#HospitalLife – In Pictures:

I am beyond thrilled to share that I have arrived HOME!  Late last night they determined that I was fit enough to return home and all of my efforts of putting up the fight of my life, certainly seems to have now paid off.  There is quite a descriptive post in the works, to walk through my latest health journey in words and how I feel that I have once again been afforded a chance at life. This has been an entirely transformative experience and one that I never imagined in my wildest dreams.  Somehow, my strength and resilience is at an all time high and because of that I have been peacefully healing —- mind, body and soul.

Here are a few pictures of the

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My hemoglobin levels were considerably low, in which case I needed a blood transfusion.  It never really dawned on me how wonderful it is that people donate blood, something I have always been too ill to do even prior to my diagnosis as I have always been anemic.  I ended up using two units of blood which ran for about six hours.  Shortly after I felt like a completely different person; less fatigued, less cold and returned color to my face.  Thank you to those who donate!

Red Cross Blood Bank Centers

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The day of my surgery I snapped an #instax polaroid of my baby, Zoi.  It seemed obvious to me that if I had her adorable little mug looking at me with those eyes of hers, it would push me to do everything in order to make it back home to her.  Aside from all of the tremendous amounts of love I received from people near and far, my amazing friends, family and of course my husband — Zoila was the one little (but actually very HUGE) incentive to show up, kick ass and get back on the road of life and viola! here I am!

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Anyone who follows along on my Instagram knows that my baby Godson holds the actual key to my heart.  He stole it from day one.  When his beautiful mom — my lovely friend, Michele visited at the hospital the day after my surgery, she brought along a one of a kind flamingo and it instantly brought ridiculous amount of smiles — and not just from me, but all of the staff, fellow patients and anyone who saw my trusty IV monitor as I wheeled it by my side throughout my stay.

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I’ll admit, my biggest complaint about surgery is that you are forbidden the basic human need of drinking water (or anything for that matter), prior to the procedure.  In my case, I was told that I couldn’t have anything from midnight until later in the night after recovery.  Quickly, my mouth became a desert and my need for water seemed like life or death.  Of course that is an exaggeration, but it is certainly how I felt.  As soon as I got the green light, which was about twelve hours later, I ordered “sips and chips” and I felt like I stumbled upon an oasis.  Dreamy does not even begin to describe the feeling of when the ice water cooled my lips for the first time.  Sometimes it really only takes the small things to make you feel a sense of nirvana.

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Before I had even been transported to my room, my two best girls had flowers ready and waiting.  Prior to my surgery, I couldn’t find the strength to speak to them.  Distancing myself for selfish emotional reasons seemed to be the only way I could cope.  I felt that if I spoke with them, I might expose that I thought I was going to die and that we’d never have an ABC reunion again.  Without fail, they stood by my side no matter what and made sure that I knew they were there with me, showering me with their love and non-stop support.   I love you both.

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I felt so much power behind this operation.  Power from prayer and positivity and all of the amazing thoughts that were put out in the universe in honor of getting through this operation with a successful outcome.  I feel cheesy every time I say it, but there is no way I would have been able to do it without all of you.  Every single person that took it upon themselves to take the time out of their day to wish me well and include me in their conversations with whomever they have faith in.  It would be fair to say that I feel endlessly blessed.  Seeing this gleaming photo at St. Joe’s Hospital and Medical Center seemed like a fitting vision for the morning after the operation.  What a beautiful sight to see (I can even see my neighborhood if I look really close).  

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On the same glorious walk as pictured above, I was marching along the halls with the most important women in my universe.  They guide me through every struggle and challenge and proudly walk by my side, even in the darkest of hallways.  There are not many words that can do this picture justice, other than, thank you and LOVE.

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Further exploring the hospital, my home away from home, I walked past my favorite piece of art adorned on the walls in the lobby of the Oncology ward.  This particular wall decor always seems to catch my eye.  I appreciate creativity and try to search for it wherever I may be.  I can especially appreciate when it’s in unexpected spaces and places.  Well done, St. Joe’s.

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Just two short years ago, Steve and I spent the night at the hospital on Christmas.  It was by far one of the more depressing of holidays.  I feel very fortunate that I will be able to spend this Christmas with my family instead of inside the hospital walls.  However, they do their best to make you feel in the holiday spirit.  To those who will be spending your holiday in the hospital, my Christmas wish is that you are surrounded by love and joy.  It will get better.

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One of my favorite little cheerleaders, Kambrell joined me at the hospital a few days after the procedure.  Seeing things through her eyes and the way she expresses her love for life, makes me feel equally alive.  She is one of the most special little girls I know and I’m so grateful to be a part of her world.

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Just a few of the many gorgeous flowers I received. THANK YOU! I was able to enjoy them everyday and smile thinking of each person and the memories we have shared.  I chose to donate the flowers to the Oncology ward of the hospital once I was released.  They were all so beautiful and I wanted other cancer patients to be able to enjoy them as much as I did.  Please know that your kindness has such an impact and made many others smile, as well as me.

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Last but most certainly not least, my Steve sent this to me the second night, once he returned home to our dogs, Keg and Zoila.  He always knows how to make me laugh, as he was wearing my #ASU hoodie and my satchel to carry Zoila, all in an effort to take Keg on a walk. He takes care of all of us so very well and I am the luckiest person to have such a brave, selfless and loving man.  Thank you seems so insufficient.  What else can I say? You’re top notch, my love.

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More to come soon.

Love,

Britt x

12.05.15: Post Surgery Update

12.05.15 BKO. from Britt Ochoa on Vimeo.

Yellow, from the hospital! I hope everyone is having a beautiful weekend. Here’s a little video update from earlier today (sorry if I am in lala land). Talk soon, soon, soon.

Love,

Britt x

I F*CKING LOVE MY GIRLFRIENDS!

WHO RUNS THE WORLD

If you drink too much, cuss too much and have questionable morals, you are probably my friend. Okay, all jokes aside, I don’t take the time often enough to say “I F*CKING LOVE MY GIRLFRIENDS!” and the thing is, I do. I’ve always been one of those lucky ducks when it comes to friends, whether past or present, I’ve always had solid girlfriends of all shapes, sizes and opinions. Absolutely there have been a few sour apples in the mix, but the rest of the batch has been unmatched.

After going through the trenches of cancer for the past two years, I realize that I have not been the greatest girlfriend in return. I’m notorious for forgetting to respond to text messages, I make plans and bail and even sometimes become self consumed with my own, crazy life that I don’t spend enough time expressing interest in yours. Yet all the while, without a doubt I still get love and you never fail to leave me off the invite list, even though you know I most likely won’t leave my house (((because, because))) and we can go days, weeks, months and even at times a whole year without spending more than an hour together, but at the drop of a hat I know you’d be there.

This one is for my girls;

Thank you for keeping it real when I have a tendency to do the most ridiculous things or have the most outlandish ideas. I come to you because I know you are wise and honest and will always have my best interest at heart.

To my friends that are now Mom’s — GOD BLESS YOU! None of you will ever truly know how in awe I am of you. I can barely remember to brush my hair and take my crazy pills and yet you manage to not only take the best care of your kid(s), but you also look crazy beautiful and effortless while doing it. I endlessly praise you!

To my friends who have traveling souls, you may not realize this but as a cancer patient I live vicariously. I have been very fortunate to be able to travel even going to Hawaii and the UK just this year, but it’s difficult due to energy levels, treatments, etc. It’s so lovely to see photos or hear stories of your travels, its beautiful to see the thirst people have for adventure and living life to its fullest and the way you see the world is wildly contagious and inspiring.

To all my #Girlboss friends out there, no matter what profession you are in, you work damn hard and deserve it all. Your insane ability to manage squillions of things at once and be on point as a friend is beyond me. Get it!

The fearless friends that hone in on things they love to do and put effort into practicing their craft. With having the attention span of a fly and the energy of a snail, the fact that, unlike me, you take the time to run a marathon or belly dance at the nearest coffee shop means you took the time to learn something, to better yourself and immerse yourself into your passions. How truly motivating, I mean, really.

My point is, I’ve been blessed with friends from all ends of the earth and all walks of life. We may not talk everyday or laugh over brunch and a mimosa(sss) on a regular basis, but in some way you all do what you do and still manage to be a brilliant friend. So, I guess what I am trying to say is, THANKS. On days that are a bit darker than others, I can still smile knowing that I can call the most kick ass babes, my friends.

Cheers, GIRLS!

Love, Britt x

A BROAD, ABROAD WITH A BLOG, ✈

Hello, my shining moonbeams. It’s been a minute. Within that minute I have entered what I feel to be a new phase in my life, a freeing phase that is catapulted by happiness. For nearly a month, I spent time across the pond and rediscovered my life and the things I want out of it.

To start off, wow. Can I just say – I LOVE ENGLAND! I’ve always known that and I had been there times before, but this time felt different. As most of you know, if you follow my story, I have been on travel lock down since my cancer diagnosis in the summer of 2013. By nature I am a jetsetter. I enjoy being in unknown places, without being attached to my “real” life and the troubles within. When I travel, there is a certain romance to it, a freedom that allows you to be whomever you want and for me, that is living without a terminal illness. I’m able to go back to being me; an adventurer with thirst in my blood for worldly experiences. When I was diagnosed, I felt that one of the biggest losses to having cancer was the fact that I could no longer be as free as I wished to be. My citizen of the world passport would no longer apply and I’d be stuck doing treatment after treatment without an escape. My escape had become writing. If I were no longer going to be able to leave and experience life, then I’d write about it, which I have.

This year, 2015, I vowed to myself that it would be different than the last two, that I would yet again spread my wings and live a little. In the beginning of the year I approached my Doctor and pleaded for some independence from my chemotherapy week after week, to which she obliged and advised that 2015 could be my year of travel with chemo squeezed in between. It was the best news I had heard in quite some time and immediately booked a trip to Hawaii with Steve-O and planned the trip for Nan and I go travel to the UK together to attend my beautiful cousin’s wedding and share laughs and love with the family over there that we don’t get to see often enough.

The trip was so important to me and I wanted to ensure that I soaked everything in. My Nan in her very own way was my wish-granting factory, as she made the trip happen. Being that we were returning to her home town, I was fortunate enough to visit her previous homes, where she grew up, the house she was born in, the hospital she had my Mum and Auntie Bev in, where my Granddad went to college, where the two of them were married and so much more. Being able to experience England through her eyes was more than my hearts desire and something I will never be able to thank her enough for.

There were endless amounts of stories, laughs, fish and chips, tea and best of all time with family on both my Nan’s side and my Granddad’s side.   My roots are in full force over there and it was lovely to get to know that side of myself so much more. The posh wedding of my cousin, which we attended, has built memories that will last a life time, as well as traveling to Chester, Liverpool and all over the Wirral with my cousin’s and their other halves, of course also visiting London with the best company and seeing each and every friend and family member. Howls were had, love was expressed and England will forever hold the key to my heart. Quite literally, as Nan and I locked our love on Albert Dock in Liverpool and threw the key into the River Mersey. Our loved ones can continue to visit us in Liverpool, even though we may not physically be there, our spirit will always remain.

Since I’ve been back I have been reliving each moment in my head and finding it difficult to write about. My time spent there was so special, that it is difficult to express. I feel rejuvenated and feel I have a new sense of direction for my life.   Suddenly gears have started moving upon my return and from that, fresh goals have emerged. I’m super excited about the future and what it holds and as things get closer, I’ll share more deets.

In the meantime, check out some photos from my trip and watch out for some upcoming projects and collabos. Big Kiss x.

Follow me on Instagram for daily updates: bestillmyheartblog

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Love, Britt x

Remission ☚ ☚ ☚

Remission

Ochoa, Britt- Cancer Timeline

Ochoa, Britt- 12 Chemo Rounds

If you shake me hard enough, I will appear, yet it feels as though I have been in an unceasing dream, or shall I say nightmare since July 1st, 2013. It has taken me a couple of days to regain surreal consciousness as I was sluggishly coming out of the dark tunnel that has been my existence for the last nine months. In fact, I became used to the dark tunnel, my eyes adjusted to the dimness and although I imagined the light at the end, I grew to accept my new reality as a Stage IV cancer patient. Somehow, I knew by some means I’d eventually see the glistening light but in the mean time I vigorously challenged my mind, body and spirit for the fight of my life.

My new identity and only distinctiveness became that of a Stage IV cancer patient. Prior to being diagnosed, I held a good deal of individual characteristics that made up my identity in my profile as a human being. Twenty-seven years had crafted me into an abundance of roles to which I found myself identifying with; a lover of all mediums of art, a frequent concert goer, a best friend to Crystal, wife of Steve, daughter of Karen and Tom, loyal employee of American Express, a shoe collector, a clothing coinsure, frequent traveler and student of the world. However, as of July 1st, 2013, my identity splintered and all of the things that once made me who I was, became superseded as I hastily shed my foregoing self to become a cancer patient, which immeasurably became my whole universe.

The last month had become soberly temperament in the realm of ways I was deteriorating both physically and mentally. For weeks I was vomiting between fifteen to twenty times per day and in some cases even greater than twenty. I was unable to keep anything down, even water. Much like many other times within the last nine months, I was forced to shelter myself like a recluse, as my symptoms disallowed me to be a part of the rest of the world for fear I would be sick, pass out and assassinate any remaining cool factor that I was clinging onto for my ego’s sake. Nevertheless it became very apparent that my inflated coolness was overstepped by my Exorcist’s style of retching. I passed the indications along to my Oncologist and she had many calculations as to what she believed it could be, even at one point believing that my symptoms were synonymous with the possibility of a brain tumor. Needless to say, I endlessly underwent every assessment and scan known to man in this so called game of “practicing medicine”. Fortunately, but frustratingly everything was coming back negative and to no avail we discouragingly found ourselves at a stand still. I cursed and I cried. I spent several nights in the Emergency Room and still no sign of the culprit or any form of developments in the hunt of what was remotely off beam as they were all returning to us unfounded. Conclusively, after kicking and screaming, my Oncologist decided it would be best to admit me to the hospital, and just like that I once again became an occupant of the Oncology Ward. The plan of action was to monitor me in the ongoing effort to uncover my unusual and erratic symptoms, which was liable for draining my body of any remaining strength by the minute.

As Murphy’s Law would have it, I did not vomit once during the recurring visit to the hospital. Ultimately, the Doctor’s were unable to categorically figure out the vile symptoms I had been having over the last month and determined that the only conceivable cause was myself. Yes, that is correct, the medical professionals reasoned that due to all of the negative testing and scans; the unremitting vomit activity was due to my very own irrational brain, or psychological anxiety, as they prefer to define it. My brain was the dam and the levee ruptured leaving me with an overflow of anxiety and self-made symptoms that could not be contained.

Now with the understanding that the monsters in my head were making me sick, I was about to be discharged from what had become my natural habitat, but not before my lovely Oncologist entered the room. Making herself comfortable at the foot of the hospital bed, as I lay sitting up waiting for her to address any further information pertaining to my current circumstances, she reached for my hand, squeezing it in a fashion as though she was about to share something of great magnitude. I took a deep breath preparing myself for her words and she then began to speak in her soft, gentle tone, “Britt, your last PET scan came back remarkable and while there is still a small tumor, there is no evidence of disease”. Confused, yet delighted, I once again found myself emerging straight into business mode. I had so many questions and my brain was scrambling to connect all of my overwhelming thoughts. Was I cancer free? Did I beat Stage IV cancer? Is this hellish nightmare over? Did I redeem the clean bill of health I had so hoped for? I was quickly shut down on all of the above questions. My Oncologist went on to say that I am in the early stages of remission, the tumor still exists, and if it weren’t for my debilitating neuropathy I’d still be on chemo going forward. She proceeded to keep it real with me and explained that the tumor still resides in my body and that there is a high probability that the cancer could return at anytime, being that my diagnosis was Stage IV. Yet, for now it is dormant and by a small margin, I am well enough to proceed with my young life at the moment without any evidence of disease living inside of me. It wasn’t the exact way I had envisioned myself receiving such news, however to know that the chemotherapy treatments proved to be a success and I was now able to carry on with a quality of life, came to be first class news and the greatest news I had heard in almost a year.

It’s been nearly five days since I have been gifted this news and to be perfectly honest I have not been able to make sense of it all in my head. But, more significantly I am hesitant as to how I should refer to myself– Am I still a cancer patient, or now a cancer survivor, or perhaps neither? Yet, I am more than willing to accept the news and feel vigorous that I survived this war that has been waged upon my body and robbed me of good health for the last 290 days, 41 weeks, 417,600 minutes, 6,960 hours and 9 months + 16 days.

After we had finally arrived home, Steve hugged and inhaled me while whispering, “I finally have my wife back”. Tears streaming from his eyes, I kissed the salt that was streaming down his cheek. Somehow, I felt as though I was the only one who wasn’t bursting at the seams with ultimate ecstasy. Cancer had managed to take possession of my life and suddenly I didn’t know how to go back to my life after the cancer surrendered. Following a steaming hot shower to wash away my bewilderment, I stood in the doorway of our bedroom that met the living room where Steve was gleefully revealing the remarkable news with all of our family and friends. In my disoriented state of mind, Steve detected that the best news we had received since my diagnosis was not sinking in for me and he wanted me to completely take in the concept that I was now a healthy twenty-eight year old woman. Resembling that of a movie, Steve enticed me to chant and scream and repeat at the top of my lungs, “I’M HEALTHY, I’M HEALTHY, I’M HEALHY…I, Britt Ochoa am H-E-A-L-T-H-Y”. It was an unfamiliar declaration, as even so much as decent health had been a stranger for so long. Somehow, I was the only one needing convincing of this news and felt guilt-ridden that I was not reacting in a more gratified and wound up manner. Sure, I knew I should be jumping for joy, showcasing tears of happiness and taking the news in a gifted way, but I was unable to parade my sudden liberation; perhaps out of shock or perhaps because I felt unconvinced.

The first few days of my new “branded identity” as someone in remission did not go as expected. Unable to get myself out of bed, I found myself wanting to be completely alone and still felt as though I was in the never ending dark tunnel that I somehow became comfortable in. The thing is, as I would lay in bed over the last nine months, it became a frequent daydream as to when the day remission would be mentioned and how I would feel in that very instant. I pictured myself to feel well, feel 100% and back to the Britt that once was. But, in turn, I felt the opposite, still reeling from the brutal pains of neuropathy, as well as the poisonous chemo that remains in my body, a “welcome home” to your old self, was not arising. Were all of the nightmares over my health supposed to escape my head by the mere mention of remission? Was I supposed to peel away the mental scars and put them in a mason jar for safekeeping? Pessimistically, my head seemed to be splitting at the seams and I found myself having an identity crisis; who was I, if not Britt, the Stage IV cancer patient?

So, as I sit here now, I can honestly tell you that I am still very jumbled over how I am presumed to emote over such rewarding news. However, alongside the confusion, I am eternally grateful that I was able to go on this journey, for I truly believe that I am a better person for it, whomever that person may now be. I now understand the meaning of “life is too short”, I comprehend that life can change in an instant and that no matter the situation; you must go at it in its full entirety. I am humbled by this experience and realize that people are truly mind-blowing, ranging from close friends and family, to complete and utter strangers. When I didn’t have the strength to pray for myself or inflate myself to keep fighting, so many soldiers in my corner took it upon themselves to keep me in their pleas to God and blessed me with good vibrations. The love and encouragement will forever be in my heart and mean more to me than anyone will ever understand.

As for my next steps, I am going to focus on healing and manifesting the idea that nothing is permanent, much like my identity as a Stage IV cancer patient. I’m not sure who I am now since finding myself post cancer, or how I will come to define myself, but what I am damn sure of is that I am a relentless fighter and if cancer shows its dreadful face again, I will be well equipped to handle it and terminate its existence.

Thank you, to everyone for being an unwavering support system through this turbulent trek. I am going to get busy living and embrace the new Britt, while rekindling some of my former identities. I now revere my life similar to that of a semi colon; a sentence that was supposed to end but didn’t. My sentence in life came close to an end and I was given the opportunity for it to continue. Therefore, I will be upmost grateful for this gift called life and continue on with my life’ s story.

Until next time,

Love- Britt x

Love, Britt x