Thursday, May 8, 2014

Conditioning Chemo, Day -5

We are finally here.  In some ways you can look at this transplant as the hopeful end to a story, or the beginning of another -- either way, we're finally here to complete this form of treatment.

I was admitted yesterday (Wednesday) and had a small surgery in which a medical team placed a triple lumen catheter  (basically like my port but it has three different access points for fluids, chemo, and antibiotics to travel through) in my chest.  My site is pretty sore and tender; however, it's very helpful.

I've just completed my first round of in-patient conditioning chemo.  Today is considered day -5 in the transplant world, -4, -3, -2, -1 will also be conditioning chemo days.  Once we hit zero, next Tuesday, we will celebrate my rebirthday since it'll be the day Jacob donates his stem cells to me and my whole immune system will be completely brand new.

As for the transplant and recovery time itself, I have many, many fears about the future, graft versus host disease, surviving, and quality of life.  But, for now, I'm attempting to put all of those fears in a small box and up on a shelf.  Right now, I'm looking at this journey through very specific lenses.  I want and need to take things a day, or even an hour at a time, and all I can do is just that.  Take each day as it comes.

Luckily, yesterday and today have been extremely easy.  The brand new Columbia Prespyterian Hospital's BMT unit is gorgeous -- if such a thing can be possible.  It is an 18 patient unit on the 11th floor over looking the city and the Hudson River.  At night the city lights are mesmerizing, during the day you can watch Ferry boats pass through the waters… The floor itself is extremely quiet, everyone is very respectful, caring and attentive. The 46 flat screen TV, personal chef and menu (just for BMT patients), smoothie carts, caregivers futon, and beautifully tiled bathrooms don't make it that bad either ;)

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My favorite PA is on this week, and the nurses have been an absolute breath of fresh air.  They check in on us every hour, without fail.  I find BMT nurses to be the best of the best, most of them have an awesome sense of humor and are brutally sarcastic.  I imagine you have to be, working in this field.  Everything I've needed from nausea to pain meds have been given without questions.  They trust me, and my needs, which is so empowering as a patient facing such a huge obstacle, such as transplant.  The social workers appear to know their shit, which is always helpful, and everyone in general gives off lots of positive vibes.  And most importantly, the areas surrounding the hospitals all are filled with tulip beds… red, white, and purple tulips everywhere. Good signs.



For now, it is smooth sailing.  The Flubaradine (chemo) that I received today and will receive the next four days went well.  No side effects to speak of yet (knock on wood), and hopefully it'll be well tolerated.  Most allo-transplanters say this is the easy part, the chemotherapy and treatment, it's really the recovery when your counts are non existent from Day 0 and on…. that are the darkest and most difficult.  But we will see.

One day at a time.  One hour at a time.  One minute at a time.
That's how we'll roll these days :)

In addition, I just wanted to take the time to endlessly thank ALL of you.  Your love, laughter, pictures, reminders, strong positive vibes, and caring words motivate me every single minute of the day.  I am so, so lucky to have every single one of you in my life.  You care for me, empower me, and love me -- and for that, I thank you.

This next year we'll be kicking off our fundraising goals into high gear to pay for this transplant.  Right now if you'd like to help out with the financial journey, or just buy some cool and delicious things, to check out my fundraising page at HelpHopeLive where most of the fundraisers will be listed.  Right now there is a 5k 'Stepping out for Support' that my in-laws are participating in, which you can sponsor donations as they dedicate their walk to me.  There is also a carmel-chocolate covered pretzel sale going on (possibly a great gift for momma's day!).  And we have a few more days that you're able to pick up your own B-Strong T-shirt or B-Strong Sweatshirt .  The T-shirts/sweatshirt sales will end on May 12th, so get 'em while their hot!  My fundraising team and I encourage you to share all of these goodies with friends and family too :)

Preview of the delicious pretzels that you're going to buy :)



Also, if any of you are one of those fabulous motivated people, we are looking for individuals to fundraise in their areas.  There is no time limit here.  We will fundraise for years if we have to -- what fun, right! ;)  So think carefully and simply: could you throw a car wash? a bake sale? hold a jeans day at your work? Go to a local bar and present them with my story/information/flyers (all of which we can provide you) to ask for a percentage of proceeds on a specific night? Do you belong to a gym? -- could you ask them to add five dollars to a class offered at the gym, and those proceeds go towards my fund?.  Are you running or participating in another athletic event -- if you are, would you mind asking friends and family to donate 5 dollars a mile to save a life? Do you have a vacation home or time share? -- can you raffle off a weekend (10 or 20 dollars a ticket) to your friends/family/coworkers and donate the proceeds to my fund?

My fundraising team has SO many ideas, so if you are stuck, no worries, we can help you find something.  If you want to run your own fundraiser, or need help thinking of an idea, please email one of my best friends, Karen, who's helping coordinate all of this at TrueBeautyFundraising@gmail.com.
She will give you all the information needed, she will direct/help you set up a flyer with HelpHopeLive, and then we can advertise it on my blog so others can help out too.  It's an easy process, and doesn't take too much energy but will go a LONG way.  So think about it :) Again, there is no time constraint.  Also, please remember all donations to my HelpHOPELive fund are tax-deductible.  You can find most of the fundraisers, and direct donations to my HelpHOPELive fund by clicking HERE.

So my hope? My hope for you today is if you live in the PA area is to go exercise on May 17th :) Join my in-laws on their 5k walk 'Stepping out for Support.'  If you don't live in PA, go clothe yourself already! ;) With one of our cool T-shirts/sweatshirts.  And above all, go treat someone you love to something sweet and send them some chocolate…or order some for just you -- you deserve it!


Any questions about the above: please email TruebeautyFundraising@gmail.com.
Sending love to all of you,
xoxox,
B.

20 comments:

Unknown said...

Love you so much Bekah and thinking of you constantly!!! Keep fighting.

Skye said...

Love you to the moon and back, sweet warrior! Your post reminded me of so many of the details of my own auto-transplant that I had forgotten--or, more likely, had tucked away in the back of my mind. I had the opportunity to go on a canoeing trip during my out-patient conditioning chemo (which I didn't tell my onc about until just this last year! ). Anyway, it was an extremely trying canoe trip--and not at ALL relaxing, as I had been promised! So many times I wanted to give up, thinking I simply didn't have any more strength to keep going-paddling that 100+ pound boat against 30 mph winds for 30 miles! I wanted to give up SO many times, but the encouragement of my husband and friends kept me pushing forward. I tell you this because that canoeing trip taught me a VERY valuable lesson that I NEEDED in going into my transplant--I COULD DO THIS! No matter what, I could "just keep paddling" just a little longer. During my worst days of the transplant--approximately days +4--+7, I found myself saying over and over, "just keep paddling Skye. Just a little longer. "

Sweetie-i KNOW you have the strength to do this. One minute at a time, if/when necessary. You are SO much stronger than you think you are! I'll even let you borrow my phrase-"JUST KEEP PADDLING!!" I wrote it in the dry erase board in my hospital room and I invite you to do the same.

I'm thinking about you every single day, hun! And I'm sending you every single positive thought and warm, healing vibe I can muster into that hospital room for you. You. Can. Do. This.

MUCH love to you!!!!

Skye

juthale said...

Hi Bekah. I truly admire your courage!!! I'm a dad helping his son finish chemo for NSHL and I pray each day he will not have to face what you have gone through. Yet I admire the cheerful and optimistic way you face such adversity. You're inspiring!

Anonymous said...

Hi Bekah....You are a true warrior! After reading your blog I feel like a whimp when I complain about the "problems" in my life. It is so true, you are an inspiration. You have a sweet, beautiful face and the heart of a warrior! You have many people sending you love and prayers.

Wendy

Austin said...

Hi Bekah. It's been several years, but I just wanted to drop you a note wishing you the very best.

Also I wanted to say that I'm truly inspired and astonished by what you've accomplished since the last time I stopped by.

I hope your recovery is going well.

Anonymous said...

Bekah,

You have been a light in the dark for so many people. Your light and beauty will continue to shine. Your life was too short. To Bekahs family I am so very sorry for your loss. I can not begin to imagine your pain.

Wendy

Karen "keltik" Tully said...

Bekah, you were a light in the darkness for so many people. You maintained a grace that would be almost impossible under the circumstances for anyone else. You maintained your zest for life, even when there were times that others would have given up. You will be missed by so many. There is joy and comfort in the love that surrounded you from your family and friends and all the lives you touched with your pure spirit and heart. I will miss you deeply. My thoughts and prayers are with your family. Your pain is gone, but theirs remains. Your love will fill the gaps. Love for always!

Skymist said...

Rebekah Furey passed away on June 8, 2014, from complications due to her allogeneic stem cell transplant procedure. Her inspiring spirit and supportive work will be missed by all of us.

Karen Tully said...

Still think of you often Bekah! We miss you so much. There is a hole in our hearts where you resided in life. May we fill that hole with our love for you even in death! HUGS! My wish is that your family and loved ones are comforted in the knowledge that you will not be forgotten!

Anonymous said...

Sweet Bekah.... RIP and thank you for your courage and hope that you have shared so openly to so many people. I am so sad as I have just learned of your passing...... <3 be free

Anonymous said...

missing you bekah...every minute of every day
love
Darlene
bekah's mom

Unknown said...

Dearest Bekah, I was going to post a while ago but wasn't sure what to say. I read your words often and always found them helpful and inspiring. You had that balance of being full of positivity and loving life, but also being able to be honest about things that weren't good - so it wasn't a false positivity. I'm glad for all the things you enjoyed and achieved in life, but sorry for the time you had to spend dealing with illness and so sorry you didn't have longer.

Both your life and your passing are reminders to me to be so grateful for what I have and not fret over small things (not that I always achieve this but I keep trying!).

To Bekah's family, I'm so sorry and I'm thinking of you.

Katy x

grendelle said...

I'm so glad this blog is still here. I think of Bekah and her family and loved one's often. She is still very much missed.

Jillian said...

Miss you every day, B.

Anonymous said...

miss you bekah
every minute of every day

mom

Anonymous said...

A FB "memory" post from 2012 for mileage needed to go to Texas, brings me right back to you Bekah. Still broken hearted.

Anonymous said...

I followed this blog when I was sick. I thought about Bekah today.

Anonymous said...

I’ve been thinking of Bekah lately. She was such a bright light to so many. And what a great writer she was. She encouraged me during treatment for Hodgkins and as I transitioned back to life after cancer. I am grateful for her and will always remember her. Lots of love to her family and friends. Anastasia (Spiecker) Forrest

Anonymous said...

I can’t believe it’s been over ten years. I hope your family and friends know your spirit is remembered. I feel lucky to have been your friend

Anonymous said...

Still miss you Bekah
Every minute of every day
You have a niece now. Zoey Iris
She has your spirit and your sass💜