about cancer being cured someday.  Let’s make someday today, for all of us.  Please make a commitment to fighting cancers today by putting on the red blood drop pin at your place setting.  It is a symbol that together, we are committed to finding cures.   I hope as you go about your day today and people ask you about your pin, you’ll share what you’ve learned here today.
We brought Nicholas with us.  He was very chatty and active during the 45 minute presentation, so unfortunately Jonathan had to be out of the room during my speech (Nicholas actually wanted to be up at the podium with me).  But he was able to snap a few pics beforehand!

Nicholas wearing "Da da's" shirt