Monday, May 30, 2011

Relapse.

I write this with bittersweet tears, as I know all of you have cheered with me these last six months that I've held a remission. I received a Pet/CT for a six-month post remission scan on Thursday, and the news revealed shows two new nodes of 2cm with a SUV of 10-13. My disease is one sneaky sucker, and most of us were a bit shocked with this news: the caner is officially back, and relapse has occurred.

I have gained all my weight (and continue) and am at 135 (over my normal weight) no symptoms, nothing. Normally I am very in-tune with my results. However, with the disease very small and not spreading like wild-fire it might just be because its just beginning to grow back again.

My team, family, my partner and I were a bit caught off guard as I walked into that scan overly confident that my remission held. I haven't felt this good in years; however, I also haven't been so happy in my professional or personal life as I am now so that could contribute to this.

But all of this, every moment of it is bittersweet. Am I upset that this relapsed occurred? Absolutely. There were snapshots and flashes of the future that were in my head since the first words of remission -- and not that all of those are now thrown out the window. They're more or less put on a bit of pause, or viewed with caution. The bittersweetness is surrounding my entire family, loved ones, and friends. We are absolutely extatic that I acheived remission for six entire months. This: A) Gives us hope for the future B) Allowed me to gain my weight, strength (both mental and physical) back to where I was years ago. and C) Gave us six months of non-cancer festivities, such as me beginning an amazing relationship with a ridiculously supportive man, my brother and sisters graduations from college, finishing up all of my grad school course work, and just life in general. I have sucked the most marrow I could out of every day, and I don't regret anything from it.

So now -- this is me, signing back on -- we are back. (Feels like I'm signing back on to a radio/tv show, :) ). Another aspect of this relapse is the fact that my partner, came with me to receive this news -- with both of us preparing for another three months of remission. With the sudden hit, (and him with zero experience in the cancer world), he supported me beyond my expectations, communicating with my family and friends after the news, talking to my doctors, fetching food, drinks, and anything I needed, and then pushing me to go to CT for the holiday weekend to visit all of my college friends, as planned. With a confirming "we are now in this together," I couldn't (oddly enough) have asked for a better response or relapse now that this has occurred.

On top of speaking of a 'good time to relapse' Whether I was in remission or not, I was set to receive my EBV+ trial vaccine on June 17th and July 1st (that Marsha has been in! and others are not moving towards), in Houston. The timing could not be better, as we had this set up and nothing in my treatment plan has changed. So life, continues to be normal, and I continue to build my strength so I can battle it out when/if those heavy chemo's must reenter my life again.

Truth be told, I am shaken, and disappointed. I had visions of moving further away from home when I graduate next spring, visions of someday being a mom again (since my menstrual cycle is temporarily back) and visions of a healthy life again... however, I am extremely, extremely grateful and feel privildged to have had these six months as I know so many other refractory kids never have that opportunity -- it does not go unnoticed that so many of us go for years and years on treatment with hardly any break. Or those, such as Anne or Andy (who are now on hospice), or Chris and Zach (who have just recently changed their treatment again) are out there in the trenches every day. I see them, I see all of us, no matter what, and I hope it does not come off in this post that I am kevetching ;) in any way. I am grateful, for these moments. And I wish for all of us (in this refractory group) that they existed more frequently.

For now we focus on: me feeling physically well, and many options for the future...

I will definitely be updating information and anything else I can to contribute to Houston trial for those who would like more information, as it is definitely another avenue/option that many people who are positive are going towards, and many of Dr. O's patients are starting to be tested for as well.


Love & Light,
B.

17 comments:

lisah said...

While saddened to hear this news, I can hear the strength and determination in your words. Please know that I will keep you in my thoughts.

grendelle said...

Oh, Bekah! So sorry to hear this, and so amazed at how you jump straight to the silver lining- sending light.

Darcy Davidson said...

Love you, B.

laulausmamma said...

Always optimistic for you sweet Bekah! Sending loving prayers and strength as always. Give that great guy of yours a big ((HUG)) for being such a special man : )

((HUGS))
Susan

Tim Mayer said...

Bekah, I know the feeling of a relapse, 5x, you will dig into the trenches once again, and you will get through this with the wonderful support team you have. Just remember their is a "new normal" and to live within it as normal as possible, which I know you will.

Emily said...

I'm so sorry to hear this. You are inspiring and exquisite as always.

Anonymous said...

i have no wrrds, truth.
evrything i try to say sounds stupid. i hav a photo i will show yuo on th bord tho . jus cos it is th only plase i think i can show yuo. but heer, on yuor blog...i can only say we love yuo, we care and we are liftng yuo up in all prayr and positiv thots. heers to hope indeed

Marlene said...

Dear Bekah - I am so very very sad -words cannot express. Your post is beautiful despite the content tho - to appreciate it's 'a good time to replase' is just plain inspiring - only those who've relapsed would understand that one! Glass half full - has to be that way.

Sending you love, hugs, healing thoughts and buckets of hope.

Marlene

Veronica said...

Love and hugs, B.....lots of love and hugs........<3

Anonymous said...

Bekah,

Im so sorry. I hate the roller coaster of cancer...it is so cruel.
Stay positive and tough.

Love,
Wendy

Johanna said...

Dear Bekah,just want to let you know that i am thinking about you,and that you are very close to my heart.
Lots of love,
Johanna,
Anne's mum from Australia.

Anonymous said...

Bekah, I've been thinking about you since I saw your status update. I'm so sorry (and upset that this disease is so d*** persistent!) I hope your next treatment will quickly and easily get you into remission again--you deserve it! Hugs to you! Janet (Quetzal)

Jessie O said...

Thinking about you with lots of love.

JoAnn said...

I am sad for you and angry with the cancer. You will be in my thoughts. I hope that this ends up being a small bump and you go quickly into remission again.

JoAnn

EEEEMommy said...

I found your blog through the Hodgkin's forum (I'm just a lurker, never signed on myself). I was so glad to read you were in remission, and am so sad to hear that the Hodge has returned. You continue to inspire with your grateful attitude. You're beautiful! I will be praying for you.

Grace and Peace,
Angel

L. Meredith said...

Bekah,
I've been thinking about you for the past week and finally came around to the blog today. I'm so sorry you are back on the roller coaster.
Sending lots of love your way.

Heather said...

Awe Bekah, I'm sorry. You are truly a bright shining light in this world. And you amaze me, have for years and will continue to do so. Much love.