Thursday, March 28, 2013

Transplant Meetings & Flight Donations

Rich and I are planning an informative allo-transplant meeting at the best transplant facility in the world.  We want to do some research, become more informed with allo (donor) transplants, and familiarize ourselves with the types of transplants and the protocols associated with them.  We want to stay ahead of the game, dot our I's and cross our T's when it comes to the future.  To do this thoroughly we need to go to the Fred Hutchinson Cancer Research Center in Seattle, Washington.





We are hoping to make this trip in mid to late June and are looking for the amazing kindness of strangers and friends to possibly donate two round trip tickets/their frequent flyer miles, from Newark to Seattle this summer.  If you cannot donate an entire flight, but would like to help out in someway when we do go to Seattle, feel free to click on the paypal account to your right. (scroll down the page, and look to the right of the blog, where you see "Donations to Treatment Travel" and click on the big yellow button that says DONATE!)  Every penny helps -- trust me.

If you know of anyone, or you yourself could possibly consider donating.
Please email me at:  RebekahFurey@mac.com

We unfortunately will not be able to book flights for three more weeks due to figuring out work and treatment schedules.  But we are hoping to figure out the logistics ahead of time.

Also, if you have been treated at the Hutch for an allo-transplant, I would love to personally hear from you.  Just a small email (email address above) would be incredible, as I would really appreciate anyone who could share personal experience.

I thank you in advance everyone, those who send their love, positive energy, and so much more.  And to those who even consider or think about this donation, I sincerely cannot even begin to thank you for your generosity, huge heart, and the kindness that lays within you.

Sending Love,
B

Friday, March 22, 2013

a whole new meaning

Birthdays have a whole new meaning when you have to fight so hard to get to them. 
-- Jacinta Allen, caregiver/fellow friend

March ninth confirmed that I have survived and thrived on this earth for twenty eight years, as I entered my twenty ninth birthday.  The weeks leading up to this celebratory week were ones filled with exhaustion, frustration, fatigue, weight loss, low counts, anemia, fear, anxiety, instability, and disappointment.  With blood counts changing results just as quickly as a flip of a coin, the numbers being different every day, Revlimid causing issues, high heart rates, low blood pressures, and my hemoglobin tanking... something had to give.

I had planned to vacation with my other half for a few days, and then have a girls weekend with my three best friends in Florida for my birthday.  My amazing, generous, and kind Uncle Jay and Aunt Bob, generously allow me to go down to their property in March and receive a mental break -- that all of us, cancer patients so desperately need.  For months, this was the break I had been holding onto.  However, due to all the obstacles from this month, I feared that I would not have any energy to even enjoy myself in the sun with my love or friends.  Sadness ensued.

Two days before we left, however, O made an important call.  He took me off the Revlimid, I (between NYC and PA) received two units of blood, and was put on a high dose of steroids.  And just like that, something gave.  The shift began.

The week in Florida between the steroids, sun, seafood, people who I love more than life itself, smell of the ocean, being on the harbor, snorkeling, eating, eating, and more eating.  Was literally one of the best weeks of my life this year.  In fact, when I sat down with my NP this week she asked how my trip was, and through telling her I literally couldn't stop crying of grateful tears.  As both her and Rich looked at me probably thinking, 'what the heck is this woman crying about?"  It was just such an amazing trip and even thinking about it overwhelms me with appreciation and gratitude.




It has been a long road since June, between the relapse last summer, getting on Revlimid, discontinuing Revlimid, and now facing this shift.   I soaked up every meal, every moment, every piece of sunshine, conversation, sound of music, and smile I possibly could.  And with that, I started to regain some strength.  With the steroids I gained five pounds in seven days.  I'm so grateful that my friends helped me continue to eat (even though they felt stuffed most meals!).  Because with every pound, I felt stronger, refreshed, re-energized, renewed.  And with every day that was spent with my love and friends from childhood, I began to feel like my old self again.   I firmly believe that so much of my recovery is always due to people who continue to lift me higher throughout all of this adversity, and for that, I am so grateful.










By the end of the week, I felt clarity and strength.  Two visions I did not have in my mind before this trip.  Which brings us to these next two weeks, and what is to come.  Since returning from FL renewed, I met with O and the team on Wednesday for a bone marrow biopsy and blood tests.  For this week, everything appears normal (this is wonderful); however, we know how easily things can change.  We discussed next steps due to the fact that we both agree Revlimid just hasn't agreed with me and my quality of life, and we will have a PET/CT scan next week to see how large my tumor burden appears in my body.  Currently (due to steroids for a week) my SED rate is 8, but most likely that will not hold for much longer.

Florida reminded me how to breathe again, how to take a step back when you are in the midst of hell and can not seem to figure a way to look elsewhere.  Both my partner and I were beginning to dictate our lives only around doctors appointments, tests, meds, ect.  We were losing sight of the mental piece, taking a breath, and stepping back to regain clarity over the situation.   Luckily, I have wonderful family who encourages us to do just that.

Now I am five pounds heavier (117lbs!), filled with beautiful memories, energy, and the ability to make informed decisions over our next steps.  We will PET/CT on Wednesday, and most likely begin a small-baby dose of Bendamustine to bridge to a CD30 Trial at Baylor College of Medicine, similar to the EBV+ Trial that I participated in over a year ago.  I welcome these changes, am grateful to put Revlimid behind us, and look forward to deep breaths, more sunshine, and a calmness I haven't felt in quite a while.




I ate during 90 percent of this trip and it was amazing.



Prepping for our snorkel day... 




Water-taxi to Peanut Island, obviously deep in thought :)








Peanut Island



A windy-St. Patty's Day...

































For those who have been asking and keeping tabs on me, I apologize for this delayed post and thank you for checking in about my health.  I am so grateful for the HL community and support.  Here's to a spring filled with great change, deep breaths and smiles.








Sending Love,
B.